Potency of novel oximes to reactivate sarin inhibited human cholinesterases.

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Potency of novel oximes to reactivate sarin inhibited human cholinesterases.

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2008 nî lūn-bûn

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2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

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2008年论文

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2008年论文

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Potency of novel oximes to reactivate sarin inhibited human cholinesterases.

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Potency of novel oximes to reactivate sarin inhibited human cholinesterases.

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prefLabel

Potency of novel oximes to reactivate sarin inhibited human cholinesterases.

@en

P1476

Potency of novel oximes to reactivate sarin inhibited human cholinesterases

@en

P2093

Jan Marek

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

Jan Picha

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

Kamil Kuca

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Vit Koleckar

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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.

Organophosphate poisoning.

Structural requirements of acetylcholinesterase reactivators.

Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds.

Reactivation of sarin-inhibited pig brain acetylcholinesterase using oxime antidotes

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

Pralidoxime iodide (2-pAM) penetrates across the blood-brain barrier.

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.

Quaternary salts of 4,3' and 4,4' bis-pyridinium monooximes: synthesis and biological activity.

P304

1-9

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P31

scholarly article

P356

10.1080/01480540701688238

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P433

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

P478

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

P50

Daniel Jun

P577

2008-01-01T00:00:00Z

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P698

18161504

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