Type : Imidazole, Pyrrolidine
Chemical_Nomenclature : 4-[2-(1H-imidazol-1-yl)ethyl]-2-{[(2R)-2-methylpyrrolidin-1-yl]methyl}phenol
Canonical SMILES : C1(=CC=C(C(=C1)CN2CCC[C@H]2C)O)CC[N]3C=CN=C3
InChI : InChI=1S\/C17H23N3O\/c1-14-3-2-8-20(14)12-16-11-15(4-5-17(16)21)6-9-19-10-7-18-13-19\/h4-5,7,10-11,13-14,21H,2-3,6,8-9,12H2,1H3\/t14-\/m1\/s1
InChIKey : LPXHWVDATIAJNV-CQSZACIVSA-N
Other name(s) : Compound 5 || 4-[2-(1-Imidazolyl)ethyl]-2-{[(R)-2-methyl-1-pyrrolidinyl]methyl}phenol || (R)-4-(2-(1H-imidazol-1-yl)ethyl)-2-((2-methylpyrrolidin-1-yl)methyl)phenol
Structure : No structure
Families : No family
| Title : Imidazole as a Pendant Reactivation Ligand Increases Efficacy Scope for Reactivation and Resurrection of Organophosphorus-Inhibited\/Aged Cholinesterases by Quinone Methide Precursors - Lovins_2026_ACS.Chem.Neurosci__ |
| Author(s) : Lovins AR , Miller KA , Homoelle RK , Hoover HJ , McElroy CA , Callam CS , Hadad CM |
| Ref : ACS Chem Neurosci , : , 2026 |
| Abstract : |
| PubMedSearch : Lovins_2026_ACS.Chem.Neurosci__ |
| PubMedID: 41712538 |