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N-(1-hydroxy-3-oxopentan-2-yl)acetamide

中文名称
——
中文别名
——
英文名称
N-(1-hydroxy-3-oxopentan-2-yl)acetamide
英文别名
——
N-(1-hydroxy-3-oxopentan-2-yl)acetamide化学式
CAS
——
化学式
C7H13NO3
mdl
——
分子量
159.18
InChiKey
HHQNAFXDPXZQRW-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:
    11
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • PROCESS FOR THE SYNTHESIS OF LACOSAMIDE
    申请人:Euticals S.P.A.
    公开号:EP2528892B1
    公开(公告)日:2014-06-04
  • Azoline Compound and Azole Compound Library and Method for Producing Same
    申请人:Suga Hiroaki
    公开号:US20140113830A1
    公开(公告)日:2014-04-24
    An object of the present invention is to provide a method of efficiently constructing a library abundant in diversity and also usable for screening of a compound that binds to a target substance having protease activity. The present invention provides a method of constructing an azoline compound library containing two or more azoline compounds having an azoline backbone introduced into at least one of Cys, Ser, Thr, and 2,3-diamino acid, and analogs thereof of Xaa 0 of a peptide represented by the following formula (I): A-(Xaa 0 ) n -B  (I) [wherein, m numbers of Xaa 0 s respectively represent arbitrary amino acids, at least one of which is an amino acid selected from the group consisting of Cys, Ser, Thr, and 2,3-diamino acid, and analogs thereof, m represents an inter selected from 2 to 40, and A and B each independently represent a peptide composed of from 0 to 100 amino acids].
  • Method for Producing Compound Containing Heterocycle
    申请人:THE UNIVERSITY OF TOKYO
    公开号:US20160083719A1
    公开(公告)日:2016-03-24
    An object of the present invention is to provide a method of stably introducing a heterocycle into a substrate peptide by using an azoline backbone introducing enzyme. The present invention provides a method of introducing a heterocycle into a leader-sequence-free substrate peptide by using an azoline backbone introducing enzyme to which a leader sequence of the substrate has been bound.
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