| Literature DB >> 21795053 |
Hirotaka Kashiwagi1, Yoshiyuki Ono, Kazuki Shimizu, Tsuyoshi Haneishi, Susumu Ito, Shigeyuki Iijima, Takamitsu Kobayashi, Fumihiko Ichikawa, Suguru Harada, Hideki Sato, Nobuo Sekiguchi, Masaki Ishigai, Tadakatsu Takahashi.
Abstract
Novel vitamin D(3) analogs with carboxylic acid were explored, focusing on a nonsecosteroidal analog, LG190178, with a bisphenyl skeleton. From X-ray analysis of these analogs with vitamin D receptor (VDR), the carboxyl groups had very unique hydrogen bonding interactions in VDR and mimicked 1α-hydroxy group and/or 3β-hydroxy group of 1α,25-dihydroxyvitamin D(3). A highly potent analog, 6a, with good in vitro activity and pharmacokinetic profiles was identified from an SAR study. Compound 6a showed significant prevention of bone loss in a rat osteoporosis model by oral administration.Entities:
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Year: 2011 PMID: 21795053 DOI: 10.1016/j.bmc.2011.07.001
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641