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Anticancer Inhibitors
Anticancer Inhibitors
Autore Fantacuzzi Marialuigia
Pubbl/distr/stampa Basel, : MDPI Books, 2022
Descrizione fisica 1 electronic resource (216 p.)
Soggetto topico Research & information: general
Chemistry
Soggetto non controllato breast cancer
tamoxifen
LY294002
synergism
apoptosis
cell cycle
tea (Camellia sinensis) flowers
BTFS
A2780/CP70 ovarian cancer cells
S phase cell cycle arrest
nicotinamide phosphoribosyltransferase
NAD+ biosynthesis
inhibitor
azacyclohexane
anticancer drug
drug design
enthalpy effect
NSCLC
Cathepsin K
cell proliferation
cell migration
cell invasion
mTOR
isatin-hydrazones
cytotoxicity
CDK2 inhibitor
ATP competitive inhibitor
ADME analysis
receptor tyrosine kinases
protein-protein interactions
protein engineering
directed evolution
angiogenesis
binding affinity
agonistic activity
saponins
phytochemicals
tea (Camellia sinensis) flower
ovarian cancer
autophagy
ZMYND8
tumorigenesis
epigenetic regulation
pro-oncogenic effects
tumor suppression
tacrine-coumarin derivatives
DNA
topoisomerases I, II
lung carcinoma cells
A549
chemotherapy
prodrug
drug targeting
overexpressed enzymes
ADC
ADEPT
GDEPT
LEAPT
PROTAC
cyclin-dependent kinase
cancer
resistance
small molecule inhibitors
PROTACs
statins
pancreatic cancer
DNA microarray
pitavastatin
cerivastatin
simvastatin
fluvastatin
atorvastatin
pravastatin
HMG-CoA reductase inhibitors
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910595069203321
Fantacuzzi Marialuigia  
Basel, : MDPI Books, 2022
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 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
Molecular Modeling in Drug Design
Molecular Modeling in Drug Design
Autore Wade Rebecca
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 online resource (220 p.)
Soggetto topico Chemistry
Soggetto non controllato adenosine
adenosine receptor
adenosine receptors
adhesion
aggregation
all-atom molecular dynamics simulation
allosterism
Alzheimer's disease
amyloid fibrils
AR ligands
artificial intelligence
AutoGrid
binding affinity
biophenols
boron cluster
cosolvent molecular dynamics
de novo design
deep learning
density-based clustering
docking
drug design
drug discovery
dynamic light scattering
enzymatic assays
EphA2-ephrin A1
extracellular loops
FimH
fragment screening
grid maps
human ecto-5?-nucleotidase
hyperlipidemia
in silico screening
interaction energy
ligand binding
ligand-protofiber interactions
mechanical stability
metadynamics
method development
molecular docking
molecular dynamics
molecular dynamics simulation
molecular modeling
molecular recognition
natural compounds
neural networks
PPI inhibition
probe energies
promiscuous mechanism
property prediction
protein protein interactions
protein-peptide interactions
proteins
quantitative structure-activity relationship (QSAR)
quantitative structure-property prediction (QSPR)
rational drug design
resultant dipole moment
scoring function
solvent effect
squalene synthase (SQS)
steered molecular dynamics
structure-based drug design
target-focused pharmacophore modeling
Traditional Chinese Medicine
turbidimetry
virtual screening
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346839403321
Wade Rebecca  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Novel Natural-based Biomolecules Discovery for Tackling Chronic Diseases
Novel Natural-based Biomolecules Discovery for Tackling Chronic Diseases
Autore Kwok Hang Fai
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (180 p.)
Soggetto topico Humanities
Social interaction
Soggetto non controllato AKT
amphibian Bowman-Birk inhibitor
amyloidogenesis
anionic lipids
anti-inflammation
anticancer therapy
anticancer therapy/cancer treatment
antifungal
antioxidant
apoptosis
Asteraceae
Astragalus membranaceus
Bcl-2 family proteins
binding affinity
branched-chain fatty acids
cell cycle arrest
colorectal cancer
Conidiobolus heterosporus
COX-2
DAPK1
docetaxel
drug delivery system
drug design
endoplasmic reticulum
F23R variant
fatty acid oxidation
fibroblasts
fucoidan
G-protein activation
gingiva
hepatocyte
hIAPP
iNOS
insulin
insulin granules
kynurenines
lignan
lipid metabolism
lung cancer
molecular cloning
molecular docking
n/a
natural-based compound
NO
orientin
PDX-1
peptides
peroxisome proliferator-activated receptor α
Petasites japonicus
PGE2
pharmacophore
PI3K
PLGA
pomegranate
post-translational modification
PPARγ
protease inhibitor
protein degradation
punicalagin
SENP
STAT3
SUMO
survivin
tannins
Tat peptide
unfolded protein response
wound healing
β-cell cytotoxicity
β-sheet transitions
μ-opioid receptor
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557607403321
Kwok Hang Fai  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Opioids and Their Receptors : Present and Emerging Concepts in Opioid Drug Discovery
Opioids and Their Receptors : Present and Emerging Concepts in Opioid Drug Discovery
Autore Spetea Mariana
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (358 p.)
Soggetto topico Medicine
Soggetto non controllato (−)-N-phenethylnorhydromorphone analogs
[35S]GTPgammaS assay
[Dmt1]DALDA
14-methoxycodeine-6-O-sulfate
1H-NMR experiments
6β-naltrexol
abuse
agonist
allodynia
analgesia
analgesics
antagonist
arrestin recruitment
beta-arrestin
bias factor
biased agonism
biased agonist
biased agonists
biased ligands
biased signaling
bifunctional ligands
binding
binding affinity
BNTX
buprenorphine
chronic constriction injury (CCI)
codeine
codeine-6-O-sulfate
DADLE
DALDA
DAMGO
delta opioid receptor
dependence
design and synthesis
dihydrocodeine
diphenethylamines
docking
dysbiosis
fentanyl
forskolin-induced cAMP accumulation assays
functional assay
G-protein bias
heteromer
hyperalgesia
interaction fingerprints
internalization
inverse agonist
ischemia
kappa opioid receptor
KGOP01
Leu-enkephalin
loperamide
lysosomes
macrocyclic tetrapeptide
mechanism elucidation
misuse
mitragynine
molecular docking
molecular dynamics
molecular modeling &
MOR and DOR agonists
morphinan
morphine
mu opioid receptor
mu receptor
multifunctional ligands
n/a
naltrexone
neonatal opioid withdrawal syndrome
neurokinin-1 receptor
neutral antagonist
NTI derivative
opioid
opioid drugs
opioid liabilities
opioid peptide
opioid peptides
opioid peptides and peptidomimetics
opioid receptors
opioid side effects
opioids
over-the-counter drugs
pain therapy
partial agonism
partial agonist
peptide synthesis
peripheral analgesic tolerance
peripheral antinociception
peripheral µ-opioid receptors
pharmacology
plasma stability
potassium channels
primary hippocampal culture
PZM21
racemic synthesis of β2-amino acids
receptor binding studies
receptor model
respiration
respiratory depression
selectivity
simulation
SR-17018
structure-activity relationships
sulfonamide
TAPP
tolerance
writhing test
zerumbone
β-arrestin recruitment assays
β2-amino acids
β2-Homo-amino acids
δ opioid receptor
δ opioid receptor antagonist
μ opioid receptor
µ opioid receptor
µ-opioid receptor
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Opioids and Their Receptors
Record Nr. UNINA-9910557108003321
Spetea Mariana  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui