Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10592456 | Bioorganic & Medicinal Chemistry Letters | 2012 | 6 Pages |
Abstract
A series of 1,3-thiazole derivatives were synthesized as potent, orally bioavailable S1P3-sparing S1P1 agonists. One of them, 24c, exhibited favorable efficacy in rat on host versus graft reaction (HvGR). The pharmacokinetic data for other compounds are shown as well.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masayoshi Asano, Tsuyoshi Nakamura, Yukiko Sekiguchi, Yumiko Mizuno, Takahiro Yamaguchi, Kazuhiko Tamaki, Takaichi Shimozato, Hiromi Doi-Komuro, Takashi Kagari, Wataru Tomisato, Ryotaku Inoue, Hiroshi Yuita, Keiko Oguchi-Oshima, Reina Kaneko,