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
SMILES
Cl.Cl.CC1=C(CSCCNC2=NC(=O)C(CC3=CC4=C(OCO4)C=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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Successful drug development despite adverse preclinical findings part 1: processes to address issues and most important findings. | 2010-12 |
|
| Mechanism of inhibition of rat liver mitochondrial respiration by oxmetidine, an H2-receptor antagonist. | 1990-03 |
|
| Oxmetidine in the short term treatment of active duodenal ulcer. A review and commentary. | 1989 |
|
| Mechanism of oxmetidine (SK&F 92994) cytotoxicity in isolated rat hepatocytes. | 1985-06 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2861279
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.
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ACTIVE MOIETY
SUBSTANCE RECORD