Document Detail


5-[(Aminoalkyl)amino]imidazo[4,5,1-de]acridin-6-ones as a novel class of antineoplastic agents. Synthesis and biological activity.
MedLine Citation:
PMID:  2296035     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A new class of antineoplastic agents, the 5-substituted imidazo[4,5,1-de]acridin-6-ones with an (aminoalkyl)amino group in the side chain, has been made. These compounds were synthesized by reduction of 1-substituted 4-nitroacridin-9(10H)-ones and subsequent reaction of the derived amines with carboxylic acids. Their cytotoxic activity against HeLaS3 cells in tissue culture and in vivo antitumor activity against P388 leukemia in mice was demonstrated. A strict relationship between the antineoplastic activity and the number of methylene spacers between proximal and distal nitrogens in the side chain was established.
Authors:
W M Cholody; S Martelli; J Paradziej-Lukowicz; J Konopa
Related Documents :
19719235 - Synthesis, in vitro and in vivo evaluation, and radiolabeling of aryl anandamide analog...
20053485 - Synthesis of highly functionalized barbituric acids and study of their interactions wit...
3754585 - Synthesis and biological activities of 5-deaza analogues of aminopterin and folic acid.
7945515 - Pharmacological studies of the two new hypoglycaemic compounds 4-(3-methyl-5-oxo-2-pyra...
20507455 - Characterization of arabidopsis thaliana-fusarium graminearum interactions and identifi...
1623955 - Effects of intravenous acetazolamide on retinal ph in the cat.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of medicinal chemistry     Volume:  33     ISSN:  0022-2623     ISO Abbreviation:  J. Med. Chem.     Publication Date:  1990 Jan 
Date Detail:
Created Date:  1990-02-22     Completed Date:  1990-02-22     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  9716531     Medline TA:  J Med Chem     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  49-52     Citation Subset:  IM    
Affiliation:
Department of Pharmaceutical Technology and Biochemistry, Technical University of Gdansk, Poland.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Acridines / chemical synthesis,  therapeutic use*
Animals
Antineoplastic Agents*
Chemical Phenomena
Chemistry
Chemistry, Physical
Hela Cells
Humans
Imidazoles / chemical synthesis,  therapeutic use*
Leukemia P388 / drug therapy
Mice
Molecular Structure
Physicochemical Phenomena
Structure-Activity Relationship
Chemical
Reg. No./Substance:
0/Acridines; 0/Antineoplastic Agents; 0/Imidazoles

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Synthesis, structure, and antiparasitic activity of sulfamoyl derivatives of ribavirin.
Next Document:  Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and ...