ml133 hydrochloride

ML133 hydrochloride (ML133 HCl) 是选择性的Kir2家族通道抑制剂，在pH 7.4 和pH 8.5 时的IC50值分别为1.8 μM 和290 nM。

ML 10302 hydrochloride 是一种特异性激动剂 5-HT4 并结合 5-HT 受体，5-HT4 和 5-HT3 的 Kis 分别为 1.07 nM 和 782 nM。

ML-7 hydrochloride (ML-7 HCl) 是一种可渗透细胞的、可逆的、有效的、ATP 竞争性的肌球蛋白轻链激酶(MLCK) 特异性抑制剂，IC50为300 nM。它还抑制平滑肌肌球蛋白轻链激酶、PKA 和 PKC。

ML-095 hydrochloride (CID-25067483 hydrochloride) 是一种特异性胎盘碱性磷酸酶抑制剂。它抑制 PLAP、TNAP 和 IAP，IC50 分别为 2.1、>100 和 53 μM。

phospholipase D2 (PLD2) inhibitor

ML-309 is an inhibitor of mutant isocitrate dehydrogenase 1 (IDH1). It reversibly and selective inhibits IDH1R132H over wild-type IDH1 (IC50s = 96 and 36,500 nM, respectively). ML-309 reduces 2-hydroxyglutarate production in U87 MG glioblastoma cells (EC50 = 55 nM).

ML-252 is a potent, selective inhibitor of the Kv7.2 voltage-gated potassium channel, demonstrating an IC50 value of 69 nM in patch clamp assays. It exists as the (S)-enantiomer, which is significantly more effective than both its (R)-enantiomer counterpart and the racemic mixture, with respective IC50 values of 944 nM and 160 nM. ML-252 exhibits high selectivity for Kv7.2 over other potassium channel subtypes and shows minimal activity against more than 68 G protein-coupled receptors, various transporters, L- and N-type calcium channels, K_ATP, and hERG potassium channels. However, it does inhibit the melatonin MT1 receptor by 61% at a 10 µM concentration.

ML 315为CDK和DYRK的双重选择性抑制剂，其IC50值分别为68 nM和282 nM，应用于癌症和神经系统疾病的研究。

ML-00253764 hydrochloride is an antagonist of nonpeptidic melanocortin receptor 4 (MC4R) (Ki and IC50 of 0.16 µM and 0.103 µM, respectively).