Drug General Information |
Drug ID |
D00PYW
|
Former ID |
DNC004238
|
Drug Name |
4-[2-(4-Imidazol-1-yl-phenoxy)-ethyl]-morpholine
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
Download
2D MOL
3D MOL
|
Formula |
C15H19N3O2
|
Canonical SMILES |
C1COCCN1CCOC2=CC=C(C=C2)N3C=CN=C3
|
InChI |
1S/C15H19N3O2/c1-3-15(4-2-14(1)18-6-5-16-13-18)20-12-9-17-7-10-19-11-8-17/h1-6,13H,7-12H2
|
InChIKey |
PXFGMZGVHWPLCC-UHFFFAOYSA-N
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Cytochrome P450 3A4 |
Target Info |
Inhibitor |
[1]
|
Cytochrome P450 2D6 |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
Steroid hormone biosynthesis
|
Linoleic acid metabolism
|
Retinol metabolism
|
Metabolism of xenobiotics by cytochrome P450
|
Drug metabolism - cytochrome P450
|
Drug metabolism - other enzymes
|
Metabolic pathways
|
Bile secretion
|
Chemical carcinogenesishsa00980:Metabolism of xenobiotics by cytochrome P450
|
Serotonergic synapse
|
PathWhiz Pathway
|
Caffeine Metabolism
|
Retinol Metabolism
|
Reactome
|
Xenobiotics
|
Aflatoxin activation and detoxificationR-HSA-211981:Xenobiotics
|
WikiPathways
|
Metapathway biotransformation
|
Aflatoxin B1 metabolism
|
Estrogen metabolism
|
Benzo(a)pyrene metabolism
|
Tamoxifen metabolism
|
Tryptophan metabolism
|
Oxidation by Cytochrome P450
|
Nuclear Receptors in Lipid Metabolism and Toxicity
|
Nuclear Receptors Meta-Pathway
|
Farnesoid X Receptor Pathway
|
Vitamin D Receptor Pathway
|
Felbamate Metabolism
|
Lidocaine metabolism
|
Nifedipine Activity
|
Colchicine Metabolic Pathway
|
Irinotecan Pathway
|
Drug Induction of Bile Acid Pathway
|
Fatty Acid Omega Oxidation
|
Codeine and Morphine MetabolismWP702:Metapathway biotransformation
|
Aripiprazole Metabolic Pathway
|
Codeine and Morphine Metabolism
|
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. |