Idaira Hueso-Falcón

Synthesis and induction of apoptosis signaling pathway of ent-kaurane derivatives.

Á. Ravelo, S. Hortelano, A. Estévez-Braun, 2010, Bioorganic & medicinal chemistry.

Indium catalyzed solvent-free multicomponent synthesis of cytotoxic dibenzo[a,h]anthracenes from aldehydes, 2-hydroxy-1,4-naphthoquinone, and 2-naphthol

A. Estévez-Braun, L. Fernández-Pérez, Idaira Hueso-Falcón, 2014 .

Synthesis and biological evaluation of naphthoquinone-coumarin conjugates as topoisomerase II inhibitors.

A. Estévez-Braun, F. Machín, Idaira Hueso-Falcón, 2017, Bioorganic & medicinal chemistry letters.

Indium Catalyzed Solvent‐Free Multicomponent Synthesis of Cytotoxic Dibenzo[a,h]anthracenes from Aldehydes, 2‐Hydroxy‐1,4‐naphthoquinone, and 2‐Naphthol.

A. Estévez-Braun, L. Fernández-Pérez, Idaira Hueso-Falcón, 2015 .

Antiproliferative and quinone reductase-inducing activities of withanolides derivatives.

J. Pezzuto, R. V. van Breemen, J. Padrón, 2014, European journal of medicinal chemistry.

A Novel Naphthoquinone-Coumarin Hybrid That Inhibits BCR-ABL1-STAT5 Oncogenic Pathway and Reduces Survival in Imatinib-Resistant Chronic Myelogenous Leukemia Cells

B. Guerra, A. Estévez-Braun, F. Estévez, 2019, Front. Pharmacol..

CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia

J. Montero, A. Pandiella, R. Blanco, 2016, Oncotarget.

CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia

Leandro, J. Montero, A. Pandiella, 2016, Oncotarget.

Synthesis and anti-inflammatory activity of ent-kaurene derivatives.

Á. Ravelo, S. Hortelano, A. Estévez-Braun, 2011, European journal of medicinal chemistry.