A-1210477

CAS号

1668553-26-1

分子式

C46H55N7O7S

主要靶点

BCL|Apoptosis

仅限科研使用

Cat No : CM03108

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Synonyms

A 1210477|A1210477|A-1210477|Apoptosis|Bcl-2 Family|inhibit|Inhibitor|Mcl-1



产品信息

CAS号 1668553-26-1
分子式 C46H55N7O7S
主要靶点 BCL|Apoptosis
主要通路 凋亡|凋亡
分子量 850.04
纯度 99.76%, 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 | Shipping with blue ice.
别名 A 1210477|A1210477|A-1210477|Apoptosis|Bcl-2 Family|inhibit|Inhibitor|Mcl-1

靶点活性

MCL1:26.2 nM

体外活性

在H929细胞中,A-1210477高亲和力结合于MCL-1,并促使MCL-1蛋白表达升高。在H929、H2110和H23细胞中,A-1210477引起凋亡的典型特征,并抑制依赖MCL-1的细胞生存能力。此外,A-1210477与navitoclax协同作用,有效杀灭多种癌症细胞系。[1] 在SKBR3细胞中,A-1210477抑制MCL-1–BIM相互作用,并诱导经典凋亡特征。[2] 另外,A-1210477还使非霍奇金淋巴瘤细胞系对venetoclax (ABT-199)更为敏感。[3]

溶解度

H2O:10 mM;DMSO:Insoluble

细胞实验

Adherent cell lines are seeded at 50?000 cells per well in 96-well plates and treated for 48?h with compounds diluted in half-log steps starting at 30?μM and ending at 0.001?μM. Multiple myeloma cell lines were seeded at 15?000–20?000 cells per well and treated similarly. Effects on proliferation and viability were determined using CellTiter-Glo reagent according to the manufacturer's instructions. IC50 values are determined by non-linear regression analysis of the concentration response data.(Only for Reference)

参考文献

1.Leverson JD, et al. Cell Death Dis. 2015, 6:e1590. doi: 10.1038/cddis.2014.561.
2.Xiao Y, et al. Mol Cancer Ther. 2015, 14(8), 1837-1847.
3.Phillips DC, et al. Blood Cancer J. 2015, 5:e368. doi: 10.1038/bcj.2015.88.

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