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5-(4-chlorophenyl)-1,2-dimethyl-N-(methylsulfonyl)-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxamide | 1428146-03-5

中文名称
——
中文别名
——
英文名称
5-(4-chlorophenyl)-1,2-dimethyl-N-(methylsulfonyl)-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxamide
英文别名
5-(4-chlorophenyl)-1,2-dimethyl-N-methylsulfonyl-4-[3-[4-(4-nitrophenyl)piperazin-1-yl]phenyl]pyrrole-3-carboxamide
5-(4-chlorophenyl)-1,2-dimethyl-N-(methylsulfonyl)-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxamide化学式
CAS
1428146-03-5
化学式
C30H30ClN5O5S
mdl
——
分子量
608.118
InChiKey
OEAKSBTYPBRXLR-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):
    5.4
  • 重原子数:
    42
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    129
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    5-(4-chlorophenyl)-1,2-dimethyl-N-(methylsulfonyl)-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxamide吡啶 、 palladium 10% on activated carbon 、 氢气N,N-二异丙基乙胺 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 0.75h, 生成 C48H53ClN8O7S3
    参考文献:
    名称:
    A Potent and Highly Efficacious Bcl-2/Bcl-xL Inhibitor
    摘要:
    Our previously reported Bcl-2/Bcl-xL inhibitor, 4, effectively inhibited tumor growth but failed to achieve complete regression in vivo. We have now performed extensive modifications on its pyrrole core structure, which has culminated in the discovery of 32 (BM-1074). Compound 32 binds to Bcl-2 and Bcl-xL proteins with K-i values of <1 nM and inhibits cancer cell growth with IC50 values of 1-2 nM in four small-cell lung cancer cell lines sensitive to potent and specific Bcl-2/Bcl-xL inhibitors. Compound 32 is capable of achieving rapid, complete, and durable tumor regression in vivo at a well-tolerated dose schedule. Compound 32 is the most potent and efficacious Bcl-2/Bcl-xL inhibitor reported to date.
    DOI:
    10.1021/jm4001105
  • 作为产物:
    描述:
    ethyl 2-acetyl-4-(4-chlorophenyl)-3-(3-iodophenyl)-4-oxobutanoate 在 4-二甲氨基吡啶copper(l) iodide草酰氯N,N-二甲基甲酰胺L-脯氨酸 、 sodium hydroxide 作用下, 以 1,4-二氧六环甲醇乙醇二氯甲烷二甲基亚砜1,2-二氯乙烷 为溶剂, 反应 24.08h, 生成 5-(4-chlorophenyl)-1,2-dimethyl-N-(methylsulfonyl)-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxamide
    参考文献:
    名称:
    A Potent and Highly Efficacious Bcl-2/Bcl-xL Inhibitor
    摘要:
    Our previously reported Bcl-2/Bcl-xL inhibitor, 4, effectively inhibited tumor growth but failed to achieve complete regression in vivo. We have now performed extensive modifications on its pyrrole core structure, which has culminated in the discovery of 32 (BM-1074). Compound 32 binds to Bcl-2 and Bcl-xL proteins with K-i values of <1 nM and inhibits cancer cell growth with IC50 values of 1-2 nM in four small-cell lung cancer cell lines sensitive to potent and specific Bcl-2/Bcl-xL inhibitors. Compound 32 is capable of achieving rapid, complete, and durable tumor regression in vivo at a well-tolerated dose schedule. Compound 32 is the most potent and efficacious Bcl-2/Bcl-xL inhibitor reported to date.
    DOI:
    10.1021/jm4001105
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文献信息

  • A Potent and Highly Efficacious Bcl-2/Bcl-xL Inhibitor
    作者:Angelo Aguilar、Haibin Zhou、Jianfang Chen、Liu Liu、Longchuan Bai、Donna McEachern、Chao-Yie Yang、Jennifer Meagher、Jeanne Stuckey、Shaomeng Wang
    DOI:10.1021/jm4001105
    日期:2013.4.11
    Our previously reported Bcl-2/Bcl-xL inhibitor, 4, effectively inhibited tumor growth but failed to achieve complete regression in vivo. We have now performed extensive modifications on its pyrrole core structure, which has culminated in the discovery of 32 (BM-1074). Compound 32 binds to Bcl-2 and Bcl-xL proteins with K-i values of <1 nM and inhibits cancer cell growth with IC50 values of 1-2 nM in four small-cell lung cancer cell lines sensitive to potent and specific Bcl-2/Bcl-xL inhibitors. Compound 32 is capable of achieving rapid, complete, and durable tumor regression in vivo at a well-tolerated dose schedule. Compound 32 is the most potent and efficacious Bcl-2/Bcl-xL inhibitor reported to date.
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