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Antitumor and Anti-HIV Agents from Natural Products
Antitumor and Anti-HIV Agents from Natural Products
Autore Nakagawa-Goto Kyoko
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (338 p.)
Soggetto topico Research & information: general
Soggetto non controllato acute toxicity
allyl isothiocyanate
Angelica dahurica
anti-HIV
antiangiogenic
antioxidants
antiproliferation
antiproliferative activity
antiretroviral agents
antitumor activity
apoptosis
Artemisia absinthium L.
aspidosperma-type
benzyl isothiocyanate
bladder cancer
Bousigonia mekongensis
BRAF inhibitor
breast cancer
butanolides
caffeic acid
cancer
cancer multidrug resistance
cancer stem cell
Carpesium divaricatum
cell cycle
cell cycle arrest
cervical cancer
chemistry
chemoprevention
cisplatin
coumarins
curcumin analog
cytotoxicity
delcosine
delpheline
diterpenoid alkaloids
DOTA
drug development
drug-drug interaction
epithelial-to-mesenchymal transition
essential oil
flavonoids
G2/M phase cell cycle arrest
HaCaT cells
HEF cell line
hepatocellular carcinoma
hepatoma cells
Hernandia nymphaeifolia
human tumor cell lines
human tumor cells
inflammation
Ivalin
kobusine
lignan glycosides
lipojesaconitine
marine metabolites
matrix metalloproteinase
medicine
melanoma
melanoma and breast cancer cell line
Mentha aquatica var. Kenting Water Mint
metastasis
mitochondria-mediated apoptosis
monoterpenoid indole alkaloids
natural agents
natural phaeosphaeride A
natural products
NF-κB
oral squamous cell carcinoma cells
oxidative stress
oxypeucedanin
P-glycoprotein
p53
phenethyl isothiocyanate
phenolic acid
pseudokobusine
pterostilbene
quercetin
reactive oxygen species
resveratrol
SK-Hep-1
sulforaphane
tamoxifen
taxol
total phenolic content
transforming growth factor-β1
triterpenoids
tubulin inhibitor
tumor suppression
two-stage skin carcinogenesis
ursolic acid
β-lapachone
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557504803321
Nakagawa-Goto Kyoko  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
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 online resource (82 p.)
Soggetto topico Research and information: general
Soggetto non controllato (+)-camphor
1,2,3-triazole
7-hydroxy-2H-chromen-2-one
ADMET
aminoquinoline
anticancer
anticonvulsant activity
antidiabetic
benzylidene derivative
C. dichotoma
Clusiaceae
coumarin
curcumin analog
DFT calculation
docking
flavonoids
Garcinia porrecta
hybrid compound
hydrazone
kokosanolide
Lansium domesticum
lupeol derivative
MCF-7
Meliaceae
molecular modeling
n/a
O-acylation reaction
organic synthesis
Oxone®
PDE
photophysical properties
quercetin
semi-synthetic
sildenafil
steady-state fluorescence
technology
terpenoid
tetranortriterpenoid
triterpene onoceranoid
valproic acid
xanthone
α-amylase
α-glucosidase
α-glucosidase inhibition
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