(1S,3S,4R,5S)-3-tetrahydropyranyl-4-tert-butyldiphenylsilyloxymethyl-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo[3.1.0]hexane | 873780-49-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: (1S,3S,4R,5S)-3-tetrahydropyranyl-4-tert-butyldiphenylsilyloxymethyl-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo[3.1.0]hexane
• 英文别名: 1-[(1S,3S,4R,5S)-4-[[tert-butyl(diphenyl)silyl]oxymethyl]-3-(oxan-2-yloxy)-1-bicyclo[3.1.0]hexanyl]pyrimidine-2,4-dione
• CAS: 873780-49-5
• 化学式: C₃₂H₄₀N₂O₅Si
• 分子量: 560.765
• InChiKey: BXVCWEUEZYYOFA-HGEQHWDGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.76
• 重原子数：
  40
• 可旋转键数：
  9
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  77.1
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (1S,3S,4R,5S)-3-tetrahydropyranyl-4-tert-butyldiphenylsilyloxymethyl-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo[3.1.0]hexane 在 四氮唑 、 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 1.75h， 生成 (1S,3S,4R,5S)-3-tetrahydropyranyl-4-di-tert-butylphosphatomethyl-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo[3.1.0]hexane
  参考文献：
  名称：

  Human P2Y₆ Receptor:  Molecular Modeling Leads to the Rational Design of a Novel Agonist Based on a Unique Conformational Preference

  摘要：

  Combining molecular dynamics (MD) in a hydrated phospholipid (DOPC) bilayer, a Monte Carlo search, and synthesis of locked nucleotide analogues, we discovered that the Southern conformation of the ribose is preferred for ligand recognition by the P2Y(6) receptor. 2'-Deoxy-(S)-methanocarbaUDP was found to be a full agonist of the receptor and displayed a 10-fold higher potency than that for the corresponding flexible 2'-deoxyUDP. MD results also suggested a conformational change of the second extracellular loop consequent to agonist binding.

  DOI：

  10.1021/jm050911p
• 作为产物：
  描述：

  (S)-2'-deoxymethanocarba uridine 在 咪唑 、 对甲苯磺酸 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 5.0h， 生成 (1S,3S,4R,5S)-3-tetrahydropyranyl-4-tert-butyldiphenylsilyloxymethyl-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo[3.1.0]hexane
  参考文献：
  名称：

  Human P2Y₆ Receptor:  Molecular Modeling Leads to the Rational Design of a Novel Agonist Based on a Unique Conformational Preference

  摘要：

  Combining molecular dynamics (MD) in a hydrated phospholipid (DOPC) bilayer, a Monte Carlo search, and synthesis of locked nucleotide analogues, we discovered that the Southern conformation of the ribose is preferred for ligand recognition by the P2Y(6) receptor. 2'-Deoxy-(S)-methanocarbaUDP was found to be a full agonist of the receptor and displayed a 10-fold higher potency than that for the corresponding flexible 2'-deoxyUDP. MD results also suggested a conformational change of the second extracellular loop consequent to agonist binding.

  DOI：

  10.1021/jm050911p

文献信息

• Human P2Y₆ Receptor:  Molecular Modeling Leads to the Rational Design of a Novel Agonist Based on a Unique Conformational Preference
  作者：Stefano Costanzi、Bhalchandra V. Joshi、Savitri Maddileti、Liaman Mamedova、Maria J. Gonzalez-Moa、Victor E. Marquez、T. Kendall Harden、Kenneth A. Jacobson

  DOI：10.1021/jm050911p

  日期：2005.12.1

  Combining molecular dynamics (MD) in a hydrated phospholipid (DOPC) bilayer, a Monte Carlo search, and synthesis of locked nucleotide analogues, we discovered that the Southern conformation of the ribose is preferred for ligand recognition by the P2Y(6) receptor. 2'-Deoxy-(S)-methanocarbaUDP was found to be a full agonist of the receptor and displayed a 10-fold higher potency than that for the corresponding flexible 2'-deoxyUDP. MD results also suggested a conformational change of the second extracellular loop consequent to agonist binding.