Hydroxypyridinone Derivatives: Synthesis And Cytotoxic Evaluation

Authors

Hojjat Sadeghi-Aliabadi1, Lotfollah Saghaie-Aliabadi1,*, Nariman Tadayonnia2, Mina Mirian2
1Department of Pharmaceutical Chemistry, School of Pharmacy, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran
2Isfahan Pharmaceutical Research Center, Isfahan University of Medical Sciences, Isfahan, I. R. Iran
*Corresponding Author: Corresponding author: Department of Pharmaceutical Chemistry, School of Pharmacy, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 2, issue 1; 5-15
Published online:Feb 08, 2013
Article type:Research Article
Received:Jan 08, 2013
Accepted:Jan 29, 2013
How to Cite:Sadeghi-Aliabadi H, Saghaie-Aliabadi L, Tadayonnia N, Mirian M. Hydroxypyridinone Derivatives: Synthesis And Cytotoxic Evaluation. J Rep Pharm Sci. 2013;2(1):e147757. doi:

Abstract

A series of 3-hydroxypyridin-4-one derivatives (HPOs) as bidentate iron (III) chelating agents were synthesized from 3-hydroxypyran-4-ones (maltol and ethyl maltol) in three steps through protection of hydroxyl group. The protected compounds were then reacted with suitable primary amines to give benzylated pyridinones. Finally, the benzyl group was removed by catalytic hydrogenation to produce the desired products. The partition coefficient of the free ligands and their iron (III) complexes were determined in an aqueous/octanol system using shakeflask method. The cytotoxic effects of these iron chelators against MCF-7 and MDA-MB-231 cancer cells were also evaluated using MTT assay. The results revealed that cytotoxicity of synthesized compounds were closely related to the lipophilycity of them so that the most lipophilic compound (4f) showed the highest activity; whereas compound 4a as a more hydrophilic agent showed the lowest cytotoxic effect; Although these compounds were cytotoxic at high concentration (≥ 0.1 mM). 

Copyright

© 2013, 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

7
Oct
2020

Synthesis and Comparison of Anti-Leishmania major Activity of Antimony and Iron Complexes of 3-Hydroxypyran-4-One and 3-Hydroxypyridine-4- One as Bi-Dentate Ligands

Zeynab Zarrabi,
Latfollah Saghaie,
Afshin Fassihi,
Nader Pestechian,
Sedigheh Saberi

Zarrabi Z, Saghaie L, Fassihi A, Pestechian N, Saberi S. Synthesis and Comparison of Anti-Leishmania major Activity of Antimony and Iron Complexes of 3-Hydroxypyran-4-One and 3-Hydroxypyridine-4- One as Bi-Dentate Ligands. J Rep Pharm Sci. 2020;9(2):e147110. doi: https://doi.org/10.4103/jrptps.JRPTPS_64_18

7
Sep
2023
Ruthenium (II) Complexes Based on Phenanthroline-Tetrazole as Possible Anticancer Agents

Ruthenium (II) Complexes Based on Phenanthroline-Tetrazole as Possible Anticancer Agents

Saeid Abaspour,
Behzad Soltani,
Hamed Hamishehkar,
Moayad Hossaini Sadr

Abaspour S, Soltani B, Hamishehkar H, Hossaini Sadr M. Ruthenium (II) Complexes Based on Phenanthroline-Tetrazole as Possible Anticancer Agents. Iran J Pharm Res. 2023;22(1):e136738. doi: https://doi.org/10.5812/ijpr-136738

20
Nov
2010

Investigation of Intestinal Absorption of Pyridinones in Rat

Masiholah Taher,
Lotfollah Saghaie,
Maryam Abrahilmi

Taher M, Saghaie L, Abrahilmi M. Investigation of Intestinal Absorption of Pyridinones in Rat. Iran J Pharm Res. 2022;3(4):e128208. doi: https://doi.org/10.22037/ijpr.2010.602

20
Nov
2010

Synthesis and Determination of Partition Coefficients of Zinc Complexes with Clinical Potential application

Lotfollah Saghaie,
Gholamal Houshfar,
Mostafa Neishabor

Saghaie L, Houshfar G, Neishabor M. Synthesis and Determination of Partition Coefficients of Zinc Complexes with Clinical Potential application. Iran J Pharm Res. 2022;5(3):e128283. doi: https://doi.org/10.22037/ijpr.2010.673

31
Dec
2019

Synthesis of 4-Phenyl-4,5-dihydropyranopyrazolone Derivatives with Activated Potassium Carbonate: Evaluation of Anticancer Activity on Cancer Cell Lines and Apoptosis Mechanism

Leila Hosseinzadeh,
Navid Mahmoudian,
Farahnaz Ahmadi,
Hadi Adibi

Hosseinzadeh L, Mahmoudian N, Ahmadi F, Adibi H. Synthesis of 4-Phenyl-4,5-dihydropyranopyrazolone Derivatives with Activated Potassium Carbonate: Evaluation of Anticancer Activity on Cancer Cell Lines and Apoptosis Mechanism. J Rep Pharm Sci. 2019;8(2):e147411. doi: https://doi.org/10.4103/jrptps.JRPTPS_82_19

More by these authors

Hojjat Sadeghi-AliabadiPubMedScholar
Lotfollah Saghaie-AliabadiPubMedScholar
Nariman TadayonniaPubMedScholar
Mina MirianPubMedScholar
Share
Cited by
Metrics