Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR
Introduction Casearia is an essential source of cytotoxic highly oxidised clerodane diterpenes, in addition to phenolics, flavonoids, and glycoside derivatives. Here we identify flavonoid‐3‐O‐glycoside derivatives in the ethyl acetate (EtOAc) fraction of the methanolic extract from leaves C. arborea...
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description | Introduction
Casearia is an essential source of cytotoxic highly oxidised clerodane diterpenes, in addition to phenolics, flavonoids, and glycoside derivatives. Here we identify flavonoid‐3‐O‐glycoside derivatives in the ethyl acetate (EtOAc) fraction of the methanolic extract from leaves C. arborea leaves.
Objective
To characterise the EtOAc phase from the methanolic extract of C. arborea leaves using ultra‐high‐performance liquid chromatography diode array detector high‐resolution tandem mass spectrometry (UHPLC‐DAD‐HRMS/MS) and molecular networking‐based dereplication.
Methodology
We identified compounds not annotated in the GNPS platform by co‐injection of standards in HPLC‐DAD or by isolation and characterisation of the metabolites using nuclear magnetic resonance (NMR) spectroscopy. A workflow on the GNPS platform aided the organisation of spectral data and dereplication by annotations. We subjected the EtOAc phase to HPLC‐DAD analysis using standard compound co‐injection to corroborate the GNPS annotations. We isolated unidentified compounds with semi‐preparative HPLC‐DAD for structural identification using NMR.
Results
We annotated a molecular family of flavonoid‐3‐O‐glycosides in the molecular networking created using the GNPS platform. These included avicularin, cacticin, isoquercitrin, quercitrin, rutin, and a quercetin‐3‐O‐pentoside cluster. We confirmed the annotations with standard compounds using HPLC‐DAD co‐injection analysis, besides identifying quercetin‐3‐O‐robinobioside and kaempferol. We isolated three flavonoid‐3‐O‐pentosides and characterised them using one‐ and two‐dimensional NMR; we identified them as reynoutrin, guaijaverin, and avicularin.
Conclusion
This work describes the isolation of kaempferol and nine known flavonoid‐3‐O‐glycosides from the polar fraction of the methanolic extract (EtOAc) from C. arborea leaves using molecular networking to guide the chromatographic procedures. We identified eight compounds for the first time in Casearia that amplify and reinforce the genus' chemotaxonomy with the presence of glycosylated flavonoids.
Kaempferol and nine flavonoid‐3‐O‐glycosides were isolated from the polar fraction of methanolic extract (EtOAc) from Casearia arborea leaves. Molecular networking‐based dereplication and co‐injection analysis was used to guide the chromatographic procedures. Eight compounds were isolated for the first time in Casearia amplifying the genus’ chemotaxonomy with the presence of glycosylated flavon |
doi_str_mv | 10.1002/pca.3032 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2487429192</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2487429192</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3492-21ffad6935f1d051050d478331e5ade086139c0902784a004fda43d9ea7e89913</originalsourceid><addsrcrecordid>eNp1kc9uEzEQh1cIRENB4gmQJS7lsO14bSfrY5QWEimhVUPPq8l6trh416m92yg3HoG34L14ElxaQELiMH-k-fRppF-WveZwzAGKk22NxwJE8SQbcdA652qsnmYj0KrMQUh5kL2I8QYg3fT4eXYghFJSghhl3xeGut42tsbe-o75hjUO73znrfnx9ZtIdZ7q2u1rH62hyJrgW-YI79Ke6BlGwmCRYdj4QMiO1uiSrSakd2yzZ1fzi-UsKU6np6mfrRepzy9X65PVmtW-3diODNvZ_jNrvaN6cBhYR_3Ohy-2u2bYGfZxdfkye9agi_TqcR5mV-_PPs3m-fL8w2I2Xea1kLrIC940aMZaqIYbUBwUGDkpheCk0BCUYy50DRqKSSkRQDYGpTCacEKl1lwcZkcP3m3wtwPFvmptrMk57MgPsSpkOZGF5rpI6Nt_0Bs_hC59VxWqBKVBKPlXWAcfY6Cm2gbbYthXHKr78KoUXnUfXkLfPAqHTUvmD_g7rQTkD8DOOtr_V1RdzKa_hD8BFMKnFw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2580590354</pqid></control><display><type>article</type><title>Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR</title><source>Wiley Online Library All Journals</source><creator>Santos, Augusto L. ; Soares, Marisi G. ; Medeiros, Lívia S. ; Ferreira, Marcelo J.P. ; Sartorelli, Patricia</creator><creatorcontrib>Santos, Augusto L. ; Soares, Marisi G. ; Medeiros, Lívia S. ; Ferreira, Marcelo J.P. ; Sartorelli, Patricia</creatorcontrib><description>Introduction
Casearia is an essential source of cytotoxic highly oxidised clerodane diterpenes, in addition to phenolics, flavonoids, and glycoside derivatives. Here we identify flavonoid‐3‐O‐glycoside derivatives in the ethyl acetate (EtOAc) fraction of the methanolic extract from leaves C. arborea leaves.
Objective
To characterise the EtOAc phase from the methanolic extract of C. arborea leaves using ultra‐high‐performance liquid chromatography diode array detector high‐resolution tandem mass spectrometry (UHPLC‐DAD‐HRMS/MS) and molecular networking‐based dereplication.
Methodology
We identified compounds not annotated in the GNPS platform by co‐injection of standards in HPLC‐DAD or by isolation and characterisation of the metabolites using nuclear magnetic resonance (NMR) spectroscopy. A workflow on the GNPS platform aided the organisation of spectral data and dereplication by annotations. We subjected the EtOAc phase to HPLC‐DAD analysis using standard compound co‐injection to corroborate the GNPS annotations. We isolated unidentified compounds with semi‐preparative HPLC‐DAD for structural identification using NMR.
Results
We annotated a molecular family of flavonoid‐3‐O‐glycosides in the molecular networking created using the GNPS platform. These included avicularin, cacticin, isoquercitrin, quercitrin, rutin, and a quercetin‐3‐O‐pentoside cluster. We confirmed the annotations with standard compounds using HPLC‐DAD co‐injection analysis, besides identifying quercetin‐3‐O‐robinobioside and kaempferol. We isolated three flavonoid‐3‐O‐pentosides and characterised them using one‐ and two‐dimensional NMR; we identified them as reynoutrin, guaijaverin, and avicularin.
Conclusion
This work describes the isolation of kaempferol and nine known flavonoid‐3‐O‐glycosides from the polar fraction of the methanolic extract (EtOAc) from C. arborea leaves using molecular networking to guide the chromatographic procedures. We identified eight compounds for the first time in Casearia that amplify and reinforce the genus' chemotaxonomy with the presence of glycosylated flavonoids.
Kaempferol and nine flavonoid‐3‐O‐glycosides were isolated from the polar fraction of methanolic extract (EtOAc) from Casearia arborea leaves. Molecular networking‐based dereplication and co‐injection analysis was used to guide the chromatographic procedures. Eight compounds were isolated for the first time in Casearia amplifying the genus’ chemotaxonomy with the presence of glycosylated flavonoids.</description><identifier>ISSN: 0958-0344</identifier><identifier>EISSN: 1099-1565</identifier><identifier>DOI: 10.1002/pca.3032</identifier><identifier>PMID: 33554403</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Acetic acid ; Annotations ; Casearia ; Chemotaxonomy ; Cytotoxicity ; dereplication ; Ethyl acetate ; flavonoid 3‐O‐glycosides ; Flavonoids ; Glycosides ; High performance liquid chromatography ; HRMS/MS ; Injection ; Kaempferol ; Liquid chromatography ; Mass spectrometry ; Mass spectroscopy ; Metabolites ; molecular networking ; Networking ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Phenols ; Quercetin ; Rutin ; Workflow</subject><ispartof>Phytochemical analysis, 2021-11, Vol.32 (6), p.891-898</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3492-21ffad6935f1d051050d478331e5ade086139c0902784a004fda43d9ea7e89913</citedby><cites>FETCH-LOGICAL-c3492-21ffad6935f1d051050d478331e5ade086139c0902784a004fda43d9ea7e89913</cites><orcidid>0000-0001-8743-3340 ; 0000-0001-9221-9867 ; 0000-0003-1877-1762 ; 0000-0003-1590-8145 ; 0000-0002-1624-8145</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpca.3032$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpca.3032$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33554403$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santos, Augusto L.</creatorcontrib><creatorcontrib>Soares, Marisi G.</creatorcontrib><creatorcontrib>Medeiros, Lívia S.</creatorcontrib><creatorcontrib>Ferreira, Marcelo J.P.</creatorcontrib><creatorcontrib>Sartorelli, Patricia</creatorcontrib><title>Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR</title><title>Phytochemical analysis</title><addtitle>Phytochem Anal</addtitle><description>Introduction
Casearia is an essential source of cytotoxic highly oxidised clerodane diterpenes, in addition to phenolics, flavonoids, and glycoside derivatives. Here we identify flavonoid‐3‐O‐glycoside derivatives in the ethyl acetate (EtOAc) fraction of the methanolic extract from leaves C. arborea leaves.
Objective
To characterise the EtOAc phase from the methanolic extract of C. arborea leaves using ultra‐high‐performance liquid chromatography diode array detector high‐resolution tandem mass spectrometry (UHPLC‐DAD‐HRMS/MS) and molecular networking‐based dereplication.
Methodology
We identified compounds not annotated in the GNPS platform by co‐injection of standards in HPLC‐DAD or by isolation and characterisation of the metabolites using nuclear magnetic resonance (NMR) spectroscopy. A workflow on the GNPS platform aided the organisation of spectral data and dereplication by annotations. We subjected the EtOAc phase to HPLC‐DAD analysis using standard compound co‐injection to corroborate the GNPS annotations. We isolated unidentified compounds with semi‐preparative HPLC‐DAD for structural identification using NMR.
Results
We annotated a molecular family of flavonoid‐3‐O‐glycosides in the molecular networking created using the GNPS platform. These included avicularin, cacticin, isoquercitrin, quercitrin, rutin, and a quercetin‐3‐O‐pentoside cluster. We confirmed the annotations with standard compounds using HPLC‐DAD co‐injection analysis, besides identifying quercetin‐3‐O‐robinobioside and kaempferol. We isolated three flavonoid‐3‐O‐pentosides and characterised them using one‐ and two‐dimensional NMR; we identified them as reynoutrin, guaijaverin, and avicularin.
Conclusion
This work describes the isolation of kaempferol and nine known flavonoid‐3‐O‐glycosides from the polar fraction of the methanolic extract (EtOAc) from C. arborea leaves using molecular networking to guide the chromatographic procedures. We identified eight compounds for the first time in Casearia that amplify and reinforce the genus' chemotaxonomy with the presence of glycosylated flavonoids.
Kaempferol and nine flavonoid‐3‐O‐glycosides were isolated from the polar fraction of methanolic extract (EtOAc) from Casearia arborea leaves. Molecular networking‐based dereplication and co‐injection analysis was used to guide the chromatographic procedures. Eight compounds were isolated for the first time in Casearia amplifying the genus’ chemotaxonomy with the presence of glycosylated flavonoids.</description><subject>Acetic acid</subject><subject>Annotations</subject><subject>Casearia</subject><subject>Chemotaxonomy</subject><subject>Cytotoxicity</subject><subject>dereplication</subject><subject>Ethyl acetate</subject><subject>flavonoid 3‐O‐glycosides</subject><subject>Flavonoids</subject><subject>Glycosides</subject><subject>High performance liquid chromatography</subject><subject>HRMS/MS</subject><subject>Injection</subject><subject>Kaempferol</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolites</subject><subject>molecular networking</subject><subject>Networking</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Phenols</subject><subject>Quercetin</subject><subject>Rutin</subject><subject>Workflow</subject><issn>0958-0344</issn><issn>1099-1565</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kc9uEzEQh1cIRENB4gmQJS7lsO14bSfrY5QWEimhVUPPq8l6trh416m92yg3HoG34L14ElxaQELiMH-k-fRppF-WveZwzAGKk22NxwJE8SQbcdA652qsnmYj0KrMQUh5kL2I8QYg3fT4eXYghFJSghhl3xeGut42tsbe-o75hjUO73znrfnx9ZtIdZ7q2u1rH62hyJrgW-YI79Ke6BlGwmCRYdj4QMiO1uiSrSakd2yzZ1fzi-UsKU6np6mfrRepzy9X65PVmtW-3diODNvZ_jNrvaN6cBhYR_3Ohy-2u2bYGfZxdfkye9agi_TqcR5mV-_PPs3m-fL8w2I2Xea1kLrIC940aMZaqIYbUBwUGDkpheCk0BCUYy50DRqKSSkRQDYGpTCacEKl1lwcZkcP3m3wtwPFvmptrMk57MgPsSpkOZGF5rpI6Nt_0Bs_hC59VxWqBKVBKPlXWAcfY6Cm2gbbYthXHKr78KoUXnUfXkLfPAqHTUvmD_g7rQTkD8DOOtr_V1RdzKa_hD8BFMKnFw</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Santos, Augusto L.</creator><creator>Soares, Marisi G.</creator><creator>Medeiros, Lívia S.</creator><creator>Ferreira, Marcelo J.P.</creator><creator>Sartorelli, Patricia</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8743-3340</orcidid><orcidid>https://orcid.org/0000-0001-9221-9867</orcidid><orcidid>https://orcid.org/0000-0003-1877-1762</orcidid><orcidid>https://orcid.org/0000-0003-1590-8145</orcidid><orcidid>https://orcid.org/0000-0002-1624-8145</orcidid></search><sort><creationdate>202111</creationdate><title>Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR</title><author>Santos, Augusto L. ; Soares, Marisi G. ; Medeiros, Lívia S. ; Ferreira, Marcelo J.P. ; Sartorelli, Patricia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3492-21ffad6935f1d051050d478331e5ade086139c0902784a004fda43d9ea7e89913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetic acid</topic><topic>Annotations</topic><topic>Casearia</topic><topic>Chemotaxonomy</topic><topic>Cytotoxicity</topic><topic>dereplication</topic><topic>Ethyl acetate</topic><topic>flavonoid 3‐O‐glycosides</topic><topic>Flavonoids</topic><topic>Glycosides</topic><topic>High performance liquid chromatography</topic><topic>HRMS/MS</topic><topic>Injection</topic><topic>Kaempferol</topic><topic>Liquid chromatography</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Metabolites</topic><topic>molecular networking</topic><topic>Networking</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Phenols</topic><topic>Quercetin</topic><topic>Rutin</topic><topic>Workflow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santos, Augusto L.</creatorcontrib><creatorcontrib>Soares, Marisi G.</creatorcontrib><creatorcontrib>Medeiros, Lívia S.</creatorcontrib><creatorcontrib>Ferreira, Marcelo J.P.</creatorcontrib><creatorcontrib>Sartorelli, Patricia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Phytochemical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santos, Augusto L.</au><au>Soares, Marisi G.</au><au>Medeiros, Lívia S.</au><au>Ferreira, Marcelo J.P.</au><au>Sartorelli, Patricia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR</atitle><jtitle>Phytochemical analysis</jtitle><addtitle>Phytochem Anal</addtitle><date>2021-11</date><risdate>2021</risdate><volume>32</volume><issue>6</issue><spage>891</spage><epage>898</epage><pages>891-898</pages><issn>0958-0344</issn><eissn>1099-1565</eissn><abstract>Introduction
Casearia is an essential source of cytotoxic highly oxidised clerodane diterpenes, in addition to phenolics, flavonoids, and glycoside derivatives. Here we identify flavonoid‐3‐O‐glycoside derivatives in the ethyl acetate (EtOAc) fraction of the methanolic extract from leaves C. arborea leaves.
Objective
To characterise the EtOAc phase from the methanolic extract of C. arborea leaves using ultra‐high‐performance liquid chromatography diode array detector high‐resolution tandem mass spectrometry (UHPLC‐DAD‐HRMS/MS) and molecular networking‐based dereplication.
Methodology
We identified compounds not annotated in the GNPS platform by co‐injection of standards in HPLC‐DAD or by isolation and characterisation of the metabolites using nuclear magnetic resonance (NMR) spectroscopy. A workflow on the GNPS platform aided the organisation of spectral data and dereplication by annotations. We subjected the EtOAc phase to HPLC‐DAD analysis using standard compound co‐injection to corroborate the GNPS annotations. We isolated unidentified compounds with semi‐preparative HPLC‐DAD for structural identification using NMR.
Results
We annotated a molecular family of flavonoid‐3‐O‐glycosides in the molecular networking created using the GNPS platform. These included avicularin, cacticin, isoquercitrin, quercitrin, rutin, and a quercetin‐3‐O‐pentoside cluster. We confirmed the annotations with standard compounds using HPLC‐DAD co‐injection analysis, besides identifying quercetin‐3‐O‐robinobioside and kaempferol. We isolated three flavonoid‐3‐O‐pentosides and characterised them using one‐ and two‐dimensional NMR; we identified them as reynoutrin, guaijaverin, and avicularin.
Conclusion
This work describes the isolation of kaempferol and nine known flavonoid‐3‐O‐glycosides from the polar fraction of the methanolic extract (EtOAc) from C. arborea leaves using molecular networking to guide the chromatographic procedures. We identified eight compounds for the first time in Casearia that amplify and reinforce the genus' chemotaxonomy with the presence of glycosylated flavonoids.
Kaempferol and nine flavonoid‐3‐O‐glycosides were isolated from the polar fraction of methanolic extract (EtOAc) from Casearia arborea leaves. Molecular networking‐based dereplication and co‐injection analysis was used to guide the chromatographic procedures. Eight compounds were isolated for the first time in Casearia amplifying the genus’ chemotaxonomy with the presence of glycosylated flavonoids.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33554403</pmid><doi>10.1002/pca.3032</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8743-3340</orcidid><orcidid>https://orcid.org/0000-0001-9221-9867</orcidid><orcidid>https://orcid.org/0000-0003-1877-1762</orcidid><orcidid>https://orcid.org/0000-0003-1590-8145</orcidid><orcidid>https://orcid.org/0000-0002-1624-8145</orcidid></addata></record> |
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subjects | Acetic acid Annotations Casearia Chemotaxonomy Cytotoxicity dereplication Ethyl acetate flavonoid 3‐O‐glycosides Flavonoids Glycosides High performance liquid chromatography HRMS/MS Injection Kaempferol Liquid chromatography Mass spectrometry Mass spectroscopy Metabolites molecular networking Networking NMR NMR spectroscopy Nuclear magnetic resonance Phenols Quercetin Rutin Workflow |
title | Identification of flavonoid‐3‐O‐glycosides from leaves of Casearia arborea (Salicaceae) by UHPLC‐DAD‐ESI‐HRMS/MS combined with molecular networking and NMR |
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