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血管生成

2-Methoxyestradiol (2-MeOE2)

品牌 厂商性质 产地 货期
阿拉丁 生产商 上海 现货

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产品参数
货号 CAS号 操作
M125960-100mg 362-07-2 询底价
M125960-50mg 362-07-2 询底价
M125960-10mg 362-07-2 询底价
M125960-25mg 362-07-2 询底价
M125960-500mg 362-07-2 询底价
产品介绍

属性

溶解性 Soluble in DMSO (10 mg/mL), ethanol (10 mg/mL), chloroform, ethanol (1 mg/ml), and 1:1DMF:PBS(pH7.2) (0.5 mg/ml). Insoluble in water.

描述

应用 A disruptor of microtubule function and HIF-1 inhibitor
产品介绍 2-Methoxyestradiol (2-MeOE2)使微管解聚,且抑制HIF-1α核积累和HIF转录活性。Phase 2。
备注 2-Methoxyestradiol depolymerizes microtubules and blocks HIF-1α nuclear accumulation and HIF-transcriptional activity. Phase 2.
生化机理 2-methoxyestradiol (2ME2) is a natural metabolite of estrogen that is known to inhibit HIF-1 alpha with an IC50 of 0.71 ± 0.11 μM for the inhibition of BPAEC migration.2-Methoxyestradiol is an endogenous estrogen metabolite with low affinity for the estrogen receptor but which disrupts microtubule function. 2-Methoxyestradiol is formed by CYP450-mediated hydroxylation followed by catechol-O-methyltransferase (COMT) methylation of estradiol. 2-Methoxyestradiol is a derivative of an oestrogenic steroidal hormone and has demonstrated: potent inhibition of endothelial cell proliferation and migration and inhibition of bFGF and VEGF-induced corneal neovascularization in mice. In MDA-MB-231 cells, 2-Methoxyestradiol inhibits HIF mediated transcriptional activation of target genes without affecting the transcription of HIF-1α itself. 2-Methoxyestradiol has been shown to induce apoptosis through activation of the p53 pathway through either activation of p38 and NF-κ
别名 2-MeOE2;2-甲氧基-β-雌二醇;2-甲氧基雌二醇;2-ME2;(8R,9S,13S,14S,17S)-2-methoxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol;2-Methoxy-β-estradiol

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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途