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- 文献和实验
- 技术资料
- 英文名:
Vorinostat
- 供应商:
上海恪敏生物科技有限公司
- CAS号:
149647-78-9
- 规格:
5mg
Vorinostat is a Histone Deacetylase Inhibitor. Vorinostat is a synthetic hydroxamic acid derivative with antineoplastic activity. This allows the hydroxamic moiety to chelate zinc ion located in the catalytic pockets of HDAC, thereby inhibiting deacetylation and leading to an accumulation of both hyperacetylated histones and transcription factors. Hyperacetylation of histone proteins results in the upregulation of the cyclin-dependent kinase p21, followed by G1 arrest. Hyperacetylation of non-histone proteins such as tumor suppressor p53, alpha tubulin, and heat-shock protein 90 produces additional anti-proliferative effects. This agent also induces apoptosis and sensitizes tumor cells to cell death processes. Vorinostat crosses the blood-brain barrier.
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文献和实验相关实验
,PDX101 (Bellinostat)作为一种没有客观反应的单一疗法并不有效。在MPM动物模型中,与未治疗的小鼠相比,panobinostat治疗显著降低了肿瘤生长。迄今为止,最大的间皮瘤试验之一是VANTAGE 14。这是一项III期研究,使用的是vorinostat或安慰剂,研究对象为661名曾接受过化疗的患者。与安慰剂相比,Vorinostat并没有提高生存率,中位生存期分别为31周和27周。然而,无进展生存期得到改善,但与临床无关(来源:欧洲多学科癌症大会)。MPM细胞系,DAC诱导衰老
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¥100 - 9999






