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6,7-diphenyl-1-β-D-ribofuranosyl-1H-pteridine-2,4-dione | 35777-58-3

中文名称
——
中文别名
——
英文名称
6,7-diphenyl-1-β-D-ribofuranosyl-1H-pteridine-2,4-dione
英文别名
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6,7-diphenylpteridine-2,4-dione
6,7-diphenyl-1-β-<i>D</i>-ribofuranosyl-1<i>H</i>-pteridine-2,4-dione化学式
CAS
35777-58-3
化学式
C23H20N4O6
mdl
——
分子量
448.435
InChiKey
MZTVKIFKQDHTFH-RCAWKPMRSA-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):
    1
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    145
  • 氢给体数:
    4
  • 氢受体数:
    8

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:
    描述:
    6,7-diphenyl-1-β-D-ribofuranosyl-1H-pteridine-2,4-dione吡啶碳酸二苯酯碳酸氢钠 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 (7aS)-8c-acetoxy-9t-acetoxymethyl-2,3-diphenyl-(7ar,10ac)-7a,8,9,10a-tetrahydro-furo[2',3':4,5]oxazolo[3,2-a]pteridin-5-one
    参考文献:
    名称:
    Hutzenlaub,W. et al., Chemische Berichte, 1976, vol. 109, p. 3217 - 3227
    摘要:
    DOI:
  • 作为产物:
    描述:
    1-(O2,O3-isopropylidene-β-D-ribofuranosyl)-6,7-diphenyl-1H-pteridine-2,4-dione盐酸三乙胺 作用下, 以 甲醇 为溶剂, 以75%的产率得到6,7-diphenyl-1-β-D-ribofuranosyl-1H-pteridine-2,4-dione
    参考文献:
    名称:
    Novel and Facil Synthesis and Evaluation of Antitumor Activities of 6,7-Bisaryl-1-(β-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones
    摘要:
    Novel 6,7-bisaryl-1-(beta-D-ribofuranosyl)pteridine-2,4( 1H,3H)-dione derivatives were synthesized by condensation of 5,6-diamino-2',3'-O-isopropylideneuridine, which was derived from uridine, with an appropriate alpha,beta-diketon, followed by acidic hydrolysis allowing removal of the isopropylidene group of the sugar moiety as a protecting group. Moreover, several N-3 alkyl derivatives of the 6,7-bisaryl-1-(beta-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones were obtained by alkylation of the 6,7-bisaryl-l-(2',3'-O-isopropylidene-beta-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones with alkyl halides and by their acidic hydrolysis for deprotection. The antitumor activities of all synthesized compounds against CCRF-HSB-2 and KB cell lines were also investigated in vitro and some of the compounds showed prospective antitumor activities.
    DOI:
    10.3987/com-09-s(s)77
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文献信息

  • Novel and Facil Synthesis and Evaluation of Antitumor Activities of 6,7-Bisaryl-1-(β-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones
    作者:Tomohisa Nagamatsu、Rafiya Khan Kandahary、Abugafar M. L. Hossion、Noriyuki Ashida
    DOI:10.3987/com-09-s(s)77
    日期:——
    Novel 6,7-bisaryl-1-(beta-D-ribofuranosyl)pteridine-2,4( 1H,3H)-dione derivatives were synthesized by condensation of 5,6-diamino-2',3'-O-isopropylideneuridine, which was derived from uridine, with an appropriate alpha,beta-diketon, followed by acidic hydrolysis allowing removal of the isopropylidene group of the sugar moiety as a protecting group. Moreover, several N-3 alkyl derivatives of the 6,7-bisaryl-1-(beta-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones were obtained by alkylation of the 6,7-bisaryl-l-(2',3'-O-isopropylidene-beta-D-ribofuranosyl)pteridine-2,4(1H,3H)-diones with alkyl halides and by their acidic hydrolysis for deprotection. The antitumor activities of all synthesized compounds against CCRF-HSB-2 and KB cell lines were also investigated in vitro and some of the compounds showed prospective antitumor activities.
  • Hutzenlaub,W. et al., Chemische Berichte, 1976, vol. 109, p. 3217 - 3227
    作者:Hutzenlaub,W. et al.
    DOI:——
    日期:——
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