McHardy_2014_Bioorg.Med.Chem.Lett_24_1711

Reference

Title : Design, synthesis, and characterization of novel, nonquaternary reactivators of GF-inhibited human acetylcholinesterase - McHardy_2014_Bioorg.Med.Chem.Lett_24_1711
Author(s) : McHardy SF , Bohmann JA , Corbett MR , Campos B , Tidwell MW , Thompson PM , Bemben CJ , Menchaca TA , Reeves TE , Cantrell WR, Jr. , Bauta WE , Lopez A , Maxwell DM , Brecht KM , Sweeney RE , McDonough J
Ref : Bioorganic & Medicinal Chemistry Lett , 24 :1711 , 2014
Abstract :

The goal of this research was to identify structurally novel, non-quaternarypyridinium reactivators of GF (cyclosarin)-inhibited hAChE that possess the capacity to mediate in vitro reactivation of GF-inhibited human acetylcholinesterase (hAChE). New compounds were designed, synthesized and assessed in GF-inhibited hAChE assays. Structure activity relationships for AChE binding and reactivation of GF-inhibited hAChE were developed. Lead compounds from two different chemical series, represented by compounds 17 and 38, displayed proficient in vitro reactivation of GF-inhibited hAChE, while also possessing low inhibition of native enzyme.

PubMedSearch : McHardy_2014_Bioorg.Med.Chem.Lett_24_1711
PubMedID: 24630558

Related information

Reactivator CHEMBL3235213-Cpd17

Citations formats

McHardy SF, Bohmann JA, Corbett MR, Campos B, Tidwell MW, Thompson PM, Bemben CJ, Menchaca TA, Reeves TE, Cantrell WR, Jr., Bauta WE, Lopez A, Maxwell DM, Brecht KM, Sweeney RE, McDonough J (2014)
Design, synthesis, and characterization of novel, nonquaternary reactivators of GF-inhibited human acetylcholinesterase
Bioorganic & Medicinal Chemistry Lett 24 :1711

McHardy SF, Bohmann JA, Corbett MR, Campos B, Tidwell MW, Thompson PM, Bemben CJ, Menchaca TA, Reeves TE, Cantrell WR, Jr., Bauta WE, Lopez A, Maxwell DM, Brecht KM, Sweeney RE, McDonough J (2014)
Bioorganic & Medicinal Chemistry Lett 24 :1711