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依拉司群 | 722533-56-4

中文名称
依拉司群
中文别名
——
英文名称
RAD-1901
英文别名
elacestrant;(R)-6-(2-(ethyl(4-(2-(ethylamino)ethyl)benzyl)amino)-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol;(6R)-6-[2-[ethyl-[[4-[2-(ethylamino)ethyl]phenyl]methyl]amino]-4-methoxyphenyl]-5,6,7,8-tetrahydronaphthalen-2-ol
依拉司群化学式
CAS
722533-56-4
化学式
C30H38N2O2
mdl
——
分子量
458.644
InChiKey
SIFNOOUKXBRGGB-AREMUKBSSA-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):
    6.3
  • 重原子数:
    34
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    44.7
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    依拉司群盐酸 作用下, 以 乙醇乙酸乙酯 为溶剂, 生成 (6R)-6-(2-(N-(4-(2-(ethylamino)ethyl)benzyl)-N-ethylamino)-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol dihydrochloride
    参考文献:
    名称:
    WO2023/64519
    摘要:
    公开号:
  • 作为产物:
    描述:
    生成 依拉司群
    参考文献:
    名称:
    Selective Estrogen Receptor Modulator
    摘要:
    本发明提供一种由以下式(I)表示的化合物; [其中T表示单键,可能具有取代基的C1-C4烷基和类似物;式(I-1)表示单键或双键;A表示单键,可能具有取代基的双价5-至14-成员杂环基和类似物;Y表示单键和类似物;Z表示亚甲基基团和类似物;环G表示苯基团和类似物,可能与5-至6-成员环缩合并可能具有杂原子;Ra和Rb相同或不同,表示氢原子和类似物;W表示单键和类似物;R'表示1到4个独立的氢原子和类似物;R''表示1到4个独立的氢原子和类似物]或其盐或水合物。
    公开号:
    US20120004315A1
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文献信息

  • [EN] ESTROGEN RECEPTOR MODULATORS<br/>[FR] MODULATEURS DU RÉCEPTEUR DES ŒSTROGÈNES
    申请人:KALYRA PHARMACEUTICALS INC
    公开号:WO2017172957A1
    公开(公告)日:2017-10-05
    Compounds of Formula (I) are estrogen receptor alpha modulators, where the variables in Formula (I) are described in the disclosure. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions that are estrogen receptor alpha dependent and/or estrogen receptor alpha mediated, including conditions characterized by excessive cellular proliferation, such as breast cancer.
    化合物的化学式(I)是雌激素受体α调节剂,其中化学式(I)中的变量在披露中有描述。这些化合物以及其药学上可接受的盐和组合物对于治疗依赖雌激素受体α和/或由雌激素受体α介导的疾病或症状是有用的,包括由细胞过度增殖所特征化的疾病,如乳腺癌。
  • [EN] ACRYLIC ACID ANALOGS<br/>[FR] ANALOGUES DE L'ACIDE ACRYLIQUE
    申请人:ZENO ROYALTIES & MILESTONES LLC
    公开号:WO2019023481A1
    公开(公告)日:2019-01-31
    Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
    本文提供了化学式(I)的化合物。这些化合物以及其药用盐和组合物对治疗疾病或病况具有用处,包括那些以细胞过度增殖为特征的病症,如乳腺癌。
  • SULFONAMIDES AS SELECTIVE ESTROGEN RECEPTOR
    申请人:Katzenellenbogen A. John
    公开号:US20070021495A1
    公开(公告)日:2007-01-25
    Compounds, pharmaceutically acceptable salts, stereoisomers and prodrugs thereof, that are ER ligands and particularly to such compounds that are ER beta-selective and/or ER beta-specific ligands. Compounds herein include certain compounds which are ER beta-selective agonists. Compounds herein include ER beta-selective agonists which exhibit minimal agonist or antagonist effect on ER alpha. Compounds of the invention include those of formula I: and any pharmaceutically acceptable salts, stereoisomers and prodrugs thereof wherein AR, R 1 , R 3 , and X 1 —X 4 are as defined hereinabove.
    本发明涉及化合物、药学上可接受的盐、立体异构体和前药,它们是ER配体,特别是这些化合物是ER beta选择性和/或ER beta特异性配体。本文化合物包括某些ER beta选择性激动剂。本文化合物包括ER beta选择性激动剂,其在ER alpha上表现出最小的激动或拮抗作用。本发明的化合物包括式I的化合物:以及它们的任何药学上可接受的盐、立体异构体和前药,其中AR、R1、R3和X1-X4如上所定义。
  • Selective Estrogen Receptor Modulator
    申请人:Hamaoka Shinichi
    公开号:US20120004315A1
    公开(公告)日:2012-01-05
    The present invention provides a compound represented by the following formula (I); [wherein T represents a single bond, a C1-C4 alkylene group which may have a substituent and the like; formula (I-1) represents a single bond or a double bond; A represents a single bond, a bivalent 5- to 14-membered heterocyclic group which may have a substituent and the like; Y represents a single bond and the like; Z represents a methylene group and the like; ring G represents a phenylene group and the like which may condense with a 5- to 6-membered ring and may have a heteroatom; R a and R b are the same as or different from each other and represent a hydrogen atom and the like; W represents a single bond and the like; R′ represents 1 to 4 independent hydrogen atoms and the like; and R″ represents 1 to 4 independent hydrogen atoms and the like] or a salt thereof, or a hydrate thereof.
    本发明提供一种由以下式(I)表示的化合物; [其中T表示单键,可能具有取代基的C1-C4烷基和类似物;式(I-1)表示单键或双键;A表示单键,可能具有取代基的双价5-至14-成员杂环基和类似物;Y表示单键和类似物;Z表示亚甲基基团和类似物;环G表示苯基团和类似物,可能与5-至6-成员环缩合并可能具有杂原子;Ra和Rb相同或不同,表示氢原子和类似物;W表示单键和类似物;R'表示1到4个独立的氢原子和类似物;R''表示1到4个独立的氢原子和类似物]或其盐或水合物。
  • Selective estrogen receptor modulator
    申请人:Hamaoka Shinichi
    公开号:US20060116364A1
    公开(公告)日:2006-06-01
    The present invention provides a compound represented by the following formula [wherein T represents a single bond, a C1-C4 alkylene group which may have a substituent and the like; formula (I-1) represents a single bond or a double bond; A represents a single bond, a bivalent 5- to 14-membered heterocyclic group which may have a substituent and the like; Y represents a single bond and the like; Z represents a methylene group and the like; ring G represents a phenylene group and the like which may condense with a 5- to 6-membered ring and may have a heteroatom; R a and R b are the same as or different from each other and represent a hydrogen atom and the like; W represents a single bond and the like; R′ represents 1 to 4 independent hydrogen atoms and the like; and R″ represents 1 to 4 independent hydrogen atoms and the like] or a salt thereof, or a hydrate thereof
    本发明提供了一种化合物,其表示为以下式子[其中T表示单键,C1-C4的烷基,可能带有取代基等;式(I-1)表示单键或双键;A表示单键,二价的5-至14-成员杂环基团,可能带有取代基等;Y表示单键等;Z表示亚甲基等;环G表示苯基团等,可与5-至6-成员环缩合并且可能具有杂原子;Ra和Rb相同或不同,表示氢原子等;W表示单键等;R'表示1至4个独立的氢原子等;R"表示1至4个独立的氢原子等]或其盐,或其水合物。
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