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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 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
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 electronic resource (146 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato thiodiketopiperazines
Geosmithia pallida
deep-sea-derived fungus
antioxidant
biological control
ecological role
gentisyl alcohol
multi-gene phylogeny
tyrosinase inhibition
marine fungi
isolation
culturing
identification
natural products
secondary metabolites
isocoumarin
tryptamine
Botryosphaeria ramose
antifungal activity
carotenoids
optimization
red yeast
Rhodotorula sp
marine-derived Aspergillus fumigatus
spiro-heterocyclic γ-lactam
cephalimysins
ophiobolins
marine fungus
Aspergillus flocculosus
anti-proliferation
biosynthetic gene cluster (BGC)
indole-diketopiperazine
Penicillium brasilianum
cytotoxicities
fungal community
phylogenetic analysis
saltwork
tidal flat
chemotaxonomy
phylogeny
mamiellales
galactolipids
betaine lipids
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