Showing results (11-20 of 145) with videos related to
Sort By:
Pageof 15
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|June 27, 2008
Cysteine-based chiral selectors for the ligand-exchange separation of amino acidsBenedetto Natalini, Roccaldo Sardella, Antonio Macchiarulo, et al.Journal of Medicinal Chemistry|October 28, 2005
Is antagonism of E/Z-guggulsterone at the farnesoid X receptor mediated by a noncanonical binding site? A molecular modeling studyUdo Meyer, Gabriele Costantino, Antonio Macchiarulo, et al.Journal of Separation Science|February 13, 2008
S-trityl-(R)-cysteine, a powerful chiral selector for the analytical and preparative ligand-exchange chromatography of amino acidsBenedetto Natalini, Roccaldo Sardella, Antonio Macchiarulo, et al.Bioorganic & Medicinal Chemistry|January 27, 2005
Docking studies on PARP-1 inhibitors: insights into the role of a binding pocket water moleculeDaniele Bellocchi, Antonio Macchiarulo, Gabriele Costantino, et al.Journal of Chemical Information and Modeling|March 19, 2009
Charting the chemical space of target sites: insights into the binding modes of amine and amidine groupsAntonio Macchiarulo, Roberto Nuti, Gokcen Eren, et al.Journal of Computer-Aided Molecular Design|September 15, 2006
Pharmacophore model for bile acids recognition by the FPR receptorCristina Ferrari, Antonio Macchiarulo, Gabriele Costantino, et al.ACS Combinatorial Science|March 22, 2013
Building a sulfonamide library by eco-friendly flow synthesisAntimo Gioiello, Emiliano Rosatelli, Michela Teofrasti, et al.Nature Reviews. Drug Discovery|August 2, 2008
Targeting bile-acid signalling for metabolic diseasesCharles Thomas, Roberto Pellicciari, Mark Pruzanski, et al.Expert Opinion on Therapeutic Patents|October 9, 2012
Patented TGR5 modulators: a review (2006 - present)Antimo Gioiello, Emiliano Rosatelli, Roberto Nuti, et al.The Journal of Organic Chemistry|August 2, 2011
Exploring the synthetic versatility of the Lewis acid induced decomposition reaction of α-diazo-β-hydroxy esters. The case of ethyl diazo(3-hydroxy-2-oxo-2,3-dihydro-1H-indol-3-yl)acetateAntimo Gioiello, Francesco Venturoni, Maura Marinozzi, et al.Pageof 15