M. Remuiñán

发表

The small-molecule SMARt751 reverses Mycobacterium tuberculosis resistance to ethionamide in acute and chronic mouse models of tuberculosis

G. Drewes, Pablo Gamallo, Markus Boesche, 2022, Science Translational Medicine.

Mycobacterium tuberculosis Gyrase Inhibitors as a New Class of Antitubercular Drugs

J. Lavandera, David Barros, Lluís Ballell, 2015, Antimicrobial Agents and Chemotherapy.

Synthesis and luminiscence properties of europium(III) and terbium(III) complexes with polyacid chelates derived from 2,6-bis(N-pyrazolyl)pyridine

M. Alonso, J. Rodríguez-Ubis, M. Remuiñán, 1993 .

University of Birmingham Identification of Novel Imidazo[1,2-a]pyridine Inhibitors Targeting M. tuberculosis QcrB

N. Loman, C. Constantinidou, M. Pallen, 2012 .

New enantioselective approach to α-allokainoids by Michael addition to chiral 4-substituted 2,3-didehydroprolinate

A. Escribano, J. Ezquerra, A. Rubio, 1995 .

Asymmetric aza-Henry reactions from N-p-tolylsulfinylimines.

J. Alemán, J. L. García Ruano, M. B. Cid, 2005, Organic letters.

4-benzyl-2,3-didehydroprolinate as a homochiral template for michael additions. Synthesis of enantiopure α-allokainoids, β-kainoids, 2,3-methanoprolines and other 3,4-disubstituted prolines

J. J. Vaquero, J. Ezquerra, A. Rubio, 1996 .

Asymmetric aza-Henry reactions from N-p-tolylsulfinylimines.

J. Alemán, J. L. García Ruano, M. B. Cid, 2005, Organic letters.

Total synthesis of ()-pateamine, a novel polyene bis-macrolide with immunosuppressive activity from the sponge Mycale sp.

G. Pattenden, M. Remuiñán, 2000 .

New enantioselective approach to the total synthesis of (−)-α-Kainic Acid

J. J. Vaquero, J. Ezquerra, A. Rubio, 1998 .

Easy Microwave Assisted Deprotection of N-Boc Derivatives

J. Vaquero, Justina Martín, M. Remuiñán, 1998 .

Total synthesis of ()-pateamine A, a novel immunosuppressive agent from Mycale sp

G. Pattenden, M. Remuiñán, D. Critcher, 2004 .

THPP target assignment reveals EchA6 as an essential fatty acid shuttle in mycobacteria

G. Drewes, M. Bantscheff, G. Besra, 2016, Nature Microbiology.

The role of the sulfinyl group in the copper catalyzed benzyl reactions from 2-p-tolylsulfinylbenzylstannanes

J. Alemán, J. L. García Ruano, M. B. Cid, 2009 .

Encoded library technology as a source of hits for the discovery and lead optimization of a potent and selective class of bactericidal direct inhibitors of Mycobacterium tuberculosis InhA.

Hongfang Yang, William McDowell, Paolo A Centrella, 2014, Journal of medicinal chemistry.

Tetrahydropyrazolo[1,5-a]Pyrimidine-3-Carboxamide and N-Benzyl-6′,7′-Dihydrospiro[Piperidine-4,4′-Thieno[3,2-c]Pyran] Analogues with Bactericidal Efficacy against Mycobacterium tuberculosis Targeting MmpL3

N. Loman, C. Constantinidou, M. Pallen, 2013, PloS one.

Easy Microwave Assisted Deprotection of N-Boc Derivatives

J. Vaquero, Justina Martín, M. Remuiñán, 1998 .

N‐Benzyl‐4‐((heteroaryl)methyl)benzamides: A New Class of Direct NADH‐Dependent 2‐trans Enoyl–Acyl Carrier Protein Reductase (InhA) Inhibitors with Antitubercular Activity

J. Sacchettini, M. Convery, Delia Blanco, 2016, ChemMedChem.

Easy-To-Synthesize Spirocyclic Compounds Possess Remarkable in Vivo Activity against Mycobacterium tuberculosis.

Katrina A. Badiola, M. Todd, P. Rutledge, 2018, Journal of medicinal chemistry.

Small-molecule SMARt751 hypersensitizes M. tuberculosis resistant to ethionamide by upregulating the mymA operon

G. Drewes, Markus Boesche, R. Wintjens, 2022 .

Identification of Novel Imidazo[1,2-a]pyridine Inhibitors Targeting M. tuberculosis QcrB

N. Loman, C. Constantinidou, M. Pallen, 2012, PloS one.