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Ethyl 2-amino-5-hydroxy-4-methylsulfanyl-furo[2,3-f]quinazoline-3-carboxylate | 1355613-27-2

中文名称
——
中文别名
——
英文名称
Ethyl 2-amino-5-hydroxy-4-methylsulfanyl-furo[2,3-f]quinazoline-3-carboxylate
英文别名
ethyl 2-amino-5-hydroxy-4-methylsulfanylfuro[2,3-f]quinazoline-3-carboxylate
Ethyl 2-amino-5-hydroxy-4-methylsulfanyl-furo[2,3-f]quinazoline-3-carboxylate化学式
CAS
1355613-27-2
化学式
C14H13N3O4S
mdl
——
分子量
319.341
InChiKey
LGEUPMUDQVANSY-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):
    2.5
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    137
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and antifungal activity of 6,7-bis(arylthio)-quinazoline-5,8-diones and furo[2,3-f]quinazolin-5-ols
    摘要:
    6,7-Bis(arylthio)-quinazoline-5,8-dione and furo[2,3-f]quinazolin-5-ol derivatives were synthesized and tested for in vitro antifungal activity against Candida, Aspergillus species, and Cryptococcus neoformans. Among them tested, many of furo[2,3-f]quinazolin-5-ols and 6,7-bis(arylthio)-quinazoline-5,8-diones showed good antifungal activity. The compounds 4a and 4e completely inhibited the growth of all against Candida and Aspergillus species tested at the MIC level of 12.5 mu g/mL. The results suggest that furo[2,3-f]quinazolin-5-ols and 6,7-bis(arylthio)-quinazoline-5,8-diones would be promising antifungal agents. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.10.099
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文献信息

  • Synthesis and antifungal activity of 6,7-bis(arylthio)-quinazoline-5,8-diones and furo[2,3-f]quinazolin-5-ols
    作者:Chung-Kyu Ryu、Yang Hui Kim、Hyun Ah Im、Ji Young Kim、Joo Hee Yoon、Aram Kim
    DOI:10.1016/j.bmcl.2011.10.099
    日期:2012.1
    6,7-Bis(arylthio)-quinazoline-5,8-dione and furo[2,3-f]quinazolin-5-ol derivatives were synthesized and tested for in vitro antifungal activity against Candida, Aspergillus species, and Cryptococcus neoformans. Among them tested, many of furo[2,3-f]quinazolin-5-ols and 6,7-bis(arylthio)-quinazoline-5,8-diones showed good antifungal activity. The compounds 4a and 4e completely inhibited the growth of all against Candida and Aspergillus species tested at the MIC level of 12.5 mu g/mL. The results suggest that furo[2,3-f]quinazolin-5-ols and 6,7-bis(arylthio)-quinazoline-5,8-diones would be promising antifungal agents. (C) 2011 Elsevier Ltd. All rights reserved.
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