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Biochemical Society Transactions
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November 18, 2014
C1 domain-targeted isophthalates as protein kinase C modulators: structure-based design, structure-activity relationships and biological activities
Virpi Talman, Riccardo Provenzani, Gustav Boije af Gennäs, et al.
Analytical and Bioanalytical Chemistry
|
March 23, 2019
Immobilization of proteolytic enzymes on replica-molded thiol-ene micropillar reactors via thiol-gold interaction
Sari Tähkä, Jawad Sarfraz, Lauri Urvas, et al.
Scientific Reports
|
April 13, 2021
Multisubstituted pyrimidines effectively inhibit bacterial growth and biofilm formation of Staphylococcus aureus
Riccardo Provenzani, Paola San-Martin-Galindo, Ghada Hassan, et al.
Journal of Chemical Information and Modeling
|
September 11, 2020
Rigorous Computational Study Reveals What Docking Overlooks: Double Trouble from Membrane Association in Protein Kinase C Modulators
Saara Lautala, Riccardo Provenzani, Artturi Koivuniemi, et al.
International Journal of Pharmaceutics
|
November 13, 2019
Design, synthesis and characterization of a PEGylated stanozolol for potential therapeutic applications
Cristian Vergallo, Giulia Torrieri, Riccardo Provenzani, et al.
Plos One
|
April 12, 2018
Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C
Riccardo Provenzani, Ilari Tarvainen, Giulia Brandoli, et al.
Journal of Medicinal Chemistry
|
April 3, 2023
Expanding the Paradigm of Structure-Based Drug Design: Molecular Dynamics Simulations Support the Development of New Pyridine-Based Protein Kinase C-Targeted Agonists
Saara Lautala, Riccardo Provenzani, Ilari Tarvainen, et al.
Briefings in Bioinformatics
|
December 28, 2021
Computationally prioritized drugs inhibit SARS-CoV-2 infection and syncytia formation
Angela Serra, Michele Fratello, Antonio Federico, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Biochemical Society Transactions
|
November 18, 2014
C1 domain-targeted isophthalates as protein kinase C modulators: structure-based design, structure-activity relationships and biological activities
Virpi Talman, Riccardo Provenzani, Gustav Boije af Gennäs, et al.
Analytical and Bioanalytical Chemistry
|
March 23, 2019
Immobilization of proteolytic enzymes on replica-molded thiol-ene micropillar reactors via thiol-gold interaction
Sari Tähkä, Jawad Sarfraz, Lauri Urvas, et al.
Scientific Reports
|
April 13, 2021
Multisubstituted pyrimidines effectively inhibit bacterial growth and biofilm formation of Staphylococcus aureus
Riccardo Provenzani, Paola San-Martin-Galindo, Ghada Hassan, et al.
Journal of Chemical Information and Modeling
|
September 11, 2020
Rigorous Computational Study Reveals What Docking Overlooks: Double Trouble from Membrane Association in Protein Kinase C Modulators
Saara Lautala, Riccardo Provenzani, Artturi Koivuniemi, et al.
International Journal of Pharmaceutics
|
November 13, 2019
Design, synthesis and characterization of a PEGylated stanozolol for potential therapeutic applications
Cristian Vergallo, Giulia Torrieri, Riccardo Provenzani, et al.
Plos One
|
April 12, 2018
Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C
Riccardo Provenzani, Ilari Tarvainen, Giulia Brandoli, et al.
Journal of Medicinal Chemistry
|
April 3, 2023
Expanding the Paradigm of Structure-Based Drug Design: Molecular Dynamics Simulations Support the Development of New Pyridine-Based Protein Kinase C-Targeted Agonists
Saara Lautala, Riccardo Provenzani, Ilari Tarvainen, et al.
Briefings in Bioinformatics
|
December 28, 2021
Computationally prioritized drugs inhibit SARS-CoV-2 infection and syncytia formation
Angela Serra, Michele Fratello, Antonio Federico, et al.
Page
of 1