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izvor podataka: crosbi

Structure of novel mannoconjugates with heterocyclic oximes and their interaction with acetylcholinesterase (CROSBI ID 596235)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Primožič, Ines ; Baumann, Krešimir ; Tomić- Pisarović, Srđanka Structure of novel mannoconjugates with heterocyclic oximes and their interaction with acetylcholinesterase // 13th Medical Chemical Defence Conference 2011 : Current Status of Terapeutic Approaches to Nerve Agent Poisoning. München, 2011. str. 47-47

Podaci o odgovornosti

Primožič, Ines ; Baumann, Krešimir ; Tomić- Pisarović, Srđanka

engleski

Structure of novel mannoconjugates with heterocyclic oximes and their interaction with acetylcholinesterase

In the attempt to improve the quality of antidotes against organophosphorus poisoning, heterocyclic oxime reactivators of inhibited AChE were linked to the sugar moiety. It was found that the attachement of a glucose to the oxime derivative increases the bioavailability of the antidote because they can mor easily cross blood-brain barrier and the antidote is retained longer in the blood circulation. Moreover, sugar analogs are in principle less toxic than the non-sugar analogs.

antidotes ; mannoconjugates ; oximes ; AChE

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Podaci o prilogu

47-47.

2011.

objavljeno

Podaci o matičnoj publikaciji

13th Medical Chemical Defence Conference 2011 : Current Status of Terapeutic Approaches to Nerve Agent Poisoning

München:

Podaci o skupu

13th Medical Chemical Defence Conference 2011

poster

13.04.2011-14.04.2011

München, Njemačka

Povezanost rada

Kemija