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

Method of selectively inhibiting prostaglandin G/H synthase-2

Patent 5571825 Issued on November 5, 1996. Estimated Expiration Date: Icon_subject March 31, 2015. 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

3558640

New benzhydrysulphinyl derivatives
Patent #: 4066686
Issued on: 01/03/1978
Inventor: Lafon

Acetic acid derivatives
Patent #: 4205087
Issued on: 05/27/1980
Inventor: Waring

Halogenobenzhydrylsulfinylacetohydroxamic acids
Patent #: 4489095
Issued on: 12/18/1984
Inventor: Lafon

Benzhydryl compounds as herbicide antidotes
Patent #: 4964893
Issued on: 10/23/1990
Inventor: Brannigan, et al.

Substituted bicyclic bis-aryl compounds exhibiting selective leukotriene B4 antagonist activity, their preparation and use in pharmaceutical compositions Patent #: 5366982
Issued on: 11/22/1994
Inventor: Dereu, et al.

Inventors

Application

No. 414394 filed on 03/31/1995

US Classes:

514/332, Plural six-membered hetero rings consisting of one nitrogen and five carbon atoms514/335, Chalcogen bonded directly to a ring carbon of the six-membered hetero ring514/437, Tricyclo ring system having the hetero ring as one of the cyclos514/444, Additional hetero ring514/455, Chalcogen bonded directly to ring carbon of the hetero ring514/461, The hetero ring is five-membered514/471, Nitrogen containing514/472, The nitrogen bonded directly to the hetero ring514/473, Chalcogen bonded directly to the hetero ring514/530, Z contains a cyclopentyl or cyclopentene ring514/532, Z-C(=O)-O-Y, wherein Z contains a benzene ring514/538, Nitrogen bonded to carbon in Z moiety514/539Plural separated benzene rings in Z moiety

Examiners

Primary: Cintins, Marianne M.
Assistant: Jarvis, William R. A.

Attorney, Agent or Firm

Foreign Patent References

  • 94/13635 WO. 06/25/1994
  • 94/15932 WO. 07/25/1994
  • 94/20480 WO. 09/25/1994

International Classes

A61K 031/44
A61K 031/38
A61K 031/34
A61K 031/235
A61K 031/24
A61K 031/215
A61K 031/35

Abstract

The present invention provides a method of selectively inhibiting prostaglandin G/H synthase-2 that comprises administering to a patient in need of such inhibition an inhibiting amount of a compound having the Formula I, II or III ##STR1## wherein the R groups and heterocycles are defined in the disclosure.

Other References

  • Remingtons Pharmaceutical Sciences, 16th Ed., 1980, p. 43
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