Showing results (91-100 of 156) with videos related to

Sort By:
Pageof 16
ACS Medicinal Chemistry Letters|April 19, 2019
Exploiting Chemical Toolboxes for the Expedited Generation of Tetracyclic Quinolines as a Novel Class of PXR AgonistsBruno Cerra, Andrea Carotti, Daniela Passeri, et al.
Chemmedchem|October 2, 2015
Concepts and Molecular Aspects in the Polypharmacology of PARP-1 InhibitorsDaniela Passeri, Emidio Camaioni, Paride Liscio, et al.
Future Medicinal Chemistry|August 4, 2017
Binding properties of different categories of IDO1 inhibitors: a microscale thermophoresis studyFrancesco Antonio Greco, Alice Coletti, Chiara Custodi, et al.
Nucleic Acids Research|December 16, 2006
Glucocorticoid-induced leucine zipper (GILZ)/NF-kappaB interaction: role of GILZ homo-dimerization and C-terminal domainBarbara Di Marco, Michela Massetti, Stefano Bruscoli, et al.
Journal of Separation Science|July 13, 2023
Estimating the hydrophobicity extent of molecular fragments using reversed-phase liquid chromatographyAndrea Carotti, Ina Varfaj, Ilaria Pruscini, et al.
Chemmedchem|October 21, 2020
The Stone Guest: How Does pH Affect Binding Properties of PD-1/PD-L1 Inhibitors?Alessandra Riccio, Alice Coletti, Daniela Dolciami, et al.
Molecular Informatics|August 5, 2016
Pharmacophore-Based Virtual Screening to Discover New Active Compounds for Human Choline Kinase α1Lucía Serrán-Aguilera, Roberto Nuti, Luisa C López-Cara, et al.
European Journal of Medicinal Chemistry|July 18, 2016
Synthesis and biological evaluation of C(5)-substituted derivatives of leukotriene biosynthesis inhibitor BRP-7Serkan Levent, Jana Gerstmeier, Abdurrahman Olgaç, et al.
Journal of Chemical Information and Modeling|August 14, 2008
Molecular field analysis and 3D-quantitative structure-activity relationship study (MFA 3D-QSAR) unveil novel features of bile acid recognition at TGR5Antonio Macchiarulo, Antimo Gioiello, Charles Thomas, et al.
Pageof 16