Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D04XPJ
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| Former ID |
DNC011638
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| Drug Name |
Biphenyl-4-carboxylic acid hydroxyamide
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| Synonyms |
Biphenylhydroxamic acid; UNII-R3GRG20IPQ; R3GRG20IPQ; CHEMBL154585; 106359-54-0; Biphenyl-4-carboxylic acid hydroxyamide; 4-biphenyl hydroxamic acid; (1,1'-Biphenyl)-4-carboxamide, N-hydroxy-; 4-Phenylbenzohydroximic acid; SCHEMBL2143958; DTXSID00147585; JWLKPHOMARIZAB-UHFFFAOYSA-N; BDBM50015086
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
 |
Download2D MOL |
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| Formula |
C13H11NO2
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| Canonical SMILES |
C1=CC=C(C=C1)C2=CC=C(C=C2)C(=O)NO
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| InChI |
1S/C13H11NO2/c15-13(14-16)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,16H,(H,14,15)
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| InChIKey |
JWLKPHOMARIZAB-UHFFFAOYSA-N
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| CAS Number |
CAS 106359-54-0
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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 | Hydroxamic acid inhibitors of 5-lipoxygenase: quantitative structure-activity relationships. J Med Chem. 1990 Mar;33(3):992-8. | |||
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