Ranitidine Hydrochloride
The hydrochloride salt form of ranitidine used to reduce stomach acid and treat conditions like peptic ulcers and gastroesophageal reflux disease. This formulation was widely prescribed before safety concerns led to its market withdrawal.
Peso molecular
350,8700 g/mol
TPSA
112,00 Ų
Áreas terapéuticas
Mecanismo de acción
Competitive H2 receptor antagonist.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitive H2 receptor antagonist.
Estructura 2D
Cite this structure
Embed this structure
SMILES
CNC(=C[N+](=O)[O-])NCCSCc1ccc(CN(C)C)o1.Cl
InChI
InChI=1S/C13H22N4O3S.ClH/c1-14-13(9-17(18)19)15-6-7-21-10-12-5-4-11(20-12)8-16(2)3;/h4-5,9,14-15H,6-8,10H2,1-3H3;1H
Molecular Formula
C13H23ClN4O3S
HBD / HBA
3 / 7
Enlaces Rotables
9
Átomos Pesados
22
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Preguntas frecuentes
The hydrochloride salt form of ranitidine used to reduce stomach acid and treat conditions like peptic ulcers and gastroesophageal reflux disease. This formulation was widely prescribed before safety concerns led to its market withdrawal.
Competitive H2 receptor antagonist.
Yes, Ranitidine Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2110372. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3033332. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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