Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D05GZI
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| Former ID |
DNC014509
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| Drug Name |
N-(4-Ethylphenyl)benzo[d]oxazol-2-amine
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| Synonyms |
CHEMBL1269619; N-(4-Ethylphenyl)benzo[d]oxazol-2-amine; SCHEMBL11966141; MolPort-009-215-967; BDBM50329392; ZINC32686273; N-(4-Ethylphenyl)benzoxazole-2-amine; AKOS034448323; MCULE-8409538696; SC-56930; N-(4-ethylphenyl)-1,3-benzoxazol-2-amine; BENZOOXAZOL-2-YL-(4-ETHYL-PHENYL)-AMINE; Z55890479
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C15H14N2O
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| Canonical SMILES |
CCC1=CC=C(C=C1)NC2=NC3=CC=CC=C3O2
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| InChI |
1S/C15H14N2O/c1-2-11-7-9-12(10-8-11)16-15-17-13-5-3-4-6-14(13)18-15/h3-10H,2H2,1H3,(H,16,17)
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| InChIKey |
KKIDKWUGBUWNPR-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Arachidonate 5-lipoxygenase (5-LOX) | Target Info | Inhibitor | [1] |
| BioCyc | Aspirin-triggered lipoxin biosynthesis | |||
| Resolvin D biosynthesis | ||||
| Leukotriene biosynthesis | ||||
| Lipoxin biosynthesis | ||||
| Aspirin triggered resolvin D biosynthesis | ||||
| Aspirin triggered resolvin E biosynthesis | ||||
| KEGG Pathway | Arachidonic acid metabolism | |||
| Metabolic pathways | ||||
| Serotonergic synapse | ||||
| Ovarian steroidogenesis | ||||
| Toxoplasmosis | ||||
| NetPath Pathway | IL4 Signaling Pathway | |||
| Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
| WikiPathways | Vitamin D Receptor Pathway | |||
| Arachidonic acid metabolism | ||||
| Eicosanoid Synthesis | ||||
| Selenium Micronutrient Network | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Synthesis and evaluation of benzoxazole derivatives as 5-lipoxygenase inhibitors. Bioorg Med Chem. 2010 Nov 1;18(21):7580-5. | |||
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