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| 1421757-18-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1421757-18-7
化学式
C22H20N2O3S
mdl
——
分子量
392.478
InChiKey
QBZSEROZPMITTB-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):
    4.43
  • 重原子数:
    28.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    76.13
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Discovery of a novel series of 4-quinolone JNK inhibitors
    摘要:
    A novel series of highly selective JNK inhibitors based on the 4-quinolone scaffold was designed and synthesized. Structure based drug design was utilized to guide the compound design as well as improvements in the physicochemical properties of the series. Compound (13c) has an IC50 of 62/170 nM for JNK1/2, excellent kinase selectivity and impressive efficacy in a rodent asthma model. Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2012.10.066
  • 作为产物:
    描述:
    2-氯-N-甲氧基-N,6-二甲基吡啶-3-羧基酰胺 在 palladium diacetate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 生成
    参考文献:
    名称:
    Discovery of a novel series of 4-quinolone JNK inhibitors
    摘要:
    A novel series of highly selective JNK inhibitors based on the 4-quinolone scaffold was designed and synthesized. Structure based drug design was utilized to guide the compound design as well as improvements in the physicochemical properties of the series. Compound (13c) has an IC50 of 62/170 nM for JNK1/2, excellent kinase selectivity and impressive efficacy in a rodent asthma model. Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2012.10.066
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