Synthesis and biological evaluation of new 4β-anilino- and 4β-imido-substituted podophyllotoxin congeners

dc.contributor.author Kamal, Ahmed
dc.contributor.author Gayatri, N. Lakshmi
dc.contributor.author Rajasekhar Reddy, D.
dc.contributor.author Murali Mohan Reddy, P. S.
dc.contributor.author Arifuddin, M.
dc.contributor.author Dastidar, Sunanda G.
dc.contributor.author Kondapi, Anand K.
dc.contributor.author Rajkumar, M.
dc.date.accessioned 2022-03-27T05:16:18Z
dc.date.available 2022-03-27T05:16:18Z
dc.date.issued 2005-11-15
dc.description.abstract A series of C-4-anilino- and C-4-imido-substituted new podophyllotoxin congeners have been designed, synthesized, and evaluated for their cytotoxicity and DNA topoisomerase-II (topo-II) inhibition potential. Some of these compounds have exhibited promising in vitro anticancer and topo-II inhibition activity. © 2005 Elsevier Ltd. All rights reserved.
dc.identifier.citation Bioorganic and Medicinal Chemistry. v.13(22)
dc.identifier.issn 09680896
dc.identifier.uri 10.1016/j.bmc.2005.06.032
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0968089605005705
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/7592
dc.subject DNA topoisomerase-II
dc.subject Etoposide
dc.subject Podophyllotoxin
dc.subject Substituted 2-aminobenzophenone
dc.title Synthesis and biological evaluation of new 4β-anilino- and 4β-imido-substituted podophyllotoxin congeners
dc.type Journal. Article
dspace.entity.type
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