Drug Information
| Drug General Information | |||||
|---|---|---|---|---|---|
| Drug ID |
D09YJS
|
||||
| Former ID |
DNC008017
|
||||
| Drug Name |
2-hydroxyphenethyl 3,4,5-trihydroxybenzoate
|
||||
| Drug Type |
Small molecular drug
|
||||
| Indication | Discovery agent | Investigative | [1] | ||
| Structure |
|
Download2D MOL |
|||
| Formula |
C15H14O6
|
||||
| Canonical SMILES |
C1=CC=C(C(=C1)CCOC(=O)C2=CC(=C(C(=C2)O)O)O)O
|
||||
| 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
|
||||
| InChIKey |
BFCLPURLRKZMCC-UHFFFAOYSA-N
|
||||
| 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 | Bioorg Med Chem Lett. 2007 Oct 1;17(19):5462-4. Epub 2007 Jul 25.Synthetic tyrosyl gallate derivatives as potent melanin formation inhibitors. | ||||
If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.