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盐酸西托硫胺 | 616-96-6

中文名称
盐酸西托硫胺
中文别名
——
英文名称
Ethyl [2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-ethoxycarbonyloxypent-2-en-3-yl]sulfanylformate;hydrochloride
英文别名
——
盐酸西托硫胺化学式
CAS
616-96-6
化学式
C18H27ClN4O6S
mdl
——
分子量
462.9
InChiKey
LIOJHMDIELWKFZ-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

物化性质

  • 熔点:
    121-123 °C

计算性质

  • 辛醇/水分配系数(LogP):
    2.341
  • 重原子数:
    30
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    159
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • CRYSTALLINE CONDITION DISLOCATING METHOD
    申请人:NIPPON SHINYAKU COMPANY, LIMITED
    公开号:EP0665009A1
    公开(公告)日:1995-08-02
    An object of this invention is to provide a method of dislocating the crystalline condition of crystalline medicine simply, speedily and homogeneously, and, moreover, in large quantities at once. This invention is directed to a method using an extruder when crystalline medicine in a certain crystalline condition (△ is dislocated to another crystalline condition (○), i.e., when the dislocation of crystalline condition (△->○) is carried out.
    本发明的目的是提供一种简单、快速和均匀地将结晶药物的结晶状态变位的方法,而且是一次性大量变位。本发明针对的是一种使用挤压机将某种结晶状态(△)的结晶药物变位到另一种结晶状态(○)的方法,即结晶状态(△->○)变位的方法。
  • SACCHARIDE-CONTAINING COMPOSITIONS
    申请人:FUJI CHEMICAL INDUSTRY CO., LTD.
    公开号:EP1008353A1
    公开(公告)日:2000-06-14
    Spray-dried powders containing calcium hydrogen phosphate and saccharides having excellent powder-fluidity and compression-moldability, being quickly disintegrated/dissolved when put into the oral cavity or water in the form of granules, tablets, etc., being useful as fillers, compression-moldability improvers, disintegration aids, administration-facilitating agents, solubilizers in the oral cavity, etc. and being applicable to drugs, foods, etc.
    含有磷酸糖类的喷雾干燥粉末,具有极佳的粉末流动性和压模性,以颗粒、片剂等形式放入口腔或中时可迅速崩解/溶解,可用作填充剂、压模性改进剂、崩解辅助剂、给药促进剂、口腔增溶剂等,适用于药物、食品等。
  • Composition for rapid disintegrating tablet in oral cavity
    申请人:FUJI CHEMICAL INDUSTRY CO., LTD.
    公开号:EP1523974A1
    公开(公告)日:2005-04-20
    The present invention provides rapid disintegrating tablets in oral cavity having a shortened disintegration time in oral cavity as well as a sufficient hardness with compared to rapid disintegrating tablets of the prior art. The above objective is solved by a composition for rapid disintegrating tablets in oral cavity, wherein components (a) to (c) are contained in such manner that (a) saccharides consisting of a combination of mannitol and xylitol is 40 to 90 parts by weight; (b) the inorganic excipient is 1 to 30 parts by weight; and (c) the disintegrating agent is 5 to 40 parts by weight, provided that the total amount of (a), (b) and (c) is 100 parts by weight.
    本发明提供的口腔快速崩解片与现有技术的口腔快速崩解片相比,具有更短的口腔崩解时间和足够的硬度。 本发明通过一种口腔快速崩解片剂组合物来实现上述目标,其中组分(a)至(c)的含有方式为 (a) 糖类甘露糖醇和木糖醇组合而成,按重量计占 40 至 90%; (b) 无机赋形剂按重量计为 1 至 30 份;以及 (c) 以重量計,崩解劑為 5 至 40 份、 条件是(a)、(b)和(c)的总用量以重量计为 100 份。
  • TABLET QUICKLY DISINTEGRATING IN ORAL CAVITY
    申请人:FUJI CHEMICAL INDUSTRY CO., LTD.
    公开号:EP1674083A1
    公开(公告)日:2006-06-28
    The present invention provides rapid disintegrating tablets in oral cavity having a shortened disintegration time in oral cavity as well as a sufficient hardness compared to rapid disintegrating tablets of the prior art. The above objective is solved by a composition in which the inorganic excipient and the disintegrating agent are dispersed in the complex particles consisting of mannitol and other saccharide(s) in a specific ratio, and rapid disintegrating tablets in oral cavity obtained by direct compression of the composition.
    本发明提供的口腔快速崩解片与现有技术的口腔快速崩解片相比,具有更短的口腔崩解时间和足够的硬度。 解决上述问题的方法是将无机辅料和崩解剂按特定比例分散在由甘露醇和其他糖类组成的复合颗粒中,通过直接压缩该组合物获得口腔快速崩解片。
  • ANTIPYRETIC/ANALGESIC COMPOSITION
    申请人:Kowa Co., Ltd.
    公开号:EP2659889A1
    公开(公告)日:2013-11-06
    Provided is a stable pharmaceutical composition comprising ibuprofen and butylscopolamine bromide. The pharmaceutical composition comprises ibuprofen, butylscopolamine bromide, and a moisture-absorbing polymer.
    本发明提供了一种由布洛芬化丁基东莨菪碱组成的稳定药物组合物。该药物组合物由布洛芬化丁基东莨菪碱和吸湿聚合物组成。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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