Drug Information
Drug General Information | Top | |||
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Drug ID |
D0R4FM
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Former ID |
DNC013602
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Drug Name |
DIHYDROKAEMPFEROL
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Synonyms |
aromadendrin; 480-20-6; (+)-Dihydrokaempferol; dihydrokaempferol; katuranin; (+)-aromadendrin; Aromadendrol; (2R,3R)-3,5,7-Trihydroxy-2-(4-hydroxyphenyl)chroman-4-one; (+)-Aromadendrol; UNII-7YA4640575; (2R,3R)-3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one; CHEMBL9323; CHEBI:15401; PADQINQHPQKXNL-LSDHHAIUSA-N; 4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-, (2R,3R)-; 7YA4640575; Arbo 14; AC1L3VDW; AC1Q6KIF; (2R,3R)-dihydrokaempferol; MLS000697722
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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 |
C15H12O6
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Canonical SMILES |
C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O
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InChI |
1S/C15H12O6/c16-8-3-1-7(2-4-8)15-14(20)13(19)12-10(18)5-9(17)6-11(12)21-15/h1-6,14-18,20H/t14-,15+/m0/s1
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InChIKey |
PADQINQHPQKXNL-LSDHHAIUSA-N
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CAS Number |
CAS 480-20-6
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PubChem Compound ID | ||||
ChEBI ID |
CHEBI:15401
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Target and Pathway | Top | |||
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Target(s) | Xanthine dehydrogenase/oxidase (XDH) | Target Info | Inhibitor | [1] |
BioCyc | Purine nucleotides degradation | |||
Urate biosynthesis/inosine 5'-phosphate degradation | ||||
Guanosine nucleotides degradation | ||||
Adenosine nucleotides degradation | ||||
Retinoate biosynthesis II | ||||
KEGG Pathway | Purine metabolism | |||
Caffeine metabolism | ||||
Drug metabolism - other enzymes | ||||
Metabolic pathways | ||||
Peroxisome | ||||
Panther Pathway | Adenine and hypoxanthine salvage pathway | |||
Purine metabolism | ||||
Pathwhiz Pathway | Caffeine Metabolism | |||
Purine Metabolism | ||||
Reactome | Purine catabolism | |||
WikiPathways | Oxidative Stress | |||
Effects of Nitric Oxide | ||||
Metabolism of nucleotides | ||||
Selenium Micronutrient Network |
References | Top | |||
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REF 1 | Inhibition of cow's milk xanthine oxidase by flavonoids. J Nat Prod. 1988 Mar-Apr;51(2):345-8. |
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