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methyl 11-(N-acryloylamino)undecanoate | 172102-69-1

中文名称
——
中文别名
——
英文名称
methyl 11-(N-acryloylamino)undecanoate
英文别名
11-acryloylamino-undecanoic acid methyl ester;11-Acryloylamino-undecansaeure-methylester;Methyl 11-(prop-2-enoylamino)undecanoate
methyl 11-(N-acryloylamino)undecanoate化学式
CAS
172102-69-1
化学式
C15H27NO3
mdl
——
分子量
269.384
InChiKey
HCULTCAVVATMEC-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):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

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
  • 下游产品
    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:
    methyl 11-(N-acryloylamino)undecanoatesodium hydroxide 作用下, 以 四氢呋喃 为溶剂, 以94%的产率得到11-(丙-2-烯酰氨基)十一烷酸
    参考文献:
    名称:
    Bioactive molecular sheets from self-assembly of polymerizable peptides
    摘要:
    我们已经证明,可聚合的多肽能够在浓溶液中自发组装成一种独特的片状二维结构,这种结构可以通过共价键固定下来,形成二维分子实体。这些实体已被证明在向活细胞输送货物方面非常有效,并且几乎无毒,相比之下,非聚合的纳米结构在这方面表现不佳。
    DOI:
    10.1039/b806559d
  • 作为产物:
    描述:
    参考文献:
    名称:
    Polyanion Inhibitors of Human Immunodeficiency Virus and Other Viruses. 5. Telomerized Anionic Surfactants Derived from Amino Acids
    摘要:
    omega-Acryloyl anionic surfactants, whose polar heads are derived from amino acids, have been telomerized to prepare polyanions of a predetermined molecular weight. The main goal of this study was to verify whether the antiviral activity is influenced by the degree of polymerization of the polyanions. The oligomeric polyanions were evaluated for their activity against human immunodeficiency virus (HIV-1 or HIV-2) and various other RNA and DNA viruses. With regard to their anti-HIV activity, a minimum number of anionic groups was necessary to achieve an inhibitory effect. Moreover, to be active the overall conformation of the polyanion must be such that the anionic groups are located on the external site of the molecule. With some of the polyanions, a 50% inhibition concentration (IC50) as low as 1 mu g/mL, or even 0.1 mu g/mL, was noted against HIV-1 in CEM-4 and MT-4 cells, respectively. The most potent polyanions also proved active against human cytomegalovirus and herpex simplex virus at concentrations of 5-10 and 20-40 mu g/mL, respectively. No activity was observed against any of the other viruses tested (i.e., vesicular stomatitis, Sindbis, Semliki forest, parainfluenza, Junin, Tacaribe, Coxsackie, polio, reo, and vaccinia). No toxicity for the host cells was observed at concentrations up to 200 mu g/mL.
    DOI:
    10.1021/jm960493b
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