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SC57666
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
SC57666图片
CAS NO:158959-32-1
规格:98%
分子量:316.39
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议
20mg电议

产品介绍
SC57666是选择性的COX2抑制剂,IC50值为26nM。
CAS:158959-32-1
分子式:C18H17FO2S
分子量:316.39
纯度:98%
存储:Store at -20°C

Background:

SC57666 is a selective COX2 inhibitor with an IC50 of 26 nM.


SC57666 inhibits COX2 with an IC50 of 3.2±0.8 nM in CHO cells stably transfected with human COX isozymes, with 1000 fold or more selectivity over COX1 (IC50=6000±1900 nM)[2].


SC57666 has been shown to be orally active (ED50=1.7 mpk) in the adjuvant-induced arthritis model. No gastric lesions are observed in mice after 5 h when SC57666 is administered intragastrically at 600 mpk. No intestinal damage is observed in rats after 72 h when SC57666 is administered intragastrically at 200 mpk[1].


[1]. Reitz DB, et al. Selective cyclooxygenase inhibitors: novel 1,2-diarylcyclopentenes are potent and orally activeCOX2 inhibitors. J Med Chem. 1994 Nov 11;37(23):3878-81. [2]. Riendeau D, et al. Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX2 inhibitor. Br J Pharmacol. 1997 May;121(1):105-17.