Ixabepilone

产品编号: DCAPI1510 Featured
Ixabepilone
结构式
219989-84-1
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中国地区超过5000个高品质化合物库存
应用领域
Ixabepilone 是一种可口服的 microtubule抑制剂,能够与微管蛋白结合,促进微管蛋白的聚合和微管的稳定,因此使细胞停滞在 G2-M 期,诱导细胞凋亡。
Cas No.: 219989-84-1
名称:
别名:
SMILES: [C@](C)12[C@]([H])(O1)C[C@H](/C(/C)=C/C1=CSC(C)=N1)NC(=O)C[C@@H](O)C(C)(C)C(=O)[C@@H](C)[C@H](O)[C@H](C)CCC2
分子式: C27H42N2O5S
分子量: 506.7
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: Ixabepilone (Azaepothilone B; BMS 247550) is an epothilone B analog and nontaxane microtubule-stabilizing compound with clinical activity in a range of solid tumors. in vitro: BMS-247550 (EpoB), a novel epothilone B analogue, induces cell cycle arrest at the G(2)-M phase transition and subsequent apoptotic cell death of MDA-MB-468 (468) cells. in vivo: Ixabepilone, on a once every 21-day schedule, is modestly active against metastatic gastric cancer previously treated with a taxane. The days 1-5 every 21 days schedule had a more favorable safety profile but no activity. The results of this study suggest that once every 21-day ixabepilone schedule should be pursued further in untreated gastric or gastroesophageal adenocarcinoma patients. Ixabepilone has demonstrated activity in patients with chemotherapy-naive metastatic HRPC. Major toxicities were neutropenia and neuropathy. Further testing to define its activity relative to standard therapy is warranted. For the detailed information of Ixabepilone, the solubility of Ixabepilone in water, the solubility of Ixabepilone in DMSO, the solubility of Ixabepilone in PBS buffer, the animal experiment(test) (test) of Ixabepilone, the cell expriment (test) of Ixabepilone, the in vivo, in vitro and clinical trial test of Ixabepilone, the EC50, IC50,and Affinity of Ixabepilone,, please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DCAPI1510 Ixabepilone Ixabepilone 是一种可口服的 microtubule抑制剂,能够与微管蛋白结合,促进微管蛋白的聚合和微管的稳定,因此使细胞停滞在 G2-M 期,诱导细胞凋亡。