TY - JOUR
T1 - Pyrazolo[3,4-d]pyrimidine Derivatives as COX-2 Selective Inhibitors: Synthesis and Molecular Modelling Studies
AU - Plescia, Fabiana
AU - Cascioferro, Stella Maria
AU - Plescia, Salvatore
AU - Maggio, Benedetta
AU - Raffa, Demetrio
AU - Raimondi, Maria Valeria
AU - Cusimano, Maria Grazia
AU - Raffa, Demetrio
PY - 2009
Y1 - 2009
N2 - The pyrazolo[3,4-d]pyrimidine system shows a multitude of interesting pharmacological properties.Owing to the potential anti-inflammatory activity of 5-benzamido-pyrazolo[3,4-d]pyrimidin-4-one derivatives and considering the easy synthesis of this class of compounds, a set of new 5-benzamido-1H-pyrazolo[3,4-d]pyrimidin-4-ones has been prepared in 42-80% yields by reacting 5-aminopyrazole-4(N-benzoyl)carbohydrazide derivatives and the opportune triethylorthoesters.Compounds 8a, b, 10a–d, and 11a, b revealed a superior inhibitory profile against COX-2, whencompared to that of reference standards NS398 and indomethacin. Molecular modelling studies confirmed the obtained biological results.
AB - The pyrazolo[3,4-d]pyrimidine system shows a multitude of interesting pharmacological properties.Owing to the potential anti-inflammatory activity of 5-benzamido-pyrazolo[3,4-d]pyrimidin-4-one derivatives and considering the easy synthesis of this class of compounds, a set of new 5-benzamido-1H-pyrazolo[3,4-d]pyrimidin-4-ones has been prepared in 42-80% yields by reacting 5-aminopyrazole-4(N-benzoyl)carbohydrazide derivatives and the opportune triethylorthoesters.Compounds 8a, b, 10a–d, and 11a, b revealed a superior inhibitory profile against COX-2, whencompared to that of reference standards NS398 and indomethacin. Molecular modelling studies confirmed the obtained biological results.
KW - 4-d]pyrimidine; 4(3H)-Quinazolinone
KW - COX-2 inhibitors; Docking
KW - Pyrazolo[3
KW - 4-d]pyrimidine; 4(3H)-Quinazolinone
KW - COX-2 inhibitors; Docking
KW - Pyrazolo[3
UR - http://hdl.handle.net/10447/38966
M3 - Article
SN - 0365-6233
VL - 2009
SP - 321
EP - 326
JO - Archiv der Pharmazie
JF - Archiv der Pharmazie
ER -