AKT-IN-2

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

AKT-IN-2 

AKT-IN-2 是一种有效的,选择性和口服生物可利用的 AKT 抑制剂,抑制 AKT1IC50 为 5 nM。

AKT-IN-2

AKT-IN-2 Chemical Structure

CAS No. : 1295514-91-8

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生物活性

AKT-IN-2 is a potent, selective and orally bioavailable AKT inhibitor with an IC50 of 5 nM for AKT1[1].

IC50 & Target[1]

Akt1

5 nM (IC50)

P70S6K

399 nM (IC50)

PKA

84 nM (IC50)

PKCβ2

3.98 μM (IC50)

RSK1

568 nM (IC50)

pGSK3β

92 nM (IC50)

体外研究
(In Vitro)

AKT-IN-2 (Compound 8) also inhibits P70S6K, PKA, PKCβ2, RSK1, and pGSK3β with IC50s of 0.399, 0.084, 3.98, 0.568, and 0.092 μM, respectively[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

505.58

Formula

C25H34F3N7O

CAS 号

1295514-91-8

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.

参考文献
  • [1]. Parthasarathy S, et al. Discovery of chiral dihydropyridopyrimidinones as potent, selective and orally bioavailable inhibitors of AKT. Bioorg Med Chem Lett. 2018 Jun 1;28(10):1887-1891.

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