Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H16N4 |
| Molecular Weight | 228.2929 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)N\C=N\C1=CC=C(C=C1)C2=CN=CN2
InChI
InChIKey=GOZUADYOHPCXLE-UHFFFAOYSA-N
InChI=1S/C13H16N4/c1-10(2)15-9-16-12-5-3-11(4-6-12)13-7-14-8-17-13/h3-10H,1-2H3,(H,14,17)(H,15,16)
| Molecular Formula | C13H16N4 |
| Molecular Weight | 228.2929 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P25021 Gene ID: 3274.0 Gene Symbol: HRH2 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/8931893 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| In vitro studies on the metabolic fate of mifentidine, a novel histamine H2-receptor antagonist. | 1997-04-01 |
|
| In vivo-in vitro correlations with a commercial dissolution simulator. Studies on the H2 receptor antagonist mifentidine. | 1996-10 |
|
| The effect of the new H2-receptor antagonist mifentidine on gastric secretion, gastric emptying and experimental gastric and duodenal ulcers in the rat: comparison with cimetidine and ranitidine. | 1986 |
|
| Mifentidine: evaluation of antiandrogen effects and kidney function studies. | 1985 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1981748
mifentidine 20 mg at night
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:57:33 GMT 2025
by
admin
on
Mon Mar 31 17:57:33 GMT 2025
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| Record UNII |
2F70KF5S0K
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C29578
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83184-43-4
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C66149
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100000080609
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5370
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C039796
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2F70KF5S0K
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SUB08955MIG
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71263
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DTXSID00232208
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CHEMBL308005
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