| Literature DB >> 17467986 |
Takashi Yamamoto1, Koichi Fujita, Sayaka Asari, Akira Chiba, Yuka Kataba, Koji Ohsumi, Naoko Ohmuta, Yuko Iida, Chiori Ijichi, Satoshi Iwayama, Naoyuki Fukuchi, Masataka Shoji.
Abstract
A series of isoxazole derivatives were synthesized and their antagonistic activities against LPA stimulation on both LPA(1)/CHO cells and rHSC cells were evaluated. Among them, 3-(4-[4-[1-(2-chloro-cyclopent-1-enyl)-ethoxycarbonylamino]-isoxazol-3- y]]-benzylsulfanyl)-propionic acid (34) showed the most potent activities.Entities:
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Year: 2007 PMID: 17467986 DOI: 10.1016/j.bmcl.2007.04.024
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823