U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Soft steroids having anti-inflammatory activity

Patent 4710495 Issued on December 1, 1987. Estimated Expiration Date: Icon_subject April 8, 2005. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3558675

3856828

Pharmaceutical compositions of 6଱,9଱-difluoro-androst-4-ene-17ଲ-carboxylates and derivatives thereof
Patent #: 4093721
Issued on: 06/06/1978
Inventor: Phillipps, et al.

Thio etianic acid derivatives Patent #: 4263289
Issued on: 04/21/1981
Inventor: Edwards

Inventor

Assignee

Application

No. 06/721282 filed on 04/08/1985

US Classes:

514/174, -O-C-O- is part of a hetero ring (e.g., acetonide, etc.)514/179, Modified C-ring (except methyl in 13-position) (e.g., double bond containing, substituted, etc.)514/180, 9-position substituted540/36, Nitrogen attached directly or indirectly to the cyclopentanohydrophenanthrene ring system by nonionic bonding540/38, Chalcogen bonded directly at the 11-position of the cyclopentanohydrophenanthrene ring system552/528, The carbon is double bonded directly at the 16-position552/610Acyclic carbon bonded directly at the 17 beta-position of the cyclopentanohydrophenanthrene ring system (e.g., etiocholanic acids, 17 cyanoetiocholanes, 17-aldehydrostanes, etc.)

Examiners

Primary: Schenkman, Leonard
Assistant: Lipovsky, Joseph A.

Attorney, Agent or Firm

International Classes

C07J 31/00 (20060101)
C07J 33/00 (20060101)
C07J 43/00 (20060101)
C07J 3/00 (20060101)

Abstract

Novel soft steroid anti-inflammatory agents, said agents being esters or thioesters of 17଱-alkoxy-11ଲ-hydroxyandrost-4-en-3-one-17ଲ-carboxylic acids, pharmaceutical compositions containing said agents, novel chemical intermediates useful in the preparation of said agents and methods of administering same to mammals in the treatment of inflammation. Preferred compounds are the haloalkyl esters of 17଱-alkoxy-11ଲ-hydroxyandrost-4-en-3-one-17ଲ-carboxylic acids.

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