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6-[4-(4-butoxy-3-fluorophenyl)piperazin-1-yl]sulfonyl-N-hydroxy-2,3-dimethoxybenzamide

中文名称
——
中文别名
——
英文名称
6-[4-(4-butoxy-3-fluorophenyl)piperazin-1-yl]sulfonyl-N-hydroxy-2,3-dimethoxybenzamide
英文别名
——
6-[4-(4-butoxy-3-fluorophenyl)piperazin-1-yl]sulfonyl-N-hydroxy-2,3-dimethoxybenzamide化学式
CAS
——
化学式
C23H30FN3O7S
mdl
——
分子量
511.6
InChiKey
GFWJKFWFRAEFCE-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):
    2.7
  • 重原子数:
    35
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    126
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • Use of sulfonyl aryl or heteroaryl hydroxamic acids and derivatives thereof as aggrecanase inhibitors
    申请人:——
    公开号:US20030171404A1
    公开(公告)日:2003-09-11
    This invention is directed to a process for inhibiting aggrecanase activity. The process comprises administering a therapeutically effective amount of a sulfonyl aromatic or heteroaromatic hydroxamic acid, a derivative thereof, or a pharmaceutically acceptable salt of the hydroxamic acid or derivative to a host animal. The compound generally corresponds in structure to the following formula: 1 wherein W and the R groups are described in more detail in Applicants' specification.
    这项发明涉及一种抑制聚集素酶活性的过程。该过程包括向宿主动物施用一定治疗有效量的磺酰芳香或杂芳羟肟酸、其衍生物或羟肟酸或其衍生物的药用盐。该化合物通常与以下结构对应:1其中W和R基的详细描述在申请人的说明书中。
  • Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors
    申请人:——
    公开号:US20030073845A1
    公开(公告)日:2003-04-17
    This invention is directed to sulfonyl aromatic hydroxamic acid compounds and salts thereof that, inter alia, inhibit matrix metalloprotease (MMP) activity and/or aggrecanase activity. In some particularly preferred embodiments, the compound corresponds in structure to one of the following formulas: 1 wherein W 2 , the R groups, and —A—R—E—Y are described in more detail in Applicants' specification. This invention also is directed to a process that comprises administering such a compound or pharmaceutically acceptable salt thereof to a host animal having a condition associated with MMP activity.
    本发明涉及磺酰基芳基羟肟酸化合物及其盐,这些化合物在抑制基质金属蛋白酶(MMP)活性和/或聚集素酶活性方面具有作用。在一些特别优选的实施方式中,该化合物的结构符合以下公式之一:其中W2、R基团和—A—R—E—Y在申请人的说明书中有更详细的描述。本发明还涉及一种过程,该过程包括向患有与MMP活性相关的病况的宿主动物施用这种化合物或其药用可接受盐。
  • USE OF SULFONYL ARYL OR HETEROARYL HYDROXAMIC ACIDS AND DERIVATIVES THEREOF AS AGGRECANASE INHIBITORS
    申请人:Pharmacia Corporation
    公开号:EP1406602A2
    公开(公告)日:2004-04-14
  • SULPHONYL ARYL HYDROXAMATES AND THEIR USE AS MMP INHIBITORS
    申请人:Pharmacia Corporation
    公开号:EP1406626A2
    公开(公告)日:2004-04-14
  • US6696449B2
    申请人:——
    公开号:US6696449B2
    公开(公告)日:2004-02-24
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