Drug Information
Drug General Information | Top | |||
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Drug ID |
D01IFR
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Former ID |
DNC014396
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Drug Name |
5-benzhydryl-1,3,4-oxadiazole-2(3H)-thione
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Synonyms |
CHEMBL593832; 5-benzhydryl-1,3,4-oxadiazole-2-thiol; 93073-39-3; 5-(diphenylmethyl)-1,3,4-oxadiazole-2-thiol; AC1MJWI7; 5-benzhydryl-3H-1,3,4-oxadiazole-2-thione; 5-benzhydryl-1,3,4-oxadiazole-2(3H)-thione; MolPort-001-902-005; ZINC17946026; STK803293; BDBM50320727; BBL012648; AKOS002344283; MCULE-6937439472; BAS 00805225; 5-Benzhydryl-[1,3,4]oxadiazole-2-thiol; SR-01000312098; 5-Diphenylmethyl-1,3,4-oxadiazole-2(3H)-thione
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C15H12N2OS
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Canonical SMILES |
C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=NNC(=S)O3
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InChI |
1S/C15H12N2OS/c19-15-17-16-14(18-15)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H,(H,17,19)
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InChIKey |
YCCKTVQLIQQBMK-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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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 | |||
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REF 1 | New potent inhibitors of tyrosinase: novel clues to binding of 1,3,4-thiadiazole-2(3H)-thiones, 1,3,4-oxadiazole-2(3H)-thiones, 4-amino-1,2,4-triaz... Bioorg Med Chem. 2010 Jun 1;18(11):4042-8. |
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