Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice

A new class of chiral pyranone fused indole derivatives were prepared by means of N-heterocyclic carbene (NHC) organocatalysis and demonstrated notable antibacterial activity against Xanthomonas oryzae pv oryzae (Xoo). Bioassays showed that compounds (3S,4R)-5b, (3S,4R)-5d, and (3S,4R)-5l exhibited...

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Main Authors: Teng, Kunpeng, Liu, Qian, Zhang, Meng, Naz, Hira, Zheng, Pengcheng, Wu, Xingxing, Chi, Robin Yonggui
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/174249
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1742492024-03-29T15:31:52Z Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice Teng, Kunpeng Liu, Qian Zhang, Meng Naz, Hira Zheng, Pengcheng Wu, Xingxing Chi, Robin Yonggui School of Chemistry, Chemical Engineering and Biotechnology Agricultural Sciences Chiral indole derivatives Bacterial activity A new class of chiral pyranone fused indole derivatives were prepared by means of N-heterocyclic carbene (NHC) organocatalysis and demonstrated notable antibacterial activity against Xanthomonas oryzae pv oryzae (Xoo). Bioassays showed that compounds (3S,4R)-5b, (3S,4R)-5d, and (3S,4R)-5l exhibited promising in vitro efficacy against Xoo, with EC50 values of 9.05, 9.71, and 5.84 mg/L, respectively, which were superior to that of the positive controls with commercial antibacterial agents, bismerthiazol (BT, EC50 = 27.8 mg/L) and thiodiazole copper (TC, EC50 = 70.1 mg/L). Furthermore, single enantiomer (3S,4R)-5l was identified as an optimal structure displaying 55.3% and 52.0% curative and protective activities against Xoo in vivo tests at a concentration of 200 mg/L, which slightly surpassed the positive control with TC (curative and protective activities of 47.2% and 48.8%, respectively). Mechanistic studies through molecular docking analysis revealed preliminary insights into the distinct anti-Xoo activity of the two single enantiomers (3S,4R)-5l and (3R,4S)-5l, wherein the (3S,4R)-configured stereoisomer could form a more stable interaction with XooDHPS (dihydropteroate synthase). These findings underscore the significant anti-Xoo potential of these chiral pyranone fused indole derivatives, and shall inspire further exploration as promising lead structures for a novel class of bactericides to combat bacterial infections and other plant diseases. Submitted/Accepted version We acknowledge the financial support from the National Key Research and Development Program of China (2022YFD1700300), the National Natural Science Foundation of China (22071036), the National Natural Science Fund for Excellent Young Scientists Fund Program (Overseas) (NSFC-YQHW), the starting grant of Guizhou University [(2022)47)], the 10 Talent Plan (Shicengci) of Guizhou Province ([2016]5649), the Science and Technology Department of Guizhou Province ([2019]1020, Qiankehe-jichu-ZK[2022]zhongdian024), the Program of Introducing Talents of Discipline to Universities of China (111 Program, D20023) at Guizhou University, Frontiers Science Center for Asymmetric Synthesis and Medicinal Molecules, Department of Education, Guizhou Province [Qianjiaohe KY (2020)004], the Basic and Applied Research Foundation of Guangdong Province (2019A1515110906), the Guizhou Province First-Class Disciplines Project [(Yiliu Xueke Jianshe Xiangmu)-GNYL(2017)008], Guizhou University of Traditional Chinese Medicine, and Guizhou University (China). 2024-03-25T00:26:10Z 2024-03-25T00:26:10Z 2024 Journal Article Teng, K., Liu, Q., Zhang, M., Naz, H., Zheng, P., Wu, X. & Chi, R. Y. (2024). Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice. Journal of Agricultural and Food Chemistry, 72(9), 4622-4629. https://dx.doi.org/10.1021/acs.jafc.3c07491 0021-8561 https://hdl.handle.net/10356/174249 10.1021/acs.jafc.3c07491 38386000 2-s2.0-85186200502 9 72 4622 4629 en Journal of Agricultural and Food Chemistry © 2024 American Chemical Society. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1021/acs.jafc.3c07491. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Agricultural Sciences
Chiral indole derivatives
Bacterial activity
spellingShingle Agricultural Sciences
Chiral indole derivatives
Bacterial activity
Teng, Kunpeng
Liu, Qian
Zhang, Meng
Naz, Hira
Zheng, Pengcheng
Wu, Xingxing
Chi, Robin Yonggui
Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
description A new class of chiral pyranone fused indole derivatives were prepared by means of N-heterocyclic carbene (NHC) organocatalysis and demonstrated notable antibacterial activity against Xanthomonas oryzae pv oryzae (Xoo). Bioassays showed that compounds (3S,4R)-5b, (3S,4R)-5d, and (3S,4R)-5l exhibited promising in vitro efficacy against Xoo, with EC50 values of 9.05, 9.71, and 5.84 mg/L, respectively, which were superior to that of the positive controls with commercial antibacterial agents, bismerthiazol (BT, EC50 = 27.8 mg/L) and thiodiazole copper (TC, EC50 = 70.1 mg/L). Furthermore, single enantiomer (3S,4R)-5l was identified as an optimal structure displaying 55.3% and 52.0% curative and protective activities against Xoo in vivo tests at a concentration of 200 mg/L, which slightly surpassed the positive control with TC (curative and protective activities of 47.2% and 48.8%, respectively). Mechanistic studies through molecular docking analysis revealed preliminary insights into the distinct anti-Xoo activity of the two single enantiomers (3S,4R)-5l and (3R,4S)-5l, wherein the (3S,4R)-configured stereoisomer could form a more stable interaction with XooDHPS (dihydropteroate synthase). These findings underscore the significant anti-Xoo potential of these chiral pyranone fused indole derivatives, and shall inspire further exploration as promising lead structures for a novel class of bactericides to combat bacterial infections and other plant diseases.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Teng, Kunpeng
Liu, Qian
Zhang, Meng
Naz, Hira
Zheng, Pengcheng
Wu, Xingxing
Chi, Robin Yonggui
format Article
author Teng, Kunpeng
Liu, Qian
Zhang, Meng
Naz, Hira
Zheng, Pengcheng
Wu, Xingxing
Chi, Robin Yonggui
author_sort Teng, Kunpeng
title Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
title_short Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
title_full Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
title_fullStr Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
title_full_unstemmed Design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against Xanthomonas oryzae pv oryzae for protection of rice
title_sort design and enantioselective synthesis of chiral pyranone fused indole derivatives with antibacterial activities against xanthomonas oryzae pv oryzae for protection of rice
publishDate 2024
url https://hdl.handle.net/10356/174249
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