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3-{[3-(2-furoyl)-2-thioxoimidazolidin-1-yl]methylene}pentane-2,4-dione | 1135237-13-6

中文名称
——
中文别名
——
英文名称
3-{[3-(2-furoyl)-2-thioxoimidazolidin-1-yl]methylene}pentane-2,4-dione
英文别名
3-[[3-(Furan-2-carbonyl)-2-sulfanylideneimidazolidin-1-yl]methylidene]pentane-2,4-dione
3-{[3-(2-furoyl)-2-thioxoimidazolidin-1-yl]methylene}pentane-2,4-dione化学式
CAS
1135237-13-6
化学式
C14H14N2O4S
mdl
——
分子量
306.342
InChiKey
MQOOWTQPTCJGRV-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):
    0.7
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    103
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    呋喃甲酰氯 、 3-[(2-Sulfanylideneimidazolidin-1-yl)methylidene]pentane-2,4-dione 在 吡啶四甲基乙二胺 作用下, 以64%的产率得到3-{[3-(2-furoyl)-2-thioxoimidazolidin-1-yl]methylene}pentane-2,4-dione
    参考文献:
    名称:
    N-Acylated and N,N′-diacylated imidazolidine-2-thione derivatives and N,N′-diacylated tetrahydropyrimidine-2(1H)-thione analogues: Synthesis and antiproliferative activity
    摘要:
    Fifty-one acylthioureas (ATUs) incorporating imidazolidine-2-thione or its upper cyclohomologue were prepared by parallel synthesis and evaluated against a high number of human cancer cell lines for antiproliferative activity. ATUs 1o (3,5-dichlorobenzoyl), 1s (2-furoyl), 3s (2-furoyl) and 1t (2-thenoyl) displayed activity against leukemia, melanoma LOX IMVI, non-small cell lung NCI-H522, renal 786-0, CAKI-1, SN12C, UO-31 and breast MCF7, MDA-MB-435, T-47D cancer cell lines in the 0.3-9.7 mu M concentration range. Compound 14s exhibited selectivity for melanoma SK-MEL-5 (GI(50) < 5 nM); 1s for leukemia MOLT-4 (GI(50): 300 nM); 1q, 3b and 3q for renal cancer UO-31 (GI(50): 70200 nM); 8s, 9s for non-small cell lung cancer EKVX (GI(50): 300, 10 nM) and 3j for HOP-92 (GI(50): 700 nM) cell line. (C) 2008 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2008.06.010
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