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1-[(quinoxalin-6-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-amino-piperidin-1-yl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purine | 668270-40-4

中文名称
——
中文别名
——
英文名称
1-[(quinoxalin-6-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-amino-piperidin-1-yl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purine
英文别名
8-(3-Aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(quinoxalin-6-ylmethyl)purine-2,6-dione
1-[(quinoxalin-6-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-amino-piperidin-1-yl)-2,6-dioxo-2,3,6,7-tetrahydro-1H-purine化学式
CAS
668270-40-4
化学式
C24H26N8O2
mdl
——
分子量
458.523
InChiKey
GFMVACPPQCXLGW-UHFFFAOYSA-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):
    1.1
  • 重原子数:
    34
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • PHARMACEUTICAL COMPOSITION COMPRISING A GLUCOPYRANOSYL-SUBSTITUTED BENZENE DERIVATIVE
    申请人:Boehringer Ingelheim International GmbH
    公开号:EP3939577A1
    公开(公告)日:2022-01-19
    The invention relates to a pharmaceutical composition according to the claim 1 comprising a glucopyranosyl-substituted benzene derivative in combination with a DPP IV inhibitor which is suitable in the treatment or prevention of one or more conditions selected from type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance and hyperglycemia. In addition the present invention relates to methods for preventing or treating of metabolic disorders and related conditions.
    该发明涉及根据权利要求1的药物组合物,包括一种葡萄糖喃基取代苯衍生物与一种适用于治疗或预防从以下选定的一种或多种疾病的DPP IV抑制剂的组合物,所述疾病包括1型糖尿病、2型糖尿病、糖耐量受损和高血糖。此外,本发明涉及预防或治疗代谢紊乱及相关疾病的方法。
  • 8-[3-AMINO-PIPERIDIN-1-YL]-XANTHINES, THE PREPARATION THEREOF AND THEIR USE AS PHARMACEUTICAL COMPOSITIONS
    申请人:Himmelsbach Frank
    公开号:US20080255159A1
    公开(公告)日:2008-10-16
    The present invention relates to substituted xanthines of general formula wherein R 1 to R 3 are defined as in claims 1 to 16 , the tautomers, the stereoisomers, the mixtures, the prodrugs thereof and the salts thereof which have valuable pharmacological properties, particularly an inhibiting effect on the activity of the enzyme dipeptidylpeptidase-IV (DPP-IV).
    本发明涉及一般式的取代黄嘌呤,其中R1至R3的定义如权利要求1至16所述,其互变异构体、立体异构体、混合物、前药和盐具有有价值的药理特性,特别是对酶二肽基肽酶-IV(DPP-IV)的抑制作用。
  • 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
    申请人:Boehringer Ingelheim Pharma GmbH & Co. KG
    公开号:US20040097510A1
    公开(公告)日:2004-05-20
    The present invention relates to substituted xanthines of general formula 1 wherein R 1 to R 3 are defined as in claims 1 to 16, the tautomers, the stereoisomers, the mixtures, the prodrugs thereof and the salts thereof which have valuable pharmacological properties, particularly an inhibiting effect on the activity of the enzyme dipeptidylpeptidase-IV (DPI-IV).
    本发明涉及一般式1的取代黄嘌呤,其中R1至R3的定义如权利要求1至16所述,其互变异构体、立体异构体、混合物、前药及其盐具有有价值的药理学特性,特别是对酶二肽基肽酶-IV(DPI-IV)的抑制作用。
  • PHARMACEUTICAL COMPOSITION COMPRISING A GLUCOPYRANOSYL-SUBSTITUTED BENZENE DERIVATE
    申请人:Dugi Klaus
    公开号:US20110195917A1
    公开(公告)日:2011-08-11
    The invention relates to a pharmaceutical composition according to the claim 1 comprising a glucopyranosyl-substituted benzene derivative in combination with a DPP IV inhibitor which is suitable in the treatment or prevention of one or more conditions selected from type 1 diabetes mellitus, type 2 diabetes mellitus, impaired glucose tolerance and hyperglycemia. In addition the present invention relates to methods for preventing or treating of metabolic disorders and related conditions.
    该发明涉及一种药物组合物,根据权利要求1,包括一种葡萄糖喃基取代的苯衍生物和一种适用于治疗或预防从以下选择的一种或多种疾病的DPP IV抑制剂:1型糖尿病,2型糖尿病,糖耐量受损和高血糖。此外,本发明还涉及预防或治疗代谢紊乱和相关疾病的方法。
  • 8-[3-AMINO-PIPERIDIN-1-YL]-XANTHINES, THEIR PREPARATION AND THEIR USE AS PHARMACEUTICAL COMPOSITIONS
    申请人:HIMMELSBACH Frank
    公开号:US20090137801A1
    公开(公告)日:2009-05-28
    Disclosed are substituted xanthines of the formula wherein R is defined as in claim 1 , the tautomers, the stereoisomers, the mixtures thereof and the salts thereof, which have valuable pharmacological properties, particularly an inhibiting effect on the activity of the enzyme dipeptidylpeptidase-IV (DPP-IV).
    本发明涉及一种公式如下的取代黄嘌呤:其中R如权利要求1所定义,其互变异构体、立体异构体、混合物及其盐,具有有价值的药理学特性,特别是对酶二肽基肽酶-IV(DPP-IV)的抑制作用。
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