Drug General Information |
Drug ID |
D0B0LC
|
Former ID |
DNC004257
|
Drug Name |
2-(4-Imidazol-1-yl-phenoxymethyl)-pyridine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C15H13N3O
|
Canonical SMILES |
C1=CC=NC(=C1)COC2=CC=C(C=C2)N3C=CN=C3
|
InChI |
1S/C15H13N3O/c1-2-8-17-13(3-1)11-19-15-6-4-14(5-7-15)18-10-9-16-12-18/h1-10,12H,11H2
|
InChIKey |
IMJROXJEYNKELD-UHFFFAOYSA-N
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PubChem Compound ID |
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Target and Pathway |
Target(s) |
Cytochrome P450 2D6 |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 3A4 |
Target Info |
Inhibitor |
[1]
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KEGG Pathway
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Metabolism of xenobiotics by cytochrome P450
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Drug metabolism - cytochrome P450
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Serotonergic synapsehsa00140:Steroid hormone biosynthesis
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Linoleic acid metabolism
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Retinol metabolism
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Drug metabolism - other enzymes
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Metabolic pathways
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Bile secretion
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Chemical carcinogenesis
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PathWhiz Pathway
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Caffeine Metabolism
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Retinol Metabolism
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Reactome
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XenobioticsR-HSA-211981:Xenobiotics
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Aflatoxin activation and detoxification
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WikiPathways
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Metapathway biotransformation
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Tamoxifen metabolism
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Oxidation by Cytochrome P450
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Vitamin D Receptor Pathway
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Aripiprazole Metabolic Pathway
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Fatty Acid Omega Oxidation
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Codeine and Morphine MetabolismWP702:Metapathway biotransformation
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Aflatoxin B1 metabolism
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Estrogen metabolism
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Benzo(a)pyrene metabolism
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Tryptophan metabolism
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Nuclear Receptors in Lipid Metabolism and Toxicity
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Nuclear Receptors Meta-Pathway
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Farnesoid X Receptor Pathway
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Felbamate Metabolism
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Lidocaine metabolism
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Nifedipine Activity
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Colchicine Metabolic Pathway
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Irinotecan Pathway
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Drug Induction of Bile Acid Pathway
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Codeine and Morphine Metabolism
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References |
REF 1 | Bioorg Med Chem Lett. 2004 Jan 19;14(2):333-6.Imidazole derivatives as new potent and selective 20-HETE synthase inhibitors. |