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(R)-2-allyl-1-(7-ethyl-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-2-yl)-6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one | 2376146-48-2

中文名称
——
中文别名
——
英文名称
(R)-2-allyl-1-(7-ethyl-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-2-yl)-6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one
英文别名
ZN-c3;azenosertib;1-[(7R)-7-ethyl-7-hydroxy-5,6-dihydrocyclopenta[b]pyridin-2-yl]-6-[4-(4-methylpiperazin-1-yl)anilino]-2-prop-2-enylpyrazolo[3,4-d]pyrimidin-3-one
(R)-2-allyl-1-(7-ethyl-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-2-yl)-6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one化学式
CAS
2376146-48-2
化学式
C29H34N8O2
mdl
——
分子量
526.641
InChiKey
OXTSYWDBUVRXFF-GDLZYMKVSA-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

物化性质

  • 沸点:
    766.7±70.0 °C(Predicted)
  • 密度:
    1.311±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    39
  • 可旋转键数:
    7
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    101
  • 氢给体数:
    2
  • 氢受体数:
    9

反应信息

点击查看最新优质反应信息

文献信息

  • Discovery of ZN-c3, a Highly Potent and Selective Wee1 Inhibitor Undergoing Evaluation in Clinical Trials for the Treatment of Cancer
    作者:Peter Q. Huang、Brant C. Boren、Sayee G. Hegde、Hui Liu、Aditya K. Unni、Sunny Abraham、Chad D. Hopkins、Sunil Paliwal、Ahmed A. Samatar、Jiali Li、Kevin D. Bunker
    DOI:10.1021/acs.jmedchem.1c01121
    日期:2021.9.9
    inhibition has received great attention in the past decade as a promising therapy for cancer treatment. Therefore, a potent and selective Wee1 inhibitor is highly desirable. Our efforts to make safer and more efficacious Wee1 inhibitors led to the discovery of compound 16, a highly selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties. The chiral ethyl moiety of compound
    Wee1 抑制作为一种有前途的癌症治疗方法在过去十年中受到了极大的关注。因此,非常需要一种有效且选择性的 Wee1 抑制剂。我们为制造更安全、更有效的 Wee1 抑制剂所做的努力导致了化合物16的发现,这是一种具有平衡效力、ADME 和药代动力学特性的高度选择性 Wee1 抑制剂。化合物16的手性乙基部分提供了 Wee1 效力的意外改善。化合物16,称为 ZN-c3,显示出优异的体内功效,目前正在 2 期临床试验中进行评估。
  • Substituted 1,2-dihydro-3H-pyrazolo[3,4-D]pyrimidin-3-ones
    申请人:Recurium IP Holdings, LLC
    公开号:US11261192B2
    公开(公告)日:2022-03-01
    Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
    本文提供了式(I)化合物。此类化合物及其药学上可接受的盐和组合物可用于治疗疾病或病症,包括以细胞过度增殖为特征的病症,如乳腺癌。
  • WO2019173082A5
    申请人:——
    公开号:WO2019173082A5
    公开(公告)日:2022-03-07
  • SUBSTITUTED 1,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONES
    申请人:Recurium IP Holdings, LLC
    公开号:EP3762385A1
    公开(公告)日:2021-01-13
  • [EN] SUBSTITUTED L,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONES<br/>[FR] L,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONES SUBSTITUÉES
    申请人:ZENO ROYALTIES & MILESTONES LLC
    公开号:WO2019173082A1
    公开(公告)日:2019-09-12
    Compounds of Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive cellular proliferation, such as breast cancer.
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