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Potent and selective TF/FVIIa inhibitors containing a neutral P1 ligand
Authors:Miura Masanori  Seki Norio  Koike Takanori  Ishihara Tsukasa  Niimi Tatsuya  Hirayama Fukushi  Shigenaga Takeshi  Sakai-Moritani Yumiko  Kawasaki Tomihisa  Sakamoto Shuichi  Okada Minoru  Ohta Mitsuaki  Tsukamoto Shin-ichi
Institution:Institute for Drug Discovery Research, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba-shi, Ibaraki 305-8585, Japan. masannori-miura@jp.astellas.com
Abstract:Inhibition of tissue factor/factor VIIa complex (TF/FVIIa) is an attractive strategy for antithrombotic therapies. We began with an investigation of a non-amidine TF/FVIIa inhibitor based on a modification of amidine compound 1. Optimization of the substituents on the P1 phenyl portion of the compound 1 led to a neutral or less basic alternative for the 4-amidinophenyl moiety. By further optimization of the substituents on the central phenyl ring, a highly potent and selective TF/FVIIa inhibitor 17d was discovered.
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