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3-[2(R)-{ethoxycarbonylpropyl-amino}-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)-benzyl]pyrimidine-2,4-(1H,3H)-dione | 832720-88-4

中文名称
——
中文别名
——
英文名称
3-[2(R)-{ethoxycarbonylpropyl-amino}-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)-benzyl]pyrimidine-2,4-(1H,3H)-dione
英文别名
3-[2(R)-{ethoxycarbonylpropyl-amino}-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]pyrimidine-2,4(1H,3H)-dione;ethyl 4-[[(2R)-1-[5-(2-chloro-3-methoxyphenyl)-3-[[2-fluoro-6-(trifluoromethyl)phenyl]methyl]-2,6-dioxopyrimidin-1-yl]-4-methylpentan-2-yl]amino]butanoate
3-[2(R)-{ethoxycarbonylpropyl-amino}-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)-benzyl]pyrimidine-2,4-(1H,3H)-dione化学式
CAS
832720-88-4
化学式
C31H36ClF4N3O5
mdl
——
分子量
642.091
InChiKey
DROHQRYFROJXSL-HXUWFJFHSA-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

  • 沸点:
    672.4±65.0 °C(Predicted)
  • 密度:
    1.272±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    44
  • 可旋转键数:
    15
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    88.2
  • 氢给体数:
    1
  • 氢受体数:
    10

SDS

SDS:ea546db50523494ffe57037af1bee538
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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

  • Gonadotropin-releasing hormone receptor antagonists and methods relating thereto
    申请人:Guo Zhiqiang
    公开号:US20050038057A1
    公开(公告)日:2005-02-17
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R 1a , R 1b , R 1c , R 2a , R 2b , R 3 , R 4 , R 5 , R 6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    本发明揭示了GnRH受体拮抗剂,其在治疗男性和女性的各种性激素相关疾病中具有用途。本发明的化合物具有以下结构:其中R1a,R1b,R1c,R2a,R2b,R3,R4,R5,R6和X如本文所定义,包括立体异构体,前药和其药物可接受的盐。还揭示了含有本发明化合物的组合物与药物可接受的载体的组合物,以及与此有关的方法,用于在需要拮抗促性腺激素释放激素的受体的个体中使用。
  • GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS AND METHODS RELATING THERETO
    申请人:Guo Zhiqiang
    公开号:US20070191403A1
    公开(公告)日:2007-08-16
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R 1a , R 1b , R 1c , R 2a , R 2b , R 3 , R 4 , R 5 , R 6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    本发明公开了具有治疗男女性激素相关疾病的效用的GnRH受体拮抗剂。本发明的化合物具有以下结构:其中,R1a、R1b、R1c、R2a、R2b、R3、R4、R5、R6和X的定义如本文所述,包括立体异构体、前药和其药物可接受的盐。本发明还公开了含有本发明化合物与药物可接受载体结合的组合物,以及与拮抗需要拮抗性腺激素释放激素的受试者相关的使用方法。
  • Gonadotropin-releasing hormone receptor antagonists and methods related thereto
    申请人:Neurocrine Biosciences, Inc.
    公开号:US07419983B2
    公开(公告)日:2008-09-02
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R1a, R1b, R1c, R2a, R2b, R3, R4, R5, R6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    本发明公开了GnRH受体拮抗剂,其在治疗男女性激素相关疾病方面具有实用性。本发明化合物具有以下结构:其中R1a、R1b、R1c、R2a、R2b、R3、R4、R5、R6和X的定义如本文所述,包括立体异构体、前药和其药学上可接受的盐。本发明还公开了含有该化合物与药学上可接受的载体组合的组合物,以及与拮抗性促性腺激素释放激素有关的使用方法,用于需要该方法的受体。
  • [EN] PYRIMIDINE-2, 4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS<br/>[FR] DERIVES DE PYRIMIDINE-2, 4-DIONE UTILISES COMME ANTAGONISTES DU RECEPTEUR D'HORMONE LIBERANT DE LA GONADOTROPHINE
    申请人:NEUROCRINE BIOSCIENCES INC
    公开号:WO2005007165A1
    公开(公告)日:2005-01-27
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R1a, R1b, R1c, R2a, R2b, R3, R4, R5, R6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    GnRH受体拮抗剂被披露,对男性和女性的各种与性激素相关的疾病具有治疗作用。本发明的化合物具有以下结构:其中R1a、R1b、R1c、R2a、R2b、R3、R4、R5、R6和X的定义如本文所述,包括立体异构体、前药和其药用可接受盐。还披露了含有本发明化合物的组合物与药用可接受载体的组合物,以及与在需要时对抗性腺激素释放激素的使用方法。
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