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Hydroxy Camptothecine 64439-81-2

简要描述:Hydroxy Camptothecine 64439-81-2
An alkaloid isolated from the stem wood of the Chinese tree, Camptotheca acuminata.

  • 产品型号:abs47027739
  • 厂商性质:生产厂家
  • 更新时间:2025-12-26
  • 访  问  量:656

详细介绍

品牌absinCAS64439-81-2
分子式C20H16N2O5纯度99%
分子量364.35货号abs47027739
规格5mg供货周期现货
主要用途This compound selectively inhibits the n应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

Hydroxy Camptothecine 64439-81-2

产品描述
描述

An alkaloid isolated from the stem wood of the Chinese tree, Camptotheca acuminata. This compound selectively inhibits the nuclear enzyme DNA topoisomerase, type I. Several semisynthetic analogs of camptothecin have demonstrated antitumor activity.

纯度
99%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
可溶性/溶解性
Soluble in DMSO
生物活性
靶点
DNA topoisomerase I
In vitro(体外研究)
10-HCPT has an inhibitory effect on phosphorylation of histone H1 and H3 in murine hepatoma cells and also exhibits a differentiation inducing effect in human HepG2 cells. 10-HCPT inhibits the cell growth, reduces the cell viability and disturbs the cell cycle distribution of human colon cancer cell line Colo 205. It induces cell cycle arrest in the G2/M phase.
In vivo(体内研究)
10-HCPT can be safely orally administered and, alternatively, a low-dose long-term treatment. Prolonged elimination of HCPT in vivo may have a significant impact on its therapeutic effects. HCPT is metabolized to its carboxylate form and glucuronides. Dose-dependent toxicity is observed with i.v. administration of HCPT.
参考文献
参考文献
  • 1. Zhang S, et al. Anticancer Drugs. 2014 Jul;25(6):614-23.

  • 2. Chen ZH, et al. PLoS One. 2013; 8(1):e53291.

  • 3. Tan H, et al. Bioorg Med Chem. 2015 Jan 1; 23(1):118-25.

研究领域
研究领域
CancerDrug resistanceTopoisomerases
EpigeneticsDNA / RNADNA SynthesisTopoisomerases
Drug DiscoverySmall Molecule DrugLead Compound Discovery
Hydroxy Camptothecine 64439-81-2温馨提示:本产品仅作科研实验使用,不支持临床等研究

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