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4-Methyl-2-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]oxypyridine

中文名称
——
中文别名
——
英文名称
4-Methyl-2-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]oxypyridine
英文别名
4-methyl-2-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]oxypyridine
4-Methyl-2-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]oxypyridine化学式
CAS
——
化学式
C13H17F3N2O
mdl
——
分子量
274.28
InChiKey
BLRGZXZSJYMEDS-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):
    3.2
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    25.4
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • [EN] PRMT5 INHIBITORS CONTAINING A DIHYDRO- OR TETRAHYDROISOQUINOLINE AND USES THEREOF<br/>[FR] INHIBITEURS DE LA PRMT5 CONTENANT UNE DIHYDRO- OU TÉTRAHYDRO-ISOQUINOLÉINE ET LEURS UTILISATIONS
    申请人:EPIZYME INC
    公开号:WO2014100730A1
    公开(公告)日:2014-06-26
    Described herein are compounds of Formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5- mediated disorders are also described.
    本文描述了式(A)的化合物,其药学上可接受的盐以及药物组合物。本发明的化合物对抑制PRMT5活性是有用的。还描述了利用这些化合物治疗PRMT5介导的疾病的方法。
  • [EN] PRMT5 INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE PRMT5 ET LEURS UTILISATIONS
    申请人:EPIZYME INC
    公开号:WO2014100734A1
    公开(公告)日:2014-06-26
    Described herein are compounds of formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.
    本文描述了式(A)的化合物,其药学上可接受的盐以及药物组成物。本发明的化合物对抑制PRMT5活性是有用的。还描述了利用这些化合物治疗PRMT5介导的疾病的方法。
  • [EN] TETRAHYDROISOQUINOLINES AS PRMT5 INHIBITORS<br/>[FR] TÉTRAHYDRO-ISOQUINOLÉINES EN TANT QU'INHIBITEURS DE PRMT5
    申请人:CTXT PTY LTD
    公开号:WO2017153513A1
    公开(公告)日:2017-09-14
    A compound of formula (I) wherein: n is 1 or 2; p is 0 or 1; R1a, R1b, R1c and R1d are independently selected from the group consisiting of H, halo, C1-4 alkoxy, C1-4 alkyl, C1-4 fluoroalkyl, C3-4 cycloalkyl, NH-C1-4 alkyl and cyano; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2e is H or Me; R3a and R3b are independently selected from H and Me; R4 is either H or Me; R5 is either H or Me; R6a and R6b are independently selected from H and Me; A is either (i) optionally substituted phenyl; (ii) optionally substituted naphthyl; or (iii) optionally substituted C5-12 heteroaryl; wherein when R2e is H, at least one of R1a, R1b, R1c and R1d is selected from C1-4 alkoxy, C2-4 alkyl, C1-4 fluoroalkyl, C3-4 cycloalkyl, NH-C1-4 alkyl and cyano.
    式(I)的化合物中:n为1或2;p为0或1;R1a、R1b、R1c和R1d分别独立地选自H、卤素、C1-4烷氧基、C1-4烷基、C1-4氟烷基、C3-4环烷基、NH-C1-4烷基和基组成的群;R2a和R2b分别独立地选自以下组成的群:(i)F;(ii)H;(iii)Me;和(iv)CH2OH;R2c和R2d分别独立地选自以下组成的群:(i)F;(ii)H;(iii)Me;和(iv)CH2OH;R2e为H或Me;R3a和R3b分别独立地选自H和Me;R4为H或Me;R5为H或Me;R6a和R6b分别独立地选自H和Me;A为(i)可选择地取代的苯基;(ii)可选择地取代的基;或(iii)可选择地取代的C5-12杂环芳基;其中当R2e为H时,至少有一个R1a、R1b、R1c和R1d选自C1-4烷氧基、C2-4烷基、C1-4氟烷基、C3-4环烷基、NH-C1-4烷基和基。
  • PRMT5 INHIBITORS AND USES THEREOF
    申请人:Epizyme, Inc.
    公开号:US20140329794A1
    公开(公告)日:2014-11-06
    Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.
    本文描述了公式(I)的化合物,其药学上可接受的盐以及其制药组合物。本发明的化合物可用于抑制PRMT5活性。还描述了使用这些化合物治疗PRMT5介导的疾病的方法。
  • TETRAHYDRO- AND DIHYDRO-ISOQUINOLINE PRMT5 INHIBITORS AND USES THEREOF
    申请人:EPIZYME, INC.
    公开号:US20150344434A1
    公开(公告)日:2015-12-03
    Described herein are compounds of Formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5 mediated disorders are also described.
    本文描述了公式(A)的化合物,其药学上可接受的盐以及它们的药物组合物。本发明的化合物对于抑制PRMT5活性是有用的。还描述了使用这些化合物治疗PRMT5介导的疾病的方法。
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