Title of article :
Design, synthesis, and evaluation of new type of l-amino acids containing pyridine moiety as nitric oxide synthase inhibitor Original Research Article
Author/Authors :
Ryosuke Ijuin، نويسنده , , Naoki Umezawa، نويسنده , , Tsunehiko Higuchi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Abstract :
New amino acids 7–12 were designed and synthesized as candidate inhibitors of human nitric oxide synthase (NOS). The 2-aminopyridine-containing l-amino acids 8 had potent inhibitory activity toward all of the human NOS isozymes. However, the regioisomers 9 and 10, and 2-methylpyridine-containing compound 11 had much lower inhibitory activity. Human NOS isozymes were also inhibited by 7, which lacks an amino group on the pyridine moiety. A computational docking study was carried out to investigate the mechanism of the inhibitory effect.
Keywords :
Computational docking study , Amino acid , Citrulline assay , Isozyme , Inhibitor , Competitive , Human , nitric oxide , Pyridine , IC50 , Picoline , design , regioisomer , 2-Aminopyridine , cysteine , Arginine , Synthesis , Nitric oxide synthase , Structure–activity relationship
Journal title :
Bioorganic and Medicinal Chemistry
Journal title :
Bioorganic and Medicinal Chemistry