Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0UH6R
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| Former ID |
DNC009729
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| Drug Name |
(N-(3-phenoxycinnamyl)-acetohydroxamic acid
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| Synonyms |
CHEMBL529218
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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 |
C17H15NO4
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| Canonical SMILES |
CC(=O)N(C(=O)C=CC1=CC(=CC=C1)OC2=CC=CC=C2)O
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| InChI |
1S/C17H15NO4/c1-13(19)18(21)17(20)11-10-14-6-5-9-16(12-14)22-15-7-3-2-4-8-15/h2-12,21H,1H3/b11-10+
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| InChIKey |
REDOCAPSVCSQLX-ZHACJKMWSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | LOX-5 messenger RNA (ALOX5 mRNA) | 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 | Arachidonic acid metabolism | |||
| Eicosanoid Synthesis | ||||
| Selenium Micronutrient Network | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Structural optimization and biological evaluation of 2-substituted 5-hydroxyindole-3-carboxylates as potent inhibitors of human 5-lipoxygenase. J Med Chem. 2009 Jun 11;52(11):3474-83. | |||
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