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diethyl (4-bromo-6-cyano-2-naphthyl)methylphosphonate | 371220-26-7

中文名称
——
中文别名
——
英文名称
diethyl (4-bromo-6-cyano-2-naphthyl)methylphosphonate
英文别名
8-Bromo-6-(diethoxyphosphorylmethyl)naphthalene-2-carbonitrile
diethyl (4-bromo-6-cyano-2-naphthyl)methylphosphonate化学式
CAS
371220-26-7
化学式
C16H17BrNO3P
mdl
——
分子量
382.194
InChiKey
RXUUBFQODVILKD-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):
    3.4
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    59.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    diethyl (4-bromo-6-cyano-2-naphthyl)methylphosphonate 在 palladium diacetate 、 lithium hexamethyldisilazane 作用下, 以 四氢呋喃乙醚 为溶剂, 生成 8-Bromo-6-((1S,2S)-2-phenyl-cyclopropyl)-naphthalene-2-carbonitrile
    参考文献:
    名称:
    Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties
    摘要:
    A series of non-amide-linked 6-substituted-2-naphthamidine urokinase plasminogen activator (uPA) inhibitors are described. These compounds possess excellent binding activities and selectivities with significantly improved pharmacokinetic profiles versus previously described amide-linked inhibitors. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.10.026
  • 作为产物:
    描述:
    4-溴-6-氰基-2-萘甲酸甲酯 在 sodium tetrahydroborate 、 N-溴代丁二酰亚胺(NBS)三苯基膦 、 calcium chloride 作用下, 以 乙醇二氯甲烷 为溶剂, 生成 diethyl (4-bromo-6-cyano-2-naphthyl)methylphosphonate
    参考文献:
    名称:
    Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties
    摘要:
    A series of non-amide-linked 6-substituted-2-naphthamidine urokinase plasminogen activator (uPA) inhibitors are described. These compounds possess excellent binding activities and selectivities with significantly improved pharmacokinetic profiles versus previously described amide-linked inhibitors. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.10.026
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文献信息

  • Naphthamidine urokinase inhibitors
    申请人:——
    公开号:US06504031B1
    公开(公告)日:2003-01-07
    Compounds having the formula: are inhibitors of urokinase and are useful in the treatment of diseases in which urokinase plays a role. Also disclosed are urokinase-inhibiting compositions, methods for the preparation of urokinase-inhibitors, and a method of inhibiting urokinase in a mammal.
    具有以下化学式的化合物是尿激酶的抑制剂,对于尿激酶在某些疾病治疗中起作用是有用的。还公开了抑制尿激酶的组合物、制备尿激酶抑制剂的方法,以及在哺乳动物中抑制尿激酶的方法。
  • Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties
    作者:Milan Bruncko、William J. McClellan、Michael D. Wendt、Daryl R. Sauer、Andrew Geyer、Christopher R. Dalton、Michele A. Kaminski、Moshe Weitzberg、Jane Gong、Joseph F. Dellaria、Robert Mantei、Xumiao Zhao、Vicki L. Nienaber、Kent Stewart、Vered Klinghofer、Jennifer Bouska、Todd W. Rockway、Vincent L. Giranda
    DOI:10.1016/j.bmcl.2004.10.026
    日期:2005.1
    A series of non-amide-linked 6-substituted-2-naphthamidine urokinase plasminogen activator (uPA) inhibitors are described. These compounds possess excellent binding activities and selectivities with significantly improved pharmacokinetic profiles versus previously described amide-linked inhibitors. (C) 2004 Elsevier Ltd. All rights reserved.
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