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4-(3-Diethylamino-propylamino)-6-methoxy-quinazoline-5,8-dione | 120075-58-3

中文名称
——
中文别名
——
英文名称
4-(3-Diethylamino-propylamino)-6-methoxy-quinazoline-5,8-dione
英文别名
4-[3-(Diethylamino)propylamino]-6-methoxyquinazoline-5,8-dione
4-(3-Diethylamino-propylamino)-6-methoxy-quinazoline-5,8-dione化学式
CAS
120075-58-3
化学式
C16H22N4O3
mdl
——
分子量
318.376
InChiKey
IVAIQEVRSWQBGS-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):
    2.2
  • 重原子数:
    23
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    84.4
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    4-(3-Diethylamino-propylamino)-6-methoxy-quinazolin-5-ol 在 potassium dihydrogenphosphate 、 potassium nitrososulfonate 作用下, 以 甲醇 为溶剂, 反应 24.0h, 以30%的产率得到4-(3-Diethylamino-propylamino)-6-methoxy-quinazoline-5,8-dione
    参考文献:
    名称:
    Heterocyclic quinones. XVII. A new in vivo active antineoplastic drug: 6,7-bis(1-aziridinyl)-4-[[3-(N,N-dimethylamino)propyl]amino]-5,8-quinazolinedione
    摘要:
    A series of heterocyclic quinones 6-substituted and 6,7-disubstituted 4-(alkylamino)-5,8-quinazolinediones, have been synthesized in order to evaluate their in vitro cytotoxicity on L1210 leukemia cells. Among 14 derivatives that have been prepared and studied for the structure-activity relationship, the most potent cytotoxic compound on L1210 leukemia cells was the 6,7-bis(1-aziridinyl)-4-[[3-(N,N-dimethylamino)propyl]amino]-5,8-quinazolinedione (24). This compound has been tested with the use of a cell-image processor on MCF-7 human mammary and HBL human melanoma cell lines. The results show that compound 24 influences cell proliferation and blocks both cells lines in the S phase. In vivo antineoplastic activity of compound 24 has been demonstrated on a broad spectrum of murine experimental models, but it was found highly toxic and produced long-delayed deaths.
    DOI:
    10.1021/jm00105a007
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文献信息

  • GIORGI-RENAULT, SYLVIANE;RENAULT, JEAN;CEBEL-SERVOLLES, PATRICIA;BARON, M+, J. MED. CHEM., 34,(1991) N, C. 38-46
    作者:GIORGI-RENAULT, SYLVIANE、RENAULT, JEAN、CEBEL-SERVOLLES, PATRICIA、BARON, M+
    DOI:——
    日期:——
  • Heterocyclic quinones. XVII. A new in vivo active antineoplastic drug: 6,7-bis(1-aziridinyl)-4-[[3-(N,N-dimethylamino)propyl]amino]-5,8-quinazolinedione
    作者:Sylviane Giorgi-Renault、Jean Renault、Patricia Gebel-Servolles、Michel Baron、Claude Paoletti、Suzanne Cros、Marie Christine Bissery、Francois Lavelle、Ghanem Atassi
    DOI:10.1021/jm00105a007
    日期:1991.1
    A series of heterocyclic quinones 6-substituted and 6,7-disubstituted 4-(alkylamino)-5,8-quinazolinediones, have been synthesized in order to evaluate their in vitro cytotoxicity on L1210 leukemia cells. Among 14 derivatives that have been prepared and studied for the structure-activity relationship, the most potent cytotoxic compound on L1210 leukemia cells was the 6,7-bis(1-aziridinyl)-4-[[3-(N,N-dimethylamino)propyl]amino]-5,8-quinazolinedione (24). This compound has been tested with the use of a cell-image processor on MCF-7 human mammary and HBL human melanoma cell lines. The results show that compound 24 influences cell proliferation and blocks both cells lines in the S phase. In vivo antineoplastic activity of compound 24 has been demonstrated on a broad spectrum of murine experimental models, but it was found highly toxic and produced long-delayed deaths.
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