Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0S6NP
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| Former ID |
DNC008863
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| Drug Name |
Kaempferol-3-O-methyl ether
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| Synonyms |
Isokaempferide; 1592-70-7; 3-Methylkaempferol; 3-O-Methylkaempferol; Kaempferol 3-methyl ether; kaempferol-3-O-methyl ether; CHEBI:1579; CHEMBL165064; 4H-1-BENZOPYRAN-4-ONE, 5,7-DIHYDROXY-2-(4-HYDROXYPHENYL)-3-METHOXY-; 3-Methylkempferol; AC1NQXOY; MLS000877008; SCHEMBL4637442; SCHEMBL1628023; MEGxp0_000171; 3-MK; cid_5280862; ACon1_001687; DTXSID90166609; MolPort-001-740-349; HMS2271C11; ZINC5732268; BDBM50240899; LMPK12112688; AKOS032949069
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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 |
C16H12O6
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| Canonical SMILES |
COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O
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| InChI |
1S/C16H12O6/c1-21-16-14(20)13-11(19)6-10(18)7-12(13)22-15(16)8-2-4-9(17)5-3-8/h2-7,17-19H,1H3
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| InChIKey |
VJJZJBUCDWKPLC-UHFFFAOYSA-N
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| CAS Number |
CAS 1592-70-7
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| PubChem Compound ID | ||||
| ChEBI ID |
CHEBI:1579
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Debrisoquine 4-hydroxylase (CYP2D6) | Target Info | Inhibitor | [1] |
| KEGG Pathway | Metabolism of xenobiotics by cytochrome P450 | |||
| Drug metabolism - cytochrome P450 | ||||
| Serotonergic synapse | ||||
| Reactome | Xenobiotics | |||
| WikiPathways | Metapathway biotransformation | |||
| Tamoxifen metabolism | ||||
| Oxidation by Cytochrome P450 | ||||
| Vitamin D Receptor Pathway | ||||
| Aripiprazole Metabolic Pathway | ||||
| Fatty Acid Omega Oxidation | ||||
| Codeine and Morphine Metabolism | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Sesquiterpenes and flavonol glycosides from Zingiber aromaticum and their CYP3A4 and CYP2D6 inhibitory activities. J Nat Prod. 2004 Jul;67(7):1079-83. | |||
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