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Anna Vulpetti

Showing results (31-40 of 60) with videos related to

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Journal of the American Chemical Society|April 10, 2007
Polyfluorinated amino acids for sensitive 19F NMR-based screening and kinetic measurementsGianluca Papeo, Patrizia Giordano, Maria Gabriella Brasca, et al.
ACS Medicinal Chemistry Letters|May 26, 2018
Discovery and Design of First Benzylamine-Based Ligands Binding to an Unlocked Conformation of the Complement Factor DAnna Vulpetti, Nils Ostermann, Stefan Randl, et al.
Angewandte Chemie (International Ed. in English)|May 5, 2020
Comprehensive and High-Throughput Exploration of Chemical Space Using Broadband <sup>19</sup> F NMR-Based ScreeningAndreas Lingel, Anna Vulpetti, Tony Reinsperger, et al.
Chemmedchem|December 1, 2016
Synthesis and Biological Evaluation of New Triazolo- and Imidazolopyridine RORγt Inverse AgonistsSamuel Hintermann, Christine Guntermann, Henri Mattes, et al.
Chemmedchem|March 9, 2023
The European Federation for Medicinal Chemistry and Chemical Biology (EFMC) Best Practice Initiative: Hit GenerationJean Quancard, Anna Vulpetti, Anders Bach, et al.
Journal of Chemical Information and Computer Sciences|May 25, 2004
Assessment of docking poses: interactions-based accuracy classification (IBAC) versus crystal structure deviationsRomano T Kroemer, Anna Vulpetti, Joseph J McDonald, et al.
ACS Medicinal Chemistry Letters|October 18, 2019
Design of Potent and Selective Covalent Inhibitors of Bruton's Tyrosine Kinase Targeting an Inactive ConformationRobert Pulz, Daniela Angst, Janet Dawson, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2005
Benzodipyrazoles: a new class of potent CDK2 inhibitorsRoberto D'Alessio, Alberto Bargiotti, Suzanne Metz, et al.
Journal of Medicinal Chemistry|February 4, 2017
Structure-Based Library Design and Fragment Screening for the Identification of Reversible Complement Factor D Protease InhibitorsAnna Vulpetti, Stefan Randl, Simon Rüdisser, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles: a new class of CDK2 inhibitorsPaolo Pevarello, Daniele Fancelli, Anna Vulpetti, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Journal of the American Chemical Society|April 10, 2007
Polyfluorinated amino acids for sensitive 19F NMR-based screening and kinetic measurementsGianluca Papeo, Patrizia Giordano, Maria Gabriella Brasca, et al.
ACS Medicinal Chemistry Letters|May 26, 2018
Discovery and Design of First Benzylamine-Based Ligands Binding to an Unlocked Conformation of the Complement Factor DAnna Vulpetti, Nils Ostermann, Stefan Randl, et al.
Angewandte Chemie (International Ed. in English)|May 5, 2020
Comprehensive and High-Throughput Exploration of Chemical Space Using Broadband <sup>19</sup> F NMR-Based ScreeningAndreas Lingel, Anna Vulpetti, Tony Reinsperger, et al.
Chemmedchem|December 1, 2016
Synthesis and Biological Evaluation of New Triazolo- and Imidazolopyridine RORγt Inverse AgonistsSamuel Hintermann, Christine Guntermann, Henri Mattes, et al.
Chemmedchem|March 9, 2023
The European Federation for Medicinal Chemistry and Chemical Biology (EFMC) Best Practice Initiative: Hit GenerationJean Quancard, Anna Vulpetti, Anders Bach, et al.
Journal of Chemical Information and Computer Sciences|May 25, 2004
Assessment of docking poses: interactions-based accuracy classification (IBAC) versus crystal structure deviationsRomano T Kroemer, Anna Vulpetti, Joseph J McDonald, et al.
ACS Medicinal Chemistry Letters|October 18, 2019
Design of Potent and Selective Covalent Inhibitors of Bruton's Tyrosine Kinase Targeting an Inactive ConformationRobert Pulz, Daniela Angst, Janet Dawson, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2005
Benzodipyrazoles: a new class of potent CDK2 inhibitorsRoberto D'Alessio, Alberto Bargiotti, Suzanne Metz, et al.
Journal of Medicinal Chemistry|February 4, 2017
Structure-Based Library Design and Fragment Screening for the Identification of Reversible Complement Factor D Protease InhibitorsAnna Vulpetti, Stefan Randl, Simon Rüdisser, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
3-Amino-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles: a new class of CDK2 inhibitorsPaolo Pevarello, Daniele Fancelli, Anna Vulpetti, et al.
Pageof 6