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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...
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Published in: | Pest management science 2023-05, Vol.79 (5), p.1977-1986 |
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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 |
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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 & 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 & 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 & 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> |
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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 |
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