Isolation and quantitation of ecologically important phloroglucinols and other compounds from Eucalyptus jensenii

dc.contributor.authorSidana, Jasmeen
dc.contributor.authorFoley, William
dc.contributor.authorSingh, Inder Pal
dc.date.accessioned2015-12-10T23:18:35Z
dc.date.issued2012
dc.date.updated2016-02-24T08:38:38Z
dc.description.abstractIntroduction Eucalyptus jensenii has not been explored for its phytoconstituents except for its essential oil although a formylated phloroglucinol compound jensenone has been the focus of several ecological studies. Objective i) To optimise the extraction conditions for preparative scale isolation of jensenone and other secondary metabolites from leaves. (ii) To develop an RP-HPLC method for simultaneous determination of phloroglucinols and other compounds in Eucalyptus leaves. Methodology Jensenone and other compounds were isolated from acetone extract using VLC over TLC grade silica. HPLC quantitation of isolated compounds was undertaken on a C 18-column using acetonitrile-water (2% formic acid) gradient elution. Results Extraction conditions for isolation of jensenone were optimised and more than 99% pure jensenone was obtained in a yield of 2.1% from the dried leaves. Ten phloroglucinol compounds, including a new nuclear methylated phloroglucinol named 4-O-demethyl miniatone, and two triterpenoids were also isolated. A RP-HPLC method was developed for simultaneous quantitation of phloroglucinols and other compounds in different extracts of E. jensenii leaves. A total of 19 compounds reported from different species of Eucalyptus was separated by this method. Conclusion The method described for isolation of jensenone is a simple, rapid and low-cost procedure amenable to the preparative scale. A new monomeric phloroglucinol compound was isolated and characterised from the acetone extract of E. jensenii leaves. The HPLC method developed can be applied successfully to different eucalypt matrices for precise and accurate determination of 19 secondary metabolites belonging to different chemical classes.
dc.identifier.issn0958-0344
dc.identifier.urihttp://hdl.handle.net/1885/65691
dc.publisherJohn Wiley & Sons Inc
dc.sourcePhytochemical Analysis
dc.subjectKeywords: 4 o demethyl miniatone; acetone; acetonitrile; Eucalyptus extract; Eucalyptus jensenii extract; euglobal g1; euglobal g2; euglobal g3; euglobal g4; grandinol; hyperin; jensenone; miniatone; phloroglucinol derivative; sideroxylin; unclassified drug; water; 4-O-demethyl miniatone; Anti-feedant; Eucalyptus jensenii; formylated phloroglucinols; Jensenal
dc.titleIsolation and quantitation of ecologically important phloroglucinols and other compounds from Eucalyptus jensenii
dc.typeJournal article
local.bibliographicCitation.issue5
local.bibliographicCitation.lastpage491
local.bibliographicCitation.startpage483
local.contributor.affiliationSidana, Jasmeen, National Institute of Pharmaceutical Education and Research (NIPER)
local.contributor.affiliationFoley, William, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationSingh, Inder Pal, National Institute of Pharmaceutical Education and Research (NIPER)
local.contributor.authoremailu9616309@anu.edu.au
local.contributor.authoruidFoley, William, u9616309
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030502 - Natural Products Chemistry
local.identifier.absfor060799 - Plant Biology not elsewhere classified
local.identifier.absfor060299 - Ecology not elsewhere classified
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciences
local.identifier.ariespublicationf5625xPUB1145
local.identifier.citationvolume23
local.identifier.doi10.1002/pca.2345
local.identifier.scopusID2-s2.0-84865068448
local.identifier.thomsonID000307546500010
local.identifier.uidSubmittedByf5625
local.type.statusPublished Version

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