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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Veröffentlicht in:Phytochemical analysis 2015-09, Vol.26 (5), p.339-345
Hauptverfasser: 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
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container_issue 5
container_start_page 339
container_title Phytochemical analysis
container_volume 26
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. 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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. 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. 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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. 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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 &amp; 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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source MEDLINE; Access via Wiley Online Library
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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