Literature DB >> 8482483

NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesions.

N Futaki1, K Yoshikawa, Y Hamasaka, I Arai, S Higuchi, H Iizuka, S Otomo.   

Abstract

1. NS-398 (N-[2-cyclohexyloxy-4-nitrophenyl] methanesulfonamide) is a new non-steroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic effects. 2. The anti-inflammatory potency of NS-398 in rat carrageenin-induced edema was as potent as that of indomethacin and 8 times more potent than diclofenac. In rat adjuvant arthritis, NS-398 showed a therapeutic effect comparable to that seen with loxoprofen but less than that seen with indomethacin and diclofenac. 3. The analgesic potency of NS-398 in rat adjuvant arthritic pain was much the same as that of indomethacin, and was about 3-5 times higher than that of diclofenac and loxoprofen. In the Randall-Selitto method in rats, NS-398 was 2-7 times as potent as loxoprofen, diclofenac and indomethacin. In acetic acid-induced writhing in mice, NS-398 was equipotent to indomethacin and diclofenac. 4. In LPS-induced fever in rats, NS-398 was 1.5-4.5 times as potent as loxoprofen and indomethacin, but less potent than diclofenac. 5. NS-398 produced little gastric ulceration in doses of up to 1000 mg/kg, while reference drugs produced distinct stomach lesions in doses of 10-30 mg/kg. 6. NS-398 inhibited prostaglandin (PG) endoperoxide synthase from sheep seminal vesicle microsomes less potent than that of ibuprofen.

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Year:  1993        PMID: 8482483     DOI: 10.1016/0306-3623(93)90018-s

Source DB:  PubMed          Journal:  Gen Pharmacol        ISSN: 0306-3623


  49 in total

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2.  Cyclooxygenase-2 contributes to functional hyperemia in whisker-barrel cortex.

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3.  Dual, but not selective, COX-1 and COX-2 inhibitors, attenuate acetic acid-evoked bladder irritation in the anaesthetised female cat.

Authors:  Alexandra Wibberley; Gerald P McCafferty; Christopher Evans; Richard M Edwards; J Paul Hieble
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4.  A human whole blood assay for clinical evaluation of biochemical efficacy of cyclooxygenase inhibitors.

Authors:  C Brideau; S Kargman; S Liu; A L Dallob; E W Ehrich; I W Rodger; C C Chan
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5.  Rapid and transient induction of cyclo-oxygenase 2 by epidermal growth factor in human amnion-derived WISH cells.

Authors:  D J Perkins; D A Kniss
Journal:  Biochem J       Date:  1997-02-01       Impact factor: 3.857

Review 6.  Cyclo-oxygenase isoenzymes. How recent findings affect thinking about nonsteroidal anti-inflammatory drugs.

Authors:  J Y Jouzeau; B Terlain; A Abid; E Nédélec; P Netter
Journal:  Drugs       Date:  1997-04       Impact factor: 9.546

7.  An accessory role for ceramide in interleukin-1beta induced prostaglandin synthesis.

Authors:  K Kirtikara; S J Laulederkind; R Raghow; T Kanekura; L R Ballou
Journal:  Mol Cell Biochem       Date:  1998-04       Impact factor: 3.396

8.  Dual inhibition of nitric oxide and prostaglandin production contributes to the antiinflammatory properties of nitric oxide synthase inhibitors.

Authors:  D Salvemini; P T Manning; B S Zweifel; K Seibert; J Connor; M G Currie; P Needleman; J L Masferrer
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9.  Diverse methyl sulfone-containing benzo[b]thiophene library via iodocyclization and palladium-catalyzed coupling.

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Journal:  J Comb Chem       Date:  2010-03-08

10.  The effects of cyclooxygenase 2 inhibitors on cartilage erosion and bone loss in a model of Mycobacterium tuberculosis-induced monoarticular arthritis in the rat.

Authors:  D W Gilroy; A Tomlinson; K Greenslade; M P Seed; D A Willoughby
Journal:  Inflammation       Date:  1998-10       Impact factor: 4.092

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