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Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives
Ten antifouling 14-membered resorcylic acid lactones 1–10 were isolated previously with low or trace natural abundance from the zoanthid-derived Cochliobolus lunatus fungus. Further optimization of fermentation conditions led to the isolation of two major natural compounds 7 and 8 with multi-gram qu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603512/ https://www.ncbi.nlm.nih.gov/pubmed/28924201 http://dx.doi.org/10.1038/s41598-017-12336-0 |
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author | Zhang, Xue-Qing Spadafora, Carmenza Pineda, Laura M. Ng, Michelle G. Sun, Ji-Hong Wang, Wei Wang, Chang-Yun Gu, Yu-Cheng Shao, Chang-Lun |
author_facet | Zhang, Xue-Qing Spadafora, Carmenza Pineda, Laura M. Ng, Michelle G. Sun, Ji-Hong Wang, Wei Wang, Chang-Yun Gu, Yu-Cheng Shao, Chang-Lun |
author_sort | Zhang, Xue-Qing |
collection | PubMed |
description | Ten antifouling 14-membered resorcylic acid lactones 1–10 were isolated previously with low or trace natural abundance from the zoanthid-derived Cochliobolus lunatus fungus. Further optimization of fermentation conditions led to the isolation of two major natural compounds 7 and 8 with multi-gram quantities. By one or two steps, we semisynthesized the six trace natural compounds 1–6 and a series of derivatives 11–27 of compounds 7 and 8 with high yields (65–95%). Compounds 11–13 showed strong antiplasmodial activity against Plasmodium falciparum with IC(50) values of 1.84, 8.36, and 6.95 μM, respectively. Very importantly, 11 and 12 were non-toxic with very safety and high therapeutic indices (CC(50)/IC(50) > 180), and thus representing potential promising leads for antiplasmodial drug discovery. Furthermore, 11 was the only compound showed obvious antileishmanial activity against Leishmania donovani with an IC(50) value of 9.22 μM. Compounds 11 and 12 showed the values of IC(50) at 11.9 and 17.2 μM against neglected Chagas’ disease causing Trypanosoma cruzi, respectively. |
format | Online Article Text |
id | pubmed-5603512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56035122017-09-20 Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives Zhang, Xue-Qing Spadafora, Carmenza Pineda, Laura M. Ng, Michelle G. Sun, Ji-Hong Wang, Wei Wang, Chang-Yun Gu, Yu-Cheng Shao, Chang-Lun Sci Rep Article Ten antifouling 14-membered resorcylic acid lactones 1–10 were isolated previously with low or trace natural abundance from the zoanthid-derived Cochliobolus lunatus fungus. Further optimization of fermentation conditions led to the isolation of two major natural compounds 7 and 8 with multi-gram quantities. By one or two steps, we semisynthesized the six trace natural compounds 1–6 and a series of derivatives 11–27 of compounds 7 and 8 with high yields (65–95%). Compounds 11–13 showed strong antiplasmodial activity against Plasmodium falciparum with IC(50) values of 1.84, 8.36, and 6.95 μM, respectively. Very importantly, 11 and 12 were non-toxic with very safety and high therapeutic indices (CC(50)/IC(50) > 180), and thus representing potential promising leads for antiplasmodial drug discovery. Furthermore, 11 was the only compound showed obvious antileishmanial activity against Leishmania donovani with an IC(50) value of 9.22 μM. Compounds 11 and 12 showed the values of IC(50) at 11.9 and 17.2 μM against neglected Chagas’ disease causing Trypanosoma cruzi, respectively. Nature Publishing Group UK 2017-09-18 /pmc/articles/PMC5603512/ /pubmed/28924201 http://dx.doi.org/10.1038/s41598-017-12336-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Xue-Qing Spadafora, Carmenza Pineda, Laura M. Ng, Michelle G. Sun, Ji-Hong Wang, Wei Wang, Chang-Yun Gu, Yu-Cheng Shao, Chang-Lun Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title | Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title_full | Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title_fullStr | Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title_full_unstemmed | Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title_short | Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives |
title_sort | discovery, semisynthesis, antiparasitic and cytotoxic evaluation of 14-membered resorcylic acid lactones and their derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603512/ https://www.ncbi.nlm.nih.gov/pubmed/28924201 http://dx.doi.org/10.1038/s41598-017-12336-0 |
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