Sequence-selectivity of 5,11-dimethyl-5 H -indolo[2,3- b ]quinoline binding to DNA. Footprinting and molecular modeling studies-Reference-Cited by-同舟云学术

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Sequence-selectivity of 5,11-dimethyl-5 H -indolo[2,3- b ]quinoline binding to DNA. Footprinting and molecular modeling studies

Published:2000-05 Issue:5 Volume:8 Page:937-943
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Osiadacz Jarosław,Majka Jerzy,Czarnecki Kamil,Peczyńska-Czoch Wanda,Zakrzewska-Czerwińska Jolanta,Kaczmarek Łukasz,Sokalski W.Andrzej

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference18 articles.

1. Neidle, S.; Jenkins, T. C. In Methods in Enzymology; Langone, J. J.; Ed.; Academic Press, 1991, Vol. 203B, p 433.

2. Cancerostatics, VI. Synthesis and Antineoplastic Properties of Some Benzo-iso-α-carbolines

3. A carboline derivative as a novel mammalian DNA topoisomerase II targeting agent

4. Synthesis and Structure-Activity Relationship of Methyl-Substituted Indolo[2,3-b]quinolines: Novel Cytotoxic, DNA Topoisomerase II Inhibitors

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2. Neocryptolepine: A Promising Indoloisoquinoline Alkaloid with Interesting Biological Activity. Evaluation of the Drug and its Most Relevant Analogs;Current Topics in Medicinal Chemistry;2015-06-04

3. Design, Synthesis, and Biological Evaluation of Artemisinin-Indoloquinoline Hybrids as Potent Antiproliferative Agents;Molecules;2014-11-18

4. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; structure–activity relationships of neocryptolepines and 6-methyl congeners;Bioorganic & Medicinal Chemistry;2012-08

5. Membrane Perturbations Induced by New Analogs of Neocryptolepine;Biological & Pharmaceutical Bulletin;2012

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