Ilomastat,GM6001,Galardin142880-36-2伊洛馬司他（GM6001） 返回列表頁

Ilomastat,GM6001,Galardin142880-36-2伊洛馬司他(GM6001)

伊洛馬司他(GM6001)
分子式：C20H28N4O4   分子量：388.46
 
產(chǎn)品描述
GM6001 (galardin, ilomastat) 是廣譜matrix metalloprotease (MMP)抑制劑，作用于MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-12, MMP-14, 和 MMP-26，Ki分別為0.4 nM, 0.5 nM, 27 nM, 3.7 nM, 0.1 nM, 0.2 nM, 3.6 nM, 13.4 nM, 和0.36 nM。
靶點
MMP
         
IC50
0.4-27 nM (Ki)
         
體外研究
GM 600l inhibits human skin fibroblast collagenase with Ki of 0.4 nM when assayed with a synthetic thio ester substrate at pH 6.5, with 50-fold selectivity over two bacterial enzymes, thermolysin and Pseudomonas aeruginosa elastase. GM 6001 (0.1 nM - 10 nM) inhibits gelatinase A and gelatinase B produced by T-cells, thus inhibits T-cell homing.
體內(nèi)研究
Topical application of GM6001 (400 μg/ml) prevents corneal ulceration after severe alkali injury. [3] In rabbit model after stenting, GM6001 significantly inhibits intimal hyperplasia and intimalcollagen content, and it increases lumen area in stented arteries without effects on proliferation rates.
溶解性
DMSO ≥25 mM，乙醇 10 mg/ml
穩(wěn)定性
2年 -20°C粉狀，6月-80°C溶于DMSO