Drug Information
Drug General Information | Top | |||
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Drug ID |
D03SKE
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Former ID |
DNC014507
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Drug Name |
2,2',3-Tribromo-4,4',5,5'-tetrahydroxybibenzyl
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Synonyms |
CHEMBL1270043; SCHEMBL15511567; BDBM50329699; 2,2'',3-Tribromo-4,4'',5,5''-tetrahydroxybibenzyl
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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 |
C14H11Br3O4
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Canonical SMILES |
C1=C(C(=CC(=C1O)O)Br)CCC2=CC(=C(C(=C2Br)Br)O)O
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InChI |
1S/C14H11Br3O4/c15-8-5-10(19)9(18)3-6(8)1-2-7-4-11(20)14(21)13(17)12(7)16/h3-5,18-21H,1-2H2
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InChIKey |
NFQMJMJFBMIAAK-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Mycobacterium Isocitrate lyase (MycB icl) | Target Info | Inhibitor | [1] |
KEGG Pathway | Glyoxylate and dicarboxylate metabolism | |||
Metabolic pathways | ||||
Biosynthesis of secondary metabolites | ||||
Microbial metabolism in diverse environments | ||||
Carbon metabolism |
References | Top | |||
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REF 1 | Bromophenols as Candida albicans isocitrate lyase inhibitors. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6644-8. |
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