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Details

Stereochemistry ACHIRAL
Molecular Formula C19H21N5O3S.2CH4O3S
Molecular Weight 591.678
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXMETIDINE MESYLATE

SMILES

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

InChI

InChIKey=KSTYTCDFRHRFLH-UHFFFAOYSA-N
InChI=1S/C19H21N5O3S.2CH4O3S/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;2*1-5(2,3)4/h2-3,7-8,10H,4-6,9,11H2,1H3,(H,22,23)(H2,20,21,24,25);2*1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula C19H21N5O3S
Molecular Weight 399.467
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Mechanism of oxmetidine (SK&F 92994) cytotoxicity in isolated rat hepatocytes.
1985 Jun
Mechanism of inhibition of rat liver mitochondrial respiration by oxmetidine, an H2-receptor antagonist.
1990 Mar
Successful drug development despite adverse preclinical findings part 1: processes to address issues and most important findings.
2010 Dec

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.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:53 UTC 2023
Edited
by admin
on Fri Dec 15 15:24:53 UTC 2023
Record UNII
6804GYV3YS
Record Status Validated (UNII)
Record Version
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Name Type Language
OXMETIDINE MESYLATE
USAN  
USAN  
Official Name English
OXMETIDINE MESYLATE [USAN]
Common Name English
SK&F 92994-J2
Code English
SKF-92994-J2
Code English
4(1H)-PYRIMIDINONE, 5-(1,3-BENZODIOXOL-5-YLMETHYL)-2-((2-(((5-METHYL-1H-IMIDAZOL-4-YL)METHYL)THIO)ETHYL)AMINO)-, DIMETHANESULFONATE
Systematic Name English
4(1H)-PYRIMIDINONE, 5-(1,3-BENZODIOXOL-5-YLMETHYL)-2-((2-(((5-METHYL-1H-IMIDAZOL-4-YL)METHYL)THIO)ETHYL)AMINO)-, DIMETHANESULPHONATE
Systematic Name English
2-((2-(((5-METHYLIMIDAZOL-4-YL)METHYL)THIO)ETHYL)AMINO)-5-PIPERONYL-4(1H)-PYRIMIDINONE DIMETHANESULPHONATE
Systematic Name English
2-[[2-[[(5-Methylimidazol-4-yl)methyl]thio]ethyl]amino]-5-piperonyl-4(1H)-pyrimidinone dimethanesulfonate
Systematic Name English
4(3H)-PYRIMIDINONE, 5-(1,3-BENZODIOXOL-5-YLMETHYL)-2-((2-(((4-METHYL-1H-IMIDAZOL-5-YL)METHYL)THIO)ETHYL)AMINO)-, METHANESULFONATE (1:2)
Systematic Name English
OXMETIDINE MESILATE
Common Name English
SK&F-92994-J2
Code English
Code System Code Type Description
NCI_THESAURUS
C166913
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
FDA UNII
6804GYV3YS
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
CAS
84455-52-7
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID401004718
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
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ChEMBL
CHEMBL2110657
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
USAN
U-61
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
PUBCHEM
13186930
Created by admin on Fri Dec 15 15:24:53 UTC 2023 , Edited by admin on Fri Dec 15 15:24:53 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY