Roberto Quesada, PhD
Affiliations: | Chemistry | University of Burgos |
Website:
http://otri.datacom.st/cien_biotec/suprabur/personal/rquesada.htmGoogle:
"Roberto Quesada"Mean distance: 9.12 | S | N | B | C | P |
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Publications
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| Scorciapino MA, Picci G, Quesada R, et al. (2022) A Simulation Model for the Non-Electrogenic Uniport Carrier-Assisted Transport of Ions across Lipid Membranes. Membranes. 12 |
| Pomorski R, García-Valverde M, Quesada R, et al. (2021) Transmembrane anion transport promoted by thioamides. Rsc Advances. 11: 12249-12253 |
| Valls A, Altava B, Aseyev V, et al. (2021) Structure-antitumor activity relationships of tripodal imidazolium-amino acid based salts. Effect of the nature of the amino acid, amide substitution and anion. Organic & Biomolecular Chemistry. 19: 10575-10586 |
| Picci G, Kubicki M, Garau A, et al. (2020) Simple squaramide receptors for highly efficient anion binding in aqueous media and transmembrane transport. Chemical Communications (Cambridge, England) |
| Davis JT, Gale PA, Quesada R. (2020) Advances in anion transport and supramolecular medicinal chemistry. Chemical Society Reviews |
| Gianotti A, Capurro V, Delpiano L, et al. (2020) Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia. International Journal of Molecular Sciences. 21 |
| Carreira-Barral I, Mielczarek M, Alonso-Carrillo D, et al. (2020) Click-tambjamines as efficient and tunable bioactive anion transporters. Chemical Communications (Cambridge, England) |
| Picci G, Carreira-Barral I, Alonso-Carrillo D, et al. (2020) Simple isophthalamides/dipicolineamides as active transmembrane anion transporters Supramolecular Chemistry. 32: 112-118 |
| Quesada R, Dutzler R. (2019) Alternative chloride transport pathways as pharmacological targets for the treatment of cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |
| Carreira-Barral I, Rumbo C, Mielczarek M, et al. (2019) Small molecule anion transporters display in vitro antimicrobial activity against clinically relevant bacterial strains. Chemical Communications (Cambridge, England) |