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CJ-1037 | 1062467-99-5

中文名称
——
中文别名
——
英文名称
CJ-1037
英文别名
trans-N-(4-(2-(((S)-2-amino-4,5,6,7-tetrahydrobenzo[d]thiazol-6-yl)(propyl)amino)ethyl)cyclohexyl)cinnamamide
CJ-1037化学式
CAS
1062467-99-5
化学式
C27H38N4OS
mdl
——
分子量
466.691
InChiKey
VEYJQJYLFDMMTQ-BUWVWOCESA-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):
    5.07
  • 重原子数:
    33.0
  • 可旋转键数:
    9.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    71.25
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

反应信息

  • 作为产物:
    描述:
    肉桂酸 、 (6S)-N6-[2-(trans-4-Aminocyclohexyl)ethyl]-N6-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine 在 1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺N,N-二异丙基乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以75 mg的产率得到CJ-1037
    参考文献:
    名称:
    Design, Synthesis, and Evaluation of Potent and Selective Ligands for the Dopamine 3 (D3) Receptor with a Novel in Vivo Behavioral Profile
    摘要:
    A series of compounds structurally related to pramipexole were designed, synthesized, and evaluated as ligands for the dopamine 3 (D-3) receptor. Compound 12 has a K-i value of 0.41 nM to D3 and a selectivity of > 30000- and 800-fold over the D-1-like and D-2 receptors, respectively. Our in vivo functional assays showed that this compound is a partial agonist at the D-3 receptor with no detectable activity at the D-2 receptor.
    DOI:
    10.1021/jm800471h
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文献信息

  • Selective Ligands for the Dopamine 3 (D3) Receptor and Methods of using the Same
    申请人:Wang Shaomeng
    公开号:US20110184033A1
    公开(公告)日:2011-07-28
    Potent and selective ligands for the dopamine 3 (D 3 ) receptor are disclosed. The D3 receptor ligands have a structural formula (I) wherein X is C═O or SO 2 , R 1 is C 1-6 alkyl, R 2 is aryl, heteroaryl, aryl, —(CH 2 ) 1-3 aryl, or —(CH 2 ) 1-3 heteroaryl, and n is 0 or 1. Methods of using the D 3 receptor ligands in the treatment of diseases and conditions wherein modulation of the D 3 receptor provides a benefit also are disclosed.
    揭示了对多巴胺3(D3)受体具有强效和选择性的配体。D3受体配体具有结构式(I),其中X是C═O或SO2,R1是C1-6烷基,R2是芳基,杂环芳基,芳基,—(CH2)1-3芳基或—(CH2)1-3杂环芳基,n为0或1。还揭示了在调节D3受体提供益处的疾病和病况的治疗中使用D3受体配体的方法。
  • US8283368B2
    申请人:——
    公开号:US8283368B2
    公开(公告)日:2012-10-09
  • Design, Synthesis, and Evaluation of Potent and Selective Ligands for the Dopamine 3 (D<sub>3</sub>) Receptor with a Novel in Vivo Behavioral Profile
    作者:Jianyong Chen、Gregory T. Collins、Jian Zhang、Chao-Yie Yang、Beth Levant、James Woods、Shaomeng Wang
    DOI:10.1021/jm800471h
    日期:2008.10.9
    A series of compounds structurally related to pramipexole were designed, synthesized, and evaluated as ligands for the dopamine 3 (D-3) receptor. Compound 12 has a K-i value of 0.41 nM to D3 and a selectivity of > 30000- and 800-fold over the D-1-like and D-2 receptors, respectively. Our in vivo functional assays showed that this compound is a partial agonist at the D-3 receptor with no detectable activity at the D-2 receptor.
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