Drug Information
Drug General Information | |||||
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Drug ID |
D02LHQ
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Former ID |
DNC013261
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Drug Name |
3-(2,4-dihydroxyphenyl)propionic acid
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C9H10O4
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Canonical SMILES |
C1=CC(=C(C=C1O)O)CCC(=O)O
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InChI |
1S/C9H10O4/c10-7-3-1-6(8(11)5-7)2-4-9(12)13/h1,3,5,10-11H,2,4H2,(H,12,13)
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InChIKey |
HMCMTJPPXSGYJY-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Tyrosine oxidase | Target Info | Inhibitor | [1] | |
BioCyc Pathway | (S)-reticuline biosynthesis | ||||
Eumelanin biosynthesis | |||||
L-dopachrome biosynthesis | |||||
KEGG Pathway | Tyrosine metabolism | ||||
Riboflavin metabolism | |||||
Metabolic pathways | |||||
Melanogenesis | |||||
PathWhiz Pathway | Riboflavin Metabolism | ||||
Tyrosine Metabolism | |||||
WikiPathways | Dopamine metabolism | ||||
References | |||||
REF 1 | J Med Chem. 2007 May 31;50(11):2676-81. Epub 2007 Apr 21.Enhanced substituted resorcinol hydrophobicity augments tyrosinase inhibition potency. | ||||
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