2,10-diamino-thiochromeno[3,2-b]thioxanthene-12,14-dione | 112506-55-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 硫色烯
• 英文名称: 2,10-diamino-thiochromeno[3,2-b]thioxanthene-12,14-dione
• 英文别名: 2,10-diamino-thiochromeno[3,2-b]thioxanthene-12,14-dione；2,10-Diamino-thiochromeno[3,2-b]thioxanthen-12,14-dion
• CAS: 112506-55-5
• 化学式: C₂₀H₁₂N₂O₂S₂
• 分子量: 376.459
• InChiKey: ASKGCILWXIIVSL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.31
• 重原子数：
  26.0
• 可旋转键数：
  0.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  86.18
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  2,10-diamino-thiochromeno[3,2-b]thioxanthene-12,14-dione 、 N,N-二乙基氯乙胺 生成 2,10-bis-[(2-diethylamino-ethyl)-amino]-thiochromeno[3,2-b]thioxanthene-12,14-dione
  参考文献：
  名称：

  Effect of the control proliferation of astrocyte on the formation of glial scars by antisenseGFAP retrovirus

  摘要：

  Astrocytes play an important role in the formation of glial scars. In order to investigate the effect of inhibiting GFAP gene expression on normal, reactive astrocytes and on glial scar formation, the efficiency of the recombinant antisense GFAP retrovirus (PLBskG) on the growth, cell cycle, morphology and GFAP gene expression of astrocytes in vitro and on the formation of glial scars in vivo has been studied by cell growth curves, flow cytometry, immunocytochemistry, in situ hybridization, RT-PCR and Southern blot. The results confirm the recombinant retrovirus (PLBskG) produced growth suppression and G1 arrest of the normal and injured astrocytes. The infected cells become round or ellipoid. The cell processes become fine or retracted. The intensity of staining of GFAP is reduced. Expression of GFAP mRNA is down regulated. However, in the control experiment, no obvious effects on the morphology or synthesis of GFAP on cultured normal and scratched astrocytes infected by primary retrovirus vector (PLXSN) have been observed. The supernatant of PLBskG has been injected into an injured site by microinjection in vivo. The number and process lengths of GFAP positive cells are obviously reduced around the injured site. The formation of the glial scar is inhibited, showing that the recombinant antisense GFAP retrovirus can effectively inhibit the growth and GFAP expression of normal and injured astrocytes in vitro and the formation of glial scar in vivo. It is suggested that GFAP plays an important role in glial scar formation.

  DOI：

  10.1007/bf02884900
• 作为产物：
  描述：

  5,5'-diamino-2,2'-m-phenylenedimercapto-di-benzoic acid 在 PPA 作用下， 生成 2,10-diamino-thiochromeno[3,2-b]thioxanthene-12,14-dione
  参考文献：
  名称：

  Effect of the control proliferation of astrocyte on the formation of glial scars by antisenseGFAP retrovirus

  摘要：

  Astrocytes play an important role in the formation of glial scars. In order to investigate the effect of inhibiting GFAP gene expression on normal, reactive astrocytes and on glial scar formation, the efficiency of the recombinant antisense GFAP retrovirus (PLBskG) on the growth, cell cycle, morphology and GFAP gene expression of astrocytes in vitro and on the formation of glial scars in vivo has been studied by cell growth curves, flow cytometry, immunocytochemistry, in situ hybridization, RT-PCR and Southern blot. The results confirm the recombinant retrovirus (PLBskG) produced growth suppression and G1 arrest of the normal and injured astrocytes. The infected cells become round or ellipoid. The cell processes become fine or retracted. The intensity of staining of GFAP is reduced. Expression of GFAP mRNA is down regulated. However, in the control experiment, no obvious effects on the morphology or synthesis of GFAP on cultured normal and scratched astrocytes infected by primary retrovirus vector (PLXSN) have been observed. The supernatant of PLBskG has been injected into an injured site by microinjection in vivo. The number and process lengths of GFAP positive cells are obviously reduced around the injured site. The formation of the glial scar is inhibited, showing that the recombinant antisense GFAP retrovirus can effectively inhibit the growth and GFAP expression of normal and injured astrocytes in vitro and the formation of glial scar in vivo. It is suggested that GFAP plays an important role in glial scar formation.

  DOI：

  10.1007/bf02884900