Follow
Lu Lu
Lu Lu
icm
Verified email at icm.uu.se
Title
Cited by
Cited by
Year
Boronic ester-linked macrocyclic lipopeptides as serine protease inhibitors targeting Escherichia coli type I signal peptidase
N Szałaj, L Lu, A Benediktsdottir, E Zamaratski, S Cao, G Olanders, ...
European Journal of Medicinal Chemistry 157, 1346-1360, 2018
172018
Design, synthesis and in vitro biological evaluation of oligopeptides targeting E. coli type I signal peptidase (LepB)
M De Rosa, L Lu, E Zamaratski, N Szałaj, S Cao, H Wadensten, ...
Bioorganic & Medicinal Chemistry 25 (3), 897-911, 2017
172017
Antibacterial sulfonimidamide-based oligopeptides as type I signal peptidase inhibitors: Synthesis and biological evaluation
A Benediktsdottir, L Lu, S Cao, E Zamaratski, A Karlén, SL Mowbray, ...
European Journal of Medicinal Chemistry 224, 113699, 2021
112021
Synthesis and In Vitro Biological Evaluation of Quinolinyl Pyrimidines Targeting Type II NADH-Dehydrogenase (NDH-2)
L Lu, L Åkerbladh, S Ahmad, V Konda, S Cao, A Vocat, L Maes, ST Cole, ...
ACS Infectious Diseases 8 (3), 482-498, 2022
22022
Structural and Biochemical Characterizations of Three Potential Drug Targets from Pathogens
L Lu
Acta Universitatis Upsaliensis, 2021
2021
MEPicides: α, β-Unsaturated Fosmidomycin N-acyl Analogsas inhibitors that selectively target DXR from Plasmodium falciparum, the deadliest causative parasite of human Malaria
L Lu, X Wang, RL Edwards, S Sooriyaarachchi, A Haymond, T Bergfors, ...
2021
Novel macrocyclic lipopeptides as serine protease inhibitors targeting Escherichia coli type I signal peptidase
A Benediktsdottir, NN Szalaj, L Lu, E Zamaratski, S Cao, G Olanders, ...
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 258, 2019
2019
Synthesis and in vitro biological evaluation of quinolinyl pyrimidines targeting type II NADH-dehydrogenase (NDH-2)
L Åkerbladh, L Lu, K Konda, S Cao, A Vocat, L Maes, ST Cole, D Hughes, ...
2017
The system can't perform the operation now. Try again later.
Articles 1–8