top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.
Coumarin and Its Derivatives
Coumarin and Its Derivatives
Autore Matos Maria João
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (406 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato 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
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557577003321
Matos Maria João  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Lignans
Lignans
Autore Barker David
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (384 p.)
Soggetto non controllato taste-active compound
heilaohu
9-norlignans
antioxidant activity
drug-like
human health
chemometrics
lignan
bitterness
red-flowered Chinese magnolia vine
antioxidant
ruminant
secoisolariciresinol diglucoside
quantification
intermolecular interactions
cattle
anti-inflammatory activity
acyl-Claisen
LOX
seed
food groups
microtubules
anti-proliferative
acetylcholinesterase inhibitors
flax
arylnaphthalene lignan
epiboly
aryldihydronaphthalene lignan
multiple bioactive components
enterolignan
total synthesis
genetic
synthesis
cultivated
cell cycle
chronic diseases
national databases
oxidation
chemical components
molecular dynamics
COX
lignans
hydroxycinnamic acid
chemical structures
Chinese magnolia vine
stereoselective synthesis
sPLA2
Bursera fagaroides
in silico studies
antibacterial activity
semisynthesis
dibenzyl butyrolactones
flavonoid glycoside
lignan glycoside
chemical characterization
hydroxymatairesinol
podophyllotoxin
Lespedeza cuneata
Bursera
oak ageing
Schisandrae Chinensis Fructus
F-actin
cultivar
UHPLC-MS/MS
bioactivity
podophyllotoxin-type lignans
harmonized databases
graph theory
antioxidants
health promotion
simultaneous quantitation
natural products
dietary intake
cell migration
Lignan
chemical space
diet
Lauraceae
pharmacokinetic
cytotoxicity
tujia ethnomedicine
flavonolignans
flavonol
adipocyte and osteoblast differentiation
Burseraceae
environment
dietary lignans
phytochemical analysis
Schisandra chinensis
animal health
neolignans
Schisandra rubriflora
cancer
norlignans
wild
ISBN 3-03897-909-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346692503321
Barker David  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui