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N-[4-(acetylamino)phenyl]acrylamide

中文名称
——
中文别名
——
英文名称
N-[4-(acetylamino)phenyl]acrylamide
英文别名
4-acrylamidephenylacetamide;N-[4-(acetylamino)phenyl]prop-2-enamide;N-(4-acetamidophenyl)prop-2-enamide
N-[4-(acetylamino)phenyl]acrylamide化学式
CAS
——
化学式
C11H12N2O2
mdl
——
分子量
204.228
InChiKey
AMUXEICCQPAHAS-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):
    0.9
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    2

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:
    N-[4-(acetylamino)phenyl]acrylamide 、 5,11,17,23-tetraiodocalix[4]arene-25,26,27,28-tetra-n-butyl ether 在 palladium diacetate 三乙胺二苯基丙基膦 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 275.0h, 以49%的产率得到5,11,17,23-tetrakis[(E)-N-(4-acetamidophenyl)-acrylamido]-25,26,27,28-tetra-n-butoxycalix[4]arene
    参考文献:
    名称:
    Synthesis and capsule formation of upper rim substituted tetra-acrylamido calix[4]arenes
    摘要:
    利用钯催化的 Heck 反应,将上缘取代的四碘钙[4]炔与多种丙烯酰胺偶联。四丙烯酰胺基上边缘取代的钙并[4]炔能以良好的收率和极高的立体选择性生成全反式异构体。研究表明,从仲丙烯酰胺中提取的四丙烯酰胺基钙钛矿[4]炔能通过八个氢键进行二聚,形成二聚胶囊,其中能包含小分子有机物。
    DOI:
    10.1039/b502378e
  • 作为产物:
    描述:
    丙烯酰氯4′-氨基乙酰苯胺吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以41%的产率得到N-[4-(acetylamino)phenyl]acrylamide
    参考文献:
    名称:
    A Potent Isoprenylcysteine Carboxylmethyltransferase (ICMT) Inhibitor Improves Survival in Ras-Driven Acute Myeloid Leukemia
    摘要:
    Blockade of Ras activity by inhibiting its post-translational methylation catalyzed by isoprenylcysteine carboxylmethyltransferase (ICMT) has been suggested as a promising antitumor strategy. However, the paucity of inhibitors has precluded the clinical validation of this approach. In this work we report a potent ICMT inhibitor, compound 3 [UCM-1336, IC50 = 2 mu M], which is selective against the other enzymes involved in the post-translational modifications of Ras. Compound 3 significantly impairs the membrane association of the four Ras isoforms, leading to a decrease of Ras activity and to inhibition of Ras downstream signaling pathways. In addition, it induces cell death in a variety of Ras-mutated tumor cell lines and increases survival in an in vivo model of acute myeloid leukemia. Because ICMT inhibition impairs the activity of the four Ras isoforms regardless of its activating mutation, compound 3 surmounts many of the common limitations of available Ras inhibitors described so far. In addition, these results validate ICMT as a valuable target for the treatment of Ras-driven tumors.
    DOI:
    10.1021/acs.jmedchem.9b00145
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文献信息

  • Temperature-responsive polymer compound and process for producing the same
    申请人:Akiyama Yoshikatsu
    公开号:US20050224415A1
    公开(公告)日:2005-10-13
    A temperature-responsive polymer and polymer material which has ester bond(s) and/or acid amide bond(s) respectively at one or more sites in the side chain and can be arbitrarily controlled by varying the side chain is provided. The process for production thereof and the use thereof are also provided.
    提供了一种温度敏感的聚合物和聚合物材料,其在侧链中的一个或多个位置具有酯键和/或酸酰胺键,并且可以通过改变侧链任意控制。同时还提供了其生产过程和使用方法。
  • TEMPERATURE-RESPONSIVE POLYMER COMPOUND AND PROCESS FOR PRODUCING THE SAME
    申请人:Amersham Pharmacia Biotech K.K.
    公开号:EP1153049A1
    公开(公告)日:2001-11-14
  • US6956077B1
    申请人:——
    公开号:US6956077B1
    公开(公告)日:2005-10-18
  • [EN] TEMPERATURE-RESPONSIVE POLYMER COMPOUND AND PROCESS FOR PRODUCING THE SAME<br/>[FR] POLYMERE SENSIBLE A LA TEMPERATURE ET PROCEDE DE FABRICATION CORRESPONDANT
    申请人:AMERSHAM PHARMACIA BIOTECH K K
    公开号:WO2000044800A1
    公开(公告)日:2000-08-03
    A temperature-responsive polymer and polymer material which has ester bond(s) and/or acid amide bond(s) respectively at one or more sites in the side chain and can be arbitrarily controlled by varying the side chain is provided. The process for production thereof and the use thereof are also provided.
  • A Potent Isoprenylcysteine Carboxylmethyltransferase (ICMT) Inhibitor Improves Survival in Ras-Driven Acute Myeloid Leukemia
    作者:Nagore I. Marín-Ramos、Moisés Balabasquer、Francisco J. Ortega-Nogales、Iván R. Torrecillas、Ana Gil-Ordóñez、Beatriz Marcos-Ramiro、Pedro Aguilar-Garrido、Ian Cushman、Antonio Romero、Francisco J. Medrano、Consuelo Gajate、Faustino Mollinedo、Mark R. Philips、Mercedes Campillo、Miguel Gallardo、Mar Martín-Fontecha、María L. López-Rodríguez、Silvia Ortega-Gutiérrez
    DOI:10.1021/acs.jmedchem.9b00145
    日期:2019.7.11
    Blockade of Ras activity by inhibiting its post-translational methylation catalyzed by isoprenylcysteine carboxylmethyltransferase (ICMT) has been suggested as a promising antitumor strategy. However, the paucity of inhibitors has precluded the clinical validation of this approach. In this work we report a potent ICMT inhibitor, compound 3 [UCM-1336, IC50 = 2 mu M], which is selective against the other enzymes involved in the post-translational modifications of Ras. Compound 3 significantly impairs the membrane association of the four Ras isoforms, leading to a decrease of Ras activity and to inhibition of Ras downstream signaling pathways. In addition, it induces cell death in a variety of Ras-mutated tumor cell lines and increases survival in an in vivo model of acute myeloid leukemia. Because ICMT inhibition impairs the activity of the four Ras isoforms regardless of its activating mutation, compound 3 surmounts many of the common limitations of available Ras inhibitors described so far. In addition, these results validate ICMT as a valuable target for the treatment of Ras-driven tumors.
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