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1-phenyl-2H-pyrrolo[3,2-c]pyrazole

中文名称
——
中文别名
——
英文名称
1-phenyl-2H-pyrrolo[3,2-c]pyrazole
英文别名
——
1-phenyl-2H-pyrrolo[3,2-c]pyrazole化学式
CAS
——
化学式
C11H9N3
mdl
——
分子量
183.21
InChiKey
HCZPUQOTVFWFKG-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    33.6
  • 氢给体数:
    1
  • 氢受体数:
    1

文献信息

  • NOVEL AZABENZIMIDAZOLE HEXAHYDROFURO[E,2-B]FURAN DERIVATIVES
    申请人:APGAR James M.
    公开号:US20150284411A1
    公开(公告)日:2015-10-08
    Novel compounds of the structural formula (I) are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPK activated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
    结构式(I)的新化合物是AMP-蛋白激酶的激活剂,可能在治疗、预防和抑制由AMPK激活的蛋白激酶介导的疾病中有用。本发明的化合物可能在治疗2型糖尿病、高血糖、代谢综合征、肥胖、高胆固醇血症和高血压方面有用。
  • NOVEL AZABENZIMIDAZOLE TETRAHYDROPYRAN DERIVATIVES
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20150210685A1
    公开(公告)日:2015-07-30
    Novel compounds of the structural formula (I) are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPKactivated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
    结构式(I)的新化合物是AMP-蛋白激酶的激活剂,可能在治疗、预防和抑制由AMPK激活的蛋白激酶介导的疾病方面有用。本发明的化合物可能在治疗2型糖尿病、高血糖、代谢综合征、肥胖、高胆固醇血症和高血压方面有用。
  • NOVEL AZABENZIMIDAZOLE TETRAHYDROFURAN DERIVATIVES
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20150203487A1
    公开(公告)日:2015-07-23
    Novel compounds of the structural formula (I) are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
    结构式(I)的新化合物是AMP-蛋白激酶的激活剂,可能在治疗、预防和抑制由AMPK激活的蛋白激酶介导的疾病中有用。本发明的化合物可能在治疗2型糖尿病、高血糖、代谢综合征、肥胖、高胆固醇和高血压方面有用。
  • [EN] NOVEL BENZIMIDAZOLE HEXAHYDROFURO[3,2-B]FURAN DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS DE BENZIMIDAZOLE HEXAHYDROFURO[3,2-B] FURANE
    申请人:MERCK SHARP & DOHME
    公开号:WO2014031468A1
    公开(公告)日:2014-02-27
    The novel benzimidazole hexahydrofuro[3,2-B]furan derivatives of the present invention are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
    本发明的新型苯并咪唑六氢呋喃[3,2-B]呋喃生物AMP-蛋白激酶的激活剂,可用于治疗、预防和抑制由AMPK激活的蛋白激酶介导的疾病。本发明的化合物可用于治疗2型糖尿病、高血糖、代谢综合征、肥胖症、高胆固醇血症和高血压。
  • NOVEL BENZIMIDAZOLE HEXAHYDROFURO[3,2-B]FURAN DERIVATIVES
    申请人:Merck Sharp & Dohme Avenue
    公开号:US20150218183A1
    公开(公告)日:2015-08-06
    The novel benzimidazole hexahydrofuro[3,2-B]furan derivatives of the present invention are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
    本发明的新型苯并咪唑六氢呋喃[3,2-B]呋喃生物AMP-蛋白激酶的激动剂,并可用于治疗、预防和抑制由AMPK激活的蛋白激酶介导的疾病。本发明的化合物可用于治疗2型糖尿病、高血糖、代谢综合征、肥胖症、高胆固醇血症和高血压。
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