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2-[3-[4-(4-Hydroxyphenyl)phenyl]propanoylamino]-4-(1,3-thiazol-2-yl)cyclohexene-1-carboxylic acid | 946113-29-7

中文名称
——
中文别名
——
英文名称
2-[3-[4-(4-Hydroxyphenyl)phenyl]propanoylamino]-4-(1,3-thiazol-2-yl)cyclohexene-1-carboxylic acid
英文别名
——
2-[3-[4-(4-Hydroxyphenyl)phenyl]propanoylamino]-4-(1,3-thiazol-2-yl)cyclohexene-1-carboxylic acid化学式
CAS
946113-29-7
化学式
C25H24N2O4S
mdl
——
分子量
448.543
InChiKey
SDAHOUDLTUCYOV-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):
    4.4
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    128
  • 氢给体数:
    3
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • COMBINATION TABLET WITH CHEWABLE OUTER LAYER
    申请人:Vitalis LLC
    公开号:US20170042821A1
    公开(公告)日:2017-02-16
    A pharmaceutical composition in the form of a combination tablet is described. The tablet has a rapidly absorbed component that enters the circulation by traversing the buccal mucosa, oral mucosa and combinations thereof, and a more slowly absorbed component that is swallowed. The therapeutic agent in the swallowed portion is absorbed across the gastric mucosa. The combination tablet may be modified, by varying the specific combinations of excipients, fillers, and the like to effect distinct release rates. In addition, the rapid and slow components may have identical or different therapeutic agents depending on the application to a specific medical condition. One embodiment of the combination tablet includes a prostaglandin inhibitor in the rapidly absorbed component in order to mitigate the side effects of immediate release niacin that is in the slow absorbing component. Such combination compositions will increase patient compliance with various dosing regimens due to the resultant decrease in the number of tablets that a patient would need to take on a daily basis.
  • Combination Tablet With Chewable Outer Layer
    申请人:Vitalis LLC
    公开号:US20200046644A1
    公开(公告)日:2020-02-13
    A pharmaceutical composition in the form of a combination tablet is described. The tablet has a rapidly absorbed component that enters the circulation by traversing the buccal mucosa, oral mucosa and combinations thereof, and a more slowly absorbed component that is swallowed. The therapeutic agent in the swallowed portion is absorbed across the gastric mucosa. The combination tablet may be modified, by varying the specific combinations of excipients, fillers, and the like to effect distinct release rates. In addition, the rapid and slow components may have identical or different therapeutic agents depending on the application to a specific medical condition. One embodiment of the combination tablet includes a prostaglandin inhibitor in the rapidly absorbed component in order to mitigate the side effects of immediate release niacin that is in the slow absorbing component. Such combination compositions will increase patient compliance with various dosing regimens due to the resultant decrease in the number of tablets that a patient would need to take on a daily basis.
  • [EN] NIACIN RECEPTOR AGONISTS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT<br/>[FR] AGONISTES DU RECEPTEUR DE LA NIACINE, COMPOSITIONS CONTENANT DE TELS COMPOSES ET PROCEDES DE TRAITEMENT
    申请人:MERCK & CO INC
    公开号:WO2007092364A2
    公开(公告)日:2007-08-16
    [EN] The present invention encompasses compounds of Formula I: as well as pharmaceutically acceptable salts and hydrates thereof, that are useful for treating atherosclerosis, dyslipidemias and the like. Pharmaceutical compositions and methods of use are also included.
    [FR] La présente invention concerne des composés de formule (I) : de même que leurs sels et hydrates pharmaceutiquement acceptables, utilisables pour le traitement de l'athérosclérose, des dyslipidémies et des maladies similaires. L'invention concerne également des compositions pharmaceutiques et des procédés d'utilisation.
  • [EN] GPR109A AGONISTS FOR THE TREATMENT OF CEREBRAL ISCHEMIA<br/>[FR] AGONISTES DE GPR109A POUR LE TRAITEMENT DE L'ISCHÉMIE CÉRÉBRALE
    申请人:UNIV RUPRECHT KARLS HEIDELBERG
    公开号:WO2011057110A1
    公开(公告)日:2011-05-12
    The present invention describes agonists for G Protein-coupled receptor 109A (GPR109A), compositions comprising the GPR109A agonists, and methods of using them. GPR109A agonists are used in methods for the treatment, prevention, and alleviation of an ischemic condition, such as cerebral ischemia.
  • Niacin Receptor Agonists, Compositions Containing Such Compounds and Methods of Treatment
    申请人:Raghavan Subharekha
    公开号:US20090062269A1
    公开(公告)日:2009-03-05
    The present invention encompasses compounds of Formula I: as well as pharmaceutically acceptable salts and hydrates thereof, that are useful for treating atherosclerosis, dyslipidemias and the like. Pharmaceutical compositions and methods of use are also included.
    本发明涵盖了Formula I的化合物,以及其药用盐和水合物,可用于治疗动脉粥样硬化、血脂异常等疾病。药物组合物和使用方法也包括在内。
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