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4-[2-(4-bromophenyl)ethyl]-1H-pyrazolo[3,4-b]pyridin-3-ol | 864845-26-1

中文名称
——
中文别名
——
英文名称
4-[2-(4-bromophenyl)ethyl]-1H-pyrazolo[3,4-b]pyridin-3-ol
英文别名
4-[2-(4-Bromophenyl)ethyl]-1,2-dihydropyrazolo[3,4-b]pyridin-3-one
4-[2-(4-bromophenyl)ethyl]-1H-pyrazolo[3,4-b]pyridin-3-ol化学式
CAS
864845-26-1
化学式
C14H12BrN3O
mdl
——
分子量
318.173
InChiKey
YVGCCZPUVZDYOF-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):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    54
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • NITROGENOUS FUSED-RING DERIVATIVES, MEDICINAL COMPOSITIONS CONTAINING THE DERIVATIVES, AND USE THEREOF AS DRUGS
    申请人:FUSHIMI Nobuhiko
    公开号:US20080188426A1
    公开(公告)日:2008-08-07
    The present invention provides nitrogen-containing fused-ring derivatives represented by the following general formula, or pharmaceutically acceptable salts thereof, or prodrugs thereof, which exhibit an excellent inhibitory activity in human SGLT and are useful as agents for the prevention or treatment of a disease associated with hyperglycemia such as diabetes, postprandial hyperglycemia, impaired glucose tolerance, diabetic complications or obesity, in the formula R 1 represent H, an optionally substituted alkyl group, an alkenyl group, etc.; R 2 represent H, a halogen atom or an alkyl group; R 3 and R 4 represent H, OH, a halogen atom, an optionally substituted alkyl group, etc.; Y represents CH or N; Q represents alkylene, alkenylene, etc.; ring A represents an aryl group or a heteroaryl group; G represents a group represented by the following general formula (G-1) or (G-2) (in which E 1 represents H, F or OH; and E 2 represents H, F, a methyl group, etc.), and pharmaceutical compositions comprising the same, and pharmaceutical uses thereof.
    本发明提供以下通式所表示的含氮融合环衍生物,或其药学上可接受的盐或前药,它们在人类SGLT中表现出优异的抑制活性,并可用作预防或治疗与高血糖相关的疾病,如糖尿病、餐后高血糖、糖耐量受损、糖尿病并发症或肥胖症的药物。其中,通式中R1代表H,可选取代的烷基,烯基等;R2代表H,卤素原子或烷基;R3和R4代表H,OH,卤素原子,可选取代的烷基等;Y代表CH或N;Q代表烷基,烯基等;环A代表芳基或杂芳基;G代表下列通式(G-1)或(G-2)所表示的基团(其中E1代表H,F或OH;E2代表H,F,甲基基团等),以及包含它们的制药组合物和制药用途。
  • Nitrogenous fused-ring derivatives, medicinal compositions containing the derivatives, and use thereof as drugs
    申请人:Fushimi Nobuhiko
    公开号:US20070191289A1
    公开(公告)日:2007-08-16
    The present invention provides nitrogen-containing fused-ring derivatives represented by the following general formula, or pharmaceutically acceptable salts thereof, or prodrugs thereof, which exhibit an excellent inhibitory activity in human SGLT and are useful as agents for the prevention or treatment of a disease associated with hyperglycemia such as diabetes, postprandial hyperglycemia, impaired glucose tolerance, diabetic complications or obesity, in the formula R 1 represent H, an optionally substituted alkyl group, analkenyl group, etc.; R 2 represent H, a halogen atom or an alkyl group; R 3 and R 4 represent H, OH, a halogen atom, an optionally substituted alkyl group, etc.; Y represents CH or N; Q represents alkylene, alkenylene, etc.; ring A represents an aryl group or a heteroaryl group; G represents a group represented by the following general formula (G-1) or (G-2) (in which E 1 represents H, F or OH; and E 2 represents H, F, a methyl group, etc.), and pharmaceutical compositions comprising the same, and pharmaceutical uses thereof.
    本发明提供以下通式所表示的含氮融合环衍生物,或其药学上可接受的盐或前药,该衍生物在人体SGLT中表现出优异的抑制活性,并可用作预防或治疗与高血糖相关的疾病,如糖尿病、餐后高血糖、糖耐量受损、糖尿病并发症或肥胖症的药物。其中,通式中R1代表H、可选的取代烷基、烯基等;R2代表H、卤素原子或烷基;R3和R4代表H、OH、卤素原子、可选的取代烷基等;Y代表CH或N;Q代表烷基、烯基等;环A代表芳基或杂芳基;G代表以下通式(G-1)或(G-2)所表示的基团(其中E1代表H、F或OH;E2代表H、F、甲基基团等),以及包含上述衍生物的制药组合物和制药用途。
  • EP1724278B1
    申请人:——
    公开号:EP1724278B1
    公开(公告)日:2014-05-07
  • US7375113B2
    申请人:——
    公开号:US7375113B2
    公开(公告)日:2008-05-20
  • US7998975B2
    申请人:——
    公开号:US7998975B2
    公开(公告)日:2011-08-16
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