Direct infusion ESI‐IT‐MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae)
INTRODUCTION: The Annonaceae family is known as a promising abundant source of secondary metabolites, especially annonaceous acetogenins, terpenoids and isoquinoline‐derived alkaloids. Although widely investigated from the phytochemical viewpoint, this family still presents some largely unexplored g...
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creator | Soares, Elzalina R Silva, Felipe M. A Almeida, Richardson A Lima, Bruna R Silva Filho, Francinaldo A Barison, Andersson Koolen, Hector H. F Pinheiro, Maria Lúcia B Souza, Afonso D. L |
description | INTRODUCTION: The Annonaceae family is known as a promising abundant source of secondary metabolites, especially annonaceous acetogenins, terpenoids and isoquinoline‐derived alkaloids. Although widely investigated from the phytochemical viewpoint, this family still presents some largely unexplored genera, e.g. the Bocageopsis. OBJECTIVE: To investigate the alkaloid content of Bocageopsis pleiosperma Maas using direct infusion electrospray ionisation ion trap tandem mass spectrometry (ESI‐IT‐MSⁿ) analysis. METHODOLOGY: Dichloromethane extracts of aerial parts were subjected to acid–base partitioning to yield the alkaloidal fractions. These fractions were analysed by direct infusion into a (+)ESI‐IT‐MSⁿ system. The alkaloidal fraction from the leaves was also obtained on a large scale and subjected to chromatographic separation. RESULTS: The tentative MSⁿ‐based identification of alkaloids in leaves, twigs and trunk bark showed that aporphine alkaloids were restricted to the leaves and twigs, tetrahydroprotoberberine alkaloids were only found in the twigs and trunk bark while benzylisoquinoline alkaloids were found in the leaves, twigs and trunk bark. Chromatographic separation of the leaf alkaloidal fraction yielded the aporphine alkaloids nornuciferine, asimilobine and isoboldine, the β‐carboline alkaloid tetrahydroharman and some mixtures containing benzylisoquinoline and aporphine alkaloids, all described for the first time in the Bocageopsis genus. Furthermore, tetrahydroharman has not previously been reported in the Magnoliales order. CONCLUSION: Direct infusion ESI‐IT‐MSⁿ analysis of alkaloids allowed fast recognition of alkaloidal classes previously reported in the Annonaceae family, aiding the chromatographic step and allowing a selective isolation of compounds previously not identified in the Bocageopsis genus. Copyright © 2015 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/pca.2568 |
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A ; Almeida, Richardson A ; Lima, Bruna R ; Silva Filho, Francinaldo A ; Barison, Andersson ; Koolen, Hector H. F ; Pinheiro, Maria Lúcia B ; Souza, Afonso D. L</creator><creatorcontrib>Soares, Elzalina R ; Silva, Felipe M. A ; Almeida, Richardson A ; Lima, Bruna R ; Silva Filho, Francinaldo A ; Barison, Andersson ; Koolen, Hector H. F ; Pinheiro, Maria Lúcia B ; Souza, Afonso D. L</creatorcontrib><description>INTRODUCTION: The Annonaceae family is known as a promising abundant source of secondary metabolites, especially annonaceous acetogenins, terpenoids and isoquinoline‐derived alkaloids. Although widely investigated from the phytochemical viewpoint, this family still presents some largely unexplored genera, e.g. the Bocageopsis. OBJECTIVE: To investigate the alkaloid content of Bocageopsis pleiosperma Maas using direct infusion electrospray ionisation ion trap tandem mass spectrometry (ESI‐IT‐MSⁿ) analysis. METHODOLOGY: Dichloromethane extracts of aerial parts were subjected to acid–base partitioning to yield the alkaloidal fractions. These fractions were analysed by direct infusion into a (+)ESI‐IT‐MSⁿ system. The alkaloidal fraction from the leaves was also obtained on a large scale and subjected to chromatographic separation. RESULTS: The tentative MSⁿ‐based identification of alkaloids in leaves, twigs and trunk bark showed that aporphine alkaloids were restricted to the leaves and twigs, tetrahydroprotoberberine alkaloids were only found in the twigs and trunk bark while benzylisoquinoline alkaloids were found in the leaves, twigs and trunk bark. Chromatographic separation of the leaf alkaloidal fraction yielded the aporphine alkaloids nornuciferine, asimilobine and isoboldine, the β‐carboline alkaloid tetrahydroharman and some mixtures containing benzylisoquinoline and aporphine alkaloids, all described for the first time in the Bocageopsis genus. Furthermore, tetrahydroharman has not previously been reported in the Magnoliales order. CONCLUSION: Direct infusion ESI‐IT‐MSⁿ analysis of alkaloids allowed fast recognition of alkaloidal classes previously reported in the Annonaceae family, aiding the chromatographic step and allowing a selective isolation of compounds previously not identified in the Bocageopsis genus. Copyright © 2015 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0958-0344</identifier><identifier>EISSN: 1099-1565</identifier><identifier>DOI: 10.1002/pca.2568</identifier><identifier>PMID: 26108161</identifier><identifier>CODEN: PHANEL</identifier><language>eng</language><publisher>England: Wiley</publisher><subject>acetogenins ; aerial parts ; Alkaloid profiling ; alkaloids ; Alkaloids - analysis ; Alkaloids - chemistry ; Alkaloids - isolation & purification ; Annonaceae ; Annonaceae - chemistry ; Bark ; Bocageopsis pleiosperma ; branches ; Chemical Fractionation - methods ; chromatography ; extracts ; Harmaline - analogs & derivatives ; Harmaline - analysis ; Harmaline - chemistry ; Harmaline - isolation & purification ; isoquinoline-derived alkaloids ; Leaves ; Magnetic Resonance Spectroscopy - methods ; Mass spectrometry ; Metabolites ; methylene chloride ; mixtures ; Molecular Structure ; Plant Bark - chemistry ; Plant Components, Aerial - chemistry ; Plant Leaves - chemistry ; Reproducibility of Results ; Secondary metabolites ; Spectrometry, Mass, Electrospray Ionization - methods ; tandem mass spectrometry ; Tandem Mass Spectrometry - methods ; terpenoids ; tetrahydroharman</subject><ispartof>Phytochemical analysis, 2015-09, Vol.26 (5), p.339-345</ispartof><rights>Copyright © 2015 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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.2568$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpca.2568$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26108161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soares, Elzalina R</creatorcontrib><creatorcontrib>Silva, Felipe M. A</creatorcontrib><creatorcontrib>Almeida, Richardson A</creatorcontrib><creatorcontrib>Lima, Bruna R</creatorcontrib><creatorcontrib>Silva Filho, Francinaldo A</creatorcontrib><creatorcontrib>Barison, Andersson</creatorcontrib><creatorcontrib>Koolen, Hector H. F</creatorcontrib><creatorcontrib>Pinheiro, Maria Lúcia B</creatorcontrib><creatorcontrib>Souza, Afonso D. L</creatorcontrib><title>Direct infusion ESI‐IT‐MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae)</title><title>Phytochemical analysis</title><addtitle>Phytochem. Anal</addtitle><description>INTRODUCTION: The Annonaceae family is known as a promising abundant source of secondary metabolites, especially annonaceous acetogenins, terpenoids and isoquinoline‐derived alkaloids. Although widely investigated from the phytochemical viewpoint, this family still presents some largely unexplored genera, e.g. the Bocageopsis. OBJECTIVE: To investigate the alkaloid content of Bocageopsis pleiosperma Maas using direct infusion electrospray ionisation ion trap tandem mass spectrometry (ESI‐IT‐MSⁿ) analysis. METHODOLOGY: Dichloromethane extracts of aerial parts were subjected to acid–base partitioning to yield the alkaloidal fractions. These fractions were analysed by direct infusion into a (+)ESI‐IT‐MSⁿ system. The alkaloidal fraction from the leaves was also obtained on a large scale and subjected to chromatographic separation. RESULTS: The tentative MSⁿ‐based identification of alkaloids in leaves, twigs and trunk bark showed that aporphine alkaloids were restricted to the leaves and twigs, tetrahydroprotoberberine alkaloids were only found in the twigs and trunk bark while benzylisoquinoline alkaloids were found in the leaves, twigs and trunk bark. Chromatographic separation of the leaf alkaloidal fraction yielded the aporphine alkaloids nornuciferine, asimilobine and isoboldine, the β‐carboline alkaloid tetrahydroharman and some mixtures containing benzylisoquinoline and aporphine alkaloids, all described for the first time in the Bocageopsis genus. Furthermore, tetrahydroharman has not previously been reported in the Magnoliales order. CONCLUSION: Direct infusion ESI‐IT‐MSⁿ analysis of alkaloids allowed fast recognition of alkaloidal classes previously reported in the Annonaceae family, aiding the chromatographic step and allowing a selective isolation of compounds previously not identified in the Bocageopsis genus. Copyright © 2015 John Wiley & Sons, Ltd.</description><subject>acetogenins</subject><subject>aerial parts</subject><subject>Alkaloid profiling</subject><subject>alkaloids</subject><subject>Alkaloids - analysis</subject><subject>Alkaloids - chemistry</subject><subject>Alkaloids - isolation & purification</subject><subject>Annonaceae</subject><subject>Annonaceae - chemistry</subject><subject>Bark</subject><subject>Bocageopsis pleiosperma</subject><subject>branches</subject><subject>Chemical Fractionation - methods</subject><subject>chromatography</subject><subject>extracts</subject><subject>Harmaline - analogs & derivatives</subject><subject>Harmaline - analysis</subject><subject>Harmaline - chemistry</subject><subject>Harmaline - isolation & purification</subject><subject>isoquinoline-derived alkaloids</subject><subject>Leaves</subject><subject>Magnetic Resonance Spectroscopy - methods</subject><subject>Mass spectrometry</subject><subject>Metabolites</subject><subject>methylene chloride</subject><subject>mixtures</subject><subject>Molecular Structure</subject><subject>Plant Bark - chemistry</subject><subject>Plant Components, Aerial - chemistry</subject><subject>Plant Leaves - chemistry</subject><subject>Reproducibility of Results</subject><subject>Secondary metabolites</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><subject>tandem mass spectrometry</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>terpenoids</subject><subject>tetrahydroharman</subject><issn>0958-0344</issn><issn>1099-1565</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c1u1DAQAGALgehSkHgCsMSlHFLGcewkx-32b6UWirYVR2uSOF23iR3srOjeeAQOPCFPgpcti4Qs2ZLnm5E9Q8hrBocMIP0w1HiYClk8IRMGZZkwIcVTMoFSFAnwLNsjL0K4A4ixUj4ne6lkUDDJJuTnsfG6Hqmx7SoYZ-nJYv7r-4_5ddwuF5Zid4-dMw0dvGtNpynahprgOhw32rV01KPH5brxbom-R_tHuHGp_S450Na7nh65Gm-1G4IJdOi0cWHQMYP2iIEeTK11FmuN-v1L8qzFLuhXj-c-uTk9uZ6dJxefzuaz6UXSprIskrRFjk1b5sBzVhaM83gDKMqGAXJZVSDytqok1E2uoZAQl6iKNIO85IJXfJ8cbOvGz31d6TCq3oRadx1a7VZBsRwyLmIX00jf_Ufv3Mrb-LqtkoJxFtWbR7Wqet2owZse_Vr97XcEyRZ8i71c7-IM1GaOKs5RbeaormbTzfnPmzDqh51Hf69kznOhvnw8U5dXR0J8Pj9WefRvt75Fp_DWm6BuFikwEaunAljGfwO8yalK</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Soares, Elzalina R</creator><creator>Silva, Felipe M. A</creator><creator>Almeida, Richardson A</creator><creator>Lima, Bruna R</creator><creator>Silva Filho, Francinaldo A</creator><creator>Barison, Andersson</creator><creator>Koolen, Hector H. F</creator><creator>Pinheiro, Maria Lúcia B</creator><creator>Souza, Afonso D. L</creator><general>Wiley</general><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</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></search><sort><creationdate>201509</creationdate><title>Direct infusion ESI‐IT‐MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae)</title><author>Soares, Elzalina R ; Silva, Felipe M. A ; Almeida, Richardson A ; Lima, Bruna R ; Silva Filho, Francinaldo A ; Barison, Andersson ; Koolen, Hector H. F ; Pinheiro, Maria Lúcia B ; Souza, Afonso D. 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A</creatorcontrib><creatorcontrib>Almeida, Richardson A</creatorcontrib><creatorcontrib>Lima, Bruna R</creatorcontrib><creatorcontrib>Silva Filho, Francinaldo A</creatorcontrib><creatorcontrib>Barison, Andersson</creatorcontrib><creatorcontrib>Koolen, Hector H. F</creatorcontrib><creatorcontrib>Pinheiro, Maria Lúcia B</creatorcontrib><creatorcontrib>Souza, Afonso D. 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A</au><au>Almeida, Richardson A</au><au>Lima, Bruna R</au><au>Silva Filho, Francinaldo A</au><au>Barison, Andersson</au><au>Koolen, Hector H. F</au><au>Pinheiro, Maria Lúcia B</au><au>Souza, Afonso D. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct infusion ESI‐IT‐MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae)</atitle><jtitle>Phytochemical analysis</jtitle><addtitle>Phytochem. Anal</addtitle><date>2015-09</date><risdate>2015</risdate><volume>26</volume><issue>5</issue><spage>339</spage><epage>345</epage><pages>339-345</pages><issn>0958-0344</issn><eissn>1099-1565</eissn><coden>PHANEL</coden><abstract>INTRODUCTION: The Annonaceae family is known as a promising abundant source of secondary metabolites, especially annonaceous acetogenins, terpenoids and isoquinoline‐derived alkaloids. Although widely investigated from the phytochemical viewpoint, this family still presents some largely unexplored genera, e.g. the Bocageopsis. OBJECTIVE: To investigate the alkaloid content of Bocageopsis pleiosperma Maas using direct infusion electrospray ionisation ion trap tandem mass spectrometry (ESI‐IT‐MSⁿ) analysis. METHODOLOGY: Dichloromethane extracts of aerial parts were subjected to acid–base partitioning to yield the alkaloidal fractions. These fractions were analysed by direct infusion into a (+)ESI‐IT‐MSⁿ system. The alkaloidal fraction from the leaves was also obtained on a large scale and subjected to chromatographic separation. RESULTS: The tentative MSⁿ‐based identification of alkaloids in leaves, twigs and trunk bark showed that aporphine alkaloids were restricted to the leaves and twigs, tetrahydroprotoberberine alkaloids were only found in the twigs and trunk bark while benzylisoquinoline alkaloids were found in the leaves, twigs and trunk bark. Chromatographic separation of the leaf alkaloidal fraction yielded the aporphine alkaloids nornuciferine, asimilobine and isoboldine, the β‐carboline alkaloid tetrahydroharman and some mixtures containing benzylisoquinoline and aporphine alkaloids, all described for the first time in the Bocageopsis genus. Furthermore, tetrahydroharman has not previously been reported in the Magnoliales order. CONCLUSION: Direct infusion ESI‐IT‐MSⁿ analysis of alkaloids allowed fast recognition of alkaloidal classes previously reported in the Annonaceae family, aiding the chromatographic step and allowing a selective isolation of compounds previously not identified in the Bocageopsis genus. Copyright © 2015 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Wiley</pub><pmid>26108161</pmid><doi>10.1002/pca.2568</doi><tpages>7</tpages></addata></record> |
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subjects | acetogenins aerial parts Alkaloid profiling alkaloids Alkaloids - analysis Alkaloids - chemistry Alkaloids - isolation & purification Annonaceae Annonaceae - chemistry Bark Bocageopsis pleiosperma branches Chemical Fractionation - methods chromatography extracts Harmaline - analogs & derivatives Harmaline - analysis Harmaline - chemistry Harmaline - isolation & purification isoquinoline-derived alkaloids Leaves Magnetic Resonance Spectroscopy - methods Mass spectrometry Metabolites methylene chloride mixtures Molecular Structure Plant Bark - chemistry Plant Components, Aerial - chemistry Plant Leaves - chemistry Reproducibility of Results Secondary metabolites Spectrometry, Mass, Electrospray Ionization - methods tandem mass spectrometry Tandem Mass Spectrometry - methods terpenoids tetrahydroharman |
title | Direct infusion ESI‐IT‐MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae) |
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