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2-Propenoic acid,3-[4-[[[2-[(4-nitrophenyl)amino]-2-oxoethyl]propylamino]sulfonyl]phenyl]-,methyl ester | 916336-31-7

中文名称
——
中文别名
——
英文名称
2-Propenoic acid,3-[4-[[[2-[(4-nitrophenyl)amino]-2-oxoethyl]propylamino]sulfonyl]phenyl]-,methyl ester
英文别名
(E)-3-(4-{[(4-Nitro-phenylcarbamoyl)-methyl]-propyl-sulfamoyl}-phenyl)-acrylic acid methyl ester
2-Propenoic acid,3-[4-[[[2-[(4-nitrophenyl)amino]-2-oxoethyl]propylamino]sulfonyl]phenyl]-,methyl ester化学式
CAS
916336-31-7
化学式
C21H23N3O7S
mdl
——
分子量
461.496
InChiKey
APQFHXHWOUEARH-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

物化性质

  • 密度:
    1.364±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.82
  • 重原子数:
    32.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    135.92
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    2-Propenoic acid,3-[4-[[[2-[(4-nitrophenyl)amino]-2-oxoethyl]propylamino]sulfonyl]phenyl]-,methyl ester铁粉氯化铵N,N-二异丙基乙胺 作用下, 以 四氢呋喃甲醇 为溶剂, 生成 (Z)-3-[4-({[4-(4-Hydroxy-8-nitro-quinazolin-5-ylamino)-phenylcarbamoyl]-methyl}-propyl-sulfamoyl)-phenyl]-acrylic acid methyl ester
    参考文献:
    名称:
    4′-Alkoxyl substitution enhancing the anti-mitotic effect of 5-(3′,4′,5′-substituted)anilino-4-hydroxy-8-nitroquinazolines as a novel class of anti-microtubule agents
    摘要:
    Mitosis inhibitors are powerful anticancer drugs. Based on a novel anti-microtubule agent of 5-(4'-methoxy)anilino-4-hydroxy-8-nitroquinazoline, a series of 5-(3',4',5'-substituted)anilino-4-hydroxy-8- nitroquinazolines were designed and synthesized to investigate the effect of the substitution on the inhibitory activity against mitotic progression of tumor cells. The large alkoxyl substitution on the 4'-position of 5-anilino ring is beneficial for the potency. The 5-(3',4,5'-trimethoxy)anilino-8-nitroquinazoline (1h) displays an overwhelming activity in arresting the cells at the G2/M phase, providing a promising new template for further development of potent microtubule-targeted anti-mitotic drugs. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.058
  • 作为产物:
    描述:
    2-氯-4’-硝基乙酰苯胺 在 bis-triphenylphosphine-palladium(II) chloride 、 N,N-二异丙基乙胺 、 zinc dibromide 作用下, 以 四氢呋喃 为溶剂, 生成 2-Propenoic acid,3-[4-[[[2-[(4-nitrophenyl)amino]-2-oxoethyl]propylamino]sulfonyl]phenyl]-,methyl ester
    参考文献:
    名称:
    4′-Alkoxyl substitution enhancing the anti-mitotic effect of 5-(3′,4′,5′-substituted)anilino-4-hydroxy-8-nitroquinazolines as a novel class of anti-microtubule agents
    摘要:
    Mitosis inhibitors are powerful anticancer drugs. Based on a novel anti-microtubule agent of 5-(4'-methoxy)anilino-4-hydroxy-8-nitroquinazoline, a series of 5-(3',4',5'-substituted)anilino-4-hydroxy-8- nitroquinazolines were designed and synthesized to investigate the effect of the substitution on the inhibitory activity against mitotic progression of tumor cells. The large alkoxyl substitution on the 4'-position of 5-anilino ring is beneficial for the potency. The 5-(3',4,5'-trimethoxy)anilino-8-nitroquinazoline (1h) displays an overwhelming activity in arresting the cells at the G2/M phase, providing a promising new template for further development of potent microtubule-targeted anti-mitotic drugs. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.08.058
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