rdf:type |
|
lifeskim:mentions |
umls-concept:C0020926,
umls-concept:C0025664,
umls-concept:C0205263,
umls-concept:C0205314,
umls-concept:C0220781,
umls-concept:C0220825,
umls-concept:C0439596,
umls-concept:C0441655,
umls-concept:C0600115,
umls-concept:C0679622,
umls-concept:C1148673,
umls-concept:C1511636,
umls-concept:C1516044,
umls-concept:C1883254,
umls-concept:C2603343
|
pubmed:issue |
5
|
pubmed:dateCreated |
2007-5-15
|
pubmed:abstractText |
Versatile method has been developed for synthesis of N-substituted imides. Thus, acid anhydrides, imides and dicarboxylic acids were successfully subjected to dehydrative cyclization with substituted amines using DPPOx and Et(3)N to afford N-substituted imides under mild conditions. The DNA binding and apoptosis induction were investigated with regard to their potential utility as cytotoxic agents. Molecular modeling methods are used to study the cytotoxic activity of the active compounds by means of molecular and quantum mechanics.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0223-5234
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
42
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
614-26
|
pubmed:meshHeading |
pubmed-meshheading:17234303-Antineoplastic Agents,
pubmed-meshheading:17234303-Apoptosis,
pubmed-meshheading:17234303-DNA,
pubmed-meshheading:17234303-Humans,
pubmed-meshheading:17234303-Imides,
pubmed-meshheading:17234303-Magnetic Resonance Spectroscopy,
pubmed-meshheading:17234303-Models, Molecular,
pubmed-meshheading:17234303-Quantitative Structure-Activity Relationship,
pubmed-meshheading:17234303-Tumor Cells, Cultured
|
pubmed:year |
2007
|
pubmed:articleTitle |
Novel and versatile methodology for synthesis of cyclic imides and evaluation of their cytotoxic, DNA binding, apoptotic inducing activities and molecular modeling study.
|
pubmed:affiliation |
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia. alaa_moenes@yahoo.com
|
pubmed:publicationType |
Journal Article
|