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Analysis of Chemical Contaminants in Food
Analysis of Chemical Contaminants in Food
Autore Medana Claudio
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (138 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 5-hydroxymethylfurfural
acrylamide
aluminium
antibiotic residues
blueberries
breast milk
cadmium
carcinogens
chromium
coffee
conazole fungicides
fishery product
furan
furfuryl alcohol
GC-MS/MS
grilled pork
high performance liquid chromatography
high-resolution mass spectrometry
hydrogen peroxide
hydroxymethylfurfural
illicit treatment
infant foods
infant formulae
LC-MS/MS
lead
lingonberries
liquid-liquid extraction
magnetic stirring assisted demulsification dispersive liquid-liquid microextraction
mass spectrometry methods
matcha
mediteranean fish
minerals
n/a
nickel
non-alcoholic beverages
occurrence
Orbitrap
perfluorooctane acid
perfluorooctane sulfonate
pesticide residue analysis
pesticide residues
PFOA
PFOS
phthalate
polycyclic aromatic hydrocarbons
pressurized solvent extraction
provisional tolerable intake
response surface methodology
risk assessment
rose hips
safety
storage conditions
structure elucidation
toxic metals
toxicological risk
β-myrcene
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557376803321
Medana Claudio  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Molecules from Side Reactions
Molecules from Side Reactions
Autore D'Errico Stefano
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (100 p.)
Soggetto topico History of engineering and technology
Soggetto non controllato (E,Z)-isomerization
19F NMR spectroscopy
1H-pyrazolo[3,4-b]pyridine
3-acetyl-2,3-dihydro-1,3,4-oxadiazole
8-Fluoro-2'-deoxyguanosine
acadesine
AICAR
allenic compounds
AMPK
azaheterocycles
benzamides
bidentate directing groups
bis-chelates
C-glycosylation
C-H bond functionalization
caprazamycins
carbohydrate
chelation assistance
chlorinated nucleosides
conjugated diyne
copper
cyanide
cyclization
diacetal
epoxide
ester group migration
fluorinated nucleosides
fluorination
furan
glycosyl sulfoxide
guanidinium
heterocycle
hydroxy methylation
ketose
LAH reduction
ligand
mannose
modified nucleosides
muraymycins
N-alkylation
N-C bond cleavage
N'-acetylhydrazide
n/a
network
nitration
nucleoside analogues
nucleosides
organic synthesis
oxazole
oxetane
pent-1,2,3,4-tetraene intermediate
phosphoramidite
phosphorylation
psicose
pyridine derivatives
pyridine-imidazolium
rare sugar
rearrangement
ribose
RORC reaction
seven-membered rings
solid phase synthesis
spiro-oxetane
thioglycoside oxidation
unexpected iminium cation
uridine
uronate
X-ray structure determination
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910674046603321
D'Errico Stefano  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui