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Kinase inhibitors from marine spongesDeep-sea natural productsAdvancement of Sialyltransferase Inhibitors: Therapeutic Challenges and OpportunitiesAsymmetric synthesis and reactivity of potent sialyltransferase inhibitors based on transition-state analogues: supplementary data.The effect of individual N-glycans on enzyme activity.Recent advances in deep-sea natural products.Computational Glycobiology: Mechanistic Studies of Carbohydrate-Active Enzymes and Implication for Inhibitor Design.Parameters affecting the analytical profile of fatty acids in the macroalgal genus Ulva.Bioassays for anticancer activities.Targeting urokinase and the transferrin receptor with novel, anti-mitotic N-alkylisatin cytotoxin conjugates causes selective cancer cell death and reduces tumor growth.Synthesis and hydrolytic evaluation of acid-labile imine-linked cytotoxic isatin model systems.N-phenethyl and N-naphthylmethyl isatins and analogues as in vitro cytotoxic agents.Calenzanane sesquiterpenes from the red seaweed Laurencia microcladia from the Bay of Calenzana, Elba Island: acid-catalyzed stereospecific conversion of calenzanol into indene- and guaiazulene-type sesquiterpenes.Asymmetric synthesis and affinity of potent sialyltransferase inhibitors based on transition-state analogues.Transition state-based ST6Gal I inhibitors: Mimicking the phosphodiester linkage with a triazole or carbamate through an enthalpy-entropy compensation.Computer-aided design of human sialyltransferase inhibitors of hST8Sia III.(Chemotaxonomic) Implications of Postharvest/Storage-Induced Changes in Plant Volatile Profiles--the Case of Artemisia absinthium L. Essential Oil.Eyes in the sea: Unlocking the mysteries of the ocean using industrial, remotely operated vehicles (ROVs).Computational characterisation of the interactions between human ST6Gal I and transition-state analogue inhibitors: insights for inhibitor designN-Glycosylation regulates endothelial lipase-mediated phospholipid hydrolysis in apoE- and apoA-I-containing high density lipoproteinsN,O-Isopropylidenated Threonines as Tools for Peptide Cyclization: Application to the Synthesis of Mahafacyclin BStereoselective synthesis of phosphoramidate α(2-6)Sialyltransferase transition-State analogue inhibitorsAcetylcholinesterase-inhibitory activity of Iranian plants: Combined HPLC/bioassay-guided fractionation, molecular networking and docking strategies for the dereplication of active compounds
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description
researcher ORCID ID = 0000-0002-2293-7916
@en
wetenschapper
@nl
name
Danielle Skropeta
@ast
Danielle Skropeta
@en
Danielle Skropeta
@es
Danielle Skropeta
@nl
type
label
Danielle Skropeta
@ast
Danielle Skropeta
@en
Danielle Skropeta
@es
Danielle Skropeta
@nl
prefLabel
Danielle Skropeta
@ast
Danielle Skropeta
@en
Danielle Skropeta
@es
Danielle Skropeta
@nl
P1053
G-3761-2015
P106
P1153
6505973067
P1960
g0H5d24AAAAJ
P31
P3829
P496
0000-0002-2293-7916