1. GPCR/G Protein Neuronal Signaling Immunology/Inflammation Anti-infection Metabolic Enzyme/Protease
  2. Histamine Receptor Bacterial Cytochrome P450
  3. Ranitidine

Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion. Ranitidine is a weak inhibitor of CYP2C19 and CYP2C9.

For research use only. We do not sell to patients.

Ranitidine Chemical Structure

Ranitidine Chemical Structure

CAS No. : 66357-35-5

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Based on 1 publication(s) in Google Scholar

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Description

Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion. Ranitidine is a weak inhibitor of CYP2C19 and CYP2C9[1][2].

IC50 & Target[1][2]

H2 Receptor

3.3 μM (IC50)

CYP2C19

 

CYP2C9

 

Clinical Trial
Molecular Weight

314.40

Formula

C13H22N4O3S

CAS No.
SMILES

O=[N+](/C=C(NC)/NCCSCC1=CC=C(CN(C)C)O1)[O-]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Ranitidine
Cat. No.:
HY-B0693
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