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19-Hydroxy-PGE2 | 55123-68-7

中文名称
——
中文别名
——
英文名称
19-Hydroxy-PGE2
英文别名
(Z)-7-[(1R,2R,3R)-2-[(E,3S,7R)-3,7-dihydroxyoct-1-enyl]-3-hydroxy-5-oxocyclopentyl]hept-5-enoic acid
19-Hydroxy-PGE2化学式
CAS
55123-68-7
化学式
C20H32O6
mdl
——
分子量
368.5
InChiKey
WTJYDBMHYPQFNJ-ZUVVJKHESA-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

  • 物理描述:
    Solid

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    26
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    115
  • 氢给体数:
    4
  • 氢受体数:
    6

文献信息

  • SUBSTITUTED CYCLOPENTANES HAVING PROSTAGLANDIN ACTIVITY
    申请人:Burk Robert M.
    公开号:US20090143461A1
    公开(公告)日:2009-06-04
    Disclosed herein are compounds having a formula: Therapeutic methods, medicaments, and compositions related thereto are also disclosed.
    本文披露了具有以下化学式的化合物:同时还披露了相关的治疗方法、药物和组合物。
  • 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金森病。
  • ERECTILE DYSFUNCTION REMEDIES CONTAINING PROSTAGLANDIN DERIVATIVES AS THE ACTIVE INGREDIENT
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1306087A1
    公开(公告)日:2003-05-02
    Therapeutic agents for erectile dysfunction containing as the active ingredient prostaglandin derivatives of formula (I) (wherein, R1 is ethyl or n-2-propenyl.), esters thereof, nontoxic salts thereof, or cyclodextrin clathrate compounds thereof. The compounds of the formula (I) are useful for the treatment of erectile dysfunction.
    治疗勃起功能障碍的药物,其活性成分为式(I)的前列腺素衍生物(其中 R1 为乙基或 n-2-丙烯基)、其酯类、其无毒盐类或其环糊精凝块化合物。 (其中,R1 为乙基或 n-2-丙烯基)、其酯类、其无毒盐类或其环糊精凝块化合物。 式(I)化合物可用于治疗勃起功能障碍。
  • 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。
  • PROSTAGLANDIN RECEPTOR AGONISTS FOR USE IN THE TREATMENT OF A CORONAVIRUS INFECTION SUCH AS COVID-19
    申请人:Medetia
    公开号:EP3981410A1
    公开(公告)日:2022-04-13
    The present invention relates to prostaglandin receptor agonists, such as EP2 and/or EP4 agonists, preferably EP2 agonists, for treating a disease caused by a coronavirus infection, such as COVID-19, in a subject in need thereof, especially in a subject at risk to develop a severe form and/or a complication of said disease.
    本发明涉及前列腺素受体激动剂,如EP2和/或EP4激动剂,优选EP2激动剂,用于治疗由冠状病毒感染(如COVID-19)引起的疾病,适用于有需要的受试者,特别是有可能患上上述疾病的严重形式和/或并发症的受试者。
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