[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[2-(benzylamino)-2-oxoethyl]sulfanyloxan-2-yl]methyl acetate | 1058156-06-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: [(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[2-(benzylamino)-2-oxoethyl]sulfanyloxan-2-yl]methyl acetate
• CAS: 1058156-06-1
• 化学式: C₂₃H₂₉NO₁₀S
• 分子量: 511.55
• InChiKey: ZXNZWPXKFPLKEX-IFPLKCGESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  35
• 可旋转键数：
  14
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.52
• 拓扑面积：
  169
• 氢给体数：
  1
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  [(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[2-(benzylamino)-2-oxoethyl]sulfanyloxan-2-yl]methyl acetate 在 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 反应 1.67h， 以93%的产率得到N-benzyl-2-(2,3,4,6-tetra-O-acetyl-1-sulfonyl-β-D-glucopyranosyl)acetamide
  参考文献：
  名称：

  Synthesis and evaluation of antitubercular activity of glycosyl thio- and sulfonyl acetamide derivatives

  摘要：

  A series of glycosyl thioacetamide and glycosyl sulfonyl acetamide derivatives have been prepared following a convenient reaction protocol and evaluated for their antitubercular activity against Mycobacterium tuberculosis H(37)Rv. Amongst 32 compounds evaluated 3 compounds were effective in inhibiting mycobacterial growth at MIC of 6.25 mu g/mL, 6 compounds at MIC of 3.125 mu g/mL and 1 compound at MIC of 1.56 mu g/mL. All active compounds were found nontoxic in Vero cell lines and mice bone marrow macrophages. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.06.004
• 作为产物：
  描述：

  、 N-苄基-2-氯乙酰胺 在 三乙胺 作用下， 以 乙腈 为溶剂， 反应 0.5h， 以90%的产率得到[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-[2-(benzylamino)-2-oxoethyl]sulfanyloxan-2-yl]methyl acetate
  参考文献：
  名称：

  Synthesis and evaluation of antitubercular activity of glycosyl thio- and sulfonyl acetamide derivatives

  摘要：

  A series of glycosyl thioacetamide and glycosyl sulfonyl acetamide derivatives have been prepared following a convenient reaction protocol and evaluated for their antitubercular activity against Mycobacterium tuberculosis H(37)Rv. Amongst 32 compounds evaluated 3 compounds were effective in inhibiting mycobacterial growth at MIC of 6.25 mu g/mL, 6 compounds at MIC of 3.125 mu g/mL and 1 compound at MIC of 1.56 mu g/mL. All active compounds were found nontoxic in Vero cell lines and mice bone marrow macrophages. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.06.004

文献信息

• Synthesis and evaluation of antitubercular activity of glycosyl thio- and sulfonyl acetamide derivatives
  作者：Samir Ghosh、Pallavi Tiwari、Shashi Pandey、Anup Kumar Misra、Vinita Chaturvedi、Anil Gaikwad、Shalini Bhatnagar、Sudhir Sinha

  DOI：10.1016/j.bmcl.2008.06.004

  日期：2008.7

  A series of glycosyl thioacetamide and glycosyl sulfonyl acetamide derivatives have been prepared following a convenient reaction protocol and evaluated for their antitubercular activity against Mycobacterium tuberculosis H(37)Rv. Amongst 32 compounds evaluated 3 compounds were effective in inhibiting mycobacterial growth at MIC of 6.25 mu g/mL, 6 compounds at MIC of 3.125 mu g/mL and 1 compound at MIC of 1.56 mu g/mL. All active compounds were found nontoxic in Vero cell lines and mice bone marrow macrophages. (c) 2008 Elsevier Ltd. All rights reserved.