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(S)-3-methyl-4-(piperidin-4-yl)piperazine-1-carboxylic acid tert-butyl ester | 1477815-58-9

中文名称
——
中文别名
——
英文名称
(S)-3-methyl-4-(piperidin-4-yl)piperazine-1-carboxylic acid tert-butyl ester
英文别名
(S)-3-methyl-4-piperidin-4-yl-piperazine-1-carboxylic acid tert-butyl ester;tert-butyl (3S)-3-methyl-4-piperidin-4-ylpiperazine-1-carboxylate
(S)-3-methyl-4-(piperidin-4-yl)piperazine-1-carboxylic acid tert-butyl ester化学式
CAS
1477815-58-9
化学式
C15H29N3O2
mdl
——
分子量
283.414
InChiKey
HFQRBLYMOWCSQM-LBPRGKRZSA-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):
    1.5
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    44.8
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF BROMODOMAIN-CONTAINING PROTEINS<br/>[FR] COMPOSÉS ET PROCÉDÉS POUR LA DÉGRADATION CIBLÉE DE PROTÉINES CONTENANT UN BROMODOMAINE
    申请人:ARVINAS INC
    公开号:WO2017030814A1
    公开(公告)日:2017-02-23
    The present invention relates to bifunctional compounds, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present invention. In particular, the present invention is directed to compounds, which contain on one end a VHL ligand which binds to the ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of targeted polypeptides.
    本发明涉及双功能化合物,其作为靶向泛素化的调节剂具有实用性,特别是根据本发明抑制各种多肽和其他蛋白质的化合物。具体而言,本发明涉及一端含有结合泛素连接酶的VHL配体,另一端含有结合靶蛋白的基团的化合物,使得靶蛋白靠近泛素连接酶以促使该蛋白的降解(和抑制)。根据本发明的化合物表现出与靶向多肽的降解/抑制一致的广泛的药理活性。
  • Piperazine-piperidine compounds as hepatitis C virus inhibitors
    申请人:Long Daniel D.
    公开号:US09206159B2
    公开(公告)日:2015-12-08
    The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.
    该发明提供式(I)的化合物:其中变量在规范中定义,或其药学上可接受的盐,它们是乙型肝炎病毒复制抑制剂。该发明还提供包含这些化合物的药物组合物,使用这些化合物治疗乙型肝炎病毒感染的方法,以及用于制备这些化合物的过程和中间体。
  • US9206159B2
    申请人:——
    公开号:US9206159B2
    公开(公告)日:2015-12-08
  • [EN] PIPERAZINE-PIPERIDINE COMPOUNDS AS HEPATITIS C VIRUS INHIBITORS<br/>[FR] COMPOSÉS DE PIPÉRAZINE-PIPÉRIDINE EN TANT QU'INHIBITEURS DU VIRUS DE L'HÉPATITE C
    申请人:THERAVANCE INC
    公开号:WO2013163262A1
    公开(公告)日:2013-10-31
    The invention provides compounds of formula (I) wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.
  • PIPERAZINE-PIPERIDINE COMPOUNDS AS HEPATITIS C VIRUS INHIBITORS
    申请人:Long Daniel D.
    公开号:US20130287730A1
    公开(公告)日:2013-10-31
    The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.
    这项发明提供了式(I)的化合物: 其中变量在规范中定义,或其药用盐,这些化合物是乙型肝炎病毒复制的抑制剂。该发明还提供了包括这些化合物的药物组合物,使用这些化合物治疗乙型肝炎病毒感染的方法,以及用于制备这些化合物的工艺和中间体。
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