Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D00VQZ
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| Former ID |
DNC013591
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| Drug Name |
1-hydroxy-3-(4-nitrophenyl)urea
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| Synonyms |
1-hydroxy-3-(4-nitrophenyl)urea; CHEMBL259979; 53731-88-7; NSC163567; AC1NQIZ7; SCHEMBL16005844; CTK1H3407; DTXSID10411168; BDBM50377113
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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 |
C7H7N3O4
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| Canonical SMILES |
C1=CC(=CC=C1NC(=O)NO)[N+](=O)[O-]
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| InChI |
1S/C7H7N3O4/c11-7(9-12)8-5-1-3-6(4-2-5)10(13)14/h1-4,12H,(H2,8,9,11)
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| InChIKey |
DXBVARSUKIUCDK-UHFFFAOYSA-N
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| CAS Number |
CAS 53731-88-7
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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 | Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation. Bioorg Med Chem Lett. 2008 Jun 15;18(12):3607-10. | |||
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