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2-azido-N-[[4-[(1,3-dioxobenzo[de]isoquinolin-4-yl)methyl]phenyl]methyl]acetamide

中文名称
——
中文别名
——
英文名称
2-azido-N-[[4-[(1,3-dioxobenzo[de]isoquinolin-4-yl)methyl]phenyl]methyl]acetamide
英文别名
——
2-azido-N-[[4-[(1,3-dioxobenzo[de]isoquinolin-4-yl)methyl]phenyl]methyl]acetamide化学式
CAS
——
化学式
C22H17N5O3
mdl
——
分子量
399.4
InChiKey
GXFXSICRNVLNCZ-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):
    4.1
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    89.6
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • NUCLEOTIDES AND APTAMERS CONTAINING BORONIC ACID GROUPS HAVING BIASED BINDING TO GLYCOSYLATED PROTEINS, AND USES THEREOF
    申请人:Georgia State University Research Foundation, Inc.
    公开号:EP2176277A2
    公开(公告)日:2010-04-21
  • [EN] NUCLEOTIDES AND APTAMERS CONTAINING BORONIC ACID GROUPS HAVING BIASED BINDING TO GLYCOSYLATED PROTEINS, AND USES THEREOF<br/>[FR] NUCLÉOTIDES ET APTAMÈRES CONTENANT DES GROUPES ACIDE BORONIQUE AYANT UNE LIAISON SOLLICITÉE À DES PROTÉINES GLYCOSYLÉES ET LEURS UTILISATIONS
    申请人:UNIV GEORGIA STATE RES FOUND
    公开号:WO2009012363A2
    公开(公告)日:2009-01-22
    The present disclosure encompasses oligonucleotide aptamers selectively binding a target glycosylated polypeptide or protein, and having biased affinity for the glycan through a boronic acid linked to a nucleosidic base of a nucleotide(s). The disclosure further encompasses methods for isolating an aptamer(s) selectively binding a target glycosylated polypeptide, where, from a population of randomized oligonucleotides that have at least one nucleotide having a boronic acid label linked to a base, is selected a first subpopulation of aptamers binding to the target glycosylated polypeptide or protein. This subpopulation is then amplified without using boronic acid-modified TTP, and amplification products not binding to a target glycosylated polypeptide or protein are selected. The second subpopulation of aptamers is then amplified using boronic acid-modified TTP to provide a population of boronic acid-modified aptamers capable of selectively binding to a glycosylation site of a target polypeptide or protein. Other aspects of the disclosure encompass methods for the use of the modified aptamers to detect glycosylated species of a polypeptide or protein.
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