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1-[5-(benzyloxy)-1-(cyclohexylmethyl)-1H-pyrazol-3-yl]-N-methylmethanamine | 1355348-69-4

中文名称
——
中文别名
——
英文名称
1-[5-(benzyloxy)-1-(cyclohexylmethyl)-1H-pyrazol-3-yl]-N-methylmethanamine
英文别名
US10183913, Example 5;1-[1-(cyclohexylmethyl)-5-phenylmethoxypyrazol-3-yl]-N-methylmethanamine
1-[5-(benzyloxy)-1-(cyclohexylmethyl)-1H-pyrazol-3-yl]-N-methylmethanamine化学式
CAS
1355348-69-4
化学式
C19H27N3O
mdl
——
分子量
313.443
InChiKey
KRMVDUWYWGAWOH-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):
    3.7
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    39.1
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • PYRAZOLE COMPOUND
    申请人:Sasaki Izumi
    公开号:US20130116296A1
    公开(公告)日:2013-05-09
    The present invention relates to a novel serotonin reuptake inhibitor which also exhibits 5-HT 2C antagonistic action (antidepressive and anxiolytic effects), in particular, 5-HT 2C inverse agonistic action comprising Compound (1): or a pharmaceutically acceptable salt thereof wherein R 1 , R 2 , R 3 and R 4 are independently hydrogen or C 1-6 alkyl etc.; R 5 is C 4-7 alkyl or —(CR 8 R 9 ) r -E; R 6 , R 7 , R 8 and R 9 are independently hydrogen, fluorine or C 1-6 alkyl; A is C 6-10 aryl or heteroaryl etc.; r is 1, 2, 3 or 4; E is C 3-8 cycloalkyl or C 6-10 aryl etc.; L is oxygen, sulfur or —NR 10 —; n is 1, 2 or 3; R 10 is hydrogen or C 1-6 alkyl etc.; and X is hydrogen or halogen etc.
    本发明涉及一种新型的血清素再摄取抑制剂,同时还表现出5-HT2C拮抗作用(抗抑郁和抗焦虑效果),特别是包括化合物(1)的5-HT2C逆作动作:或其药学上可接受的盐,其中R1、R2、R3和R4独立地为氢或C1-6烷基等;R5为C4-7烷基或—(CR8R9)r-E;R6、R7、R8和R9独立地为氢、或C1-6烷基;A为C6-10芳基或杂环芳基等;r为1、2、3或4;E为C3-8环烷基或C6-10芳基等;L为氧、或—NR10—;n为1、2或3;R10为氢或C1-6烷基等;X为氢或卤素等。
  • THERAPEUTIC AGENT FOR NON-MOTOR SYMPTOMS ASSOCIATED WITH PARKINSON'S DISEASE
    申请人:Sumitomo Dainippon Pharma Co., Ltd.
    公开号:EP3569233A1
    公开(公告)日:2019-11-20
    The purpose of the present invention is to provide: a therapeutic agent or a recurrence preventive agent for serotonergic system- or dopaminergic system-related diseases, in particular, mental dysfunction symptoms and other non-motor symptoms of Parkinson's disease; and a method for treating the aforesaid symptoms or preventing the recurrence of the same. A compound represented by formula (1) [wherein each symbol is as defined in the description] or a pharmaceutically acceptable salt thereof can exhibit an effect of treating serotonergic system- or dopaminergic system-related diseases, in particular, mental dysfunction symptoms and other non-motor symptoms of Parkinson's disease and/or an effect of preventing the recurrence of the same.
    本发明的目的是提供:一种治疗5-羟色胺能系统或多巴胺能系统相关疾病,特别是帕森病的精神功能障碍症状和其他非运动症状的治疗剂或复发预防剂;以及一种治疗上述症状或预防上述症状复发的方法。由式(1)代表的化合物[其中各符号如描述中所定义]或其药学上可接受的盐可以显示出治疗血清素能系统或多巴胺能系统相关疾病的效果,特别是精神功能障碍症状和帕森病的其他非运动症状,和/或防止其复发的效果。
  • Pyrazole compound
    申请人:Sumitomo Dainippon Pharma Co., Ltd.
    公开号:US10087146B2
    公开(公告)日:2018-10-02
    The present invention relates to a novel serotonin reuptake inhibitor which also exhibits 5-HT2C antagonistic action (antidepressive and anxiolytic effects), in particular, 5-HT2C inverse agonistic action comprising Compound (1): or a pharmaceutically acceptable salt thereof wherein R1, R2, R3 and R4 are independently hydrogen or C1-6 alkyl etc.; R5 is C4-7 alkyl or —(CR8R9)r-E; R6, R7, R8 and R9 are independently hydrogen, fluorine or C1-6 alkyl; A is C6-10 aryl or heteroaryl etc.; r is 1, 2, 3 or 4; E is C3-8 cycloalkyl or C6-10 aryl etc.; L is oxygen, sulfur or —NR10—; n is 1, 2 or 3; R10 is hydrogen or C1-6 alkyl etc.; and X is hydrogen or halogen etc.
    本发明涉及一种新型血清素再摄取抑制剂,它还具有 5-HT2C 拮抗作用(抗抑郁和抗焦虑作用),特别是 5-HT2C 反激动作用,由化合物(1)组成: 或其药学上可接受的盐 其中R1、R2、R3和R4独立地为氢或C1-6烷基等;R5为C4-7烷基或-(CR8R9)r-E;R6、R7、R8和R9独立地为氢、或C1-6烷基; A 是 C6-10 芳基或杂芳基等;r 是 1、2、3 或 4;E 是 C3-8 环烷基或 C6-10 芳基等;L 是氧、或-NR10-;n 是 1、2 或 3;R10 是氢或 C1-6 烷基等; X 是氢或卤素等。
  • US8569353B2
    申请人:——
    公开号:US8569353B2
    公开(公告)日:2013-10-29
  • US8809383B2
    申请人:——
    公开号:US8809383B2
    公开(公告)日:2014-08-19
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