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| 69674-66-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
69674-66-4
化学式
C17H15NNaO3
mdl
——
分子量
304.29
InChiKey
SOZGOLIIBOWMKT-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):
    2.65
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    57.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Oral solid pharmaceutical form with sequential action for the administering of drugs with ulcerogenic side effect
    申请人:LABORATORIO ITALIANO BIOCHIMICO FARMACEUTICO LISAPHARMA S.P.A.
    公开号:EP0167958A2
    公开(公告)日:1986-01-15
    Oral solid pharmaceutical form with antiinflammatory and analgesic activity, with sequential action, with protective effect on the gastric and duodenal mucosa against the action of the active principles having ulcerogenic effect, contained in the same pharmaceutical form. Said pharmaceutical form is constituted by a tablet comprising: (a) a centre core containing an active principle provided with antiinflammatory and analgesic activity, with ulcerogenic side effects; (b) a layer coating of said core, containing a second active principle provided with protective action for said gastric and duodenal mucosa, which is immediately released.
    具有消炎和镇痛活性的口服固体药剂,具有连续作用,对胃和十二指肠粘膜具有保护作用,防止具有致溃疡作用的活性成分对胃和十二指肠粘膜的作用,包含在同一药剂中。 所述药剂由片剂构成,片剂包括:(a)中心芯,内含具有消炎和镇痛活性的活性成分,具有致溃疡副作用;(b)所述中心芯的包衣层,内含对所述胃和十二指肠粘膜具有保护作用的第二种活性成分,可立即释放。
  • METHOD OF INCREASING EPITHELIAL PERMEABILITY USING NANOPARTICLES
    申请人:Carnegie Mellon University
    公开号:EP3651789A1
    公开(公告)日:2020-05-20
  • EXTRACTS FOR THE REGENERATION OF LIGAMENTS
    申请人:University of Pittsburgh - of the Commonwealth System of Higher Education
    公开号:EP3755267A1
    公开(公告)日:2020-12-30
  • Method of Increasing Epithelial Permeability Using Nanoparticles
    申请人:Carnegie Mellon University
    公开号:US20200129444A1
    公开(公告)日:2020-04-30
    Provided herein are devices and dosage forms useful in delivering macromolecular active ingredients or drugs, such as proteins, peptides and nucleic acids, through epithelial membranes, such as intestinal epithelium. Also provided are trans-epithelial drug delivery methods and methods of treatment of diabetes or insulin resistance, or to induce weight loss.
  • Compositions and Methods for Modulating Permeability of Biological Barriers
    申请人:Carnegie Mellon University
    公开号:US20210113519A1
    公开(公告)日:2021-04-22
    A method of reversibly increasing intestinal epithelium permeability is provided. A plant polyphenol composition, such as a pelargonidin-containing composition is enterically-administered, e.g., with a high molecular weight therapeutic agent, such as insulin, such that therapeutic agents having high molecular weights can be delivered enterically. An oral dosage form for enteric delivery of high molecular weight therapeutic agents also is provided.
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