Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0V1DW
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| Former ID |
DNC009162
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| Drug Name |
3,4,5-tribromo-2-(2', 4'-dibromo-phenoxy)phenol
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| Synonyms |
CHEMBL464577; CHEBI:68326; 3,4,5-tribromo-2-(2,4-dibromophenoxy)phenol; 35162-01-7; Dysidea substance A; 6-hydroxy-2,2',3,4,4'-pentabromodiphenyl ether; SCHEMBL5527228; CTK1B7172; DTXSID60474586; BDBM50292443; ACM35162017; 3,4,5-tribromo-2-(2',4'-dibromophenoxy)phenol; Phenol, 3,4,5-tribromo-2-(2,4-dibromophenoxy)-; 3,4,5-tribromo-2-(2'', 4''-dibromo-phenoxy)phenol
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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 |
C12H5Br5O2
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| Canonical SMILES |
C1=CC(=C(C=C1Br)Br)OC2=C(C(=C(C=C2O)Br)Br)Br
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| InChI |
1S/C12H5Br5O2/c13-5-1-2-9(6(14)3-5)19-12-8(18)4-7(15)10(16)11(12)17/h1-4,18H
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| InChIKey |
LNZHBUPVHNJGJG-UHFFFAOYSA-N
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| CAS Number |
CAS 35162-01-7
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| PubChem Compound ID | ||||
| ChEBI ID |
CHEBI:68326
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Glutamine amidotransferase (GMPS) | Target Info | Inhibitor | [1] |
| BioCyc | Guanosine nucleotides de novo biosynthesis | |||
| Superpathway of purine nucleotide salvage | ||||
| Purine nucleotides de novo biosynthesis | ||||
| Guanosine ribonucleotides de novo biosynthesis | ||||
| KEGG Pathway | Purine metabolism | |||
| Drug metabolism - other enzymes | ||||
| Metabolic pathways | ||||
| Panther Pathway | De novo purine biosynthesis | |||
| Pathwhiz Pathway | Glutamate Metabolism | |||
| Purine Metabolism | ||||
| Reactome | Purine ribonucleoside monophosphate biosynthesis | |||
| WikiPathways | Metabolism of nucleotides | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Enzyme inhibitors: new and known polybrominated phenols and diphenyl ethers from four Indo-Pacific Dysidea sponges. J Nat Prod. 1995 Sep;58(9):1384-91. | |||
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