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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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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