Prostaglandin synthase-2 inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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514375, 514443, 514394, 514465, 514464, 514469, 514415, 548178, 548217, 5483044, 548469, 549471, 549437, 549 51, C07D27762, C07D26356, C07D33354, C07D23508

Patent

active

056818424

ABSTRACT:
The present invention provides a compound of the formula: ##STR1## such compounds are useful for inhibiting prostaglandin synthesis. Pharmaceutical compositions and methods for inhibiting prostaglandin synthesis are also disclosed.

REFERENCES:
patent: 3840597 (1974-10-01), Moore et al.
patent: 4375479 (1983-03-01), Schroeder
patent: 4866091 (1989-09-01), Matsuo et al.
Mitchell et al; Cyclooxygenase-2: Regulation and Relevance in Inflammation; Biochemical Pharmacology. vol. 50 No. 10 pp. 1535-1542, 1995.
Battistini et al; Cox-1 and Cox-2:"Toward the Development of More Selective Nsaids" (1994) Drug News and Perspectives, 7(8), 501-512.
DeWitt et al; The Differential Susceptibility of Prostaglandin Endoperoxide H Synthases-1 and -2 to Nonsteroidal Anti-Inflammatory Drugs: Aspirin Derivatives as Selective Inhibitors; Med Chem Res (1995) 5:325-343.

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