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3-methyl-10-o-tolyl-10H-benzo[g]pteridine-2,4-dione | 35919-98-3

中文名称
——
中文别名
——
英文名称
3-methyl-10-o-tolyl-10H-benzo[g]pteridine-2,4-dione
英文别名
Benzo[g]pteridine-2,4(3H,10H)-dione, 3-methyl-10-(2-methylphenyl)-;3-methyl-10-(2-methylphenyl)benzo[g]pteridine-2,4-dione
3-methyl-10-<i>o</i>-tolyl-10<i>H</i>-benzo[<i>g</i>]pteridine-2,4-dione化学式
CAS
35919-98-3
化学式
C18H14N4O2
mdl
——
分子量
318.335
InChiKey
GTJWDRBWXVWTEL-UHFFFAOYSA-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):
    2.6
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    65.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Flavins as potential antimalarials. 2. 3-Methyl-10-(substituted-phenyl)flavins
    摘要:
    A series of 3-methyl-10-(substituted-phenyl)flavins was prepared and tested for antimalarial activity against the lethal parasite Plasmodium vinckei in mice. Several of these analogues were found to be effective antimalarial agents. A quantitative structure-activity relationship study was undertaken with 44 analogues and no satisfactory relationship could be established.
    DOI:
    10.1021/jm00110a009
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文献信息

  • A New and Improved<b><i>N</i></b>-3 Alkylation of 10-Substituted Isoalloxazines Using 1,8-Diazabicyclo[5.4.0]undec-7-ene in Benzene
    作者:Geetanjali、Ram Singh、S. M. S. Chauhan
    DOI:10.1081/scc-120015816
    日期:2003.1.4
    Abstract 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) has been identified as a remarkable base for the alkylation at N-3 position of 10-substituted isoalloxazines with alkyl halides in dry benzene.
    摘要 1,8-二氮杂双环[5.4.0]十一碳-7-烯(DBU) 已被鉴定为在无水苯中用烷基卤在10-取代异恶嗪的N-3 位进行烷基化反应的显着碱。
  • Microwave-Assisted Synthesis of 10-Substituted Isoalloxazines in the Presence of Solid Acids
    作者:S. M. S. Chauhan、Ram Singh、Geetanjali
    DOI:10.1081/scc-120017194
    日期:2003.1.5
    Abstract The microwave-enhanced synthesis of 10-substituted isoalloxazines is achieved rapidly (˜4 min) and in good yield (>80–95%) via the cyclocondensation of 2-substituted aminoanilines with alloxan or N-methylalloxan monohydrate in the presence of acidic alumina or montmorillonite clays (KSF and K10).
    摘要 通过 2-取代氨基苯胺与四氧嘧啶或 N-甲基四氧嘧啶一水合物在酸性存在下的环缩合反应,10-取代异咯嗪的微波增强合成可快速(约 4 分钟)且收率良好(>80-95%)。氧化铝或蒙脱石粘土(KSF 和 K10)。
  • COWDEN, WILLIAM B.;HALLADAY, PETER K.;CUNNINGHAM, ROSS B.;HUNT, NICHOLAS +, J. MED. CHEM., 34,(1991) N, C. 1818-1822
    作者:COWDEN, WILLIAM B.、HALLADAY, PETER K.、CUNNINGHAM, ROSS B.、HUNT, NICHOLAS +
    DOI:——
    日期:——
  • Flavins as potential antimalarials. 2. 3-Methyl-10-(substituted-phenyl)flavins
    作者:William B. Cowden、Peter K. Halladay、Ross B. Cunningham、Nicholas H. Hunt、Ian A. Clark
    DOI:10.1021/jm00110a009
    日期:1991.6
    A series of 3-methyl-10-(substituted-phenyl)flavins was prepared and tested for antimalarial activity against the lethal parasite Plasmodium vinckei in mice. Several of these analogues were found to be effective antimalarial agents. A quantitative structure-activity relationship study was undertaken with 44 analogues and no satisfactory relationship could be established.
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