產(chǎn)品目錄

規(guī)格	10mg 50mg
CAS	116686-15-8
別名	FK-3311;FK3311
化學(xué)名	N-[4-acetyl-2-(2,4-difluorophenoxy)phenyl]methanesulfonamide
分子式	C15H13F2NO4S
分子量	341.33
溶解度	DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 5 mg/ml
儲存條件	Store at -20°C
General tips	For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition	Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request

產(chǎn)品描述：

FK 3311, a cell-permeable and orally available sulfonanilide, is a highly selective inhibitor of cyclooxygenase (COX)-2 with IC 50 value of 1.6 μM.

Cyclooxygenase-2 (COX-2) is a membrane bound enzyme that transfers the electrons from cytochrome c to the catalytic subunit 1. The expression of COX-2 is tightly regulated and induced by different mediators such as cytokine, growth factor, and endotoxin.

FK3311 was shown to selectively inhibit consititutive and inducible COX-2 activity in human platelets and mononuclear cells [1].

The component has also been used extensively in various animal models to study the role of COX-2. In ischemia-reperfusion rat model, administration of FK 3311 via the penile vein can significantly reduce the serum levels of aspartate aminotransferase (AST), lactate dehydrogenase (LDH), alanine aminotransferase (ALT) and thromboxane (Tx) B2. However, FK 3311 treatment did not reduce the 6-keto-PG F1a levels in these rats[2]. In addition, liver tissue blood flow was remarkably better in the FK3311 treated rat compared with their control group. Histological examination of the livers revealed that FK3311 treatment reduced the hepatic tissue damage and improved the liver graft function [3]. In the canine lung transplantation model, treatment of FK3311 reduced lung damage, neutrophil infiltration into lung, technetium-99m-albumin accumulation and thromboxane B2 level. The lung with FK3311 treatment had better pulmonary gas exchange and hemodynamics [4].

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原創(chuàng)作者：上海莼試生物技術(shù)有限公司

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