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CAS No. : 2230757-47-6
MCE 国际站:ACP-5862
产品活性:ACP-5862 是 Acalabrutinib 的主要活性的,循环的,吡咯烷开环代谢产物,对 Bruton 酪氨酸激酶 (BTK) 的 IC50 为 5.0 nM。ACP-5862 是时间依赖性的 CYP3A4 和 CYP2C8 弱抑制剂。Acalabrutinib 是一种口服有效的,选择性的 BTK 抑制剂,IC50 和 EC50 分别为 3 nM 和 8 nM。
研究领域:Metabolic Enzyme/Protease | Protein Tyrosine Kinase/RTK
作用靶点:Drug Metabolite | Btk | Cytochrome P450
In Vivo: Following a single oral dose of 100 mg Acalabrutinib, the half‐life of ACP‐5862 is 6.9 hours and the mean exposure is approximately twofold to threefold higher than that of Acalabrutinib.
ACP-5862 (M27) is the major single metabolite in the systemic circulation and accountes for 57.4% and 42.1% of the AUC0-t total radioactivity in male and female rat plasma, respectively. ACP-5862, the major human metabolite, is a relatively minor component in the systemic circulation and accountes for 6.1% and 8.1% of the AUC0-t total radioactivity in male and female dog plasma, respectively.
ACP-5862 (1 or 10 μM) has reversible protein binding of 98.6%, 99.8%, 94.3%, 98.6% in mouse, rat, dog, and human plasma.
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