IP Library Granted Patent US 7,385,083
Granted Patent B2
US 7,385,083 · App. 10/664,165 · Granted Jun 10, 2008

Potassium channel opener

Assignee: Tanabe Seiyaku Co., Ltd.
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Quick Facts
Patent No.
US 7,385,083
App. No.
10/664,165
Granted
Jun 10, 2008
Kind
B2
Abstract

A potassium channel opener comprising a compound (e.g., pimaric acid) represented by the formula [I]: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are each independently hydrogen, alkyl, alkenyl, halogen, hydroxy, halogenated alkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, heteroaryl, acyl, carboxyl, alkoxycarbonyl, hydroxamate, sulfo, carbamoyl, sulfonamide, aldehyde, or nitrile; or R 4 and R 5 may be bonded to each other to form a ring; or R 6 and R 7 may be bonded to each other to form a ring; and all of three bonds represented by are single bonds, or one of the three bonds is double bond and the other bonds are single bonds, or a physiologically acceptable salt thereof as an effective ingredient.

Claims (7)

1. A method of treatment of hypertension, tonic bladder, disturbances of peripheral circulation, airway hyperresponsiveness, sensory neuron hypersensitivity, central spasm or ischemic central nervous system disorder, which comprises administering a compound, or a physiologically acceptable salt thereof as an active ingredient, wherein the compound is represented by the formula:

wherein R 12 is acyl, carboxyl, hydroxamate, sulfo, carbamoyl, sulfonamide or nitrile;

wherein R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 and R 21 are each independently hydrogen, alkyl, alkenyl, halogen, hydroxy, halogenated alkyl, hydroxyalkyl, aminoalkyl, alkoxy, aryl, heteroaryl, acyl, carboxyl, carboxyl, alkoxycarbonyl, hydroxamate, sulfo, carbamoyl, sulfonamide, aldehyde or nitrile; or R 20 and R 21 may be bonded to each other to form oxo.

2. The method according to claim 1 , wherein R 11 , R 13, and R 18 are alkyls, R 12 is carboxyl, R 14 , R 15 and R 16 are hydrogen, or a physiologically acceptable salt thereof.

3. The method according to claim 1 , wherein R 11 , R 13 and R 18 are alkyls, R 12 is carboxyl, R 14 , R 15 , R 16 , R 20 , and R 21 are hydrogen, and R 17 and R 19 are halogen, or a physiologically acceptable salt thereof.

4. The method according to claim 1 , which method is for treatment of essential hypertension, tonic bladder, airway hyperresponsiveness, or ischemic central nervous system disorder.

5. The method according to claim 1 , wherein said compound is dichlorodehydroabietic acid.

Assignments (2)
CHANGE OF NAME Recorded Oct 26, 2007
From: TANABE SEIYAKU CO., LTD.
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 020021/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2003
From: IMAIZUMI, YUJI; OHWADA, TOMOHIKO
To: TANABE SEIYAKU CO., LTD.
Reel/Frame 014516/0332 →
Priority Claims (2)
JP 2001-127054 · Apr 25, 2001 · national
JP 2001-337723 · Nov 2, 2001 · national
Continuity (2)
Continuation In Part PCTJP020408500 · Apr 24, 2002
Related Publication 20040116482A1 · Jun 17, 2004