Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin.

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In vitro oxime-assisted reactivation of paraoxon-inhibited human acetylcholinesterase and butyrylcholinesterase.The role of the oximes HI-6 and HS-6 inside human acetylcholinesterase inhibited with nerve agents: a computational study.

P2860

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Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin.

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http://www.wikidata.org/entity/Q48167739

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2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年学术文章

@wuu

2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh

2007年學術文章

@zh-hant

name

Potency of five structurally d ...... rases inhibited by cyclosarin.

@en

Potency of five structurally d ...... rases inhibited by cyclosarin.

@nl

type

Item

label

Potency of five structurally d ...... rases inhibited by cyclosarin.

@en

Potency of five structurally d ...... rases inhibited by cyclosarin.

@nl

prefLabel

Potency of five structurally d ...... rases inhibited by cyclosarin.

@en

Potency of five structurally d ...... rases inhibited by cyclosarin.

@nl

P1476

Potency of five structurally d ...... rases inhibited by cyclosarin.

@en

P2093

Jiri Cabal

http://www.w3.org/2001/XMLSchema#string

Kamil Kuca

http://www.w3.org/2001/XMLSchema#string

P2860

Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents.

Specification of the structure of oximes able to reactivate tabun-inhibited acetylcholinesterase.

Structural requirements of acetylcholinesterase reactivators.

Signs of cyclosarin-induced neurotoxicity and its pharmacological treatment with quaternary pyridinium-oximes reactivators.

In vitro and in vivo evaluation of pyridinium oximes: mode of interaction with acetylcholinesterase, effect on tabun- and soman-poisoned mice and their cytotoxicity.

Reactivation kinetics of acetylcholinesterase from different species inhibited by highly toxic organophosphates.

Rational design of alkylene-linked bis-pyridiniumaldoximes as improved acetylcholinesterase reactivators.

A comparison of the ability of a new bispyridinium oxime--1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium)butane dibromide and currently used oximes to reactivate nerve agent-inhibited rat brain acetylcholinesterase by in vitro methods.

Reactivation of cyclosarin-inhibited rat brain acetylcholinesterase by pyridinium--oximes.

Antidotal treatment of GF-agent intoxication in mice with bispyridinium oximes.

P304

512-515

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

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10.1080/15563650701354234

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Daniel Jun

Martina Hrabinova

P577

2007-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

17503257

http://www.w3.org/2001/XMLSchema#string

Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin.

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P2860

P2860

Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698