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Details

Stereochemistry ACHIRAL
Molecular Formula C19H21N5O3S.2ClH
Molecular Weight 472.389
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXMETIDINE HYDROCHLORIDE

SMILES

Cl.Cl.CC1=C(CSCCNC2=NC(=O)C(CC3=CC=C4OCOC4=C3)=CN2)N=CN1

InChI

InChIKey=RBNMEHBTDUJJJM-UHFFFAOYSA-N
InChI=1S/C19H21N5O3S.2ClH/c1-12-15(23-10-22-12)9-28-5-4-20-19-21-8-14(18(25)24-19)6-13-2-3-16-17(7-13)27-11-26-16;;/h2-3,7-8,10H,4-6,9,11H2,1H3,(H,22,23)(H2,20,21,24,25);2*1H

HIDE SMILES / InChI
Oxmetidine is an H2-receptor antagonist that was studied as a gastrointestinal agent. Oxmetidine possesses efficacy in the treatment of peptic ulcers. However, information about the further development of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Oxmetidine in the short term treatment of active duodenal ulcer. A review and commentary.
1989

Sample Use Guides

In Vitro Use Guide
Oxmetidine (50 microM) blocked pyruvate/malate-supported state 3 (ADP-stimulated) respiration, caused a decrease in the ADP:0 ratio and a loss of respiratory control in isolated rat liver mitochondria.
Name Type Language
OXMETIDINE HYDROCHLORIDE
USAN  
USAN  
Official Name English
2-[[2-[[(5-Methylimidazol-4-yl)methyl]thio]ethyl]amino]-5-piperonyl-4(1H)-pyrimidinone dihydrochloride
Systematic Name English
SK&F-92994-A2
Code English
4(1H)-PYRIMIDINONE, 5-(1,3-BENZODIOXOL-5-YLMETHYL)-2-((2-(((5-METHYL-1H-IMIDAZOL-4-YL)METHYL)THIO)ETHYL)AMINO)-, DIHYDROCHLORIDE
Common Name English
SK&F 92994-A2
Code English
SK&F 92994-A(SUB 2)
Code English
SKF-92994-A2
Code English
OXMETIDINE HCL
Common Name English
OXMETIDINE HYDROCHLORIDE [USAN]
Common Name English
Code System Code Type Description
PUBCHEM
162998
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
263-997-3
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
FDA UNII
W93O1FK310
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
CAS
63204-23-9
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110657
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID70212572
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY
NCI_THESAURUS
C170274
Created by admin on Sat Dec 16 06:42:02 GMT 2023 , Edited by admin on Sat Dec 16 06:42:02 GMT 2023
PRIMARY