T. Mena-Barragán

发表

Unprecedented inhibition of glycosidase-catalyzed substrate hydrolysis by nanodiamond-grafted O-glycosides

R. Boukherroub, S. Szunerits, C. O. Mellet, 2015 .

Inhibitor versus chaperone behaviour of d-fagomine, DAB and LAB sp(2)-iminosugar conjugates against glycosidases: A structure-activity relationship study in Gaucher fibroblasts.

K. Higaki, E. Nanba, C. Ortiz Mellet, 2016, European journal of medicinal chemistry.

A bicyclic 1-deoxygalactonojirimycin derivative as a novel pharmacological chaperone for GM1 gangliosidosis.

Kei Yura, Yasubumi Sakakibara, Katsumi Higaki, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

Stereoselective synthesis of 2-acetamido-1,2-dideoxyallonojirimycin (DAJNAc), a new potent hexosaminidase inhibitor.

A. Riera, C. Ortiz Mellet, J. G. García Fernández, 2013, Organic letters.

Tuning glycosidase inhibition through aglycone interactions: pharmacological chaperones for Fabry disease and GM1 gangliosidosis.

Y. Sakakibara, K. Yura, K. Higaki, 2012, Chemical communications.

Iminosugar-based glycopolypeptides: glycosidase inhibition with bioinspired glycoprotein analogue micellar self-assemblies.

C. Ortiz Mellet, Colin Bonduelle, S. Lecommandoux, 2014, Chemical communications.

Fluorinated hydroxypiperidines as selective β-glucosidase inhibitors.

C. Ortiz Mellet, D. Gueyrard, T. Mena-Barragán, 2015, Organic & biomolecular chemistry.

Probing the Inhibitor versus Chaperone Properties of sp2-Iminosugars towards Human β-Glucocerebrosidase: A Picomolar Chaperone for Gaucher Disease

K. Higaki, E. Nanba, R. Pieters, 2018, Molecules.

Stereoselective synthesis of 2-acetamido-1,2-dideoxynojirimycin (DNJNAc) and ureido-DNJNAc derivatives as new hexosaminidase inhibitors.

A. Riera, C. Ortiz Mellet, J. G. García Fernández, 2015, Organic & biomolecular chemistry.

Unexpected loss of stereoselectivity in glycosylation reactions during the synthesis of chondroitin sulfate oligosaccharides

P. Nieto, J. D. de Paz, T. Mena-Barragán, 2019, Beilstein journal of organic chemistry.

pH-Responsive Pharmacological Chaperones for Rescuing Mutant Glycosidases.

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2015, Angewandte Chemie.

Molecular basis of 1-deoxygalactonojirimycin arylthiourea binding to human α-galactosidase a: pharmacological chaperoning efficacy on Fabry disease mutants.

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2014, ACS chemical biology.

PDA-Based Glyconanomicelles for Hepatocellular Carcinoma Cells Active Targeting Via Mannose and Asialoglycoprotein Receptors

J. Muntané, E. Navarro-Villarán, E. Romero-Ben, 2021 .