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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 online resource (406 p.)
Soggetto topico Biology, life sciences
Research & information: general
Soggetto non controllato 3-aroylcoumarines
4-hydroxy-7-methoxycoumarin
4-hydroxycoumarin
6'-(4-biphenyl)-β-iso-cinchonine
acenocoumarol
adenosine receptors
analytical methods
anti-HIV
antibacterial activity
anticancer activity
anticoagulation
antiplatelet activity
apoptosis
autophagy
benzopyrones
benzyl 2,3-butadienoate
binding affinity
bioactivity
biological applications
biosynthesis
biotransformation
calanolide A
calanolides
Calophyllaceae
Calophyllum
chalcocoumarin
chalcone
chalepensin
chalepin
charge transfer
cholinesterase inhibition
cholinesterases
Chromobacterium violaceum
complementary therapies
constitutive androstane receptor
coumarin
coumarin dyes
coumarin3-carboxamides
coumarins
COX
Crohn's disease
curcumin
curcumin-coumarin hybrids
dihydrocoumarin-fused dihydropyranones
direct laser write
docking
docking simulation
drug discovery
dye-sensitized solar cells
electrophilic compounds
Escherichia coli
esculetin
esculin
ethynylaryl
ferulenol
five-membered aromatic heterocycles
fluorescent probes
free radical polymerization
furan
glutathione
glycyrol
Glycyrrhiza uralensis
human monoamine oxidases
hydroxyl-modified coumarin
imidazole
immunoproteasome
impedance aggregometry
in silico studies
in silico tools
inflammation
inflammatory bowel disease
intestinal inflammation
isocoumarin
kinetics
LED
liquiritigenin
macrophage
MAO-B
MAPK
mechanical valve
model plant
molecular dynamics
monoamine oxidase inhibition
n/a
natural genetic variation
natural products
neurodegenerative diseases
neuroprotection
NF-κB
non-nucleoside reverse transcriptase inhibitors (NNRTIs)
non-peptidic
osthole
oxazole
oxidative stress
photocomposites
photophysical
plant-derived molecules
polyphenols
pseudocalanolides
psoralen core
pyranocoumarins
pyrazole
pyrrole
QS inhibitors
quorum sensing
reverse transcriptase
Ruta chalepensis
Rutaceae
scavenging activity
scoparone
selenophen
simple coumarins
sorafenib
structural annotation
thermal and structural characterization
thiadiazole
thiazole
thieno [3,2-b] thiophene
thiophene
time in therapeutic range
triazole
ulcerative colitis
umbelliferone
warfarin
warhead scan
Yin Chen Hao
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
Marine Microbial Diversity as a Source of Bioactive Natural Products
Marine Microbial Diversity as a Source of Bioactive Natural Products
Autore Stien Didier
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (146 p.)
Soggetto topico Biology, life sciences
Research & information: general
Soggetto non controllato anti-proliferation
antifungal activity
antioxidant
Aspergillus flocculosus
betaine lipids
biological control
biosynthetic gene cluster (BGC)
Botryosphaeria ramose
carotenoids
cephalimysins
chemotaxonomy
culturing
cytotoxicities
deep-sea-derived fungus
ecological role
fungal community
galactolipids
gentisyl alcohol
Geosmithia pallida
identification
indole-diketopiperazine
isocoumarin
isolation
mamiellales
marine fungi
marine fungus
marine-derived Aspergillus fumigatus
multi-gene phylogeny
n/a
natural products
ophiobolins
optimization
Penicillium brasilianum
phylogenetic analysis
phylogeny
red yeast
Rhodotorula sp
saltwork
secondary metabolites
spiro-heterocyclic γ-lactam
thiodiketopiperazines
tidal flat
tryptamine
tyrosinase inhibition
xanthophylls
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557737703321
Stien Didier  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui