Alclofenac


CAS No. : 22131-79-9

(Synonyms: Allopydin; W-7320)

22131-79-9
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Cat. No. : HY-W009706
M.Wt: 226.66
Formula: C11H11ClO3
Purity: >98 %
Solubility: DMSO : 16.67 mg/mL (ultrasonic;warming;heat to 60°C)
Introduction of 22131-79-9 :

Alclofenac (Allopydin) is an orally active prostaglandin synthase inhibitor with anti-inflammatory, analgesic and antipyretic activities. Alclofenac irreversibly inhibits platelet aggregation. Alclofenac can be used in research related to rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, low back pain and sciatica[1]. In Vitro:Alclofenac inhibits prostaglandin biosynthesis in vitro in ram seminal vesicle microsomes[1].
Alclofenac inhibits oxidative phosphorylation in rat liver mitochondria in vitro[1].
Alclofenac exerts cytostatic and cytotoxic effects on mammalian cells in vitro[1].
Alclofenac inhibits collagen- or epinephrine-induced human platelet aggregation in vitro[1]. In Vivo:Alclofenac (20-100 mg/kg; p.o./s.c.) exhibits dose-dependent anti-inflammatory activity against carrageenan-induced paw edema in rats[1].
Alclofenac (25-100 mg/kg; p.o./s.c.) prevents and treats adjuvant-induced arthritis in rats[1].
Alclofenac exhibits analgesic activity in rats[1].
Alclofenac (100-200 mg/kg; p.o.) exerts a dose-dependent antipyretic effect in febrile rabbits[1].
Alclofenac (100-200 mg/kg; p.o./i.p.) exerts central nervous system depressant activity in rats, which is manifested by prolonged pentobarbital-induced sleep time[1].
Alclofenac (10-960 mg/kg; p.o.; once daily; for 5 consecutive days) inhibits acute inflammation in rats in a dose-dependent manner[2].

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