Drug Information
| Drug General Information | |||||
|---|---|---|---|---|---|
| Drug ID |
D0B2NG
|
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| Former ID |
DNC014506
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| Drug Name |
Bis(3-bromo-4,5-dihydroxyphenyl)methanone
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent | Investigative | [1] | ||
| Structure |
|
Download2D MOL |
|||
| Formula |
C13H8Br2O5
|
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| Canonical SMILES |
C1=C(C=C(C(=C1O)O)Br)C(=O)C2=CC(=C(C(=C2)Br)O)O
|
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| InChI |
1S/C13H8Br2O5/c14-7-1-5(3-9(16)12(7)19)11(18)6-2-8(15)13(20)10(17)4-6/h1-4,16-17,19-20H
|
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| InChIKey |
QWGGKBRLOGNRAY-UHFFFAOYSA-N
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| PubChem Compound ID | |||||
| Target and Pathway | |||||
| Target(s) | Isocitrate lyase | Target Info | Inhibitor | [1] | |
| KEGG Pathway | Glyoxylate and dicarboxylate metabolism | ||||
| Metabolic pathways | |||||
| Biosynthesis of secondary metabolites | |||||
| Microbial metabolism in diverse environments | |||||
| Carbon metabolism | |||||
| References | |||||
| REF 1 | Bioorg Med Chem Lett. 2010 Nov 15;20(22):6644-8. Epub 2010 Sep 21.Bromophenols as Candida albicans isocitrate lyase inhibitors. | ||||
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