Coumarin and Its Derivatives

Coumarins 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 extra...

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Language:English
Published: MDPI - Multidisciplinary Digital Publishing Institute 2022
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Online Access:ONIX_20220111_9783036527758_999
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description Coumarins 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.
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spelling doab-20.500.12854ir-771682024-03-28T03:33:55Z Coumarin and Its Derivatives Matos, Maria João coumarin hydroxyl-modified coumarin photophysical thermal and structural characterization Glycyrrhiza uralensis glycyrol liquiritigenin cholinesterases human monoamine oxidases kinetics docking simulation chalcone neurodegenerative diseases adenosine receptors binding affinity docking 4-hydroxy-7-methoxycoumarin macrophage inflammation NF-κB MAPK calanolides pseudocalanolides calanolide A Calophyllum Calophyllaceae anti-HIV reverse transcriptase non-nucleoside reverse transcriptase inhibitors (NNRTIs) osthole umbelliferone esculin 4-hydroxycoumarin sorafenib apoptosis autophagy Yin Chen Hao constitutive androstane receptor scoparone coumarins quorum sensing QS inhibitors plant-derived molecules Chromobacterium violaceum immunoproteasome psoralen core non-peptidic electrophilic compounds warhead scan inflammatory bowel disease isocoumarin Crohn’s disease ulcerative colitis glutathione oxidative stress complementary therapies intestinal inflammation benzopyrones five-membered aromatic heterocycles furan pyrrole thiophene selenophen dihydrocoumarin-fused dihydropyranones 3-aroylcoumarines benzyl 2,3-butadienoate 6’-(4-biphenyl)-β-iso-cinchonine biological applications drug discovery fluorescent probes warfarin acenocoumarol mechanical valve time in therapeutic range anticoagulation Ruta chalepensis Rutaceae chalepin chalepensin bioactivity biosynthesis coumarin3-carboxamides pyranocoumarins anticancer activity antibacterial activity free radical polymerization LED photocomposites direct laser write analytical methods model plant natural genetic variation natural products simple coumarins chalcocoumarin MAO-B molecular dynamics in silico studies dye-sensitized solar cells coumarin dyes thieno [3,2-b] thiophene charge transfer ethynylaryl esculetin antiplatelet activity impedance aggregometry COX polyphenols pyrazole imidazole thiazole oxazole triazole thiadiazole curcumin curcumin–coumarin hybrids neuroprotection monoamine oxidase inhibition cholinesterase inhibition scavenging activity Escherichia coli biotransformation ferulenol structural annotation in silico tools n/a thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences Coumarins 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. 2022-01-11T13:54:35Z 2022-01-11T13:54:35Z 2021 book ONIX_20220111_9783036527758_999 9783036527758 9783036527741 https://directory.doabooks.org/handle/20.500.12854/77168 eng image/jpeg Attribution 4.0 International https://mdpi.com/books/pdfview/book/4786 https://mdpi.com/books/pdfview/book/4786 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-2774-1 10.3390/books978-3-0365-2774-1 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036527758 9783036527741 406 Basel, Switzerland open access
spellingShingle coumarin
hydroxyl-modified coumarin
photophysical
thermal and structural characterization
Glycyrrhiza uralensis
glycyrol
liquiritigenin
cholinesterases
human monoamine oxidases
kinetics
docking simulation
chalcone
neurodegenerative diseases
adenosine receptors
binding affinity
docking
4-hydroxy-7-methoxycoumarin
macrophage
inflammation
NF-κB
MAPK
calanolides
pseudocalanolides
calanolide A
Calophyllum
Calophyllaceae
anti-HIV
reverse transcriptase
non-nucleoside reverse transcriptase inhibitors (NNRTIs)
osthole
umbelliferone
esculin
4-hydroxycoumarin
sorafenib
apoptosis
autophagy
Yin Chen Hao
constitutive androstane receptor
scoparone
coumarins
quorum sensing
QS inhibitors
plant-derived molecules
Chromobacterium violaceum
immunoproteasome
psoralen core
non-peptidic
electrophilic compounds
warhead scan
inflammatory bowel disease
isocoumarin
Crohn’s disease
ulcerative colitis
glutathione
oxidative stress
complementary therapies
intestinal inflammation
benzopyrones
five-membered aromatic heterocycles
furan
pyrrole
thiophene
selenophen
dihydrocoumarin-fused dihydropyranones
3-aroylcoumarines
benzyl 2,3-butadienoate
6’-(4-biphenyl)-β-iso-cinchonine
biological applications
drug discovery
fluorescent probes
warfarin
acenocoumarol
mechanical valve
time in therapeutic range
anticoagulation
Ruta chalepensis
Rutaceae
chalepin
chalepensin
bioactivity
biosynthesis
coumarin3-carboxamides
pyranocoumarins
anticancer activity
antibacterial activity
free radical polymerization
LED
photocomposites
direct laser write
analytical methods
model plant
natural genetic variation
natural products
simple coumarins
chalcocoumarin
MAO-B
molecular dynamics
in silico studies
dye-sensitized solar cells
coumarin dyes
thieno [3,2-b] thiophene
charge transfer
ethynylaryl
esculetin
antiplatelet activity
impedance aggregometry
COX
polyphenols
pyrazole
imidazole
thiazole
oxazole
triazole
thiadiazole
curcumin
curcumin–coumarin hybrids
neuroprotection
monoamine oxidase inhibition
cholinesterase inhibition
scavenging activity
Escherichia coli
biotransformation
ferulenol
structural annotation
in silico tools
n/a
thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
Coumarin and Its Derivatives
title Coumarin and Its Derivatives
title_full Coumarin and Its Derivatives
title_fullStr Coumarin and Its Derivatives
title_full_unstemmed Coumarin and Its Derivatives
title_short Coumarin and Its Derivatives
title_sort coumarin and its derivatives
topic coumarin
hydroxyl-modified coumarin
photophysical
thermal and structural characterization
Glycyrrhiza uralensis
glycyrol
liquiritigenin
cholinesterases
human monoamine oxidases
kinetics
docking simulation
chalcone
neurodegenerative diseases
adenosine receptors
binding affinity
docking
4-hydroxy-7-methoxycoumarin
macrophage
inflammation
NF-κB
MAPK
calanolides
pseudocalanolides
calanolide A
Calophyllum
Calophyllaceae
anti-HIV
reverse transcriptase
non-nucleoside reverse transcriptase inhibitors (NNRTIs)
osthole
umbelliferone
esculin
4-hydroxycoumarin
sorafenib
apoptosis
autophagy
Yin Chen Hao
constitutive androstane receptor
scoparone
coumarins
quorum sensing
QS inhibitors
plant-derived molecules
Chromobacterium violaceum
immunoproteasome
psoralen core
non-peptidic
electrophilic compounds
warhead scan
inflammatory bowel disease
isocoumarin
Crohn’s disease
ulcerative colitis
glutathione
oxidative stress
complementary therapies
intestinal inflammation
benzopyrones
five-membered aromatic heterocycles
furan
pyrrole
thiophene
selenophen
dihydrocoumarin-fused dihydropyranones
3-aroylcoumarines
benzyl 2,3-butadienoate
6’-(4-biphenyl)-β-iso-cinchonine
biological applications
drug discovery
fluorescent probes
warfarin
acenocoumarol
mechanical valve
time in therapeutic range
anticoagulation
Ruta chalepensis
Rutaceae
chalepin
chalepensin
bioactivity
biosynthesis
coumarin3-carboxamides
pyranocoumarins
anticancer activity
antibacterial activity
free radical polymerization
LED
photocomposites
direct laser write
analytical methods
model plant
natural genetic variation
natural products
simple coumarins
chalcocoumarin
MAO-B
molecular dynamics
in silico studies
dye-sensitized solar cells
coumarin dyes
thieno [3,2-b] thiophene
charge transfer
ethynylaryl
esculetin
antiplatelet activity
impedance aggregometry
COX
polyphenols
pyrazole
imidazole
thiazole
oxazole
triazole
thiadiazole
curcumin
curcumin–coumarin hybrids
neuroprotection
monoamine oxidase inhibition
cholinesterase inhibition
scavenging activity
Escherichia coli
biotransformation
ferulenol
structural annotation
in silico tools
n/a
thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
topic_facet coumarin
hydroxyl-modified coumarin
photophysical
thermal and structural characterization
Glycyrrhiza uralensis
glycyrol
liquiritigenin
cholinesterases
human monoamine oxidases
kinetics
docking simulation
chalcone
neurodegenerative diseases
adenosine receptors
binding affinity
docking
4-hydroxy-7-methoxycoumarin
macrophage
inflammation
NF-κB
MAPK
calanolides
pseudocalanolides
calanolide A
Calophyllum
Calophyllaceae
anti-HIV
reverse transcriptase
non-nucleoside reverse transcriptase inhibitors (NNRTIs)
osthole
umbelliferone
esculin
4-hydroxycoumarin
sorafenib
apoptosis
autophagy
Yin Chen Hao
constitutive androstane receptor
scoparone
coumarins
quorum sensing
QS inhibitors
plant-derived molecules
Chromobacterium violaceum
immunoproteasome
psoralen core
non-peptidic
electrophilic compounds
warhead scan
inflammatory bowel disease
isocoumarin
Crohn’s disease
ulcerative colitis
glutathione
oxidative stress
complementary therapies
intestinal inflammation
benzopyrones
five-membered aromatic heterocycles
furan
pyrrole
thiophene
selenophen
dihydrocoumarin-fused dihydropyranones
3-aroylcoumarines
benzyl 2,3-butadienoate
6’-(4-biphenyl)-β-iso-cinchonine
biological applications
drug discovery
fluorescent probes
warfarin
acenocoumarol
mechanical valve
time in therapeutic range
anticoagulation
Ruta chalepensis
Rutaceae
chalepin
chalepensin
bioactivity
biosynthesis
coumarin3-carboxamides
pyranocoumarins
anticancer activity
antibacterial activity
free radical polymerization
LED
photocomposites
direct laser write
analytical methods
model plant
natural genetic variation
natural products
simple coumarins
chalcocoumarin
MAO-B
molecular dynamics
in silico studies
dye-sensitized solar cells
coumarin dyes
thieno [3,2-b] thiophene
charge transfer
ethynylaryl
esculetin
antiplatelet activity
impedance aggregometry
COX
polyphenols
pyrazole
imidazole
thiazole
oxazole
triazole
thiadiazole
curcumin
curcumin–coumarin hybrids
neuroprotection
monoamine oxidase inhibition
cholinesterase inhibition
scavenging activity
Escherichia coli
biotransformation
ferulenol
structural annotation
in silico tools
n/a
thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
url ONIX_20220111_9783036527758_999