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MN-001
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。
MN-001图片
CAS NO:125961-82-2
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议

产品介绍
MN-001 (KCA 757) 是一种硫肽白三烯受体拮抗剂,一种口服生物可利用的抗炎剂,用于治疗哮喘。
Cas No.125961-82-2
别名4-[6-乙酰基-3-[3-[(4-乙酰基-3-羟基-2-丙基苯基)硫]丙氧基]-2-丙基苯氧基]丁酸,KCA 757, Tipelukast
化学名4-[6-acetyl-3-[3-[(4-acetyl-3-hydroxy-2-propylphenyl)thio]propoxy]-2-propylphenoxy]-butanoic acid
Canonical SMILESCC(C1=C(O)C(CCC)=C(SCCCOC2=C(CCC)C(OCCCC(O)=O)=C(C(C)=O)C=C2)C=C1)=O
分子式C29H38O7S
分子量530.67
溶解度1mg/ml in ethanol, sparingly soluable in chloroform & ethyl acetate
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

Tipelukast (KCA 757) is a sulfidopeptide leukotriene receptor antagonist, an orally bioavailable anti-inflammatory agent and used for the treatment of asthma.

Tipelukast inhibits the binding of [3H] LTD4 to the LTD4 receptors on pul-monary cell membrane of guinea-pigs (IC50 = 2.3 μmol)[2].

Fiftheen min after an aerosolized antigen challenge, and UNDW inhaled 5 min later into the guinea pigs, Tipelukast significantly alters the UNDW-induced bronchoconstriction[1]. Tipelukast (1 and 5 mg/kg) administered intravenously 15 min after antigen challenge reduces the propranolol-induced bronchoconstriction (PIB) in a dose-dependent manner in guinea-pigs[2].

[1]. Fujimura M, et al. No involvement of lipid mediators in a guinea pig model of ultrasonically nebulized distilled water-induced bronchoconstriction. Prostaglandins Other Lipid Mediat. 2000 Jan;60(1-3):49-58. [2]. Fujimura M, et al. Role of leukotrienes in post-allergic propranolol-induced bronchoconstriction in guinea-pigs. Clin Exp Allergy. 1997 Oct;27(10):1219-26.