10-methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8-one | 36441-69-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氮杂环庚烷
• 英文名称: 10-methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8-one
• 英文别名: 10-Methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8-on；(1R,2S,5R,6S)-10-methyl-10-azatricyclo[4.3.1.12,5]undecan-8-one
• CAS: 36441-69-7
• 化学式: C₁₁H₁₇NO
• 分子量: 179.262
• InChiKey: DUINGRBTGMDCEY-YDRMRZIKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  10-methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8-one 在 乙醇 、 sodium 作用下， 生成 10-methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8c-ol 、 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  The Stereochemical Course of a Robinson-Schöpf Biogenetic-Type Reaction. The Conformation of Certain Tricyclic Tropane Congeners¹

  摘要：

  DOI：

  10.1021/ja00956a029
• 作为产物：
  描述：

  bicyclo<2.2.1>heptane-2,3-dione 在 lead(IV) acetate 、 lithium aluminium tetrahydride 、 乙醚 、 乙酸甲酯 、 水 作用下， 生成 10-methyl-(1rN,2tC¹¹)-10-aza-tricyclo[4.3.1.1^2,5]undecan-8-one
  参考文献：
  名称：

  Improved yield and functionality of parathyroid cells separated by using collagenase-digestion with cold pre-incubation

  摘要：

  Preparation of cells from solid organs often induces a functional impairment due to the proteolytic cell damage by the applied digestive enzyme like collagenase, trypsin or dispase. To preserve the tissue and to enhance the yield of cells, Laue et al. reported an islet cell isolation with pre-incubation at 4 C permitting the enzyme to diffuse into the tissue and explicite activity equally throughout the whole particle. The aim of this study was to investigate whether this procedure can be applied to parathyroid glands. Therefore porcine parathyroid glands were dissected into 1 mm(3) pieces. Subsequently one group of these pieces was incubated 22 h at 4 C in 2 mg/ml collagenase before activating the enzyme by elevating the temperature to 37 C for 30 min. The other group was incubated directly at 37 C for 30 min. The yield of cells and their viability was assessed by light-microscopy and staining with trypan-blue. After the cells were immobilized in barium-alginate and cultivated for 7 days, the function was tested by incubation in different calcium concentrations and PTH-measurement. Finally, the viability was assessed by histology. Using a cold pre-incubation with collagenase, a significantly higher number of isolated cells was retrieved compared with collagenase-digestion without pre-incubation. The viability was about 100% and did not differ between both groups. After immobilization and cultivation the viability decreased to less than 30%, with and without pre-incubation. In contrast to viability the PTH-secretion of the cells differed significantly between both procedures. By preincubation with collagenase at 4 C a gentle method is presented resulting in an enhancement of yield and function of single cells of parathyroid glands. (C)2001, Editrice Kurtis .

  DOI：

  10.1007/bf03343821

文献信息

• The Stereochemical Course of a Robinson-Schöpf Biogenetic-Type Reaction. The Conformation of Certain Tricyclic Tropane Congeners¹
  作者：Leo A. Paquette、John W. Heimaster

  DOI：10.1021/ja00956a029

  日期：1966.2
• Improved yield and functionality of parathyroid cells separated by using collagenase-digestion with cold pre-incubation
  作者：M. Laudes、A. Gaumann、C. Laue、J. Schrezenmeir

  DOI：10.1007/bf03343821

  日期：2001.2

  Preparation of cells from solid organs often induces a functional impairment due to the proteolytic cell damage by the applied digestive enzyme like collagenase, trypsin or dispase. To preserve the tissue and to enhance the yield of cells, Laue et al. reported an islet cell isolation with pre-incubation at 4 C permitting the enzyme to diffuse into the tissue and explicite activity equally throughout the whole particle. The aim of this study was to investigate whether this procedure can be applied to parathyroid glands. Therefore porcine parathyroid glands were dissected into 1 mm(3) pieces. Subsequently one group of these pieces was incubated 22 h at 4 C in 2 mg/ml collagenase before activating the enzyme by elevating the temperature to 37 C for 30 min. The other group was incubated directly at 37 C for 30 min. The yield of cells and their viability was assessed by light-microscopy and staining with trypan-blue. After the cells were immobilized in barium-alginate and cultivated for 7 days, the function was tested by incubation in different calcium concentrations and PTH-measurement. Finally, the viability was assessed by histology. Using a cold pre-incubation with collagenase, a significantly higher number of isolated cells was retrieved compared with collagenase-digestion without pre-incubation. The viability was about 100% and did not differ between both groups. After immobilization and cultivation the viability decreased to less than 30%, with and without pre-incubation. In contrast to viability the PTH-secretion of the cells differed significantly between both procedures. By preincubation with collagenase at 4 C a gentle method is presented resulting in an enhancement of yield and function of single cells of parathyroid glands. (C)2001, Editrice Kurtis .