Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marco Bartoloni"'
Autor:
Marco Bartoloni, Sandro Waltersperger, Mario Bumann, Achim Stocker, Tamis Darbre, Jean-Louis Reymond
Publikováno v:
ARKIVOC, Vol 2014, Iss 3, Pp 113-123 (2014)
Externí odkaz:
https://doaj.org/article/dd2d4902de1d465db90d7303445b2ccf
Autor:
Julien Furrer, Georg Süss-Fink, Lydia E. H. Paul, Marco Bartoloni, Jean-Louis Reymond, Federico Giannini
Publikováno v:
MedChemCom
In order to improve the water-solubility of dinuclear thiolato-bridged arene ruthenium complexes, a new series was synthesized by conjugating octaarginine, octalysine, and cyclo[Lys-Arg-Gly-Asp-D-Phe] using chloroacetyl thioether (ClAc) ligation, res
Autor:
Ana Ardá, Sabine André, Cristina Nativi, Barbara Richichi, Marco Fragai, Jesús Jiménez-Barbero, Claudio Luchinat, Blanca E. Domínguez, Marco Bartoloni, Hans-Joachim Gabius, Elisa Dragoni
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal; Vol 19
Chemistry-A European Journal; Vol 19
A new strategy to exploit galectin presence to target matrix metalloproteinases (MMPs) is presented. A bifunctional conjugate with lactose and an inhibitor for MMPs is able to bind MMP and Gal-3 simultaneously. This compound might allow the lectin to
Autor:
Rameshwar U. Kadam, Tamis Darbre, Marco Bartoloni, Jean-Louis Reymond, Julien Furrer, Julian Schwartz
Publikováno v:
Chemical Communications
Norbornapeptides (bicyclo[2.2.1]heptapeptides) and related bicyclic homodetic peptides were prepared by solid-phase peptide synthesis using an orthogonal protection scheme. These conformationally rigid peptides cover an almost pristine area of peptid
Autor:
Ivan Dibonaventura, Kathrin Bartho, Olivia Gräbner, Jean-Louis Reymond, Tamis Darbre, Joao Banha, Swathi Bongoni, Michael Sefkow, Marco Bartoloni, Xian Jin, Maria J. Marcaida
Publikováno v:
Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Di Bonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis (2015). Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability. Chemical Science, 6(10), pp. 5473-5490. The Royal Society of Chemistry 10.1039/C5SC01699A
CHEMICAL SCIENCE
CHEMICAL SCIENCE
Double cyclization of short linear peptides obtained by solid phase peptide synthesis was used to prepare bridged bicyclic peptides (BBPs) corresponding to the topology of bridged bicyclic alkanes such as norbornane. Diastereomeric norbornapeptides w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1920ae5ca6de88fec46c9aa9e8ef21f5
https://infoscience.epfl.ch/record/214286
https://infoscience.epfl.ch/record/214286