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22-Oxo-tricosanoic acid

中文名称
——
中文别名
——
英文名称
22-Oxo-tricosanoic acid
英文别名
22-oxotricosanoic acid
22-Oxo-tricosanoic acid化学式
CAS
——
化学式
C23H44O3
mdl
——
分子量
368.6
InChiKey
DWIGCHXTZQHDFF-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):
    8.8
  • 重原子数:
    26
  • 可旋转键数:
    21
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • PROTEASE STABILIZED, ACYLATED INSULIN ANALOGUES
    申请人:Madsen Peter
    公开号:US20110105720A1
    公开(公告)日:2011-05-05
    Novel acylated insulin analogues exhibiting resistance towards proteases can, effectively, be administered pulmonary or orally. The insulin analogues contain B25H and A14E or A14H.
    具有对蛋白酶抵抗力的新型酰化胰岛素类似物可以通过肺部或口服有效地给予。胰岛素类似物包含B25H和A14E或A14H。
  • PROTEASE STABILIZED ACYLATED INSULIN ANALOGUES
    申请人:NOVO NORDISK A/S
    公开号:US20150210748A1
    公开(公告)日:2015-07-30
    Novel acylated insulin analogues exhibiting resistance towards proteases can, effectively, be administered pulmonary or orally. The insulin analogues contain B25H and A14E or A14H.
    具有对蛋白酶抗性的新型酰化胰岛素类似物可以有效地通过肺部或口服给药。胰岛素类似物包含B25H和A14E或A14H。
  • Protease stabilized, acylated insulin analogues
    申请人:Novo Nordisk A/S
    公开号:EP2910570B1
    公开(公告)日:2016-10-12
  • Novel antibacterial agents
    申请人:Christensen G. Burton
    公开号:US20070154948A1
    公开(公告)日:2007-07-05
    This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands has a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.
  • N-Terminally Modified Insulin Derivatives
    申请人:Novo Nordisk A/S
    公开号:US20140357838A1
    公开(公告)日:2014-12-04
    The invention is related to novel N-terminally modified insulin derivatives comprising extra disulphide bond(s), pharmaceutical compositions comprising such and methods of making such.
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