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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
Opac: Controlla la disponibilità qui
Anticancer Drugs 2021
Anticancer Drugs 2021
Autore Meegan Mary J
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (594 p.)
Soggetto topico Research & information: general
Chemistry
Soggetto non controllato thymidylate synthase
cytotoxicity
1,2,3-triazole
1,3,4-oxadiazole
5-fluoruracil
pemetrexed
docking
3,4'-bis-guanidino
3-amino-4'-guanidino
diphenyl ether
phenyl pyridyl ether
intramolecular hydrogen bond
cancer cell viability
HL-60
BRAF
apoptosis
thieno[2,3-d][1,2,3]triazine
acetamide
H1299
HER2
EGFR
Bcl-2 inhibitors
Indole-based analogues
benzimidazole
MTT cytotoxic assay
cell cycle analysis
DNA fragmentation
ELISA
solid/lipid nanoparticles
phenstatin
letrozole
tubulin polymerisation inhibitor
aromatase inhibitor
breast cancer
hybrid molecule
dual-targeting molecule
designed multiple ligand
NaMSA
cyclophosphamide
histopathology
testis
urinary bladder
anticancer agents
enantioselective synthesis
gastric adenocarcinoma
tryptophanol
concentration-guided dosing
model informed dosing
physiologically based pharmacokinetics
sorafenib
tyrosil-DNA-phosphodiesterase 1
adamantane
resin acid
TDP1
cytotoxic agents
apoptosis induction
HT-29 cells
MDA-MB-231 cells
mechanism prediction
STAT inhibitors
miR-21
hydrazide derivatives
nitrogen scaffolds
mitoxantrone
cardiotoxicity
inflammation
oxidative stress
age
cumulative dose
Trk
NTRK
tissue-agnostic
larotrectinib
entrectinib
Trk fusion
protein kinase inhibitors
USFDA
cancer
patent review
generic product
doxazosin
MD simulations
combretastatin A-4
cytotoxic activity
hybrid compounds
indazole
mucin
MUC1
MUC16
immunotherapy
cancer vaccine
CAR (chimeric antigen receptor)
ADC (antibody-drug conjugate)
thiourea
interleukin-6
trypan blue assay
chalcones
exportin-1
covalent binding
CovDock
anticancer activity
xanthone
in vitro
in vivo
isolation
synthesis
heterocyclic compound
benzenesulfonamides
imidazoles
alkylated
colony formation
tumor spheroids
HDAC inhibitors
chalcone
dual inhibitors
carvedilol
kidney
toxicity
7-deaza-4'-thioadenosine derivatives
multi-kinase inhibitor
anticancer
nucleoside
Imiquimod
drug efflux
multidrug resistance
Toll-Like Receptor
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910576874303321
Meegan Mary J  
Basel, : 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 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
Opac: Controlla la disponibilità qui