1443221-48-4Relevant academic research and scientific papers
An efficient one-pot synthesis of functionally diverse 2-aminothiazoles from isothiocyanates, amidines/guanidines and halomethylenes
Jalani, Hitesh B.,Pandya, Amit N.,Pandya, Dhaivat H.,Sharma, Jayesh A.,Sudarsanam,Vasu, Kamala K.
, p. 5403 - 5406 (2013/09/12)
An efficient one-pot method for the synthesis of 2-aminothiazoles using simple starting materials like isothiocyanates, amidines/guanidines and various halomethylenes is reported. The synthesis of 2-aminothiazoles involves reactions such as nucleophilic a
New insight into adenosine receptors selectivity derived from a novel series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamides and furamides
Inamdar, Gajanan S.,Pandya, Amit N.,Thakar, Hardik M.,Sudarsanam, Vasudevan,Kachler, Sonja,Sabbadin, Davide,Moro, Stefano,Klotz, Karl-Norbert,Vasu, Kamala K.
, p. 924 - 934 (2013/07/27)
A series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamide and furamide analogues were investigated in radioligand binding studies at adenosine receptor subtypes with an aim to obtain potent and selective adenosine receptor ligands. Benzamide and furamide linked to thiazole was found to be crucial for high adenosine receptor affinity. The most potent compound indentified in this study was 5d with low nanomolar affinity for all four adenosine receptor subtypes. Compounds 5a and 5g showed moderate selectivity for A2A adenosine receptors. Molecular docking versus all four human adenosine receptors combined with membrane molecular dynamics studies were performed to rationalise the peculiar selectivity profile of 5d antagonist.
