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GV-196771A
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
GV-196771A图片
CAS NO:166974-23-8
规格:98%
分子量:423.22
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议
20mg电议

产品介绍
GV-196771A是GV196771的钠盐形式。是NMDA受体拮抗剂。
CAS:166974-23-8
分子式:C20H13Cl2N2NaO3
分子量:423.22
纯度:98%
存储:Store at -20°C

Background:

GV-196771A is the sodium salt form of GV196771, is an NMDA receptor antagonist.



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 (