搜索结果

"M 25" 的搜索结果

目录号	产品详情		靶点
T22958	M 25		Others
T22958	Smoothened (Smo) receptor antagonist		Others
T71299	M-25
T71299	M-25 is a Smoothened antagonist and inhibitor of the Hedgehog pathway.
T10432L	AZD-8529 mesylate		GluR
T10432L	AZD-8529 mesylate 是高度选择性的可口服mGluR2正向调节剂，EC50值为 285 nM。它在 20-25 M 时，对 mGluR1、3、4、5、6、7 和 8 亚型没有显示正变构调节剂反应。		GluR
T71297	TT15
T71297	TT15 is an agonist of the GLP-1R.
T18173	m-PEG25-acid		Others
T18173	m-PEG25-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].		Others
T18174	m-PEG25-Hydrazide		Others
T18174	m-PEG25-Hydrazide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].		Others
T18176	m-PEG25-Propargyl		Others
T18176	m-PEG25-Propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].		Others
T14197L	Alvameline maleate	Lu 25-109-M
T14197L	Alvameline maleate is used as a Partial M1 Agonist and M2/M3 Antagonist.
T18175	m-PEG25-NHS ester		Others
T18175	m-PEG25-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].		Others
T38293	4-CPPC		Others
T38293	4-CPPC 是一种巨噬细胞迁移抑制因子 2 (MIF-2; IC50= 27 μM) 的抑制剂。它对 MIF-2 的选择性高于 MIF-1 (IC50= 450 μM)。当以 10 μM 浓度使用时，它在体外抑制 MIF-2，但不抑制 MIF-1，与 CD74 结合。 4-CPPC（5、10 和 25 μM）抑制原代人皮肤成纤维细胞中 MIF-2 诱导的 ERK1/2 磷酸化。		Others