CAS NO: | 1818393-16-6 |
生物活性 | Alrizomadlin (APG-115) is an orally activeMDM2protein inhibitor binding toMDM2protein withIC50andKivalues of 3.8 nM and 1 nM, respectively[1]. Alrizomadlin blocks the interaction ofMDM2and p53 and induces cell-cycle arrest andapoptosisin a p53-dependent manner[2][3]. | ||||||||||||||||||||||||||||||||||||||||
IC50& Target | IC50: 3.8 nm (APG-115)[1] | ||||||||||||||||||||||||||||||||||||||||
体外研究 (In Vitro) | Alrizomadlin (0.001-100 μM; 72 hours) inhibits cell proliferation in concentration-dependent manner, with IC50s of 18.9 ± 15.6 nM and 103.5 ± 18.3 nM respectively in AGS and MKN45 cells[3].Alrizomadlin (0.02 μM, 0.2 μM; 48 hours) enhances the anti-proliferative effect of radiotherapy at different radiation dose[3].Alrizomadlin (0.02 μM, 0.2 μM; 48 hours) affects progression by inducing cells arrested at G0/G1 phase in AGS and MKN45 cell with wild p53[3].Alrizomadlin (0.02 μM, 0.2 μM; 24 hours) activates p53 to enhance radiosensitivity in AGS and MKN45 cells; stable knockout of p53 abrogates expression of MDM2, p53, p21, PUMA, BAX, Cleaved-caspase3, γH2AX[3].Alrizomadlin (0.3 μM, 1 μM, 3 μM, 10 μM; 24 hours) leads to a concentration-dependent cell cycle arrest in G2/M phases and a decreasing in S-phase in p53 wide-type cell lines (TPC-1, KTC-1)[4]. Cell Proliferation Assay[3]
RT-PCR[3]
Cell Cycle Analysis[3]
Apoptosis Analysis[4]
Western Blot Analysis[3]
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体内研究 (In Vivo) | Alrizomadlin (Delivered orally; 100 mg/kg; once daily; 10 days) enhances radiation antitumor effect in gastric adenocarcinoma in vivo[3].
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Clinical Trial | |||||||||||||||||||||||||||||||||||||||||
分子量 | 642.59 | ||||||||||||||||||||||||||||||||||||||||
性状 | Solid | ||||||||||||||||||||||||||||||||||||||||
Formula | C34H38Cl2FN3O4 | ||||||||||||||||||||||||||||||||||||||||
CAS 号 | 1818393-16-6 | ||||||||||||||||||||||||||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||||||||||||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 100 mg/mL(155.62 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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