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dc.contributor.editorTringali, Corrado
dc.date.accessioned2021-05-01T15:30:19Z
dc.date.available2021-05-01T15:30:19Z
dc.date.issued2020
dc.identifierONIX_20210501_9783039367047_579
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/68833
dc.description.abstractThis Special Issue is focused on natural polyphenols and their synthetic bioactive analogues. It is composed of one review on aza- and azo-stilbenes as bioisosteric analogs of the stilbenoid resveratrol and four original articles, including studies on synthetic (bisphenol neolignans inspired by honokiol, multicomponent synthesis of polyphenols), and natural polyphenols (polyphenols from Tamarix ramosissima and Melanoleuca styphelioides) as antiproliferative, anti-Alzheimer’s, antioxidant, antimicrobial, or anti-inflammatory agents.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.otherMelaleuca styphelioides
dc.subject.otherpolyphenols
dc.subject.otherLC/MS-MS
dc.subject.otheranti-oxidant activity
dc.subject.otheranti-inflammatory activity
dc.subject.otherkeratinocytes
dc.subject.otherTamarix ramosissima
dc.subject.otherpolyphenolics
dc.subject.otherantioxidant activity
dc.subject.otherantimicrobial activity
dc.subject.otherisorhamnetin
dc.subject.otherhispidulin
dc.subject.othercirsimaritin
dc.subject.othermulticomponent reactions
dc.subject.otherβ-amyloid proteins
dc.subject.otherAlzheimer’s disease
dc.subject.otherUgi reaction
dc.subject.otherβ-lactams
dc.subject.othertrans-resveratrol
dc.subject.otheraza-stilbene
dc.subject.otherazo-stilbene
dc.subject.otherbio-isosterism
dc.subject.otherstructure-activity relationship
dc.subject.otherhonokiol
dc.subject.otherbisphenol neolignans
dc.subject.otherSuzuki–Miyaura cross-coupling
dc.subject.otherantitumor activity
dc.subject.otherapoptosis
dc.subject.othern/a
dc.titleFrom Natural Polyphenols to Synthetic Bioactive Analogues
dc.typebook
oapen.identifier.doi10.3390/books978-3-03936-705-4
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783039367047
oapen.relation.isbn9783039367054
oapen.pages98
oapen.place.publicationBasel, Switzerland


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