(S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-5,9-dimethyldeca-4,9-dien-1-one | 1376709-17-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: (S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-5,9-dimethyldeca-4,9-dien-1-one
• 英文别名: (3S,4E)-3-hydroxy-5,9-dimethyl-1-[(4R)-4-propan-2-yl-2-sulfanylidene-1,3-thiazolidin-3-yl]deca-4,9-dien-1-one
• CAS: 1376709-17-9
• 化学式: C₁₈H₂₉NO₂S₂
• 分子量: 355.566
• InChiKey: QYDWSTPAPWAKIS-MMJTVPDGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  23
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  97.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-5,9-dimethyldeca-4,9-dien-1-one 在 2,6-二甲基吡啶 、 potassium carbonate 作用下， 以 二氯甲烷 为溶剂， 反应 6.25h， 生成 (S,E)-methyl 3-((tert-butyldimethylsilyl)oxy)-5,9-dimethyldeca-4,9-dienoate
  参考文献：
  名称：

  Total Synthesis of the Potent cAMP Signaling Agonist (−)-Alotaketal A

  摘要：

  We have developed a convergent synthetic route to the potent cAMP signaling agonist (-)-alotaketal A that employs two stages of SmI2-mediated reductive allylation reactions for assembling the polycycle and fragment coupling. Also notable are a Hg(OAc)(2)-mediated selective alkene oxidation and the subtlety of the formation of the unprecedented spiroketal ring system. The probes AKAR4 and ICUE3 were used to evaluate the cAMP singaling agonistic activity of (-)-alotaketal A and elucidate its structure-activity relationship.

  DOI：

  10.1021/ja303529z
• 作为产物：
  描述：

  (E)-6-chloro-3,7-dimethylocta-2,7-dien-1-ol 在 manganese(IV) oxide 、 lithium aluminium tetrahydride 、 tin(II) trifluoromethanesulfonate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 为溶剂， 反应 21.5h， 生成 (S,E)-3-hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)-5,9-dimethyldeca-4,9-dien-1-one
  参考文献：
  名称：

  Total Synthesis of Alotaketal A

  摘要：

  The total synthesis of the cAMP signaling pathway activator (-)-alotaketal A is reported. A convergent approach to the unusual alotane sesterterpenoid skeleton was employed, exploiting a remarkable LiDBB-mediated coupling of an (R)-carvone-derived delta-lactone with an allyl bromide side chain, followed by spiroacetalization.

  DOI：

  10.1021/ol302570k

文献信息

• Total synthesis and structure–activity relationship study of the potent cAMP signaling agonist (−)-alotaketal A
  作者：Jinhua Huang、Jessica R. Yang、Jin Zhang、Jiong Yang

  DOI：10.1039/c3ob40120k

  日期：——

  A detailed account of the first total synthesis of alotaketal A, a tricyclic spiroketal sesterterpenoid that potently activates the cAMP signaling pathway, is provided. The synthesis employs both intra- and intermolecular reductive allylation of esters for assembling one of the fragments and their coupling. A Hg(OAc)2-mediated allylic mercuration is used to introduce the C22-hydroxyl group. The subtle influence of substituents over the course of the spiroketalization process is revealed. The synthesis confirms the relative and absolute stereochemistry of (−)-alotaketal A and allows verification of alotaketal A's effect over cAMP signaling using reporter-based FRET imaging assays with HEK 293T cells. Our studies also revealed alotaketal A's unique activity in selectively targeting nuclear PKA signaling in living cells.

  提供了对alotaketal A的首次完全合成的详细描述。alotaketal A是一种三环螺烯糖甙类化合物，能够有效激活cAMP信号通路。该合成采用了酯的分子内和分子间还原烯丙基化反应来组装其中一个片段及其耦合。通过Hg(OAc)2介导的烯丙基汞化反应引入了C22-羟基。合成过程中取代基的微妙影响被揭示出来。此合成确认了(−)-alotaketal A的相对和绝对立体化学，并可以使用HEK 293T细胞的报告基FRET成像实验验证alotaketal A对cAMP信号的影响。我们的研究还揭示了alotaketal A在活细胞中选择性靶向核PKA信号的独特活性。
• Total Synthesis of Alotaketal A
  作者：Mengyang Xuan、Ian Paterson、Stephen M. Dalby

  DOI：10.1021/ol302570k

  日期：2012.11.2

  The total synthesis of the cAMP signaling pathway activator (-)-alotaketal A is reported. A convergent approach to the unusual alotane sesterterpenoid skeleton was employed, exploiting a remarkable LiDBB-mediated coupling of an (R)-carvone-derived delta-lactone with an allyl bromide side chain, followed by spiroacetalization.
• Total Synthesis of the Potent cAMP Signaling Agonist (−)-Alotaketal A
  作者：Jinhua Huang、Jessica R. Yang、Jin Zhang、Jiong Yang

  DOI：10.1021/ja303529z

  日期：2012.5.30

  We have developed a convergent synthetic route to the potent cAMP signaling agonist (-)-alotaketal A that employs two stages of SmI2-mediated reductive allylation reactions for assembling the polycycle and fragment coupling. Also notable are a Hg(OAc)(2)-mediated selective alkene oxidation and the subtlety of the formation of the unprecedented spiroketal ring system. The probes AKAR4 and ICUE3 were used to evaluate the cAMP singaling agonistic activity of (-)-alotaketal A and elucidate its structure-activity relationship.