Synthesis of Pyrimidine Schiff Bases as Anticancer Agents

Main Authors: M. S. SHINGARE, D. B. INGLE
Format: Article Journal
Bahasa: eng
Terbitan: , 1976
Subjects:
Online Access: https://zenodo.org/record/6396396
ctrlnum 6396396
fullrecord <?xml version="1.0"?> <dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><creator>M. S. SHINGARE</creator><creator>D. B. INGLE</creator><date>1976-10-31</date><description>Department of Chemistry, Marathwada University, Aurangabad. Manuscript received 17 March 1976 ; revised 17 May 1976 ; accepted 15 July 1976 Some pyrimidine Schiff's bases were synthesised by condensing 6-amino uracil with different substituted benzaldehydes and few heterocyelic aldehydes. The compounds were also tested for anticancer activity and were found inactive against WM-256 tumour system.</description><identifier>https://zenodo.org/record/6396396</identifier><identifier>10.5281/zenodo.6396396</identifier><identifier>oai:zenodo.org:6396396</identifier><language>eng</language><relation>doi:10.5281/zenodo.6396395</relation><rights>info:eu-repo/semantics/openAccess</rights><rights>https://creativecommons.org/licenses/by/4.0/legalcode</rights><source>Journal of Indian Chemical Society Vol. 53(Oct 1976) 1036-1037</source><subject>Synthesis</subject><subject>Nitrogen</subject><title>Synthesis of Pyrimidine Schiff Bases as Anticancer Agents.</title><type>Journal:Article</type><type>Journal:Article</type><recordID>6396396</recordID></dc>
language eng
format Journal:Article
Journal
Journal:Journal
author M. S. SHINGARE
D. B. INGLE
title Synthesis of Pyrimidine Schiff Bases as Anticancer Agents
publishDate 1976
topic Synthesis
Nitrogen
url https://zenodo.org/record/6396396
contents Department of Chemistry, Marathwada University, Aurangabad. Manuscript received 17 March 1976 ; revised 17 May 1976 ; accepted 15 July 1976 Some pyrimidine Schiff's bases were synthesised by condensing 6-amino uracil with different substituted benzaldehydes and few heterocyelic aldehydes. The compounds were also tested for anticancer activity and were found inactive against WM-256 tumour system.
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