SAR study to find optimal cholinesterase reactivator against organophosphorous nerve agents and pesticides

. 2016 Dec ; 90 (12) : 2831-2859. [epub] 20160831

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid27582056
Odkazy

PubMed 27582056
DOI 10.1007/s00204-016-1827-3
PII: 10.1007/s00204-016-1827-3
Knihovny.cz E-zdroje

Irreversible inhibition of acetylcholinesterase (AChE) by organophosphates leads to many failures in living organism and ultimately in death. Organophosphorus compounds developed as nerve agents such as tabun, sarin, soman, VX and others belong to the most toxic chemical warfare agents and are one of the biggest threats to the modern civilization. Moreover, misuse of nerve agents together with organophosphorus pesticides (e.g. malathion, paraoxon, chlorpyrifos, etc.) which are annually implicated in millions of intoxications and hundreds of thousand deaths reminds us of insufficient protection against these compounds. Basic treatments for these intoxications are based on immediate administration of atropine and acetylcholinesterase reactivators which are currently represented by mono- or bis-pyridinium aldoximes. However, these antidotes are not sufficient to ensure 100 % treatment efficacy even they are administered immediately after intoxication, and in general, they possess several drawbacks. Herein, we have reviewed new efforts leading to the development of novel reactivators and proposition of new promising strategies to design novel and effective antidotes. Structure-activity relationships and biological activities of recently proposed acetylcholinesterase reactivators are discussed and summarized. Among further modifications of known oximes, the main attention has been paid to dual binding site ligands of AChE as the current mainstream strategy. We have also discussed new chemical entities as potential replacement of oxime functional group.

Citace poskytuje Crossref.org

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Strategies for enhanced bioavailability of oxime reactivators in the central nervous system

. 2023 Nov ; 97 (11) : 2839-2860. [epub] 20230829

Development of versatile and potent monoquaternary reactivators of acetylcholinesterase

. 2021 Mar ; 95 (3) : 985-1001. [epub] 20210131

Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators

. 2020 Dec ; 35 (1) : 478-488.

Understanding the Interaction Modes and Reactivity of Trimedoxime toward MmAChE Inhibited by Nerve Agents: Theoretical and Experimental Aspects

. 2020 Sep 05 ; 21 (18) : . [epub] 20200905

Safety and Efficacy of New Oximes to Reverse Low Dose Diethyl-Paraoxon-Induced Ventilatory Effects in Rats

. 2020 Jul 03 ; 25 (13) : . [epub] 20200703

Trends in the Recent Patent Literature on Cholinesterase Reactivators (2016-2019)

. 2020 Mar 12 ; 10 (3) : . [epub] 20200312

Acetylcholinesterase: The "Hub" for Neurodegenerative Diseases and Chemical Weapons Convention

. 2020 Mar 07 ; 10 (3) : . [epub] 20200307

Reactivation of VX-Inhibited Human Acetylcholinesterase by Deprotonated Pralidoxime. A Complementary Quantum Mechanical Study

. 2020 Jan 27 ; 10 (2) : . [epub] 20200127

Cysteine-Targeted Insecticides against A. gambiae Acetylcholinesterase Are Neither Selective nor Reversible Inhibitors

. 2020 Jan 09 ; 11 (1) : 65-71. [epub] 20191126

Molecular modeling studies on the interactions of 7-methoxytacrine-4-pyridinealdoxime, 4-PA, 2-PAM, and obidoxime with VX-inhibited human acetylcholinesterase: a near attack conformation approach

. 2019 Dec ; 34 (1) : 1018-1029.

Acute Toxic Injuries of Rat's Visceral Tissues Induced by Different Oximes

. 2019 Nov 11 ; 9 (1) : 16425. [epub] 20191111

Toxic Injury to Muscle Tissue of Rats Following Acute Oximes Exposure

. 2019 Feb 06 ; 9 (1) : 1457. [epub] 20190206

Synthesis, Biological Evaluation, and Docking Studies of Novel Bisquaternary Aldoxime Reactivators on Acetylcholinesterase and Butyrylcholinesterase Inhibited by Paraoxon

. 2018 May 07 ; 23 (5) : . [epub] 20180507

A newly developed oxime K203 is the most effective reactivator of tabun-inhibited acetylcholinesterase

. 2018 Feb 21 ; 19 (1) : 8. [epub] 20180221

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...