DNA Binding Study of Dihydropyrano [3, 4-C] Chromene Derivative by some Spectroscopic Techniques

Author(s):
Mahvash Farajzadeh DehkordiMahvash Farajzadeh Dehkordi1, Gholamreza DehghanGholamreza Dehghan1,*, Majid MahdaviMajid Mahdavi1, Mohammad Ali Hosseinpour FeiziMohammad Ali Hosseinpour Feizi1
1Department of Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran
*Corresponding Author: Corresponding author: Department of Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 5, issue 2; 80-82
Published online:Aug 23, 2016
Article type:Research Article
Received:Jun 17, 2016
Accepted:Aug 15, 2016
How to Cite:Farajzadeh Dehkordi M, Dehghan G, Mahdavi M, Hosseinpour Feizi MA. DNA Binding Study of Dihydropyrano [3, 4-C] Chromene Derivative by some Spectroscopic Techniques. J Rep Pharm Sci. 2016;5(2):e147649. doi:

Abstract

This study was designed to examine the interaction of dihydropyranochromene derivative, 2-amino-4-phenyl-5-oxo-4H, 5H-pyrano-[3, 2-c] chromene-3-carbonitrile (4-PC) with calf thymus DNA (ctDNA) by absorption spectroscopy, competitive fluorescence studies, circular dichroism (CD) and viscosity measurements. It was found that 4-PC could interact with ctDNA through non- intercalative mode and the intrinsic binding constant, Kb, for 4-PC with ctDNA was estimated to be 2.74 ×103 M-1. Methylene blue (MB) displacement studies revealed that 4-PC could not replace ctDNA bounded MB, which is indicative of groove binding mode of 4-PC with DNA. Furthermore, 4-PC induced detectable changes in the CD spectrum of ctDNA as well as changes in its viscosity, corroborate the above experimental results.

Copyright

© 2016, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

31
Jan
2015

Study on the Interaction between Isatin-β-Thiosemicarbazone and Calf Thymus DNA by Spectroscopic Techniques

Parvaneh Pakravan,
Shahla Masoudian

Pakravan P, Masoudian S. Study on the Interaction between Isatin-β-Thiosemicarbazone and Calf Thymus DNA by Spectroscopic Techniques. Iran J Pharm Res. 2015;14(1):e125264. doi: https://doi.org/10.22037/ijpr.2015.1634

18
Apr
2023
Innov J Pharm Res

Synthesis, Antioxidant, Cytotoxicity, Induce Apoptosis Investigation and Docking Study of New Halogenated Dihydropyrano[3,2-b]Chromene-3-Carbonitrile Derivatives on MCF-7 Breast Cancer Cell Line

Touba Eslaminejad,
Ehsan Faghih Mirzaei,
Mehdi Abaszadeh

Eslaminejad T, Faghih Mirzaei E, Abaszadeh M. Synthesis, Antioxidant, Cytotoxicity, Induce Apoptosis Investigation and Docking Study of New Halogenated Dihydropyrano[3,2-b]Chromene-3-Carbonitrile Derivatives on MCF-7 Breast Cancer Cell Line. Iran J Pharm Res. 2023;22(1):e132932. doi: https://doi.org/10.5812/ijpr-132932

31
Jul
2021

Chromium (III) Complexes of 4,5-diazafluoren-9-one Ligand as Potential Anti-proliferative Agents: Synthesis, Characterization, DNA Binding, Molecular Docking and In-vitro Cytotoxicity Evaluation

Omolbanin Shahraki,
Habib Ghaznavi,
Niloufar Akbarzadeh-T,
Sheida Shahraki,
Roghayeh Sheervalilou,
Tahere Kondori

Shahraki O, Ghaznavi H, Akbarzadeh-T N, Shahraki S, Sheervalilou R, et al. Chromium (III) Complexes of 4,5-diazafluoren-9-one Ligand as Potential Anti-proliferative Agents: Synthesis, Characterization, DNA Binding, Molecular Docking and In-vitro Cytotoxicity Evaluation. Iran J Pharm Res. 2021;20(3):e124504. doi: https://doi.org/10.22037/ijpr.2021.114685.14996

29
Oct
2013

Growth inhibition and Induction of apoptosis in K562 Chronic Myeloid Leukaemia cells by the derivatives of dihydropyrano[c]chromenes family

Sina Pejman,
Majid Mahdavi,
Saeed Balalaei

Pejman S, Mahdavi M, Balalaei S. Growth inhibition and Induction of apoptosis in K562 Chronic Myeloid Leukaemia cells by the derivatives of dihydropyrano[c]chromenes family. J Kermanshah Univ Med Sci. 2013;17(7):e74458. doi:

31
Oct
2013

2-Amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles as New Cytotoxic Agents

Afsaneh Zonouzi,
Roghieh Mirzazadeh,
Maliheh Safavi,
Sussan Kabudanian Ardestani,
Saeed Emami,
Alireza Foroumadi

Zonouzi A, Mirzazadeh R, Safavi M, Kabudanian Ardestani S, Emami S, et al. 2-Amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles as New Cytotoxic Agents. Iran J Pharm Res. 2013;12(4):e125751. doi: https://doi.org/10.22037/ijpr.2013.1396

Download PDF1.92 MB
Share on
Cited by
Metrics

Ordering Reprints

Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC 

Search Relations

Author(s):

Related Articles