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dc.contributor.editorMatos, Maria João
dc.date.accessioned2022-01-11T13:54:35Z
dc.date.available2022-01-11T13:54:35Z
dc.date.issued2021
dc.identifierONIX_20220111_9783036527758_999
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/77168
dc.description.abstractCoumarins are widely distributed in nature and can be found in a large number of naturally occurring and synthetic bioactive molecules. The unique and versatile oxygen-containing heterocyclic structure makes them a privileged scaffold in Medicinal Chemistry. Many coumarin derivatives have been extracted from natural sources, designed, synthetized, and evaluated on different pharmacological targets. In addition, coumarin-based ion receptors, fluorescent probes, and biological stains are growing quickly and have extensive applications to monitor timely enzyme activity, complex biological events, as well as accurate pharmacological and pharmacokinetic properties in living cells. The extraction, synthesis, and biological evaluation of coumarins have become extremely attractive and rapidly developing topics. A large number of research and review papers have compiled information on this important family of compounds in 2020. Research articles, reviews, communications, and concept papers focused on the multidisciplinary profile of coumarins, highlighting natural sources, most recent synthetic pathways, along with the main biological applications and theoretical studies, were the main focus of this book. The huge and growing range of applications of coumarins described in this book is a demonstration of the potential of this family of compounds in Organic Chemistry, Medicinal Chemistry, and different sciences related to the study of natural products. This book includes 23 articles: 17 original papers and six review papers.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciencesen_US
dc.subject.othercoumarin
dc.subject.otherhydroxyl-modified coumarin
dc.subject.otherphotophysical
dc.subject.otherthermal and structural characterization
dc.subject.otherGlycyrrhiza uralensis
dc.subject.otherglycyrol
dc.subject.otherliquiritigenin
dc.subject.othercholinesterases
dc.subject.otherhuman monoamine oxidases
dc.subject.otherkinetics
dc.subject.otherdocking simulation
dc.subject.otherchalcone
dc.subject.otherneurodegenerative diseases
dc.subject.otheradenosine receptors
dc.subject.otherbinding affinity
dc.subject.otherdocking
dc.subject.other4-hydroxy-7-methoxycoumarin
dc.subject.othermacrophage
dc.subject.otherinflammation
dc.subject.otherNF-κB
dc.subject.otherMAPK
dc.subject.othercalanolides
dc.subject.otherpseudocalanolides
dc.subject.othercalanolide A
dc.subject.otherCalophyllum
dc.subject.otherCalophyllaceae
dc.subject.otheranti-HIV
dc.subject.otherreverse transcriptase
dc.subject.othernon-nucleoside reverse transcriptase inhibitors (NNRTIs)
dc.subject.otherosthole
dc.subject.otherumbelliferone
dc.subject.otheresculin
dc.subject.other4-hydroxycoumarin
dc.subject.othersorafenib
dc.subject.otherapoptosis
dc.subject.otherautophagy
dc.subject.otherYin Chen Hao
dc.subject.otherconstitutive androstane receptor
dc.subject.otherscoparone
dc.subject.othercoumarins
dc.subject.otherquorum sensing
dc.subject.otherQS inhibitors
dc.subject.otherplant-derived molecules
dc.subject.otherChromobacterium violaceum
dc.subject.otherimmunoproteasome
dc.subject.otherpsoralen core
dc.subject.othernon-peptidic
dc.subject.otherelectrophilic compounds
dc.subject.otherwarhead scan
dc.subject.otherinflammatory bowel disease
dc.subject.otherisocoumarin
dc.subject.otherCrohn’s disease
dc.subject.otherulcerative colitis
dc.subject.otherglutathione
dc.subject.otheroxidative stress
dc.subject.othercomplementary therapies
dc.subject.otherintestinal inflammation
dc.subject.otherbenzopyrones
dc.subject.otherfive-membered aromatic heterocycles
dc.subject.otherfuran
dc.subject.otherpyrrole
dc.subject.otherthiophene
dc.subject.otherselenophen
dc.subject.otherdihydrocoumarin-fused dihydropyranones
dc.subject.other3-aroylcoumarines
dc.subject.otherbenzyl 2,3-butadienoate
dc.subject.other6’-(4-biphenyl)-β-iso-cinchonine
dc.subject.otherbiological applications
dc.subject.otherdrug discovery
dc.subject.otherfluorescent probes
dc.subject.otherwarfarin
dc.subject.otheracenocoumarol
dc.subject.othermechanical valve
dc.subject.othertime in therapeutic range
dc.subject.otheranticoagulation
dc.subject.otherRuta chalepensis
dc.subject.otherRutaceae
dc.subject.otherchalepin
dc.subject.otherchalepensin
dc.subject.otherbioactivity
dc.subject.otherbiosynthesis
dc.subject.othercoumarin3-carboxamides
dc.subject.otherpyranocoumarins
dc.subject.otheranticancer activity
dc.subject.otherantibacterial activity
dc.subject.otherfree radical polymerization
dc.subject.otherLED
dc.subject.otherphotocomposites
dc.subject.otherdirect laser write
dc.subject.otheranalytical methods
dc.subject.othermodel plant
dc.subject.othernatural genetic variation
dc.subject.othernatural products
dc.subject.othersimple coumarins
dc.subject.otherchalcocoumarin
dc.subject.otherMAO-B
dc.subject.othermolecular dynamics
dc.subject.otherin silico studies
dc.subject.otherdye-sensitized solar cells
dc.subject.othercoumarin dyes
dc.subject.otherthieno [3,2-b] thiophene
dc.subject.othercharge transfer
dc.subject.otherethynylaryl
dc.subject.otheresculetin
dc.subject.otherantiplatelet activity
dc.subject.otherimpedance aggregometry
dc.subject.otherCOX
dc.subject.otherpolyphenols
dc.subject.otherpyrazole
dc.subject.otherimidazole
dc.subject.otherthiazole
dc.subject.otheroxazole
dc.subject.othertriazole
dc.subject.otherthiadiazole
dc.subject.othercurcumin
dc.subject.othercurcumin–coumarin hybrids
dc.subject.otherneuroprotection
dc.subject.othermonoamine oxidase inhibition
dc.subject.othercholinesterase inhibition
dc.subject.otherscavenging activity
dc.subject.otherEscherichia coli
dc.subject.otherbiotransformation
dc.subject.otherferulenol
dc.subject.otherstructural annotation
dc.subject.otherin silico tools
dc.subject.othern/a
dc.titleCoumarin and Its Derivatives
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-2774-1
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036527758
oapen.relation.isbn9783036527741
oapen.pages406
oapen.place.publicationBasel, Switzerland


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