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Chem Pharm Bull (Tokyo) ; 55(2): 317-23, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17268108

ABSTRACT

In the course of development of factor Xa (FXa) inhibitors, we have found unique compounds containing an N,O- and an N,N-spiro acetal structure. It appeared that the difference in overall conformation due to the N,X-spiro acetal structure might be important for FXa inhibitory activity. Therefore, other N,X-spiro acetal structures, an N,S- and an N,SO2-spiro acetal, were developed as analogues of the N,X-spiro acetal structure. Compound 7b (N,S-spiro acetal structure) was found to have the strongest activity in these series of N,X-spiro acetal compounds, which had ever been synthesized.(4,5)).


Subject(s)
Acetals/chemistry , Antithrombin III/chemical synthesis , Nitrogen/chemistry , Oxygen/chemistry , Piperidines/chemical synthesis , Spiro Compounds/chemical synthesis , Anticoagulants/pharmacology , Antithrombin III/pharmacology , Molecular Conformation , Molecular Structure , Piperidines/pharmacology , Serine Proteinase Inhibitors/pharmacology , Spiro Compounds/pharmacology
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