benzyl 5-O-pivaloyl-2-O-methoxymethyl-3-deoxy-3-C-hydroxymethyl-α-D-lyxo-pentofuranose | 288380-76-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: benzyl 5-O-pivaloyl-2-O-methoxymethyl-3-deoxy-3-C-hydroxymethyl-α-D-lyxo-pentofuranose
• 英文别名: [(2S,3S,4S,5S)-3-(hydroxymethyl)-4-(methoxymethoxy)-5-phenylmethoxyoxolan-2-yl]methyl 2,2-dimethylpropanoate
• CAS: 288380-76-7
• 化学式: C₂₀H₃₀O₇
• 分子量: 382.454
• InChiKey: GMSKEONFBKSOHX-MHORFTMASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  27
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  83.4
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  benzyl 5-O-pivaloyl-2-O-methoxymethyl-3-deoxy-3-C-hydroxymethyl-α-D-lyxo-pentofuranose 在 20percent Pd(OH)2/C 咪唑 、 2,6-二甲基吡啶 、 4-二甲氨基吡啶 、 sodium tetrahydroborate 、 正丁基锂 、 三氟化硼乙醚 、 四丁基氟化铵 、 氢气 、 4-甲基苯磺酸吡啶 、 二异丁基氢化铝 作用下， 以 四氢呋喃 、 吡啶 、 甲醇 、 乙醇 、 正己烷 、 二氯甲烷 、 二甲基亚砜 、 N,N-二甲基甲酰胺 、 甲苯 、 叔丁醇 为溶剂， 反应 81.68h， 生成 (5S,6R)-6-(tert-butyldimethylsilanyloxy)-5-[(R)-1-(tert-butyldimethylsilanyloxy)allyl]non-8-ynnitrile
  参考文献：
  名称：

  Efficient and Versatile Synthesis of Novel 2α-Substituted 1α,25-Dihydroxyvitamin D₃ Analogues and Their Docking to Vitamin D Receptors

  摘要：

  Novel 2 alpha -substituted 1 alpha ,25-dihydroxyvitamin D-3 analogues with 2 alpha -alkyl and 2 alpha -hydroxyalkyl groups were systematically synthesized from D-xylose. Their conformation on binding to the ligand binding domain (LBD) of the vitamin D receptor was analyzed. It has been found that the 2 alpha -hydroxypropyl group best fits the cavity of the LBD, and the binding activity is three times higher than that for the natural hormone.

  DOI：

  10.1021/jo010375i
• 作为产物：
  描述：

  1,2-O-异亚丙基-alpha-D-呋喃木糖 在 盐酸 、 sodium hydroxide 、 4 A molecular sieve 、 sodium hexamethyldisilazane 、 四丁基碘化铵 、 N,N-二异丙基乙胺 、 9-硼双环[3.3.1]壬烷 、 三苯基膦 、 pyridinium chlorochromate 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 吡啶 、 甲醇 、 二氯甲烷 、 水 、 甲苯 为溶剂， 反应 53.75h， 生成 benzyl 5-O-pivaloyl-2-O-methoxymethyl-3-deoxy-3-C-hydroxymethyl-α-D-lyxo-pentofuranose
  参考文献：
  名称：

  Efficient and Versatile Synthesis of Novel 2α-Substituted 1α,25-Dihydroxyvitamin D₃ Analogues and Their Docking to Vitamin D Receptors

  摘要：

  Novel 2 alpha -substituted 1 alpha ,25-dihydroxyvitamin D-3 analogues with 2 alpha -alkyl and 2 alpha -hydroxyalkyl groups were systematically synthesized from D-xylose. Their conformation on binding to the ligand binding domain (LBD) of the vitamin D receptor was analyzed. It has been found that the 2 alpha -hydroxypropyl group best fits the cavity of the LBD, and the binding activity is three times higher than that for the natural hormone.

  DOI：

  10.1021/jo010375i

文献信息

• Syntheses and biological evaluation of novel 2α-substituted 1α,25-dihydroxyvitamin D3 analogues
  作者：Yoshitomo Suhara、Ken-ichi Nihei、Hirokazu Tanigawa、Toshie Fujishima、Katsuhiro Konno、Kimie Nakagawa、Toshio Okano、Hiroaki Takayama

  DOI：10.1016/s0960-894x(00)00189-x

  日期：2000.5

  Novel 2 alpha-substituted 1 alpha,25-dihydroxyvitamin D-3 analogues were efficiently synthesized and their biological activities were evaluated. 2 alpha-Methyl-1 alpha,25-dihydroxyvitamin D-3 (2), whose unique biological activities were previously reported, was modified to 2 alpha-alkyl (ethyl and propyl) and 2 alpha-hydroxyalkyl (hydroxymethyl, hydroxyethyl, and hydroxypropyl) analogues 3-7 by elongation of the alkyl chain and/or introduction of a terminal hydroxyl group. 2 alpha-Hydroxypropyl-1 alpha,25-dihydroxyvitamin D-3 (7) exhibited an exceptionally potent calcium-regulating effect and a unique activity profile. (C) 2000 Elsevier Science Ltd. All rights reserved.
• Efficient and Versatile Synthesis of Novel 2α-Substituted 1α,25-Dihydroxyvitamin D₃ Analogues and Their Docking to Vitamin D Receptors
  作者：Yoshitomo Suhara、Ken-ichi Nihei、Masaaki Kurihara、Atsushi Kittaka、Kentaro Yamaguchi、Toshie Fujishima、Katsuhiro Konno、Naoki Miyata、Hiroaki Takayama

  DOI：10.1021/jo010375i

  日期：2001.12.1

  Novel 2 alpha -substituted 1 alpha ,25-dihydroxyvitamin D-3 analogues with 2 alpha -alkyl and 2 alpha -hydroxyalkyl groups were systematically synthesized from D-xylose. Their conformation on binding to the ligand binding domain (LBD) of the vitamin D receptor was analyzed. It has been found that the 2 alpha -hydroxypropyl group best fits the cavity of the LBD, and the binding activity is three times higher than that for the natural hormone.