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(5R,8R,10R)-6-allyl-N-[3-(morpholino)propyl]ergoline-8-carboxamide | 1419268-44-2

中文名称
——
中文别名
——
英文名称
(5R,8R,10R)-6-allyl-N-[3-(morpholino)propyl]ergoline-8-carboxamide
英文别名
(5R,8R,10R)-6-Allyl-N-[3-(morpholino)propyl]ergoline-8-carboxamide;(6aR,9R,10aR)-N-(3-morpholin-4-ylpropyl)-7-prop-2-enyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
(5R,8R,10R)-6-allyl-N-[3-(morpholino)propyl]ergoline-8-carboxamide化学式
CAS
1419268-44-2
化学式
C25H34N4O2
mdl
——
分子量
422.571
InChiKey
BOEUMVJAHQQUPU-KJXAQDMKSA-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):
    2.3
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    60.6
  • 氢给体数:
    2
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of Novel Analogs of Cabergoline: Improving Cardiovascular Safety by Removing 5-HT2B Receptor Agonism
    摘要:
    The dopamine agonist cabergoline has been used to treat prolactinomas, Parkinson's disease, Cushing's disease, and sexual dysfunction. However, its clinical use was severely curtailed when it was found that patients taking cabergoline had an increased risk of developing cardiac-valve regurgitation. This potentially life-threatening condition has been associated with drugs, such as cabergoline, that are 5-HT2B receptor agonists. We prepared analogs of cabergoline and have identified several that have limited or no agonism at the 5-HT2B receptor.
    DOI:
    10.1021/ml3003814
  • 作为产物:
    描述:
    N-(3-氨丙基)吗啉卡麦角林氮气磷酸肌酸N-(3-氨丙基)吗啉二氯甲烷 作用下, 以 二氯甲烷 为溶剂, 反应 144.0h, 以to afford 30 mg of compound 4 as a brown solid (80% yield)的产率得到(5R,8R,10R)-6-allyl-N-[3-(morpholino)propyl]ergoline-8-carboxamide
    参考文献:
    名称:
    ERGOLINE DERIVATIVES AS DOPAMINE RECEPTOR MODULATORS
    摘要:
    本发明提供公式(I)的化合物,其中R1-R4具有规范中定义的任何值,以及其盐。这些化合物可用作多巴胺受体调节剂,用于治疗多巴胺受体调节与相关的疾病(例如性功能障碍,垂体瘤,帕金森病和库欣病)。
    公开号:
    US20150307486A1
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文献信息

  • [EN] ERGOLINE DERIVATIVES AS DOPAMINE RECEPTOR MODULATORS<br/>[FR] DÉRIVÉS D'ERGOLINE EN TANT QUE MODULATEURS D'UN RÉCEPTEUR DE LA DOPAMINE
    申请人:UNIV MINNESOTA
    公开号:WO2014078857A1
    公开(公告)日:2014-05-22
    The invention provides compounds of formula (I) wherein R1-R4 have any of the values defined in the specification, and salts thereof. The compounds are useful as dopamine receptor modulators for the treatment of diseases where modulation of dopamine receptors is implicated (e.g. sexual dysfunction, prolactinoma, Parkinson's disease, and Cushings disease).
    该发明提供了式(I)的化合物,其中R1-R4具有规范中定义的任何值,以及其盐。这些化合物可用作多巴胺受体调节剂,用于治疗多巴胺受体调节受牵扯的疾病(例如性功能障碍、垂体催乳素瘤、帕金森病和库欣氏症)。
  • US9670199B2
    申请人:——
    公开号:US9670199B2
    公开(公告)日:2017-06-06
  • Synthesis of Novel Analogs of Cabergoline: Improving Cardiovascular Safety by Removing 5-HT<sub>2B</sub> Receptor Agonism
    作者:Peter I. Dosa、Tim Ward、Michael A. Walters、Suck Won Kim
    DOI:10.1021/ml3003814
    日期:2013.2.14
    The dopamine agonist cabergoline has been used to treat prolactinomas, Parkinson's disease, Cushing's disease, and sexual dysfunction. However, its clinical use was severely curtailed when it was found that patients taking cabergoline had an increased risk of developing cardiac-valve regurgitation. This potentially life-threatening condition has been associated with drugs, such as cabergoline, that are 5-HT2B receptor agonists. We prepared analogs of cabergoline and have identified several that have limited or no agonism at the 5-HT2B receptor.
  • ERGOLINE DERIVATIVES AS DOPAMINE RECEPTOR MODULATORS
    申请人:REGENTS OF THE UNIVERSITY OF MINNESOTA
    公开号:US20150307486A1
    公开(公告)日:2015-10-29
    The invention provides compounds of formula (I) wherein R 1 -R 4 have any of the values defined in the specification, and salts thereof. The compounds are useful as dopamine receptor modulators for the treatment of diseases where modulation of dopamine receptors is implicated (e.g. sexual dysfunction, prolactinoma, Parkinson's disease, and Cushings disease).
    本发明提供公式(I)的化合物,其中R1-R4具有规范中定义的任何值,以及其盐。这些化合物可用作多巴胺受体调节剂,用于治疗多巴胺受体调节与相关的疾病(例如性功能障碍,垂体瘤,帕金森病和库欣病)。
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