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2,4,6-Trimethyl-piperazin | 4406-09-1

中文名称
——
中文别名
——
英文名称
2,4,6-Trimethyl-piperazin
英文别名
1,3,5-trimethyl-piperazine;1,3,5-Trimethylpiperazine
2,4,6-Trimethyl-piperazin化学式
CAS
4406-09-1
化学式
C7H16N2
mdl
MFCD18902342
分子量
128.217
InChiKey
CLPZHEDSMNQBPP-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):
    0.5
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    15.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • PYRIMIDINE-FUSED CYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
    申请人:SHANGHAI BLUERAY BIOPHARMA CO., LTD.
    公开号:US20210053989A1
    公开(公告)日:2021-02-25
    Disclosed in the present disclosure are a pyrimidine-fused cyclic compound or a pharmaceutically acceptable salt, hydrate, prodrug, stereoisomer, solvate or isotope labeled compound thereof. Also provided in the present disclosure are a preparation method for the compound, a composition comprising the compound and a use of the compound for the preparation of a medicament for the prevention and/or treatment of a disease or condition associated with abnormal SHP2 activity.
    本公开涉及一种嘧啶融合的环状化合物或其药用可接受的盐、合物、前药、立体异构体、溶剂合物或同位素标记化合物。本公开还提供了该化合物的制备方法、包含该化合物的组合物以及该化合物用于制备与异常SHP2活性相关的疾病或病况的药物的用途。
  • 2-Amino-quinazolin-5-ones
    申请人:Bellamacina R. Cornelia
    公开号:US20070027150A1
    公开(公告)日:2007-02-01
    2-Amino-quinazolin-5-one compounds, stereoisomers, tautomers, pharmaceutically acceptable salts, and prodrugs thereof; compositions that include a pharmaceutically acceptable carrier and one or more of the 2-amino-quinazolin-5-one compounds, either alone or in combination with at least one additional therapeutic agent. Methods of using the 2-amino-quinazolin-5-one compounds, either alone or in combination with at least one additional therapeutic agent, in the prophylaxis or treatment of cell proliferative diseases.
    2-氨基喹唑啉-5-酮化合物,立体异构体,互变异构体,药学上可接受的盐及其前药;包括药学上可接受的载体和一种或多种2-氨基喹唑啉-5-酮化合物的组合物,可以单独使用或与至少一种额外治疗剂结合使用。使用2-氨基喹唑啉-5-酮化合物的方法,可以单独使用或与至少一种额外治疗剂结合使用,用于预防或治疗细胞增殖性疾病。
  • [EN] NOVEL COMPOUNDS FOR TREATMENT OF DISEASES RELATED TO DUX4 EXPRESSION<br/>[FR] NOUVEAUX COMPOSÉS POUR LE TRAITEMENT DE MALADIES LIÉES À L'EXPRESSION DE DUX4
    申请人:FACIO INTELLECTUAL PROPERTY B V
    公开号:WO2021105481A1
    公开(公告)日:2021-06-03
    The present invention relates to compounds that act as DUX4 repressors, suitable for the treatment of diseases related to DUX4 expression, such as muscular dystrophies. It also relates to use of such compounds, or to methods of use of such compounds.
    本发明涉及作为DUX4抑制剂的化合物,适用于治疗与DUX4表达相关的疾病,如肌肉萎缩症。它还涉及使用这些化合物,或者使用这些化合物的方法。
  • [EN] NOVEL THIENOPYRIMIDINE DERIVATIVES, PROCESSES FOR THE PREPARATION THEREOF AND THERAPEUTIC USES THEREOF<br/>[FR] NOUVEAUX DÉRIVÉS DE THIÉNOPYRIMIDINE, LEURS PROCÉDÉS DE PRÉPARATION ET LEURS UTILISATIONS THÉRAPEUTIQUES
    申请人:SANOFI SA
    公开号:WO2013150036A1
    公开(公告)日:2013-10-10
    The present invention relates to compounds of formula (I): wherein R6 is -CONH2 or a -C(Rα)(Rβ)(OH) group; R is a substituted phenyl or heteroaryl group; R7 is an optionally substituted aryl or heteroaryl group. Process for the preparation thereof and therapeutic use thereof.
    本发明涉及式(I)化合物的制备过程及其治疗用途:其中R6是-CONH2或一个-C(Rα)(Rβ)(OH)基团;R是一个取代的苯基或杂芳基团;R7是一个可选地取代的芳基或杂芳基团。
  • [EN] AMINOPYRIMIDINE HETEROCYCLIC COMPOUND WITH ADENOSINE RECEPTOR ANTAGONISTIC ACTIVITY<br/>[FR] COMPOSÉ AMINOPYRIMIDINE HÉTÉROCYCLIQUE PRÉSENTANT UNE ACTIVITÉ ANTAGONISTE DU RÉCEPTEUR DE L'ADÉNOSINE
    申请人:SUZHOU YUNXUAN YIYAO KEJI YOUXIAN GONGSI
    公开号:WO2017088755A1
    公开(公告)日:2017-06-01
    Disclosed hereinis an aminopyrimidine heterocyclic compound with adenosine receptor antagonistic activity, comprising a compound of the general formula (I), or a pharmaceutically acceptable salt thereof. The aminopyrimidine heterocyclic compound with adenosine receptor antagonistic activitydisclosed herein can be used as an effective adenosine receptor antagonist, and can be used for the treatment or prevention of disorders caused by abnormal level of adenosine.
    本文披露了一种具有腺苷受体拮抗活性的氨基嘧啶杂环化合物,包括一般式(I)的化合物或其药学上可接受的盐。本文披露的具有腺苷受体拮抗活性的氨基嘧啶杂环化合物可用作有效的腺苷受体拮抗剂,并可用于治疗或预防由腺苷平异常引起的疾病。
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