抄録
We synthesized new vitamin K analogues with demethylation or reduction of the double bonds of the side chain of menaquinone-4 (MK-4) and evaluated their SXR-mediated transcriptional activity as well as the extent of their conversion to MK-4. The results indicated that the analogue with the methyl group deleted at the 7′ site of the side chain part affected conversion activity to MK-4. In contrast, a decrease in the number of the double bonds in the side chain moiety appeared to decrease the SXR-mediated transcriptional activity.
本文言語 | English |
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ページ(範囲) | 1553-1558 |
ページ数 | 6 |
ジャーナル | Journal of Medicinal Chemistry |
巻 | 55 |
号 | 4 |
DOI | |
出版ステータス | Published - 2012 2月 23 |
外部発表 | はい |
ASJC Scopus subject areas
- 分子医療
- 創薬