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Natural Products Chemistry: Advances in Synthetic, Analytical and Bioactivity Studies
Natural Products Chemistry: Advances in Synthetic, Analytical and Bioactivity Studies
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2023
Descrizione fisica 1 online resource (228 p.)
Soggetto topico Chemistry
Research & information: general
Soggetto non controllato 1,2,3-triazole
5-HT
anti-metastasis
antibacterial
anticancer activity
apoptosis
Arthrinium sp
Aspergillus
bioactivity
biocatalysis
chemoenzymatic
chrysin
curcumin
curcuminoids
cyclophosphamide
cytotoxicity
D-IBS
deuterium labeling
docosahexaenoic acids
endophytic fungus
expression analysis
flavones
GI dysfunction
granulosa cells
gut microbiota
hybrids
kaempferol
larvae of Musca domestica
liquid-chromatography tandem mass spectrometry
loonamycin
macamide
marine fungi
measurement of vitamin D metabolites in blood
medicinal chemistry
molecular cloning
n/a
natural compounds
natural product synthesis
O-glycan
ovarian cancer
ovary
p53
phenolics
PI3K/AKT/mTOR
protocatechuic
pyridone alkaloids
quinones
semi-synthetic compounds
sesquiterpenoids
stilbenes
TbUGGT
Trapa bispinosa Roxb
triple negative breast cancer
vitamin D
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Natural Products Chemistry
Record Nr. UNINA-9910743279003321
MDPI - Multidisciplinary Digital Publishing Institute, 2023
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds
Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds
Autore Matiadis Dimitrios
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (124 p.)
Soggetto topico Research & information: general
Soggetto non controllato [1,3]-H shift
11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine
15N-NMR
4-anilino-quin(az)olines
alkyne
amino-substituted fused oxazolocoumarin
aminocyclopentitol
anion radical
Au-nanoparticles
aza-Michael addition
azopyridine
benzimidazole
bicyclic aziridine
bromination
C-C bond length
carbocyclic hydantoins
carbonyl complex
catechol
chalcogenophene
chemoselective reduction
chlorination
condensation
conformational flexibility
Cu(II) complex
curcuminoids
cytotoxic
DABCO
DFT calculations
dimethyl acetylenedicarboxylate
disulfur dichloride
DNA binding
domino reactions
electronic structure
fused oxazolocoumarins
gamma-amino acid
GIAO
heterocycle
heterocycles
hinge binder
homopiperazine
HRMS
imidazolidine-2,4-diones
imine
intramolecular SN displacement
isoxazolo[3,4-b]quinolin-3(1H)-one
kinase inhibitor design
ligands
magnetic properties
MDR reversal
N-1 substituted hydantoin
n/a
NaBH4
nitrogen heterocycles
NMR
nucleophilic aromatic substitution
nucleophilic displacement
nucleophilic substitution
o-aminophenol
o-hydroxynitrocoumarins
oxygen-nitrogen heterocycles
piperazine
pyrazolines
pyridine derivatives
pyrimidine
ring closing
ruthenium
Schiff base
spiro hydantoins
stereochemistry
thiol-alkyne click reaction
thiophene derivatives
thiosemicarbazone
water chemistry
X-ray crystallographic analysis
X-ray structure
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Nitrogen-Containing Molecules
Record Nr. UNINA-9910557605603321
Matiadis Dimitrios  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Qualitative and Quantitative Analysis of Bioactive Natural Products 2018
Qualitative and Quantitative Analysis of Bioactive Natural Products 2018
Autore Marcotullio Maria Carla
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 online resource (374 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato 1-triacontanol
aleuritolic acid
Alzheimer's disease
amino acids content
anthocyanins
antibacterial activity
antioxidant
antioxidant activity
antioxidant capacity
apoptosis
artificial neural network
autophagy
bioactive compounds
bioactive natural compounds
biostimulant
Bolbostemma paniculatum
C-glycosylflavone
cannabidiol
capsaicinoids
carotenoids
CBD oil
cerebral ischemia reperfusion injury
chemometrics
chili
chromatogram-bioactivity correlation
crocins
Curcuma longa
curcuminoids
decursin
decursinol
decursinol angelate
endothelial function
Erigeron breviscapus extract
essential oil
extraction
flavonoids
food traceability
free radical-scavenging
fruit powders
gas chromatography
GC-MS
GC/MS
geographical origin
geographical variation
Ginkgo biloba Extract (GBE)
ginseng berry extract
ginsenosides
hemp seed oil
HPLC
HPLC analysis
HPLC methods
HPLC-ELSD
HPLC-Q-Exactive-Orbitrap-MS
HPLC-Q-TOF-MS/MS
hydrodistillation
identification
ionic liquids
Iris lactea Pall. var. chinensis (Fisch.) Koidz
liquid chromatography
liquid chromatography-mass spectrometry
LTQ-Orbitrap
macrodiolides
mass spectrometry
metabolic profiling
method validation
MODDE experimental design
Moroccan region
multivariate statistical analysis
Myristica fragrans
nodakenin
nutmeg
odor-activity values
Olea europaea L.
olive leaves
oral administration
organic acids
pharmacokinetics
phenolic acids
phenolic compounds
phenolics
Podospermum
proanthocyanidins
qualitative analysis
quality evaluation
quantification
quantitative analysis
Quercus acuta leaf
recycling preparative high performance liquid chromatography
red cabbage
response surface methodology
rice
Rossa da inverno sel. Rojo Duro onion cultivar
saffron
Scorzonera
scutellarein
scutellarin
secondary metabolites
separation optimisation
ShenFu prescription decoction
Sorbus
SPME-GC/MS
Spondias spp
stability
Staphylococcus aureus
statistical evaluations
stereoselective and simultaneous analysis
sugars
talarodiolide
Talaromyces pinophilus
terpenes
terrain conditions
traditional Chinese medicine decoction
triterpenes
turmeric
turmerone
UFLC-QQQ-MS
UHPLC analysis
UHPLC-MS/MS
UPLC
UPLC-ESI-MS/MS
UPLC-MS
UPLC-QTOF-MS
volatile compounds
wine
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346662303321
Marcotullio Maria Carla  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui