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Quinoxaline-2-carboxylic acid 2-[(2S,4R,5R,6R)-5-[(2R,4R,5S,6R)-4-amino-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-4-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-ethyl ester | 729592-67-0

中文名称
——
中文别名
——
英文名称
Quinoxaline-2-carboxylic acid 2-[(2S,4R,5R,6R)-5-[(2R,4R,5S,6R)-4-amino-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-4-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-ethyl ester
英文别名
——
Quinoxaline-2-carboxylic acid 2-[(2S,4R,5R,6R)-5-[(2R,4R,5S,6R)-4-amino-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-4-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-ethyl ester化学式
CAS
729592-67-0
化学式
C35H59N3O8Si2
mdl
——
分子量
706.04
InChiKey
VAJFIGIYRNIDPS-BFPWXIDPSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.57
  • 重原子数:
    48.0
  • 可旋转键数:
    11.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    133.48
  • 氢给体数:
    1.0
  • 氢受体数:
    11.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline–carbohydrate hybrids
    摘要:
    The novel DNA interactive quinoxaline-carbohydrate hybrids possessing disaccharides as the carbohydrate moieties were designed and synthesized, and their DNA photocleaving abilities were evaluated in order to examine the effect of the disaccharide structures. The configurations of the glycosidic bonds in the disaccharide strongly affected the DNA photocleaving ability, and two P-glycosidic bond linkages were very effective for the DNA photocleavage. Furthermore, the quinoxaline-disaccharide hybrids exhibited selective cytotoxicity against cancer cells with photoirradiation. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.03.065
  • 作为产物:
    描述:
    Quinoxaline-2-carboxylic acid 2-[(2S,4R,5R,6R)-5-[(2R,4R,5S,6R)-4-azido-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-4-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-ethyl ester三苯基膦 作用下, 以 四氢呋喃 为溶剂, 反应 13.0h, 以79%的产率得到Quinoxaline-2-carboxylic acid 2-[(2S,4R,5R,6R)-5-[(2R,4R,5S,6R)-4-amino-5-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-4-(tert-butyl-dimethyl-silanyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-ethyl ester
    参考文献:
    名称:
    The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline–carbohydrate hybrids
    摘要:
    The novel DNA interactive quinoxaline-carbohydrate hybrids possessing disaccharides as the carbohydrate moieties were designed and synthesized, and their DNA photocleaving abilities were evaluated in order to examine the effect of the disaccharide structures. The configurations of the glycosidic bonds in the disaccharide strongly affected the DNA photocleaving ability, and two P-glycosidic bond linkages were very effective for the DNA photocleavage. Furthermore, the quinoxaline-disaccharide hybrids exhibited selective cytotoxicity against cancer cells with photoirradiation. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.03.065
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