F. Cortés-Selva

Celastraceae Sesquiterpenes as a New Class of Modulators That Bind Specifically to Human P-Glycoprotein and Reverse Cellular Multidrug Resistance

J. M. Pérez-Victoria, Á. Ravelo, S. Castanys, 2004, Cancer Research.

Dihydro-beta-agarofuran sesquiterpenes: a new class of reversal agents of the multidrug resistance phenotype mediated by P-glycoprotein in the protozoan parasite Leishmania.

L. Pardo, Á. Ravelo, S. Castanys, 2005, Current pharmaceutical design.

Functional expression of a multidrug P-glycoprotein transporter of Leishmania.

S. Castanys, F. Gamarro, F. Muñoz-Martínez, 2005, Biochemical and Biophysical Research Communications - BBRC.

SAR studies of dihydro-beta-agarofuran sesquiterpenes as inhibitors of the multidrug-resistance phenotype in a Leishmania tropica line overexpressing a P-glycoprotein-like transporter.

L. Pardo, Á. Ravelo, S. Castanys, 2004, Journal of medicinal chemistry.

Chemosensitization of a multidrug-resistant Leishmania tropica line by new sesquiterpenes from Maytenus magellanica and Maytenus chubutensis.

M. L. Kennedy, J. M. Pérez-Victoria, Á. Ravelo, 2001, Journal of medicinal chemistry.

Absolute configuration and complete assignment of 13C NMR data for new sesquiterpenes from Maytenus chiapensis.

Á. Ravelo, I. L. Bazzocchi, J. Gavín, 2003, Journal of natural products.

Combination of Suboptimal Doses of Inhibitors Targeting Different Domains of LtrMDR1 Efficiently Overcomes Resistance of Leishmania spp. to Miltefosine by Inhibiting Drug Efflux

Maria Paola Costi, J. M. Pérez-Victoria, A. di Pietro, 2006, Antimicrobial Agents and Chemotherapy.

Leishmanicidal constituents from the leaves of Piper rusbyi.

J. Piñero, A. Giménez, I. L. Bazzocchi, 2007, Planta medica.