Name | N-(3-bromophenyl)-3-methylimidazo[4,5-g]quinazolin-8-amine |
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Synonyms |
HMS3229C05
8-[(3-Bromophenyl)amino]-3-methyl-3H-imidazo[4,5-g]-quinazoline Imidazoquinazoline deriv. 12 IN1402 bpiq-i |
Description | BPIQ-I (PD 159121) is a potent and ATP-competitive EGFR tyrosine kinase inhibitor.. BPIQ-I shows anti-proliferative actively[1][2]. |
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Related Catalog | |
In Vitro | BPIQ-I (0-50 µM; 3 days) 具有抗增殖活性,对 A-431, MDA-MB-468, U-87, SKOV-3, MDAMB-231 细胞的 EC50 值分别为 >50、30、>50、6.5、>50 µM [1]. BPIQ-I (10 nM) 通过与 ATP 竞争来阻断 erbB RTK,从而消除 CO2 敏感性[2]。 Cell Viability Assay [1] Cell Line: A-431, MDA-MB-468, U-87, SKOV-3, MDAMB-231 cells Concentration: 0-50 µM Incubation Time: 3 days Result: Inhibited cells growth with EC50s of >50, 30, >50, 6.5, >50 µM for A-431, MDA-MB-468, U-87, SKOV-3, MDAMB-231 cells, respectively. |
References |
Molecular Formula | C16H12BrN5 |
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Molecular Weight | 354.20400 |
Exact Mass | 353.02800 |
PSA | 55.63000 |
LogP | 4.09560 |