A series of thiazole based amides have been designed and synthesized by solution-phase amide coupling of 2-aminothiazole and its derivatives with naturally occurring aromatic and heteroaromatic acids in excellent yield via DIC/HOBt protocol All the compounds have been evaluated for their antitubercular activity against M. tuberculosis virulent strain M. tuberculosis H37Rv and PknG inhibitory activity in the presence and absence of the inhibitors The compounds display moderate to significant PknG inhibitory activity (9.1-15.6% inhibition at 100 µM) as compared to the standard inhibitors and very moderate in vitro antitubercular activities against M. tuberculosis virulent strain M. tuberculosis H37Rv.
AbstractA small library of compounds are synthesized and evaluated for their in vitro antitubercular...
The recent emergence of drug-resistant strains of Mycobacterium tuberculosis (Mtb) has complicated a...
Objective: The objective of the paper was to synthesize and characterize new derivatives of thiazole...
To determine antimycobacterium and dTDP rhamnose inhibitor activity of the synthesized azetidinone, ...
Molecular design: The novel molecule of 2,4-substituted thiazolidine derivatives are designed by us...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
1388-1399The history of incessant struggle and the current global burden associated with emerging in...
The history of incessant struggle and the current global burden associated with emerging infectious ...
International audienceThe recent emergence of drug-resistant strains of Mycobacterium tuberculosis (...
International audienceThe recent emergence of drug-resistant strains of Mycobacterium tuberculosis (...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusTuberculosis (TB), caused...
Glutamine synthetase I is a vital enzyme present in the cell wall of Mycobacterium tuberculosis H37R...
A series of substituted 2-amino-1,3-thiazines were synthesized as amides (9a-9i), carbamates (9j-9m)...
AbstractA small library of compounds are synthesized and evaluated for their in vitro antitubercular...
The recent emergence of drug-resistant strains of Mycobacterium tuberculosis (Mtb) has complicated a...
Objective: The objective of the paper was to synthesize and characterize new derivatives of thiazole...
To determine antimycobacterium and dTDP rhamnose inhibitor activity of the synthesized azetidinone, ...
Molecular design: The novel molecule of 2,4-substituted thiazolidine derivatives are designed by us...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
Purpose: To synthesize and characterize novel thiazolidinone derivatives and screen them for antitub...
1388-1399The history of incessant struggle and the current global burden associated with emerging in...
The history of incessant struggle and the current global burden associated with emerging infectious ...
International audienceThe recent emergence of drug-resistant strains of Mycobacterium tuberculosis (...
International audienceThe recent emergence of drug-resistant strains of Mycobacterium tuberculosis (...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusTuberculosis (TB), caused...
Glutamine synthetase I is a vital enzyme present in the cell wall of Mycobacterium tuberculosis H37R...
A series of substituted 2-amino-1,3-thiazines were synthesized as amides (9a-9i), carbamates (9j-9m)...
AbstractA small library of compounds are synthesized and evaluated for their in vitro antitubercular...
The recent emergence of drug-resistant strains of Mycobacterium tuberculosis (Mtb) has complicated a...
Objective: The objective of the paper was to synthesize and characterize new derivatives of thiazole...