Probing linker design in citric acid–ciprofloxacin conjugates
-
Add time:09/07/2019 Source:sciencedirect.com
A series of structurally related citric acid–ciprofloxacin conjugates was synthesised to investigate the influence of the linker between citric acid and ciprofloxacin on antibacterial activities. Minimum inhibitory concentrations (MICs) were determined against a panel of reference strains and clinical isolates of bacteria associated with infection in humans and correlated with the DNA gyrase inhibitory activity. The observed trend was rationalised by computational modelling.
We also recommend Trading Suppliers and Manufacturers of Citric Acid tert-Butyl Ester (cas 114340-52-2). Pls Click Website Link as below: cas 114340-52-2 suppliers
Prev:Enzymatic resolution of Z-γ,γ′-di-tert-butyl-D,L-carboxyglutamic acid methyl ester
Next:An efficient synthesis of methyl N-[2-(R)-(1-napthylmethyl)-3-(morpholinocarbonyl)propionyl]-(S)-histidinate, the key synthetic intermediate of renin inhibitors) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Enzymatic resolution of Z-γ,γ′-di-tert-butyl-D,L-carboxyglutamic acid methyl ester09/06/2019
- Impact of thermooxidation of phytosteryl and phytostanyl fatty acid esters on cholesterol micellarization in vitro09/05/2019
- Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters09/04/2019
-
Health and Chemical more >


