产品
编 号：F200048
分子式：C20H13Cl2N2NaO3
分子量：423.22
分子式：C20H13Cl2N2NaO3
分子量：423.22
产品类型
规格
价格
是否有货
结构图
CAS No: 166974-23-8
产品详情
生物活性：
GV-196771A is the sodium salt form of GV196771, is an NMDA receptor antagonist.
体内研究：
GV196771 is a potent antagonist of the modulatory glycine site of the N-methyl-D-aspartate receptor. GV196771 is a potent antagonist of the modulatory glycine site of the NMDA receptor developed for treatment of neuropathic pain. GV196771 is an NMDA receptor antagonist with low oral bioavailability in rats and mice. GV196771 has low oral bioavailability (<10%) and plasma clearance (~2 mL/min/kg) in rats.
GV-196771A is the sodium salt form of GV196771, is an NMDA receptor antagonist.
体内研究：
GV196771 is a potent antagonist of the modulatory glycine site of the N-methyl-D-aspartate receptor. GV196771 is a potent antagonist of the modulatory glycine site of the NMDA receptor developed for treatment of neuropathic pain. GV196771 is an NMDA receptor antagonist with low oral bioavailability in rats and mice. GV196771 has low oral bioavailability (<10%) and plasma clearance (~2 mL/min/kg) in rats.
产品资料
Copyright©2015-2024 沪ICP备2022026524号-1
沪公网安备