摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(R)-普鲁前列素,游离酸 | 215168-33-5

中文名称
(R)-普鲁前列素,游离酸
中文别名
——
英文名称
(R)-Butaprost (free acid)
英文别名
7-[(1R,2R,3R)-3-hydroxy-2-[(E,4R)-4-hydroxy-4-(1-propylcyclobutyl)but-1-enyl]-5-oxocyclopentyl]heptanoic acid
(R)-普鲁前列素,游离酸化学式
CAS
215168-33-5
化学式
C23H38O5
mdl
——
分子量
394.5
InChiKey
PAYNQYXOKJDXAV-NMXQQJQMSA-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):
    3.9
  • 重原子数:
    28
  • 可旋转键数:
    13
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    94.8
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • PROSTAGLANDIN ANALOGS AND USES THEREOF
    申请人:Lifex Biolabs, Inc.
    公开号:US20210139435A1
    公开(公告)日:2021-05-13
    The present invention relates to pharmaceutical composition for the prevention or treatment of a disease, disorder, or condition associated with Nurr1, including, as an active ingredient, a prostaglandin analog or a pharmaceutically acceptable salt thereof, wherein the compound has excellent effects in inducing Nurr1, and thus, can be useful as a pharmaceutical composition for the prevention or treatment of a disease, disorder, or condition associated with Nurr1, in particular, cancer, autoimmune disease such as rheumatoid arthritis, schizophrenia, manic depression and neurodegenerative disease such as Alzheimers disease or Parkinson's disease.
    本发明涉及一种药物组合物,用于预防或治疗与Nurr1相关的疾病、紊乱或状况,其中包括作为活性成分的前列腺素类似物或其药学上可接受的盐,该化合物具有良好的诱导Nurr1的效果,因此,可用作预防或治疗与Nurr1相关的疾病、紊乱或状况的药物组合物,特别是癌症、自身免疫性疾病如类风湿关节炎、精神分裂症、躁郁症以及神经退行性疾病如阿尔茨海默病或帕森病。
  • Ep2 Receptor Agonists
    申请人:Borman Richard Anthony
    公开号:US20080045596A1
    公开(公告)日:2008-02-21
    A compound selected from one of the following: or a salt, solvate, chemically protected form or prodrug thereof, and its use in treating conditions alleviated by agonism of an EP 2 receptor.
    从以下化合物中选择一个:或其盐、溶剂化物、化学保护形式或前药,以及其在治疗通过EP2受体激动缓解的疾病中的应用。
  • Synergistic combination of an anti-IgE antibody and an EP2 receptor agonist
    申请人:Universitat Autònoma de Barcelona
    公开号:EP2818484A1
    公开(公告)日:2014-12-31
    The present invention relates to synergistic combinations, including immunoconjugates, of an anti-IgE antibody, such as omalizumab, with an EP2 receptor agonist and their use in the prevention or treatment of an IgE-mediated disorder, preferably asthma.
    本发明涉及抗 IgE 抗体(例如奥马珠单抗)与 EP2 受体激动剂的协同组合(包括免疫结合剂),以及它们在预防或治疗 IgE 介导的疾病(最好是哮喘)中的用途。
  • [EN] SYNERGISTIC COMBINATION OF AN ANTI-IGE ANTIBODY AND AN EP2 RECEPTOR AGONIST<br/>[FR] COMBINAISON SYNERGIQUE D'UN ANTICORPS ANTI-IGE ET D'UN AGONISTE DU RÉCEPTEUR EP2
    申请人:UNIV BARCELONA AUTONOMA
    公开号:WO2014206808A1
    公开(公告)日:2014-12-31
    The present invention relates to synergistic combinations, including immunoconjugates, of an anti-IgE antibody, such as omalizumab, with an EP2 receptor agonist and their use in the prevention or treatment of an IgE-mediated disorder, preferably asthma.
查看更多