Ciencias Biomédicas
Departamento
Pedro Alejandro
Sánchez Murcia
Publikationen, an denen er mitarbeitet Pedro Alejandro Sánchez Murcia (40)
2024
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The repertoire of iron superoxide dismutases from Leishmania infantum as targets in the search for therapeutic agents against leishmaniasis
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 39, Núm. 1
2022
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Identification of 1,2,3-triazolium salt-based inhibitors of Leishmania infantum trypanothione disulfide reductase with enhanced antileishmanial potency in cellulo and increased selectivity
European Journal of Medicinal Chemistry, Vol. 244
2021
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Efficient Dimerization Disruption of Leishmania infantum Trypanothione Reductase by Triazole-phenyl-thiazoles
Journal of Medicinal Chemistry, Vol. 64, Núm. 9, pp. 6137-6160
2020
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A Supramolecular Stabilizer of the 14-3-3ζ/ERα Protein-Protein Interaction with a Synergistic Mode of Action
Angewandte Chemie - International Edition, Vol. 59, Núm. 13, pp. 5284-5287
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Peptides mimicking the β7/β8 loop of HIV'1 reverse transcriptase p51 as “hotspot-targeted” dimerization inhibitors
ACS Medicinal Chemistry Letters, Vol. 11, Núm. 5, pp. 811-817
2019
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Cold-induced aldimine bond cleavage by Tris in: Bacillus subtilis alanine racemase
Organic and Biomolecular Chemistry, Vol. 17, Núm. 17, pp. 4350-4358
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Identification of NEK3 and MOK as novel targets for lithium
Chemical Biology and Drug Design
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Pyrrolopyrimidine vs Imidazole-Phenyl-Thiazole Scaffolds in Nonpeptidic Dimerization Inhibitors of Leishmania infantum Trypanothione Reductase
ACS Infectious Diseases, Vol. 5, Núm. 6, pp. 873-891
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Reaction mechanism of nucleoside 2′-deoxyribosyltransferases: Free-energy landscape supports an oxocarbenium ion as the reaction intermediate
Organic and Biomolecular Chemistry, Vol. 17, Núm. 34, pp. 7891-7899
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Unravelling the covalent binding of zampanolide and taccalonolide AJ to a minimalist representation of a human microtubule
Journal of Computer-Aided Molecular Design, Vol. 33, Núm. 7, pp. 627-644
2018
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A Series of Enthalpically Optimized Docetaxel Analogues Exhibiting Enhanced Antitumor Activity and Water Solubility
Journal of Natural Products, Vol. 81, Núm. 3, pp. 524-533
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Characterization of an atypical, thermostable, organic solvent- and acid-tolerant 2′-deoxyribosyltransferase from Chroococcidiopsis thermalis
Applied Microbiology and Biotechnology, Vol. 102, Núm. 16, pp. 6947-6957
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Engineering Erg10 Thiolase from Saccharomyces cerevisiae as a Synthetic Toolkit for the Production of Branched-Chain Alcohols
Biochemistry, Vol. 57, Núm. 8, pp. 1338-1348
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Enzymatic Synthesis of Therapeutic Nucleosides using a Highly Versatile Purine Nucleoside 2’-DeoxyribosylTransferase from Trypanosoma brucei
ChemCatChem, Vol. 10, Núm. 19, pp. 4406-4416
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Trypanothione reductase inhibition and anti-leishmanial activity of all-hydrocarbon stapled α-helical peptides with improved proteolytic stability
European Journal of Medicinal Chemistry, Vol. 149, pp. 238-247
2017
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2′-Deoxyribosyltransferase from Leishmania mexicana, an efficient biocatalyst for one-pot, one-step synthesis of nucleosides from poorly soluble purine bases
Applied Microbiology and Biotechnology, Vol. 101, Núm. 19, pp. 7187-7200
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First example of peptides targeting the dimer interface of Leishmania infantum trypanothione reductase with potent in vitro antileishmanial activity#
European Journal of Medicinal Chemistry, Vol. 135, pp. 49-59
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Improved proteolytic stability and potent activity against Leishmania infantum trypanothione reductase of α/β-peptide foldamers conjugated to cell-penetrating peptides
European Journal of Medicinal Chemistry, Vol. 140, pp. 615-623
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Making sense of the past: Hyperstability of ancestral thioredoxins explained by free energy simulations
Physical Chemistry Chemical Physics, Vol. 19, Núm. 34, pp. 23239-23246
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Structural rationale for the cross-resistance of tumor cells bearing the A399V variant of elongation factor eEF1A1 to the structurally unrelated didemnin B, ternatin, nannocystin A and ansatrienin B
Journal of Computer-Aided Molecular Design, Vol. 31, Núm. 10, pp. 915-928