BMS-962212 是直接的，可逆的，选择性 FXIa 抑制剂。 BMS-962212 具有良好的耐受性，快速起效的药效 (PD) 反应和快速消除。 BMS-962212 在活化的部分促凝血酶原激酶时间内依赖性地增加暴露，并且在 FXI 凝血活性中依赖性地降低暴露。
CAS：1430114-34-3
分子式：C32H28ClFN8O5
分子量：659.07
纯度：98%
存储：Store at -20°C

Background:

BMS-962212 is a direct, reversible, selective factor XIa (FXIa) inhibitor . BMS-962212 is well tolerated, with fast onset of pharmacodynamic (PD) responses and rapid elimination. BMS-962212 increases exposure dependently in activated partial thromboplastin time, and decreases exposure dependently in FXI clotting activity[1].

[1]. Perera V, et al. First-in-human study to assess the safety, pharmacokinetics and pharmacodynamics of BMS-962212, a direct, reversible, small molecule factor XIa inhibitor in non-Japanese and Japanese healthy subjects. Br J Clin Pharmacol. 2018 May;84(5):876-887.