FK 3311
(Synonyms: N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺,FK-3311;FK3311) 目录号 : GC11768A COX-2 inhibitor
Cas No.:116686-15-8
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
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].
References:
1.Grossman CJ, Wiseman J, Lucas FS, Trevethick MA, Birch PJ. Inhibition of constitutive and inducible cyclooxygenase activity in human platelets and mononuclear cells by NSAIDs and Cox 2 inhibitors. Inflamm Res 1995,44:253-257.
2.Kobayashi M, Takeyoshi I, Kurabayashi M, Matsumoto K, Morishita Y. The effects of a cyclooxygenase-2 inhibitor, FK3311, on total hepatic ischemia-reperfusion injury of the rat. Hepatogastroenterology 2007,54:522-526.
3.Oshima K, Yabata Y, Yoshinari D, Takeyoshi I. The effect of cyclooxygenase (COX)-2 inhibition on ischemia-reperfusion injury in liver transplantation. J Invest Surg 2009,22:239-245.
4.Sunose Y, Takeyoshi I, Tsutsumi H, Ohwada S, Oriuchi N, Matsumoto K, et al. Effect of a cyclooxygenase-2 inhibitor, FK3311, in a canine lung transplantation model. Ann Thorac Surg 2001,72:1165-1171; discussion 1171-1162.
Cas No. | 116686-15-8 | SDF | |
别名 | N-[4-乙酰基-2-(2,4-二氟苯氧基)苯基]-甲烷磺酰胺,FK-3311;FK3311 | ||
化学名 | N-[4-acetyl-2-(2,4-difluorophenoxy)phenyl]methanesulfonamide | ||
Canonical SMILES | CC(=O)C1=CC(=C(C=C1)NS(=O)(=O)C)OC2=C(C=C(C=C2)F)F | ||
分子式 | C15H13F2NO4S | 分子量 | 341.33 |
溶解度 | DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 5 mg/ml | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 2.9297 mL | 14.6486 mL | 29.2972 mL |
5 mM | 0.5859 mL | 2.9297 mL | 5.8594 mL |
10 mM | 0.293 mL | 1.4649 mL | 2.9297 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
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工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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