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Acitrel | 774595-73-2

中文名称
——
中文别名
——
英文名称
Acitrel
英文别名
sodium;hydrogen carbonate;6-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]-1H-benzimidazole
Acitrel化学式
CAS
774595-73-2
化学式
C18H20N3NaO6S
mdl
——
分子量
429.4
InChiKey
UUYQXLQNUVEFGD-UHFFFAOYSA-M
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):
    -1.21
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    157
  • 氢给体数:
    2
  • 氢受体数:
    9

文献信息

  • A NOVEL FORMULATION, OMEPRAZOLE ANTACID COMPLEX-IMMEDIATE RELEASE FOR RAPID AND SUSTAINED SUPRESSION OF GASTRIC ACID
    申请人:SANTARUS, INC.
    公开号:EP1603537A2
    公开(公告)日:2005-12-14
  • PHARMACEUTICAL FORMULATION AND METHOD FOR TREATING ACID-CAUSED GASTROINTESTINAL DISORDERS
    申请人:SANTARUS, INC.
    公开号:EP1648417A2
    公开(公告)日:2006-04-26
  • A NOVEL FORMULATION, OMEPRAZOLE ANTACID COMPLEX-IMMEDIATE RELEASE FOR RAPID AND SUSTAINED SUPPRESSION OF GASTRIC ACID
    申请人:Santarus, Inc.
    公开号:EP1796641A1
    公开(公告)日:2007-06-20
  • ORALE ZUBEREITUNGEN MIT OMEPRAZOL ODER PANTOPRAZOL
    申请人:Symrise AG
    公开号:EP3380085A1
    公开(公告)日:2018-10-03
  • Novel formulation, omeprazole antacid complex-immediate release for rapid and sustained suppression of gastric acid
    申请人:——
    公开号:US20040248942A1
    公开(公告)日:2004-12-09
    The present invention is directed to methods, kits, combinations, and compositions for treating, preventing or reducing the risk of developing a gastrointestinal disorder or disease, or the symptoms associated with, or related to a gastrointestinal disorder or disease in a subject in need thereof. In one aspect, the present invention provides a pharmaceutical composition comprising a proton pump inhibiting agent and a buffering agent for oral administration and ingestion by a subject. Upon administration, the composition contacts the gastric fluid of the stomach and increases the gastric fluid pH of the stomach to a pH that substantially prevents or inhibits acid degradation of the proton pump inhibiting agent in the gastric fluid and allows a measurable serum concentration of the proton pump inhibiting agent to be absorbed into the blood serum of the subject.
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