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4-Quinolone derivatives and their activities against Gram positive pathogens
GF Zhang, S Zhang, B Pan, X Liu, LS Feng - European Journal of Medicinal …, 2018 - Elsevier
Gram-positive bacteria are responsible for a broad range of infectious diseases, and the
emergency and wide spread of drug-resistant Gram-positive pathogens including MRSA …
emergency and wide spread of drug-resistant Gram-positive pathogens including MRSA …
Recent developments of quinolone-based derivatives and their activities against Escherichia coli
F Gao, P Wang, H Yang, Q Miao, L Ma, G Lu - European Journal of …, 2018 - Elsevier
Escherichia coli (E. coli) is the most common pathogen in both hospital and community
settings, and is capable of causing infections that can lead to serious consequences …
settings, and is capable of causing infections that can lead to serious consequences …
Amino acid or peptide conjugates of acridine/acridone and quinoline/quinolone-containing drugs. A critical examination of their clinical effectiveness within a twenty …
M Kukowska - European Journal of Pharmaceutical Sciences, 2017 - Elsevier
Abstract Acridines/acridones, quinolines/quinolones (chromophores) and their derivatives
constitute extremely important family of compounds in current medicine. Great significance …
constitute extremely important family of compounds in current medicine. Great significance …
Molecular modeling studies of novel fluoroquinolone molecules
TR Allaka, NK Katari, V Veeramreddy… - Current Drug …, 2018 - benthamdirect.com
Background: Fluoroquinolones have been the centre of considerable scientific and clinical
interest due to their broad spectrum pharmacological activities. Pefloxacin is an analogue of …
interest due to their broad spectrum pharmacological activities. Pefloxacin is an analogue of …
Synthesis of 6‐Fluoro‐7‐cyclic Amino‐substituted Dicarboxylic Acid Quinolones and their Antibacterial Activity
A Ravi Kumar, G Sathaiah… - Journal of …, 2014 - Wiley Online Library
Novel 1‐carboxymethyl‐6‐fluoro‐7‐cyclic amino‐substituted‐4‐oxo‐1, 4‐dihydroquinolone‐
3‐carboxylic acids 7a, 7b, 7c, 7d, 7e, 7f, 7g, 7h, 7i, 7j, 7k, 7l, 7m, 7n were synthesized as a …
3‐carboxylic acids 7a, 7b, 7c, 7d, 7e, 7f, 7g, 7h, 7i, 7j, 7k, 7l, 7m, 7n were synthesized as a …
Design, synthesis and biological evaluation of novel fluorinated heterocyclic hybrid molecules based on triazole & quinoxaline scaffolds lead to highly potent …
A Chandra Shekhar… - Letters in Drug …, 2015 - ingentaconnect.com
A series of novel fluorinated heterocyclic hybrid molecules based on triazole & quinoxaline
scaffold were designed, synthesized and evaluated for inhibition of Plasmodium falciparum …
scaffold were designed, synthesized and evaluated for inhibition of Plasmodium falciparum …
Synthesis of Novel N‐Triazolo Methyl Substituted Fluoroquinolones and Their Antimicrobial Activity
A Ravi Kumar, G Sathaiah… - Journal of …, 2015 - Wiley Online Library
An elegant synthetic strategy was adopted for the preparation of N‐triazolo methyl
substituted fluoroquinolones 4 and screened for their antimicrobial activity. The synthetic …
substituted fluoroquinolones 4 and screened for their antimicrobial activity. The synthetic …
Synthesis of Novel Trifluoromethyl Substituted Imidazo Fused Quinolone Analogues and their Antibacterial Activity
G Sathaiah, BPV Lingaiah… - Anti-Infective …, 2016 - benthamdirect.com
A series of novel trifluoromethyl substituted imidazo fused quinolone analogues were
prepared, isolated and characterized. The title compounds, thus ob-tained, were …
prepared, isolated and characterized. The title compounds, thus ob-tained, were …