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5-Methyl-2-(piperazin-1-yl)pyrimidine | 262847-57-4

中文名称
——
中文别名
——
英文名称
5-Methyl-2-(piperazin-1-yl)pyrimidine
英文别名
5-methyl-2-piperazin-1-ylpyrimidine
5-Methyl-2-(piperazin-1-yl)pyrimidine化学式
CAS
262847-57-4
化学式
C9H14N4
mdl
——
分子量
178.23
InChiKey
ZXPTZVHHGCYNHT-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):
    0.4
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    41
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • [EN] 3-((HETERO-)ARYL)-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DECANE DERIVATIVES<br/>[FR] DÉRIVÉS DE 3-((HÉTÉRO-)ARYL)-8-AMINO-2-OXO-1,3-DIAZA-SPIRO-[4.5]-DÉCANE
    申请人:GRUENENTHAL GMBH
    公开号:WO2017121647A1
    公开(公告)日:2017-07-20
    The invention relates to 3-((hetero-)aryl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives, their preparation and their use in medicine, particularly in the treatment of pain.
    本发明涉及3-(杂)芳基-8-氨基-2-氧代-1,3-二氮杂螺[4.5]癸烷衍生物,它们的制备方法以及它们在医药中的应用,特别是在治疗疼痛方面的应用。
  • [EN] GLYCOSIDASE INHIBITORS<br/>[FR] INHIBITEURS DE GLYCOSIDASES
    申请人:ASCENEURON S A
    公开号:WO2017144639A1
    公开(公告)日:2017-08-31
    Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.
    式(I)中A、R、W、Q、n和m的含义如权利要求书所述,可用于治疗tau病和阿尔茨海默病。
  • [EN] BENZOTHIAZOLES AND AZA-ANALOGUES THEREOF USE AS ANTIBACTERIAL AGENTS<br/>[FR] BENZOTHIAZOLES ET LEURS ANALOGUES AZA UTILISÉS COMME AGENTS ANTIBACTÉRIENS
    申请人:RANBAXY LAB LTD
    公开号:WO2009156966A1
    公开(公告)日:2009-12-30
    The present invention provides Gyrase B and/or Topoisomerase IV par E inhibitors, which can be used as antibacterial agents. Compounds disclosed herein can be used for treating or preventing conditions caused by or contributed by gram positive, gram negative and anaerobic bacteria, more particularly against, for example, Staphylococci, Streptococci, Enterococci, Haemophilus, Pseudomonas spp., Acenetobacter spp., Moraxalla spp., Chlamydia spp., Mycoplasma spp., Legionella spp., Ktycobacterium spp., Helicobacter, Clostridium spp., Bacteroides spp., Coryne bacterium, Bacillus spp., Enterobactericeae,' (E.coli, Klebsiella spp., Proteus spp.,etc. ) or any combination thereof Also provided, are processes for preparing compounds disclosed herein, pharmaceutical compositions containing compounds disclosed herein, and methods of treating bacterial infections. (Formula)
    本发明提供了Gyrase B和/或Topoisomerase IV par E抑制剂,可用作抗菌剂。本文披露的化合物可用于治疗或预防由革兰氏阳性、革兰氏阴性和厌氧菌引起或促成的疾病,更具体地针对例如葡萄球菌、链球菌、肠球菌、流感嗜血杆菌、假单胞菌、阿氏耶森氏菌、摩拉氏菌、沙雷菌、支原体、支原体、军团菌、肺结核杆菌、幽门螺杆菌、梭菌、拮抗杆菌、克雷伯菌科(大肠杆菌、克雷伯菌等)、或其任意组合。还提供了制备本文披露的化合物的方法、含有本文披露的化合物的药物组合物,以及治疗细菌感染的方法。
  • PYRAZOLOQUINOLINONE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
    申请人:SANOFI
    公开号:US20140235616A1
    公开(公告)日:2014-08-21
    The invention relates to compounds corresponding to formula (I), in which R1, R2 and R3 are as defined in Claim 1 , and also to the process for preparing them and to their therapeutic use.
    这项发明涉及与式(I)相对应的化合物,其中R1、R2和R3如权利要求1中所定义,并且还涉及它们的制备方法及其治疗用途。
  • [EN] TRIAZOLOPYRIDINE INHIBITORS OF MYELOPEROXIDASE<br/>[FR] INHIBITEURS DE TRIAZOLOPYRIDINE DE LA MYÉLOPEROXYDASE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2017040450A1
    公开(公告)日:2017-03-09
    The present invention provides compounds of Formula (I): wherein A, Y and R1 are each as defined in the specification, and compositions comprising any of such novel compounds. These compounds are myeloperoxidase (MPO) inhibitors and/or eosinophil peroxidase (EPX) inhibitors, which may be used as medicaments.
    本发明提供了式(I)的化合物:其中A、Y和R1如规范中所定义,并包括任何此类新化合物的组合物。这些化合物是髓过氧化物酶(MPO)抑制剂和/或嗜酸性粒细胞过氧化物酶(EPX)抑制剂,可用作药物。
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