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8-(trifluoromethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione | 620948-90-5

中文名称
——
中文别名
——
英文名称
8-(trifluoromethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
英文别名
8-(trifluoromethyl)-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione
8-(trifluoromethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione化学式
CAS
620948-90-5
化学式
C10H7F3N2O2
mdl
——
分子量
244.173
InChiKey
IKSLCIHAAZNANL-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):
    0.8
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 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:
    描述:
    8-(trifluoromethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione四氢呋喃盐酸1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺N,N-二异丙基乙胺diborane(6) 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 15.0h, 生成 (S)-3-amino-3-((S)-5,6-difluoro-2,3-dihydro-1H-inden-1-yl)-1-(8-(trifluoromethyl)-2,3-dihydro-1H-benzo[e][1,4]diazepin-4(5H)-yl)propan-1-one
    参考文献:
    名称:
    Design, Synthesis, and Pharmacological Evaluation of Fused β-Homophenylalanine Derivatives as Potent DPP-4 Inhibitors
    摘要:
    Dipeptidyl peptidase-4 (DPP-4) inhibitors are accepted as a favorable class of agents for the treatment of type 2 diabetes. Herein, a series of fused beta-homophenylalanine derivatives as novel DPP-4 inhibitors were designed, synthesized, and evaluated for their inhibitory activities against DPP-4. Most of them displayed excellent DPP-4 inhibitory activities and good selectivity. Among them, 9aa, 18a, and 18m also showed good efficacy in an oral glucose tolerance test (OGTT) in ICR mice. Moreover, when dosed 8 h prior to glucose challenge, 18m showed significantly greater potency than sitagliptin. It thus provides potential candidates for the further development into potent drugs targeting DPP-4.
    DOI:
    10.1021/acsmedchemlett.5b00074
  • 作为产物:
    参考文献:
    名称:
    Design, Synthesis, and Pharmacological Evaluation of Fused β-Homophenylalanine Derivatives as Potent DPP-4 Inhibitors
    摘要:
    Dipeptidyl peptidase-4 (DPP-4) inhibitors are accepted as a favorable class of agents for the treatment of type 2 diabetes. Herein, a series of fused beta-homophenylalanine derivatives as novel DPP-4 inhibitors were designed, synthesized, and evaluated for their inhibitory activities against DPP-4. Most of them displayed excellent DPP-4 inhibitory activities and good selectivity. Among them, 9aa, 18a, and 18m also showed good efficacy in an oral glucose tolerance test (OGTT) in ICR mice. Moreover, when dosed 8 h prior to glucose challenge, 18m showed significantly greater potency than sitagliptin. It thus provides potential candidates for the further development into potent drugs targeting DPP-4.
    DOI:
    10.1021/acsmedchemlett.5b00074
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文献信息

  • [1,4]Diazepino[6,7,1-ij]quinoline derivatives as antipsychotic and antiobesity agents
    申请人:Wyeth
    公开号:US20040009970A1
    公开(公告)日:2004-01-15
    Compounds of Formula I or a pharmaceutically acceptable salt thereof are provided: 1 where R 1 through R 7 are defined herein. The compounds of Formula I are 5HT2c agonists or partial agonists, and are useful for treating a variety of disorders.
    提供公式I的化合物或其药用可接受的盐:其中R1至R7在此处定义。公式I的化合物是5HT2c受体激动剂或部分激动剂,可用于治疗多种疾病。
  • [EN] [1,4]DIAZEPINO[6,7,1-IJ]QUINOLINE DERIVATIVES AS ANTI PSYCHOTIC AND ANTIOBESITY AGENTS<br/>[FR] DERIVES DE [1,4]DIAZEPINO[6,7,1-IJ]QUINOLINE EN TANT QU'AGENTS ANTIPSYCHOTIQUES ET CONTRE L'OBESITE
    申请人:WYETH CORP
    公开号:WO2003091250A1
    公开(公告)日:2003-11-06
    Compounds of formula 1 or a pharmaceutically acceptable salt thereof are provided: I where R1 through R7 are defined herein. The compounds of formula I are 5HT2c agonists or partial agonists, and are useful for treating a variety of disorders.
    提供公式1或其药学上可接受的盐的化合物:I,其中R1到R7在此定义。公式I的化合物是5HT2c激动剂或部分激动剂,可用于治疗各种疾病。
  • [1,4]Diazepino[6,7,1-IJ]quinoline derivatives as antipsychotic and antiobesity agents
    申请人:Ramamoorthy Sivaramakrishnan P.
    公开号:US20070004707A1
    公开(公告)日:2007-01-04
    Compounds of Formula I or a pharmaceutically acceptable salt thereof are provided: where R 1 through R 7 are defined herein. The compounds of Formula I are 5HT2c agonists or partial agonists, and are useful for treating a variety of disorders.
    提供公式I的化合物或其药学上可接受的盐:其中R1到R7在此定义。公式I的化合物是5HT2c激动剂或部分激动剂,并且可用于治疗各种疾病。
  • [1,4]diazepino[6,7,1-IJ]quinoline derivatives as antipsychotic and antiobesity agents
    申请人:Wyeth LLC
    公开号:US07687620B2
    公开(公告)日:2010-03-30
    Compounds of Formula I or a pharmaceutically acceptable salt thereof are provided: where R1 through R7 are defined herein. The compounds of Formula I are 5HT2c agonists or partial agonists, and are useful for treating a variety of disorders.
    提供公式I或其药学上可接受的盐的化合物:其中R1到R7在此定义。公式I的化合物是5HT2c激动剂或部分激动剂,可用于治疗各种疾病。
  • (1,4)DIAZEPINO(6,7,1-IJ)QUINOLINE DERIVATIVES AS ANTI PSYCHOTIC AND ANTIOBESITY AGENTS
    申请人:Wyeth
    公开号:EP1497293B1
    公开(公告)日:2008-06-11
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