Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D07ZAV
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| Former ID |
DNC014499
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| Drug Name |
2-(butylthiomethyl)-5-hydroxy-4H-pyran-4-one
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| Synonyms |
CHEMBL1269398; 204503-10-6; 2-(butylthiomethyl)-5-hydroxy-4H-pyran-4-one; CTK0J0428; DTXSID10680655; BDBM50330110; AKOS030554091; 4H-Pyran-4-one, 2-[(butylthio)methyl]-5-hydroxy-
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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 |
C10H14O3S
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| Canonical SMILES |
CCCCSCC1=CC(=O)C(=CO1)O
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| InChI |
1S/C10H14O3S/c1-2-3-4-14-7-8-5-9(11)10(12)6-13-8/h5-6,12H,2-4,7H2,1H3
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| InChIKey |
PJEUFTMKXABORH-UHFFFAOYSA-N
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| CAS Number |
CAS 204503-10-6
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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 | Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6569-71. | |||
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