Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H12N2 |
| Molecular Weight | 220.2692 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N1C=NC(=C1C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=CPHGOBGXZQKCKI-UHFFFAOYSA-N
InChI=1S/C15H12N2/c1-3-7-12(8-4-1)14-15(17-11-16-14)13-9-5-2-6-10-13/h1-11H,(H,16,17)
| Molecular Formula | C15H12N2 |
| Molecular Weight | 220.2692 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://patents.com/us-4670185.htmlCurator's Comment: https://www.ncbi.nlm.nih.gov/pubmed/13756443; https://www.ncbi.nlm.nih.gov/pubmed/13768238; https://www.ncbi.nlm.nih.gov/pubmed/2863106
Sources: http://patents.com/us-4670185.html
Curator's Comment: https://www.ncbi.nlm.nih.gov/pubmed/13756443; https://www.ncbi.nlm.nih.gov/pubmed/13768238; https://www.ncbi.nlm.nih.gov/pubmed/2863106
4,5-diphenylimidazole is an antihistaminic and antiallergic drug. It was shown to be an inhibitor of phenytoin p-hydroxylation in rat hepatic microsomes, however 1-imidazoles had higher inhibitory potency observed at submicromolar concentrations.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13756443
Curator's Comment: Diphenylimidazole (DIT) activity as an antiallergic drug is mentioned in the literature from the early 1960s
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Zinc(II) and Nickel(II) Benzoate Complexes from the Use of 1-methyl-4,5-diphenylimidazole. | 2010 |
|
| QSAR Studies on antiepileptic and locomotor in vivo activities of 4,5-diphenyl-1H-imidazoles. | 2009-08 |
|
| Molecular and electronic structure of five-coordinate complexes of iron(II/III) containing o-diiminobenzosemiquinonate(1-) pi radical ligands. | 2005-10-03 |
|
| From model compounds to protein binding: syntheses, characterizations and fluorescence studies of [RuII(bipy)(terpy)L]2+ complexes (bipy = 2,2'-bipyridine; terpy = 2,2':6',2''-terpyridine; L = imidazole, pyrazole and derivatives, cytochrome c). | 2005-01-21 |
|
| Photosensitized oxidation of 13C,15N-labeled imidazole derivatives. | 2002-08-14 |
| Substance Class |
Chemical
Created
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admin
on
Edited
Mon Mar 31 18:06:48 GMT 2025
by
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on
Mon Mar 31 18:06:48 GMT 2025
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| Record UNII |
398688L26Z
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| Record Status |
Validated (UNII)
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| Record Version |
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