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| 1201809-53-1

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1201809-53-1
化学式
C24H30N8S*ClH
mdl
——
分子量
499.083
InChiKey
UOBJMFWSKCGAJJ-YHSIFKNPSA-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):
    5.25
  • 重原子数:
    34.0
  • 可旋转键数:
    7.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    106.57
  • 氢给体数:
    3.0
  • 氢受体数:
    9.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Heterobiaryl purine derivatives as potent antiproliferative agents: Inhibitors of cyclin dependent kinases. Part II
    摘要:
    C-6 Biarylmethylamino purine derivatives of roscovitine (1) inhibit cyclin dependent kinases and demonstrate potent antiproliferative activity. Replacement of the aryl rings of the C-6 biarylmethylamino group with heterobiaryl rings has provided compounds with significantly improved activity. In particular, derivatives 18g and 9c demonstrated 1000-fold and 1250-fold improvements, respectively, in the growth inhibition of HeLa cells compared to roscovitine (1). (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.011
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文献信息

  • Heterobiaryl purine derivatives as potent antiproliferative agents: Inhibitors of cyclin dependent kinases. Part II
    作者:Michael P. Trova、Keith D. Barnes、Luis Alicea、Travis Benanti、Mark Bielaska、Joseph Bilotta、Brian Bliss、Thuy Nguyen Duong、Simon Haydar、R. Jason Herr、Yu Hui、Matthew Johnson、John M. Lehman、Denise Peace、Matthew Rainka、Patricia Snider、Susan Salamone、Steven Tregay、Xiaozhang Zheng、Thomas D. Friedrich
    DOI:10.1016/j.bmcl.2009.10.011
    日期:2009.12
    C-6 Biarylmethylamino purine derivatives of roscovitine (1) inhibit cyclin dependent kinases and demonstrate potent antiproliferative activity. Replacement of the aryl rings of the C-6 biarylmethylamino group with heterobiaryl rings has provided compounds with significantly improved activity. In particular, derivatives 18g and 9c demonstrated 1000-fold and 1250-fold improvements, respectively, in the growth inhibition of HeLa cells compared to roscovitine (1). (C) 2009 Elsevier Ltd. All rights reserved.
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