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Steroids in natural matrices: Chemical features and bioactive properties

dc.contributor.authorBarreira, João C.M.
dc.contributor.authorFerreira, Isabel C.F.R.
dc.date.accessioned2018-01-25T10:00:00Z
dc.date.accessioned2018-02-02T10:30:05Z
dc.date.available2018-01-25T10:00:00Z
dc.date.available2018-02-02T10:30:05Z
dc.date.issued2015
dc.description.abstractSince the establishment of their structure, the potential of steroids to act as structural cornerstone for the design of derived drugs became evident. This potential was confirmed by pharmacological studies, which highlighted broad biological effects. Nevertheless, the term steroid is commonly associated with androgenic-anabolic compounds, but the latter compounds comprise only a single, relatively small, class of biologically active steroids. In fact, all steroids share the same three-dimensional backbone. Many of their chemical properties are determined by steric configuration of the steroid nucleus. Despite the high number of chiral centers, steroids occur in nature essentially as a single chiral species. These structural characteristics are closely related with the biological activity of steroids. In this chapter, a review work on different steroids found in natural matrices is presented, aiming to provide a state-of-the-art overview of specific concerns of the biochemistry and physiology of these isoprenoid lipids. The work is organized according to different classes (cholesterol, anabolic steroids, sex steroids, corticosteroids, phytosterols, brassinosteroids, ecdysteroids, among others) and natural sources (animals, plants, fungi) of steroids. Besides structural considerations, the key features leading the information throughout the text include the analytical techniques (chromatography, spectroscopy, hyphenated techniques) used for their identification and/or quantification and regulation of biosynthesis (considering the derivatives from lanosterol and cycloartenol) emphasizing human steroidogenesis. Special attention is paid to the bioactivity of different sterols, focusing on the physiological role of oxidized derivatives of cholesterol and oxysterols in normal and pathological cellular processes, influence of endogenous sex steroids in the regulation of inflammatory processes, anticancer properties, antioxidative effects, and activation of the expression of defense genes.en_EN
dc.description.sponsorshipThe authors are grateful to CIMO (Strategic Project No. PEst-OE/AGR/ UI0690/2011). João C.M. Barreira also thanks Fundação para a Ciência e a Tecnologia, POPH-QREN, and FSE for his grant (No. SFRH/BPD/72802/2010).
dc.description.versioninfo:eu-repo/semantics/publishedVersionen_EN
dc.identifier.citationBarreira, João C.M.; Ferreira, Isabel C.F.R. (2015). Steroids in natural matrices: Chemical features and bioactive properties. In Biotechnology of Bioactive Compounds: Sources and Applications. p. 395-431. ISBN 9781118733103.en_EN
dc.identifier.doi10.1002/9781118733103.ch16en_EN
dc.identifier.isbn9781118733103
dc.identifier.urihttp://hdl.handle.net/10198/15436
dc.language.isoeng
dc.peerreviewedyesen_EN
dc.relationStrategic Project - UI 690 - 2011-2012
dc.relationBIOACTIVE PROPERTIES & CYTOPROTECTIVE POTENTIAL OF NATURAL EXTRACTS/INDIVIDUAL COMPOUNDS: APPLICATION OF SINGLE CELL GEL ELECTROPHORESIS AND OTHER BIOCHEMICAL, CHEMICAL AND ELECTROCHEMICAL ASSAYS
dc.subjectAnalytical techniquesen_EN
dc.subjectBioactivityen_EN
dc.subjectBiosynthesisen_EN
dc.subjectStructureen_EN
dc.titleSteroids in natural matrices: Chemical features and bioactive propertiesen_EN
dc.typebook part
dspace.entity.typePublication
oaire.awardTitleStrategic Project - UI 690 - 2011-2012
oaire.awardTitleBIOACTIVE PROPERTIES & CYTOPROTECTIVE POTENTIAL OF NATURAL EXTRACTS/INDIVIDUAL COMPOUNDS: APPLICATION OF SINGLE CELL GEL ELECTROPHORESIS AND OTHER BIOCHEMICAL, CHEMICAL AND ELECTROCHEMICAL ASSAYS
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/PEst-OE%2FAGR%2FUI0690%2F2011/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBPD%2F72802%2F2010/PT
oaire.fundingStream6817 - DCRRNI ID
person.familyNameBarreira
person.familyNameFerreira
person.givenNameJoão
person.givenNameIsabel C.F.R.
person.identifier144781
person.identifier.ciencia-id9418-CF95-9919
person.identifier.orcid0000-0003-1233-0990
person.identifier.orcid0000-0003-4910-4882
person.identifier.ridD-8269-2013
person.identifier.ridE-8500-2013
person.identifier.scopus-author-id54895546900
person.identifier.scopus-author-id36868826600
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccessen_EN
rcaap.typebookParten_EN
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relation.isAuthorOfPublicationbd0d1537-2e03-41fb-b27a-140af9c35db8
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