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Anti-inflammatory compounds oxicams

Another compound structurally related to the oxicams is RU 43526 (159) [387], which gave approximately equipotent inhibition of seminal vesicle CO (2.1 //M) and of rat ISN (3.0 //M). Removal of the 2-substituent had no effect on the CO inhibition, but drastically reduced 5-LO potency. RU 43526 was orally active, but only in NSAID-sensitive models (CPE 4 mg/kg, RAA 0.7 mg/kg). It was unknown whether the 5-LO inhibition made any contribution to the anti-inflammatory activity of this compound. [Pg.38]

Oxicames are representatives of another series of anti-inflammatory, analgesic, and fever-reducing compounds whose mechanisms of action are most likely the suppression of prostaglandin synthesis. These drugs are capable of relieving painful symptoms of medium intensity. [Pg.51]

Literature reports on heterocyclic compounds containing a 1,2- or 2,1-benzothiazine ring have appeared in increasing numbers in recent years. This trend is likely to continue as a result of the anti-inflammatory activity of 4-hydroxy-2H-l,2-benzothiazine-3-carboxamide 1,1-dioxides (the oxicams ). [Pg.125]


See other pages where Anti-inflammatory compounds oxicams is mentioned: [Pg.557]    [Pg.557]    [Pg.613]    [Pg.453]    [Pg.425]    [Pg.249]   
See also in sourсe #XX -- [ Pg.613 , Pg.614 ]




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