SAR study to find optimal cholinesterase reactivator against organophosphorous nerve agents and pesticides
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, přehledy
PubMed
27582056
DOI
10.1007/s00204-016-1827-3
PII: 10.1007/s00204-016-1827-3
Knihovny.cz E-zdroje
- Klíčová slova
- Acetylcholinesterase, Nerve agents, Organophosphate, Pyridinium oximes, Reactivation, Uncharged reactivator,
- MeSH
- acetylcholinesterasa chemie metabolismus MeSH
- antidota chemie farmakologie terapeutické užití MeSH
- cholinesterasové inhibitory chemie toxicita MeSH
- katalytická doména MeSH
- konformace proteinů MeSH
- lidé MeSH
- ligandy MeSH
- molekulární konformace MeSH
- molekulární struktura MeSH
- nervová bojová látka chemie toxicita MeSH
- organofosforové sloučeniny antagonisté a inhibitory toxicita MeSH
- otrava organofosfáty farmakoterapie etiologie metabolismus MeSH
- pesticidy antagonisté a inhibitory toxicita MeSH
- pyridinové sloučeniny chemie farmakologie MeSH
- racionální návrh léčiv * MeSH
- reaktivátory cholinesterasy chemie farmakologie terapeutické užití MeSH
- vazebná místa MeSH
- vztahy mezi strukturou a aktivitou MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- acetylcholinesterasa MeSH
- antidota MeSH
- cholinesterasové inhibitory MeSH
- ligandy MeSH
- nervová bojová látka MeSH
- organofosforové sloučeniny MeSH
- pesticidy MeSH
- pyridinové sloučeniny MeSH
- reaktivátory cholinesterasy MeSH
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
Strategies for enhanced bioavailability of oxime reactivators in the central nervous system
Development of versatile and potent monoquaternary reactivators of acetylcholinesterase
Trends in the Recent Patent Literature on Cholinesterase Reactivators (2016-2019)
Acetylcholinesterase: The "Hub" for Neurodegenerative Diseases and Chemical Weapons Convention
Acute Toxic Injuries of Rat's Visceral Tissues Induced by Different Oximes
Toxic Injury to Muscle Tissue of Rats Following Acute Oximes Exposure