Synthesis of a new reactivator of tabun inhibited acetylcholinesterase

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG16__%2F03%3A00000901" target="_blank" >RIV/60162694:G16__/03:00000901 - isvavai.cz</a>

Alternative codes found

RIV/60162694:G38__/03:00000901

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Synthesis of a new reactivator of tabun inhibited acetylcholinesterase

Original language description

Synthesis of a new asymmetric bisquaternary reactivator of tabun-inhibited acetylcholinesterase-1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoyl pyridinium)butane dibromide is described.Reactivation potency of this oxime is compared to the currently used reactivators .pralidoxime,obidoxime and H-oxime HI-6

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FP - Other medical fields

OECD FORD branch

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Project

<a href="/en/project/OBVLAJEP20032" target="_blank" >OBVLAJEP20032: C-AGENTS - Medical problem of human being, animal andplant protection against topical types of military useable chemical agents</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2003

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Bioorganic and Medicinal Chemistry Letters

ISSN

0960-894X

e-ISSN

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Volume of the periodical

13

Issue of the periodical within the volume

20

Country of publishing house

GB - UNITED KINGDOM

Number of pages

3

Pages from-to

3545-3547

UT code for WoS article

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EID of the result in the Scopus database

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