0000000000015132

AUTHOR

Paolo Rovero

0000-0001-9577-5228

showing 3 related works from this author

Triterpene glycosides from Blighia welwitschii and evaluation of their antibody recognition capacity in multiple sclerosis

2020

Multiple sclerosis (MS) in a multifactorial autoimmune disease in which reliable biomarkers are needed for therapeutic monitoring and diagnosis. Autoantibodies (autoAbs) are known biomarker candidates although their detection in biological fluids requires a thorough characterization of their associated antigens. Over the past twenty years, a reverse chemical-based approach aiming to screen putative autoantigens has underlined the role of glycans, in particular glucose, in MS. Despite the progress achieved, a lack of consensus regarding the nature of innate antigens as well as difficulties proposing new synthetic glucose-based structures have proved to be obstacles. Here is proposed a strate…

0106 biological sciencesGlycanMultiple SclerosisPlant ScienceHorticultureBiology01 natural sciencesBiochemistryEpitopeAntigenTriterpenemedicineHumansGlycosidesMolecular BiologyAutoimmune diseasechemistry.chemical_classificationmedicine.diagnostic_test010405 organic chemistryAutoantibodyGlycosideGeneral MedicineSaponinsmedicine.diseaseTriterpenes0104 chemical sciencesBiochemistrychemistryImmunoassaybiology.proteinBlighia010606 plant biology & botanyPhytochemistry
researchProduct

Synthesis, structural aspects and bioactivity of the marine cyclopeptide hymenamide C

2001

Abstract Head-to-tail proline containing cyclopeptide hymenamide C [cyclo(Leu-Trp-Pro 3 -Phe-Gly-Pro 6 -Glu); 1 ], isolated from a marine sponge and for which a preliminary immunomodulating activity was reported, was efficiently synthesized by a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/Allyl) via anchoring the ω -carboxyl function of the glutamic acid to the solid support (PAC–PEG–PS). The linear precursor was entirely assembled and subsequently cyclized on resin, yielding a major product identical to the natural hymenamide C and a minor one, a geometric isomer of hymenamide C ( 2 ), differing for the geometry of peptide linkages at Pro residues. Both the ‘proline-rich’ c…

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryElastaseDegranulationPeptideBiological activityGlutamic acidBiochemistryIn vitroSolid-phase synthesisDrug DiscoveryProlineTetrahedron
researchProduct

Synthesis and biological properties of the seven alanine-modified analogues of the marine cyclopeptide hymenamide C

2002

The synthesis and biological activity of the marine cyclopeptide hymenamide C(1), showing an inhibitory effect on human neutrophil elastase degranulation release, were recently described. Based on this result, it was decided to undertake a systematic structure-activity relationship study of this cyclopeptide, based on the Ala-scan technique, in order to obtain useful information for the rational design of additional analogues. The synthesis and characterization of the seven Ala modified analogues are reported and their biological and pharmacological properties are described.

PharmacologyAlanineHuman neutrophilStereochemistryChemistryOrganic ChemistryElastaseRational designBiological activityGeneral MedicineBiochemistrySolid-phase synthesisBiochemistryStructural BiologyBiological propertyDrug DiscoveryMolecular MedicineMolecular BiologyInhibitory effectJournal of Peptide Science
researchProduct