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US4474804A Expired / Lapsed US ⏱️ 0.0 years remaining

7-Oxabicyclo substituted prostaglandin phenyl carboxylic acid derivatives useful as cardiovascular agents

Assignee: ER Squibb and Sons LLC
•
Filing: 1983-09-19
•
Granted: 1984-10-02
•
Expires: 2003-09-19
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Abstract

Abstract 7-Oxabicyclo substituted prostaglandin phenyl carboxylic acid derivatives are provided having the structural formula ##STR1## and including all stereoisomers thereof. The compounds are cardiovascular agents useful, for example, in the treatment of thrombolytic disease.

Inventors

  • 👤 Jagabandhu Das
  • 👤 Martin F. Haslanger

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 01:45
CPC Classifications
C; C07; C07D; C07D493/00; C07D493/02; C07D493/08; A; A61; A61P; A61P7/00; A61P7/02

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 106 words
A compound having the structural formula ##STR18## and including all stereoisomers thereof, wherein; R is H, lower alkyl or alkali metal; A is --CH═CH--, or (CH 2 ) 2 ; R 1 is lower alkyl, aryl-lower alkyl, aryl, cycloalkyl or cycloalkylalkyl; m is 0 or 1 and n is 0 or 1; wherein the term "aryl" used by itself or as part of another group refers to monocyclic or bicyclic aromatic groups containing from 6 to 10 carbons in the ring portion and the term "cycloalkyl" used by itself or as part of another group refers to saturated cyclic hydrocarbon groups containing 3 to 12 carbons.
Claim 2
Dependent Claim 106 words
A compound having the structural formula ##STR18## and including all stereoisomers thereof, wherein; R is H, lower alkyl or alkali metal; A is --CH═CH--, or (CH 2 ) 2 ; R 1 is lower alkyl, aryl-lower alkyl, aryl, cycloalkyl or cycloalkylalkyl; m is 0 or 1 and n is 0 or 1; wherein the term "aryl" used by itself or as part of another group refers to monocyclic or bicyclic aromatic groups containing from 6 to 10 carbons in the ring portion and the term "cycloalkyl" used by itself or as part of another group refers to saturated cyclic hydrocarbon groups containing 3 to 12 carbons.
Claim 3
Dependent Claim 11 words
The compound as defined in claim 1 wherein A is --CH═CH.
Claim 4
Dependent Claim 12 words
The compound as defined in claim 1 wherein R 1 is cycloalkyl.
Claim 5
Dependent Claim 13 words
The compound as defined in claim 1 wherein --COOR is in the meta-position.
Claim 6
Dependent Claim 11 words
The compound as defined in claim 1 wherein R is H.
Claim 7
Dependent Claim 15 words
The compound as defined in claim 1 wherein A is (CH 2 ) 2 .
Claim 8
Dependent Claim 21 words
The compound as defined in claim 1 wherein R 1 is cyclohexyl, A is --CH═CH-- and COOR is in the meta-position.
Claim 9
Dependent Claim 15 words
The compound as defined in claim 1 wherein m is 1 and n is 0.
Claim 10
Dependent Claim 21 words
The compound as defined in claim 1 having the name [1β,2α(Z),3α(1E),4β]-3-[3-[3-(3-cyclohexyl-3-hydroxy-1-propenyl)-7-oxabicyclo[2.2.1]hept-2-yl]-1-propenyl]benzoic acid or its methyl ester, including all isomers of each.
Claim 11
Dependent Claim 21 words
The compound as defined in claim 1 having the name [1β,2α(E),3α(1E),4β]-3-[3-[3-(3-cyclohexyl-3-hydroxy-1-propenyl)-7-oxabicyclo[2.2.1]hept-2-yl]-1-propenyl]benzoic acid or its methyl ester, including all isomers of each.
Claim 12
Dependent Claim 30 words
A method of inhibiting platelet aggregation which comprises administering to a mammalian host an effective amount of a compound as defined in claim 1 or a pharmaceutically acceptable salt thereof.
Claim 13
Dependent Claim 30 words
A composition for inhibiting platelet aggregation comprising an effective amount of a compound as defined in claim 1 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier therefor.
Claim 14
Dependent Claim 26 words
The method as defined in claim 11 wherein said compound is administered in an amount within the range of from about 1 to about 100 mg/kg.

References Cited (Backward Citations)

US4143054A Cited
US4187236A Cited
US4220594A Cited
US4254044A Cited
GB2039909A Cited
US4228180A Cited
EP0043292A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-10-02 1988-04-02 1988-10-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-10-02 1992-04-02 1992-10-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-10-02 1996-04-02 1996-10-02 $7700.00 Window Closed / Lapsed

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