埃博霉素B

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本试剂(埃博霉素B)
仅供科研实验使用,不得用于其他用途！

简介：
货 号：LC2-E-5500
名 称：埃博霉素B
别 名：Epothilone B Free Base
C A S ：152044-54-7
分子量：507.68
分子式：C27H41NO6S
纯 度：HPLC/TLC:>99%
说 明：Storage: Store at or below -20 ºC. Solubility: Soluble in DMSO at 40 mg/mL; soluble in ethanol at 40 mg/mL; very poorly soluble in water; maximum solubility in plain water is estimated to be about 10-50 µM buffers, serum, or other additives may increase or decrease the aqueous solubility. Disposal: A.
文 献：Epothilones A-F are anticancer drugs. They induce microtubule polymerization at submicromolar concentrations and lead to death of cancer cells. Goodin, S., et al. "Epothilones: mechanism of action and biologic activity." J. Clin. Oncol. 22: 2015-2025 (2004). Epothilone B possess essentially all the biological effects of taxol both in vitro and in cultured cells. Epothilone B caused cell cycle arrest at the G2-M transition (EC50 = 32 nM for Hela cells and 3 nM for Hs578T), similar to taxol (EC50 = 7 nM for Hela cells and 10 nM for Hs578T). Epothilone B leads to cytotoxicity (EC50 = 40 nM for Hela cells and 6 nM for Hs578T), also similar to taxol (EC50 = 20 nM for Hela cells and 15 nM for Hs578T). However, epothilone B retains a much greater mitotic arrest at the G2-M transition and toxicity against P-glycoprotein-expressing multiple drug resistant KBV-1 cells (EC50 = 92 nM and 58 nM, respectively) than paclitaxel (EC50 = 17 µM and 23 µM, respectively). Bollag, D.M., et al. "Epothilones, a new class of microtubule-stabilizing agents with a taxol-like mechanism of action." Cancer Res. 55: 2325-2333 (1995). Two acquired β-tubulin mutations [β274(Thr-->Ile) and β282(Arg-->Gln)] near the taxane binding site exhibit impaired epothilone- and taxane-driven tubulin polymerization. Giannakakou, P., et al. "A common pharmacophore for epothilone and taxanes: molecular basis for drug resistance conferred by tubulin mutations in human cancer cells." Proc. Natl. Acad. Sci. USA 97: 2904-2909 (2000). Purified tubulin from parental 1A9 human ovarian carcinoma cells demonstrated paclitaxel-driven increased polymerization while the resistant cell tubulin with a mutation at 270 (Phe --> Val) or 364 (Ala --> Thr) barely polymerized under identical conditions. In contrast, the resistant cells retained sensitivity to epothilone B and the assembly was increased. Giannakakou, P., et al. "Paclitaxel-resistant human ovarian cancer cells have mutant beta-tubulins that exhibit impaired paclitaxel-driven polymerization." J. Biol. Chem. 272: 17118-17125 (1997). Epothilone B inhibited the growth of paclitaxel-sensitive human carcinoma cell lines including A549 (lung), NCI-H460 (Lung), HCT-116 (colon), DU145 (prostate), PC-3M (prostate), MDA-MB-231 (breast), BT-20 (breast), ZR-75-1 (breast), T-24 (bladder), and A-431 (epidermoid) with IC50's ranging from 0.13 nM to 0.64 nM. It also inhibited the growth of paclitaxel-resistant human cancer cell lines including CCRF-CEM (leukemia), CCRF-CEM/VBL100, SW620 (colon), SW620AD-300, KB-31, KB-8511, 1A9 (ovarian), 1A9PTX22, MCF-7 (breast), MCF-7/ADR, and HCT-15 (colon) with IC50's of 0.06 nM to 2.9 nM. Altmann, K.H., et al. "Epothilones and related structures--a new class of microtubule inhibitors with potent in vivo antitumor activity." Biochim. Biophys. Acta 1470: M79-M91 (2000). Diarrhea is the dose-limiting toxicity for epothilone B in clinical trials for patients with lung, ovarian and prostate cancers. Larkin, J.M.G., et al. "Patupilone" Drugs Fut. 32: 323 (2007).