SBI-0206965

SBI-0206965 是一种强效,选择性和细胞渗透性自噬激酶ULK1抑制剂,对 ULK1 激酶活性的 IC50 为 108 nM,对 ULK2 的 IC50 为 711 nM。

CAS号

1884220-36-3

分子式

C21H21BrN4O5

主要靶点

Autophagy|Apoptosis

仅限科研使用

Cat No : CM06824

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Synonyms

SBI0206965



产品信息

SBI-0206965 is a potent, selective and cell-permeable autophagy kinase ULK1 inhibitor with IC50 of 108 nM for ULK1 kinase activity and 711 nM for ULK2.

CAS号 1884220-36-3
分子式 C21H21BrN4O5
主要靶点 Autophagy|Apoptosis
主要通路 自噬|凋亡
分子量 489.32
纯度 98.86%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 SBI0206965

靶点活性

ULK1:108 nM|ULK2:711 nM

体外活性

In HEK293T transfected with WT or KI Myc-tagged ULK1 and WT Vps34, SBI-0206965 inhibits Ser249 phosphorylation of overexpressed Vps34 and Beclin1 Ser15 phosphorylation. SBI-0206965 suppresses autophagy induced by mTOR inhibition in A549 cells, and prevents ULK1-dependent cell survival in WT MEFs. In addition, SBI-0206965 also synergizes with mTOR inhibition to induce cancer cell death. [1]

溶解度

DMSO:20 mg/mL

参考文献

1.Elokdah H, et al. J Med Chem. 2004, 47(14), 3491-3494.
2.Zhang H, Cui Z, Cheng D, et al. RNF186 regulates EFNB1 (ephrin B1)-EPHB2-induced autophagy in the colonic epithelial cells for the maintenance of intestinal homeostasis[J]. Autophagy . 2020

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