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sPLA2 Inhibitor
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。
sPLA2 Inhibitor图片
CAS NO:393569-31-8
包装与价格:
包装价格(元)
500μg询价
1mg询价
5mg询价
10mg询价

sPLA2 Inhibitor 是一种 D-酪氨酸衍生物,是一种口服有效的分泌型磷脂酶 A2 (sPLA2) 抑制剂,对人非胰腺分泌型 PLA2 异构体 IIa (hnpsPLA2-IIa) 的 IC50 为 29 nM。
Cas No.393569-31-8
Canonical SMILESO=C(CCCCCCC1=CC=CC=C1)N[C@@H](CCC(O)=O)CC(C=C2)=CC=C2OCC3=CC=CC=C3
分子式C31H37NO4
分子量487.6
溶解度DMF: 5 mg/ml,DMSO: 2 mg/ml,Ethanol: 5 mg/ml,Ethanol:PBS (pH 7.2) (1:6): 0.1 mg/ml
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

Secreted phospholipases A2 (sPLA2s) are a diverse family of low molecular weight PLA2s with tissue-specific expression patterns and actions. The group IIA sPLA2 (sPLA2-IIA) was originally purified from platelets and exudates from patients with rheumatoid arthritis. Its expression can be induced by inflammatory mediators, and mouse studies suggest that it may play roles in colorectal polyposis, atherosclerosis, and bacterial infections. sPLA2 inhibitor is an orally active inhibitor of sPLA2-IIA. It protects against intestinal reperfusion injury in rats when given at 10 mg/kg orally. sPLA2 inhibitor also attenuates NF-κB signaling in lung cancer cells and protects against diet-induced metabolic syndrome in rats.

 
 
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