AU5257699A - Use of thiazolidinediones to prevent or delay onset of NIDDM - Google Patents

Description

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Applicant: SANKYO COMPANY LIMITED Invention Title: USE OF THIAZOLIDINEDIONES TO PREVENT OR DELAY ONSET OF NIDDM eb S S

S

5* 5

*S

S.

S S SI.. S S S SS S 55 55555.

55555S The following statement is a full description of this invention, including the best method of performing it known to

US:

-1A- USE OF THIAZOLIDINEDIONES TO PREVENT OR DELAY ONSET OF NIDDM FIELD OF TEE INVENTION The present invention pertains to a number of S" compounds which can be used to treat impaired glucose intolerance in order to prevent or delay the onset of noninsulin-dependent diabetes mellitus -(NIDDM). More specifically, the present invention involves in one embodiment administering to a patient certain known thiazolidinedione derivatives and related antihyperglycemic agents which reduce fasting insulin levels and return normal glucose tolerance to an o:*o individual, thus preventing or delaying the onset of NIDDM or complications resulting therefrom.

BACKGROUND

Diabetes is one of the most prevalent chronic disorders worldwide with significant personal and financial costs for patients and their families, as well as for society. Different types of diabetes exist with distinct etiologies and pathogeneses. For example, diabetes mellitus is a disorder of carbohydrate metabolism, characterized by hyperglycemia -2and glycosuria and resulting from inadequate production or utilization of insulin.

Diabetes mellitus often develops from certain at risk populations, one such population is individuals with impaired glucose tolerance (IGT). Impaired glucose tolerance is a condition intermediate between frank, noninsulin-dependent diabetes mellitus and normal glucose tolerance in which the affected person's postprandial glucose response is abnormal as assessed by 2-hour postprandial plasma glucose levels. This

IGT

population progresses to a certain form of diabetes mellitus, specifically noninsulin-dependent diabetes mellitus

(NIDDM)...

NIDDM or otherwise referred to as Type ii diabetes is the form of diabetes mellitus which occurs .predominantly in adults in whom adequate production of insulin is available for use, yet a defect exists in insulin-mediated utilization and metabolism of glucose -n erph-- ral tisues. it has been shown that for some people with diabetes a genetic predisposition results in a mutation in the gene(s) coding for insulin and/or the insulin receptor and/or insulin-mediated signal transduction factor(s), thereby resulting in ineffective insulin and/or insulin-mediated effects thus impairing the utilization or metabolism of glucose. The population with impaired glucose tolerance progresses to NIDDM at a rate of 51 to 10 of cases per year.

Failure to treat NIDDM can result in mortality due to cardiovascular disease and in other diabetic complications including retinopathy, nephropathy, and peripheral neuropathy. For many years treatment of NIDDM has involved a program aimed at lowering blood sugar with a combination of diet and exercise.

Alternatively, treatment of NIDDM involved oral hypoglycemic agents, such as sulfonylureas alone or in -3combination with insulin injections. Recently, alphaglucosidase inhibitors, such as acarbose, have been shown to be effective in reducing the postprandial rise in blood glucose (Lefevre, et al., Drugs 1992;44: 29-38). In Europe and Canada another treatment used primarily in obese diabetics is metformin, a biguanide.

In any event, what is required is a method of treating populations experiencing impaired glucose tolerance in order to prevent or delay the onset of NIDDM thereby bringing relief of symptoms, improving the quality of life, preventing acute and long-term complications, reducing mortality and treating accompanying disorders of those at risk for NIDDM. The methods of using the disclosed compounds for treating populations experiencing impaired glucose tolerance to prevent or delay the onset of IIDDM as taught herein oe: meet these objectives.

Compounds useful for practicing the present invention, and methods of making these compounds are known. Some of these compounds are disclosed in W• Oo o 91/07107; WO 92/02520; WO 94/01433; WO 89/08651; JP Kokai 69383/92; U.S. Patent Nos. 4,287,200; 4,340,605; .0o.

4,438,141; 4,444,779; 4,461,902; 4,572,912; 4,687,777; 4,703,052; 4,725,610; 4,873,255; 4,897,393; 4,897,405; 4,918,091; 4,948,900; 5,002,953; 5,061,717; 5,120,754; 5,132,317; 5,194,443; 5,223,522; 5,232,925; and 5,260,445. The active compounds disclosed in these publications are useful as therapeutic agents for the treatment of diabetes, hyperglycemia, hypercholesterolemia, and hyperlipidemia. The disclosure of these publications are incorporated herein by reference in particular with respect to the active compounds disclosed therein, and methods of preparation thereof. These compounds are useful for the treatment of impaired glucose tolerance (IGI) in order to prevent or delay onset of NIDDM and complications resulting therefrom, in accordance with the present invention.

-4- There is no disclosure in the above-identified references to use the compounds identified in this present application in the treatment of populations experiencing impaired glucose tolerance in order to prevent or delay the onset of NIDDM and complications resulting therefrom.

SUMMARY OF THE INVENTION The present invention provides a method for the treatment of impaired glucose tolerance in order to Prevent or delay the onset of NIDDM. It is known that persons with impaired glucose tolerance have a much higher rate of progression to NIDDM than persons with normal glucose tolerance. Saad, et al., New Enql J Med 1988; 319:1500-6. If impaired glucose tolerance can be normalized, it is likely that the progression to NIDDM will be delayed or prevented in this population.

Compounds useful for practicing the present invention reduce fasting insulin levels, improve insulin sensitivity, and return glucose tolerance to the normal range for many individuals. As agents having:the aforementioned effects (in the return of glucose tolerance), the compounds of the following formulas are useful in prophylactically treating individuals to prevent or delay the onset of NIDDM.

5 Accordingly, the present invention is the use of compounds of Formula I wherein R 1 and R 2 are the same or different and each represents a hydrogen atom or a CI-Cs alkyl group;

R

3 represents a hydrogen atom, a Ci-C 6 aliphatic acyl group, an alicyclic acyl group, an aromatic acyl group, a 15 heterocyclic acyl group, an araliphatic acyl group, a (Ci-C 6 alkoxy)carbonyl group, or an aralkyloxycarbonyl group; R and R 5 are the same or different and each represents a hydrogen atom, a Ci-C 5 alkyl group or a Ci-C 20 alkoxy group, or R and R' together represent a Ci-C 4 alkylenedioxy group; n is 1, 2, or 3 W represents the -CH 2 >CO, or CH-OR 6 group (in which R 6 represents any one of the atoms or groups defined for R 3 and may be the same as or different from R 3 and Y and Z are the same or different and each represents an oxygen atom or an imino group; and pharmaceutically acceptable salts thereof.

Also, according to the present invention there is provided a compound according to Formula IX

^IX

3 5

O

E:\LCo1eS\Keep\Speci\div of 17709-97.doe 1/10/99 6 or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically acceptable solvate thereof, wherein: As represents a substituted or unsubstituted aromatic heterocyclyl group; As represents a benzene ring having in total up to substituents; Xg represents O,S, or NR 32 wherein R 32 represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;

Y

2 represents 0 or S; 15 R 31 represents a hydrogen atom or an alkyl, aralkyl, or aryl group; and n represents an integer in the range from 2 to 6 in the manufacture of a medicament used for the prevention or delay of the onset of noninsulin-dependent diabetes S- 20 mellitus in a subject suffering from impaired glucose intolerance.

The present invention is also the use of compounds of the Formula II

II

wherein R 11 is substituted or unsubstituted alkyl, alkoxy, E:\LColes\Keep\Speci\div of 17709-97.doc 1/10/99 6a cycloalkyl, phenylalkyl, phenyl, aromatic acyl group, a or 6-membered heterocyclic group including 1 or 2 heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur or a group of the formula wherein R 13 and R 14 are the same or different and each is lower alkyl or R 13 and R 14 are combined to each other either directly or as interrupted by a heteroatom selected from the group consisting of nitrogen, oxygen, and sulfur to 15 form a 5- or 6-membered ring; wherein R12 means a bond or a lower alkylene group; and wherein Li and L 2 are the same or different and each is hydrogen or lower alkyl or Li and L2 are combined to form an alkylene group; or a pharmaceutically acceptable salt thereof.

The present invention is also the use of *compounds of the Formula III E:\LCo1es\1eep\Speci\div of 17709-97.doc 1/10/99 -7- /0 I A 0 s 16 wherein Ris and R 1 5 are independently hydrogen, lower alkyl containing 1 to 6 carbon atoms, alkoxy containing I to 6 carbon atoms, halogen, ethynyl, nitrile, methylthio, trifluoromethyl, vinyl, nitro, or halogen substituted benzyloxy; n is 0 to 4 and the pharmaceutically .acceptable salts thereof.

~The present invention is also directed to the use of compounds of the Formula

IV

O

wherein the dotted line represents a bond or no bond; V is -CH CH-, -N CH-, -CH N- or S; D is CH2, CHO, CO, C NOR, or CH

CH;

x is S, O, NR1,, -CH N or -N

CH;

Y is CH or N; Z is hydrogen, alkyl, (C-C7) cycloalkyl, phenyl, naphthyl, pyridyl, furyl, thienyl, or phenyl mono- or disubstituted with the same or different groups which are (CI-C3)alkyl, trifluoromethyl, (Cl-C3)alkoxy, fluoro, chloro, or bromo; Z, is hydrogen or (C,-C,)alkyl; R,7 and R, are each independently hydrogen or methyl; and n is 1, 2, or 3; -8the pharmaceutically acceptable cationic salts thereof; and the pharmaceutically acceptable acid addition salts thereof when the compound contains a basic nitrogen.

The present invention is also directed to the use of compounds of the Formula V x 2 o 0 wherein the dotted line represents a bond or no bond; A and B. are each independently CH or N, with the proviso that when A or B is N, the other is CH;

X

1 is S, SO, SO 2

CH

2 CHOH, or CO; n is 0 or 1;

Y

1 is CHR, or R 21 with the proviso that when n is 1 and SY is NR2,, X, is so onr CO; is CHR22 CHCH, C-C

OCH

2 SCH2, SOCH 2 or SO 2

CH,;

:"19 R2o, RV, and R 22 are each independently hydrogen or methyl; and

X

2 and X 3 are each independently hydrogen, methyl, trifluoromethyl, phenyl, benzyl, hydroxy, methoxy, phenoxy, benzyloxy, bromo, chloro, or fluoro; a pharmaceutically acceptable cationic salt thereof; or a pharmaceutically acceptable acid addition salt thereof when A or B is N.

The present invention also relates to the use of compounds of the Formula VI -9c 3

O

or a pharmaceutically acceptable salt thereof wherein R 23 is alkyl of 1 to 6 carbon atoms, cycloalkyl of 3 to 7 carbon atoms, phenyl or mono- or di-substituted phenyl wherein said substituents are independently alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 3 carbon atoms, halogen, or trifluoromethyl.

The present invention also provides the use of a compound of Formula VII

*S

OO L* NE VII or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically acceptable solvate thereof, wherein:

A

2 represents an alkyl group, a substituted or unsubstituted aryl group, or an aralkyl group wherein the alkylene or the aryl moiety may be substituted or unsubstituted;

A

3 represents a benzene ring having in total up to 3 optional substituents;

R

2 4 represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group wherein the alkyl or the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group; or A. together with represents substituted or unsubstituted

C

2 polymethylene group, optional substituents for the polymethylene group being selected from alkyl or aryl or adjacent substituents together with the methylene carbon atoms to which they are attached form a substituted or unsubstituted phenylene group;

R

2 s and R 2 d each represent hydrogen, or R 25 and R together represent a bond;

X

4 represents 0 or S; and n represents an integer in the range of from 2 to 6.

The present invention also provides the use of a compound of. Formula VIII or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutical'I acceptable solvate therefor, wherein:

R

27 and R 28 each independently represent an alkyl group, a substituted or unsubstituted aryl group, or an aralkyl group being substituted or unsubstituted in the aryl or alkyl moiety; or R 7 together with R 28 represents a linking group, the linking group consisting of an optionally substituted methylene group and .either a further optionally substituted methylene group or an 0 or S atom, ooo *optional substituents for the said methylene groups being selected from alkyl-, aryl, or aralkyl, or substituents oo.. of adjacent methylene groups together with the carbon atoms to which they are attached form a substituted or unsubstituted phenylene group; R9 and R30 each represent hydrogen, or R 2 9 and R 30 together represent a bond;

A

4 represents a benzene ring having in total up to 3 optional substituents; -11- Xs represents 0 or S; and n represents an integer in the range of from 2 to 6.

The present invention also provides the use of a compound of Formula

IX

D 0 0 or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically acceptable solvate thereof, wherein: A. represents a substituted or unsubstituted aromatic heterocyclyl group; A, represents a benzene ring having -in total up to 5 substituents; X, represents o, S, or NRa 2 wherein represents ahydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;

Y

2 represents 0 or S; represents an alkyl, aralkyl, or aryl group; and n represents an integer in the range of from 2 to 6.

Suitable aromatic heterocyclyl groups include substituted or unsubstituted, single or fused ring aromatic heterocyclyl groups comprising up to 4 hetero atoms'in each ring selected from oxygen, sulphur, or nitrogen.

Favored aromatic heterocyclyl groups include substituted or unsubstituted single ring aromatic heterocyclyl groups having 4 to 7 ring atoms, preferably or 6 ring atoms.

-12- In particular, the aromatic heterocyclyl group comprises i, 2, or 3 heteroatoms, especially 1 or 2, selected from oxygen, sulphur, or nitrogen.

Suitable values for As when it represents a -membered aromatic heterocyclyl group include thiazolyl and oxazoyl, especially oxazoyl.

Suitable values for As when it represents a 6-membered aromatic heterocyclyl group include pyridyl or pyrimidinyl.

Suitable R. represents an alkyl group, in particular a C,_ 8 alkyl group, for example a methyl group.

Preferably, A. represents a moiety of formula or N

N

KN

s a^ 'Y N (a (b wherein: and R4 each independently represents a hydrogen atom, an alkyl group, or a substituted or unsubstituted aryl roup or when Rand R4 are each attached to adjacent Scarbon atoms, then P and R 3 together with the carbon atoms to which they are attached form a benzene ring *wherein each carbon atom represented by R. and R S• together may be substituted or unsubstituted; and in the moiety of Formula

X

7 represents oxygen or sulphur.

In one favored aspect R3 and R 34 together represent a moiety of Formula -13- (d) wherein R3 5 and R3, each independently represent hydrogen, halogen, substituted or unsubstituted alkyl, or alkoxy.

The present invention also provides for the use of compounds for Formula X or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically :.:acceptable solvate thereof, wherein:

A

7 represents a substituted or unsubstituted aryl\group; A. represents a benzene ring having in total up to 5 substituents; X. represents o, S, or NR:z wherein R 39 represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;

Y

3 represents 0 or S;

R

37 represents hydrogen; R3. represents hydrogen or an alkyl, aralkyl, or aryl group or R 3 7 together with R3 represents a bond; and n represents an integer in the range of from 2 to 6.

-14- The present invention is also directed to the use of compounds of the Formula 0 _o A'

A

2 0 or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically acceptable solvate thereof, wherein:

A

1 represents a substituted or unsubstituted aromatic heterocyclyl group;

R

i represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group;

A

2 represents a benzene ring navng in total uptp five S: substituents; and n represents an integer in the range of from 2 to 6.

Ssuitable aromatic heterocyclyl groups include substituted or unsubstituted, single or fused ring aromatic heterocyclyl groups comprising up to 4 hetero atoms in each ring selected from oxygen, sulphur or nitrogen.

Favoured aromatic heterocyclyl groups include substituted or unsubstituted single ring aromatic heterocyclyl groups having 4 to 7 ring atoms, preferably 5 or 6 ring atoms.

In particular, the aromatic heterocyclyl group comprises 1, 2 or 3 heteroatoms, especially 1 or 2, selected from oxygen, sulphur or nitrogen.

Suitable values for A' when it represents aromatic heterocyclyl group include thiazolyl and oxazolyl, especially oxazolyl.

Suitable values for A' when it represents a 6-membered aromatic heterocyclyl group include pyridyl or pyrimidinyl.

Preferably, A' represents a moiety of formula (b) or R 4 Cb) (C) wherein: R4and R 6 each independently represents a hydrogen atom, an alkyl group or a substituted or unsubstituted aryl group or when R4 and R 5 are each attached to adjacent carbon .atoms, then R 4 and R s together with the carbon atoms to which they are attached form a benzene ring wherein each carbon atom represented by R 4 and R 5 together may be substituted or unsubstituted; and in the moiety of formula (a) X represents oxygen or sulphur.

The present invention is also directed to the use of compounds of the Formulas -16or a pharmaceutically acceptable salt thereof wherein the dotted line represents a bond or no bond; R is cycloalkyl of three to seven carbon atoms, naphthyl, thienyl, furyl, phenyl or substituted phenyl wherein said substituent is alkyl of one to three carbon atoms, alkoxy of one to three carbon atoms, trifluoromethyl, chloro, fluoro or bis(trifluoromethyl); R, is alkyl of one to three carbon atoms;'X is O or C=0; a is 0 or S; and B is N or CH.

A preferred group of compounds are those of formula XI wherein the dotted line represents no bond, R, is methyl, X is 0 and A is O. Especially preferred within this group are the compounds where R is phenyl, 2-naphthyl and A second group of preferred compounds are those of formula XII wherein the dotted line represents no bond, R i is methyl and A is 0. Especially preferred within this groupare compounds where B is CH and R is phenyl, p-tolyl, -tolyl, cyclohexyl and 2-naphthyl. Also especially preferred is the compound where B is N and R is phenyl.

A still further embodiment of the present invention is the use of pharmaceutical composition for administering an effective amount of a compound of -17the preceding Formulas I through XIII along with a pharmaceutically acceptable carrier in unit dosage form in the treatment methods mentioned above.

DETAILED DESCRIPTION OF THE PREFERRED

EMBODIMENTS

The compounds used in the treatment methods of the invention, which are 5-[4-(chromoanalkoy) benzyljthiazolidene deijivatives, may be represented by the Formulas and (Ic)

R

R

9* 4 N )(CHzh) CH-CH-C==Y (Ib) :RO C

R

2 1a *9 z

R

N(CH

2 CHF-~CH -C -y (1c) RO C

NH

R OR (in which R 2 R 3 R 4

R

5 Ra, n, Y, and Z are as defined above) and include pharmaceutically acceptable salts thereof.

In the compounds of the invention, where R 1 or R 2 represents an alkyl group, this may be a straight or branched chain alkyl group having from 1 to 5 carbon -18atoms and is preferably a primary or secondary alkyl group, for example the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, or isopentyl group.

Where R 3

R

e or R e represents an aliphatic acyl group, this preferably has from 1 to 6 carbon atoms and may include one or more carbon-carbon double or triple bonds. Examples of such groups include the formyl, acetyl, propionyl, butyryl, isobutyryl, pivaloyl, hexanoyl, acryloyl, methacryloyl, and crotonyl groups.

Where R 3 Re, or Re' represents an alicyclic acyl group, it is preferably a cyclopentanecarbonyl, cyclohexanecarbonyl, or cycloheptanecarbonyl group.

Where R 3 Re, or R 8 represents an aromatic acyl group, the aromatic moiety thereof may optionally have one or.more substituents (for example, nitro, amino, alkylamino, dialkylamino, alkoxy, halo, alkyl, or hydroxy substituents); examples of such aromatic acyl groups Sincluded the benzoyl, p-nitrobenzoyl, m-fluorobenzoyl, o-chlorobenzoyl, p-aminobenzoyl, m-(dimethylamino)benzoyl, o-methoxybenzoyl, 3,4-dichlorobenzoyl, t-butyl-4-hydroxybenzoyl, and 1-naphthoyl groups.

Where R 3 Re, or R e represents a heterocyclic acyl group, the heterocyclic moiety thereof preferably has one or more, preferably one, oxygen, sulfur, or nitrogen hetero atoms and has from 4 to 7 ring atoms; examples of such heterocyclic acyl groups include the 2-furoyl, 3-thenoyl, 3-pyridinecarbonyl (nicotinoyl), and 4 -pyridinecarbonyl groups.

Where

R

3 Re, or R 8 represents an araliphatic acyl group, the aliphatic moiety thereof may optionally have one or more carbon-carbon double or triple bonds and the aryl moiety thereof may optionally have one or more substituents (for example, nitro, amino, alkylamino, dialkylamino, alkoxy, halo, alkyl, or hydroxy substituents); examples of such araliphatic acyl groups -19include the phenylacetyl, p-chlorophenylacetyl, phenylpropionyl, and cinnamoyl groups.

Where R 3

R

6 or R 8 represents a (C-C alkoxy)carbonyl group, the alkyl moiety thereof may be any one of those alkyl groups as defined for R' and R 2 but is preferably a methyl or ethyl group, and the alkoxycarbonyl group represented by R 3

R

e or is therefore preferably a methoxycarbonyl or ethoxycarbonyl group.

Where R 3 Re, or R' represents an aralkyloxycarbonyl group, the aralkyl moiety thereof may be any one of those included within the araliphatic acyl group represented by

R

3

R

8 or Re', but is preferably a benzyloxycarbonyl group.

Where R 4 and R 5 represent alkyl groups, they may be the same or different and may be straight or branched chain alkyl groups. They preferably have from 1 to 5 carbon atoms and examples include the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, and isopentyl groups.

SWhere R 4 and R 5 represent alkoxy groups, these may be the same or different and may be straight or branched chain groups, preferably having from 1 to 4 carbon atoms.

Examples include the methoxy, ethoxy, propoxy, isopropoxy, and butoxy groups. Alternatively, R 4 and R may together represent a C 1

-C

4 alkylenedioxy group, more preferably a methylenedioxy or ethylenedioxy group.

Preferred classes of compounds of Formula I are as follows: Compounds in which R 3 represents a hydrogen atom, a aliphatic acyl group, an aromatic acyl group, or a heterocyclic acyl group.

Compounds in which Y represents an oxygen atom;

R

1 and R 2 are the same or different and each represents a hydrogen atom or a C,-C s alkyl group; R 3 represents a hydrogen atom, a aliphatic acyl group, an aromatic acyl group, or a pyridinecarbonyl group; and R 4 and R 5 are the same or different and each represents a hydrogen atom, a C 1

-C

5 alkyl group, or a C, or C 2 alkoxy group.

Compounds as defined in above, in which: R 1

R

2

R

4 and R 5 are the same or different and each represents a hydrogen atom or a C,-C s alkyl group; n is 1 or 2; and W represents the -CH 2 or >CO group.

Compounds as defined in above, in which R 3 represents a hydrogen atom, a C,-C 5 aliphatic acyl group, a benzoyl group, or a nicotinyl group.

Compounds as defined in above, in which: R' and R 4 are the same or different and each represents a

C,-C

5 alkyl group; R 2 and R 5 are the same or different and each represents the hydrogen atom or the methyl group; and R 3 represents a hydrogen atom or a C 1

-C

4 aliphatic acyl group.

Compounds in which: W represents the -CH 2 or >CO group; Y and Z both represent oxygen atoms; n is 1 or 2; R 1 and R 4 are the same or different and each. represents a C,-C 4 alkyl group; R 2 and R 5 are the same or different and each represents the hydrogen atom or the methyl group;, and R 3 represents a hydrogen atom or a C-C 4 aliphatic acyl group.

Compounds as defined in above, in which n is 1.

Compounds as defined in or above, in 'which W represents the -CH 2 group.

Preferred compounds among the compounds of Formula I are those wherein: 9 9* R' is a C -C 4 alkyl group, more preferably a methyl o* r isobutyl group, most preferably a methyl group;

R

2 is a hydrogen atom or a C,-C 4 alkyl group, preferably a hydrogen atom, or a methyl or isopropyl group, more preferably a hydrogen atom or a methyl group, most preferably a methyl group; -21-

R

3 is a hydrogen atom, a C,-C 4 aliphatic acyl group, an aromatic acyl group or a pyridinecarbonyl group, preferably a hydrogen atom, or an acetyl, butyryl, benzoyl, or nicotinyl group, more preferably a hydrogen atom or an acetyl, butyryl or benzoyl group, most preferably a hydrogen atom or an acetyl group;

R

4 is a hydrogen atom, a C,-C 4 alkyl group or a C, or C; alkoxy group, preferably a methyl, isopropyl, t-butyl, or methoxy group, more preferably a methyl or t-butyl group, most preferably a methyl group;

R

5 is a hydrogen atom, a C,-C 4 alkyl group or a C, or C, alkoxy group, preferably a hydrogen atom, or a methyl or methoxy group, more preferably a hydrogen atom or a methyl group, and most preferably a methyl group; n'is 1 or 2, preferably 1; Y is an oxygen atom; Z is an oxygen atom or an imino group, most preferably an oxygen atom; and W is a -CH 2 or >C=O group, preferably a -CH 2 group.

Referring to the general Formula II, the substituents may be any from 1 to 3 selected from nitro, amino, alkylamino, dialkylamino, alkoxy, halo, alkyl, or hydroxy, the aromatic acyl group may be benzoyl and S naphthoyl. The alkyl group R 11 may be a straight chain or

S

branched alkyl of 1 to 10 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, i-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, and n-decyl; the cycloalkyl group R 11 may be a cycloalkyl groupsof 3 to 7 carbon atoms, such as cyclopropyl, cyclopentyl, cyclohexyl, and cycloheptyl; and the phenylalkyl group R, 1 may be a phenylalkyl group of 7 to 11 carbon atoms such as benzyl and phenethyl. As examples of the heterocyclic group R 11 may be mentioned or 6-membered groups each including 1 or 2 hetero-atoms -22selected from among nitrogen, oxygen, and sulfur, such as pyridyl, thienyl, furyl, thiazolyl, etc. When R 11 is N3 the lower alkyls R 13 and R 14 may each be a lower alkyl of 1 to 4 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, and n-butyl. When R 13 and R 14 are combined to each other to form a 5- or 6-membered heterocyclic group as taken together with the adjacent N atom, in the form of

H

'N-x o o this heterocyclic group may further include a heteroatom selected from among nitrogen, oxygen, and sulfur as exemplified by piperidino, morpholino, pyrrolidino, and piperazino. The lower alkylene group R 12 may contain 1 to 3 carbon atoms and thus may be, for example, methylene, ethylene, or trimethylene. The bond R 12 is equivalent to the symbol or the like which is used in i*i chemical structural formulas, and when R 12 represents such a bond, the compound of general Formula II is represented by the following general Formula II(a) iliafllwn enrlFrml Ia M 0 -23- Li 11 I I (a) Thus, when R 12 is a bond, the atoms adjacent thereto on both sides are directly combined together. As examples of the lower alkyls L, and there may be mentioned lower alkyl groups of 1 to 3 carbon atoms, such as methyl and ethyl. The alkylene group formed as L, and L. are joined together is a group of the formula

-(CH

2 n [where n is an integer of 2 to The cycloalkyl, phenylalkyl, phenyl, and heterocyclic groups mentioned above, as well as said heterocyclic group

L

.F C- C- C may have 1 to 3 substituents in optional positions on the respective rings. As examples of such substituents may be mentioned lower alkyls methyl, ethyl, etc.), lower alkoxy groups methoxy, ethoxy, etc.), halogens chlorine, bromine, etc.), and hydroxyl.

The case also falls within the scope of the general Formula II that an alkylenedioxy group of the formula

-(CH

2 (is an integer of 1 to such as methylenedioxy, is attached to the two adjacent carbon atoms on the ring to form an additional ring.

The preferred compounds of Formula III are those wherein R 1 s and are independently hydrogen, lower alkyl containing I to 6 carbon atoms, alkoxy containing 1 to 6 carbon atoms, halogen, ethynyl, nitrile, -24trifluoromethyl, vinyl, or nitro; n is 1 or 2 and the pharmaceutically acceptable salts thereof.

Preferred in Formula IV are compounds wherein the dotted line represents no bond, particularly wherein D is CO or CHOH. More preferred are compounds wherein V is -CH CH-, -CH N- or S and n is 2, particularly those compounds wherein X is O and Y is N, X is S and Y is N, X is S and Y is CH or X is -CH N- and Y is CH. In the most preferred compounds X is 0 or S and Y is N forming an oxazol-4-yl, oxazol-5-yl, thiazol-4-yl, or thiazolgroup; most particularly a 2 -[(2-thienyl), (2-furyl), phenyl, or substituted 4-oxazolyl group.

The preferred compounds in Formula V are: a) those wherein the dotted line represents no bond, A and B are each CH, X, is CO, n is 0, R 19 is hydrogen,

Z

2 is CHCH 2 or CH=CH and X 3 is hydrogen, particularly when X 2 is hydrogen, 2-methoxy, 4-benzyloxy, or 4-phenylZ.

b) those wherein A and B are each CH, X, is S or

SO

2 n is 0, R 19 is hydrogen, Z 2 is CH 2

CH

2 and X 3 is hydrogen, particularly when X 2 is hydrogen or 4-chloro.

A preferred group of compounds is that of Formula VI wherein R 23 is alkyl, (C 3

-C

7 cycloalkyl, phenyl, halophenyl, or (C,-C,)alkylphenyl. Especially preferred within this group are the compounds where R 2 3 is phenyl, *o methylphenyl, fluorophenyl, chlorophenyl, or cyclohexyl.

When used herein with regard to Formulas VII *through X, the term "aryl" includes phenyl and naphthyl, suitably phenyl, optionally substituted with up to preferably up to 3, groups selected from halogen, alkyl, phenyl, alkoxy, haloalkyl, hydroxy, amino, nitro, carboxy, alkoxycarbonyl, alkoxycarbonylalkyl, alkylcarbonyloxy, or alkylcarbonyl groups.

The term "halogen" refers to fluorine, chlorine, bromine, and iodine; preferably chlorine.

The terms "alkyl"' and "alkoxy"l relate to groups having straight or branched carbon chains, containing up to 12 carbon atoms.

Suitable alkyl groups are Cl- 12 alikyl groups, especially Cl.a alkyl groups, e.g. methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, or tert-butyl groups.I Suitable substituents for any alkyl group include those indicated above-in relation to the term "aryl".

Suitable substituents for any heterocyclyl group include up to 4 substituents selected from the group consisting of alkyl., alkoxy, aryl, and halogen or any 2 substituents on adjacent carbon atoms, together with the carbon atoms to which they are attached, may form an aryl 'group, preferably a benzene ring, and wherein the carbon atoms of the aryl group represented by the said 2 substituents may themselves be substituted or unsubstituted.

Specific examples of compounds of the present invention are given in the following list: (3,4-dihydro- 6-hydroxy- 2,5,7, 8-tetramethyl-2H-l-benzopyran-2-yl) methoxy) phenyl]methyl) 4-thiazolidinedione: (troglitazone); 4- (2-naphthylmethyl) -1,2,3 ,5-oxathiadiazole-2-oxide; 5-(4-[2-(N-(benzoxazol-2-yl)-N-methylamino]ethoxy]benzyl.)-5-methylthiazolidine-2 ,4-dione; 5-j4-2-(2,4-dioxo-5-phenylthiazolidin-3-yl)ethoxy]benzyl] thiazolidine-2, 4-dione; 5-(4-[2-(N-methyl-N- (phenoxycarbonyl) amino] ethoxy] benzyl]thiazolidine-2 ,4-dione; 5-[4-(2-phenoxyethoxy) benzyl~thiazolidine-2 ,4-dione; -26-

E(

4 -(2-(4-chlorophenyl) ethylsulfonyl]benzyl>thiazolidine.2 4-dione; -[4-3-(5methyl2-phenyloxazol4.yl)propionyl]benzylj thiazolidine-2, 4-dione; 4-f (l-methylcyclohexyl)mnethoxy]benzyljthiadiao lidine-2,4-dione: (ciglitazone); 5.[4(-rx--mehlycoey~mtoy ezlthiadiazolidine.2,4-dione; 4 -2-(5-methyl2-phenyloxazol.

4 -yl) ethoxyl]benzyljthiadizolidione- 2 ,4-dione; 4 f2-(-ethylpyridin-2-yl) ethoxyl]benzyl] thiadiazolidine2, 4 dione: (pioglitazone); (2-benzyl-2, 3-dihydrobenzopyran) thiadiazoline.2,4..dione: (englitazone); 2 thiadiazoline-2,4-dione;.

4-f2- (3-phenylureido) ethoxyl]benzyl~thia-.

'-diazoline-2, 4-dione; Sf 4 [2-(fN-(benzoxazo1.-2-yl>N-.methVlamilethn5benzyj thiadiazoline-2 ,4-diane;.

4 f[3-(-methyl-2-phenyoxazol.4-yl)propionyl]benzyl]thiadiazolne.2,4:do 5-2(5-methyl-2-phenyoxazol.4..ylmethyl)- ~benzofuran-5..ylmethyl] oxazolidine-2 ,4-dione; f[ 4 2 -N-methyl-N-.(2-pyridyl) amino] ethoxy] benzylj thiazoljdine-2, 4-diane; and 5-4[-N(ezxzl2y)Nmtyaioehx] benzyl] oxazolidine-2, 4-diane.

As defined herein, "compl ications of NIDDM"I is referred to as cardiovascular complications or several of the metabolic and circulatory disturbances that are associated with hyperglycemia, insulin resistance, hyperinsulinemia and/or hyperproinsulinemij, delayed insulin release, dyslipidemia, retinopathy, peripheral neuropathy, nephropathy, and hypertension- -27- The compounds of Formulas I through XIII are capable of further forming pharmaceutically acceptable base salts.

The compounds of Formulas I through XIII are capable of further forming both pharmaceutically acceptable acid addition and/or base salts. All of these forms are within the scope of the present invention.

Pharmaceutically acceptable acid addition salts of the compounds of Formulas I through XIII include salts derived from nontoxic inorganic acids such as hydrochloric, nitric, phosphoric, sulfuric, hydrobromic, hydriodic, hydrofluoric, phosphorous, and the like, as well as the salts derived from nontoxic organic acids, such as aliphatic mono- and dicarboxylic acids, phenylsubstituted alkanoic acids, hydroxy alkanoic acids, alkanedioic acids, aromatic acids, aliphatic and aromatic sulfonic acids, etc. Such salts thus include sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, nitrate, phosphate, monohydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, trifluoroacetate, propionate, caprylate, o. isobutyrate, oxalate, malonate, succinate, suberate, sebacate, fumarate, maleate, mandelate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, phthalate, benzenesulfonate, toluenesulfonate, phenylacetate, citrate, lactate, maleate, tartrate, methanesulfonate, and the like. Also contemplated are salts of amino acids such as arginate and the like and gluconate, galacturonate, n-methyl glucamine (see, for example, Berge et al., "Pharmaceutical Salts," Journal of Pharmaceutical Science 1977;66:1-19).

The acid addition salts of said basic compounds are prepared by contacting the free base form with a sufficient amount of the desired acid to produce the salt in the conventional manner. The free base form may be regenerated by contacting the salt form with a base and -28isolating the free base in the conventional manner or as above. The free base forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free base for purposes of the present invention.

Pharmaceutically acceptable base addition salts are formed with metals or amines, such as alkali and alkaline earth metals or organic amines. Examples of metals used as cations are sodium, potassium, magnesium, calcium, and the like. Examples of suitable amines are N,N'-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, dicyclohexylamine, ethylenediamine, N-methylglucamine, and procaine (see, for example, Berge et al., "Pharmaceutical Salts," Journal of Pharmaceutical Science 1977;66:1-19).

The base addition salts of said acidic compounds are prepared by contacting the free acid form with a sufficient amount of the desired base to prodUUUce the salt in the conventional manner. The free acid form may be regenerated by contacting the salt form with an acid and isolating the free acid in the conventional manner or as above. The free acid forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid for purposes of the present invention.

Certain of the compounds of the present invention can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms, including hydrated forms, are equivalent to unsolvated forms and are intended to be encompassed within the scope of the present invention. Certain of the compounds of the present invention possess one or more chiral centers and each center may exist in different configurations. The compounds can, therefore, form stereoisomers. Although these are all represented herein -29by a limited number of molecular formulas, the present invention includes the use of both the individual, isolated isomers and mixtures, including racemates, thereof. Where stereospecific synthesis techniques are employed or optically active compounds are employed as starting materials in the preparation of the compounds, individual isomers may be prepared directly; on the other hand, if a mixture of isomers is prepared, the individual isomers may be obtained by conventional resolution techniques, 6r the mixture may be used as it is, without resolution.

Furthermore, the thiazolidene or oxazolidene part of the compounds of Formulas I through XIII can exist in the form of tautomeric isomers. All of the tautomers are represented by Formulas I through XIII, and are intended to be a part of the present invention.

For preparing pharmaceutical compositions from the compounds of the present invention, pharmaceutically .acceptable carriers cadn be either solid or liquid; Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules. A solid carrier can be one or more substances which may also act as diluents, flavoring agents, binders, preservatives, tablet disintegrating agents, or an encapsulating material.

In powders, the carrier is a finely divided solid which is in a mixture with the finely divided active component.

In tablets, the active component is mixed with the carrier having the necessary binding properties in suitable proportions and compacted in the shape and size desired.

The powders and tablets preferably contain from five or ten to about seventy percent of the active compound.

Suitable carriers are magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch,

__M

gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose, a low melting wax, cocoa butter, and the like. The term "preparation" is intended to include the formulation of the active compound with encapsulating material as a carrier providing a capsule in which the active component with or without other carriers, is surrounded by a carrier, which is thus in association with it. Similarly, cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid dosage forms suitable for oral administration.

For preparing suppositories, a low melting wax, such as a mixture of fatty acid glycerides or cocoa butter, is first melted and the active component is dispersed homogeneously therein, as by stirring. The molten homogenous mixture is then poured into convenient sized molds, allowed to cool, and thereby to solidify.

Liquid form preparations include solutions, suspensions, and emulsions for example, wat r water w Qa L o r water propylene glycol solutions. For parenteral injection liquid preparations can be formulated in solution in aqueous polyethylene glycol solution.

Aqueous solutions suitable for oral use can be prepared by dissolving the active component in water and adding suitable colorants, flavors, stabilizing and thickening agents as desired.

Aqueous suspensions suitable for oral use can be o made by dispersing the finely divided active component in water with viscous material, such as natural or synthetic S* gums, resins, methylcellulose, sodium a.o. carboxymethylcellulose, and other well-known suspending agents.

Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for oral administration. Such liquid forms include solutions, suspensions, and emulsions.

-31- These preparations may contain, in addition to the active component, colorants, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.

The pharmaceutical preparation is preferably in unit dosage form. In such form the preparation is subdivided into unit doses containing appropriate quantities of the active component. The unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules. Also, the unit dosage form can be a capsules, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.

The quantity of active component in a unit dose preparation may be varied or adjusted from 0.1 mg to 100 mg preferably 0.5 mg to 100 mg according to the particular application and the potency of the active component. The composition can, if desired, also contain other compatible therapeutic agents.

o. In therapeutic use in the treatment of at risk populations such as those with impaired glucose tolerance, to prevent or delay the onset of NIDDM and complications arising therefrom, the compounds utilized in the pharmaceutical methods of this invention are administered along with a pharmaceutically acceptable carrier at the initial dosage of about 0.01 mg to about 20 mg per kilogram daily. A daily dose range of about 0.01 mg to about 10 mg per kilogram is preferred. The dosages, however, may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compound being employed.

Determination of the proper dosage for a particular situation is within the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, 32 the dosage is increased by small increments until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day, if desired.

The compounds of Formulas I through XIII are valuable agents in returning an individual to a state of glucose tolerance and therefore preventing or delaying the onset of NIDDM. The following illustrates testing to show that compounds have the disclosed activity, using the preferred compound troglitazone.

EXAMPLE 1 In a blinded, randomized, fixed-dose, parallel-group, placebo-controlled, outpatient trial, the effects of the test compound (compound hydroxy-2,5,7,8-tetramethyl-2H-l-benzopyran-2yl)methoxy]phenly]-methyl]-2,4-thiazolidinedione- (troglitazone), was compared with that of a placebo on glucose tolerance and on insulin sensitivity. The trial in impaired glucose tolerance (IGT) included a 2-week screening period and a 12-week treatment period. Fifty-six patients were randomized to treatment with placebo or 400 mg/day of troglitazone. Oral glucose tolerance tests (OGTT) and frequently sampled intravenous glucose tolerance tests (FSIGTT) to assess insulin sensitivity were performed before study medication, and after 6 weeks and after 12 weeks of randomized treatment.

Patients included in this study were adults in reasonably good health who have IGT by the WHO criteria as demonstrated by OGTT (Harris Hadden Knowler Berrett International Criteria for

M

-33the Diagnosis of Diabetes and Impaired Glucose Tolerance, Diabetes Care 1985;8(6):562-7). Most of the patients that were recruited were relatives of patients with NIDDM, patients with a history of gestational diabetes mellitus, patients with a history of prior abnormal OGTT, or patients with other indicators of insulin resistance (coronary artery disease, obesity, hypertriglyceridemia, and hypertension).

The OGTT was carried out according to the following procedure: Test was administered in the morning after a 10- to 14-hour fast. Water, but not coffee, could be consumed during the fast. Patients were required to remain seated during the test. Study medication was omitted on the morning of the test and taken with lunch.

mL of venous blood was collected into a serum separation tube for baseline.

1.75-g/kg body weight, up to a maximum of 75 g of glucose was administered orally as a liquid beverage to be consumed over no more than 5 minutes.

5 mL of venous blood was collected into a serum separation tube every 30 minutes up to 2 hours, timing from the start of ingestion of the glucose.

Each blood specimen was allowed to clot for minutes. The specimens were centrifuged until clot and serum were separated by a well-formed polymer barrier. Serum was transferred from each specimen, using separate pipettes for each, into plastic vials and frozen immediately. If centrifuging of specimens was delayed for any reason, specimens were refrigerated and centrifuged as soon as possible.

Frozen specimens were examined for oral glucose tolerance according to the WHO diagnostic criteria.

-34- WHO Diagnostic Criteria Serum Glucose mq/dL (mmol/L) Normal IGT Diabetes Fasting <140 <140 z140 (27.8) 2 hour <140 140-199 (7.8-11.1) 2200 (all.l) PROTOCOL 1 Treatment Effects 2-Hour Glucose Fasting Insulin (mg/dL) (UIU/mL) Test Compound A Baseline 6 Week Baseline 6 Week 1 167.00 81.00 14.40 2.00 2 143.00 146.00 9.10 25.70 3 143.00 106.00 4.00 6.20 4 167.00 85.00 12.70 11.30 166.00 113.00 13.20 13.30 6 158.00 101.00 20.00 11.30 7 148.00 81.00 8.30 2.00 8 166.00 172.00 21.80 9.30 9 187.00 158.00 22.50 12.20 147.00 98.00 12.00 7.70 Placebo 1 182.00 155.00 20.70 17.20 2 154.00 125.00 10.30 10.90 3 145.00 155.00 12.30 12.10 4 160.00 133.00 25.90 11.60 184.00 177.00 27.70 20.20 6 160.00 193.00 23.90 50.30 7 144.00 145.00 5.50 8.60 8 148.00 132.00 15.40 12.20 9 181.00 229.00 18.10 27.70 170.00 141.00 19.80 13.50 r r The results of the OGTTs show that treatment with the test compound correlates to reduction of fasting insulin levels and return of glucose tolerance to the normal range for approximately 70% of the subjects. With the exception of one placebo-responder, treatment with placebo does not change significantly the fasting insulin and glucose tolerance profiles.

-PROTOCOL 1 SU~MmarY of OGTT Glucose (mg/dL) Treatment a Screening We ek1 (N 1 8) (N -37) (N 19) Compound A 0 105 88 173 153 157 18S 151 16.2 170 145 152 2.o 160 12313 Placebo 0 102 100 9 169 164 163 184 191 186 175 181 176 162 155' IS0 These results show that the average value for 2-hour ~.glucose from the OGTT returns to the normal range for *patients treated for 6 weeks an d 12 weeks with Test Compound A compared to placebo which shows no significant :::change in the average value for 2-hou glucose.

6* PROTOCOL

I

Conversion After 6 Weeks of Treatment From IGT to Normal by WHO Classification Treatment IGT at Screening Converted to Normal Compound A 18 12 (67%) Placebo 19 7 (37%) The results show that on a patient-by-patient analysis, significantly more persons classified with IGT convert to normal glucose tolerance after treatment with Test Compound A (67ts) than with placebo 36 EXAMPLE 2 Usually, ZDF rats develop glucose intolerance between 3 and 8 weeks of age and become overtly diabetic between 8 and weeks (ref. DIABETES, vol.44, pp1447-1457, 1995).

We started to treat ZDF rats with BRL-49653, 2-[Nmethyl-N-(2-pyridyl)amino]-ethoxy]benzyl]thiazolidine-2,4dione, as a food admixture from 6 weeks of age in which ZDF rats shows impaired glucose tolerance but normal glucose level in basal state (no difference in plasma glucose between ZDF and control rats).

Therefore, following Figure 1 suggest that BRL-49653 improved impaired glucose tolerance and suppressed development of overt diabetes through this effect.

o -111 -0-

-A-

ZDF rats prevention Control BRL-49653, 0.0006% QA43mglkglday BRL-49653, 0,003% 2.I'Bmglkg/day 800- 700- 600J 500 400- 300- 200- 100-~ I i 56 7 10 11 Time 1:2 1:3 14 (weeks) 9 1 1 15 16 17 18 19 Me SE (6i=4-Al) I, CC C C CC C C C *uI C

CCC

C C C

CCC

C C C C

CC

CCC C C C C C C C C CC C 38 The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.

P.e

C

*o o

Claims (5)

1. 2. The method according to claim 1 comprising administering to a host a therapeutically effective amount of 5-[4-[2-[N-methyl-N-(2-pyridyl)amino]- ethoxy]benzyl]thiazolidine-2,4-dione.
2. 3. Use of a compound according to Formula IX 0 0 or a tautomeric form thereof and/or a pharmaceutically acceptable salt thereof, and/or a pharmaceutically acceptable solvate thereof, wherein: Airepresents a substituted or unsubstituted aromatic S, heterocyclyl group; As represents a benzene ring having in total up to substituents; X 6 represents O,S, or NR 32 wherein R 32 represents a hydrogen atom, an alkyl group, an acyl group, an aralkyl group, wherein the aryl moiety may be substituted or unsubstituted, or a substituted or unsubstituted aryl group; 0 Y 2 represents O or S; R 3 1 represents a hydrogen atom or an alkyl, aralkyl, or aryl group; and n represents an integer in the range from 2 to 6 in the manufacture of a medicament used for the prevention or delay of the onset of noninsulin-dependent diabetes mellitus in a subject suffering from impaired glucose intolerance.
3. 4. Use of a compound according to claim 3 wherein the compound is 5-[4-[2-[N-methyl-N-(2-pyridyl)amino]- 41 ethoxy]benzyl]thiazolidine-2,4-dione. A method of treating impaired glucose tolerance substantially as herein before described with reference to anyone of the foregoing examples.
4. 6. Use of a compound according to Formula IX as defined in claim 3 substantially as herein before described with reference to anyone of the foregoing examples.
5. 7. Every novel feature disclosed herein either alone or in combination, including every novel compound, composition, method, treatment and use disclosed in this specification. Dated this 1st day of October 1999 SANKYO COMPANY LIMITED °By their Patent Attorneys GRIFFITH HACK S S. *Y Fellows Institute of Patent and Trade Mark Attorneys of Australia *0 I 0 *r