Drug Information
Drug General Information | |||||
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Drug ID |
D0H5XP
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Former ID |
DNC014497
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Drug Name |
2-(ethylthiomethyl)-5-hydroxy-4H-pyran-4-one
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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 |
C8H10O3S
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Canonical SMILES |
CCSCC1=CC(=O)C(=CO1)O
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InChI |
1S/C8H10O3S/c1-2-12-5-6-3-7(9)8(10)4-11-6/h3-4,10H,2,5H2,1H3
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InChIKey |
BOZGBIVLELURMD-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 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. Epub 2010 Sep 21.Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. | ||||
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