Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D07HYL
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| Former ID |
DNC007075
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| Drug Name |
2,4,3',5'-tetrahydroxybibenzyl
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| Synonyms |
CHEMBL221291; 2,4,3',5'-tetrahydroxybibenzyl; SCHEMBL19433107; BDBM50193667; 2,4,3'',5''-tetrahydroxybibenzyl; 4-[2-(3,5-dihydroxyphenyl)ethyl]benzene-1,3-diol
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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 |
C14H14O4
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| Canonical SMILES |
C1=CC(=C(C=C1O)O)CCC2=CC(=CC(=C2)O)O
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| InChI |
1S/C14H14O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h3-8,15-18H,1-2H2
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| InChIKey |
IEOZKGCYMAJAHS-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 | Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. Bioorg Med Chem Lett. 2006 Nov 1;16(21):5650-3. | |||
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