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| 品牌 | absin | CAS | 64439-81-2 |
|---|---|---|---|
| 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. |
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| 研究领域 | |
| 研究领域 | CancerDrug resistanceTopoisomerases EpigeneticsDNA / RNADNA SynthesisTopoisomerases Drug DiscoverySmall Molecule DrugLead Compound Discovery |
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