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

Chemical Structure : Tariquidar methanesulfonate hydrate

CAS No.: 625375-83-9

Tariquidar methanesulfonate hydrate (XR 9576;XR-9576;XR9576)

货号: PC-42649Not For Human Use, Lab Use Only.

A potent, specific P-gp inhibitor with Kd of 5.1 nM.

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100 mg ¥3960 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

A potent, specific P-gp inhibitor with Kd of 5.1 nM; potentiates the cytotoxicity of several drugs including doxorubicin, paclitaxel, etoposide, and vincristine in a panel of human MDR cell lines at 25-80 nM; exhibits potent i.v. and p.o. activity without apparently enhancing the plasma pharmacokinetics of paclitaxel or the toxicity of coadministered drugs.

Breast Cancer

Phase 2 Discontinued

物理化学性质&存储条件

分子量 892.9887
分子式 C40H52N4O15S2
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

DMSO: ≥ 296 mg/mL; H2O: < 8.9 mg/mL

Chemical Name/SMILES

3-Quinolinecarboxamide, N-[2-[[[4-[2-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]amino]carbonyl]-4,5-dimethoxyphenyl]-, methanesulfonate, hydrate (1:2:3)

参考文献

1. Martin C, et al. Br J Pharmacol. 1999 Sep;128(2):403-11.

2. Mistry P, et al. Cancer Res. 2001 Jan 15;61(2):749-58.

3. Walker J, et al. Eur J Cancer. 2004 Mar;40(4):594-605.

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