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2-Ethyl-1-(4-chlor-benzyl)-benzimidazol | 101282-16-0

中文名称
——
中文别名
——
英文名称
2-Ethyl-1-(4-chlor-benzyl)-benzimidazol
英文别名
1-[(4-Chlorophenyl)methyl]-2-ethylbenzimidazole
2-Ethyl-1-(4-chlor-benzyl)-benzimidazol化学式
CAS
101282-16-0
化学式
C16H15ClN2
mdl
MFCD03671840
分子量
270.762
InChiKey
RMZUCBNDWOZAMQ-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):
    4.5
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • PDE10 INHIBITORS AND RELATED COMPOSITIONS AND METHODS
    申请人:Bergmann John E.
    公开号:US20080300240A1
    公开(公告)日:2008-12-04
    Compounds that inhibit PDE10 are disclosed that have utility in the treatment of a variety of conditions, including (but not limited to) psychotic, anxiety, movement disorders and/or neurological disorders such as Parkinson's disease, Huntington's disease, Alzheimer's disease, encephalitis, phobias, epilepsy, aphasia, Bell's palsy, cerebral palsy, sleep disorders, pain, Tourette syndrome, schizophrenia, delusional disorders, drug-induced psychosis and panic and obsessive-compulsive disorders. The compounds have the general structure: wherein m, n, p, x, R, R 1 , R 2 , R 3 , R 4 , R 5 , A and B, are defined herein, including pharmaceutically acceptable salts, stereoisomers, solvates or prodrugs thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for inhibiting PDE 10 in a warm-blooded animal in need of the same.
    抑制PDE10的化合物已被披露,对治疗包括(但不限于)精神病、焦虑、运动障碍和/或神经系统疾病(如帕森病、亨廷顿病、阿尔茨海默病、脑炎、恐惧症、癫痫、失语症、贝尔氏面瘫、脑瘫、睡眠障碍、疼痛、抽动症、精神分裂症、妄想症、药物诱发的精神病和恐慌以及强迫症)多种疾病具有用途。这些化合物具有一般结构: 其中m、n、p、x、R、R1、R2、R3、R4、R5、A和B在此定义,包括药学上可接受的盐、立体异构体、溶剂合物或其前药。还披露了含有本发明化合物的组合物,与药学上可接受的载体结合,以及与使用这些化合物抑制需要同样的PDE10的温血动物相关的方法。
  • Methods and compositions of treating a flaviviridae family viral infection
    申请人:Einav Shirit
    公开号:US20100028299A1
    公开(公告)日:2010-02-04
    Briefly described, embodiments of this disclosure include compounds, pharmaceutical compositions, methods of treating a host infected with a virus from the Flaviviridae family of viruses, methods of inhibiting HCV replication in a host, methods of inhibiting the binding of NS4B polypeptide to the 3′UTR of HCV negative strand RNA in a host, methods of treating liver fibrosis in a host, and the like.
    简要描述,本公开涉及的实施例包括化合物、制药组合物、治疗感染黄病毒科病毒的宿主的方法、抑制宿主中HCV复制的方法、抑制NS4B多肽与HCV负链RNA的3'UTR结合的方法、治疗宿主肝纤维化的方法等。
  • METHODS AND COMPOSITIONS OF TREATING A FLAVIVIRIDAE FAMILY VIRAL INFECTION
    申请人:Choong Ingrid C.
    公开号:US20120276050A1
    公开(公告)日:2012-11-01
    Clemizole and clemizole analog compounds, and pharmaceutical compositions of the same, are useful in methods of treating a host infected with a virus from the Flaviviridae family of viruses, methods of inhibiting HCV replication in a host, methods of inhibiting the binding of NS4B polypeptide to the 3′UTR of HCV negative strand RNA in a host, and methods of treating liver fibrosis in a host.
  • US7786139B2
    申请人:——
    公开号:US7786139B2
    公开(公告)日:2010-08-31
  • US8278327B2
    申请人:——
    公开号:US8278327B2
    公开(公告)日:2012-10-02
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