Document Detail


Cancerostatics. IV. On the synthesis of some noval 1-Azacarbazole derivatives as antineoplastic agents.
MedLine Citation:
PMID:  7255278     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
By condensation of 2-chloro-3-nitropyridine with some anilines the corresponding 2-anilino-3-nitropyridines 1a--11 were obtained. Hydrogenation of these compounds and subsequent diazotization of the 2-anilino-3-aminopyridine derivatives 2a--2l gave triazoles 3a--3l which thermally decomposed in PPA or in liquid paraffine afforded the required 6- and 8-substituted 1-azacarbazole derivatives 4a--3, i--l. Some of these compounds showed significant activity against transplanted mouse sarcoma 180. None of them were active against L 1210 and P 388 leukemias.
Authors:
L Kaczmarek; P Nantka-Namirski
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Polish journal of pharmacology and pharmacy     Volume:  33     ISSN:  0301-0244     ISO Abbreviation:  Pol J Pharmacol Pharm     Publication Date:    1981 Jan-Feb
Date Detail:
Created Date:  1981-09-22     Completed Date:  1981-09-22     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0366561     Medline TA:  Pol J Pharmacol Pharm     Country:  POLAND    
Other Details:
Languages:  eng     Pagination:  121-7     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Animals
Antineoplastic Agents / chemical synthesis*,  pharmacology
Indoles / chemical synthesis*
Mice
Neoplasms, Experimental / drug therapy
Pyridines / chemical synthesis
Chemical
Reg. No./Substance:
0/Antineoplastic Agents; 0/Indoles; 0/Pyridines

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


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