Bruno Catalanotti

Bruno Catalanotti

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Bruno Catalanotti

Bruno Catalanotti

Publications by authors named "Bruno Catalanotti"

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Benzylamides and piperazinoarylamides of ibuprofen as fatty acid amide hydrolase inhibitors.

J Enzyme Inhib Med Chem 2019 Dec;34(1):562-576

a Department of Life and Environmental Sciences - Unit of Pharmaceutical, Pharmacological and Nutraceutical Sciences , University of Cagliari , Cagliari , Italy.

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http://dx.doi.org/10.1080/14756366.2018.1532418DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352954PMC
December 2019

Targeting multiple G-quadruplex-forming DNA sequences: Design, biophysical and biological evaluations of indolo-naphthyridine scaffold derivatives.

Eur J Med Chem 2019 Aug 16;182:111627. Epub 2019 Aug 16.

Dipartimento di Scienze della Salute, Università "Magna Græcia", Campus Salvatore Venuta, Viale Europa, 88100, Catanzaro, Italy; Net4Science srl, Università "Magna Græcia", Campus Salvatore Venuta, Viale Europa, 88100, Catanzaro, Italy.

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http://dx.doi.org/10.1016/j.ejmech.2019.111627DOI Listing
August 2019

Novel propanamides as fatty acid amide hydrolase inhibitors.

Eur J Med Chem 2017 Aug 12;136:523-542. Epub 2017 May 12.

Department of Life and Environmental Sciences, Unit of Pharmaceutical, Pharmacological and Nutraceutical Sciences, University of Cagliari, via Ospedale 72, Cagliari I-09124, Italy.

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http://dx.doi.org/10.1016/j.ejmech.2017.05.033DOI Listing
August 2017

Insight into the mechanism of action of plakortins, simple 1,2-dioxane antimalarials.

Org Biomol Chem 2010 Feb 16;8(4):846-56. Epub 2009 Dec 16.

Dipartimento di Chimica delle Sostanze Naturali, Università di Napoli Federico II, Via D. Montesano 49, I-80131 Napoli, Italy.

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http://dx.doi.org/10.1039/b918600jDOI Listing
February 2010

Design and synthesis of potent antimalarial agents based on clotrimazole scaffold: exploring an innovative pharmacophore.

J Med Chem 2007 Feb 31;50(4):595-8. Epub 2007 Jan 31.

Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Universita' di Siena, via Aldo Moro, 53100 Siena, Italy.

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http://dx.doi.org/10.1021/jm061429pDOI Listing
February 2007

Oligonucleotides containing an acridine group covalently bonded to the nucleotide flanking the 3'-3' phosphodiester junction for alternate strand triple helix formation.

Nucleosides Nucleotides Nucleic Acids 2003 May-Aug;22(5-8):1069-71

Dipartimento di Chimica delle Sostanze Naturali, Università di Napoli Federico II, Napoli, Italy.

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http://dx.doi.org/10.1081/NCN-120022738DOI Listing
December 2003

Substrate inhibitors and blockers of excitatory amino acid transporters in the treatment of neurodegeneration: critical considerations.

Eur J Pharmacol 2003 Oct;479(1-3):291-6

Laboratory Receptor Pharmacology, Mario Negri Institute for Pharmacological Research, Via Eritrea 62, 20157, Milan, Italy.

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http://dx.doi.org/10.1016/j.ejphar.2003.08.078DOI Listing
October 2003

Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: past, present, and future perspectives.

Curr Pharm Des 2002 ;8(8):615-57

Dipartimento Farmaco Chimico Tecnologico, Universitá degli Studi di Siena, via Aldo Moro, 53100 Siena, Italy.

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http://dx.doi.org/10.2174/1381612024607207DOI Listing
July 2002

Circular dichroism and thermal melting differentiation of Hoechst 33258 binding to the curved (A(4)T(4)) and straight (T(4)A(4)) DNA sequences.

Biochim Biophys Acta 2002 Jun;1576(1-2):136-42

Centro di Studio per gli Acidi Nucleici del CNR, c/o Dipartimento di Genetica e Biologia Molecolare, Università di Roma La Sapienza, Piazzale Aldo Moro. 5, 00185 Rome, Italy.

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http://dx.doi.org/10.1016/s0167-4781(02)00338-xDOI Listing
June 2002