Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D08HFK
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| Former ID |
DNC014510
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| Drug Name |
5-Chloro-N-phenylbenzo[d]oxazol-2-amine
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| Synonyms |
CHEMBL1269620; 79558-94-4; 2-Benzoxazolamine, 5-chloro-N-phenyl-; 5-Chloro-N-phenylbenzo[d]oxazol-2-amine; AC1NKL9S; 5-chloro-N-phenyl-1,3-benzoxazol-2-amine; SCHEMBL3474865; CTK2G4049; DTXSID50406795; BDBM50329393; ZINC33559155; N-Phenyl-5-chlorobenzoxazole-2-amine; VU0404023-1; J3.559.656I
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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 |
C13H9ClN2O
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| Canonical SMILES |
C1=CC=C(C=C1)NC2=NC3=C(O2)C=CC(=C3)Cl
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| InChI |
1S/C13H9ClN2O/c14-9-6-7-12-11(8-9)16-13(17-12)15-10-4-2-1-3-5-10/h1-8H,(H,15,16)
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| InChIKey |
YWNAVPSABPGECL-UHFFFAOYSA-N
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| CAS Number |
CAS 79558-94-4
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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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