CHEMBL3093089
General
Type : Imidazole
Chemical_Nomenclature : (NE)-N-[(1,3-dibenzylimidazol-1-ium-2-yl)methylidene]hydroxylamine bromide
Canonical SMILES : C1=CC=C(C=C1)CN2C=C[N+](=C2\/C=N\/O)CC3=CC=CC=C3.[Br-]
InChI : InChI=1S\/C18H17N3O.BrH\/c22-19-13-18-20(14-16-7-3-1-4-8-16)11-12-21(18)15-17-9-5-2-6-10-17\;\/h1-13H,14-15H2\;1H
InChIKey : XULUVONPRMDBPI-UHFFFAOYSA-N
Other name(s) : oxime 3
MW : 372.3
Formula : C18H18BrN3O
CAS_number :
PubChem : 136240095
UniChem : XULUVONPRMDBPI-UHFFFAOYSA-N
Target
Structure : No structure
Families : No family
References (2)
| Title : N,N'-dibenzyl imidazolium oximes are potent reactivators of organophosphate-inhibited human butyrylcholinesterase - Kolic_2026_Eur.J.Med.Chem_313_118895 |
| Author(s) : Kolic D , Divjak T , Sinko G , Spahic Z , Ramic A , Lulic AM , Katalinic M , Macek Hrvat N , Primozic I , Kovarik Z |
| Ref : Eur Journal of Medicinal Chemistry , 313 :118895 , 2026 |
| Abstract : |
| PubMedSearch : Kolic_2026_Eur.J.Med.Chem_313_118895 |
| PubMedID: 42070449 |
| Title : Synthesis and antimicrobial profile of N-substituted imidazolium oximes and their monoquaternary salts against multidrug resistant bacteria - Odzak_2013_Bioorg.Med.Chem_21_7499 |
| Author(s) : Odzak R , Skocibusic M , Maravic A |
| Ref : Bioorganic & Medicinal Chemistry , 21 :7499 , 2013 |
| Abstract : |
| PubMedSearch : Odzak_2013_Bioorg.Med.Chem_21_7499 |
| PubMedID: 24126094 |