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N-benzyl-1-[1-butyl-2-(3-fluorophenyl)-1H-imidazol-5-yl]-N-(2,3-dichlorobenzyl)methanamine | 439558-24-4

中文名称
——
中文别名
——
英文名称
N-benzyl-1-[1-butyl-2-(3-fluorophenyl)-1H-imidazol-5-yl]-N-(2,3-dichlorobenzyl)methanamine
英文别名
N-[[3-butyl-2-(3-fluorophenyl)imidazol-4-yl]methyl]-N-[(2,3-dichlorophenyl)methyl]-1-phenylmethanamine
N-benzyl-1-[1-butyl-2-(3-fluorophenyl)-1H-imidazol-5-yl]-N-(2,3-dichlorobenzyl)methanamine化学式
CAS
439558-24-4
化学式
C28H28Cl2FN3
mdl
——
分子量
496.455
InChiKey
UAJRLQXGOCAZRQ-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):
    7.1
  • 重原子数:
    34
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    21.1
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • High affinity small molecule C5a receptor modulators
    申请人:Thurkauf Andrew
    公开号:US20070027158A1
    公开(公告)日:2007-02-01
    This invention relates to low molecular weight, non-peptidic, non-peptidomimetic, organic molecules that act as modulators of mammalian complement C5a receptors, preferably ones that act as high affinity C5a receptor ligands and also to such ligands that act as antagonists or inverse agonists of complement C5a receptors. Preferred compounds of the invention possess some or all of the following properties in that they are: 1) multi-aryl in structure, 2) heteroaryl in structure, 3) a pharmaceutically acceptable oral dose can provide a detectable in vitro effect, 4) comprise fewer than four or preferably no amide bonds, and 5) capable of inhibiting leukocyte chemotaxis at nanomolar or sub-nanomolar concentrations. This invention also relates to pharmaceutical compositions comprising such compounds and the use of such compounds in treating a variety of inflammatory and immune system disorders. Additionally, this invention relates to the use such compounds as probes for the localization of C5a receptors.
    本发明涉及低分子量、非肽、非肽类似物有机分子,其作为哺乳动物补体C5a受体的调节剂。其中,优选的化合物是作为高亲和力C5a受体配体的,也是作为补体C5a受体的拮抗剂或反向激动剂的。该发明的优选化合物具有以下一些或全部特性:1)多芳基结构,2)杂芳基结构,3)药学上可接受的口服剂量可提供可检测的体外效果,4)包含少于四个或优选不含酰胺键,5)能够在纳摩尔或亚纳摩尔浓度下抑制白细胞趋化。此外,本发明还涉及包括这些化合物的制药组合物,以及将这些化合物用于治疗各种炎症和免疫系统疾病的用途。此外,本发明还涉及将这些化合物用作C5a受体定位的探针的用途。
  • COMBINATION THERAPY FOR THE TREATMENT OF CONDITIONS WITH PATHOGENIC INFLAMMATORY COMPONENTS
    申请人:NEUROGEN CORPORATION
    公开号:EP1490044A1
    公开(公告)日:2004-12-29
  • EP1490044A4
    申请人:——
    公开号:EP1490044A4
    公开(公告)日:2008-04-16
  • US7271270B2
    申请人:——
    公开号:US7271270B2
    公开(公告)日:2007-09-18
  • [EN] COMBINATION THERAPY FOR THE TREATMENT OF CONDITIONS WITH PATHOGENIC INFLAMMATORY COMPONENTS<br/>[FR] THERAPIE COMBINATOIRE POUR LE TRAITEMENT DE MALADIES FAISANT INTERVENIR DES COMPOSANTS INFLAMMATOIRES
    申请人:NEUROGEN CORP
    公开号:WO2003084524A1
    公开(公告)日:2003-10-16
    Compositions and methods for treating diseases that are associated with inflammation are provided. Such diseases include arthritis (particularly rheumatoid arthritis) and other autoimmune disorders, asthma, cardio-and cerebrovascular disease, burns, psoriasis, reperfusion injury, and traumatic CNS and spinal cord injury. The compositions generally comprise at least one C5a antagonist and at least one C5a receptor-inactive therapeutic agent. The methods involve co-administration of at least one C5a antagonist and at least one C5a receptor-inactive therapeutic agent to a patient. The C5a antagonist and C5a receptor-inactive therapeutic agent may be present within the same composition, or may be administered separately to the patient.
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