60586-98-3Relevant academic research and scientific papers
Synthesis and biological evaluation of new 3-Aralkylamino-2-aryl-2H- 1,2,4-pyridothiadiazine 1,1-dioxides as potential CCK-Receptor ligands
De Tullio, Pascal,Pirotte, Bernard,Neven, Philippe,Masereel, Bernard,Dewalque, Daniel,Diouf, Ousmane,Podona, Tchao,Caignard, Daniel,Renard, Pierre,Delarge, Jacques
, p. 463 - 471 (2007/10/03)
A series of 2-aralkyl-4H-pyridothiadiazine 1,1-dioxides and 3-aralkylamino-2-ary1-2H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides structurally related to quinazolinone CCK receptor antagonists were synthesized and evaluated as CCK-A and CCK-B receptor ligands. The compounds were effective as cholecystokinin-ligands in the micromolar range of concentration, c.f. the cholecystokinin receptor antagonists asperlicin, lorglumide or benzotript, and were thus less potent than the best quinazolinones previously reported. Although the compounds were unsuitable for drug use, the work contributed to our understanding of the chemistry of unusual 2,3 -disubstituted pyridothiadiazinedioxides.
