| Title of Invention | NAPHTHYLSULFONIC ACIDS AND COMPOSITIONS COMPRISING THE SAME |
|---|---|
| Abstract | Methods for treating conditions associated with hyperglycemia, especially Type II diabetes, with novel naphthylsulfonic acids and related compounds are provided. Compounds of formula (1) where: R<sup>1</sup> and R<sup>2</sup> are, independently, hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, R<sup>3</sup> is a substituent on the B ring; and is -SO<sub>2</sub>OR<sup>6</sup> , -C(O)OR<sup>6</sup>, -SO<sub>2</sub>NR<sup>6</sup><sub>2</sub>-C(O)NR<sup>6</sup><sub>2</sub> or tetrazolyl; the linker -WY- between the naphthyl and phenyl intersects the A ring of the naphthyl and is, independently, -C(O)NR<sup>7</sup>-, -NR<sup>7</sup>C(O)-, -C(O)O-, -OC(O)-, -CH=CH-, -NR<sup>7</sup>CH<sub>2</sub>-, -CH<sub>2</sub>NR<sup>7</sup>-, -NR<sup>7</sup>C(O)NR<sup>7</sup>- -NR<sup>7</sup>C(O)O-, -OC(O)NR<sup>7</sup> -, -NR<sup>7</sup>SO<sub>2</sub>O-, -OSO<sub>2</sub>NR<sup>7</sup>-, -OC(O)O-, -SO<sub>2</sub>NR<sup>7</sup>-, -NR<sup>7</sup>SO<sub>2</sub>-, -OSO<sub>2</sub>-, or -SO<sub>2</sub>O-; each R<sup>6</sup> and R<sup>7</sup> is, independently, hydrogen or lower alkyl; optionally in the form of single stereoisomers or mixtures of stereoisomers, or the pharmaceutically acceptable salts thereof; are useful in methods of stimulating the kinase activity of the insulin receptor, enhancing the activation of the insulin receptor by insulin, and stimulating the uptake of glucose into cells. A variety of antidiabetic compounds and pharmaceutical compositions comprising the antidiabetic compounds are also disclosed. |
| Full Text | NOVEL NAPHTHYLSULFONIC ACIDS AND RELATED COMPOUNDS AS GLUCOSE UPTAKE AGONISTS BACKGROUND OF THE INVENTION (a) Field of the Invention The present invention relates to methods, pharmaceutical compositions, and compounds for enhancing insulin-dependent glucose uptake. The compounds of the invention activate the insulin receptor kinase, leading to an increased sensitivity to insulin and an increase in glucose uptake. The invention relates in particular to the use of the compounds in methods for the treatment of humans with hyperglycemia, and especially for the treatment of Type II diabetes. (b) Description of Related Art Among the many functions performed by peptide and protein hormones in metabolism is the ability to interact with receptors with high specificity. The insulin receptor is present on virtually all cells and at high concentrations on the cells for the liver, skeletal muscles, and adipose tissue. Stimulation of the insulin receptor with insulin is an essential element in carbohydrate metabolism and storage. Diabetics either lack sufficient endogenous secretion of the insulin hormone (Type I) or have an insulin receptor-mediated signaling pathway that is resistant to endogenous or exogenous insulin (Type II, or non-insulin-dependent diabetes mellitus (NIDDM)). Type II diabetes is the most common form of diabetes, affecting about 5% of individuals in the industrialized nations. In Type II diabetics, major insulin-responsive tissues such as liver, skeletal muscle and fat exhibit the insulin resistance (Haring and Mehnert, Diabetohgia 36:176-182 (1993); Haring etal., Diabetohgia, 37 Suppl 2:S149-54 (1994)). The resistance to insulin in Type II diabetes is complex and likely multifactorial but appears to be caused by an impaired signal from the insulin receptor to the glucose transport system and to glycogen synthase. Impairment of the insulin receptor kinase has been implicated in the pathogenesis of this signaling defect. Insulin resistance is also found in many non-diabetic individuals, and may be an underlying etiologic factor in the development of the disease (Reaven, Diabetes, 37:1595-1607(1988)). Considerable information is known concerning the insulin receptor itself. The receptor consists of four separate subunits consisting of two identical a and two identical P chains. The p subunits contain a tyrosine kinase activity and the ATP binding sites. The insulin receptor is activated by autophosphorylation of key tyrosine residues in its cytoplasmic tyrosine kinase domain. This autophosphorylation is required for subsequent activity of the insulin receptor. The autophosphorylation stabilizes the activated receptor kinase resulting in a phosphorylation cascade involving intracellular signaling proteins. At present there are limited pharmacological approaches to treatment of Type II diabetes. Insulin is currently used as a treatment, but is disadvantageous because it must be injected and because its extreme potency requires careful titration of dose. Although several peptide analogs of insulin have been described, none with a molecular weight below about 5000 Daltons retains activity. Some peptides which interact with sites on the p-subunit of the insulin receptor have shown enhancement of the activity of insulin on its receptor (KoJe et a!., J. Biol Chem., 271:31619-31626 (1996); Kasuya etal., Biochem. Biophys. Res. Commun., 200:777-83 (1994)). Kohanski and others have reported on a variety of polycationic species that generate a basal effect, but do little to enhance insulin action (Kohanski, J. Biol. Chem., 264:20984-91 (1989); Xu el al, Biochemistry 30:11811-19 (1991). These peptides apparently act on the cytoplasmic kinase domain of the insulin receptor. In addition, certain non-peptide components have been found to enhance the agonist properties of peptide hormones, but none appear to act directly on the insulin receptor kinase. For instance, the ability of thiazolidinediones, such as pioglitazone, to enhance adipocyte differentiation has been described (Kletzien, el al., Mol. Pharmacol, 41:393 (1992)). These thiazolidinediones represent a class of potential anti-diabetic compounds that enhance the response of target tissues to insulin (Kobayasfti, Diabetes, 41:476 (1992)). The thiazolidinediones act at an unknown site downstream from the insulin receptor itself and do not have a direct effect on the insulin receptor kinase. Other anti-diabetic agents currently in use include both insulin secretagogues (such as the sulfonylureas) and biguanides (such as metformin) that inhibit hepatic glucose output. To date, non-peptide substances which can mimic the activating effect of insulin on the insulin receptor have eluded discovery. A variety of polyanionic sulfonic acid derivatives including suramin, azo dyes and related compounds are known in the art and have been established as potential therapeutics for a variety of disease indications. Suramin, described in 1917, is a polysulfonic acid that has been extensively researched (Dressel, J. Chem. Ed., 38:585 (1961); Dressel, J. Chem. Ed., 39:320 (1962)). it has therapeutic uses as an anthelmintic and antiprotozoal. More recently, it has been described as an inhibitor to reverse transcriptase in certain avian and murine retroviruses (De Clercq, Cancer Letters, 8:9 (1979); Mitsuya el al. Science, 226:172 (1984)). Large numbers of compounds relating to suramin exist. Most of the suramin analogs which have been reported have multiple sulfonic acid functionality on each aryl ring. Recent studies indicate that polyanionic suramin analogs have anti-angiogenic, antiproliferative activity, and anti-viral activity (Gagliardi et al., Cancer Chemother. Pharmacol, 41:117 (1988): Doukas el al, Cancer Res., 55:5161 (1995); Mohan et al, Antiviral Chem., 2:215 (1991)). A number of other bisnaphthylsulfonic acids have been described in the patent literature as complement inhibitors (US 4132730, US 4129591, US 4120891, US 4102917, US 4051176). Additionally, there are a number of azo dye patents (DE 19521589, US 3716368, DE 2216592, FR J578556) which disclose polysulfonated naphthalene azo compounds. However, none of the suramin analogs or azo dyes have been suggested to be useful in the treatment of hyperglycemia or diabetes. SUMMARY OF THE INVENTION This invention is directed to pharmaceutical compositions comprising naphthalene sulfonic acids and related compounds which enhance glucose uptake into cells, to the naphthalene sulfonic acids and related compounds, and to methods for enhancing glucose uptake in mammals using these pharmaceutical compositions and compounds. R1 and R2 are, independently, hydrogen, alkyl, substituted alkyl, aryl, substituted aryl. -C(0)R4. -C(0)OR4, -C(0)NR4R5, -S(0)2R4. -S(0)2OR4, heteroaryl. substituted heteroaryl, heterocyclyl, substituted heterocyclyl, aryl(!ower)aIkyl, substituted aryl(lower)alkyl, heteroaryl(lower)alkyi, substituted heteroaryl(lower)alkyl, or lower alkenyl, or R1 and R2 together with the conjoining nitrogen are C3-C9 heteroaryl, C3-C5 heterocyclyl, or both R" and R2 are oxygen and together with the conjoining nitrogen forming -N02, R3 is a substituent on the B ring and is -S02OR6, -C(0)OR6, -S02NR62, -C(0)NR62 or tetrazolyl; each linker -WY- between the naphthyl and phenyl intersects the A ring on the naphthyl and is, independently, -C(0)NR7-, -NR7C(0)-, -C(0)0-, -OC(O)-, -CH=CH-, -NR7CH2-, -CH2NR7-, -NR7C(0)NR7-, -NR7C(0)0-, -OC(0)NR7-, -NR7S020-, -OS02NR7-, -OC(0)0-, -S02NR7-, -NR7SOr, -0S02-, or -SO2O-, each R4 and R5 is, independently, hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, aryl(lower)alkyl, substituted aryl(lower)alkyl, substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, or lower alkenyl, each R6 and R7 is, independently, hydrogen or lower alkyl, each R8 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl(lower)alkyl, substituted aryI(lower)alkyl, substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR92, -NR9C(0)R9, -OS02R9, -S02OR9, -S02NR92, or -NR9S02R9, each R9 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heteroaryl (lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, aryl(lower)alkyl, or substituted aryl(lower)alkyl, each Z is a non-interfering substituent, each x and v is, independently, 0, 1, 2 or 3, and R10 is aryl, substituted aryl, heteroaryl, or substituted heteroaryl, optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutically acceptable salt thereof. In a second aspect, the invention provides a method of stimulating the kinase activity of the insulin receptor comprising conlacting the insulin receptor, or the kinase portion thereof, with a compound of the first aspect of this invention, in an amount sufficient to stimulate the kinase activity of the insulin receptor. In a third aspect, this invention provides a method of activating the insulin receptor or enhancing the activation of the insulin receptor by insulin comprising contacting the insulin receptor, or the kinase portion thereof, with a compound of the first aspect of this invention, in an amount sufficient to activate the insulin receptor or enhance insulin"s activation of the insulin receptor. Enhancement of insulin"s ability to activate its receptor in a mammal may be effected by administering the compound of the first aspect of this invention to the mammal. In a fourth aspect, the invention provides the use of a compound of the first aspect of this invention in a method of stimulating the uptake of glucose into cells which display the insulin receptor. This method of stimulating the uptake of glucose into cells which display the insulin receptor comprises contacting the ceils in the presence of insulin with a compound of the first aspect of this invention in an amount sufficient to stimulate the uptake of glucose into the cells. The uptake of glucose into cells in a mammal may be effected by administering the compound of the first aspect of this invention to the mammal. Other aspects of the invention are directed to the use of a compound of the first aspect of this invention in the treatment of hyperglycemia, type I diabetes, or type II diabetes in a mammal, such as a human. These methods of treatment all comprise the step of administering a therapeutically effective amount of the a compound of the first aspect of this invention to the mammal. Optionally, the methods of treatment may also comprise administering insulin to the mammal. Another aspect of the invention is directed to compounds of formula 1, where: each R* and R5 is, independently, hydrogen, alkyl, Rn-substituted alkyl, aryl, R"-substituted aryl, aryI(iower)aIkyi, Rn-substituted aryl(lowerJalkyi, R,l-substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, substituted R11-substituted heteroaryl(lower)alkyl, heterocyclyl, R"-substituted heterocyclyl, or lower alkenyl; each Ru is, independently, aryl, substituted aryl, alkyl, substituted alkyl, substituted heteroaryl, heteroaryl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nttro, halo: cyano. -OR12, -SR"l -C(0)R12, -OC(0)R12. -C(0)OR,2; -NRI2:, -C(0)KR,!:, -NR!2C(0)R13, -OS02Ri2, -S02OR12, -SO;NRi:2, or -NR12S02R12; and each R12 and R13 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heteroaryl(lower)alkyl. substituted heteroaryl(lower)alkyl> heterocyclyl, substituted heterocyclyl, arylflower)atkyf, or substituted aryl(lower)alkyl; provided that if R10 isnaphthyl, v isO, and each -WY- is -C(0)NR7- or -NR7C(0>, then (i) Z is not -S02OH; and (ii) if R1 or R2 is -C(0)NR4Rs, then R13 is neither aryl nor substituted aryl. Pharmaceutical compositions comprising a pharmaceutical^ acceptable carrier and these compounds of the invention as active ingredients are provided in still another aspect of the invention. BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 shows the effect of a compound of the invention, compound 8, in combination with insulin on blood glucose levels in db/db mice. Figure 2 shows the effect of another compound of the invention, compound 10, in combination with insulin on blood glucose levels in db/db mice. Figure 3 shows the effect of compound 8 on 3T3 HIR cells. DETAILED DESCRIPTION OF THE INVENTION (a) Definitions and General Parameters "Alkyl", as in "alkyl" or "alkyloxy", means C1-C20 monovalent hydrocarbyl moiety which may be linear, branched, or cyclic. "Lower alkyl", as in "lower alky!", "halo-lower alkyl", "aryl(lower)alkyr, or "heteroaryl(lower)alkyI", means a Ci-C,0 alkyl. The term "lower alkyl" includes such moieties as methyl, ethyl, isopropyl, propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, hexyl, cyclopentyl, cyclopropylmethyl, cyclohexyl, orcyclohexylmethyl. Ci-C6 lower alkyls are preferred, A "substituted alkyl" or "substituted lower alkyl" is an alkyl or lower alkyl, respectively, which is typically mono-, di-, or tri-substituted with a moiety such as aryl, R"-substituted ary], heteroaryl. nitro, cyano, halo, -OR. -SR, -COR, -OC(0)R. -C(0)OR, -NR2, -S02OR, -OS02R, -S02NR2. -NRS02R, -CONR2, or -NRCOR. where each R is. independently, hydrogen, lower alky], R"-substituted lower alkyl, ary], R"-substituted ary!. heteroaryl, heteroaryl(lower)alkyl, R"-substituted aryl(lower)alkyl, or aryl(lower)alkyl and each R" is, independently, hydroxy, halo, lower alkyloxy, cyano, thio, nitro, lower alkyl, halo-lower alkyl, or amino. Substituted alkyls or substituted lower alkyls which are substituted with one to three of the substituents selected from the group consisting of cyano, halo, Jower alkyloxy, thio, nitro, amino, or hydroxy are particularly preferred. The term "halo-lower alkyl" means a lower alkyl substituted with one to three halo groups, and is further exemplified by such radicals as -CF3, -CH2CF3 and -CH2CC13. "Aryl", as in "aryl", "aryloxy", and "aryl(lower)alkyl", means a radical derived from an aromatic hydrocarbon containing 6 to 20 ring carbon atoms, having a single ring (e.g., phenyl), or two or more condensed rings, preferably 2 to 3 condensed rings (e.g., naphthyl), or two or more aromatic rings, preferably 2 to 3 aromatic rings, which are linked by a single bond (e.g., biphenyl). The aryl is preferably C6-C16 and even more preferably, C& to Cl4. A "substituted aryl" is an aryl radical which is substituted, multiply or singly, with a moiety such as an alkyl, R"-substituted alkyl, halo, cyano, nitro, -SR, -OR, -COR, -OCOR, -SO2OR, -OSO2R, -SO:NR2, -NRSO2R, -COOR, -NR2> -CONR2, or -NRCOR, where each R is, independently, hydrogen, lower alkyl, R"-substituted lower alkyl, aryl, R"-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or R"-substituted aryl(lower)alkyl and each R" is, independently hydroxy, halo, lower alkyloxy, cyano, thio, nitro, lower alkyl, halo-lower alkyl, or amino. A substituted aryl may be substituted from one to seven times with any combination of the radicals listed above. Preferably, however, the substituted aryl is mono-, di-, or tri-substituted. Especially preferred substituents on a substituted aryl are lower alkyl, halo-lower alkyl, halo, cyano, thio, nitro, amino, lower alkyloxy, or hydroxy. The radicals -S02OR, -S02NR2, -COOR, and -CONR2, where R is hydrogen or lower alkyl, are also especially preferred substituents of substituted aryls on the compounds of the present invention. "Heteroaryl", as in heteroaryl and heteroaryl(lower)alkyl, means a radical derived from an aromatic hydrocarbon containing 5 to 14 ring atoms, 1 to 5 of which are hetero atoms chosen, independently, from N, O, or S, and includes monocyclic, condensed heterocyclic, and condensed carbocyclic and heterocyclic aromatic rings (e.g., thienyl, fury], pyrrolyl, pyrimidinyl, isoxazolyl, oxazolyL indolyl, isobenzofuranyl, puriny], isoquinolyl. pteridinyl, imidazolyl. pyridyi, pyrazolyh pyrazinyl, quinolyl, etc). A ""substituted heteroaryi" may have from one to three substituents such as an alkyl, R"-substituted alkyl, halo, cyano, nitro, -SR, -OR, -COR, -OOCR, -SO:OR, -OSO:R, -S02NR:, -NRS02R, -COOR, -NR:, -CONR2, or -NRCOR, where each R is independently hydrogen, lower alkyl, R"-substituted lower alkyl, aryl, R"-substituted aryl, heteroaryi, heteroaryl(lower)alkyl, ary!(lower)alkyl, or R"-substituted aryl(lower)alkyl and each R" is, independently, hydroxy, halo, lower alkyloxy, cyano, thio, nitro, lower alkyl, halo-lower aikyl, or amino. In addition, any two adjacent substituents on the heteroaryi may optionally together form a lower alkylenedioxy. Particularly preferred substituents on the substituted heteroaryi include hydroxy, halo, lower alkyloxy, cyano, thio, nitro, lower alkyl, halo-lower alkyl, halo-lower alkyl, or amino. "Heterocyclyl" means a radical derived from an aliphatic, cyclic hydrocarbon containing 5 to 14 ring atoms, 1 to 5 of which are hetero atoms chosen, independently, from N, O, or S. Monocyclic rings (e.g., tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, etc.) are preferred. A "substituted heterocyclyl" may have from one to three substituents, preferably substituents like an alkyl, R"-substituted alkyl, halo, cyano, nitro, -SR, -OR, -COR, -OOCR, -S02OR, -OSO2R, -SO2NR2, -NRSO2R, -COOR, -NR2, -CONR2, or -NRCOR, where each R is, independently, hydrogen, lower alkyl, R"-substituted alkyl, aryl, R"-substituted aryl, heteroaryi, heteroaryl(lower)alkyl, aryl(lower)alkyl, or R"-substituted aryl(lower)alkyl and each R" is, independently hydroxy, halo, lower alkyloxy, cyano, thio, nitro, lower alkyl, halo-lower alkyl, or amino. Preferred substituents on a substituted heterocyclyl include lower alkyl, halo-lower alkyl, halo, cyano, thio, amino, lower alkyloxy, or hydroxy. "Aryl(lower)alkyl" means a lower alkyl radical which is substituted with an aryl, as previously defined. A "substituted aryl(lower)alkyl" means an aryl(lower)alkyl radical having one to three substituents on the aryl portion or the alkyl portion of the radical, or both. "Heteroaryi (lower)alkyr means a lower alkyl radical which is substituted with a heteroaryi, as previously defined. A "substituted heteroaryl(lower)aryl" means a heteroaryi{lower)alkyl radical having one to three substituents on the heteroaryi portion or the alk\l portion of the radical, or both. A "lower alkyloxy" means an -OR radical, where R is a lower alkyl. "Lower alkenyl" means any branched or unbranched unsaturated C2-Cio group having the number of carbon atoms specified, or up to i 0 carbon atoms if no limitation on the number of carbon atoms is specified; and having 1 or more double bonds in the group. Lower alkenyl is exemplified by ethenyl, propenyl, butenyl, pentenyl, and hexenyl, in their various isomeric forms, where the unsaturated bond(s) can be located anywhere in the group. "Halo" means bromo, iodo, fluoro, or chloro. A "non-interfering substituent" means a substituent which, when present on a given compound, does not substantially decrease or otherwise inhibit a particular, desired bioactivity of the compound, such as the ability of the compound to stimulate the kinase activity of the insulin receptor, to activate the insulin receptor, or to stimulate the uptake of glucose into cells displaying the insulin receptor. The presence of the non-interfering substituent should not detrimentally affect the bioactivity of the compound by more than about 30%. Preferably, the non-interfering substituent decreases the bioactivity of the compound by less than about 10%. Most preferably, the non-interfering substituent does not decrease the bioactivity of the compound to any detectable degree. However, the effect of the presence of the non-interfering substituent on the compound need not be neutral. For instance, the non-interfering substituent may optionally increase a particular bioactivity of the compound. Suitable non-interfering substituents include, but are not limited to, alkyl, substituted alkyl, cyano, halo, nitro, -SR, -OR, and -NR2, where each R is, independently, hydrogen, lower alkyl, or substituted lower alkyl. A "pharmaceutically acceptable salt" may be any salt derived from an inorganic or organic acid or an inorganic or organic base. The term "pharmaceutically acceptable anion" refers to the anion of such acid addition salts. The term "pharmaceutically acceptable cation" refers to a cation formed by addition of a base. The salt and/or the anion or cation are chosen not to be biologically or otherwise undesirable. "Stereoisomers" are compounds that have the same sequence of covalent bonds and differ in the relative disposition of their atoms in space. "Inner salts" or "Zwitterions" can be formed by transferring a proton from the carboxyl group onto the lone pair of electrons of the nitrogen atom in the amino group. J A "therapeutically effective amount" means that amount which, when administered to an animal for treating a disease, is sufficient to effect such treatment for the disease. "Treating" or ""treatment" of a disease in a mammal Includes: (1) preventing the disease from occurring in a mammal which may be predisposed to the disease but does not yet experience or display symptoms of the disease, (2) inhibiting the disease, i.e., arresting its development, or (3) relieving symptoms of the disease, i.e., causing regression of the disease. The "kinase portion thereof, with respect to the insulin receptor, means the cytoplasmic tyrosine kinase domain of the insulin receptor. The expression "in a manner known per se" employed to describe processes of preparation of the compounds of the invention refers to analagous processes or processes known in the art for the preparation of analogous compounds. heteroaryl, heterocyclyi, substituted heterocyclyl, aryl(lower)alkyl, substituted aryi(lower)aIkyl, heteroaryl(lower)aIkyl, substituted heteroaryl(Iower)aIkyl, or lower alkenyl, or R1 and R2 together with the conjoining nitrogen are C3-C9 heteroaryl, C3-C5 heterocyclyl, or both R1 and R: are oxygen and together with the conjoining nitrogen forming -NO2, R3 is a substituem on the B ring and is -S02OR6, -C(0)OR6, -S02NR6:, -C(0)NRft2 or tetrazolyl; the linker -WY- between the naphthyi and phenyl intersects the A ring on the naphlhyl and is, independently, -C(0)NR7-, -NR7C{0)-, -C(0)0-, -OC(0)-, -CH=CH-, -NR7CH2-, -CH2NR7-, -NR7C(0)NR7-, -NR7C(0)0-, -OC(0)NR7-, -NR7S020, -0S02NR7-. -0C(0)O-, -SO2NR7-, -NR7S02-, -OS02-, or -SO2O-, each R4 and R5 is, independently, hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, ary}(lower)a3ky], substituted ary](lower)alkyl, substituted heteroaryl, heteroary), heteroaryl(lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, or lower alkenyl, each R6 and R7 is, independently, hydrogen or lower alky!, each R8 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl(lower)alkyl, substituted aryl(lower)alkyl, substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryJ(lower)aJkyl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR92, -NR9C(0)R9, -OS02R9, -S02OR9, -S02NR92, or -NR9S02R9, each R9 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryI(lower)alkyl, heterocyclyl, substituted heterocyclyl, aryl(lower)alkyl, or substituted aryl(lower)alkyl, R10 is aryl, substituted aryl, heteroaryl, or substituted heteroaryl, each Z is a non-interfering substituent, and each x and v is, independently, 0, 1, 2 or 3, optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutical^ acceptable salt thereof. The left linker is written as -YW- simply in order to point out its directionality. This pharmaceutical composition is useful for stimulating the uptake of glucose into cells of a mammal or for treating a mammalian disease state such as hyperglycemia, type I diabetes, or type D diabetes. Another aspect of the invention is directed to a compound of formula I, where: each RA andR5 is, independently, hydrogen, alkyl, Rn-substituted alkyl, aryl, Rn-substituted aryl, aryI(]ower)alkyl, RH-substituted ar>r!(lower)alkyl. R1"-substituted heteroaryl. heteroaryl. heteroaryl(lower)alkyl. substituted R11-heteroaryl (lower)alkyl. heterocyclyl, Rn-substituted heterocyclyl, or lower alkenyl; each R" is, independently, aryl. substituted aryl. alky I. substituted alkyt, ary](lower)a!kyl, substituted aryl(!ower)alkyl, substituted heteroaryl, heteroaryl, heteroaryl(tower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nitro, halo, cyano, -OR12, -SR12, -C(0)Ri:. -OC(0)R12, -C(0)OR"2, -NR,22, -C(0)NR,32, -NR,2C(0)R"3, -OS02R"2, -S02OR]2, -S02NR,22, or -NRL2S02R12; and each R12 and R13 is, independently, hydrogen, lower alky], substituted lower alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, aryl(lower)alkyl, or substituted aryI(lower)alkyl; with the proviso that if R10 is naphthyl, v is 0, and each -WY- is -C(0)NR7- or -NR7C(0)-, then (i) Z is not -S02OH; and (ii) if R1 or R2 is -C(0)NR4R5, then R13 is neither aryl nor substituted aryl. R10 of the compounds of formula I-II are preferably aryl or substituted aryl. The aryl or substituted aryl is preferably naphthyl or substituted naphthyl. Alternatively, the aryl or substituted aryl may be phenyl or substituted phenyl. In an alternative preferred embodiment, R10 is a heteroaryl or substituted heteroaryl. For instance, R10 may be quinolyl. In a compound of formula I or n, if v is 1, 2, or 3, then, preferably, each R is, independently, hydrogen, lower alkyl, substituted lower alkyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR92, -NR9C(0)R9, -OSO:R9, -SO2OR9, -SOjNR 2. or -KR9S02R9. where R9 is hydrogen or lower alky]. In particularly preferred embodiments. R8 is hydrogen, lower alky], halo-lower alky], nitro, halo, cyano, amino, lower alkyloxy, thio, or -C(0)OR9. where R9 is lower alkyl or hydrogen. In the compounds of formula I and II, v is preferably zero. where each substituent R1, R2, R3, -WY-, Z and x is independently defined as for formula I, optionally in the form of single stereoisomers or mixtures of stereoisomers, or pharmaceutically acceptable salts thereof. Preferably, each non-interfering substituent Z in the compounds of formula I, n, HI, and IV is, independently, alkyl, substituted alkyl, cyano, halo, nitro, -SRU, -OR14, or -NR"42, where each R14 is, independently, hydrogen, lower alkyl, or substituted lower alkyl. Preferably each Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy. In preferred compounds of the formulas I-IV, each x is 0 or 1. In the most preferred compounds, each x is 0. In preferred compounds of formula [, II, III. and IV, R1 is alkyl, substituted alkyl. aryl, substituted aryl, -C(0)R4, -C(0)OR4, -C(0)NR4R5, -S(0):R4. -S(0)2OR4, heteroaryl aryl(lower)alkyl, substituted aryl(!ower)a]kyl, or heteroary!(]ower)a[kyl and R2 is hydrogen or lower alkyl. Most preferably, R1 is -C(0)R4, -C(0)NR4R5, or -S02R4 and R2 is hydrogen or Sower alkyl. In a preferred embodiment of the invention, R3 of the compounds of formula I-IV is -S02OR6 or -S02NR62. In preferred compounds of the invention, R3 is -SO20H. In an alternative preferred embodiment, R3 is instead -C(0)OR6, -C(0)NR62 or tetrazolyl. For instance, R3 may be -C(0)OH. In preferred compounds of formula I-IV, each R4 and R5 is, independently, hydrogen, alkyl, Rn-substituted alkyl, aryl, R11-substituted aryl, aryI(lower)alkyl, Rn-substituted aryl(lower)atkyI, Rn-substituted heteroaryl, heteroaryl, heteroarylflowerlalkyl, substituted Rn-heteroaryl(lower)alkyl, heterocyclyl, Rn-substituted heterocyclyl, or lower alkenyl, where each Rn is, independently, aryl, substituted aryl, alkyl, substituted alkyl, substituted heteroaryl, heteroaryl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nitro, halo, cyano, -OR"2, -SR"2, -C(0)R12, -OC(0)R12, -C(0)ORi2, -NR,22, -C(0)NR132, -NRl2C(0)R13, -OS02R12, -SO2OR12, -S02NRl22, or -NRl2S02Rt2 and each R12 and R13 is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryl(lower)aIkyl, heterocyclyl, substituted heterocyclyl, aryl(lower)alkyl, or substituted aryl(lower)alkyl. In further preferred compounds of formulas I-IV, R4 is lower alkyl, R!l-substituted lower alkyl* ary"" R1"-substituted aryl, aryl(Iower)alkyl, Rn-substituted aryl(Iower)alkyl, heteroaryI(Iower)alkyl, or heteroaryl and R5 is hydrogen or lower alkyl. Preferably, each R1" is, independently, aryl, Rl5-substituted aryl, lower alkyl, Rl5-substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)R12, -OC(0)R12, -C(0)OR12, -C(0)NR,32! or -NR12C(0)R13, each R12 and R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, aryl, R15-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryI(lower)alkyl, or R!i-substituted aryI(lower)alkyl, and each R is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl, halo-lower alkyl, or lower alkyloxy. In preferred compounds of formula I. II, III. and IV. each -WY- Sinker is. independently. -C(0)NR7-, -NR7C(0}-. -S02NR7-, -NR7S02-. or -NR7C(0)NR7-. In one embodiment, each -WY- linker is -SO;NiR7- or -NR7S02-. In another embodiment, each -WY- linker is -NR7C(0)NR7-. In one particularly preferred embodiment, each -WY- linker is. independently, -C(0)NR7- or -NR7C(0)-. Compounds of formula I-IV where each -WY- linker is -C(0)NR7- are most preferred. In compounds of formulas I-IV, each R7 is preferably hydrogen. Compounds of formula I-IV in which the -WY- linkers are identical are preferred. This is especially true of compounds of formula III and IV. In compounds of formula III and IV, it is also preferred that the R3 substituents be identical to each other and the naphthyl or substituted naphthyl groups to which the R3 radicals are attached also be identical to each other. This symmetry, however, is not required. For instance, in a compound of formula IV, one R3 may be -C(0)OH and the other R3 may be -S02OH. Compounds of formula I, n, III, or IV comprising more than one preferred substituent are especially preferred. If a compound comprises more preferred substituents than a second compound, then the first compound is preferred over the second. For instance, compounds of formula IV comprising preferred radicals for the substituents (Z)*, R1, R2, and-WY-are preferred over compounds of formula I comprising preferred radicals for only the substituents (Z)x and -WY-. R4isaikyLRn-5ubstitutedaIkyLar\i. R"-substituted aryl, aryI(lower)alkyi. R1""-substituted aryl(lower)alkyl. heteroaryl (lower)alkvL R;"-substituted heteroaryi(lower)afk) L heterocyclyl, R"-substituted heterocychi heteroary], or R"-S[iost["tufed fieteroarjl; each R11 is, independently, aryl, Rl5-substituted aryl. lower alkyl, Rl5-substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)R12, -OCfO)R12, -C(0)OR12, -C(0)NR]32, or-NRl2C(0)R13; each R12 and R13 is, independently, hydrogen, lower alkyl, Ris-substituted lower alkyl, aryl, R,5-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyi, or Rl5-substituted aryl(lower)alkyl; and R is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy; and xisO, 1, or 2, optionally in the form of single stereoisomers or mixtures of stereoisomers, or pharmaceutically acceptable salts thereof. A particularly preferred group of compounds are those of formula V, where: x is zero; R7 is hydrogen; R3 is -SO3H; and R4 is R" "-substituted phenyl where each R11 is independently lower alkyl, Rls-substituted lower alkyl, lower alkyloxy, cyano, halo, thio, amino, amido, nitro or hydroxy. R4 isalkyl, R"-substituted alkyl, aryl.R11-substituted aryl aryl0ower)alkyl. Rn-substituted aryl (lower) alkyl, heteroaryl(lower)aikyl. R!"-substituted heteroaryl heteroaryl, nitro, halo, cyano, amino, thio. -OR12, -C(0)R12, -OC(0)R12, -C(0)OR,:. -C(0)NRl32, or -NRl2C(0)R13; each R12 and R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, aryl, Ris-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or Rl5-substituted aryl(lower)alkyl; and R15 is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy; and xisO, l,or2, optionally in the form of single stereoisomers or mixtures of stereoisomers, or pharmaceutically acceptable salts thereof. aryl(lower)alkyl, heteroaryl(lower)alkyI, Rll-substituted heteroaryl(lower)alkyl" heterocyclyl, R11-substituted heterocyclyl, heteroaryl, orRn-substituted heteroaryl; each Rn is, independently, aryl, R1 "-substituted aryl, lower alkyl, R,5-substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)Rn, -OC(0)R12, -C(0)OR12, -C(0)NR132, or-NR12C(0)R13; each R"2 is. independently, hydrogen, lower alkyl, R1 "-substituted lower alkyl, aryl, RiJ-substituted aryl, heteroaryl, heter"oaryl(lower)alkyl, aryl(lower)alkyl, or R ^-substituted aryl(lower)alkyi; each R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, heteroaryl, heteroaryl(lower)alkyl, ary!(lower)alkyl, or R15-substituted aryl(lower)a!kyl; R 3 is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy; and x isO, 1, or 2, optionally in the form of single stereoisomers or mixtures of stereoisomers, or pharmaceutically acceptable salts thereof. aryl(lower)alkyl, heteroaryl(Iower)alkyl, Ru-substituted heteroaryl(lower)alkyl, heterocyclyl, R."-substituted heterocyclyl, heteroaryl, or R11-substituted heteroaryl; each Rs is, independently, hydrogen, lower alkyl, substituted lower alkyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR9:, -C(0)NR92, -NR9C(0)R9, -OSO2R9, -SOzOR9, -S02NR92, or-NR9S02R9; and each R9 is, independently, hydrogen or lower alkyl; R"° is aryl, R^-substituted aryl, heteroaryl, or R1 ^substituted heteroaryl; each RN is, independently, aryl, R"""-substituted an."], lower alkyi, R,5-substituted lower alkyl. heteroaryl, nitro. halo, cyaiio, amino, thio. -OR12, -C(0)R12, -OC(0)R":. -C(0)OR"-C(0)NR,32. or -KR,2C(0)R"-; each R12 and RU is, independently, hydrogen, lower alkyl, R1 ^substituted lower alkyl. aryl. R1 ^substituted aryl heteroaryl heteroaryl(Iower)a[kyl, aryi(Iower)a!kyl, or R15-substituted aryl(tower)alkyl; and R is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower aikyioxy; where 2 is lower alkyl, halo-lower alkyl, lower aikyioxy, cyano, halo, thio, amino, nitro, or hydroxy; and each x is, independently, 0, 1, or 2, optionally in the form of single stereoisomers or mixtures of stereoisomers, or pharmaceutical ly acceptable salts thereof. Compounds of the formulas V-VII1 are particularly preferred when each R3 is -SO3H or tetrazolyl and each R7 is hydrogen. Alternatively, each R3 is -COOH and each R7 is hydrogen. Compounds of the present invention which are suitable for use in pharmaceutical compositions and methods of the invention, include, but are not limited to the following compounds: 5-{{3-[(3-methylphenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoy!]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[(4-methylpheny!)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl)- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[(4-methoxyphenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[(3-chlorophenyl)carbonylamino]-5-rN-(6-sulfonaphthyl)carbamoyl]phenyI}- carbonylammo)naphthalene-2-sulfonicacid; 5 carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[(4-fluorophenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonic acid; ; 5-({3-[(3-niethoxyphenyl)carboiiylamino]-5-[X-(6-sulfonaphlh>l)carbanioy]]phenvl}- carbonylamino)naphthalene-2-sulfonic acid; 5-({3-[(4-nitrophenyI)carbonylamino]-5-[N-{6-suIfonaphthyl)carbamo>"!]phenyl}- carbonyiamino)naphtha!ene-2-sulfonic acid; 5-({3-[(3-nitropheny!)carbonylamino]-5-[N-(6-su]fonaphthyi)carbamoyi]phenyl}- carbon.ylainino)naphtha]ene-2-sulfonicacid; 5-({3-[(3-nitro-4-methylphenyi)carbonylamino]-5-[N-(6-sulfonaphthy])carbamoy]]pbenyl}- carbonylamino)naphthalene-2-sulfonicacid; 2-(N-{3,5-bis[N-(6-sulfonaphthyl)carbamoyi]phenyl}carbamoyl)benzoicacid; 2-(N-{3,5-bis[N-(6-sulfonaphthyl)carbamoyl]phenyl}carbamoyl)-4,5-dichlorobenzoic acid; 5-({3-[(4-chlorophenyl)carbonylamino]-5-[N-(6-suifonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 2-(N-{3,5-bispV-(6-suifonaphthyJ)carbamoy)]phenyl}carbamoyI)-3,5-dichJorobenzoic acid; 2-(N-{3,5-bis[N-(6-sulfonaphthyl)carbamoyl]phenyl}carbamoyl)-6-hydroxybenzoic acid; 5-({3-(phenylcarbonylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]pheny]}carbonylamino)- naphthaIene-2-sulfonic acid; 5>({3-(acetylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}carbonylamino)-naphthalene- 2-sulfonic acid; 5-({3-(2-naphthylcarbonylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}-carbonylamino)- naphthalene-2-sulfonic acid; 5-({3-(l-naphthylcarbonylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]-phenyl}carbonylamino)- naphthalene-2 -sulfonic acid; 5"({3-[(2-methylphenyl)carbony]amino]-5-[N-(6-sulfonaphthy])carbamoy}]pheny]}- carbonylamino)naphthalene-2-sulfonicacid; (3S)-3-amino-3-(N-{3,5-bis[N-(6-sulfonaphthyI)carbamoyl]phenyl}carbamoyl)propanoic acid; 3-(N-{3,5-bistN-(6-sulfonaphthyl)carbamoyl]phenyl}carbamoyl)-3-phenylpropanoicacid; 3.(N.{3,5-bis[N-(6-sulfonaphthy!)carbamoyl]phenyl}carbamoyI)-2-phenyIpropanoic acid; 5-({5-tN-(6-sulfonaphthyI)carbamoyl]-3-[(2-sulfophenyl)carbonylamino]phenyl}- carbonylamino)naphthalene-2-sulfonic acid; 3-(>].{3,5-bis[N-(6-sulfonaphthyl)carbamoyi]phenyl}carbamoyl)benzoicacid; 4_(N-{3)5-bis[N-(6-sulfonaphthyl)carbamoyl]plienyl}carbamoyl)benzoicacid; 3_(N-(3,5-bis[N-(6-su]fonaphlhyl)carbamoyl]pbeny]}carbamoy])propanoicacid; 5-({3-(cyclohexyIcarbonylamino)-5-[N-(6-sulfonaphthyl)carbamoyt]phenyi;carbon>lamino)- naphthalene-2-suIfbnic acid; 5-({3-(2-fury]carbony!amiiio)-5-[N-(6-su;fonaphthyl)carbamoyl]pheny]}carbonyiamiiio)- naphthalene-2-sulfonic acid: 5-({3-(4-pyridy]carbonylamino)-5-[N-(6-suifonaphthy])carbamoyl]phenyl}carbonylamino)- naphtbalene-2-sulfonic acid; 5-({3-(3-pyridylcarbonylamino)-5-[N-(6-sulfonaphthyi)carbamoyi]phenyl}carbonylamino)- naphthalene-2-sulfonic acid; 5-({3-(2-phenylacetylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}carbonylamino)- naphthalene-2-suIfonic acid 5-({3 naphlhalene-2-sulfonic acid; 5-({3-(2-oxo-2-(2-quinolyl)acetylamino)-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[2-(4-methylphenoxy)acetytamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-su]fonicacid; 5-({3-[2-(4-methoxyphenyl)acetylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-[(3-{3-[N-(4-methylpheny])carbamoyl]propanoytamino}-5-[N-(6-sulfonaphthyl)- carbamoyl]phenyl)carbonylamino]naphthalene-2-sulfonicacid; 5-({3-[2-(4-methylphenyl)acetylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[2-(3-chloropheny])acetylamino]-5-[N-(6-suIfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5-({5-[(3-amino-4-methylphenyl)carbonylamino]-3-[N-(6-sulfonaphthyl)carbanioyl]phenyt}- carbonyiaraino)naphtha]ene-2-su]fDnicacid; 5-({5-(2-(2-naphthyloxy)acetylamino)-3-[N-(6-sulfonaphthyl)carbamoyl]phenyI}- carbony}amino)naphtha\ene~2-sulfomcacid; 5-({5-[(7-methoxybenzo[d]fiiran-2-yl)carbonylamino]-3-[N-(6-sulfonaphthyl)carbamoyI]- phenyJ}carbonylamino)naphlhalene-2-su!fonicacid; 5-({3-[(phenylsulfonyl)amino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}-carbonylamino)- naphthalene-2-sulfonic acid; 5-f;3-f(2-naphrhj"]sLilfon\f)amJno"]-5-[N-(6-siJlfonapb[hy])carbamoy)]pheny]ll- carbony]amino)naphthalene-2-5Li!tonic acid; 5-[(3-{[(4-chiorophenyl)sulfonyl]amino/-5-[N-(6-5ulfonaphthyl)carbamoyl]phenyl)- carbonylammo]flaphtfialene-2-sulfenicacid; 5-[(3-{[(4-fluorophenyl)sulfonyl]amino}-5-[N-(6-sulfonaphlhyi)carbamoy!]pheny])- carbonylamino]naphthalene-2-sulfonicacid; 5-[(3-{[(4-methoxyphenyl)suIfonyI]aminoS-5-[N-(6-suffonaphthyl)carbamoyI]phenyI)- carbonylamino]naphlhalene-2-sulfonicacid; 5-[(3-{[(4-methyiphenyI)sulfonyl]amino}-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl)- carbonylamino]naphthalene-2-sulfonic acid; 5-({3-[(l-naphthylsuIfonyl)amino]-5-[N>(6-sulfonaphthyl)carbamoyl]pheny]}- carbonylamino)naphthalene-2-sutfonicacid; 5-[(3-{[(2,4,6-trimethylphenyl)su)fonyI]araino}-5-[N-(6-sulfonaphthyl)carbamoyl]-phenyl)- carbonylaminoJnaphthalene-2 -sulfonic acid; 5-[(5-{[benzylsulfonyl]amino}-3-[N-(6-su]fonaphthyl)carbamoyl]phenyl)carbonylainino]- naphthalene-2-sulfonic acid; 5-[(3-{[(3-chIorophenyI)amino]carbonyIamino}-5-fN-(6-sulfonaphthyi)carbamoyi]phenyi)- carbonylamino]naphthalene-2-sulfonicacid; 5-[(3-{[(4-chlorophenyl)amino]carboHylamino}-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl)- carbonylamino]naphthalene-2-su]fonicacid; 5-[(3-{[(2-chlorophenyl)amino]carbonylamino}-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl)- carbonylamino]naphthalene-2-sulfonicacid; 5-[(3-{[(2-methylphenyl)amino]carbonylamino}-5-[N-(6-sulfonaphthy!)carbamoyl]phenyt)- carbonylamino]naphtha(ene-2-sulfonicacid; 5-[(3-{[(3-methylphenyl)amino]carbonylamino}-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl)- carbonylamino]naphthalene-2-sulfonitacid; 5-[(3-{t(4-methyIphenyI)afflinoJcarbonylamino}-5-[N-(6-suIfonaphthyf)carbanioyl]phenyl)- carbonylamino]naphthalene-2-sulfonic acid; 5-[(3-{[(2-methoxyphenyl)amino]carbonylamino}-5-[N-(6-sulfonaphthyl)carbamoylJpheiiyl)- carbonylamino]naphthalene-2-sulfonicacid; 5 -[(3 - {[(3-methoxypheny])amino]carbony]amino} -5 -[N-{6-suf fojiaphthyI)carbam oy]]phenyl)- carbony]amino]naphthalene-2-5ulfonicacid; 54(3-{L(4"m^hoxyphenyl)amino]carbonylamiiio}-5-[N-(6-su!fonaphthyl)carbamoyljphenyl)- carbonylamino]naphthalene-2-sulfonicacid; 5-{{3-[(phenyIamino)carbonyIaminoj-5-[N-j6-sulfonaphthyl)carbamoyl]pheny]}- carbonylamino)naphthalene-2-sulfonicacid; 5-({3-[(3-chiorophenyl)carbony[amino]-5-[N-(6-fiydroxy-naphthyI)carbamoyi]phenyl}- carbony!ammo)naphthaIene-2-sulfonicacid; 5-({3-[(3-Chlorophenyl)carbonylamino]-5-(N-naphthylcarbamoyl)phenyl}carbony1amino)- naphthalene-2-sulfonic acid; 5-({3-[(4-methylpheny!)carbonylamino]-5-(N-(8-quinolyl)carbamoyl)phenyl}- carbonylamino)naphthalene-2-suIfonicacid; (2S)-2-({5-[(4-methylphenyl)carbonylamino]-3-fN-(6-suifonaphthyl)carbamoyl]phenyl}- carbonylamino)-3-phenylpropanoicacid; 5-({3-[(4-methylphenyl)carboiiy]amino]-5-[N-(6-sulfamoylnaphthyl)carbamoy]]phenyl}- carbonylamino)naphthalene-2-sulfonicacid; 5 -({5-[N-(6-carboxynaphthyl)carbam oyl] -3-[(4-methylpheny l)carbonylam inojphenyl} - carbonylamino)naphthalene-2-carboxylicacid; 5-({3-amino-5-|^-methyl-N-(6-sulfonaphthyl)carbamoyl]phenyl}-N-methylcarbonylamino)- naphthalene-2-sulfonic acid; and 5-({5-[(3-chlorophenyl)carbonylamino]-3-[N-methyl-N-(6-sulfonaphthyl)carbamoyl]phenyl}- N-methylcarbonylamino)naphthalene-2-sulfonicacid; optionally in the form of single stereoisomers or mixtures of stereoisomers, and the pharmaceutically acceptable salts thereof. Syntheses and descriptions of these compounds are outlined in Examples 1 through 11. Certain compounds of the invention may contain one or more chiral centers. In such cases, all stereoisomers also fall within the scope of this invention. The invention compounds include the individually isolated stereoisomers as well as mixtures of such stereoisomers. Pharmaceutically acceptable salts, cations and anions of the compounds of the invention are also encompassed by the present invention and are useful in the methods and pharmaceutical compositions described herein. Pharmaceutically acceptable salts include salts which may be formed when acidic protons present are capable of reacting with inorganic or organic bases. Typically the parent compound is treated with an excess of an alkaline reagent, such as hydroxide, carbonate or alkoxide, containing an appropriate cation. Cations such as Na"1", KT, Ca"" and MJ-J4 are examples of cations present in pharmaceutically acceptable salts. The Na" salts are especially useful. Acceptable inorganic bases, therefore, include aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate and sodium hydroxide. Salts may also be prepared using organic bases, such as salts of primary, secondary and tertiary amines, substituted amines including naturally-occurring substituted amines, and cyclic amines including isopropylamine, trimethyiamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-dimethylaminoethanol, tromethamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, N-alkylglucamines, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, and the like. If the compounds of the invention contain a basic group, an acid addition salt may be prepared. Acid addition salts of the compounds are prepared in a standard manner in a suitable solvent from the parent compound and an excess of acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid (giving the sulfate and bisuifate salts), nitric acid, phosphoric acid and the like, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, salicylic acid, p-toluenesulfonic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, lactic acid, o-(4-hydroxy-benzoyl)benzoic acid, 1,2-ethane-disulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthaIenesulfonic acid, camphorsulfonic acid, 4-methyl-bicyc!o[2.2.2.]oct-2-ene-1-carboxylic acid, glucoheptonic acid, gluconic acid, 4,4"-methylenebis(3-hydroxy-2-naphthoic)acid, 3-phenyl prop ionic acid, trimethylacetic acid, t-butylacetic acid, lauryJsulfuric acid, glucuronic acid, glutamic acid, 3-hydroxy-2-naphthoic acid, stearic acid, muconic acid and the like. Certain of the compounds form inner salts or Zwitterions. The pharmaceutical compositions of the invention preferably comprise a preferred compound of formula I. For instance, the pharmaceutical composition may comprise a compound of formula II, HI, IV, V, VI, VII, or VIE as an active ingredient. However, pharmaceutical compositions which comprise any of the compounds of the invention are contemplated. In al] cases, the pharmaceutical compositions of the invention also comprise a pharmaceutically acceptable carrier. i The pharmaceutical compositions of this invention maybe formulated as solutions or lyophilized powders for parenteral administration. Powders may be reconstituted by addition of a suitable diluent or other pharmaceutical!;" acceptable carrier prior to use. The liquid formulation is generally a buffered, isotonic, aqueous solution. Examples of suitable diluents are normal isotonic saline solution, 5% dextrose in water or buffered sodium or ammonium acetate solution. Such formulations are especially suitable for parenteral administration, but may also be used for oral administration. It may be desirable to add excipients such as polyvinylpyrrolidinone, gelatin, hydroxycellulose, acacia, polyethylene glycol, mannitol, sodium chloride or sodium citrate. Alternatively, these compounds may be encapsulated, tableted or prepared in an emulsion or syrup for oral administration. Pharmaceutically acceptable solid or liquid carriers may be added to enhance or stabilize the composition, or to facilitate preparation of the composition. Liquid carriers include syrup, peanut oil, olive oil, glycerin, saline, alcohols and water. Solid carriers include starch, lactose, calcium sulfate, dihydrate, terra alba, magnesium stearate or stearic acid, talc, pectin, acacia, agar or gelatin. The carrier may also include a sustained release material such as glyceryl monostearate or , glyceryl distearate, alone or with a wax. The amount of solid carrier varies but, preferably, will be between about 20 mg to about 1 g per dosage unit. The pharmaceutical preparations are made following the conventional techniques of pharmacy involving milling, mixing, granulation, and compressing, when necessary, for tab}et forms; or milling, mixing and filling for hard gelatin capsule forms. When a liquid carrier is use, the preparation will be in the form of a syrup, elixir, emulsion or an aqueous or non-aqueous suspension. Such a liquid formulation may be administered directly p.o. or filled into a soft gelatin capsule. Some specific examples of suitable pharmaceutical compositions are described in Examples 15-17, below. Typically, a pharmaceutical composition of the present invention would be packaged in a container with a label indicating use of the pharmaceutical composition in the treatment of hyperglycemia, type I diabetes, or type II diabetes, or a combination of the disease conditions. (c) Methods of Use of Compounds of this Invention. Compounds of the invention have been found to bind to the kinase domain and stimulate autophosphorylation of the receptor (Example 12, below). In addition, these compounds have been shown to enhance insulin"s ability to effect the transport of glucose ■ into cultured fibroblast cells (Example 13, below). The compounds have also been shown to lower blood glucose levels in db/dbmicc (Figures ] and 2, Example 14). The ability of compounds of the invention to stimulate aiitophosphorylatioh of the insulin receptor and to stimulate the uptake of glucose into cells which is demonstrated in the specific examples, Example 12-14, beiow, indicates their usefulness in the treatment and management of subjects with diabetes. Without intending to be bound by any theory, it is believed that the compounds of this invention act directly on the kinase function of the receptor and do not necessarily compete with insulin for binding at the insulin-binding site, nor do they effect activation of the receptor by a mechanism similar to that exhibited by insulin. Thus, they are directly able to activate the kinase to autophosphorylate, to potentiate the effect of insulin, to activate the kinase function of the receptor in phosphorylating exogenous substrates and to effect the increased uptake of glucose by adipocytes and insulin receptor-bearing cells in general and to lower blood glucose in diabetic subjects. Accordingly, by virtue of the activities of the compounds of the invention, they may be used to stimulate the kinase activity of an insulin receptor, to enhance the activation of the insulin receptor by insulin, to enhance the stimulation by insulin of cellular glucose uptake, and to stimulate the uptake of glucose in diabetic subjects. Thus, the compounds of this invention are useful in the treatment of diabetes. One aspect of the invention is directed to a method of stimulating the kinase activity of the insulin receptor. This method comprises contacting the insulin receptor, or the kinase portion thereof, with a compound of the invention in an amount sufficient to stimulate the kinase activity of the insulin receptor. By stimulating the kinase activity of the insulin receptor, both autophosphorylation as well as the phosphorylation of exogenous substrates is enhanced. The stimulation of the kinase activity of the insulin receptor may occur either in vivo or in vitro. The compounds of the invention have been demonstrated to exhibit stimulatory activity at the insulin receptor with subsequent lowering of circulating glucose levels for a potential therapeutic effect in diabetes illness. Similarly, other compounds which show the same effects on the insulin receptor and, thus, on circulating glucose have the potential to be useful for the treatment of diabetes diseases. The compounds claimed within this patent can be used as a model to discover other new agents that act on the insulin receptor and thereby lower circulating levels of glucose in diabetic patients. The steps in a process in which these agents can be utilized to discover new insulin receptor agonists/activators and glucose- lowering therapeutic agents may be achieved by the following. The compounds mav be utilized to validate, optimize, and standardize assays necessary for the discovery of other compounds that: 1. Activate/stimulate the cytoplasmic kinase domain of the insulin receptor kinase or the insulin receptor kinase; 2. Activate/stimulate the insulin receptor; 3. Stimulate glucose uptake into cells and tissues; 4. Lower circulating glucose levels in mammals; 5. Lower circulating glucose levels in humans; 6. Inhibit lipolysis in cells and tissues; 7. Inhibit lipolysis in mammals. These compounds can be utilized as a benchmark to discover compounds that show improved activity in assays that: 1. Activate/stimulate the cytoplasmic kinase domain of the insulin receptor kinase or the insulin receptor kinase; 2. Activate/stimulate the insulin receptor; 3. Stimulate glucose uptake into cells and tissues; 4. Lower circulating glucose levels in mammals; 5. Lower circulating glucose levels in humans; 6. Inhibit lipolysis in cells and tissues; 7. Inhibit lipolysis in mammals. Combined with algorithms that compare structures or chemical properties and/or match structures or chemical properties within libraries of test compounds, these compounds can be utilized to discover compounds that display activity in bioassays that: 1. Activate/stimulate the cytoplasmic kinase domain of the insulin receptor kinase or the insulin receptor kinase; 2. Activate/stimulate the insulin receptor; 3. Stimulate glucose uptake into cells and tissues; 4. Lower circulating glucose levels in mammals; 5. Lower circulating glucose levels in humans; 6. Inhibit lipolysis in cells and tissues; 7. Inhibit lipolysis in mammals. Combined with algorithms that compare structures and/or match structures for the purpose of modeling molecular interactions, these compounds can he utilized to discover compounds that display activity in bioassays that: 1. Activate/stimulate the cytoplasmic kinase domain of the insulin receptor kinase or the insulin receptor kinase; 2. Activate/stimulate the insulin receptor; 3. Stimulate glucose uptake into celis and tissues; 4. Lower circulating glucose levels in mammals; 5. Lower circulating glucose levels in humans; 6. Inhibit Hpolysis in cells and tissues; 7. Inhibit lipolysis in mammals. In another aspect of the invention, the insulin receptor is activated by contacting the insulin receptor, or the kinase portion thereof, with a compound of the invention in an amount sufficient to stimulate insulin"s activation of its receptor, optionally in the presence of insulin. The targeted insulin receptor may optionally be on the surface of a cell in a mammal. In such a case, the contacting is effected by administering the compound, or a pharmaceutical composition thereof, to the mammal. In still another aspect of the invention, the compounds of the invention are used to stimulate the uptake of glucose into cells displaying the insulin receptor. This method comprises contacting the cells with a compound of the invention, optionally in the presence of insulin, and in an amount sufficient to stimulate the uptake of glucose into the cells. The targeted cells may optionally be in a mammal and the step of contacting the receptor with the compound may then be effected by administering the compound, or pharmaceutical composition thereof, to the mammal. A method of treating hyperglycemia in a mammal, preferably a human, is provided by another aspect of the invention. The method of treating hyperglycemia in a mamma) comprises administering a therapeutically effective amount of a compound of the invention, or a pharmaceutical composition thereof, to the mammal. Optionally, the method may farther comprise treating the mammal with an additional form of therapy for hyperglycemia- For instance, one method may also comprise administering to the mammal with insulin in addition to the compounds of the invention. Alternatively, the compounds of the invention may be administered to the mammal in combination with a non-insulin drug or other alternative treatment for hyperglycemia. The total amount of the combination of drugs administered lo the mammal must be a therapeutically effective amount, although the amounts of each of tlie individual drugs ma> by themselves be suboptimal for therapeutic purposes. A very dangerous side-effect of the administration of insulin is insulin-induced hypoglycemia with the potential for coma and, possibly, death. This problem can become quite severe in diabetic patients who develop unpredictable responses to insulin or have hyper-variable levels of circulating glucose. For these patients, the co-administration of the compounds of the invention with sub-therapeutic doses of insulin will minimize the possibility that the diabetic patient wiU over-dose on insulin and suffer from the severe consequences such as coma and death. These compounds appear to be incapable of inducing hypoglycemia in the presence of insulin. They appear to increase the effectiveness of insulin but do not display true insulin mimetic effects like hypoglycemia. These compounds are, thus, effective insulin safeners. Still another aspect of the invention relates to a method of treating type I diabetes in a mammal. This method comprises administering a therapeutically effective amount of a compound of the invention, or a pharmaceutical composition thereof, to the mammal. In a preferred embodiment, the mammal is a human. The method may optionally further comprise treating the mammal with an additional form of therapy for type I diabetes. For instance, insulin may also be administered to the mammal. The amount of insulin which is delivered to the mammal should be in a therapeutically effective amount when used in conjunction with a compound of the invention. However, the amount delivered to a mammal in conjunction with a compound of the invention is preferably less than an amount which would be therapeutically effective if delivered to the mammal alone. It is understood that the insulin which is administered in any of the treatments of the present invention may either be isolated from a natural source or recombinant. In addition, an insulin analog may be substituted for insulin in any of the treatments of the present invention. In still further aspects of the invention, the compounds of the invention, or pharmaceutical compositions thereof, are used to treat type D diabetes in a mammal, This method comprises administering a therapeutically effective amount of a compound of the invention, or a pharmaceutical composition thereof, to the mammal. Again, the preferred subject is a human. Again, like the other treatment methods of the invention, this method may further comprise treating the mammal with an additional form of therapy for type II diabetes, such as administering insulin to the mammal. The compounds of the invention, or pharmaceutical compositions thereof, are thus used to enhance glucose uptake in patients which require such treatment. The method of treatment comprises the administration parenterally. and orally, of an effective quantity of the chosen compound, preferably dispersed in a pharmaceutical carrier. The effective doses of the compound of the invention are generally selected from the range of 0.01 to 1000 mg/kg, preferably 0.01 to 100 mg/kg and more preferably 1-30 mg/kg, but will be readily determined by one skilled in the art depending upon the route of administration, age and condition of the patient. The dosage units may be administered one to ten times daily for acute or chronic disease. No unacceptable toxicological effects are expected when compounds of the invention are administered in accordance with the present invention. The compounds of the invention, or pharmaceutical compositions thereof, may be administered by any route suitable to the subject being treated and the nature of the subject"s condition. Routes of administration include, but are not limited to, administration by injection, including intravenous, intraperitoneai, intramuscular, and subcutaneous injection, by transmucosal or transdermal delivery, through topical applications, nasal spray, suppository and the like or may be administered orally. Formulations may optionally be liposomal formulations, emulsions, formulations designed to administer the drug across mucosal membranes or transdermal formulations. Suitable formulations for each of these methods of administration may be found, for example, in Remington"s Pharmaceutical Sciences, latest edition, Mack Publishing Company, Easton, PA. (d) Processes for Preparation of the Compounds of the Invention Another aspect of the invention is a process for preparing the compounds of formula I. The compounds of the invention are prepared by conventional methods of organic chemistry in a manner known perse. In some cases, protective groups may be introduced and later removed. Suitable protective groups for amino, hydroxy), carboxyl groups are described in Greene, et a!., Protective Groups in Organic Synthesis, Second Edition, John Wiley and Sons, New York, 1991. In some cases, activation of functional groups will be required to perform a particular reaction. For example, activation of carboxylic acids can be achieved by using a number of different reagents as described in Larock, Comprehensive Organic Transformations, VCH Publishers, New York, 1989. Compounds of the invention may be prepared via acylation or alkylation of the amino group in a manner known per se. For example, particulars for the acylation are shown in Reaction Scheme I. In alkylation, an alkyl group is added to or substituted in a compound. Alkylation is carried out in a suitable solvent, such as. for example, acctonitrile, DMF. or THF. at 0 to 160°C, typically at approximately 25°C to reflux and requires some 1 to 18 hours. The compounds may likewise be synthesized via condensation reactions in a manner known per se. For example, particulars for the condensation are shown in Reaction Scheme IV. In a condensation reaction, a simple substance, such as water or HC1, is released by the combination of two or more molecules. The condensation reaction may occur upon addition of any of a number of starting materials utilized in organic syntheses at a temperature between 50 and ]25°C. A condensation reaction may also be intramolecular. In the condensation reaction, the compounds of formula I are assembled from sub¬structures a, p, and y, which make up the molecule. The sub-structures a, p, and y are shown in the main process claim. The assembly involves reactive groups capable of forming the linker -WY-. For example, the assembly may involve the condensation of activated sub¬structure a with the sub-assembly p-y or the condensation of the sub-assembly a-p with activated sub-structure y or the condensation of activated sub-structures a and y with sub¬structure p. In the latter case, identity of sub-structures a and y is preferred to avoid mixtures of reaction products. In order to assemble such components of the formula I (a-p-a), one activated sub-structure p may be reacted with two sub-structures a (see Reaction Scheme V), Components of formula I may also be prepared by reduction of the nitro group in a manner known perse, as shown in Reaction Schemes I or II. An ester form of a compound of formula I may be hydrolyzed to form the salt or free acid of the compound, as shown in Reaction Scheme IV. In hydrolysis, the ester may be saponified by reaction with water or with an alkanol in the presence of base. Hydrolysis is catalyzed by acid or base and may require as long as 18 hours. Further conventional processes for preparing compounds of formula I involve the elaboration of substituents or the conversion of substituents. For example, a bromo substituent may be converted into a hydroxy group and vice versa. Furthermore, pharmaceutically acceptable salts of the compounds of the invention may be prepared, as well as their corresponding free bases, and a racemic mixture of any proportions of a compound of the invention may be resolved to yield a stereoisomer thereof. In salt formation, a free acid is converted into a salt via addition of a basic reagent, such as aqueous sodium hydroxide or triethanolamine, that replaces all or part of the hydrogen ions of the acid with one or more cations of a base. The compounds of the invention can he synthesized as shown in the following examples or by modifying the exemplified .syntheses by means known to those of ordinary skill in the art. (e) Examples The Examples which follow serve to illustrate this invention. The Examples are intended to in no way limit the scope of this invention, but are provided to show how to make and use compounds of the invention. Example I. Synthesis of 5-({3-f(3-methvlphenvl>carbonylamino]-5-)>J-f6-sulfonaphthvlV carbamoyUphenvl}carbonylamino)naphth.alene-2-sulfonic acid (compound 7) One synthetic route according to the present invention is outlined in Reaction Scheme " f thionyl chloride in pyridine. The di-acid chloride was next reacted with 2 equivalents of 5-amino-2-naphthalene sulfonic acid, compound 3. to give the bis-amide (5-({3-nilro-5-[N-(6-suIfonaphthyI)carbamoyI]pheny[}carbony[aiTiino)-naphthaIene-2-suIfonic acid, compound 4). The nitro group of compound 4 was reduced using tin(II) chloride in aqueous acid solution to give 5-(j3-amino-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}carbonylamino)-naphthalene-2-suifonic acid, compound 5. Compound 5 was reacted with 3-methyibenzoyI chloride, compound 6, to furnish compound 7. Preparation of"5-({3-nitro-5-[N-(6-su{fonaphthyl)carbamoyl]phenyl}carbonylamino)~ naphthalene-2-sulfonic acid (compound 4) 10.56 g (0.05 mole) of 5-nitrobenzene-l,3-dicarboxylic acid was suspended in 18 mL (0.165 mol) of thionyl chloride and then added to lOmL pyridine. The mixture was stirred at room temperature until it became a clear solution and then stirred for one more hour. The excess of thionyl chloride was removed under vacuum. 22.33 g (0.10 mol) of 5-amino-2-naphthalenesulfonic acid was suspended in 150 mL of pyridine and added to the above di-acid chloride in 50 mL (50:50) of dioxane and CHC13 under vigorous stirring for 1-2 hrs. The crude product was precipitated with dioxane. The oily product was collected on a Bdchner runnel. The brown colored oily product was dissolved in 500 mL water, then allowed to precipitate out over 30 min. The solid material was collected using filtration. It yielded 16.2 g. Preparation of"5~({3~amino-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}carboriylamino)-naphthalene-2-sulfonic acid (compound 5) 7.00 g (31.0 mrool) of tin(II) chloride dihydrate was dissolved in 35 mL concentrated HC1 and cooled to 0-5°C in an ice bath. It was added to 7.5 g (9.6 mmol) of 4 in one portion. The mixture was stirred vigorously at room temperature for 2-3 hrs, then it was cooled in an ice bath. The white solid material was collected by filtration and washed with concentrated HC1 (15 mL x 3), 6 N HC1 (15 mL x 3), and 1 N HC1 (20 mL x 4). The solid was then dried in a desiccator and yielded 5.65 g. Preparation of S-({3.^(5-methylphenyijcarbo>ylamino]-5fN-(6-svlfomiphthylfcarkamoyl]-pheny]}carbonylamino)naphtha\ene~2-sulfomc acid (compound 7) 100 mg (0.17 mmol) of compound 5 was suspended in 5 mL of pyridine and 2 mL sulfolane and added 0.030 mL (0.23 mmo\) of 3-methylbenzoyl chloride, ft was stirred in room temperature for about 16 hrs. The reaction mixture became a clear solution and a solid material was precipitated out by tetrahydrofuran (THF) (100 mL). The solid material was collected using filtration and washed with THF three times. This afforded SO mg of an off white powder. Example 2. Synthesis of 5-("{3-f(3-methvlphenvllcarbonviamino)-5-fN-(,6-suIfonaphthviV carbamovl]phenyllcarbonylaminolnaphthalene-2-sulfonic acid (compound 7) To 100 mg (0.17 mmol) of compound 5 suspended in 5 mL of pyridine and 2 mL of sulfolane was added 23 |iL(0.172 mmo])of3-methylbenzoyl chloride. The reaction was allowed to stir at ambient temperature for 16 hr. An additional 12 ;JL (0.085 mmol) of 3-methylbenzoyl chloride was added and the reaction allowed to stir for an additional 2 hr. Excess acid chloride was quenched by the addition of 0.5 mL of methanol. The reaction product was precipitated upon addition of THF (100 mL) and collected by vacuum filtration to provide 78 mg of the desired compound. The products were identified by *H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Example 3. Synthesis of 2-fN-B,5-bisrN-(6-sulfonaphthvl)carbamovl1phenvUcarbamovlV benzoic acid (compound 17) To 100 mg (0.17 mmol) of compound 5 dissolved in 10 mL of dimethyl formamide was added 50 mg ( 0.337 mmol) of phthalic anhydride. The reaction was allowed to stir at ambient temperature for 16 hr. An additional 25 mg (0,17 mmol) of phthalic anhydride was added and the reaction allowed to stir for an additional 24 hr. The reaction product was precipitated upon addition of THF (100 mL) and collected by vacuum filtration to yield 74 mg of the desired compound. The product was identified by lH NMR and mass spectroscopy and purity was assessed by RP-HPLC. Example 4. Synthesis of additional compounds of formula V The following compounds shown in Table 1 were prepared using procedures similar to those outlined in Examples 1-3. The procedures described in Examples 1-3 can be readily modified by those skilled in the art to generate a wide array of compounds of formula V. Km instance, the use of various, alternative acid chlorides instead of compound 6. in Reaction Example 5. Synthesis of 5-fn-;f["4-chiQropiienviisuifonvnaminoi-5-fN-r6-suffonaphtKvl)-carbamovnphenyDcarbon\lamino|naDhthalene-2-sulfonic acid (compound 50) To 100 mg (0.17 mmol) of compound 5 suspended in 5 mL of pyridine and 2 mLof sulfolane was added 36 mg (0.172 mmol) of 4-chTorobenzenesulfonyl chloride. The reaction was allowed to stir at ambient temperature for 16 hr. An additional 18 mg (0.085 mmol) of the 4-chlorobenzenesulfonyI chloride was added and the reaction allowed to stir for an additional 2 hr. The reaction product was precipitated upon addition of THF and collected by vacuum filtration. The product was identified by "H NMR and mass spectroscopy and purity-was assessed by RP-HPLC. Example 7. Preparation of 5-f04rf2-chlorophenyi)amino1carbonylamino}-5-fN-(6-sulfo-naphthvl)carbamoyl1phenvl1carbonvlaminolnaphthalene-2-sulfonic acid (compound 591 To 100 mg (0.17 mmol) of compound 5 dissolved in 10 mL of dimethylformamide and 1 mL of pyridine was added 25 ^iL (0.207 mmol) of 2-chlorophenyl isocyanate. The reaction was allowed to stir at ambient temperature for 16 hr. An additional 12 uL (0.103 mmol) of 2-chloropheny] isocyanate was added and the reaction allowed to stir for an additional 2 hr. The reaction product was precipitated upon addition of THF and collected by vacuum filtration to provide 57 mg of the desired compound. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Example 8. Synthesis of additional compounds of formula VH By modifying the symhesis described in Example 7 using procedures well known in Preparation of3-amino-5-(methoxycarbonyl)benzoic acid (compound 68) To 2.75 g of mono-methyl-5-nitroisophthalate (or 5-(methoxycarbonv])-3-nitrobenzoicacid), compound 67, dissolved in 30 mL of THF was added 100 mg of 10% palladium on carbon. The reaction was placed in a Parr hydrogenator under a H; atmosphere of 45 psi and shaken for 16 hr. The solid palladium catalyst was removed by vacuum filtration through celite and 5 mL of IN HC1 in diethyl ether was added to the filtrate. After sitting for 12 hr, the solid was collected by vacuum filtration and was washed with ethyl acetate. This provided 1.82 g of the desired product. The product was identified by lH NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of "3-[(3-Chlorophenyl)carbonylamino]-5-(methoxycarbonyl)benzoic acid (compound 70) To 0.576 g (2.49 mmol) of compound 68 was added 10 mL of THF, 10 mL of water, and 2.6 mL of a IN aqueous solution of sodium hydroxide. To this reaction solution was added, alternately in small portions, a solution of 341 |AL (2.74 mmol) of 3-chlorobenzoyl chloride (compound 69) in 5 mL of THF and 2.6 mL of a IN aqueous solution of sodium hydroxide. During the additions, the pH of the reaction solution was checked by pH paper and the reaction was kept at a pH greater than 8. After complete addition, TLC indicated some compound 68 remained. The above procedure was repeated using 150 uL (1.21 mmol) of 3-chlorobenzoyl chloride (69) in 5 mL THF and enough IN aqueous sodium hydroxide to maintain a reaction solution pH above 8. After TLC analysis indicated complete consumption of compound 68, the reaction was extracted with ethyl acetate and 0.5 N aqueous sodium bicarbonate. Then, the aqueous layer was acidified with 6 N HC1 and extracted with ethyl acetate. The organic layer was dried (MgSCv), filtered, and volatiles removed in vacuo. The resulting residue was treated with ethyl acetate/diethyl ether 50/50 to form a white solid that was collected by vacuum filtration. This provided 0.604 g of the desired product. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of methyl 3-(chlorocarbotryl)-5-[(3-Chlorophenyl)carbonylamino]benzoate (compound 71) To 0.319 g (0.96 mmol) of compound 70 was added 8 mL of thionyl chloride and the resulting suspension was allowed to stir at ambient temperature for 2 hr. Then, 5 drops of pyridine was added. The reaction immediately became a homogenous solution. After 30 min, To 29.3 g (0.13 mol) of 5-amino-2-naphthaIenesulfonic acid (compound 72) was added 40 mL of pyridine and 26 mL of acetic anhydride. The resulting suspension was allowed to stir at ambient temperature. After 24 hr, the resulting solution was diluted with 60 mL of methanol. Then, a solution of 3.6 g (0.156 mol) of sodium in 100 mL of methanol was added. After a solid precipitate began to form, 200 mL of diethyl ether was added and the suspension allowed to stir. The solid was collected by vacuum filtration and was washed with diethyl ether. This provided 38.9 g (0.11 mol) of the desired product. The product was identified by !H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of5-(acetylamino)naphthalene-2-sulfonyl chloride (compound 74) To 38.9 g (0.11 mol) of compound 73 was added 52 mL of phosphorus oxychloride, 105 mL of sulfolane, 105 mL of acetonitrile, and 4 mL of dimethylacetamide. The resulting suspension was allowed to stir at ambient temperature for 24 hr. An additional 10 mL each of sulfolane and acetonitrile were added and the reaction temperature was raised to 50 °C. After 2 hr, the reaction became opaque. The reaction temperature was lowered to 25°C, and then the reaction contents were poured onto 1 L of ice. After all the ice melted, the resulting solid was collected by vacuum filtration and was washed with cold water. This provided 33.5 g (O.I 1 mol) of the desired product. The product was identified by "H NMR and m spectroscopy and purity was assessed by RP-HPLC. Preparation of 4-methylphenyl 5-(acetylammo)naphthalene~2-sulfonate (Compound 75) To 15.7 mL(!50 mmol) of p-cresol in ! 00 mL of pyridine cooled in an ice/water bath, was added half of 27.7 g( 97.6 mmol) of compound 74. After lOmin, the remaining half of compound 74 was added. After another 10 min, the reaction was removed from the cold bath and allowed to warm to ambient temperature. The reaction was poured unto ice and extracted with dichloromethane. The organic layer was washed with 0.1 N aqueous HC1 followed by 1.25 N aqueous NaOH. The organic layer was dried (MgS04)s filtered, and volatiles removed in vacuo. The residue was recrystallized from ethyl acetate/ t-butyl methyl ether to give 11.9 g (33.5 mmol) of the desired product. The volatiles were removed from the filtrate and an additional 10.5 g (29.5 mmol) of the desired product was isolated. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of 4-methylphenyl 5-aminonaphthalene-2-$ulfonate (compound 76) To 9.05 g (0.03 mol) of compound 75 was added 40 mL of dioxane and 120 mL of 6N aqueous HC1. The reaction suspension was heated to 75°C for 7 hr. The resulting solution was cooled to room temperature and neutralized with ION aqueous sodium hydroxide to pH of 10. The reaction was extracted with ethyl acetate. The organic layer was dried (MgS04), filtered, and reduced to a small volume in vacuo. Then, 50 mL of IN HCI in diethyl ether was added to form a solid collected by vacuum filtration. This provided 8.57 g (0.02 mol) of the desired product. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of methyl 5-[(3-ch!orophenyI)carbonylamino]-3-(N-{6-[(4-methylphenyI)-oxysulfonyl]naphthyl}carbamoyl)benzoate (compound 77) To 0.34 g (0.96 mmol) of compound 71 was added 0.33 g (0.96 mmol) of compound 76, J 5 mL of dichloromethane, and 162 (iL of pyridine. After 16 hr the reaction was extracted twice from ethyl acetate with 0.5 N aqueous HC1. The organic layer was then extracted with 1M aqueous sodium bicarbonate. The organic layer was dried (MgS04), filtered, and volatiles removed in vacuo. The resulting residue was stripped from dichloromethane twice and the resulting solid suspended in dichloromethane. The solid was collected by vacuum filtration. This provided 0.28 g (0.44 mmol) of the desired product. The product was identified by :H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of~5-[(3-chlorophenyl)carbonylamino]-3-(N-{6-[(4-meihylphenyl)ox\sulfom>lj naphthytjcarbamoyljbenzoic acid {compound 78) To 0.28 g {0.44 mmol) of compound 77 was added 50 mL of"THF to form a homogeneous solution. Then. 2.24 mL (2.24 mmol) of a IN aqueous solution of lithium hydroxide was added. This produced a solid that was dissolved by the addition of 15 mL of water. After 10 hr, the reaction pH was lowered to 1 and the volatile THF removed by rotary evaporation. The resulting solid was collected by vacuum filtration. This provided 0.28 g (0.44 mmol) of the desired product. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation oj" 4-methyiphenyl 5-({3-(chlorocarbony})-5-[(3-chlorophenyl)-carbonylamino]"-phenyl}carbonylamino)naphthatene-2-sulfonate (compound 79) To 23.4 mg (38.1 ^mol) of compound 78 was added 0.5 mL of fhiortyl chloride. The suspension was allowed to stir at ambient temperature for 1 hour. Then, 1 mL of acetonitrile was added. After another hour the reaction remained a suspension so 1 mL of THF was added. The reaction solution became homogeneous within an hour. After an additional 30 min of stirring, the volatiles were removed in vacuo and the resulting residue was stripped from chloroform two times. This gave a solid product that was used without characterization. Preparation of 4-methylphenyl 5-({3-[(3-chlorophenyl)carbonylamino]-5-[N-(6~ hydroxynaphthyl)carbamoyl]phenyl}carbonylamino)naphthalene-2-sulfanaie (compound 81) To 24.1 mg (38.1 umo!) of compound 79 was added 10 mL of dichloromefhane followed by 16.7 mg (105 umol) of 5-amino-2-naphthol (80) dissolved in 5 mL of 1:1 dichloromethane."THF. The reaction was allowed to stir at ambient temperature for 16 hr. The reaction was extracted with ethyl acetate and IN aqueous HC1. The organic layer was dried (MgS04), filtered, and volatiles removed in vacuo. The resulting residue was treated with dichloromethane and diethyl ether to form a yellow solution and a solid precipitate. The solid was collected by vacuum filtration to provide 15 mg (19.9 uunol) of the desired compound, The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of Sodium 5-({3-[ To 12-0 mg (15.0 fimol) of compound 81 was added 400 (il_ of methanol. To this stirred suspension was added 400 JJL of a 1.3 7 M solution of sodium methoxide in methanol. The suspension quickly became homogeneous. The reaction was allowed to stir at ambient temperature for 40 hr. The reaction was acidified to pH 1 with 6 N HC1 and the volatiles were removed by rotary evaporation. The resulting solid was suspended in 0.5 mL of water and the solid collected bycentrifugad"on. This provided 10 mg (15 pjnol) of the desired compound. The product was identified by !H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Example 11. Synthesis of 5-("{5-rN-f6-carboxvnaphthvncarbamovll-3-[(4-melhvlphenyl)-carbonvlaminolphenvl} carbon ylamino)naphthaIene-2-carboxylic acid (compound 91) Compound 91 was synthesized according to the procedures outlined in Reaction Scheme V and described below. To 1.20 g (5.74 mmol) of methyl 5-amino-3-(methoxycarbonyf)benzoate, compound 87, suspended in 50 mL of chloroform and 1.05 mL (6.00 mmol) of diisopropylethylamine was added 836 uL (6.32 mmol) of p-toluoyl chloride in lOmL of chloroform over 30min. The reaction was allowed to stir at ambient temperature for 2 hr. Then, another 100 (iL (0.60 mmol) of diisopropylethylamine and 100 ^L (0.76 mmol) of p-toluoyl chloride in 2 mL of chloroform was added. After an addition 30 min, the volatiles were removed by rotary evaporation and the resulting residue was dissolved in ethyl acetate and extracted with 0.1 N aqueous NaOH followed by extraction with water. The organic layer was dried (MgSO^), filtered, and volatiles removed in vacuo. This provided 1.86 g (5.68 mmol) of the desired compound. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of 5-[(4~methylphenyl)carbonylumino]benzerie-l,3-dicarboxyUc acid " (compound 89) To 1.50 g (4.58 mmol) of compound 88 suspended in 50 mL of methanol was added 11 mL (1 i mmol) of 1M aqueous LiOH. The suspension was allowed to stir at ambient temperature for 16 hr. TbJs produced a nearly dear solution that was fikered lo remove small amount of insoluble material. The methanol was removed from the filtrate by rotary evaporation and the pH of the aqueous solution was lowered to 1 with 1 N HCI. The resulting solid precipitate was collected by vacuum filtration and washed with water. This provided 1.37 g (4.57 mmol) of the desired compound. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. Preparation of"5-[(4-methy}phenyl)carbony}amino]benzene-l,3-dicarbonyl chloride (compound 90) To 40.0 mg (f 3.4 mmol) of compound 89 was added 2 mL of rhionyl chloride. The resulting suspension was allowed to stir for 16 hr. Then, 100 uL of pyridine was added. The reaction became a clear solution after 30 min. The reaction was allowed to stir for an additional 4 hr. The volatites were removed in vacuo and chloroform (10 mL) was added and removed in vacuo two times. This gave a solid product that was used without characterization. Preparation of 5-({5~[N-(6-carboxynaphthyi)carbamoyl]-3-[(4-methylphenyl)~ carbonylamino]pheny!}carbonylamino)naphthaler}e-2-carboxylic acid (compound 91) To 13.4 mmol of compound 90 dissolved in 3 mL of chloroform was added 50.0 mg (26.7 mmol) of compound (5-amino-2-naphthoic acid) (see Price, C. C; Michel, R. H. J. Amer. Chem. Soc. 74, 3652 (1952)) dissolved in 4 mL of pyridine. The reaction solution was allowed to stir at ambient temperature for 16 hr. Diethyl ether was added to form a precipitate that was collected by centrifugation. This solid was dissolved in methanol and allowed to sit for 2 days. A fine precipitate was collected by centrifugation and the desired compound was purified by RP-HPLC (buffer A: 5% acetonitrile, 95% water, 0.05% TFA, buffer B: 95% acetonitrile, 5% water, 0.05% TFA). This provided 1.1 mg (1.73 umol) of the desired compound. The product was identified by "H NMR and mass spectroscopy and purity was assessed by RP-HPLC. , Example 13. 32P-Cytoplasmic kinase domain (CKD) autophosphorvlation assay The complete p-kinase domain of the human insulin receptor (CKD) was expressed in, and purified from, baculovinis. CKD (4.0jig/mL), in a solution of 50 mM Tris-HCl, 2 mM MnCl2, 10 mM MgCl2 (50(i1 final volume), was combined with 50umol ATP, and 5 u€i 32P-ATP (3000 Ci/mmol.)- A test compound, or the vehicle (DMSO), was added to a final DMSO concentration of 1 %. The mixture was incubated for 10 minutes at room temperature. The reaction was terminated by the addition of \0\i\ of 200 mM EDTA. A 30ul volume was removed, mixed with 5^1 of 6X Laemmeli sodium dodecyl sulfate (SDS) treatment buffer, and heated to 94°C for 5 minutes. A 20u1 aliquot was then run on an SDS-PAGE gel. The radioactivity incorporated into the CKD band is quantified by phosphorimaging of the gei, u, scintillation counting of the excised bands. The results for this assay are shown in Table 11. The potency of a compound for increasing phosphorylation is expressed as a percentage of the vehicle level. Example 14. Glucose transport activity 3T3 LI fibroblasts (ATCC) were grown in Dulbccco"s modified Eagle"s medium (DMEM) with 10% fetal bovine serum (FBS, medium). The cells were plated at a density of 3x10 cells/well in 24-vvell plates. Two days after confluence was reached, the cells were treated for 3 days with 0.5 mM isobulylmethylxanthine (TBMX). 1 uM dexamethasone, supplemented with 1.7uM insulin. The cells were then transferred to medium with 1 JuM insulin for 2 more days. The cells were maintained in medium for an additional 4 days. Finally the cells were serum starved overnight in 0.1% bovine serum albumin (BSA) in DMEM. The following day, the culture medium was replaced with 150 mM NaCl, 1.7 mM KC1, 0.9 mM CaCl2, 1.47 mM K2HP04 (pH 7.4) to which was added either the experimental compounds, or their vehicle (DMSO). Insulin or its vehicle (0.01% BSA) was diluted in the assay buffer (containing test compound or vehicle, respectively) to a final concentration of 5.6 nM. After incubation for 30 min at 37°C, 5 uCi/mL ,4C-2-Dixie-D-glucose was added, and the incubation was continued for additional 30 min at 37°C. The cells were then washed 3 times with ice-cold PBS/20 mM glucose and Lysol in 250u! of lysis buffer (50 mM HEPES pH 7.6, 1% Triton X-l 00) for 30 min at room temperature. Radioactivity in the lysate was quantified by scintillation counting. Once l4C-2-deoxy-D-glucose is transported into the cell it is not released. Glucose transport is, therefore, proportional to the amount of radioactivity in the lysate. The concentration of compound necessary to produce an increase in glucose transport greater than the sum of the standard deviation of the vehicle control plus the largest standard deviation of a test sample (generally 150% of the vehicle control) was recorded as the EC (effective concentration). Example 15. Blood glucose level determination in db/db mice Seven to 9 week old male db/db mice (Jackson Laboratories, Bar Harbor, Maine), were used to the study of the effects of compounds on blood glucose levels. Animals were kept in a 12h/12h light/dark cycle, and experiments were initiated immediately after the dark period (7:00 a.m.). Food was removed at this time and returned after the final blood glucose measurement was taken. Insulin (0.5U/ml, Humulin R, Catalog HI-201, Lilly, Indianapolis, Indiana) was prepared by diluting lOOU/mL stock insulin 1:200 with PBS (phosphate buffered saline, Gibco, BRL). Compounds were prepared in a vehicle of either PBS or 20% DMSO in PBS. Five to 10 animals (average weight 40 - 50g) were used in each treatment condition. The animals were injected subcutaneously with either 0.01 U insulin in PBS, followed by 0.1 mL of compound or its vehicle delivered intraperitoneally. Blood samples were taken 0 min, 15 min, 30 min, 1 hr, 2 hr and 4 hr after the administration of the drug or vehicle by tail bleeding. Glucose measurements were made with a Glucometer and Glucose strips (Bayer). The resulting data are shown in Figures 1 and 2. Figure 1 shows the effect of compound 8 in combination with insulin on blood glucose levels in db/db mice. Blood glucose levels at various time points are shown following injections either with insulin in phosphate buffered saline (PBS) or with compound 8 and insulin in PBS. The blood glucose levels are reported as the percentage of the "0-time" values. Figure 2 shows the effect of compound 10 in combination with insulin on blood glucose levels in db/db mice. Blood glucose levels at various time points are shown following injection of db/db mice with compound 10, its vehicle (DMSO) and insulin in PBS. Blood glucose ieveis at various time points following injections either with insulin in PBS or with PBS and DMSO are also shown for comparison. Example 16. Effect on 3T3-HIR Cells 3T3-HIR cells were grown in DMEM with 10% FBS in 6 well dishes. After reaching 90% confluency, the celts were serum starved with 0.1% BSA in DMEM for 16 hr. The cells were stimulated with 3.2, 10, 32, 56 and lOOuJvl of compound in the presence or absence of 2.5 nM insulin for 15 minutes at 37°C. The cells were lysed in the lysis buffer and 20u,g of total cell lysate from each sample was resolved in a 8% SDS-PAGE, transferred onto an Immobilon-P membrane and probed with anti-phosphotyrosine antibody. Insulin receptor [3-subunit and IRS-1 protein bands were identified and quantified by using Phosphorimager (Molecular Dynamics), with the autoradiogram shown in Figure 3. Example 17. Oral pharmaceutical composition preparation - solid dosage formulation A pharmaceutical composition for oral administration may be prepared by combining the following: % w/w Compound of the invention 10% Magnesium stearate 0.5% Starch 2.0% Hydroxypropylmethylcellulose 1.0% Macrocrystalline cellulose 86.5% The mixture may be compressed to tablets, or filled into hard gelatin capsules. The tablet may be coated by applying a suspension of film former (e.g. hydroxypropytmethylcellulose), pigment (e.g. titanium dioxide) and plasticiser (e.g. diethyl phthalate) and drying the film by evaporation of the solvent. The film coat can comprise 2.0% to 6.0% of the tablet weight, preferably about 3.0%. Exampie 18. Oral pharmaceutical composilion preparation - capsule A pharmaceutical composition of a compound of the invention suitable for oral administration may also be prepared by combining the following: % w/w Compound of the invention 20% Polyethylene glycol 80% The medicinal compound is dispersed or dissolved in the liquid carrier, with a thickening agent added, if required. The formulation is then enclosed in a soft gelatin capsule by suitable technology. Example 19. Pharmaceutical composition for parenteral administration A pharmaceutical composition for parenteral administration may be prepared by combining the following: Preferred Level Compound of formula I-VHI 1.0% Saline 99.0% The solution is sterilized and sealed in sterile containers. All documents cited in the above specification are herein incorporated by reference. Various modifications and variations of the present invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in the art are intended to be within the scope of the following claims. heteroaryl, heterocycly), substituted heterocyclyl, aryl(lower)alkyl, substituted aryl(lower)alkyl, heteroaryl (lower)alkyl, substituted heteroaryl(lower)alkyl, or lower alkenyl, or R1 and R2 together with the conjoining nitrogen are C3-C9 heteroaryl, C3-C5 heterocyclyl, or both R1 and R2 are oxygen and together with the conjoining nitrogen form -NO2; R3 is a substituent on the B ring and is -S02OR6, -C(0)OR6, -S02NR62, -C(0)NR62 Or tetrazolyl; the linker -WY- between the naphthyl and phenyl intersects the A ring of the naphthyl and is, independently, -C(0)NR7-, -NR"C(O)-, -C(0)0-, -OC(O)-, -CH=CH-, -NR7CH2-, -CH2NR7-, -NR7C(0)NR7-, -NR7C(O)0-, -OC(0)NR7-, -NR7S02O, -OS02NR7-, -OC(0)0-, -S02NR7-, -NR7S02-, -OS02-, or -S020-; each R4 and Rs is, independently, hydrogen, aifcyl, R1 "-substituted alkyl, aryf, R "-substituted aryl, aryl(lower)aIky!, Rn-substituted aryl(lower)alkyl, Rn-substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, R11 -substituted heteroaryl(lower)alkyl, heterocyclyl, R1"-substituted heterocyclyl, or lower alkenyl; each R6 and R7 is, independently, hydrogen or lower alkyl; each Z is a non-interfering substituent; each x and v is, independently, 0,1, 2 or 3; each R8 is, independently, hydrogen, alkyl, substituted alkyl, aryl(lower)alkyl, substituted aryl(lower)alkyl, substituted heteroaryl, heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryl(lower)alkyl, heterocyclyl, substituted heterocyclyl, lower alkenyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR92, -NR9C(0)R9, -OS02R9, -S02OR9, -S02NfR92, or -NR9S02R9; R is aryl, substituted aryl. heteroaryl. or substituted heteroaryl; each R" is. independently. aryl, substituted aryl, alkyl, substituted alky], substituted heteroaryl, heteroaryl. heterocyclyl, substituted hcterocyclyl, lower alkenyl. nitro. halo, cyano. -OR12. -SR"2, -C(0)R"2, -OC(0)RJ2, -C(0)OR12, -NR,2:, -C(0)NRl3;, -NR12C(0)R13, -OS02R13, -S03OR12, -S02NR,22, or -NR12S02R13; and each R9, R12, and Rlj is, independently, hydrogen, lower alkyl, substituted lower alkyl, aryl, substituted ary!, heteroaryl, substituted heteroaryl, heteroaryl(lower)alkyl, substituted heteroaryi(lower)alkyl, heterocyclyl, substituted heterocyclyl, aryl(lower)aikyl, or substituted aryl(lower)alkyl; provided that if R10 is naphthyl, v is 0, and each -WY- is -C(0)NR7- or -NR7C(0>, then Z is not -S02OH; and if R1 or R2 is -C(0)NR4R5, then Ri3 is neither aryl nor substituted aryl, optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceuticaliy acceptable salt thereof. 2. The compound as claimed in claim 1, where each Z is, independently, alkyl, substituted alkyl, cyano, halo, nitro, -SR14, -OR14, or -NR14:; and each R14 is, independently, hydrogen, lower alkyl, or substituted lower alkyl. 3. The compound as claimed in claim 2, where each Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy. 4. The compound as claimed in claim 1, where each x is 0. 5. The compound as claimed in claim 1, where R3 is -S02OR6, -S02NR62, -C(0)OR6, TC(0)NR62 or tetrazolyl. or a pharmaceutiealfy acceptable salt thereof. 8. The compound as claimed in claim 7, where R10 is aryl or substituted arvl, heteroaryi or substituted heteroaryi. 9. The compound as claimed in claim 8. where R,f) is naphthyl or substituted naphthyl, phenyl or substituted phenyl. 10. The compound as claimed in claim 7, where if v is 1, 2, or 3, each RK is, independently, hydrogen, lower alkyl, substituted lower alkyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR92! -NR9C(0)R9, -OS02R9, -SO2OR9, -S02NR9: or -NR9S02R9; and each R9 is, independently, hydrogen or lower alkyl. 11. The compound as claimed in claim 10, where each R8 is, independently, hydrogen, lower alkyl, halo-lower alkyl, nitro, halo, cyano, amino, lower alkyloxy, thio, or -C(0)OR9; and each R9 is, independently, hydrogen or lower a)kyt. 15. The compound of any one as claimed in claims 1, 7, 13, or 14 where each Z is, independently, alkyl, substituted alky I, cyano, halo, nitro, -SRU, -OR"\ or -NR!43: and each R1* is, independently, hydrogen, lower alkyl, or substituted lower alkyl. 16. The compound as claimed in claim 15, where each Z is lower alkyl, halo-lower alkyl, lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy. 17. The compound of any one as claimed in claims 1, 7, or 13, where each x is 0- 18. The compound of any one as claimed in claims 1, 7, 13, or 14, where R3 is -SO2OR6 or -S02NR62, -C(0)OR6, -C(0)NR62 or tetrazolyl. 19. The compound as claimed in claim 18, where R3 is-SChOH, -C(0)OH or tetrazolyl. 20. The compound of any one as claimed in claims 1,7, 13, or 14, where R! is -C(0)R4, -C(0)NR4R5, or -S02R4; and R2 is hydrogen or lower alkyl. 21. The compound as claimed in claim 20, where R4 is lower alkyl, Rn-substituted lower alkyl, aryl, R!l-substituted aryl, aryl(lower)alkyt> R11-substituted aryl(lower)alkyl, heteroaryl(lower)alkyl, or heteroaryl; and R5 is hydrogen or lower alkyl. 22. The compound as claimed in claim 21, where each R is. independently, aryl. R5-substituted aryl, lower alkyl, Rl5-substituted lower alkyl, heteroaryl, nitro. halo, cyano. amino, thio, -ORi:. -C(0)Rt2, -OC(0)R12. -C(0)ORi:-C(0)NRl32, or -NR12C(0)R,:": each Ru and R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, aryl, R,5-substituted an."!, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or R,5-substituted ary!(lower)alkyl; and each R is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl, halo-lower alkyl, or lower alkyloxy, 23. The compound of any one as claimed in claims 1, 7, 13, or 14, where each -WY-linker is, independently, -C(0)NR7-, -NR7C(0)-, -S02NR7-, -NR7S02-, or -NR7C(0)NR7-. aryl(lower)alkyl, heteroaryl(lower)alkyl, R11 -substituted heteroaryl(lower)alkyl, heterocyclyl, R1"-substituted heterocyclyl, heteroaryl, or R!"-substituted heteroaryl; each Rn is, independently, aryl, R1S-substituted aryl, lower alkyl, R15-substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)R12, -OC(0)R12, -C(0)OR12, -C(0)NR!32, or -NR,2C(0)R13; each R12 and R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, aryl, R,5-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or Rls-substituted aryl(lower)alkyl; and R15 is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl. halo-lower alky 1. lower alkyloxy, cyano, halo, thio, amino, nitro, or hydroxy; and x is 0, 1, or 2, optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutically acceptable salt thereof. 26. The compound as claimed in claim 25, where each R3 is -S03H, -C(0)OH or tetrazoiyl; and each R7 is hydrogen. 27. The compound as claimed in claim 26, where x is zero, R3 is -SO3H, and R4 is Rn-substituted phenyl where each Ru is independently lower alkyl, Rls-substituted lower alkyl, lower alkyloxy, cyano, halo, thio, amino, arnido, nitro or hydroxy. ary!(lower)alkyl, heteroaryl(lower)alkyl, R11 -substituted heteroaryl(lower)alkyl, heterocyclyl, R11-substituted beterocyclyl, heteroaryl, or R"-substituted heteroaryl; each R" is, independently, aryl, R15 -substituted aryl, lower alkyl, R,5-substituted lower alkyl, heteroaryl, nitro, haio, cyano, amino, thio, -OR12, -C(0)RJ3, -OC(0)R12, -C(0)OR"2, -C(0)NR132, or -NR12C(0)R13; each R12 and R13 is, independently, hydrogen, lower alkyl, Rl5-substituted lower alkyl, aryl, R1 5substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or R15-substituted aryl(lower)alkyl; and R1 is, independently, baio, thio. amino, niiro. cyano, hydroxy, loueralkyl or ioweraikyloxy; " Zis lower alkyl, halo-lower alkyl. lower alkylox;. cyario, halo, thio. amino, nitro, or hydroxy: and ?i is 0, I, or 2. optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutically acceptable salt thereof. 29. The compound as claimed in claim 28, where each R3 is -S03H, -C(0)OH or tetrazoiyl; and each R7 is hydrogen. aryl(lower)alkyl, heteroaryl(lower)alkyl, R11 -substituted heteroaryl(Iower)alkyl, heterocyclyl, Rn-substituted heterocyclyl, heteroaryl, or Rn-substituted heteroaryl; each R1" is, independently, aryl, R15-substituted aryl, lower alkyl, R15-substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)R12, -OC(0)R12, -C(0)OR12, -C(0)NR,32, or-NR12C(0)Rn; each R12 is, independently, hydrogen, lower alkyl, R1 5substituted lower alkyl, aryl, R15-substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or R1 5substituted aryl(lower)alkyl; each R13 is, independently, hydrogen, lower alkyl, R1 5substituted lower alkyl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or Rl5-substituted aryl(lower)alkyl; Rl! is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl. halo-lower alky], lower alky!ox>. cyano. halo, thio. amino, nitro. or hydroxy: and xis 0, 1, or 2. optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutically acceptable salt thereof. 31. The compound as claimed in claim 30, where each R3 is -S03H, -C(0)OH or tetrazolyl; and each R7 is hydrogen. heterocyclyl, R11-substituted heterocyclyl, heteroaryl, or Rn-substituted heteroaryl; each R8 is, independently, hydrogen, lower alkyl, substituted lower alkyl, nitro, halo, cyano, -OR9, -SR9, -C(0)R9, -OC(0)R9, -C(0)OR9, -NR92, -C(0)NR93, -NR9C(0)R9, -OS02R9, -S02OR9, -S02NR92, or -NR9S02R9; and each R9 is, independently, hydrogen or lower alkyl; R10 is aryl, R15-substituted aryl, heteroaryl, or R,5-substituted heteroaryl; eachR11 is, independently, aryl, R15-substitutedaryl, lower alkyl- R1 5substituted lower alkyl, heteroaryl, nitro, halo, cyano, amino, thio, -OR12, -C(0)R12, -OC(0)R12, -C(O)0R1!, -C(0)NR132, or -NRi:C(0)Ri3; each R12 and R13 is, independently, hydrogen, lower alkyl, R,5-substituted lower alkyl, aryl, R1 5substituted aryl, heteroaryl, heteroaryl(lower)alkyl, aryl(lower)alkyl, or Rl5-substiruted arylflowerjalkyl; and R1S is, independently, halo, thio, amino, nitro, cyano, hydroxy, lower alkyl or lower alkyloxy; where Z is lower alkyl. halo-lower alkyl, lower alkyloxy, cyano, halo. thio. amino, nitro. or hydroxy; and each x is. independently, 0, 1, or 2. optionally in the form of a single stereoisomer or mixture of stereoisomers, or a pharmaceutic ally acceptable salt thereof 33. A compound as claimed in claim 32, where each R3 is -S03H, -C(0)OH or tetrazolyl; and each R7 is hydrogen. 34. The compound as claimed in claim 1, where R2 is hydrogen, R* is phenyl or naphthyl optionally substituted with lower alkyl, lower alkoxy, halo, nitro, carboxy, hydroxy, or sulfo, lower alkyl optionally substituted with phenyl, phenyloxy, lower alkylphenyloxy, lower alkoxyphenyl, lower alkylphenyl, halophenyl, amino, carboxy, naphthyloxy, or lower alkylphenylcarbamoyl, cyclohexyl, furyl, pyridyl, quinoxalyl, or benzofuranyl optionally substituted with lower alkoxy, and R"° is naphthyl optionally substituted with hydroxy or sulfonyl, quinolinyl, or lower alkyl optionally substituted with carboxy or phenyl optionally substituted with hydroxy, or a pharmaceutically acceptable salt thereof. 35. The compound as claimed in claim 34 selected from the group consisting of: 5-({3-[(4-methylphenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylamino)naphthalene-2-sulfonicacid, 5-({3-[(4-methoxyphenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonylammo)naphthalene-2-sulfonicacid, 5-({3-[(3-chIorophenyI)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonyIamino)naphthaiene-2-sulfonicacid, 5-({3-[(3-nirro5-methylphenyl)carbonylamino]-5-[N-(6-sulfonaphthyl)carbamoyl]phenyl}- carbonyIamino)naphthaIene-2-sulfonicacid, and the pharmaceutically acceptable salts thereof. 36. A pharmaceutical composition comprising: (a) a compound of any one as claimed in claims 1 to 36 as an active ingredient; and (b) a pharmaceutical \y acceptable carrier. |
|---|
in-pct-2002-0234-che abstract fig-1.jpg
in-pct-2002-0234-che abstract.pdf
in-pct-2002-0234-che claims-duplcate.pdf
in-pct-2002-0234-che claims.pdf
in-pct-2002-0234-che correspondence-others.pdf
in-pct-2002-0234-che correspondence-po.pdf
in-pct-2002-0234-che description(complete)-duplicate.pdf
in-pct-2002-0234-che description(complete).pdf
in-pct-2002-0234-che drawings.pdf
in-pct-2002-0234-che form-1.pdf
in-pct-2002-0234-che form-13.pdf
in-pct-2002-0234-che form-19.pdf
in-pct-2002-0234-che form-26.pdf
in-pct-2002-0234-che form-3.pdf
in-pct-2002-0234-che form-5.pdf
in-pct-2002-0234-che form-6.pdf
in-pct-2002-0234-che other.pdf
in-pct-2002-0234-che others.pdf
in-pct-2002-0234-che petition.pdf
in-pct-2002-234-che-triplicate claims.pdf
| Patent Number | 214147 | ||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Indian Patent Application Number | IN/PCT/2002/234/CHE | ||||||||||||||||||||||||
| PG Journal Number | 13/2008 | ||||||||||||||||||||||||
| Publication Date | 31-Mar-2008 | ||||||||||||||||||||||||
| Grant Date | 05-Feb-2008 | ||||||||||||||||||||||||
| Date of Filing | 12-Feb-2002 | ||||||||||||||||||||||||
| Name of Patentee | TELIK, INC | ||||||||||||||||||||||||
| Applicant Address | 750 Gateway Boulevard, South San Francisco, CA 94080, | ||||||||||||||||||||||||
Inventors:
|
|||||||||||||||||||||||||
| PCT International Classification Number | C07C 237/42 | ||||||||||||||||||||||||
| PCT International Application Number | PCT/US2000/020909 | ||||||||||||||||||||||||
| PCT International Filing date | 2000-07-28 | ||||||||||||||||||||||||
PCT Conventions:
|
|||||||||||||||||||||||||