Type : non-oxime, Quinone methide precursor
Chemical_Nomenclature :
Canonical SMILES : C1(=CC=C(C(=C1)CN2CCC[C@H]2C)O)NC(=O)C3=CC=C([N+](=O)[O-])C=C3
InChI : InChI=1S\/C19H21N3O4\/c1-13-3-2-10-21(13)12-15-11-16(6-9-18(15)23)20-19(24)14-4-7-17(8-5-14)22(25)26\/h4-9,11,13,23H,2-3,10,12H2,1H3,(H,20,24)\/t13-\/m1\/s1
InChIKey : LYSRLTKQEGAENE-CYBMUJFWSA-N
Other name(s) :
Structure : No structure
Families : No family
Title : 4-Amidophenol Quinone Methide Precursors: Effective and Broad-Scope Nonoxime Reactivators of Organophosphorus-Inhibited Cholinesterases and Resurrectors of Organophosphorus-Aged Acetylcholinesterase - Lovins_2024_ACS.Chem.Neurosci__ |
Author(s) : Lovins AR , Miller KA , Buck AK , Ensey DS , Homoelle RK , Murtha MC , Ward NA , Shanahan LA , Gutti G , Shriwas P , McElroy CA , Callam CS , Hadad CM |
Ref : ACS Chem Neurosci , : , 2024 |
Abstract : |
PubMedSearch : Lovins_2024_ACS.Chem.Neurosci__ |
PubMedID: 38621296 |