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6‑Halopyridylmethylidene Penicillin-Based Sulfones Efficien..:

Juan C. Vázquez-Ucha (2747002) ; Diana Rodríguez (7860584) ; Cristina Lasarte-Monterrubio (7324745)...
https://figshare.com/articles/dataset/6_Halopyridylmethylidene_Penicillin-Based_Sulfones_Efficiently_Inactivate_the_Natural_Resistance_of_Pseudomonas_aeruginosa_to_Lactam_Antibiotics/14510781. , 2021

Link: https://doi.org/10.1021/acs.jmedchem.1c00369.s007

RT Journal
T1 <Title>6‑Halopyridylmethylidene Penicillin-Based Sulfones Efficiently Inactivate the Natural Resistance of Pseudomonas aeruginosa to β‑Lactam Antibiotics</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14510781&Exemplar=1&LAN=DE
				
A1 Juan C. Vázquez-Ucha (2747002)
A1 Diana Rodríguez (7860584)
A1 Cristina Lasarte-Monterrubio (7324745)
A1 Emilio Lence (1559887)
A1 Jorge Arca-Suarez (10722972)
A1 María Maneiro (2747005)
A1 Eva Gato (8503593)
A1 Astrid Perez (10722975)
A1 Marta Martínez-Guitián (10722978)
A1 Carlos Juan (54424)
A1 Antonio Oliver (195701)
A1 German Bou (2263219)
A1 Concepción González-Bello (1358856)
A1 Alejandro Beceiro (1559890)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Microbiology
K1 Pharmacology
K1 Infectious Diseases
K1 Virology
K1 Space Science
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 antimicrobial resistance
K1 not-always-evident pocket
K1 inhibition kinetics
K1 Computational studies
K1 chromosomal cephalosporinase AmpC
K1 AmpC β- lactamase
K1 deacylation rate
K1 H 10 helix
K1 antipseudomonal ceftazidime
K1 Natural Resistance
K1 tunnel-like site
K1 AmpC enzymes
K1 drug design
K1 PAO 1
K1 ampC expression levels
K1 Bromide 2
K1 indolizine adduct
K1 Pseudomonas aeruginosa
K1 nosocomial infections
JF https://figshare.com/articles/dataset/6_Halopyridylmethylidene_Penicillin-Based_Sulfones_Efficiently_Inactivate_the_Natural_Resistance_of_Pseudomonas_aeruginosa_to_Lactam_Antibiotics/14510781
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c00369.s007
DO https://doi.org/10.1021/acs.jmedchem.1c00369.s007
SF ELIB - SuUB Bremen

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