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Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii

[Image: see text] Two new biflavanones (1 and 2), three new bichalconoids (3–5), and 11 known flavonoid analogues (6–16) were isolated from the stem bark extract (CH(3)OH–CH(2)Cl(2), 7:3, v/v) of Ochna holstii. The structures of the isolated metabolites were elucidated by NMR spectroscopic and mass...

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Autores principales: Kalenga, Thobias M., Ndoile, Monica M., Atilaw, Yoseph, Gilissen, Pieter J., Munissi, Joan J. E., Rudenko, Anastasia, Bourgard, Catarina, Sunnerhagen, Per, Nyandoro, Stephen S., Erdelyi, Mate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923207/
https://www.ncbi.nlm.nih.gov/pubmed/33511842
http://dx.doi.org/10.1021/acs.jnatprod.0c01017
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author Kalenga, Thobias M.
Ndoile, Monica M.
Atilaw, Yoseph
Gilissen, Pieter J.
Munissi, Joan J. E.
Rudenko, Anastasia
Bourgard, Catarina
Sunnerhagen, Per
Nyandoro, Stephen S.
Erdelyi, Mate
author_facet Kalenga, Thobias M.
Ndoile, Monica M.
Atilaw, Yoseph
Gilissen, Pieter J.
Munissi, Joan J. E.
Rudenko, Anastasia
Bourgard, Catarina
Sunnerhagen, Per
Nyandoro, Stephen S.
Erdelyi, Mate
author_sort Kalenga, Thobias M.
collection PubMed
description [Image: see text] Two new biflavanones (1 and 2), three new bichalconoids (3–5), and 11 known flavonoid analogues (6–16) were isolated from the stem bark extract (CH(3)OH–CH(2)Cl(2), 7:3, v/v) of Ochna holstii. The structures of the isolated metabolites were elucidated by NMR spectroscopic and mass spectrometric analyses. The crude extract and the isolated metabolites were evaluated for antibacterial activity against Bacillus subtilis (Gram-positive) and Escherichia coli (Gram-negative) as well as for cytotoxicity against the MCF-7 human breast cancer cell line. The crude extract and holstiinone A (1) exhibited moderate antibacterial activity against B. subtilis with MIC values of 9.1 μg/mL and 14 μM, respectively. The crude extract and lophirone F (14) showed cytotoxicity against MCF-7 with EC(50) values of 11 μg/mL and 24 μM, respectively. The other isolated metabolites showed no significant antibacterial activities (MIC > 250 μM) and cytotoxicities (EC(50) ≥ 350 μM).
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spelling pubmed-79232072021-03-04 Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii Kalenga, Thobias M. Ndoile, Monica M. Atilaw, Yoseph Gilissen, Pieter J. Munissi, Joan J. E. Rudenko, Anastasia Bourgard, Catarina Sunnerhagen, Per Nyandoro, Stephen S. Erdelyi, Mate J Nat Prod [Image: see text] Two new biflavanones (1 and 2), three new bichalconoids (3–5), and 11 known flavonoid analogues (6–16) were isolated from the stem bark extract (CH(3)OH–CH(2)Cl(2), 7:3, v/v) of Ochna holstii. The structures of the isolated metabolites were elucidated by NMR spectroscopic and mass spectrometric analyses. The crude extract and the isolated metabolites were evaluated for antibacterial activity against Bacillus subtilis (Gram-positive) and Escherichia coli (Gram-negative) as well as for cytotoxicity against the MCF-7 human breast cancer cell line. The crude extract and holstiinone A (1) exhibited moderate antibacterial activity against B. subtilis with MIC values of 9.1 μg/mL and 14 μM, respectively. The crude extract and lophirone F (14) showed cytotoxicity against MCF-7 with EC(50) values of 11 μg/mL and 24 μM, respectively. The other isolated metabolites showed no significant antibacterial activities (MIC > 250 μM) and cytotoxicities (EC(50) ≥ 350 μM). American Chemical Society and American Society of Pharmacognosy 2021-01-29 2021-02-26 /pmc/articles/PMC7923207/ /pubmed/33511842 http://dx.doi.org/10.1021/acs.jnatprod.0c01017 Text en © 2021 American Chemical Society and American Society of Pharmacognosy This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Kalenga, Thobias M.
Ndoile, Monica M.
Atilaw, Yoseph
Gilissen, Pieter J.
Munissi, Joan J. E.
Rudenko, Anastasia
Bourgard, Catarina
Sunnerhagen, Per
Nyandoro, Stephen S.
Erdelyi, Mate
Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title_full Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title_fullStr Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title_full_unstemmed Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title_short Biflavanones, Chalconoids, and Flavonoid Analogues from the Stem Bark of Ochna holstii
title_sort biflavanones, chalconoids, and flavonoid analogues from the stem bark of ochna holstii
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923207/
https://www.ncbi.nlm.nih.gov/pubmed/33511842
http://dx.doi.org/10.1021/acs.jnatprod.0c01017
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