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4-(2,2-Dimethylpropyl)-1-methylpiperazin-2-one

中文名称
——
中文别名
——
英文名称
4-(2,2-Dimethylpropyl)-1-methylpiperazin-2-one
英文别名
4-(2,2-dimethylpropyl)-1-methylpiperazin-2-one
4-(2,2-Dimethylpropyl)-1-methylpiperazin-2-one化学式
CAS
——
化学式
C10H20N2O
mdl
——
分子量
184.28
InChiKey
MTCXLZYZFMBZRZ-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):
    1.3
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    23.6
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • FUSED HETEROCYCLIC COMPOUND, PREPARATION METHOD THEREFOR, PHARMACEUTCIAL COMPOSITION, AND USES THEREOF
    申请人:SHANGHAI YINGLI PHARMACEUTICAL CO., LTD
    公开号:US20160244432A1
    公开(公告)日:2016-08-25
    Disclosed are a fused heterocyclic compound, a preparation method therefor, a pharmaceutical composition, and uses thereof. The fused heterocyclic compound is shown in formula I, formula II, or formula III. The preparation method of the fused heterocyclic compound and/or the pharmaceutically acceptable salt thereof in the present invention comprises three synthesizing routes. The present invention also provides a pharmaceutical composition of the fused heterocyclic compound, the pharmaceutical composition containing one or more of the fused heterocyclic compound shown in formula I, formula II, or formula III, the pharmaceutically acceptable salt thereof, hydrates, solvent compounds, polymorphs and prodrugs thereof, and a pharmaceutically acceptable carrier. The present invention also relates to an application of the fused heterocyclic compound and/or the pharmaceutical composition in preparing kinase inhibitors and in preparing drugs for preventing and treating diseases related to kinase. The fused heterocyclic compound of the present invention has selective inhibition function on PI3Kδ, and can be used for preparing drugs for preventing and treating cell proliferation diseases such as cancers, infections, inflammations, or autoimmune diseases.
    揭示了一种融合杂环化合物,其制备方法,药物组合物及其用途。所述融合杂环化合物如公式I、公式II或公式III所示。本发明的所述融合杂环化合物和/或其药用可接受盐的制备方法包括三种合成途径。本发明还提供了一种包含融合杂环化合物的药物组合物,所述药物组合物含有公式I、公式II或公式III所示的一个或多个融合杂环化合物,其药用可接受盐、合物、溶剂化合物、多型体和前药,以及药用可接受载体。本发明还涉及应用所述融合杂环化合物和/或药物组合物制备激酶抑制剂以及制备用于预防和治疗与激酶相关疾病的药物。本发明的融合杂环化合物PI3Kδ具有选择性抑制功能,可用于制备用于预防和治疗细胞增殖性疾病如癌症、感染、炎症或自身免疫疾病的药物。
  • CYCLIC PEPTIDES AND USE AS MEDICINES
    申请人:Fu Jiping
    公开号:US20140134132A1
    公开(公告)日:2014-05-15
    The present invention provides a compound of formula I; or a pharmaceutically acceptable salt thereof, wherein the variables R 1 , R 2 , R 3 , R 4 , R 5 , and A-B are defined herein, which are non-immunosuppresive, cyclophilin-binding, mPTP blockers and are therefore useful for the prevention or treatment of diseases or disorders such as HCV infection, stroke, multiple sclerosis, HBV infection, HPV infection, asthma, cancer, muscular dystrophy, sepsis, ischemia/reperfusion injury, and heart failure.
    本发明提供了一种化合物I的公式;或其药学上可接受的盐,其中变量R1、R2、R3、R4、R5和A-B在此处定义,这些化合物是非免疫抑制剂、环肽酶结合剂、mPTP阻滞剂,因此可用于预防或治疗HCV感染、中风、多发性硬化、HBV感染、HPV感染、哮喘、癌症、肌萎缩症、败血症、缺血/再灌注损伤和心力衰竭等疾病或紊乱。
  • N-LINKED LACTAM M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
    申请人:Kuduk Scott D.
    公开号:US20150065498A1
    公开(公告)日:2015-03-05
    The present invention is directed to N-linked lactam compounds of general formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.
    本发明涉及一般式(I)的N-连接内酰胺化合物,它们是M1受体正向变构调节剂,可用于治疗M1受体参与的疾病,例如阿尔茨海默病、精神分裂症、疼痛或睡眠障碍。本发明还涉及包含这些化合物的药物组合物,以及在治疗M1受体介导的疾病中使用这些化合物和组合物的方法。
  • SUBSTITUTED INDOLE MCL-1 INHIBITORS
    申请人:Vanderbilt University
    公开号:US20210283138A1
    公开(公告)日:2021-09-16
    The present disclosure provides for compounds that inhibit the activity of an anti-apoptotic Bcl-2 family member Myeloid cell leukemia-1 (Mcl-1) protein. The present disclosure also provides for pharmaceutical compositions as well as methods for using compounds for treatment of diseases and conditions (e.g., cancer) characterized by the over-expression or dysregulation of Mcl-1 protein.
  • US9072696B2
    申请人:——
    公开号:US9072696B2
    公开(公告)日:2015-07-07
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