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Lorenzo Cianni

Showing results (1-10 of 20) with videos related to

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Physical Chemistry Chemical Physics : PCCP|November 5, 2019
Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energyJerônimo Lameira, Vinícius Bonatto, Lorenzo Cianni, et al.
Journal of Medicinal Chemistry|July 31, 2019
Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity?Lorenzo Cianni, Christian Wolfgang Feldmann, Erik Gilberg, et al.
Bioorganic & Medicinal Chemistry|November 30, 2020
Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and LLorenzo Cianni, Fernanda Dos Reis Rocho, Vinícius Bonatto, et al.
Physical Chemistry Chemical Physics : PCCP|September 14, 2018
Experimental study and computational modelling of cruzain cysteine protease inhibition by dipeptidyl nitrilesAlberto Monteiro Dos Santos, Lorenzo Cianni, Daniela De Vita, et al.
Biochimie|April 18, 2016
Perylene and coronene derivatives binding to G-rich promoter oncogene sequences efficiently reduce their expression in cancer cellsEmanuela Micheli, Alessandro Altieri, Lorenzo Cianni, et al.
Bioorganic Chemistry|July 7, 2020
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteasesLorenzo Cianni, Fernanda Dos Reis Rocho, Fabiana Rosini, et al.
Bioorganic Chemistry|May 22, 2018
Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitorsLorenzo Cianni, Geraldo Sartori, Fabiana Rosini, et al.
Journal of Chemical Information and Modeling|March 4, 2020
Assessment of the Cruzain Cysteine Protease Reversible and Irreversible Covalent Inhibition MechanismJosé Rogério A Silva, Lorenzo Cianni, Deborah Araujo, et al.
Molecules (Basel, Switzerland)|June 14, 2018
Natural Aromatic Compounds as Scaffolds to Develop Selective G-Quadruplex Ligands: From Previously Reported Berberine Derivatives to New Palmatine AnaloguesMarco Franceschin, Lorenzo Cianni, Massimo Pitorri, et al.
Bioorganic & Medicinal Chemistry Letters|August 9, 2020
N-Sulfonyl dipeptide nitriles as inhibitors of human cathepsin S: In silico design, synthesis and biochemical characterizationCarina Lemke, Lorenzo Cianni, Christian Feldmann, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Physical Chemistry Chemical Physics : PCCP|November 5, 2019
Predicting the affinity of halogenated reversible covalent inhibitors through relative binding free energyJerônimo Lameira, Vinícius Bonatto, Lorenzo Cianni, et al.
Journal of Medicinal Chemistry|July 31, 2019
Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity?Lorenzo Cianni, Christian Wolfgang Feldmann, Erik Gilberg, et al.
Bioorganic & Medicinal Chemistry|November 30, 2020
Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and LLorenzo Cianni, Fernanda Dos Reis Rocho, Vinícius Bonatto, et al.
Physical Chemistry Chemical Physics : PCCP|September 14, 2018
Experimental study and computational modelling of cruzain cysteine protease inhibition by dipeptidyl nitrilesAlberto Monteiro Dos Santos, Lorenzo Cianni, Daniela De Vita, et al.
Biochimie|April 18, 2016
Perylene and coronene derivatives binding to G-rich promoter oncogene sequences efficiently reduce their expression in cancer cellsEmanuela Micheli, Alessandro Altieri, Lorenzo Cianni, et al.
Bioorganic Chemistry|July 7, 2020
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteasesLorenzo Cianni, Fernanda Dos Reis Rocho, Fabiana Rosini, et al.
Bioorganic Chemistry|May 22, 2018
Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitorsLorenzo Cianni, Geraldo Sartori, Fabiana Rosini, et al.
Journal of Chemical Information and Modeling|March 4, 2020
Assessment of the Cruzain Cysteine Protease Reversible and Irreversible Covalent Inhibition MechanismJosé Rogério A Silva, Lorenzo Cianni, Deborah Araujo, et al.
Molecules (Basel, Switzerland)|June 14, 2018
Natural Aromatic Compounds as Scaffolds to Develop Selective G-Quadruplex Ligands: From Previously Reported Berberine Derivatives to New Palmatine AnaloguesMarco Franceschin, Lorenzo Cianni, Massimo Pitorri, et al.
Bioorganic & Medicinal Chemistry Letters|August 9, 2020
N-Sulfonyl dipeptide nitriles as inhibitors of human cathepsin S: In silico design, synthesis and biochemical characterizationCarina Lemke, Lorenzo Cianni, Christian Feldmann, et al.
Pageof 2