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Florenci V. González

Affiliations: 
Universitat Jaume I, Spain 
Area:
organic synthesis, medicinal chemistry
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Parents

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Miguel Carda grad student 1991-1995 Universitat Jaume I
Alberto Marco grad student 1991-1995 Universitat de València
William R. Roush post-doc 1995-1998 Indiana University
Robert Michael Williams post-doc 1998-1998 Colorado State

Children

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Irakusne López grad student 2005-2009 Universitat Jaume I
Javi Izquierdo grad student 2006-2011 Universitat Jaume I
Juan Agut grad student 2010-2014 Universitat Jaume I
Antonio Latorre grad student 2010-2015 Universitat Jaume I
Andreu Vidal grad student 2011-2016 Universitat Jaume I
María Kneeteman post-doc 2005-2006 Universitat Jaume I
Pedro Mancini post-doc 2007-2008 Universitat Jaume I
Amitkumar C. Jain post-doc 2009-2012 Universitat Jaume I (Computer Science Tree)
Víctor Macías post-doc 2017-2018 Universitat Jaume I
Santiago Royo post-doc 2015-2020 Universitat Jaume I

Collaborators

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Publications

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Fernández-de-la-Pradilla A, Royo S, Schirmeister T, et al. (2023) Impact of the Warhead of Dipeptidyl Keto Michael Acceptors on the Inhibition Mechanism of Cysteine Protease Cathepsin L. Acs Catalysis. 13: 13354-13368
Arafet K, Royo S, Schirmeister T, et al. (2023) Impact of the Recognition Part of Dipeptidyl Nitroalkene Compounds on the Inhibition Mechanism of Cysteine Proteases Cruzain and Cathepsin L. Acs Catalysis. 13: 6289-6300
Macías-Villamizar VE, Cuca-Suárez L, Rodríguez S, et al. (2020) Formal [3+2] Cycloaddition Reactions of Electron-Rich Aryl Epoxides with Alkenes under Lewis Acid Catalysis Affording Tetrasubstituted Tetrahydrofurans. Molecules (Basel, Switzerland). 25
Bou-Iserte L, Latorre A, Rodríguez S, et al. (2019) Three-Step Telescoped Synthesis of Monosubstituted Vicinal Diamines from Aldehydes. Acs Omega. 4: 2261-2267
Royo S, Schirmeister T, Kaiser M, et al. (2018) Antiprotozoal and cysteine proteases inhibitory activity of dipeptidyl enoates. Bioorganic & Medicinal Chemistry
Latorre A, Schirmeister T, Kesselring J, et al. (2016) Dipeptidyl Nitroalkenes as Potent Reversible Inhibitors of Cysteine Proteases Rhodesain and Cruzain. Acs Medicinal Chemistry Letters. 7: 1073-1076
Royo S, Rodríguez S, Schirmeister T, et al. (2015) Dipeptidyl Enoates As Potent Rhodesain Inhibitors That Display a Dual Mode of Action. Chemmedchem. 10: 1484-7
Latorre A, Rodríguez S, González FV, et al. (2015) Synthetic Studies on the Preparation of Alanyl Epoxysulfones as Cathepsin Cysteine Protease Electrophilic Traps. The Journal of Organic Chemistry. 80: 7752-6
Willemen HL, Campos PM, Lucas E, et al. (2014) A novel p38 MAPK docking-groove-targeted compound is a potent inhibitor of inflammatory hyperalgesia. The Biochemical Journal. 459: 427-39
Fabregat-Cabello N, Sancho JV, Vidal A, et al. (2014) Development and validation of a liquid chromatography isotope dilution mass spectrometry method for the reliable quantification of alkylphenols in environmental water samples by isotope pattern deconvolution. Journal of Chromatography. A. 1328: 43-51
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