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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-P-glycoprotein (P-gp)-Elacridar hydrochloride
Elacridar hydrochloride

Chemical Structure : Elacridar hydrochloride

CAS No.: 143851-98-3

Elacridar hydrochloride (GF-120918A)

货号: PC-45888Not For Human Use, Lab Use Only.

Elacridar hydrochloride is a potent inhibitor of multidrug resistance (MDR, P-gp) that fully reverses multidrug resistance CHRC5, OV1/DXR and MCF7/ADR cells to the cytotoxicity of doxorubicin and vincristine with IC50 of 0.02 uM.

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25 mg ¥1280 In stock
50 mg ¥1980 In stock
100 mg ¥2980 In stock
250 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Elacridar hydrochloride is a potent inhibitor of multidrug resistance (MDR, P-gp) that fully reverses multidrug resistance CHRC5, OV1/DXR and MCF7/ADR cells to the cytotoxicity of doxorubicin and vincristine with IC50 of 0.02 uM.
Elacridar effectively competes with [3H]azidopine for binding P-glycoprotein.
Elacridar restores sensitivity of the tumor to a single dose of doxorubicin in mice; orally bioavailable.

物理化学性质&存储条件

分子量 600.1039
分子式 C34H34ClN3O5
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-Acridinecarboxamide, N-[4-[2-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-9,10-dihydro-5-methoxy-9-oxo-, hydrochloride (1:1)

参考文献

1. Hyafil F, et al. Cancer Res. 1993 Oct 1;53(19):4595-602.

2. den Ouden D, et al. Leukemia. 1996 Dec;10(12):1930-6.

3. Witherspoon SM, et al. Clin Cancer Res. 1996 Jan;2(1):7-12.

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