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产品价格:电议      采购度:1598      原产地:美洲
发布时间:2021/8/2 19:27:12 所属地区:上海 上海市
简要描述:
Siremadlin (NVP-HDM201) 是口服有效的选择性 p53-MDM2 抑制剂。
标签:NVP-HDM201
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CAS No. : 1448867-41-1
MCE 站:Siremadlin
产品活性:Siremadlin (NVP-HDM201) 是口服有效的选择性 p53-MDM2 抑制剂。
研究领域:Apoptosis | Metabolic Enzyme/Protease
作用靶点:MDM-2/p53 | E1/E2/E3 Enzyme
In Vitro: Siremadlin (NVP-HDM201) disrupts both human and murine TP53- MDM2 interactions, with nanomolar cellular IC50 values, blocking TP53 degradation.
In Vivo: Siremadlin (NVP-HDM201) is an imidazolopyrrolidinone analogue, showing a very advantageous in vivo profile. NVP-HDM201 has recently entered Phase 1 clinical trials in cancer patients. Constitutive PB mutagenesis in Arf?/? mice provides a collection of spontaneous tumors with characterized insertional genetic landscapes. Tumors are allografted in large cohorts of mice to assess the pharmacologic effects of Siremadlin (NVP-HDM201). Sixteen out of 21 allograft models are sensitive to Siremadlin (NVP-HDM201) but ultimately relapse under treatment. A comparison of tumors with acquired resistance to Siremadlin (NVP-HDM201) and untreated tumors identified 87 genes that are differentially and significantly targeted by the PB transposon. Siremadlin (NVP-HDM201) administered either daily at a low dose or once at a high dose revealed a differentiated engagement of the p53 molecular response. In contrast to the daily low dose treatment regimen, the single high dose Siremadlin (NVP-HDM201) regimen results in a rapid and dramatic induction of p53-dependent PUMA expression and apoptosis. This is consistent with the finding that a single high dose Siremadlin (NVP-HDM201) treatment, administered orally or intravenously, results in a robust and sustained tumor regression. Overall, both daily and once every 3 weeks dosing regimen shows comparable long term efficacy in preclinical studies. The ongoing clinical trial is currently designed to compare both dosing regimens with regard to efficacy and tolerability.
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更新时间:2024/1/2 10:17:29
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