Salicylanilide diethyl phosphates: Synthesis, antimicrobial activity and cytotoxicity

Bioorganic & Medicinal Chemistry
2014.0

Abstract

A series of 27 salicylanilide diethyl phosphates was prepared as a part of our on-going search for new antimicrobial active drugs. All compounds exhibited in vitro activity against Mycobacterium tuberculosis, Mycobacterium kansasii and Mycobacterium avium strains, with minimum inhibitory concentration (MIC) values of 0.5-62.5μmol/L. Selected salicylanilide diethyl phosphates also inhibit multidrug-resistant tuberculous strains at the concentration of 1μmol/L. Salicylanilide diethyl phosphates also exhibited mostly the activity against Gram-positive bacteria (MICs ≥1.95μmol/L), whereas their antifungal activity is significantly lower. The IC50 values for Hep G2 cells were within the range of 1.56-33.82μmol/L, but there is no direct correlation with MICs for mycobacteria.

Knowledge Graph

Similar Paper

Salicylanilide diethyl phosphates: Synthesis, antimicrobial activity and cytotoxicity
Bioorganic & Medicinal Chemistry 2014.0
Salicylanilide carbamates: Antitubercular agents active against multidrug-resistant Mycobacterium tuberculosis strains
Bioorganic & Medicinal Chemistry 2010.0
Novel derivatives of nitro-substituted salicylic acids: Synthesis, antimicrobial activity and cytotoxicity
Bioorganic & Medicinal Chemistry 2015.0
Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity
Bioorganic & Medicinal Chemistry 2017.0
Synthesis and biological activity of new salicylanilide N,N-disubstituted carbamates and thiocarbamates
Bioorganic & Medicinal Chemistry 2014.0
Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates
Bioorganic & Medicinal Chemistry 2015.0
Combating highly resistant emerging pathogen Mycobacterium abscessus and Mycobacterium tuberculosis with novel salicylanilide esters and carbamates
European Journal of Medicinal Chemistry 2015.0
Salicylanilide esters of N-protected amino acids as novel antimicrobial agents
Bioorganic & Medicinal Chemistry Letters 2009.0
Salicylanilide N-monosubstituted carbamates: Synthesis and in vitro antimicrobial activity
Bioorganic & Medicinal Chemistry 2016.0
New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species
Bioorganic & Medicinal Chemistry 2013.0