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