3AZ3
Crystal Structure Analysis of Vitamin D receptor
3AZ3 の概要
| エントリーDOI | 10.2210/pdb3az3/pdb |
| 関連するPDBエントリー | 3AZ1 3AZ2 |
| 分子名称 | Vitamin D3 receptor, (4S)-4-hydroxy-5-[4-(3-{4-[(3S)-3-hydroxy-4,4-dimethylpentyl]-3-methylphenyl}pentan-3-yl)-2-methylphenoxy]pentanoic acid (3 entities in total) |
| 機能のキーワード | vitamin d receptor, hormone receptor |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| 細胞内の位置 | Nucleus: P11473 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 29244.95 |
| 構造登録者 | |
| 主引用文献 | Kashiwagi, H.,Ono, Y.,Shimizu, K.,Haneishi, T.,Ito, S.,Iijima, S.,Kobayashi, T.,Ichikawa, F.,Harada, S.,Sato, H.,Sekiguchi, N.,Ishigai, M.,Takahashi, T. Novel nonsecosteroidal vitamin D(3) carboxylic acid analogs for osteoporosis, and SAR analysis. Bioorg.Med.Chem., 19:4721-4729, 2011 Cited by PubMed 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. PubMed: 21795053DOI: 10.1016/j.bmc.2011.07.001 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.36 Å) |
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