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Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group

[Image: see text] Introduction: With regard to the anti-mycobacterial activity of 2-pyrazinoic acid esters (POEs), recent studies have shown that both pyrazine core and alkyl part of POE interact with the fatty acid synthase type (I) (FAS (I)) precluding a complex formation between NADPH and FAS (I)...

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Autores principales: Khani-Meinagh, Hossein, Mostafavi, Hossein, Reiling, Norbert, Mahdavi, Majid, Zarrini, Gholamreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879708/
https://www.ncbi.nlm.nih.gov/pubmed/31799156
http://dx.doi.org/10.15171/bi.2019.25
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author Khani-Meinagh, Hossein
Mostafavi, Hossein
Reiling, Norbert
Mahdavi, Majid
Zarrini, Gholamreza
author_facet Khani-Meinagh, Hossein
Mostafavi, Hossein
Reiling, Norbert
Mahdavi, Majid
Zarrini, Gholamreza
author_sort Khani-Meinagh, Hossein
collection PubMed
description [Image: see text] Introduction: With regard to the anti-mycobacterial activity of 2-pyrazinoic acid esters (POEs), recent studies have shown that both pyrazine core and alkyl part of POE interact with the fatty acid synthase type (I) (FAS (I)) precluding a complex formation between NADPH and FAS (I). Methods: Considering this interaction at the reductase site of FAS (I) responsible for reduction of β-ketoacyl-CoA to β-hydroxyacyl-CoA, we hypothesized that POE containing a bioreducible center in its alkyl part might show an increased anti-tubercular activity due to the involvement of FAS (I) in extra bio-reduction reaction. Thus, we synthesized novel POEs, confirmed their structures by spectral data, and subsequently evaluated their anti-mycobacterial activity against Mycobacterium tuberculosis (Mtb) (H37Rv) strain at 10 μg/mL concentration. Results: Compounds 3c, 3j, and 3m showed higher activity with regard to the inhibition of Mtb growth by 45.4, 45.7, and 51.2% respectively. Unexpectedly, the maltol derived POE 3l having the lowest log p value among the POEs indicated the highest anti-mycobacterial growth activity with 56% prevention. Compounds 3c and 3l showed no remarkable cytotoxicity on human macrophages at 10 μg/mL concentration as analyzed by xCELLigence real-time cell analysis. In further experiments, some of the tested POEs, unlike pyrazinamide (PZA), exhibited significant antibacterial and also anti-fungal activities. POEs showed an enhanced bactericidal activity on gram-positive bacteria as shown for Staphylococcus aureus , e.g. compound 3b with a MIC value of 125 μg/mL but not E. coli as a gram-negative bacteria, except for maltol derived POE (3l) that showed an inverse activity in the susceptibility test. In the anticancer activity test against the human leukemia K562 cell lines using MTT assay, compounds 3e and 3j showed the highest cytotoxic effect with IC50 values of 25±8.0 μΜ and 25±5.0 μΜ, respectively. Conclusion: It was found that the majority of POEs containing a bioreducible center showed higher inhibitory activities on Mtb growth when compared to the similar compounds without a bio-reducible functional group.
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spelling pubmed-68797082019-12-03 Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group Khani-Meinagh, Hossein Mostafavi, Hossein Reiling, Norbert Mahdavi, Majid Zarrini, Gholamreza Bioimpacts Original Research [Image: see text] Introduction: With regard to the anti-mycobacterial activity of 2-pyrazinoic acid esters (POEs), recent studies have shown that both pyrazine core and alkyl part of POE interact with the fatty acid synthase type (I) (FAS (I)) precluding a complex formation between NADPH and FAS (I). Methods: Considering this interaction at the reductase site of FAS (I) responsible for reduction of β-ketoacyl-CoA to β-hydroxyacyl-CoA, we hypothesized that POE containing a bioreducible center in its alkyl part might show an increased anti-tubercular activity due to the involvement of FAS (I) in extra bio-reduction reaction. Thus, we synthesized novel POEs, confirmed their structures by spectral data, and subsequently evaluated their anti-mycobacterial activity against Mycobacterium tuberculosis (Mtb) (H37Rv) strain at 10 μg/mL concentration. Results: Compounds 3c, 3j, and 3m showed higher activity with regard to the inhibition of Mtb growth by 45.4, 45.7, and 51.2% respectively. Unexpectedly, the maltol derived POE 3l having the lowest log p value among the POEs indicated the highest anti-mycobacterial growth activity with 56% prevention. Compounds 3c and 3l showed no remarkable cytotoxicity on human macrophages at 10 μg/mL concentration as analyzed by xCELLigence real-time cell analysis. In further experiments, some of the tested POEs, unlike pyrazinamide (PZA), exhibited significant antibacterial and also anti-fungal activities. POEs showed an enhanced bactericidal activity on gram-positive bacteria as shown for Staphylococcus aureus , e.g. compound 3b with a MIC value of 125 μg/mL but not E. coli as a gram-negative bacteria, except for maltol derived POE (3l) that showed an inverse activity in the susceptibility test. In the anticancer activity test against the human leukemia K562 cell lines using MTT assay, compounds 3e and 3j showed the highest cytotoxic effect with IC50 values of 25±8.0 μΜ and 25±5.0 μΜ, respectively. Conclusion: It was found that the majority of POEs containing a bioreducible center showed higher inhibitory activities on Mtb growth when compared to the similar compounds without a bio-reducible functional group. Tabriz University of Medical Sciences 2019 2019-05-22 /pmc/articles/PMC6879708/ /pubmed/31799156 http://dx.doi.org/10.15171/bi.2019.25 Text en © 2019 The Author(s) This work is published by BioImpacts as an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Research
Khani-Meinagh, Hossein
Mostafavi, Hossein
Reiling, Norbert
Mahdavi, Majid
Zarrini, Gholamreza
Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title_full Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title_fullStr Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title_full_unstemmed Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title_short Design, synthesis and evaluation of biological activities of some novel anti-TB agents with bio-reducible functional group
title_sort design, synthesis and evaluation of biological activities of some novel anti-tb agents with bio-reducible functional group
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879708/
https://www.ncbi.nlm.nih.gov/pubmed/31799156
http://dx.doi.org/10.15171/bi.2019.25
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