Matías Rey-Carrizo

Easily Accessible Polycyclic Amines that Inhibit the Wild-Type and Amantadine-Resistant Mutants of the M2 Channel of Influenza A Virus

F. J. Luque, R. Lamb, W. DeGrado, 2014, Journal of medicinal chemistry.

Dimerization of pyramidalized 3,4,8,9-tetramethyltetracyclo [4.4.0.0(3,9).0(4,8)]dec-1(6)-ene to a hydrocarbon featuring four cyclohexane rings in boat conformations.

S. Vázquez, Matías Rey-Carrizo, M. Font‐Bardia, 2014, Angewandte Chemie.

Azapropellanes with anti-influenza a virus activity.

L. Naesens, Eva Torres, R. Leiva, 2014, ACS medicinal chemistry letters.

Identification of nonstandard macrocyclic peptide ligands through display screening.

H. Suga, Matías Rey-Carrizo, R. Taylor, 2017, Drug discovery today. Technologies.

Efficient synthesis of phenylene-ethynylene rods and their use as rigid spacers in divalent inhibitors

A. Bernardi, N. Varga, R. Pieters, 2013, Beilstein journal of organic chemistry.

New polycyclic dual inhibitors of the wild type and the V27A mutant M2 channel of the influenza A virus with unexpected binding mode.

F. J. Luque, L. Naesens, J. Juárez-Jiménez, 2015, European journal of medicinal chemistry.

3-Azatetracyclo[5.2.1.1(5,8).0(1,5)]undecane derivatives: from wild-type inhibitors of the M2 ion channel of influenza A virus to derivatives with potent activity against the V27A mutant.

R. Lamb, W. DeGrado, L. Naesens, 2013, Journal of medicinal chemistry.