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Search Results for " ranitidine "

Targets Recommended: P450 Antibacterial Histamine Receptor

抑制剂 & 化合物

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T3610	Ranitidine 雷尼替丁,HSDB 3925,Ranitidin	P450; Antibacterial; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience
	Ranitidine (HSDB 3925) 是一种选择性的，具有口服活性的组胺 H2 受体拮抗剂，IC50为 3.3 μM。它还一种是CYP2C19和CYP2C9的弱抑制剂，可抑制胃液分泌。
T0865	Ranitidine Hydrochloride AH19065,盐酸雷尼替丁	P450; Antibacterial; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience
	Ranitidine Hydrochloride (AH19065) 是一种具有口服活性的组胺 H2 受体选择性拮抗剂，IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂，可抑制胃液分泌。
T19929	Ranitidine-S-oxide	Others	Others
	Ranitidine-S-oxide is a metabolite of Ranitidine. It is commonly used in the treatment of peptic ulcer disease, Zollinger–Ellison syndrome，and gastroesophageal reflux disease.
T71059	Ranitidine bismuth citrate IST 622,雷尼替丁枸橼酸盐	Others	Others
	Ranitidine bismuth citrate 为一种口服活性的组胺H2受体(Histamine H2-receptor)拮抗剂，其IC50值为3.3 μM，对SARS-CoV-2感染细胞显示高选择性。该化合物还是治疗幽门螺杆菌(Helicobacter Pylori)感染的常用试剂，其MIC90为16 ng/L。
T20775	Ranitidine-N-oxide	Others	Others
	Ranitidine-N-oxide is a metabolite of Ranitidine. Ranitidine is a antagonist of histamine H2-receptor, it inhibits the normal and meal-stimulated secretion of stomach acid. Ranitidine is a medication decreaseing stomach acid production.
T71057	WF 2421	Others	Others
	WF 2421 is an aldose reductase inhibitor produced by Humicola grisea.

化合物

Ranitidine

Cat.No: T3610

Synonym: 雷尼替丁,HSDB 3925,Ranitidin

Target: P450, Antibacterial, Histamine Receptor

Ranitidine Hydrochloride

Cat.No: T0865

Synonym: AH19065,盐酸雷尼替丁

Target: P450, Antibacterial, Histamine Receptor

Ranitidine bismuth citrate

Cat.No: T71059

Synonym: IST 622,雷尼替丁枸橼酸盐

Cat. No.	Product Name	Target	Signaling Pathways
TMIJ-0189	Ranitidine-d6 HCl
	Ranitidine-d6 HCl 是 Ranitidine HCl 的氘代化合物。Ranitidine HCl 的 CAS 号为 66357-59-3。Ranitidine hydrochloride 是一种具有口服活性的组胺 H2 受体选择性拮抗剂，IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂，可抑制胃液分泌。