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Design, synthesis and biological activities of echinopsine derivatives containing acylhydrazone moiety
Based on the broad-spectrum biological activities of echinopsine and acylhydrazones, a series of echinopsine derivatives containing acylhydrazone moieties have been designed, synthesized and their biological activities were evaluated for the first time. The bioassay results indicated that most of th...
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Published in: | Scientific reports 2022-02, Vol.12 (1), p.2935-2935, Article 2935 |
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description | Based on the broad-spectrum biological activities of echinopsine and acylhydrazones, a series of echinopsine derivatives containing acylhydrazone moieties have been designed, synthesized and their biological activities were evaluated for the first time. The bioassay results indicated that most of the compounds showed moderate to good antiviral activities against tobacco mosaic virus (TMV), among which echinopsine (
I
) (inactivation activity, 49.5 ± 4.4%; curative activity, 46.1 ± 1.5%; protection activity, 42.6 ± 2.3%) and its derivatives
1
(inactivation activity, 44.9 ± 4.6%; curative activity, 39.8 ± 2.6%; protection activity, 47.3 ± 4.3%),
3
(inactivation activity, 47.9 ± 0.9%; curative activity, 43.7 ± 3.1%; protection activity, 44.6 ± 3.3%),
7
(inactivation activity, 46.2 ± 1.6%; curative activity, 45.0 ± 3.7%; protection activity, 41.7 ± 0.9%) showed higher anti-TMV activity in vivo at 500 mg/L than commercial ribavirin (inactivation activity, 38.9 ± 1.4%; curative activity, 39.2 ± 1.8%; protection activity, 36.4 ± 3.4%). Some compounds exhibited insecticidal activities against
Plutella xylostella
,
Mythimna separate
and
Spodoptera frugiperda.
Especially, compounds
7
and
27
displayed excellent insecticidal activities against
Plutella xylostell
(mortality 67 ± 6% and 53 ± 6%) even at 0.1 mg/L. Additionally, most echinopsine derivatives exhibited high fungicidal activities against
Physalospora piricola and Sclerotinia sclerotiorum
. |
doi_str_mv | 10.1038/s41598-022-06775-7 |
format | article |
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I
) (inactivation activity, 49.5 ± 4.4%; curative activity, 46.1 ± 1.5%; protection activity, 42.6 ± 2.3%) and its derivatives
1
(inactivation activity, 44.9 ± 4.6%; curative activity, 39.8 ± 2.6%; protection activity, 47.3 ± 4.3%),
3
(inactivation activity, 47.9 ± 0.9%; curative activity, 43.7 ± 3.1%; protection activity, 44.6 ± 3.3%),
7
(inactivation activity, 46.2 ± 1.6%; curative activity, 45.0 ± 3.7%; protection activity, 41.7 ± 0.9%) showed higher anti-TMV activity in vivo at 500 mg/L than commercial ribavirin (inactivation activity, 38.9 ± 1.4%; curative activity, 39.2 ± 1.8%; protection activity, 36.4 ± 3.4%). Some compounds exhibited insecticidal activities against
Plutella xylostella
,
Mythimna separate
and
Spodoptera frugiperda.
Especially, compounds
7
and
27
displayed excellent insecticidal activities against
Plutella xylostell
(mortality 67 ± 6% and 53 ± 6%) even at 0.1 mg/L. Additionally, most echinopsine derivatives exhibited high fungicidal activities against
Physalospora piricola and Sclerotinia sclerotiorum
.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-022-06775-7</identifier><identifier>PMID: 35190609</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/638/309 ; 639/638/403 ; 639/638/549 ; Animals ; Antifungal Agents ; Antiviral Agents ; Ascomycota - drug effects ; Bioassays ; Biological activity ; Design ; Drug Design - methods ; Granulovirus - drug effects ; Humanities and Social Sciences ; Hydrazones - chemistry ; Inactivation ; Insecticides ; multidisciplinary ; Natural products ; Quinolones - chemical synthesis ; Quinolones - chemistry ; Quinolones - pharmacology ; Ribavirin ; Science ; Science (multidisciplinary) ; Spodoptera - drug effects ; Tobacco ; Tobacco Mosaic Virus - drug effects ; Viruses</subject><ispartof>Scientific reports, 2022-02, Vol.12 (1), p.2935-2935, Article 2935</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-910db20685122fd2f121ad6a1aabb3a468e97fd56a4aac63c5bf11c7c34361623</citedby><cites>FETCH-LOGICAL-c540t-910db20685122fd2f121ad6a1aabb3a468e97fd56a4aac63c5bf11c7c34361623</cites><orcidid>0000-0002-6062-3766</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2630742932/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2630742932?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35190609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cui, Peipei</creatorcontrib><creatorcontrib>Cai, Mingjiang</creatorcontrib><creatorcontrib>Meng, Yanan</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Song, Hongjian</creatorcontrib><creatorcontrib>Liu, Yuxiu</creatorcontrib><creatorcontrib>Wang, Qingmin</creatorcontrib><title>Design, synthesis and biological activities of echinopsine derivatives containing acylhydrazone moiety</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Based on the broad-spectrum biological activities of echinopsine and acylhydrazones, a series of echinopsine derivatives containing acylhydrazone moieties have been designed, synthesized and their biological activities were evaluated for the first time. The bioassay results indicated that most of the compounds showed moderate to good antiviral activities against tobacco mosaic virus (TMV), among which echinopsine (
I
) (inactivation activity, 49.5 ± 4.4%; curative activity, 46.1 ± 1.5%; protection activity, 42.6 ± 2.3%) and its derivatives
1
(inactivation activity, 44.9 ± 4.6%; curative activity, 39.8 ± 2.6%; protection activity, 47.3 ± 4.3%),
3
(inactivation activity, 47.9 ± 0.9%; curative activity, 43.7 ± 3.1%; protection activity, 44.6 ± 3.3%),
7
(inactivation activity, 46.2 ± 1.6%; curative activity, 45.0 ± 3.7%; protection activity, 41.7 ± 0.9%) showed higher anti-TMV activity in vivo at 500 mg/L than commercial ribavirin (inactivation activity, 38.9 ± 1.4%; curative activity, 39.2 ± 1.8%; protection activity, 36.4 ± 3.4%). Some compounds exhibited insecticidal activities against
Plutella xylostella
,
Mythimna separate
and
Spodoptera frugiperda.
Especially, compounds
7
and
27
displayed excellent insecticidal activities against
Plutella xylostell
(mortality 67 ± 6% and 53 ± 6%) even at 0.1 mg/L. Additionally, most echinopsine derivatives exhibited high fungicidal activities against
Physalospora piricola and Sclerotinia sclerotiorum
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drug effects</topic><topic>Bioassays</topic><topic>Biological activity</topic><topic>Design</topic><topic>Drug Design - methods</topic><topic>Granulovirus - drug effects</topic><topic>Humanities and Social Sciences</topic><topic>Hydrazones - chemistry</topic><topic>Inactivation</topic><topic>Insecticides</topic><topic>multidisciplinary</topic><topic>Natural products</topic><topic>Quinolones - chemical synthesis</topic><topic>Quinolones - chemistry</topic><topic>Quinolones - pharmacology</topic><topic>Ribavirin</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Spodoptera - drug effects</topic><topic>Tobacco</topic><topic>Tobacco Mosaic Virus - drug effects</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cui, Peipei</creatorcontrib><creatorcontrib>Cai, Mingjiang</creatorcontrib><creatorcontrib>Meng, Yanan</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Song, Hongjian</creatorcontrib><creatorcontrib>Liu, Yuxiu</creatorcontrib><creatorcontrib>Wang, Qingmin</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cui, Peipei</au><au>Cai, Mingjiang</au><au>Meng, Yanan</au><au>Yang, Yan</au><au>Song, Hongjian</au><au>Liu, Yuxiu</au><au>Wang, Qingmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, synthesis and biological activities of echinopsine derivatives containing acylhydrazone moiety</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2022-02-21</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><spage>2935</spage><epage>2935</epage><pages>2935-2935</pages><artnum>2935</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Based on the broad-spectrum biological activities of echinopsine and acylhydrazones, a series of echinopsine derivatives containing acylhydrazone moieties have been designed, synthesized and their biological activities were evaluated for the first time. The bioassay results indicated that most of the compounds showed moderate to good antiviral activities against tobacco mosaic virus (TMV), among which echinopsine (
I
) (inactivation activity, 49.5 ± 4.4%; curative activity, 46.1 ± 1.5%; protection activity, 42.6 ± 2.3%) and its derivatives
1
(inactivation activity, 44.9 ± 4.6%; curative activity, 39.8 ± 2.6%; protection activity, 47.3 ± 4.3%),
3
(inactivation activity, 47.9 ± 0.9%; curative activity, 43.7 ± 3.1%; protection activity, 44.6 ± 3.3%),
7
(inactivation activity, 46.2 ± 1.6%; curative activity, 45.0 ± 3.7%; protection activity, 41.7 ± 0.9%) showed higher anti-TMV activity in vivo at 500 mg/L than commercial ribavirin (inactivation activity, 38.9 ± 1.4%; curative activity, 39.2 ± 1.8%; protection activity, 36.4 ± 3.4%). Some compounds exhibited insecticidal activities against
Plutella xylostella
,
Mythimna separate
and
Spodoptera frugiperda.
Especially, compounds
7
and
27
displayed excellent insecticidal activities against
Plutella xylostell
(mortality 67 ± 6% and 53 ± 6%) even at 0.1 mg/L. Additionally, most echinopsine derivatives exhibited high fungicidal activities against
Physalospora piricola and Sclerotinia sclerotiorum
.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35190609</pmid><doi>10.1038/s41598-022-06775-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6062-3766</orcidid><oa>free_for_read</oa></addata></record> |
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source | Publicly Available Content Database; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 639/638/309 639/638/403 639/638/549 Animals Antifungal Agents Antiviral Agents Ascomycota - drug effects Bioassays Biological activity Design Drug Design - methods Granulovirus - drug effects Humanities and Social Sciences Hydrazones - chemistry Inactivation Insecticides multidisciplinary Natural products Quinolones - chemical synthesis Quinolones - chemistry Quinolones - pharmacology Ribavirin Science Science (multidisciplinary) Spodoptera - drug effects Tobacco Tobacco Mosaic Virus - drug effects Viruses |
title | Design, synthesis and biological activities of echinopsine derivatives containing acylhydrazone moiety |
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