IP Library Granted Patent US 6,864,279
Granted Patent B2
US 6,864,279 · App. 10/132,750 · Granted Mar 8, 2005

Materials and methods for treating coagulation disorders

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Quick Facts
Patent No.
US 6,864,279
App. No.
10/132,750
Granted
Mar 8, 2005
Kind
B2
Abstract

This invention is drawn to compounds which are more easily metabolized by the metabolic drug detoxification systems. Particularly, warfarin analogs which have been designed to include esters within the structure of the compounds are taught. The invention teaches methods of reducing the toxicity of drugs comprising the introduction of ester groups into drugs during the synthesis of the drug. This invention is also drawn to methods of treating coagulation disorders comprising the administration of compounds which have been designed to be metabolized by serum or intracellular hydrolases and esterases. Pharmaceutical compositions of the ester containing warfarin, analogs are also taught.

Claims (80)

1. An anticoagulant compound, having the following formula, including salts and isomers:

wherein

X is hydrogen, alkyl, cycloalkyl, heterocyclyl, hydroxy, alkoxy, or heteroaryl or aryl optionally substituted with COOR 1 ;

R 1 is hydrogen, alkyl or alkylaryl, all optionally substituted with lower alkyl, hydroxy, or alkoxy;

Y is (CHR 3 ) n COOR 4 or aryl substituted with COOR 5 , wherein n=1-3;

R 3 is hydrogen, alkyl, alkylaryl, or aryl all optionally substituted with lower allyl, hydroxy, or alkoxy;

R 4 is alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy; and

R 5 is hydrogen, alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy.

2. The compound, according to claim 1 ,

wherein X is hydrogen, alkyl, cycloalkyl, heterocyclyl, hydroxy, alkoxy, heteroaryl or aryl optionally substituted with COOR 1 ; R 1 is hydrogen, alkyl or alkylaryl, all optionally substituted with lower alkyl, hydroxy, or alkoxy; and Y is CH 2 COOR 4.

3. The compound, according to claim 1 ,

wherein X is hydrogen and Y is aryl substituted with COOR 5 .

4. The compound, according to claim 1 , having one of the following structures:

wherein

R 1 is selected from the group consisting of CH 2 COOR 5 , CH(COOR 5 ) 2 ;

R 2 is H;

R 3 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl;

R 4 is H or a halogen; and,

R 5 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl groups.

5. A pharmaceutical composition, comprising a pharmaceutical carrier and a compound having the following formula, including salts and isomers:

wherein

X is hydrogen, alkyl, cycloalkyl, heterocyclyl, hydroxy, alkoxy, or heteroaryl or aryl optionally substituted with COOR 1 ;

R 1 is hydrogen, alkyl or alkylaryl, all optionally substituted with lower alkyl, hydroxy, or alkoxy;

Y is (CH 3 ) n COOR 4 or aryl substituted with COOR 5 , wherein n=1-3;

R 3 is hydrogen, alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy;

R 4 is alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy, and

R 5 is hydrogen, alkyl, alkyaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy; or.

6. The composition, according to claim 5 , having the following structure:

wherein

R 1 is selected from the group consisting of CH 2 COOR 5 , CH(COOR 5 ) 2 ;

R 2 is H;

R 3 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl; and,

R 4 is H or a halogen; and,

R 5 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl groups.

7. A method, for providing anticoagulant activity to a patient in need of such activity, wherein said method comprises administering to a patient in need of such treatment a compound having the following formula, including salts and isomers:

wherein

X is hydrogen, alkyl, cycloalkyl, heterocyclyl, hydroxy, alkoxy, or heteroaryl or aryl optionally substituted with COOR 1 ;

R 1 is hydrogen, alkyl or alkylaryl, all optionally substituted with lower alkyl, hydroxy, or alkoxy;

Y is (CHR 3 ) n COOR 4 or aryl substituted with COOR 5 , wherein n=1-3;

R 3 is hydrogen, alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy;

R 4 is alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy; and

R 5 is hydrogen, alkyl, alkylaryl, or aryl all optionally substituted with lower alkyl, hydroxy, or alkoxy.

8. The method, according to claim 7 , comprising administering a compound having the following structure:

wherein

R 1 is selected from the group consisting of CH 2 COOR 5 , CH(COOR 5 ) 2 ;

R 2 is H;

R 3 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl; and,

R 4 is H or a halogen; and,

R 5 is selected from the group consisting of C 1-4 alkyl, phenyl, and benzyl groups.

9. The method, according to claim 7 , wherein the patient is a human.

10. An anticoagulant compound, having the following formula, including salts and isomers:

wherein:

X is hydrogen; and

Y is aryl substituted with COOR 1 , wherein R 1 is a substituted or unsubstituted alkyl.

11. An anticoagulant compound, having the following formula, including salts and isomers:

wherein:

X is aryl substituted with more than one substituent or with a substituted alkoxy;

Y is (CHR 3 ) n COOR 4 , wherein n=1-3;

R 3 is hydrogen, or a substituted or unsubstituted alkyl; and

R 4 is hydrogen, or a substituted or unsubstituted alkyl.

12. A pharmaceutical composition, comprising a pharmaceutical carrier and a compound having the following formula, including salts and isomers:

wherein:

X is hydrogen; and

Y is aryl substituted with COOR 1 , wherein R 1 is a substituted or unsubstituted alkyl.

13. A pharmaceutical composition, comprising a pharmaceutical carrier and a compound having the following formula, including salts and isomers:

wherein

X is aryl substituted with more than one substituent or with a substituted alkoxy,

Y is (CHR 3 ) n COOR 4 , wherein=1-3;

R 3 is hydrogen, or a substituted or unsubstituted allyl; and

R 4 is hydrogen, or a substituted or unsubstituted alkyl.

14. A method, for providing anticoagulant activity to a patient in need of such activity, wherein said method comprising administering to a patient in need of such treatment a compound having the following formula, including salts and isomers:

wherein:

X is hydrogen; and

Y is aryl substituted with COOR 1 , wherein R 1 is a substituted or unsubstituted alkyl.

15. A method, for providing anticoagulant activity to a patient in need of such activity, wherein said method comprising administering to a patient in need of such treatment a compound having the following formula, including salts and isomers:

wherein:

X is aryl substituted with more t an one substituent or with a substituted alkoxy,

Y is (CHR 3 ) n COOR 4 , wherein n=1-3;

R 3 is hydrogen, or a substituted or unsubstituted alkyl; and

R 4 is hydrogen, or a substituted or unsubstituted alkyl.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Feb 6, 2013
From: AYER CAPITAL PARTNERS MASTER FUND, L.P.; MPM BIOVENTURES III, L.P.; MPM BIOVENTURES III-QP, L.P.; MPM BIOVENTURES III GMBH & CO. BETEILIGUNGS KG; MPM BIOVENTURES III PARALLEL FUND, L.P.; AYER CAPITAL PARTNERS KESTREL FUND, L.P.; MPM ASSET MANAGEMENT INVESTORS 2002 BVIII LLC
To: ARYX THERAPEUTICS, INC.
Reel/Frame 029767/0524 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2012
From: ARYX THERAPEUTICS, INC.
To: ARMETHEON, INC.
Reel/Frame 027738/0001 →
SECURITY AGREEMENT Recorded Oct 18, 2010
From: ARYX THERAPEUTICS, INC.
To: AYER CAPITAL PARTNERS MASTER FUND, L.P.; MPM BIOVENTURES III, L.P.; MPM BIOVENTURES III-QP, L.P.; MPM BIOVENTURES III GMBH & CO. BETEILIGUNGS KG; MPM BIOVENTURES III PARALLEL FUND, L.P.; AYER CAPITAL PARTNERS KESTREL FUND, L.P.; MPM ASSET MANAGEMENT INVESTORS 2002 BVIII LLC
Reel/Frame 025150/0379 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 29, 2007
From: ARYX THERAPEUTICS
To: ARYX THERAPEUTICS, INC.
Reel/Frame 020024/0545 →