Name | 1-(2-(4-fluorophenyl)cyclopenten-1-yl)-4-(methylsulfonyl)benzenee |
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Synonyms |
1-fluoro-4-(2-(4-methylsulfonylphenyl)-1-cyclopenten-1-yl)benzene
SC-57666 1-fluoro-4-[2-[4-(methylsulfonyl)phenyl]cyclopenten-1-yl] benzene 1-fluoro-4-(2-(4-(methanesulfonyl)phenyl)cyclopent-1-enyl)benzene 1-(4-methanesulphonylphenyl)-2-(4-fluorophenyl)cyclopentene 1-(2-(4-fluorophenyl)cyclopenten-1-yl)-4-(methylsulfonyl)benzene SC57666 |
Description | SC57666 is a selective COX2 inhibitor with an IC50 of 26 nM. |
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Related Catalog | |
Target |
COX-2:26 nM (IC50) |
In Vitro | 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]. |
In Vivo | 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]. |
References |
Molecular Formula | C18H17FO2S |
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Molecular Weight | 316.39000 |
Exact Mass | 316.09300 |
PSA | 42.52000 |
LogP | 5.40470 |
Storage condition | 2-8℃ |