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.
Anticancer Agents : Design, Synthesis and Evaluation
Anticancer Agents : Design, Synthesis and Evaluation
Autore Chen Qiao-Hong
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (606 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 1,2,3-triazole
2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
3,6-dibromocarbazole
4-(pyridin-4-yloxy)benzamide
5-bromoindole
5-fluorouracil
ABCB1 (P-glycoprotein)
actin
ADME
allene
amides/esters
androgen receptor
anti-cancer activity
anti-neuroinflammation
anti-ovarian cancer
anti-tumor
anticancer
anticancer activity
anticancer agent
anticancer agents
anticancer compounds
antimitotic agents
antioxidant activity
antiproliferative activity
antiproliferative agent
antitumor
antitumor activity
apalutamide
apoptosis
aromatase
benzimidazole
benzofuran-pyrazole
benzofurans
beta-lapachone
bivalency
breast cancer
c-Met
carbazole
cell cycle
chemical synthesis
chemoresistance
chrysin analogues
colchiceine
colchicine amide
colchicine analogs
colchicine sulfonamide
colon cancer
computational docking
coumarin
crystal structure
cyanopyridone
cytotoxic activity
cytotoxic properties
cytotoxicity
darolutamide
DFT study
dihydroartemisinin
dihydropyranoindole
docking
docking studies
drug discovery
drug resistance
E-stereoselective
enzalutamide
enzyme inhibition
estrone derivatives
flavonoid
flavonoids
gemcitabine
HDAC inhibitors
HeLa
HepG2
hydrates
hydrazine
IGF-1R
IL-12
immune modulation
indoleamine 2,3-dioxygenase
inflammation
inhibitor
K562
kinase inhibitor
MCF-7
MDM2-p53 interaction
migration
mimetics
molecular simulation
MOLT-4
multidrug resistance (MDR) reversal
N-substituted pyrazoline
nanoparticles
natural product
neuroblastoma
NIH3T3
o-nitro-benzyl
organosilicon compounds
ortho-quinones
ovarian cancer
overcoming drug resistance
P-glycoprotein
P-MAPA
PARP inhibitor
PARP-1 inhibition
phenylpyrazolopyrimidine
photoactivatable protecting groups
PI3Ks
PI3Kα inhibitor
PI3Kδ inhibitors
polyvalency
prodrug
prostate cancer
PROTACs
protein degradation
protein kinase
protein-protein interactions
Pyrazole
pyrazolopyridine
pyridotriazine
quinazolin-4(3H)-one
quinazolin-4(3H)-thione
regioselective
salinomycin
Schiff base
SILA-409 (Alis-409)
SILA-421 (Alis-421)
Src
substituted pyridine
synergy
synthesis
Talazoparib
tanshione IIA
taxoids
thiazolidinone
Thienopyrimidine
thienopyrimidinone
thiocolchicine
thiopene
thioxotriazopyridine
TLR signaling
topoisomerase II inhibitor
triazolothiadiazine
triple-negative breast cancer
tryptophan metabolism
tubulin inhibitors
tumor specificity
urea
virtual screening
xanthones
yeast-based assays
zampanolide
βIII-tubulin
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Anticancer Agents
Record Nr. UNINA-9910557129103321
Chen Qiao-Hong  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species
Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species
Autore Nicoletti Rosario
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 online resource (134 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato antibacterial
antibacterial activity
antifungal activity
Aspergillaceae
Aspergillus
Aspergillus candidus
Aspergillus clavatus
aspetritone
bioactive products
bis-indolyl benzenoids
BK (Maxi-K) channel
breast cancer
breviane spiroditerpenoid
candidusin
chromone
coumarin
cytotoxic
cytotoxicities
cytotoxicity
diastereomers
diterpenoid
drug discovery
ECD calculations
EGFR
endophytic fungi
gefitinib
HER2
hydroxypyrrolidine
IDH1 inhibitory activity
indole-diterpenoids
lapatinib
mangrove endophytic fungus
mangroves
marine-derived fungi
n/a
NMR data calculations
Penicillium raistrickii
Penicillium sp. TJ403-1
penitrem A
polyketides
secondary metabolites
sesquiterpenoid
sponge-associated fungus
sterone
Talaromyces
Talaromyces purpurogenus
thermo-change strategy
TNF-?
ISBN 3-03897-981-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346857703321
Nicoletti Rosario  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Biocatalytic Synthesis of Bioactive Compounds
Biocatalytic Synthesis of Bioactive Compounds
Autore Aleu Josefina
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (142 p.)
Soggetto topico Biology, life sciences
Research & information: general
Soggetto non controllato 8-hydroxydaidzein
active agent synthesis
adaptation
alkene cleavage
amylosucrase
anti-inflammation
aryl alkenes
basidiomycota
biocatalysis
biocatalyst
bioprocess
biotransformation
bromination
carotene degradation
chlorination
coumarin
Deinococcus geothermalis
dye-decolorizing peroxidase (DyP)
filamentous fungi
glycerol
Glycine max (L.) Merr
glycosyltransferase
halogenase
haloperoxidase
HPLC/MS
in situ product removal
isoflavone aglycone-rich extract
isoflavone α-glucoside
Komagataella pfaffii
limonene
lipase
manganese
mevalonate pathway
monoterpenes
oxidation
oxidative cleavage
pharmaceuticals
Pleurotus sapidus
psychrotrophs
reaction engineering
selective hydroxylation
soluble
stable
terpenes
two-liquid phase fermentation
unsaturated fatty acid
UV/NTG mutagenesis
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557380503321
Aleu Josefina  
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
Modern Seed Technology
Modern Seed Technology
Autore Taylor Alan G
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (183 p.)
Soggetto topico Biology, life sciences
Research and information: general
Technology, Engineering, Agriculture, Industrial processes
Soggetto non controllato abiotic stress
baby leaf hemp
blindness
Brassica oleracea
chemometrics
chlorophyll content
containerized transplants
corn
coumarin
crop establishment
cultivar selection
field emergence
film coat
fluorescent tracer
fruit morphology
heat and drought stresses
heatmaps
humic acids
image analysis
in vivo imaging system (IVIS)
low phytic acid
multispectral
multispectral imaging
n/a
near-infrared
oil-bodies migration
organic agriculture
pellet
pericarp
physiological maturity
piperonyl amides
potassium nitrate
relative growth rate (RGR)
seed acquisition of desiccation tolerance
seed coat
seed coating
seed dressing
seed enhancement
seed health
seed quality
seed respiration
seed testing
seed treatment
seed vigor
seed-size distribution
Solanum lycopersicum L.
sowing density
soybean
specific root length (SRL)
spectroscopy
spinach
systemic uptake
testa
tissue lipophilicity
Vigna unguiculata (L.) Walp
Zn localization
Zn priming
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557366203321
Taylor Alan G  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern Strategies for Heterocycle Synthesis
Modern Strategies for Heterocycle Synthesis
Autore Favi Gianfranco
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (372 p.)
Soggetto topico Medicine
Soggetto non controllato 1-oxa-triene
1,2,3-triazol
1,3-oxazines
1H-imidazole-2(3H)-thione
2H-imidazo[2,1-b][1,3,4]thiadiazine
2H-pyran
3-trifluoroacetyl coumarins
3,2':6',3"-terpyridine
4-bromo quinolines
5-acylamino-1,3-thiazoles
acylhydrazone group
alkynes
alkynoic acids
amine nucleophiles
antifungal activities
antitumor
aromatic substitution
arylation
asymmetric dimeric β-carboline
aza-Wittig
azides
cascade cyclization
cascade reaction
CF3CO-acetylenes
cinnolines
click reaction
condensation
copper-catalyzed azide-alkyne cycloaddition
coumarin
CuAAC
cyclic ethers
cycloalkynes
cyclohexanol derivative
cycloisomerization
cytotoxic
cytotoxicity
dienone
dihydrocoumarins
enol ethers
fluorescence
fluorinated heterocycles
fluoroalcohol
fused N-heterocycles
gold catalysis
Hantzsch reaction
heterocycles
heterocyclic
inter-molecular approach
intra-molecular approach
ketone
Knoevenagel
multicomponent reaction
multicomponent reactions
n/a
natural products
nucleobase
organic dyes
organocatalysis
oxa-electrocyclization
phenols
photocatalysis
photoredox
photoredox cyclization
propargyl Claisen
propargylic alcohols
purine
pyrazolo[3,4-b]pyridine
pyridine
pyrrolidones
Richter cyclization
saturated oxygen heterocycles
silica sulfuric acid
solid-phase synthesis
Staudinger reaction
structure-activity relationship
Suzuki coupling
synthesis
synthesis of benzofurans
terpyridines
TMSBr
total synthesis
traceless synthesis
triazoles
triazolylmethyl phosphate
triazolylmethyl phosphinate
valence isomerism
visible-light-induced catalysis
α-chloroglycinates
α-halohydrazones
γ-lactam
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557409903321
Favi Gianfranco  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Oxidative Stress Modulators and Functional Foods
Oxidative Stress Modulators and Functional Foods
Autore Taira Junsei
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (244 p.)
Soggetto topico Manufacturing industries
Medicine and Nursing
Soggetto non controllato (-)-loliolide
altitude variations
antimicrobial activity
antimutagenicity
antioxidant
antioxidant activity
antioxidant compounds
antioxidant effect
antioxidative mechanisms
apoptosis
Benzo[a]pyrene
bilberry
BPDE-DNA adduct
cardiac dysfunction
coumarin
cudratrixanthone O
dendrimer
diabetes mellitus
DPPH
electronic effect
epigallocatechin-gallate
ESR
fibrosis
fine dust
folic acid
fucoidan
gradient ethanol precipitation
HaCaT
HaCaT keratinocyte
heme oxygenase-1
hemeoxygenase-1
high sugar-fat diet
HO-1
hydrogen atom transfer (HAT)
in vivo model
inflammation
jujube pomace
kidney damage
LC/MS
lingonberry
liposomes
lycopene
mitochondria
myricetin
n/a
neural tube defects
neurodegeneration
nitric oxide
NOR3
Nrf2
nuclear transcription factor erythroid-2-like factor 2
nutricosmetic
nutrient
obesity
oxidative stress
Peucedanum japonicum Thunb
phase detoxifying enzyme
physiological conditions
polyphenols
polysaccharide
pteryxin
QM-ORSA
Quamoclit angulata
RAW264.7 cells
reaction rate constants
reactive oxygen species
Sargassum horneri
sequential proton loss electron transfer (SPLET)
single electron transfer-proton transfer (SET-PT)
structural analysis
tomato-oleoresin
type 2 diabetes
ultraviolet B
zebrafish embryo
β-adrenergic system
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557361503321
Taira Junsei  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
PPARs as Key Mediators of Metabolic and Inflammatory Regulation
PPARs as Key Mediators of Metabolic and Inflammatory Regulation
Autore Vázquez-Carrera Manuel
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (456 p.)
Soggetto topico Biochemistry
Biology, life sciences
Research and information: general
Soggetto non controllato adipose tissue
AMPK
amygdala
atopic dermatitis
bezafibrate
brain
browning
cancer
common carotid artery occlusion
coregulator
corticotropin releasing hormone
coumarin
crystal structure
cytomegalovirus
dairy animals
depression
diabetes
DNA methylation
docking
doping control
dual/pan agonist
electroretinography
ELISA
energy homeostasis
exercise
fatty acid oxidation
fatty acids
fenofibrate
fenofibric acid
fibroblast growth factor 21
fluorescent ligand
GDF15
gene transcription
glucose
GSK3787
GW0742
hepatic damage
hepatic sex-biased gene expression
histone modification
HIV
immunity
immunohistochemistry
infection
inflammation
insulin resistance
kidney fibrosis
ligand
lipid droplets
lipid metabolism
lipidomics
lipopolysaccharide (LPS)
liver damage
lung
M. leprae
M. tuberculosis
metabolic alterations
metabolic reprograming
metabolic syndrome
microglia
micronutrients
miRNA
molecular docking
mycobacteria
n/a
neural stem cells
neurogenesis
neuroinflammation
neuropathology
nitric oxide synthase
non-alcoholic fatty liver disease (NAFLD)
non-alcoholic steatohepatitis (NASH)
nonalcoholic fatty liver disease (NAFLD)
norepinephrine
nuclear factors
nuclear receptor
nuclear receptors
nucleus accumbens
nutrigenomics
obesity
oleoylethanolamide
P2Y2 receptor
palmitoylethanolamide
pattern-recognition receptors
pemafibrate
peroxisome
peroxisome proliferator-activated receptor
peroxisome proliferator-activated receptor alpha
peroxisome proliferator-activated receptor gamma (PPARγ)
peroxisome proliferator-activated receptors (PPAR)
peroxisome-proliferator-activated receptor
phagocytosis
pharmacological targets
PPAR
PPAR gamma
PPARg
PPARs
PPARα
PPARα knockout
PPARβ/δ
PPARγ
PPARγ ligand
PPRE
proliferation
psoriasis
pulmonary arterial hypertension
pulmonary artery
quercetin
real-time PCR
regulatory T cells
resveratrol
retinal ischemia
screening
sex dimorphism
signaling pathway
skeletal muscle
subgenual prefrontal cortex
substrate metabolism
TGFβ
toll-like receptor 4
type 2 diabetes mellitus
vascular injury
X-ray crystallography
Zika
β-oxidation
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910576873703321
Vázquez-Carrera Manuel  
MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Synthesis of Flavonoids or Other Nature-Inspired Small Molecules
Synthesis of Flavonoids or Other Nature-Inspired Small Molecules
Autore Ribaudo Giovanni
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (82 p.)
Soggetto topico Research and information: general
Soggetto non controllato (+)-camphor
1,2,3-triazole
7-hydroxy-2H-chromen-2-one
ADMET
aminoquinoline
anticancer
anticonvulsant activity
antidiabetic
benzylidene derivative
C. dichotoma
Clusiaceae
coumarin
curcumin analog
DFT calculation
docking
flavonoids
Garcinia porrecta
hybrid compound
hydrazone
kokosanolide
Lansium domesticum
lupeol derivative
MCF-7
Meliaceae
molecular modeling
n/a
O-acylation reaction
organic synthesis
Oxone®
PDE
photophysical properties
quercetin
semi-synthetic
sildenafil
steady-state fluorescence
technology
terpenoid
tetranortriterpenoid
triterpene onoceranoid
valproic acid
xanthone
α-amylase
α-glucosidase
α-glucosidase inhibition
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557615703321
Ribaudo Giovanni  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui