IP Library Patent Application 11913256
Patent Application
App. No. 11/913,256

Preventive and/or Therapeutic Agent for Diabetic Vascular Disorder and Respiratory Disorder

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Patent No.
US None
App. No.
11/913,256
Abstract

The present invention provides preventive and/or therapeutic agents for either one, or both, of a diabetic vascular disorder and a diabetic respiratory disorder comprising, as an active ingredient, a cyclohexenone long chain alcohol compound represented by the following formula (1): [wherein R 1 , R 2 , and R 3 each represent a hydrogen atom or a methyl group, and X represents a linear or branched C10-C28 alkylene or alkenylene group]. Since the cyclohexenone long chain alcohol of formula (1) improves diabetic vascular smooth muscle contraction and bronchial smooth muscle contraction, it is useful as a preventive and/or therapeutic agent for a diabetic vascular disorder or a respiratory disorder.

Claims (39)

1 . A method for either one, or both, of preventing and treating at least one disorder selected from the group consisting of diabetic vascular disorders and diabetic respiratory disorders, comprising the step of administering a cyclohexenone long chain alcohol compound represented by the following formula (1):

wherein R 1 , R 2 , and R 3 each represent a hydrogen atom or a methyl group, and X represents a linear or branched C10-C28 alkylene or alkenylene group.

2 . The method of claim 1 , wherein R 1 is a methyl group and X is a linear C10-C28 alkylene group.

3 . The method of claim 2 , wherein R 2 is a methyl group.

4 . The method of claim 2 , wherein R 3 is a methyl group.

5 . The method of claim 1 , wherein R 1 and R 2 are hydrogen atoms.

6 . The method of claim 1 , wherein the cyclohexenone long chain alcohol compound is selected from the group consisting of the following compounds:

3-(10-hydroxydecyl)-2-cyclohexen-1-one (3-(10-hydroxydecyl)-2-cyclohexenone);

3-(1-hydroxyundecyl)-2-cyclohexen-1-one (3-(11-hydroxyundecyl)-2-cyclohexenone);

3-(12-hydroxydodecyl)-2-cyclohexen-1-one (3-(12-hydroxydodecyl)-2-cyclohexenone);

3-(13-hydroxytridecyl)-2-cyclohexen-1-one (3-(13-hydroxytridecyl)-2-cyclohexenone);

3-(14-hydroxytetradecyl)-2-cyclohexen-1-one (3-(14-hydroxytetradecyl)-2-cyclohexenone);

3-(10-hydroxydecyl)-4-methyl-2-cyclohexen-1-one (3-(10-hydroxydecyl)-4-methyl-2-cyclohexenone);

3-(11-hydroxyundecyl)-4-methyl-2-cyclohexen-1-one (3-(11-hydroxyundecyl)-4-methyl-2-cyclohexenone);

3-(12-hydroxydodecyl)-4-methyl-2-cyclohexen-1-one (3-(12-hydroxydodecyl)-4-methyl-2-cyclohexenone);

3-(13-hydroxytridecyl)-4-methyl-2-cyclohexen-1-one (3-(13-hydroxytridecyl)-4-methyl-2-cyclohexenone);

3-(14-hydroxytetradecyl)-4-methyl-2-cyclohexen-1-one (3-(14-hydroxytetradecyl)-4-methyl-2-cyclohexenone);

4,4-dimethyl-3-(10-hydroxydecyl)-2-cyclohexen-1-one (4,4-dimethyl-3-(10-hydroxydecyl)-2-cyclohexenone);

3-(11-hydroxyundecyl)-4,4-dimethyl-2-cyclohexen-1-one (3-(11-hydroxyundecyl)-4,4-dimethyl-2-cyclohexenone);

3-(12-hydroxydodecyl)-4,4-dimethyl-2-cyclohexen-1-one (3-(12-hydroxydodecyl)-4,4-dimethyl-2-cyclohexenone);

3-(13-hydroxytridecyl)-4,4-dimethyl-2-cyclohexen-1-one (3-(13-hydroxytridecyl)-4,4-dimethyl-2-cyclohexenone);

3-(14-hydroxytetradecyl)-4,4-dimethyl-2-cyclohexen-1-one (3-(14-hydroxytetradecyl)-4,4-dimethyl-2-cyclohexenone);

3-(10-hydroxydecyl)-2-methyl-2-cyclohexen-1-one (3-(10-hydroxydecyl)-2-methyl-2-cyclohexenone);

3-(11-hydroxyundecyl)-2-methyl-2-cyclohexen-1-one (3′-(11-hydroxyundecyl)-2-methyl-2-cyclohexenone);

3-(12-hydroxydodecyl)-2-methyl-2-cyclohexen-1-one (3-(12-hydroxydodecyl)-2-methyl-2-cyclohexenone);

3-(13-hydroxytridecyl)-2-methyl-2-cyclohexen-1-one (3-(13-hydroxytridecyl)-2-methyl-2-cyclohexenone);

3-(14-hydroxytetradecyl)-2-methyl-2-cyclohexen-1-one (3-(14-hydroxytetradecyl)-2-methyl-2-cyclohexenone);

3-(12-hydroxydodecyl)-2,4,4-trimethyl-2-cyclohexen-1-one (3-(12-hydroxydodecyl)-2,4,4-trimethyl-2-cyclohexenone);

3-(13-hydroxytridecyl)-2,4,4-trimethyl-2-cyclohexen-1-one (3-(13-hydroxydodecyl)-2,4,4-trimethyl-2-cyclohexenone);

3-(14-hydroxytetradecyl)-2,4,4-trimethyl-2-cyclohexen-1-one (3-(14-hydroxytetradecyl)-2,4,4-trimethyl-2-cyclohexenone);

3-(15-hydroxypentadecyl)-2,4,4-trimethyl-2-cyclohexen-1-one (3-(15-hydroxypentadecyl)-2,4,4-trimethyl-2-cyclohexenone); and

3-(16-hydroxyhexadecyl)-2,4,4-trimethyl-2-cyclohexen-1-one (3-(16-hydroxyhexadecyl)-2,4,4-trimethyl-2-cyclohexenone).

7 . The method of claim 1 , wherein the disorder is a diabetic vascular disorder.

8 . The method of claim 1 , wherein the disorder is a diabetic respiratory disorder.

9 . The method of claim 8 , wherein the diabetic respiratory disorder is sleep apnea syndrome.

10 . The method of claim 1 , wherein the method is a therapeutic method.

11 . A preventive and/or therapeutic agent for either one, or both, of a diabetic vascular disorder and a diabetic respiratory disorder, comprising, as an active ingredient, a cyclohexenone long chain alcohol compound represented by the following formula (1):

wherein R 1 , R 2 , and R 3 each represent a hydrogen atom or a methyl group, and X represents a linear or branched C10-C28 alkylene or alkenylene group.

12 . The method of claim 3 , wherein R 3 is a methyl group.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2013
From: MEIJI CO., LTD.
To: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS); UNIVERSITE DE STRASBOURG
Reel/Frame 029788/0972 →
CHANGE OF NAME Recorded Aug 15, 2011
From: MEIJI DAIRIES CORPORATION
To: MEIJI CO., LTD
Reel/Frame 026748/0640 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2008
From: SATOH, KEISUKE; SAITO, MOTOAKI; LUU, BANG; YAMADA, MASASHI; SUZUKI, HIROTO
To: MEIJI DAIRIES CORPORATION
Reel/Frame 021460/0330 →