The structural resemblance between the fused imidazopyridine heterocyclic ring system and purines has prompted biological investigations to assess their potential therapeutic significance. They are known to play a crucial role in numerous disease conditions. The discovery of their first bioactivity as GABAA receptor positive allosteric modulators divulged their medicinal potential. Proton pump inhibitors, aromatase inhibitors, and NSAIDs were also found in this chemical group. Imidazopyridines have the ability to influence many cellular pathways necessary for the proper functioning of cancerous cells, pathogens, components of the immune system, enzymes involved in carbohydrate metabolism, etc. The collective results of biochemical and bioph...
Objective: The present study aims to synthesize a novel derivatives of Imidazo[1,2-a]pyridines and t...
For many years all six isomers of pyridopyridazines have been an interesting class of heterocyclic c...
Imidazole was first synthesized by Heinrich Debus in 1858 and was obtained by the reaction of glyoxa...
The structural resemblance between the fused imidazopyridine heterocyclic ring system and purines ha...
This review presents most of the literature data about imidazo[4,5-b]pyridine derivatives and their ...
The main goal of this article is to present selected syntheses, structures and a various biological ...
Imidazo[1,2-a]pyridine cores have increasing importance in the pharmaceutical industry with their wi...
Les produits appartenant à la famille des pyridopyrimidines sont caractérisés par leur intense utili...
BACKGROUND/AIM: Malignant diseases present a significant public health burden worldwide and their tr...
A series of novel 2-phenyl-3H-imidazo[4,5-b]pyridines and 2-phenyl-3H-imidazo[4,5-c]pyridines and th...
The synthesis of select novel imidazole and imidazopyridine compounds were examined for anti-cancer ...
A series of novel 2-phenyl-3H-imidazo[4,5-b]pyridines and 2-phenyl-3H-imidazo[4,5-c]pyridines and th...
A novel series of tetracyclic imidazo[4, 5- b]pyridine derivatives was designed and synthesized as p...
A series of imidazo[l,2-a]pyridine derivatives of formula (I), being potent modulators of human TNFa...
A series of imidazo[l,2-a]pyridine derivatives of formula (I), being potent modulators of human TNFa...
Objective: The present study aims to synthesize a novel derivatives of Imidazo[1,2-a]pyridines and t...
For many years all six isomers of pyridopyridazines have been an interesting class of heterocyclic c...
Imidazole was first synthesized by Heinrich Debus in 1858 and was obtained by the reaction of glyoxa...
The structural resemblance between the fused imidazopyridine heterocyclic ring system and purines ha...
This review presents most of the literature data about imidazo[4,5-b]pyridine derivatives and their ...
The main goal of this article is to present selected syntheses, structures and a various biological ...
Imidazo[1,2-a]pyridine cores have increasing importance in the pharmaceutical industry with their wi...
Les produits appartenant à la famille des pyridopyrimidines sont caractérisés par leur intense utili...
BACKGROUND/AIM: Malignant diseases present a significant public health burden worldwide and their tr...
A series of novel 2-phenyl-3H-imidazo[4,5-b]pyridines and 2-phenyl-3H-imidazo[4,5-c]pyridines and th...
The synthesis of select novel imidazole and imidazopyridine compounds were examined for anti-cancer ...
A series of novel 2-phenyl-3H-imidazo[4,5-b]pyridines and 2-phenyl-3H-imidazo[4,5-c]pyridines and th...
A novel series of tetracyclic imidazo[4, 5- b]pyridine derivatives was designed and synthesized as p...
A series of imidazo[l,2-a]pyridine derivatives of formula (I), being potent modulators of human TNFa...
A series of imidazo[l,2-a]pyridine derivatives of formula (I), being potent modulators of human TNFa...
Objective: The present study aims to synthesize a novel derivatives of Imidazo[1,2-a]pyridines and t...
For many years all six isomers of pyridopyridazines have been an interesting class of heterocyclic c...
Imidazole was first synthesized by Heinrich Debus in 1858 and was obtained by the reaction of glyoxa...