Loading…

Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties

BACKGROUND To study the effect of changing the piperidine ring of oxathiapiprolin on the fungicidal activity, we designed and synthesized novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties, and studied their fungicidal activities against Phytophthora capsici in vitr...

Full description

Saved in:
Bibliographic Details
Published in:Pest management science 2023-05, Vol.79 (5), p.1977-1986
Main Authors: Peng, Xing‐Jie, Tian, Xue‐Rong, Yu, Shu‐Jing, Zhao, Tong‐Tong, Bian, Qiang, Zhao, Wei‐Guang
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83
cites cdi_FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83
container_end_page 1986
container_issue 5
container_start_page 1977
container_title Pest management science
container_volume 79
creator Peng, Xing‐Jie
Tian, Xue‐Rong
Yu, Shu‐Jing
Zhao, Tong‐Tong
Bian, Qiang
Zhao, Wei‐Guang
description BACKGROUND To study the effect of changing the piperidine ring of oxathiapiprolin on the fungicidal activity, we designed and synthesized novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties, and studied their fungicidal activities against Phytophthora capsici in vitro. RESULTS These derivatives showed moderate to good fungicidal activities against Phytophthora capsici, two oxime ether derivatives showed higher fungicidal activity in vitro than dimethomorph (EC50 = 0.1331 μg mL−1) and comparable to oxathiapiprolin (EC50 = 0.0042 μg mL−1). Oxime ester derivatives showed significantly reduced activities compared with oxime ether derivatives. Most of these derivatives showed broad‐spectrum fungicidal activity against the other eight kinds of fungi. Moreover, four derivatives exhibited good antifungal activities in vivo against Phytophthora capsici, Pseudoperonospora cubensis, and Phytophthora infestans. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici. CONCLUSION The activity of 10b against Phytophthora infestans was better than that of mandipropamid, and compound 10d exhibited higher fungicidal activities against Pseudoperonospora cubensis and Phytophthora infestans than mandipropamid. These two derivatives emerged as promising candidates for antifungal drugs. © 2023 Society of Chemical Industry. Novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties were designed and synthesized, and their fungicidal activities against Phytophthora capsaicae in vitro and in vivo were studied. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici.
doi_str_mv 10.1002/ps.7374
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2768242524</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2768242524</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83</originalsourceid><addsrcrecordid>eNp10U1rFTEUBuAgiv1Q_AcScNGCvTVfk2SWpR8qFFpQwd2QSc7cpswk02Tm6u26P9xcb9uF4OqcAw8vB16E3lFyTAlhn8Z8rLgSL9AurZhciLrWL593_XMH7eV8Swip65q9RjtcSklJTXfRwxlkvwxHOK_DdFP2fIRNcLibw9Jb70yPjZ38yk8eMo4dDnEFPR79CMnc-wB4uvHmPvaAHSS_MsUWaGOYjA8-LHH87QfAUMITjunpzFM5h-hhk_sGvepMn-Ht49xHPy7Ov59-WVxeff56enK5sFxUYqFFS7SBlivKtNadUk6KDlqQTjFtqaOCthUVumulVVZT4kwnnJNgK0uN5vvocJs7png3lx-awWcLfW8CxDk3TEnNBKuYKPTDP_Q2zimU74qqOVdcM17UwVbZFHNO0DVj8oNJ64aSZlNMM-ZmU0yR7x_z5nYA9-yemijg4xb88j2s_5fTXH_7G_cHjOeYzA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2793373823</pqid></control><display><type>article</type><title>Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties</title><source>Wiley</source><creator>Peng, Xing‐Jie ; Tian, Xue‐Rong ; Yu, Shu‐Jing ; Zhao, Tong‐Tong ; Bian, Qiang ; Zhao, Wei‐Guang</creator><creatorcontrib>Peng, Xing‐Jie ; Tian, Xue‐Rong ; Yu, Shu‐Jing ; Zhao, Tong‐Tong ; Bian, Qiang ; Zhao, Wei‐Guang</creatorcontrib><description>BACKGROUND To study the effect of changing the piperidine ring of oxathiapiprolin on the fungicidal activity, we designed and synthesized novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties, and studied their fungicidal activities against Phytophthora capsici in vitro. RESULTS These derivatives showed moderate to good fungicidal activities against Phytophthora capsici, two oxime ether derivatives showed higher fungicidal activity in vitro than dimethomorph (EC50 = 0.1331 μg mL−1) and comparable to oxathiapiprolin (EC50 = 0.0042 μg mL−1). Oxime ester derivatives showed significantly reduced activities compared with oxime ether derivatives. Most of these derivatives showed broad‐spectrum fungicidal activity against the other eight kinds of fungi. Moreover, four derivatives exhibited good antifungal activities in vivo against Phytophthora capsici, Pseudoperonospora cubensis, and Phytophthora infestans. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici. CONCLUSION The activity of 10b against Phytophthora infestans was better than that of mandipropamid, and compound 10d exhibited higher fungicidal activities against Pseudoperonospora cubensis and Phytophthora infestans than mandipropamid. These two derivatives emerged as promising candidates for antifungal drugs. © 2023 Society of Chemical Industry. Novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties were designed and synthesized, and their fungicidal activities against Phytophthora capsaicae in vitro and in vivo were studied. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici.</description><identifier>ISSN: 1526-498X</identifier><identifier>EISSN: 1526-4998</identifier><identifier>DOI: 10.1002/ps.7374</identifier><identifier>PMID: 36661091</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Abnormalities ; Antifungal Agents - chemistry ; Drug development ; Esters - pharmacology ; Ether - pharmacology ; Ethers - pharmacology ; Ethyl Ethers - pharmacology ; Fungicidal activity ; Fungicides ; Fungicides, Industrial - chemistry ; Hyphae ; mode of action ; oxime ester ; oxime ether ; Oximes - pharmacology ; Phytophthora capsici ; Phytophthora infestans ; Piperazine ; piperazine thiazole derivatives ; Piperazines - pharmacology ; Piperidine ; Pseudoperonospora cubensis ; Structure-Activity Relationship ; Thiazoles - pharmacology</subject><ispartof>Pest management science, 2023-05, Vol.79 (5), p.1977-1986</ispartof><rights>2023 Society of Chemical Industry.</rights><rights>Copyright © 2023 Society of Chemical Industry</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83</citedby><cites>FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83</cites><orcidid>0000-0001-8796-4264</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36661091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Xing‐Jie</creatorcontrib><creatorcontrib>Tian, Xue‐Rong</creatorcontrib><creatorcontrib>Yu, Shu‐Jing</creatorcontrib><creatorcontrib>Zhao, Tong‐Tong</creatorcontrib><creatorcontrib>Bian, Qiang</creatorcontrib><creatorcontrib>Zhao, Wei‐Guang</creatorcontrib><title>Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties</title><title>Pest management science</title><addtitle>Pest Manag Sci</addtitle><description>BACKGROUND To study the effect of changing the piperidine ring of oxathiapiprolin on the fungicidal activity, we designed and synthesized novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties, and studied their fungicidal activities against Phytophthora capsici in vitro. RESULTS These derivatives showed moderate to good fungicidal activities against Phytophthora capsici, two oxime ether derivatives showed higher fungicidal activity in vitro than dimethomorph (EC50 = 0.1331 μg mL−1) and comparable to oxathiapiprolin (EC50 = 0.0042 μg mL−1). Oxime ester derivatives showed significantly reduced activities compared with oxime ether derivatives. Most of these derivatives showed broad‐spectrum fungicidal activity against the other eight kinds of fungi. Moreover, four derivatives exhibited good antifungal activities in vivo against Phytophthora capsici, Pseudoperonospora cubensis, and Phytophthora infestans. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici. CONCLUSION The activity of 10b against Phytophthora infestans was better than that of mandipropamid, and compound 10d exhibited higher fungicidal activities against Pseudoperonospora cubensis and Phytophthora infestans than mandipropamid. These two derivatives emerged as promising candidates for antifungal drugs. © 2023 Society of Chemical Industry. Novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties were designed and synthesized, and their fungicidal activities against Phytophthora capsaicae in vitro and in vivo were studied. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici.</description><subject>Abnormalities</subject><subject>Antifungal Agents - chemistry</subject><subject>Drug development</subject><subject>Esters - pharmacology</subject><subject>Ether - pharmacology</subject><subject>Ethers - pharmacology</subject><subject>Ethyl Ethers - pharmacology</subject><subject>Fungicidal activity</subject><subject>Fungicides</subject><subject>Fungicides, Industrial - chemistry</subject><subject>Hyphae</subject><subject>mode of action</subject><subject>oxime ester</subject><subject>oxime ether</subject><subject>Oximes - pharmacology</subject><subject>Phytophthora capsici</subject><subject>Phytophthora infestans</subject><subject>Piperazine</subject><subject>piperazine thiazole derivatives</subject><subject>Piperazines - pharmacology</subject><subject>Piperidine</subject><subject>Pseudoperonospora cubensis</subject><subject>Structure-Activity Relationship</subject><subject>Thiazoles - pharmacology</subject><issn>1526-498X</issn><issn>1526-4998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp10U1rFTEUBuAgiv1Q_AcScNGCvTVfk2SWpR8qFFpQwd2QSc7cpswk02Tm6u26P9xcb9uF4OqcAw8vB16E3lFyTAlhn8Z8rLgSL9AurZhciLrWL593_XMH7eV8Swip65q9RjtcSklJTXfRwxlkvwxHOK_DdFP2fIRNcLibw9Jb70yPjZ38yk8eMo4dDnEFPR79CMnc-wB4uvHmPvaAHSS_MsUWaGOYjA8-LHH87QfAUMITjunpzFM5h-hhk_sGvepMn-Ht49xHPy7Ov59-WVxeff56enK5sFxUYqFFS7SBlivKtNadUk6KDlqQTjFtqaOCthUVumulVVZT4kwnnJNgK0uN5vvocJs7png3lx-awWcLfW8CxDk3TEnNBKuYKPTDP_Q2zimU74qqOVdcM17UwVbZFHNO0DVj8oNJ64aSZlNMM-ZmU0yR7x_z5nYA9-yemijg4xb88j2s_5fTXH_7G_cHjOeYzA</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Peng, Xing‐Jie</creator><creator>Tian, Xue‐Rong</creator><creator>Yu, Shu‐Jing</creator><creator>Zhao, Tong‐Tong</creator><creator>Bian, Qiang</creator><creator>Zhao, Wei‐Guang</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8796-4264</orcidid></search><sort><creationdate>202305</creationdate><title>Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties</title><author>Peng, Xing‐Jie ; Tian, Xue‐Rong ; Yu, Shu‐Jing ; Zhao, Tong‐Tong ; Bian, Qiang ; Zhao, Wei‐Guang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abnormalities</topic><topic>Antifungal Agents - chemistry</topic><topic>Drug development</topic><topic>Esters - pharmacology</topic><topic>Ether - pharmacology</topic><topic>Ethers - pharmacology</topic><topic>Ethyl Ethers - pharmacology</topic><topic>Fungicidal activity</topic><topic>Fungicides</topic><topic>Fungicides, Industrial - chemistry</topic><topic>Hyphae</topic><topic>mode of action</topic><topic>oxime ester</topic><topic>oxime ether</topic><topic>Oximes - pharmacology</topic><topic>Phytophthora capsici</topic><topic>Phytophthora infestans</topic><topic>Piperazine</topic><topic>piperazine thiazole derivatives</topic><topic>Piperazines - pharmacology</topic><topic>Piperidine</topic><topic>Pseudoperonospora cubensis</topic><topic>Structure-Activity Relationship</topic><topic>Thiazoles - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Xing‐Jie</creatorcontrib><creatorcontrib>Tian, Xue‐Rong</creatorcontrib><creatorcontrib>Yu, Shu‐Jing</creatorcontrib><creatorcontrib>Zhao, Tong‐Tong</creatorcontrib><creatorcontrib>Bian, Qiang</creatorcontrib><creatorcontrib>Zhao, Wei‐Guang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pest management science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Xing‐Jie</au><au>Tian, Xue‐Rong</au><au>Yu, Shu‐Jing</au><au>Zhao, Tong‐Tong</au><au>Bian, Qiang</au><au>Zhao, Wei‐Guang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties</atitle><jtitle>Pest management science</jtitle><addtitle>Pest Manag Sci</addtitle><date>2023-05</date><risdate>2023</risdate><volume>79</volume><issue>5</issue><spage>1977</spage><epage>1986</epage><pages>1977-1986</pages><issn>1526-498X</issn><eissn>1526-4998</eissn><abstract>BACKGROUND To study the effect of changing the piperidine ring of oxathiapiprolin on the fungicidal activity, we designed and synthesized novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties, and studied their fungicidal activities against Phytophthora capsici in vitro. RESULTS These derivatives showed moderate to good fungicidal activities against Phytophthora capsici, two oxime ether derivatives showed higher fungicidal activity in vitro than dimethomorph (EC50 = 0.1331 μg mL−1) and comparable to oxathiapiprolin (EC50 = 0.0042 μg mL−1). Oxime ester derivatives showed significantly reduced activities compared with oxime ether derivatives. Most of these derivatives showed broad‐spectrum fungicidal activity against the other eight kinds of fungi. Moreover, four derivatives exhibited good antifungal activities in vivo against Phytophthora capsici, Pseudoperonospora cubensis, and Phytophthora infestans. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici. CONCLUSION The activity of 10b against Phytophthora infestans was better than that of mandipropamid, and compound 10d exhibited higher fungicidal activities against Pseudoperonospora cubensis and Phytophthora infestans than mandipropamid. These two derivatives emerged as promising candidates for antifungal drugs. © 2023 Society of Chemical Industry. Novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties were designed and synthesized, and their fungicidal activities against Phytophthora capsaicae in vitro and in vivo were studied. The hyphae morphology study showed that compound 10d might cause mycelial abnormalities of Phytophthora capsici.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>36661091</pmid><doi>10.1002/ps.7374</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8796-4264</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1526-498X
ispartof Pest management science, 2023-05, Vol.79 (5), p.1977-1986
issn 1526-498X
1526-4998
language eng
recordid cdi_proquest_miscellaneous_2768242524
source Wiley
subjects Abnormalities
Antifungal Agents - chemistry
Drug development
Esters - pharmacology
Ether - pharmacology
Ethers - pharmacology
Ethyl Ethers - pharmacology
Fungicidal activity
Fungicides
Fungicides, Industrial - chemistry
Hyphae
mode of action
oxime ester
oxime ether
Oximes - pharmacology
Phytophthora capsici
Phytophthora infestans
Piperazine
piperazine thiazole derivatives
Piperazines - pharmacology
Piperidine
Pseudoperonospora cubensis
Structure-Activity Relationship
Thiazoles - pharmacology
title Design, synthesis, and fungicidal activities of novel piperazine thiazole derivatives containing oxime ether or oxime ester moieties
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T13%3A24%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design,%20synthesis,%20and%20fungicidal%20activities%20of%20novel%20piperazine%20thiazole%20derivatives%20containing%20oxime%20ether%20or%20oxime%20ester%20moieties&rft.jtitle=Pest%20management%20science&rft.au=Peng,%20Xing%E2%80%90Jie&rft.date=2023-05&rft.volume=79&rft.issue=5&rft.spage=1977&rft.epage=1986&rft.pages=1977-1986&rft.issn=1526-498X&rft.eissn=1526-4998&rft_id=info:doi/10.1002/ps.7374&rft_dat=%3Cproquest_cross%3E2768242524%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3454-84b08aeb3712888f77d64febe6d728c1d141b5148fb6c7c810daf4dd6ec5c1a83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2793373823&rft_id=info:pmid/36661091&rfr_iscdi=true