Search results for "Side chain"

showing 5 items of 345 documents

Hyaluronan Graft Copolymers Bearing Fatty-Acid Residues as Self-Assembling Nanoparticles for Olanzapine Delivery

2019

In order to evaluate the potential of a technology platform based on hyaluronan copolymers grafted with propargylated ferulate fluorophores (HA-FA-Pg) in the development of drug delivery systems, the propargyl groups of HA-FA-Pg derivatives were employed with oleic acid (OA) or stearic acid (SA) residues across a biocompatible hexa(ethylene glycol) (HEG) spacer. The designed materials (i.e., HA-FA-HEG-OA or HA-FA-HEG-SA) showed clear-cut aggregation features in an aqueous environment, as confirmed by dynamic light scattering (DLS) and transmission electron microscopy (TEM), generating nanoaggregate systems. In fact, HA-FA-HEG-OA and HA-FA-HEG-SA derivatives showed the property to create sel…

olanzapinePharmaceutical Science02 engineering and technologyself-assembling nanocarrier010402 general chemistry01 natural sciencesArticlechemistry.chemical_compounddrug delivery systemsDynamic light scatteringhyaluronic acidCopolymerSide chainSolubilityDrug delivery systems; Ferulic acid; Hyaluronic acid; Olanzapine; Oleic acid; Self-assembling nanocarriers; Stearic acidSelf-assembling nanocarriersstearic acid021001 nanoscience & nanotechnology0104 chemical sciencesOleic acidchemistryChemical engineeringoleic acidDrug deliveryStearic acid0210 nano-technologyEthylene glycolferulic acid
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Synthesis and Molecular Modeling Studies of Derivatives of a Highly Potent Peptidomimetic Vinyl Ester as Falcipain-2 Inhibitors

2012

Herein we report the synthesis of a set of constrained peptidomimetics endowed with an electrophilic vinyl ester warhead and structurally related to a previously identified lead compound, a potent and irreversible inhibitor of falcipain-2 (FP-2). FP-2 is the main hemoglobinase of the malaria parasite P. falciparum. The new compounds were evaluated for their inhibition against FP-2, and the results were rationalized on the basis of docking experiments. These studies underscore the pivotal role of both the ester function at the P1' site and the trifluoromethyl group of the P3 side chain in determining the correct orientation of the Michael acceptor warhead in the catalytic site, and as a cons…

peptidomimeticdMolecular modelPeptidomimeticStereochemistryPlasmodium falciparumVinyl esterBiochemistrycysteine proteasesfalcipain-2 inhibitorsAntimalarialschemistry.chemical_compoundCatalytic DomainDrug DiscoverySide chainHumansEnzyme InhibitorsMalaria FalciparumGeneral Pharmacology Toxicology and PharmaceuticsPharmacologyTrifluoromethylOrganic Chemistrydocking studiescysteine proteases; peptidomimeticd; docking studies; falcipain-2 inhibitorsMolecular Docking SimulationCysteine EndopeptidaseschemistryDocking (molecular)Michael reactionMolecular MedicinePeptidomimeticsLead compoundChemMedChem
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Inulin-Based Polymeric Micelles Functionalized with Ocular Permeation Enhancers: Improvement of Dexamethasone Permeation/Penetration through Bovine C…

2021

Ophthalmic drug delivery is still a challenge due to the protective barriers of the eye. A common strategy to promote drug absorption is the use of ocular permeation enhancers, while an innovative approach is the use of polymeric micelles. In the present work, the two mentioned approaches were coupled by conjugating ocular permeation enhancers (PEG2000, carnitine, creatine, taurine) to an inulin-based co-polymer (INU-EDA-RA) in order to obtain self-assembling biopolymers with permeation enhancer properties for the hydrophobic drug dexamethasone (DEX). Inulin derivatives were properly synthetized, were found to expose about 2% mol/mol of enhancer molecules in the side chain, and resulted abl…

permeation enhancermicellesPEG2000InulinPharmaceutical SciencedexamethasoneMicelleocular drug deliveryArticlechemistry.chemical_compoundPharmacy and materia medicaSide chainEnhancerChromatographyinulinPEG<sub>2000</sub>Chemistrypermeation enhancerscarnitinePenetration (firestop)PermeationRS1-441creatineIonic strengthtaurineEx vivoPharmaceutics
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The pentafluorophenyl group as π-acceptor for anions: a case study

2015

Chemical science 6(1), 354-359 (2015). doi:10.1039/C4SC02762K

positive chargesChemistryStereochemistryChemieSolid-stateGeneral Chemistryhapticities540side-chainsstructural dataAcceptor3. Good healthIonevaluation criteriakey elementsComputational chemistryGroup (periodic table)pentafluorophenylddc:540HapticitySide chainStatistical analysiselectron-deficientta116Chemical Science
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Interaction of mushroom tyrosinase with aromatic amines, o-diamines and o-aminophenols

2004

3-Amino-L-tyrosine was found to be a substrate of mushroom tyrosinase, contrary to what had previously been reported in the literature. A series of amino derivatives of benzoic acid were tested as substrates and inhibitors of the enzyme. 3-Amino-4-hydroxybenzoic acid, 4-amino-3-hydroxybenzoic acid and 3,4-diaminobenzoic acid were oxidized by this enzyme, as previously reported for Neurospora crassa tyrosinase, but 4-aminobenzoic acid and 3-aminobenzoic acid were not. Interestingly, 3-amino-4-hydroxybenzoic acid was oxidized five times faster than 4-amino-3-hydroxybenzoic acid, confirming the importance of proton transfer from the hydroxyl group at C-4 position. All compounds inhibited the m…

proton transferStereochemistryTyrosinaseBiophysicsPlasma protein bindingDiaminestyrosinaseAminophenolsBiochemistryCatalysisNeurospora crassachemistry.chemical_compoundo-aminophenolSide chainAminesMolecular BiologyBenzoic acidchemistry.chemical_classificationbiologyMonophenol Monooxygenaseo-phenylenediamineSubstrate (chemistry)biology.organism_classificationOxygenEnzymechemistryElectrophoresis Polyacrylamide GelAgaricalesProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
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