搜索结果

Search Results for " diltiazem "

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T0112L	Diltiazem Diltiazem free base,Dilticard,地尔硫卓,CRD-401,CRD401,Dilzen,CRD 401
	Diltiazem is a non-dihydropyridine (non-DHP) calcium channel blocker that relaxes the smooth muscle in arterial walls, thus opening (dilating) arteries, allowing easier blood flow, and lowering blood pressure, and is used to treat hypertension, angina pec
T0112	Diltiazem hydrochloride CRD-401,盐酸地尔硫卓,RG 83606 HCl,Diltiazem HCl	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Diltiazem hydrochloride (RG 83606 HCl) 是一种苯并硫氮卓类钙通道阻滞剂，由于其拮抗钙离子对膜功能的作用而具有血管舒张作用。
T0112L2	Diltiazem malate Tiamate,UNII-14Y6444DRP,MK-793
	Diltiazem malate is an ACE inhibitor and non-dihydropyridine calcium channel blocker used in the treatment of hypertension.
T21008	Deacetyldiltiazem Desacetyl Diltiazem
	Deacetyldiltiazem is a metabolite product of Diltiazem which is a coronary vasodilator, and is present in the plasma of individuals taking Diltiazem.
T33781	O-Demethyldeacetyldiltiazem Deacetyl-O-demethyldiltiazem,Deacetyl-O-demethyl-D-diltiazem,Deacetyl o-desmethyl diltiazem
	O-Demethyldeacetyldiltiazem is one of the diltiazem metabolites in human plasma.
T33781L	O-Demethyldeacetyldiltiazem hydrochloride Deacetyl o-desmethyl diltiazem hydrochloride
	O-Demethyldeacetyldiltiazem hydrochloride is a biochemical.
T31248	Deacetyl-N-monodemethyldiltiazem
	Deacetyl-N-monodemethyldiltiazem is a major metabolites of diltiazem.
T31247	Deacetyl-N,O-didemethyldiltiazem
	Deacetyl-N,O-didemethyldiltiazem is a biochemical.
T68221	Clentiazem (free base)
	Clentiazem (free base) is a calcium channel blocker. It is a chlorine derivative of diltiazem.
T70037	AJG-049 free base
	AJG-049 free base is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).
T71454	Sas 1310
	Sas 1310 is a diltiazem derivative that acts as a calcium antagonist.
T70036	AJG-049 HCl
	AJG-049 HCl is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).