2012
DOI: 10.1002/chin.201248173
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ChemInform Abstract: Design, Microwave‐Assisted Synthesis and in silico Docking Studies of New 4H‐Pyrimido[2,1‐b]benzothiazole‐2‐arylamino‐3‐cyano‐4‐ones (III) as Possible Adenosine A2B Receptor Antagonists.

Abstract: Design, Microwave-Assisted Synthesis and in silico Docking Studies of New 4H-Pyrimido[2,1-b]benzothiazole-2-arylamino-3-cyano-4-ones (III) as PossibleAdenosine A2B Receptor Antagonists. -(BALAKUMAR, C.; KISHORE, D. P.; RAO, K. V.; NARAYANA, B. L.; RAJWINDER, K.; RAJKUMAR, V.; RAO*, A. R.; Indian J.

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“…Thus, it was our thought of interest to further investigate any changes in affinity and selectivity towards ARs for a novel series of triazolopyridine derivatives ( 4a–4t ) with 7‐amino (NH 2 ) and 6‐carbonitrile (CN) group, while varying the substitution pattern at the 2‐position of the scaffold with various aryl/hetero‐aryl moieties (Figure ). In continuation of our interest in the search of novel ligands for adenosine receptors (Balakumar et al., ; Chandrasekaran et al., ; Deb et al., ; Kaur et al., ; Kishore, Balakumar, Rao, Roy, & Roy, ; Prasad et al., ; Sirisha et al., ; Veeraswamy et al., ) and in the light of the above‐mentioned literature reports, some novel 5‐oxo[1,2,4]triazolo[1,5‐ a ]pyridine‐6‐carbonitrile derivatives ( 4a–4t ) have been synthesized as potential selective ligands for hA 1 AR.…”
Section: Introductionmentioning
confidence: 98%
“…Thus, it was our thought of interest to further investigate any changes in affinity and selectivity towards ARs for a novel series of triazolopyridine derivatives ( 4a–4t ) with 7‐amino (NH 2 ) and 6‐carbonitrile (CN) group, while varying the substitution pattern at the 2‐position of the scaffold with various aryl/hetero‐aryl moieties (Figure ). In continuation of our interest in the search of novel ligands for adenosine receptors (Balakumar et al., ; Chandrasekaran et al., ; Deb et al., ; Kaur et al., ; Kishore, Balakumar, Rao, Roy, & Roy, ; Prasad et al., ; Sirisha et al., ; Veeraswamy et al., ) and in the light of the above‐mentioned literature reports, some novel 5‐oxo[1,2,4]triazolo[1,5‐ a ]pyridine‐6‐carbonitrile derivatives ( 4a–4t ) have been synthesized as potential selective ligands for hA 1 AR.…”
Section: Introductionmentioning
confidence: 98%
“… 20 , 21 Similarly, thiazole orange ( Figure 1 ) and a few benzothiazole derivatives have been reported for their applications in organic and medicinal chemistry. 22 …”
Section: Introductionmentioning
confidence: 99%
“…Earlier, we have reported novel quinoline bearing dihydropyridines for their inhibition against the lung cancer cell lines and obtained potential inhibition profiles . Compounds SYBR Green I and SYBR Safe (Figure ) are mainly used as dyes for the quantification of double-stranded DNA (quantitative PCR) and to visualize DNA (gel electrophoresis). , Similarly, thiazole orange (Figure ) and a few benzothiazole derivatives have been reported for their applications in organic and medicinal chemistry …”
Section: Introductionmentioning
confidence: 99%