Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2007-5-10
pubmed:abstractText
(-)-Cytisine and its derivatives are promising alkaloids in the development of new drugs for the treatment of disorders of the central nervous system (CNS). Electron ionization (EI) mass spectral fragmentations of cytisine (1), N-methylcytisine (2), N-ethylcytisine (3), N-acetylcytisine (4), N-propionylcytisine (5) and N-benzoylcytisine (6) have been investigated. Detailed fragmentation pathways have been identified for all significant ions, including a few characteristic fragment ions. The principal fragmentation routes of compounds 1-6 have been determined on the basis of EI low-resolution, high-resolution and B2/E linked scans as well as linked scans at constant B/E.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0951-4198
pubmed:author
pubmed:copyrightInfo
Copyright (c) 2007 John Wiley & Sons, Ltd.
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1409-13
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Electron ionization mass spectral study of selected N-amide and N-alkyl derivatives of cytisine.
pubmed:affiliation
Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Pozna?, Poland. Anna.Przybyl@amu.edu.pl
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't