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ML-9 Free Base
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。
ML-9 Free Base图片
CAS NO:110448-31-2
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
ML-9 (Free Base) 是 Akt 激酶的选择性强效抑制剂,可抑制肌球蛋白轻链激酶 (MLCK) 和基质相互作用分子 1 (STIM1) 的活性。 ML-9 (Free Base) 抑制 MLCK,PKA 和 PKC 活性,Ki值分别为 4、32 和 54 μM。 ML-9 通过刺激自噬小体的形成并抑制其降解来诱导自噬 (autophagy)。
生物活性

ML-9 (Free Base) is a selective and potent inhibitor ofAktkinase, inhibitsmyosinlight-chain kinase (MLCK) and stromal interaction molecule 1 (STIM1) activity[3]. ML-9 (Free Base) inhibits inhibits MLCK,PKAandPKCactivity withKivalues of 4, 32 and 54 μM, respectively[1]. ML-9 (Free Base) inducesautophagyby stimulating autophagosome formation and inhibiting their degradation[3].

体外研究
(In Vitro)

ML9 (Free Base) (0-100 μM; 0-24 hours) has no reduction in cardiomyocyte viability, 50-100 μM significantly induces cell death[2].
ML9 (Free Base) (50 μM; 1-4 hours) significantly increases cleaved caspase-3 levels, decreased STIM1 protein levels by about 42%[2].

Cell Viability Assay[1]

Cell Line:Neonatal rat ventricular myocytes (NRVM) cells
Concentration:0, 10, 50 and 100 μM
Incubation Time:0, 1, 4, 8 and 24 hours
Result:Decreased cell viability at 50–100 μM concentration.

Apoptosis Analysis[1]

Cell Line:Neonatal rat ventricular myocytes (NRVM) cells
Concentration:50 μM
Incubation Time:0, 1, 4, 8 hours
Result:Induced cardiomyocyte death through necrosis and apoptosis.
分子量

324.83

Formula

C15H17ClN2O2S

CAS 号

110448-31-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.