136320-11-1Relevant articles and documents
4-Amino-5-vinyl-3(2H)-pyridazinones and analogues as potent antinociceptive agents: Synthesis, SARs, and preliminary studies on the mechanism of action
Vergelli, Claudia,Giovannoni, Maria Paola,Pieretti, Stefano,Giannuario, Amalia Di,Piaz, Vittorio Dal,Biagini, Pierfrancesco,Biancalani, Claudio,Graziano, Alessia,Cesari, Nicoletta
, p. 5563 - 5575 (2008/03/14)
A series of 4-amino-5-vinyl-3(2H)-pyridazinones and analogues were synthesized and their antinociceptive effect was evaluated in the mouse abdominal constriction model. Several of the novel compounds showed ED50 values in the range 6-20 mg/kg/s
REDUCTIVE CLEAVAGE OF ISOXAZOLOPYRIDAZINONES: A SYNTHETIC APPROACH TO VARIOUS 4,5-FUNCTIONALIZED 3(2H)-PYRIDAZINONES
Piaz, Vittorio Dal,Ciciani, Giovanna,Giovannoni, Maria Paola
, p. 1173 - 1179 (2007/10/02)
4-Aminopyridazin-3(2H)-ones substituted at position 5 with a variety of oxygenated carbon chains were obtained in good yields by reductive opening of the pentatomic ring of isoxazolopyridazinones (1).Starting from ethyl 4-acylisoxazole-3-carboxylat