Química Orgánica
Department
Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublications in collaboration with researchers from Instituto de Parasitología y Biomedicina López Neyra (24)
2021
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Synthesis of sp2-Iminosugar Selenoglycolipids as Multitarget Drug Candidates with Antiproliferative, Leishmanicidal and Anti-Inflammatory Properties
Molecules (Basel, Switzerland), Vol. 26, Núm. 24
2019
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Synthesis of polyfluoroalkyl sp2-iminosugar glycolipids and evaluation of their immunomodulatory properties towards anti-tumor, anti-leishmanial and anti-inflammatory therapies
European Journal of Medicinal Chemistry, Vol. 182
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Thiol-ene "click" synthesis and pharmacological evaluation of C-glycoside sp2-iminosugar glycolipids
Molecules, Vol. 24, Núm. 16
2016
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Optimization by Molecular Fine Tuning of Dihydro-β-agarofuran Sesquiterpenoids as Reversers of P-Glycoprotein-Mediated Multidrug Resistance
Journal of Medicinal Chemistry, Vol. 59, Núm. 5, pp. 1880-1890
2015
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Antileishmanial activity of sp2-iminosugar derivatives
RSC Advances, Vol. 5, Núm. 28, pp. 21812-21822
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Restoration of chemosensitivity in P-glycoprotein-dependent multidrug-resistant cells by dihydro-β-agarofuran sesquiterpenes from Celastrus vulcanicola
Journal of Natural Products, Vol. 78, Núm. 4, pp. 736-745
2011
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Leishmanicidal and reversal multidrug resistance constituents from Aeonium lindleyi
Planta Medica, Vol. 77, Núm. 1, pp. 77-80
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Overcoming human P-glycoprotein-dependent multidrug resistance with novel dihydro-β-agarofuran sesquiterpenes
European Journal of Medicinal Chemistry, Vol. 46, Núm. 10, pp. 4915-4923
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Terpenoids from maytenus species and assessment of their reversal activity against a multidrug-resistant leishmania tropica line
Chemistry and Biodiversity, Vol. 8, Núm. 12, pp. 2291-2298
2009
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Novel dihydro-β-agarofuran sesquiterpenes as potent modulators of human P-glycoprotein dependent multidrug resistance
Organic and Biomolecular Chemistry, Vol. 7, Núm. 24, pp. 5166-5172
2008
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Bis-pyranobenzoquinones as a new family of reversal agents of the multidrug resistance phenotype mediated by P-glycoprotein in mammalian cells and the protozoan parasite Leishmania
Journal of Medicinal Chemistry, Vol. 51, Núm. 22, pp. 7132-7143
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New terpenoids from Maytenus apurimacensis as MDR reversal agents in the parasite Leishmania
Bioorganic and Medicinal Chemistry, Vol. 16, Núm. 3, pp. 1425-1430
2007
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Biological evaluation, structure-activity relationships, and three-dimensional quantitative structure-activity relationship studies of dihydro-β-agarofuran sesquiterpenes as modulators of P-glycoprotein- dependent multidrug resistance
Journal of Medicinal Chemistry, Vol. 50, Núm. 20, pp. 4808-4817
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Leishmanicidal constituents from the leaves of Piper rusbyi
Planta Medica, Vol. 73, Núm. 3, pp. 206-211
2006
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Insights into the molecular mechanism of action of Celastraceae sesquiterpenes as specific, non-transported inhibitors of human P-glycoprotein
Biochimica et Biophysica Acta - Biomembranes, Vol. 1758, Núm. 1, pp. 98-110
2005
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Dihidro-β-agarofuran sesquiterpenes: A new class of reversal agents of the multidrug resistance phenotype mediated by P-glycoprotein in the protozoan parasite Leishmania
Current Pharmaceutical Design, Vol. 11, Núm. 24, pp. 3125-3159
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Functional expression of a multidrug P-glycoprotein transporter of Leishmania
Biochemical and Biophysical Research Communications, Vol. 329, Núm. 2, pp. 502-507
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Reversion of human Pgp-dependent multidrug resistance by new sesquiterpenes from Zinowiewia costaricensis
Journal of Medicinal Chemistry, Vol. 48, Núm. 13, pp. 4266-4275
2004
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Celastraceae sesquiterpenes as a new class of modulators that bind specifically to human P-glycoprotein and reverse cellular multidrug resistance
Cancer Research, Vol. 64, Núm. 19, pp. 7130-7138
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SAR Studies of Dihydro-β-agarofuran Sesquiterpenes as Inhibitors of the Multidrug-Resistance Phenotype in a Leishmania tropica Line Overexpressing a P-Glycoprotein-Like Transporter
Journal of Medicinal Chemistry, Vol. 47, Núm. 3, pp. 576-587