acetic acid-(10-aza-bicyclo[4.3.1]dec-8exo-ylester); hydrochloride | 105640-96-8

• 分子结构分类: 有机化合物 - 生物碱及其衍生物 - 托烷生物碱
• 英文名称: acetic acid-(10-aza-bicyclo[4.3.1]dec-8exo-ylester); hydrochloride
• 英文别名: Essigsaeure-(10-aza-bicyclo[4.3.1]dec-8exo-ylester); Hydrochlorid
• CAS: 105640-96-8
• 化学式: C₁₁H₁₉NO₂*ClH
• 分子量: 233.738
• InChiKey: ZPAFOBLAQLCIBL-FOBKSFJMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.03
• 重原子数：
  15.0
• 可旋转键数：
  1.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  38.33
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  水 、 acetic acid-(10-aza-bicyclo[4.3.1]dec-8exo-ylester); hydrochloride 、 furan-2,3,5(4H)-trione pyridine (1:1) 生成 10-acetyl-10-aza-bicyclo[4.3.1]decane-8exo-ol
  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
• 作为产物：
  描述：

  10-aza-bicyclo[4.3.1]decane-8exo-ol; hydrochloride 、 乙酰氯 生成 acetic acid-(10-aza-bicyclo[4.3.1]dec-8exo-ylester); hydrochloride
  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