ym-244769 hydrochloride

inhibitor of the reverse mode of Na+/Ca2+ exchange (NCX)

mGlu1 receptor antagonist

YM-58790 hydrochloride is a potent M3 muscarinic receptor antagonist(Ki of 15 nM).

YM 298198 Hydrochloride is a non-competitive antagonist with high affinity and selectivity for mGlu1 receptors (Ki = 19 nM). YM 298198 Hydrochloride is inactive at other mGlu receptor subtypes (mGlu2-7), ionotropic receptors and glutamate transporters (IC50 > 10 μM). It inhibits glutamate-induced IP production more potently than CPCCOEt (IC50 values are 16 nM and 6.3 μM respectively).

YM-244769 dihydrochloride 是一种有效的 Na+ Ca2+ exchange 3 (NCX3) 抑制剂，IC50 为 18 nM。 YM-244769 dihydrochloride 对神经元和肾脏具有有效的保护作用。

YM-244769 (3-Pyridinecarboxamide, N-[(3-aminophenyl)methyl]-6-[4-[(3-fluorophenyl)methoxy]phenoxy]-) 是一种有效的 Na+ Ca2+ exchange 3 (NCX3) 抑制剂，IC50 为 18 nM。 YM-244769 对神经元和肾脏具有有效的保护作用。

Sepantronium hydrochloride (YM-155 hydrochloride) 是一种新型survivin 抑制剂，抑制survivin 启动子的IC50为 0.54 nM。