Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Elisa Danieli"'
Autor:
Maria Rosaria Romano, Elisa Danieli, Marta Tontini, Gabriele Costantini, Francesco Berti, Daniela Proietti, Paolo Costantino, Roberto Adamo, Giulia Brogioni
Publikováno v:
Journal of Carbohydrate Chemistry. 30:249-280
Laminarin-CRM197 glycoconjugates were previously demonstrated to be immunogenic and confer protection against Candida albicans in mice. Laminarin consists of β-(1,3) glucan repeating units, with sporadic β-(1,6) branches. A set of short glucans was
Publikováno v:
Organic Letters. 13:378-381
Clostridium difficile is the most commonly diagnosed cause of nosocomial diarrhea with increasing incidence and mortality among elderly and hospitalized patients. We report the first synthesis of the surface polysaccharide PS-II repeating unit and it
Autor:
Gloria Menchi, Anna Bottoncetti, Elisa Danieli, Alberto Pupi, Antonio Guarna, S. Raspanti, Donatella Potenza, and Andrea Trabocchi, Nicoletta Cini
Publikováno v:
Amino Acids. 38:329-337
3-Aza-6,8-dioxabicyclo[3.2.1]octane-based amino acids as reverse turn inducers have been introduced into cyclic peptidomimetics containing the RGD or DGR retro-sequence, in order to achieve a stereochemical scanning of the binding capability of the r
Publikováno v:
Amino Acids. 35:37-44
Delta-amino acids are very attractive in drug discovery, especially in the peptidomimetic area, because of their capability to act as dipeptide isosteres and reverse turn mimetics. Herein we report the synthesis of a rigid delta-amino acid constraine
Publikováno v:
Tetrahedron. 63:6827-6834
Iminosugars are inhibitors of glycoprocessing and are of interest as scaffolds for medicinal chemistry, as their successful application as peptide mimetics has shown. The synthesis of novel peptidomimetics based on 1-deoxynojirimycin (DNJ) requires p
Publikováno v:
European Journal of Organic Chemistry. 2007:1659-1668
A new set of β-turn mimetics incorporating a bicyclic turn inducer was achieved by use of the solid-phase Petasis reaction in a stereoselective fashion. The stereoselectivity of the reaction turned out to be dependent on the side chain of the amino
Publikováno v:
European Journal of Organic Chemistry. 2005:4372-4381
Constrained bicyclic β- and γ/δ-amino acids using glycidol and sugar derivatives were developed. The synthetic strategies involved epoxide ring opening of a glycidol derivative, and subsequent coupling with sugar-derived amines, leading to di- or
Autor:
Osman S. Cakici, Mario A. Monteiro, Cesira Galeotti, Maria Scarselli, Elisa Danieli, Francesco Berti, Emilia Cappelletti, Roberto Adamo, Daniela Proietti, Marta Tontini, Vittoria Pinto, Maria Rosaria Romano, Barbara Brogioni, Rosanna Leuzzi, Paolo Costantino, Erwin Swennen, Luigi Lay
Publikováno v:
ACS chemical biology. 7(8)
Clostridium difficile is emerging worldwide as a major cause of nosocomial infections. The negatively charged PSII polysaccharide has been found in different strains of C. difficile and, thereby, represents an important target molecule for a possible
Autor:
Luigi Lay, Elisa Danieli, Francesco Berti, Emilia Cappelletti, Daniela Proietti, Paolo Costantino, Marta Tontini, Roberto Adamo, Giulia Brogioni, Maria Rosaria Romano
Publikováno v:
Bioorganicmedicinal chemistry. 20(21)
Staphylococcus aureus is a major cause of nosocomial infections. Glycoconjugates of type 5 and 8 capsular polysaccharides have been investigated for vaccine application. The proposed structure of type 5 polysaccharide is: →4-β-D-ManNAcA-(1→4)-α
A new phosphorylated derivative of carboxymethylcellulose and amidic carboxymethylcellulose containing one phosphate group for each disaccharide unit was synthesized using sodium trimetaphospahte (STMP) as the phosphating agent. The new polysaccharid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ee5cb67d16ce78fb3076f5416c9025
http://hdl.handle.net/11365/34264
http://hdl.handle.net/11365/34264