| Title : [Reactivation of phosphorylated acetylcholinesterase (AChE): quaternary salts of vinylogous pyridinaldoxims (author's transl)]. [German] - Hagedorn_1976_Arzneimittelforschung_26_1515 |
| Author(s) : Hagedorn I , Hohler W |
| Ref : Arzneimittelforschung , 26 :1515 , 1976 |
|
Abstract :
Application of Wittig reaction to 4-pyridinecarboxaldehyde leads to 4-beta-formylvinylpyridine (62%). The corresponding oxime (4-(2)) can be quaternized with alpha,alpha'-bis-(chloromegonin), and with methyliodide one to 4-PAM (4-(3)). In this case the formal insertion of an ethylenic double bond between the pyridinium ring and the aldoxime group decreases the ability to reactivate phosphorylated acetylcholinesterase (AChE). |
| PubMedSearch : Hagedorn_1976_Arzneimittelforschung_26_1515 |
| PubMedID: 1036947 |
Hagedorn I, Hohler W (1976)
[Reactivation of phosphorylated acetylcholinesterase (AChE): quaternary salts of vinylogous pyridinaldoxims (author's transl)]. [German]
Arzneimittelforschung
26 :1515
Hagedorn I, Hohler W (1976)
Arzneimittelforschung
26 :1515