3TKC
Design, Synthesis, Evaluation and Structure of Vitamin D Analogues with Furan Side Chains
3TKC の概要
エントリーDOI | 10.2210/pdb3tkc/pdb |
関連するPDBエントリー | 3A3Z 3A40 |
分子名称 | Vitamin D3 receptor, (1S,3R,5Z,7E,14beta,17alpha,20S)-20-[5-(1-hydroxy-1-methylethyl)furan-2-yl]-9,10-secopregna-5,7,10-triene-1,3-diol, SULFATE ION, ... (4 entities in total) |
機能のキーワード | alpha-helical sandwich, transcription, calcitriol, phosphorylation, nucleus |
由来する生物種 | Homo sapiens (human) |
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 | 30024.61 |
構造登録者 | |
主引用文献 | Fraga, R.,Zacconi, F.,Sussman, F.,Ordonez-Moran, P.,Munoz, A.,Huet, T.,Molnar, F.,Moras, D.,Rochel, N.,Maestro, M.,Mourino, A. Design, synthesis, evaluation, and structure of vitamin D analogues with furan side chains. Chemistry, 18:603-612, 2012 Cited by PubMed Abstract: Based on the crystal structures of human vitamin D receptor (hVDR) bound to 1α,25-dihydroxy-vitamin D(3) (1,25 D) and superagonist ligands, we previously designed new superagonist ligands with a tetrahydrofuran ring at the side chain that optimize the aliphatic side-chain conformation through an entropy benefit. Following a similar strategy, four novel vitamin D analogues with aromatic furan side chains (3a, 3b, 4a, 4b) have now been developed. The triene system has been constructed by an efficient stereoselective intramolecular cyclization of an enol triflate (A-ring precursor) followed by a Suzuki-Miyaura coupling of the resulting intermediate with an alkenyl boronic ester (CD-side chain, upper fragment). The furan side chains have been constructed by gold chemistry. These analogues exhibit significant pro-differentiation effects and transactivation potency. The crystal structure of 3a in a complex with the ligand-binding domain of hVDR revealed that the side-chain furanic ring adopts two conformations. PubMed: 22162241DOI: 10.1002/chem.201102695 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.75 Å) |
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