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5,8-diaminophthalazine | 502584-74-9

中文名称
——
中文别名
——
英文名称
5,8-diaminophthalazine
英文别名
Phthalazine-5,8-diamine
5,8-diaminophthalazine化学式
CAS
502584-74-9
化学式
C8H8N4
mdl
——
分子量
160.178
InChiKey
KPIVUFBRSUKPFI-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):
    -0.3
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    77.8
  • 氢给体数:
    2
  • 氢受体数:
    4

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:
    5,8-diaminophthalazine盐酸sodium chlorate 作用下, 反应 1.0h, 以76%的产率得到6,7-二氯酞嗪-5,8-二酮
    参考文献:
    名称:
    Synthesis and antifungal activity of 6-arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones
    摘要:
    6-Arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among those tested, many compounds showed good antifungal activity. The results suggest that phthalazine-5,8-diones would be potent antifungal agents. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.003
  • 作为产物:
    描述:
    5-硝基酞嗪 在 palladium on activated charcoal 氢氧化钾氢气羟胺 作用下, 以 甲醇乙醇 为溶剂, 20.0~55.0 ℃ 、20.68 kPa 条件下, 反应 5.0h, 生成 5,8-diaminophthalazine
    参考文献:
    名称:
    Synthesis and antifungal activity of 6-arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones
    摘要:
    6-Arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among those tested, many compounds showed good antifungal activity. The results suggest that phthalazine-5,8-diones would be potent antifungal agents. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.003
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文献信息

  • Synthesis and antiproliferative activity of indolizinophthalazine-5,12-dione derivatives, DNA topoisomerase IB inhibitors
    作者:De-Qing Shen、Zu-Ping Wu、Xi-Wei Wu、Zeng-Yun An、Xiang-Zhang Bu、Lian-Quan Gu、Zhi-Shu Huang、Lin-Kun An
    DOI:10.1016/j.ejmech.2010.05.048
    日期:2010.9
    A series of novel indolizinophthalazine-5,12-dione derivatives were designed and synthesized by the reaction of 6,7-dichlorophthalazine-5,8-dione with active methylene reagents (AMR) and pyridine derivatives. Some of synthesized compounds exhibited significant in vitro antiproliferative activity at micromolar level toward four human tumor cell lines, including lung adenocarcinoma cell, large-cell lung carcinoma cell, breast carcinoma cell and ardriamycin-resistance breast carcinoma cell. The DNA topoisomerase IB inhibitory assay indicated that DNA topoisomerase IB might be a biological target of the synthesized compounds. (C) 2010 Published by Elsevier Masson SAS.
  • Synthesis and antifungal activity of 6-arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones
    作者:Chung-Kyu Ryu、Rae-Eun Park、Mi-Young Ma、Ji-Hee Nho
    DOI:10.1016/j.bmcl.2007.02.003
    日期:2007.5
    6-Arylamino-phthalazine-5,8-diones and 6,7-bis(arylthio)-phthalazine-5,8-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among those tested, many compounds showed good antifungal activity. The results suggest that phthalazine-5,8-diones would be potent antifungal agents. (c) 2007 Elsevier Ltd. All rights reserved.
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