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XR 9051 HCl

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货号
XR 9051 HCl
CAS 号
[180422-22-4]
分子式
C 39 H 36 N 4 O 5 .HCl
分子量
679.2
规格
10mg; 50mg
规格(数值)
10 mg
别名
N-[4-[2-(3,4-Dihydro-6,7-dimethoxy- 2(1H)-isoquinolinyl)ethyl]phenyl]-3-[(Z)-[(5Z)-4-m ethyl-3,6-dioxo-5-(phenylmethylene)piperazinyliden e]methyl]benzamide hydrochloride
溶解性
Soluble to 100 mM in DMSO
储存条件
Store at -20°C
销量
0

产品描述

Potent modulator of P-glycoprotein-mediated multidrug resistance (MDR) that inhibits the binding of cytotoxics to P-glycoprotein (EC 50 = 134 nM). Reverses resistance to a variety of cytotoxic drugs (including doxorubicin, etoposide and vincristine) in several murine and human P-gp-overexpressing cell lines. Orally active. Purity: >98 %

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