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4-tert-butyl-N-(4-chloro-2-(4-morpholino-1H-[1,2,3]triazolo[4,5-c]pyridine-1-yl)phenyl)benzenesulfonamide | 1094757-87-5

中文名称
——
中文别名
——
英文名称
4-tert-butyl-N-(4-chloro-2-(4-morpholino-1H-[1,2,3]triazolo[4,5-c]pyridine-1-yl)phenyl)benzenesulfonamide
英文别名
4-tert-butyl-N-(4-chloro-2-(4-morpholino-1H-[1,2,3]triazolo[4,5-c]pyridin-1-yl)phenyl)benzenesulfonamide;4-tert-butyl-N-[4-chloro-2-(4-morpholin-4-yltriazolo[4,5-c]pyridin-1-yl)phenyl]benzenesulfonamide
4-tert-butyl-N-(4-chloro-2-(4-morpholino-1H-[1,2,3]triazolo[4,5-c]pyridine-1-yl)phenyl)benzenesulfonamide化学式
CAS
1094757-87-5
化学式
C25H27ClN6O3S
mdl
——
分子量
527.047
InChiKey
RVWKTSXAZSTVQX-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):
    4.6
  • 重原子数:
    36
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    111
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • N-(2-(HETARYL)ARYL) ARYLSULFONAMIDES AND N-(2-(HETARYL) HETARYL ARYLSULFONAMIDES
    申请人:Charvat Trevor T.
    公开号:US20090005410A1
    公开(公告)日:2009-01-01
    Compounds are provided that act as potent antagonists of the CCR9 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.
    提供了作为CCR9受体强效拮抗剂的化合物。动物实验表明,这些化合物对于治疗炎症非常有效,而炎症是CCR9的典型疾病特征。这些化合物通常是芳基磺酰胺衍生物,可用于制药组合物、治疗CCR9介导疾病的方法,以及作为鉴定CCR9拮抗剂的检测中的对照物。
  • N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES
    申请人:Charvat Trevor T.
    公开号:US20120245138A1
    公开(公告)日:2012-09-27
    Compounds are provided that act as potent antagonists of the CCR9 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.
    提供了作为CCR9受体的有效拮抗剂的化合物。动物实验表明这些化合物对于治疗CCR9标志性疾病炎症是有用的。这些化合物通常是芳基磺酰胺衍生物,可用于制药组合物、治疗CCR9介导的疾病的方法,以及作为鉴定CCR9拮抗剂的试验控制。
  • N-(2-(HETARYL)ARYL) ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES
    申请人:Charvat Trevor T.
    公开号:US20100331302A1
    公开(公告)日:2010-12-30
    Compounds are provided that act as potent antagonists of the CCR9 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.
    提供了一些化合物,它们作为CCR9受体的有效拮抗剂。动物实验表明,这些化合物对于治疗CCR9标志性疾病炎症非常有用。这些化合物通常是芳基磺酰胺衍生物,并且在制药组合物、治疗CCR9介导疾病的方法以及用于识别CCR9拮抗剂的测定中作为对照物质非常有用。
  • Abuse-proofed dosage form
    申请人:Bartholomaus Johannes
    公开号:US20050152843A1
    公开(公告)日:2005-07-14
    The invention relates to a solid administration form, protected from parenteral abuse and containing at least one viscosity-increasing agent in addition to one or more active substances that have parenteral abuse potential. The agent forms, when a necessary minimum amount of an aqueous liquid is added, on the basis of an extract obtained from the administration form, a preferably injectable gel that remains visually distinct when introduced into another quantity of an aqueous liquid.
    本发明涉及一种防止非肠道滥用的固体给药形式,除了一种或多种具有非肠道滥用潜能的活性物质外,还含有至少一种增粘剂。当加入必要的最低量的性液体时,该药剂在从给药形式中提取的基础上形成一种优选的可注射凝胶,该凝胶在加入另一种数量的性液体时在视觉上仍然是独特的。
  • N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES
    申请人:ChemoCentryx, Inc.
    公开号:EP2170823B1
    公开(公告)日:2014-08-06
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