Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0W2OP
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| Former ID |
DNC009617
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| Drug Name |
2-(4-benzylphenoxy)ethanamine
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| Synonyms |
2-(4-benzylphenoxy)ethanamine; CHEMBL163807; 2-(4-benzylphenoxy)ethylamine; SCHEMBL7138354; MJTXDDKAEQAMNA-UHFFFAOYSA-N; 2-(4-Benzyl-phenoxy)-ethylamine; BDBM50085290
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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 |
C15H17NO
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| Canonical SMILES |
C1=CC=C(C=C1)CC2=CC=C(C=C2)OCCN
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| InChI |
1S/C15H17NO/c16-10-11-17-15-8-6-14(7-9-15)12-13-4-2-1-3-5-13/h1-9H,10-12,16H2
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| InChIKey |
MJTXDDKAEQAMNA-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Leukotriene A-4 hydrolase (LTA4H) | Target Info | Inhibitor | [1] |
| BioCyc | Leukotriene biosynthesis | |||
| KEGG Pathway | Arachidonic acid metabolism | |||
| Metabolic pathways | ||||
| Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
| WikiPathways | Arachidonic acid metabolism | |||
| Eicosanoid Synthesis | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Activation and inhibition of leukotriene A4 hydrolase aminopeptidase activity by diphenyl ether and derivatives. Bioorg Med Chem Lett. 2008 Dec 15;18(24):6549-52. | |||
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