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New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancerInhibiting endocannabinoid biosynthesis: a novel approach to the treatment of constipation.New Indole Tubulin Assembly Inhibitors Cause Stable Arrest of Mitotic Progression, Enhanced Stimulation of Natural Killer Cell Cytotoxic Activity, and Repression of Hedgehog-Dependent Cancer.Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitorsModulation of thermo-transient receptor potential (thermo-TRP) channels by thymol-based compounds.(-)-Menthylamine derivatives as potent and selective antagonists of transient receptor potential melastatin type-8 (TRPM8) channels.Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism.New tetrazole-based selective anandamide uptake inhibitors.New N-arachidonoylserotonin analogues with potential "dual" mechanism of action against pain.Carbamoyl tetrazoles as inhibitors of endocannabinoid inactivation: a critical revisitation.The anandamide membrane transporter. Structure-activity relationships of anandamide and oleoylethanolamine analogs with phenyl rings in the polar head group region.Synthesis and biological evaluation of piperazinyl carbamates and ureas as fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channel dual ligands.Modulation of neutrophil phospholipase C activity and cyclic AMP levels by fMLP-OMe analogues.Biaryl tetrazolyl ureas as inhibitors of endocannabinoid metabolism: modulation at the N-portion and distal phenyl ring.Isopeptide bonds in chemotactic tripeptides. Synthesis and activity of lysine-containing fMLF analogs.Synthesis and activity of novel glutathione analogues containing an urethane backbone linkage.Synthesis and activity of HCO-Met-Leu-Phe-OMe analogues containing beta-alanine or taurine at the central position.Hybrid alpha/beta3-peptides with proteinogenic side chains. Monosubstituted analogues of the chemotactic tripeptide For-Met-Leu-Phe-OMe.Peptides containing 4-amino-1,2-dithiolane-4-carboxylic acid (Adt): conformation of Boc-Adt-Adt-NHMe and NH...S interactions.3-Ylidenephthalides as a new class of transient receptor potential channel TRPA1 and TRPM8 modulators.Development of a potent inhibitor of 2-arachidonoylglycerol hydrolysis with antinociceptive activity in vivo.Tetrahydro-β-carboline derivatives targeting fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channels.A 'pure' chemoattractant formylpeptide analogue triggers a specific signalling pathway in human neutrophil chemotaxisEffect of acyclic monoterpene alcohols and their derivatives on TRP channelsSynthesis and biological evaluation of [6]-gingerol analogues as transient receptor potential channel TRPV1 and TRPA1 modulators4-Amino-1,2-dithiolane-4-carboxylic acid (Adt) as cysteine conformationally restricted analogue. Synthetic protocol for Adt containing peptidesBiscarbamate analogues of the chemotactic tripeptide fMLF-OMe
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marianna Nalli
@ast
Marianna Nalli
@en
Marianna Nalli
@es
Marianna Nalli
@nl
type
label
Marianna Nalli
@ast
Marianna Nalli
@en
Marianna Nalli
@es
Marianna Nalli
@nl
prefLabel
Marianna Nalli
@ast
Marianna Nalli
@en
Marianna Nalli
@es
Marianna Nalli
@nl
P106
P1153
6602651522
P21
P31
P496
0000-0003-2774-6868