Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties

Phytochemical investigation of leaves and stembark of <i>Artocarpus</i><i>lacucha</i> collected in Thailand resulted in three yet undescribed isomeric flavan-3-ol derivatives (<b>1</b>–<b>3</b>), the four known compounds gambircatechol (<b>4</...

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Main Authors: Weerasak Songoen, Witthawat Phanchai, Lothar Brecker, Dominik Wenisch, Michael A. Jakupec, Wanchai Pluempanupat, Johann Schinnerl
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/4/1078
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spelling doaj-812ff9b11a744922811cfaf2342314ad2021-02-19T00:05:34ZengMDPI AGMolecules1420-30492021-02-01261078107810.3390/molecules26041078Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative PropertiesWeerasak Songoen0Witthawat Phanchai1Lothar Brecker2Dominik Wenisch3Michael A. Jakupec4Wanchai Pluempanupat5Johann Schinnerl6Department of Chemistry and Center of Excellence for Innovation in Chemistry, Special Research Unit for Advanced Magnetic Resonance, Faculty of Science, Kasetsart University, Bangkok 10900, ThailandDepartment of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002, ThailandDepartment of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Strasse 38, A-1090 Vienna, AustriaInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Strasse 42, A-1090 Vienna, AustriaInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Strasse 42, A-1090 Vienna, AustriaDepartment of Chemistry and Center of Excellence for Innovation in Chemistry, Special Research Unit for Advanced Magnetic Resonance, Faculty of Science, Kasetsart University, Bangkok 10900, ThailandDepartment of Botany and Biodiversity Research, Faculty of Life Science, University of Vienna, Rennweg 14, A-1030 Vienna, AustriaPhytochemical investigation of leaves and stembark of <i>Artocarpus</i><i>lacucha</i> collected in Thailand resulted in three yet undescribed isomeric flavan-3-ol derivatives (<b>1</b>–<b>3</b>), the four known compounds gambircatechol (<b>4</b>), (+)-catechin (<b>5</b>), (+)-afzelechin (<b>6</b>) and the stilbene oxyresveratrol (<b>7</b>). Compounds <b>1</b> to <b>3</b> feature 6/6/5/6/5/6 core structures. All structures were deduced by NMR and MS, while density functional theory (DFT) calculations on B3LYP theory level were performed of compounds <b>1</b> to <b>3</b> to support the stereochemistry in positions 2 and 3 in the C-ring. Possible biosynthetic pathways leading to <b>4</b> are discussed. The DPPH assay revealed high radical scavenging activities for <b>1</b> (EC<sub>50</sub> = 9.4 ± 1.0 µmol mL<sup>−1</sup>), <b>2</b> (12.2 ± 1.1), <b>3</b> (10.0 ± 1.5) and <b>4</b> (19.0 ± 2.6), remarkably lower than ascorbic acid (EC<sub>50</sub> = 34.9) and α-tocopherol (EC<sub>50</sub> = 48.6). A cytotoxicity assay revealed moderate but consistent antiproliferative properties of <b>1</b> in CH1/PA-1 (ovarian teratocarcinoma) and SW480 (colon carcinoma) cells, with IC<sub>50</sub> values of 25 ± 6 and 34 ± 4 µM, respectively, whereas effects in A549 (non-small cell lung cancer) cells were rather negligible. The performed DCFH-DA assay of <b>1</b> in the former cell lines confirmed potent antioxidative effects even in the cellular environment.https://www.mdpi.com/1420-3049/26/4/1078<i>Artocarpus lacucha</i>Moraceaeflavan-benzofuranartocarpinolradical scavenging activitiescytotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Weerasak Songoen
Witthawat Phanchai
Lothar Brecker
Dominik Wenisch
Michael A. Jakupec
Wanchai Pluempanupat
Johann Schinnerl
spellingShingle Weerasak Songoen
Witthawat Phanchai
Lothar Brecker
Dominik Wenisch
Michael A. Jakupec
Wanchai Pluempanupat
Johann Schinnerl
Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
Molecules
<i>Artocarpus lacucha</i>
Moraceae
flavan-benzofuran
artocarpinol
radical scavenging activities
cytotoxicity
author_facet Weerasak Songoen
Witthawat Phanchai
Lothar Brecker
Dominik Wenisch
Michael A. Jakupec
Wanchai Pluempanupat
Johann Schinnerl
author_sort Weerasak Songoen
title Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
title_short Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
title_full Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
title_fullStr Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
title_full_unstemmed Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical <i>Artocarpus</i><i>lacucha</i> Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties
title_sort highly aromatic flavan-3-ol derivatives from palaeotropical <i>artocarpus</i><i>lacucha</i> buch.-ham possess radical scavenging and antiproliferative properties
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-02-01
description Phytochemical investigation of leaves and stembark of <i>Artocarpus</i><i>lacucha</i> collected in Thailand resulted in three yet undescribed isomeric flavan-3-ol derivatives (<b>1</b>–<b>3</b>), the four known compounds gambircatechol (<b>4</b>), (+)-catechin (<b>5</b>), (+)-afzelechin (<b>6</b>) and the stilbene oxyresveratrol (<b>7</b>). Compounds <b>1</b> to <b>3</b> feature 6/6/5/6/5/6 core structures. All structures were deduced by NMR and MS, while density functional theory (DFT) calculations on B3LYP theory level were performed of compounds <b>1</b> to <b>3</b> to support the stereochemistry in positions 2 and 3 in the C-ring. Possible biosynthetic pathways leading to <b>4</b> are discussed. The DPPH assay revealed high radical scavenging activities for <b>1</b> (EC<sub>50</sub> = 9.4 ± 1.0 µmol mL<sup>−1</sup>), <b>2</b> (12.2 ± 1.1), <b>3</b> (10.0 ± 1.5) and <b>4</b> (19.0 ± 2.6), remarkably lower than ascorbic acid (EC<sub>50</sub> = 34.9) and α-tocopherol (EC<sub>50</sub> = 48.6). A cytotoxicity assay revealed moderate but consistent antiproliferative properties of <b>1</b> in CH1/PA-1 (ovarian teratocarcinoma) and SW480 (colon carcinoma) cells, with IC<sub>50</sub> values of 25 ± 6 and 34 ± 4 µM, respectively, whereas effects in A549 (non-small cell lung cancer) cells were rather negligible. The performed DCFH-DA assay of <b>1</b> in the former cell lines confirmed potent antioxidative effects even in the cellular environment.
topic <i>Artocarpus lacucha</i>
Moraceae
flavan-benzofuran
artocarpinol
radical scavenging activities
cytotoxicity
url https://www.mdpi.com/1420-3049/26/4/1078
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