(3-bromo-5-phenoxyphenyl)boronic-acid
General
Type : Boron compound,Phenoxyphenyl
Chemical_Nomenclature : (3-bromo-5-phenoxyphenyl)boronic acid
Canonical SMILES : B(C1=CC(=CC(=C1)Br)OC2=CC=CC=C2)(O)O
InChI : InChI=1S\/C12H10BBrO3\/c14-10-6-9(13(15)16)7-12(8-10)17-11-4-2-1-3-5-11\/h1-8,15-16H
InChIKey : AMTOJYMQDUXNJR-UHFFFAOYSA-N
Other name(s) : 3-Bromo-5-phenoxyphenylboronic acid,MFCD21332918,AKOS027349335,ZINC169964610,AK353528,Y2490
MW : 292.92
Formula : C12H10BBrO3
CAS_number :
PubChem : 74892124
UniChem : AMTOJYMQDUXNJR-UHFFFAOYSA-N
IUPHAR :
Wikipedia :
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Target
Families : (3-bromo-5-phenoxyphenyl)boronic-acid ligand of proteins in family: Carb_B_Arthropoda
Stucture : 5TYJ alpha-esterase-7 in complex with (3-bromo-5-phenoxylphenyl)boronic acid
Protein : luccu-E3aest7
References (1)
| Title : Overcoming insecticide resistance through computational inhibitor design - Correy_2019_Proc.Natl.Acad.Sci.U.S.A_116_21012 |
| Author(s) : Correy GJ , Zaidman D , Harmelin A , Carvalho S , Mabbitt PD , Calaora V , James PJ , Kotze AC , Jackson CJ , London N |
| Ref : Proc Natl Acad Sci U S A , 116 :21012 , 2019 |
| Abstract : Correy_2019_Proc.Natl.Acad.Sci.U.S.A_116_21012 |
| ESTHER : Correy_2019_Proc.Natl.Acad.Sci.U.S.A_116_21012 |
| PubMedSearch : Correy_2019_Proc.Natl.Acad.Sci.U.S.A_116_21012 |
| PubMedID: 31575743 |
| Gene_locus related to this paper: luccu-E3aest7 |