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3-ethyl-1-(4-fluoro-phenyl)-6-phenyl-1,4,5,6-tetrahydro-pyrazolo[3,4-c]pyridin-7-one | 6620-48-0

中文名称
——
中文别名
——
英文名称
3-ethyl-1-(4-fluoro-phenyl)-6-phenyl-1,4,5,6-tetrahydro-pyrazolo[3,4-c]pyridin-7-one
英文别名
3-Ethyl-1-(4-fluorophenyl)-6-phenyl-4,5-dihydropyrazolo[3,4-c]pyridin-7-one
3-ethyl-1-(4-fluoro-phenyl)-6-phenyl-1,4,5,6-tetrahydro-pyrazolo[3,4-<i>c</i>]pyridin-7-one化学式
CAS
6620-48-0
化学式
C20H18FN3O
mdl
——
分子量
335.381
InChiKey
PKFGHAIJIHZQFD-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):
    4.2
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    38.1
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:6c99fab9bd3da0cdc57c0e3d9311c432
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反应信息

  • 作为产物:
    参考文献:
    名称:
    7-Oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridines as Novel Inhibitors of Human Eosinophil Phosphodiesterase
    摘要:
    High-throughput file screening against inhibition of human lung PDE4 led to the discovery of 3-ethyl-1-(4-fluorophenyl)-6-phenyl-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine (11) as a novel PDE4 inhibitor. Subsequent SAR development, using an eosinophil PDE assay, led to analogues up to 50-fold more potent than 11 with IC50 values of 0.03-1.6 mu M. One such compound, CP-220,629 (22) (IC50 = 0.44 mu M), was efficacious in the guinea pig aerosolized antigen induced airway obstruction assay (ED50 2.0 mg/kg, po) and demonstrated a significant reduction in eosinophil (55%), neutrophil (65%), and IL-1 beta (82%) responses to antigen challenge in atopic monkeys (10 mg/kg, po).
    DOI:
    10.1021/jm9800090
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文献信息

  • Synthesis of the Novel Tetrahydropyrazolo[3,4-c]pyridin-5-one Scaffold
    作者:Nicholas Howe、Kevin Blades、Gillian Lamont
    DOI:10.1055/s-0034-1379504
    日期:——
    We report an efficient synthesis of the novel 1,4,6,7-tetrahydropyrazolo[3,4-c]pyridin-5-one scaffold with the potential for incorporation of alkyl or aryl substituents at the C-3 and N-6 positions. The route utilises a Dieckmann condensation to install the lactam ring, followed by a hydrazine cyclisation to build the fused pyrazole ring.
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