| Literature DB >> 27001232 |
Shun Katsuyama1, Kumi Sugino2, Yukiko Sasazawa1, Yoshihiko Nakano1, Harumi Aono2, Keisuke Morishita1, Makoto Kawatani2, Kazuo Umezawa3, Hiroyuki Osada2, Siro Simizu1.
Abstract
We screened small-molecule compounds that inhibit osteoclast differentiation to find new anti-osteoporosis agents and found that a novel compound, SUKU-1, suppressed osteoclastogenesis. We also synthesized 38 derivatives of SUKU-1 and discovered that nine of them had inhibitory effects on osteoclastogenesis and that SUKU-33 was the most potent inhibitor. Next, we investigated the mechanisms by which SUKU-33 suppressed osteoclast differentiation. By measuring the uptake of [(3) H]-uridine in cells, we found that SUKU-33 suppressed both equilibrative nucleoside transporters and concentrative nucleoside transporters. These results suggest that SUKU-33 inhibits osteoclast differentiation by suppressing nucleoside transporters.Entities:
Keywords: concentrative nucleoside transporter; equilibrative nucleoside transporter; osteoclast differentiation; osteoporosis
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Year: 2016 PMID: 27001232 DOI: 10.1002/1873-3468.12146
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124