Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D09YJS
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| Former ID |
DNC008017
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| Drug Name |
2-hydroxyphenethyl 3,4,5-trihydroxybenzoate
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| Synonyms |
CHEMBL399354; 2-hydroxyphenethyl 3,4,5-trihydroxybenzoate; Gallic acid 2-hydroxyphenethyl ester
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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 |
C15H14O6
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| Canonical SMILES |
C1=CC=C(C(=C1)CCOC(=O)C2=CC(=C(C(=C2)O)O)O)O
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| InChI |
1S/C15H14O6/c16-11-4-2-1-3-9(11)5-6-21-15(20)10-7-12(17)14(19)13(18)8-10/h1-4,7-8,16-19H,5-6H2
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| InChIKey |
BFCLPURLRKZMCC-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Tyrosinase (TYR) | Target Info | Inhibitor | [1] |
| BioCyc | (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 | Top | |||
|---|---|---|---|---|
| REF 1 | Synthetic tyrosyl gallate derivatives as potent melanin formation inhibitors. Bioorg Med Chem Lett. 2007 Oct 1;17(19):5462-4. | |||
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