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Biological Activity and Applications of Natural Compounds
Biological Activity and Applications of Natural Compounds
Autore Seca Ana M. L
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (206 p.)
Soggetto topico Medicine
Soggetto non controllato 5-pentylcyclohexa-1,3-diene
alantolactone
aldol condensation
almond
amino acid metabolism
anti-aging
anti-inflammatory
antibacterial activity
anticancer
anticholinesterase
antidiabetic
antidiabetic activity
antimicrobial
antioxidant
antitumor
apoptosis
arglabin
Aspergillus niger
Asteraceae
biological activity
byproducts
Caenorhabditis elegans
Candida
Candida albicans
cardioprotective
carvacrol
celastroloids
chalcones
chlorogenic acid
colorectal cancer
Cryptococcus neoformans
cytotoxic
design of experiment
essential oils
flavanones
flavonoid
fungistatic effect
GC/MS
Helianthus annuus
Helianthus strumosus
honey
in vivo study
inhibition of dimorphism
longevity
Maytenus
metabolomics data
natural compounds
NHDF cells
oleracone
osthole
oxidative stress
parthenolide
Penicillium digitatum
phenolic acids
phenolic compounds
pimenta d'água
Portulaca oleracea L.
Prangos pabularia Lindl
propolis
PTP-1B
rosemary
rosmarinic acid
Salviae miltiorrhizae radix
SAR
semisynthesis
sesquiterpene lactones
structure-activity relationship
thapsigargin
therapeutic applications
total synthesis
ultrasound-assisted extraction
volatile oil
wound-healing activity
α-pinene
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557291403321
Seca Ana M. L  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Biological and Pharmacological Activity of Plant Natural Compounds
Biological and Pharmacological Activity of Plant Natural Compounds
Autore Pezzani Raffaele
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (296 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 10-oxyderivatives of oleoside secoiridoids
acute inflammation
Ageratina havanensis
Amelanchier alnifolia Nutt
anti-ageing
anti-cancer activities
anti-inflammatory
anti-oxidant
antibacterial
antioxidant
antioxidant potential
behavioral disorders
bioactive compounds
biological activity
Bromelia antiacantha
Brosimum gaudichaudii
cancer preventive
carriers
caspase-1
catechin
colorectal cancer
cytokine storm
cytotoxicity
depression
doxorubicin
EGCG
epigallocatechin-3-gallate
flavonoids
flow cytometry
forced swim test
functional food
Genipa americana
granuloma
green tea
hesperidin
Hibiscus acetosella
histopathology
human lung adenocarcinoma
hyperuricemia
IL-18
IL-1β
immunological disorders
immunopharmacology
inflammation
juglone
KRAS
lipopolysaccharide
Mahonia aquifolium
matrix metalloproteinases
multifloroside
muscle function
n/a
nanocrystals
natural compounds
natural products
nephrotoxicity
new-clean process extraction
NLRP3 inflammasome
nootkatone
P-glycoprotein
Pharbitis nil
pharmacological activities
pharmacological activity
phenolic acids
phenolic compound
phenylpropanoids
phytochemistry
plant secondary metabolites
plant side effects
plants
powders
procalcitonin
RA-3
structure-activity relationship
Tabebuia impetiginosa
Taheebo
tail suspension test
Talisia esculenta
traditional uses
triterpene
UPLC
UPLC-ESI-MS/MS
zingerone
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557471303321
Pezzani Raffaele  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon Ligands : From Fundamental Aspects to Applications
Carbon Ligands : From Fundamental Aspects to Applications
Autore Canac Yves
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (311 p.)
Soggetto topico Research and information: general
Soggetto non controllato 195Pt NMR
alkali metals
amide
amino-acids
aromaticity
asymmetric synthesis
calixarene
carbenes
carbido complexes
carbodiphosphorane
carbon ligand
carbone
carbone complexes
catalysis
chemical bonding
chirality
coordination
coordination chemistry
copolymerization of epoxide with CO2
Cu(I) complex
cyclooctatetraene ions
dehydrogenation
density functional theory
density functional theory (DFT)
DFT calculations
drug resistance
electrochemistry
electron paramagnetic resonance (EPR) spectroscopy
electronic structure
germylene
gold
hafnium
hybrid molecules
imidazole
intramolecular C-H activation
ion pairs
ligand
ligands
lithium
macrocycle
malaria
mercury(II) complex
metal complexes
metathesis
N-heterocyclic carbene
N-heterocyclic carbenes
n/a
nanoparticle
natural bond orbitals
negative charge
NHC
NHC ligands
NHC-ligands
nitro catalysts
olefins
optical resolution
oxide
palladium catalyst
phosphonium ylide
phosphorus ylides
photoluminescence
pincer
pincer ligand
pincer ligands
Plasmodium falciparum
platinum
potassium
reactivity
rhodium
ruthenium
selenonium salts
selenonium ylides
spectroscopy
stereogenic selenium atom
structure-activity relationship
Suzuki-Miyaura reaction
T-shaped
titanium
transition metal complexes
tropylidenyl ions
water
X-ray
ylide
ylides
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Carbon Ligands
Record Nr. UNINA-9910557372703321
Canac Yves  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Forest, Foods and Nutrition
Forest, Foods and Nutrition
Autore Durazzo Alessandra
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (342 p.)
Soggetto topico Biology, life sciences
Cultural studies: food and society
Research and information: general
Soggetto non controllato ABTS
Acanthopanax
Africa
Agew and Sidama
agroforestry
aliphatic esters
Amhara
antioxidant
antioxidant activity
assessment of wild food
auxin
Ayeyarwaddy region
bioactive compounds
biocontrol
biodiversity
bioeconomy
biological activity
biologically activecompounds
blackberry
Butyrospermum parkii
Chamaemelum fuscatum
chamomile
Changbai Mountains
chaste tree
chitinase
ciwujia
community garden
Compositae
conservation
contingent valuation
cosmetics
Crataegus
Cyclocarya paliurus
dedicated databases
dimensions in science
DPPH
economic
edible forest products
edible landscape
electrochemical oxidation
Enguday
ESCC (Esophageal squamous cell carcinoma)
essential oil
essential oils
estimation of potential
ethnic groups
ethnomycology
extracts
ferns
flavonoid
flavonoids
folk taxonomy
food
food and nutrition security
food composition databases
food processing industry
food security
forest
forest foods
forests and trees
fruit
Fulani
fungal pathogen
gender
green coffee
hawthorn
health benefits
health-promoting properties
heavy metal contamination
herbal medicine
historically polluted area
in vitro studies
in vivo studies
JNK (c-Jun N-terminal kinase)
jujube
Khingan Mountains
livelihoods
local communities
Lysobacter antibioticus HS124
mangrove forest
market
marketing
Mediterranean
methacrylate
mineral concentration
mushroom
Myanmar
natural population
neglected and underutilized species (NUS)
non-edible forest products
non-wood forest product
novel food
nutraceuticals
nutritional value
p38
phenolic acids
phenolics
phenylpropanoid biosynthesis
phytonutrients
plant extracts
podophyllotoxin
Polypodiopsida
product differentiation
production
pteridophytes
Rhamnaceae
ROS (reactive oxygen species)
S. greggii
S. mellifera
S. munzii
S. officinalis
S. officinalis "Icterina"
S. rutilans
Salvia Africana
seasonal dynamic
secondary metabolite
seed development
Siberian ginseng
solvent
structure-activity relationship
sustainable agriculture
technology and innovation (STI)
transcriptome analysis
tree
triterpenoid
tropical forest areas
tyrosinase inhibition
Ulmus pumila
urban consumers
urban horticulture
UV-VIS
Vitellaria paradoxa
Vitex agnus-castus L.
walnut (Juglans regia L.)
wild edible plants
wild edible tree species
wild food
wild harvesting
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557438503321
Durazzo Alessandra  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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From Natural Polyphenols to Synthetic Bioactive Analogues
From Natural Polyphenols to Synthetic Bioactive Analogues
Autore Tringali Corrado
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (98 p.)
Soggetto topico Research and information: general
Soggetto non controllato Alzheimer's disease
anti-inflammatory activity
anti-oxidant activity
antimicrobial activity
antioxidant activity
antitumor activity
apoptosis
aza-stilbene
azo-stilbene
bio-isosterism
bisphenol neolignans
cirsimaritin
hispidulin
honokiol
isorhamnetin
keratinocytes
LC/MS-MS
Melaleuca styphelioides
multicomponent reactions
n/a
polyphenolics
polyphenols
structure-activity relationship
Suzuki-Miyaura cross-coupling
Tamarix ramosissima
trans-resveratrol
Ugi reaction
β-amyloid proteins
β-lactams
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557467903321
Tringali Corrado  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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G-quadruplex and Microorganisms / Sara N. Richter
G-quadruplex and Microorganisms / Sara N. Richter
Autore Richter Sara N
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (208 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato bacteria
folding
co-translational refolding
RecQ helicase
regulatory element
conformational dynamics
G4Hunter
NDPK
fluorescence
pseudorabies virus
Epstein-Barr virus (EBV)
structure-activity relationship
PhenDC3
eukaryotic hosts
Herpesvirus
translation suppression
turn-on ligands
co-transcriptional folding
Herpesviridae
G-quadruplex
nucleoside diphosphate kinase
nucleic acids
nucleic acids conformation
bioinformatics
protein–DNA interaction
aptamers
deinococcus
Alphaherpesvirinae
EBNA1
G4
virus
human papillomaviruses
S. cerevisiae
genome stability
G-quadruplexes
metastable structure
genome evolution
pyridostatin
alphaherpesviruses
structure
protozoa
genome
G-quadruplex ligand
NMR
microbes
DNA
protein-mRNA interactions
G-quadruplex formation
immediate early promoters
ISBN 9783039212446
3039212443
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367567503321
Richter Sara N  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Marine Bioactive Peptides : : Structure, Function, and Therapeutic Potential / / Tatiana V. Ovchinnikova
Marine Bioactive Peptides : : Structure, Function, and Therapeutic Potential / / Tatiana V. Ovchinnikova
Autore Ovchinnikova Tatiana V
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (442 p.)
Soggetto topico Biology, life sciences
Soggetto non controllato cone snail
tilapia
animal models
BRICHOS domain
recombinant peptide
calcium absorption
plastein reaction
antioxidant activity
endothelial dysfunction
C3a
lung cancer
invertebrate immunity
identification
zinc bioavailability
NA-inhibitory peptide
nuclear magnetic resonance (NMR)
review
ACE-inhibitory activity
intestinal absorption
hairtail (Trichiurus japonicas)
DU-145 cells
peptide
crustacean
venom duct
Kalloconus
drug design
molecular symmetry
arenicin
?-helix
APETx2
conotoxins
functional diversity
docking
conotoxin
neuraminidase
angiotensin II
polychaeta
influenza virus
phylogeny
gene expression
host defense peptide
Perinereis aibuhitensis
anti-diabetic activity
conopeptides
SHRs
Chlorella pyrenoidosa protein hydrolysate (CPPH)
metastasis
Caco-2 cell monolayer
Nrf2
caco-2 cells
HUVEC
PYP15
sea cucumber
decapeptide
cytotoxic
arenicin-1
marine peptides
cell proliferation
Conus
Conus ateralbus
self-production of hydrogen peroxide
antimicrobial activity
molecular dynamics
machine learning
tachyplesins
ion channels
gut microbiota
Anthopleura anjunae oligopeptide
signaling pathways
half-fin anchovy hydrolysates
NF-?B
Chlorella pyrenoidosa protein hydrolysate-calcium chelate (CPPH-Ca)
antihypertensive effect
QAGLSPVR
antimicrobial peptides
vasculogenic mimicry
antibacterial
?-hairpin
innate immunity
transcriptome sequencing
HIF-1?
Gracilariopsis lemaneiformis
function
ACE-inhibitory peptide
complement
peptide-zinc complex
structure-activity relationship
multi-functional peptides
cod skin
adsorption
Maillard reaction products
molecular docking
antibacterial peptide
PI3K/AKT/mTOR signaling pathway
Arenicola marina
antimicrobial peptide
Rana-box
acid-sensing ion channel
Neptunea arthritica cumingii
apoptosis
membrane damage
proteolytic system
toxin
polyphemusins
computational studies
muscle
oyster zinc-binding peptide
abalone
pain relief
transport routes
cytotoxicity
dexamethasone
cell death
host?microbe relationship
anti-LPS factor
MMPs
protein synthesis
structure
Pyropia yezoensis peptide
cone snails
chemical synthesis
prostate cancer
Ugr 9-1
myotube atrophy
ISBN 9783039215331
3039215337
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367750603321
Ovchinnikova Tatiana V  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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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
New Approaches for the Discovery of Pharmacologically-Active Natural Compounds / José L. Medina-Franco
New Approaches for the Discovery of Pharmacologically-Active Natural Compounds / José L. Medina-Franco
Autore Medina-Franco José L
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (158 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato immunoproteasome
ginsenoside F1
visualization
chemoinformatics
soil microorganism
molecular diversity
web service
epigenetics
bioinsecticides
Tibetan Plateau
nanoparticles
Py-GC/MS
drug discovery
consensus diversity plot
chemical data set
molecular interactions
curcumin
similarity maps
Alzheimer's disease
proteasome inhibitors
cyclodextrin glycosyltransferase (CGTase)
classification
squalene
docking
molecular docking
cholestasis
protein aggregation
brain diseases
structure-activity relationship
flavonoids
molecular fingerprints
cyclodextrin glycosyltransferase
random forest
multitarget
natural products
inflammation
natural product-likeness
chemical space
epi-informatics
molecular dynamics
machine learning
systematic review
phenylethanoid glycosides
?-glucosyl ginsenoside F1
alpine grassland
Calceolaria
marine diterpenoid
Parkinson's disease
ISBN 9783039211050
3039211056
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346860403321
Medina-Franco José L  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Parasitic Weeds : Biology and Control
Parasitic Weeds : Biology and Control
Autore Dor Evgenia
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (152 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato chemigation
drip irrigation
Egyptian broomrape
herbicide
imazapic
parasitic plants
tomato
weed control
sunflower (Helianthus annuus)
broomrape (Orobanche cumana)
broomrape resistance
transcriptomics
GC-MS analysis
holoparasitic plant
metabolic changes
parasitic organs
parasitic weeds
Striga
Orobanche
Phelipanche
chickpea
strigolactone
chickpea phenotype
chlorophyll
carotenoid
anthocyanin
Cuscuta
food chain
feeding mode
heavy metal
holoparasite
host
tRNA
mobile mRNA
crop safety
branched broomrape
imazamox
sulfosulfuron
germination stimulant
isothiocyanates
structure-activity relationship
suicidal germination
Striga hermonthica
seedbank
strigolactone analogs
witch weeds
methyl phenlactonoate
Phelipanche aegyptiaca
glyphosate
ethametsulfuron-methyl
chemical control
ISBN 3-0365-5290-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Parasitic Weeds
Record Nr. UNINA-9910637794903321
Dor Evgenia  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui