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Advances in Ginsenosides
Advances in Ginsenosides
Autore Chen Jen-Tsung
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (264 p.)
Soggetto topico Medicine
Soggetto non controllato Ginseng berries
UPLC-QTOF/MS
HR-MAS NMR spectroscopy
ginsenoside
primary metabolite
notoginseng leaf triterpenes
HMGB1
cerebral ischemia and reperfusion injury
inflammation
MAPK
NF-κB
Panax ginseng
wild ginseng
pharmacopuncture
safety
clinical trials
ocotillol type ginsenoside epimers
stereoselective ADME characteristics
molecular docking analysis
homology modeling
molecular interaction
Rg3
Th17
RORγt
EAE
Lactobacillus ginsenosidimutans
complete genome sequence
novel glycoside hydrolases
bioconversion
recombinant enzyme
ginsenoside Rg3(S)
gram unit production
Asian ginseng
American ginseng
Panax quinquefolium L.
ginsenosides
anti-inflammation
pro-resolving
ginseng
macrophage
M2 polarization
ginsenoside CK
neurogenesis
cell proliferation
neuroprotection
dammarane-type triterpene saponin
ginsenoside MT1
transglycosylation
biotransformation
biotechnology
Anxa2
epithelial-mesenchymal transition
(20S)G-Rh2
bioreactor
cell suspension
hairy root
polyploidy
protoplast
Panax sp
polysaccharides
allergy
immune system
compound M1
hepatoprotective
anti-cancer
anti-diabetic
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557766503321
Chen Jen-Tsung  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Biocatalytic Process Optimization
Biocatalytic Process Optimization
Autore Kuo Chia-Hung
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (296 p.)
Soggetto topico Research & information: general
Soggetto non controllato catechin
degalloylation
flavonol
glycoside hydrolase
optimization
tannase
immobilized DERA
statin side chain
continuous flow synthesis
alginate-luffa matrix
design of experiments
Anguilla marmorata
eel protein hydrolysates
functional properties
herbal eel extracts
agarose
agarase
agarotriose
agaropentaose
expression
calycosin
calycosin-7-O-β-D-glucoside
glucosyltransferase
sucrose synthase
UDP-glucose recycle
UGT-SuSy cascade reaction
Candida antarctica lipase A
surface-display system
shear rate
mass transfer rate
enzymatic kinetic study
enzymatic synthesis
β-amino acid esters
microreactor
aromatic amines
Michael addition
kraft pulp
cellulose
xylan
enzymatic hydrolysis
Penicillium verruculosum
glucose
xylose
lipase
acidolysis
docosahexaenoic acid ethyl ester
eicosapentaenoic acid ethyl ester
ethyl acetate
kinetics
styrene monooxygenase
indole monooxygenase
two-component system
chiral biocatalyst
solvent tolerance
biotransformation
epoxidation
NAD(P)H-mimics
superoxide dismutase (SOD)
catalase (CAT)
glutathione reductase (GR)
aluminum (Al)
selenium (Se)
mouse
brain
liver
phosphatidylcholine
3,4-dimethoxycinnamic acid
enzymatic interesterification
biocatalysis
Pleurotus ostreatus
enenzymatic hydrolysis
peptide
antioxidant
hepatoprotective activity
Yarrowia lipolytica
whole-cell biocatalysis
indolizine
cycloaddition
trehalose
viscosity
enzymes
protein dynamics
Kramers' theory
protein stabilization
enzyme inhibition
Lipase
transesterification
2-phenylethyl acetate
packed-bed reactor
solvent-free
cyclic voltammetry
electrochemical impedance spectroscopy
carbon nanotubes
redox mediators
CYP102A1
naringin dihydrochalcone
neoeriocitrin dihydrochalcone
regioselective hydroxylation
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557487503321
Kuo Chia-Hung  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
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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Carbohydrate-Active Enzymes : Structure, Activity and Reaction Products
Carbohydrate-Active Enzymes : Structure, Activity and Reaction Products
Autore Benini Stefano
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (408 p.)
Soggetto topico Research & information: general
Biology, life sciences
Soggetto non controllato glycoside hydrolase
xylanase
carbohydrate-binding module
CBM truncation
halo-tolerant
xylan hydrolysis
pectate lyase
Paenibacillus polymyxa
pectins
degradation
Lactobacillus
GH13_18
sucrose phosphorylase
glycoside phosphorylase
Ilumatobacter coccineus
Thermoanaerobacterium thermosaccharolyticum
crystallography
galactosidase
hydrolysis
reaction mechanism
complex structures
cold-adapted
GH2
Cellulase
random mutagenesis
cellulose degradation
structural analysis
α-amylase
starch degradation
biotechnology
structure
pyruvylation
pyruvyltransferase
exopolysaccharides
capsular polysaccharides
cell wall glycopolymers
N-glycans
lipopolysaccharides
biosynthesis
sequence space
pyruvate analytics
Nanopore sequencing
ganoderic acid
Bacillus thuringiensis
biotransformation
glycosyltransferase
whole genome sequencing
applied biocatalysis
enzyme cascades
chemoenzymatic synthesis
sugar chemistry
carbohydrate
Leloir
nucleotide
Enzymatic glycosylation
alkyl glycosides (AG)s
Deep eutectic solvents (DES)
Amy A
alcoholysis
methanol
circular dichroism
protein stability
alpha-amylase
biomass
hemicellulose
bioethanol
xylanolytic enzyme
hemicellulase
lysozyme
peptidoglycan cleavage
avian gut GH22
crystal structure
glycosylation
UDP-glucose pyrophosphorylase
UDP-glucose
nucleotide donors
Rhodococcus, Actinobacteria, gene redundancy
Leloir glycosyltransferases
activated sugar
UTP
thermophilic fungus
β-glucosidases
Chaetomium thermophilum
protein structure
fungal enzymes
endo-α-(1→6)-d-mannase
mannoside
Mycobacterium
lipomannan
lipoarabinomannan
phosphatidylinositol mannosides
GH68
fructosyltransferase
fructooligosaccharides
FOS biosynthesis
prebiotic oligosaccharides
Arxula adeninivorans
α-glucosidase
maltose
panose
amylopectin
glycogen
inhibition by Tris
transglycosylation
glycoside hydrolyase
Trichoderma harzianum
complete saccharification
lignocellulose
N-acetylhexosamine specificity
GH20
phylogenetic analysis
NAG-oxazoline
acceptor diversity
lacto-N-triose II
human milk oligosaccharides
NMR
molecular phylogeny
α2,8-sialyltransferases
polySia motifs
evolution
ST8Sia
functional genomics
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Carbohydrate-Active Enzymes
Record Nr. UNINA-9910557134503321
Benini Stefano  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Catalyzed Synthesis of Natural Products
Catalyzed Synthesis of Natural Products
Autore Díez David
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2019
Descrizione fisica 1 electronic resource (82 p.)
Soggetto non controllato structured phosphatidylcholine
carvone
immobilized lipases
trimyristin
3-hydroxyoxindole
green chemistry
structural revision
anticancer
triterpenoid
organocatalysis
natural products
epoxidation
benzimidazole
total synthesis
zinc
Antrodia cinnamomea
aminocatalysis
epoxide
asymmetric organocatalysis
mandelamides
STAT3
asymmetric catalysis
Psychrobacillus
isatin
chiral ?-hydroxyamide
interesterification
proline
phaeosphaeride B
biotransformation
phaeosphaeride A
myristic acid
egg-yolk phosphatidylcholine
acidolysis
antcin K
deep eutectic solvents
ISBN 3-03921-949-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910367737103321
Díez David  
MDPI - Multidisciplinary Digital Publishing Institute, 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Colloids and Interfaces in Oil Recovery / Spencer Taylor
Colloids and Interfaces in Oil Recovery / Spencer Taylor
Autore Taylor Spencer
Pubbl/distr/stampa Basel, Switzerland : , : MDPI, , 2019
Descrizione fisica 1 electronic resource (234 p.)
Soggetto non controllato multicomponent ion exchange
alcohols
polymer-enhanced foam
low salinity waterflooding
heavy oil
cyclodextrins
SAGD
nanoparticle fluids
CO2 foam
in-situ rheology
surfactants
Pickering emulsions
enhanced oil recovery
emulsions
inclusion complexes
petroleum
Bacillus halodurans
non-Newtonian flow in porous medium
oil recovery
Bacillus firmus
oil film displacement
surface and interfacial tension
naphthenic acid
Microbial Enhanced Oil Recovery
recovery factor
thermal recovery
heavy oil and bitumen
SAG
colloid and interfacial science
metal ion interactions
porous media
optical video microscopy
microfluidics
spore forming bacteria
interfacial complexation
electric double layer
dynamic interfacial tension
polymer flooding
wettability
polymers
fluid-fluid interactions
interfaces
waterflooding
oil sands
EOR
contact angles
wettability alteration
biotransformation
monolayer
asphaltene
petroleum colloids
surface charge
heavy oil recovery
ISBN 9783039211074
3039211072
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910346843003321
Taylor Spencer  
Basel, Switzerland : , : MDPI, , 2019
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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Enzymes, Biocatalysis and Chemical Biology
Enzymes, Biocatalysis and Chemical Biology
Autore Serra Stefano
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 electronic resource (152 p.)
Soggetto topico Research & information: general
Soggetto non controllato 7-hydroxycoumarin
3-(2,4-dihydroxyphenyl)-propionic acid
3-(2,3,5-trihydroxyphenyl)-propionic acid
ipso-hydroxylase
Pseudomonas mandelii
sweet potato β-amylase (SPA) 2
methoxy polyethylene glycol maleimide (Mal-mPEG) 3
chemical modification 4
enzymatic characteristics
(S)-N-Boc-3-hydroxypiperidine
carbonyl reductase
asymmetric reduction
rational design
Rhodococcus erythropolis
biotransformation
oxidation
apocarotenoids
flavours
fungi
ionone
damascone
theaspirane
enzymatic activity assay
adenylate kinase
spectrophotometry
orthogonal experiment
bromothymol blue
Botrytis cinerea
antifungal activity
laccase
2,6-dimethoxy-4-(phenylimino)cyclohexa-2,5-dienone derivatives
citral
citronellal
enantioselectivity
Old Yellow Enzyme
site-saturation mutagenesis
substrate binding mode
browning reaction
polyphenol oxidase
ultrasonic processing
structural changes
aggregation
ganoderic acid A
glucosyltransferase
acidic
Bacillus subtilis
triterpenoid
Lentinula edodes
endogenous formaldehyde
GGT
C-S lyase
expression levels
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557123003321
Serra Stefano  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fungal Nanotechnology
Fungal Nanotechnology
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (364 p.)
Soggetto topico Technology: general issues
Soggetto non controllato aflatoxins
Aspergillus section Flavi
chitosan
nanocomposites
fungal nanotechnology
Trichoderma spp
ZnO nanoparticles
antibacterial activity Xanthomonas oryzae pv. oryzae
co-cultivation
secondary metabolites
biotransformation
biomineralization
metal oxide nanoparticles
nanoparticle dissolution
nanoparticle mobility
fungal leaching
ecotoxicity
nanomaterial
nanosensors
phytopathogens
zinc
endophytic bacteria
silver nanoparticles
Magnaporthe oryzae
antifungal activity
oyster mushroom
application
antibacterial
anticancer
antioxidant
nanohybrids
polymer-metal composites
antifungal
postharvest
Fusarium
synthesis
nanoparticles
mechanism
medicine
agriculture
nanofactory
toxicity
copper (I) iodide
composites
atomic force microscopy
Vicia faba
plant disease
root rot
R. solani
Se-NPs
nano-biosynthesis
plant promotion
metal oxides
nano-fungicides
pathogenic fungi
protein profiling
radical scavenging activity
resistance
homeostasis
fungal-metal interaction
lichen
green synthesis
eco-friendly
antimicrobial
MgO-NPs
optimization
mosquitocidal and repellence activity
tannery effluents
chromium ion
nanoantifungal
mycotoxin degradation
theragnostic
veterinary
bamboo
Ag/TiO2
visible light photoactivity
energy storage
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557422403321
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Marine Bioactive Peptides II: Structure, Function, and Therapeutic Potential
Marine Bioactive Peptides II: Structure, Function, and Therapeutic Potential
Autore Ovchinnikova Tatiana V
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 electronic resource (228 p.)
Soggetto topico Medicine
Soggetto non controllato Spanish mackerel (Scomberomorous niphonius)
muscle
peptide
antioxidant activity
stability
biological activity
chemistry
marine derived fungi
peptides
biotransformation
laxaphycin
autophagy
apoptosis
cyanobacteria
bioactive peptides
marine
secondary structure
proline
mechanism of activity
marine waste
antimicrobial peptide
polychaeta
innate immunity
BRICHOS domain
recombinant peptide
β-hairpin structure
nuclear magnetic resonance (NMR)
arenicin
complement system
complement regulation
jellyfish
Rhopilema esculentum
Sanderia malayensis
proteome
venom
toxin
hydrolysate
fish protein
ageing
physical function
dietary assessment
seafood intake
healthy ageing
marine organism
anticancer medicine
small peptide
liner peptide
cyclic peptide
marine peptide
dolastatin 10
antitumor
lead exploration
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Marine Bioactive Peptides II
Record Nr. UNINA-9910557353303321
Ovchinnikova Tatiana V  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui