Valspodar(PSC833)

产品编号: DC9813 Featured
Valspodar(PSC833)
结构式
121584-18-7
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中国地区超过5000个高品质化合物库存
应用领域
Valspodar是一种选择性的P-糖蛋白抑制剂,已被用作实验性癌症治疗和化学增敏剂。
Cas No.: 121584-18-7
名称:
别名: PSC 833; PSC-833; PSC833
SMILES: C/C=C/C[C@@H](C)C(=O)[C@H]1C(=O)N[C@H](C(=O)N(CC(=O)N([C@H](C(=O)N[C@H](C(=O)N([C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N([C@H](C(=O)N([C@H](C(=O)N([C@H](C(=O)N1C)C(C)C)C)CC(C)C)C)CC(C)C)C)C)C)CC(C)C)C)C(C)C)CC(C)C)C)C)C(C)C
分子式: C63H111N11O12
分子量: 1214.62
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: Valspodar(PSC833) is a P-glycoprotein (P-gp) inhibitor widely used in preclinical and clinical studies for overcoming multidrug resistance (MDR). In rat, Valspodar showed properties of low hepatic extraction and wide distribution, similar to that of its structural analogue cyclosporine A. Administration of Valspodar to animals before mitoxantrone treatment increased the accumulation of mitoxantrone in the MDR tumors to 94% of that in the wild-type tumors. These studies have added direct in vitro and in vivo visual information on how P-gp processes anticancer compounds and how P-gp inhibitors modulate MDR in resistant cancer cells.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
TITLE DOWNLOAD
MSDS_2817_DC9813_121584-18-7
COA
LOT NO. DOWNLOAD
产品编号 产品名称 应用领域
DC9813 Valspodar(PSC833) Valspodar是一种选择性的P-糖蛋白抑制剂,已被用作实验性癌症治疗和化学增敏剂。
DC2018 LY335979 (Zosuquidar 3HCl) Zosuquidar trihydrochloride是P-糖蛋白的抑制剂, Ki值为59 nM。