Publications by authors named "Maria-Cruz Bonache"

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Skeletal Transformations Observed in the Reaction of a Tricyclic Thymine Nucleoside with Dicarbonyl Compounds.
María-Cruz Bonache, Elisa G -Doyagüez, Raúl Benito-Arenas, M Angeles Bonache, María-Luisa Jimeno

ACS Omega· August 2024

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Selective inhibition of Human Immunodeficiency Virus type 1 (HIV-1) by a novel family of tricyclic nucleosides.
María-Cruz Bonache, Alessandra Cordeiro, Ernesto Quesada, Els Vanstreels, Dirk Daelemans

Antiviral Res· October 2011

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One-pot synthesis of polycyclic nucleosides with unusual molecular skeletons.
María-Cruz Bonache, Alessandra Cordeiro, Paula Carrero, Ernesto Quesada, María-José Camarasa

J Org Chem· December 2009

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6-Amino-2-mercapto-3H-pyrimidin-4-one derivatives as new candidates for the antagonism at the P2Y12 receptors.
Pamela Crepaldi, Barbara Cacciari, Maria-Cruz Bonache, Giampiero Spalluto, Katia Varani

Bioorg Med Chem· July 2009

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Novel N-3 substituted TSAO-T derivatives: synthesis and anti-HIV-evaluation.
María-Cruz Bonache, Ernesto Quesada, Chih-Wei Sheen, Jan Balzarini, Nicolas Sluis-Cremer

Nucleosides Nucleotides Nucleic Acids· April 2008

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Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity.
Nunzia Ciliberti, Stefano Manfredini, Angela Angusti, Elisa Durini, Nicola Solaroli, Maria Cruz Bonache

Bioorg Med Chem· April 2007

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A cyclic enamine derived from 1,2-O-isopropylidene-alpha-D-xylofuranose as a novel carbohydrate intermediate to achieve skeletal diversity.
Alessandra Cordeiro, Ernesto Quesada, María-Cruz Bonache, Sonsoles Velazquez, María-José Camarasa

J Org Chem· September 2006

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Design and discovery of a novel dipeptidyl-peptidase IV (CD26)-based prodrug approach.
Carlos García-Aparicio, María-Cruz Bonache, Ingrid De Meester, Ana San-Félix, Jan Balzarini

J Med Chem· August 2006

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Improving the antiviral efficacy and selectivity of HIV-1 reverse transcriptase inhibitor TSAO-T by the introduction of functional groups at the N-3 position.
María-Cruz Bonache, Cristina Chamorro, Sonsoles Velázquez, Erik De Clercq, Jan Balzarini

J Med Chem· October 2005

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Synthesis of novel Bi-, Tri-, and tetracyclic nucleosides by reaction of a common cyclic enamine derived from TSAO-T with nucleophiles.
María-Cruz Bonache, Cristina Chamorro, Alessandra Cordeiro, María-José Camarasa, María-Luisa Jimeno

J Org Chem· December 2004

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N-3 substituted TSAO derivatives as a probe to explore the dimeric interface of HIV-1 reverse transcriptase.
María-Cruz Bonache, Cristina Chamorro, Sonsoles Velázquez, Erik De Clercq, Jan Balzarini

Nucleosides Nucleotides Nucleic Acids· December 2003

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Structure-activity relationship studies on a novel family of specific HIV-1 reverse transcriptase inhibitors.
María-Cruz Bonache, Cristina Chamorro, Esther Lobatón, Erik De Clercq, Jan Balzarini

Antivir Chem Chemother· September 2003

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Synthesis and structural characterization of pyrimidine bi- and tricyclic nucleosides with sugar puckers conformationally locked into the eastern region of the pseudorotational cycle.
Cristina Chamorro, Santos M Luengo, María-Cruz Bonache, Sonsoles Velázquez, María-Jesús Pérez-Pérez

J Org Chem· August 2003

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