938447-20-2Relevant academic research and scientific papers
Prodrug-based design, synthesis, and biological evaluation of N-benzenesulfonylpiperidine derivatives as novel, orally active factor Xa inhibitors
Ishihara, Tsukasa,Seki, Norio,Hirayama, Fukushi,Orita, Masaya,Koshio, Hiroyuki,Taniuchi, Yuta,Sakai-Moritani, Yumiko,Iwatsuki, Yoshiyuki,Kaku, Seiji,Kawasaki, Tomihisa,Matsumoto, Yuzo,Tsukamoto, Shin-ichi
, p. 4175 - 4192 (2008/03/12)
We describe here our investigation of a new series of orally active fXa inhibitors based on a prodrug strategy. Solid-phase parallel synthesis identified a unique series of fXa inhibitors with a substituted benzenesulfonyl group as a novel S4 binding elem
