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.
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
Opac: Controlla la disponibilità qui
Recent Developments on Protein–Ligand Interactions : From Structure, Function to Applications
Recent Developments on Protein–Ligand Interactions : From Structure, Function to Applications
Autore de Brevern Alexandre G
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (282 p.)
Soggetto topico Research & information: general
Biology, life sciences
Biochemistry
Soggetto non controllato pimaricin thioesterase
protein-substrate interaction
macrocyclization
molecular dynamics (MD) simulation
pre-reaction state
folate
folate receptor
peptide conjugation
click reaction
biolayer interferometry
acetylcholinesterase
resistance
organophosphorus
pesticides
molecular modeling
lepidopterous
insects
conserved patterns
similarity
3D-patterns
epigenetics
protein-RNA interaction
RRM domain inhibitor
NMR fragment-based screening
TDP-43
galectin-1
gulopyranosides
fluorescence polarization
benzamide
selective
phospholipase C gamma 1
SLP76
virtual screening
pharmacophore mapping
molecular docking
molecular dynamics
caspase inhibition
protein-ligand binding free energy
Monte Carlo sampling
docking and scoring
molecular conformational sampling
procollagen C-proteinase enhancer-1
glycosaminoglycans
computational analysis of protein-glycosaminoglycan interactions
calcium ions
fragment-based docking
protein–ligand analysis
drug discovery and design
structure–activity relationships
bioremediation
High Energy Molecules
HMX
protein design
nitroreductase
flavoprotein
substrate specificity
pharmacophore
secretoglobin
odorant-binding protein
chemical communication
pheromone
N-phenyl-1-naphthylamine
in silico docking
protein–ligand interactions
2D interaction maps
ligand-binding assays
protein-ligand complexes
dataset
clustering
structural alignment
refinement
PD-1/PD-L1
immune checkpoint inhibitors
biphenyl-conjugated bromotyrosine
amino acid conjugation
amino-X
in silico simulation
IC50
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Recent Developments on Protein–Ligand Interactions
Recent Developments on Protein–Ligand Interactions
Record Nr. UNINA-9910566462703321
de Brevern Alexandre G  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui