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2-Neopentylpiperidine

中文名称
——
中文别名
——
英文名称
2-Neopentylpiperidine
英文别名
2-(2,2-dimethylpropyl)piperidine
2-Neopentylpiperidine化学式
CAS
——
化学式
C10H21N
mdl
MFCD02663605
分子量
155.28
InChiKey
WWVIHSGXAWYJLS-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):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

文献信息

  • Pyrazolo[1,5-a]pyridine derivatives or pharmaceutically acceptable salts thereof
    申请人:Unoki Gen
    公开号:US20070072898A1
    公开(公告)日:2007-03-29
    A pyrazolo[1,5-a]pyridine derivative represented by formula (I) and salt thereof exhibit excellent MAPKAP-K2 inhibitory activity. Accordingly, medicines comprising this compound as an active ingredient are expected to be valuable for treating or preventing diseases mediated by MAPKAP-K2 such as inflammatory injury, autoimmune diseases, asteropathia destruens, cancer and/or growth of tumor.
    由式(I)表示的吡唑并[1,5-a]吡啶衍生物及其盐表现出优异的MAPKAP-K2抑制活性。因此,包含该化合物作为活性成分的药物预计对治疗或预防由MAPKAP-K2介导的疾病,如炎症损伤、自身免疫疾病、asteropathia destruens、癌症和/或肿瘤生长具有重要价值。
  • 1,6- DIAZABICYCLO [3,2,1] OCTAN-7-ONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTIONS
    申请人:Patil Vijaykumar Jagdishwar
    公开号:US20150203503A1
    公开(公告)日:2015-07-23
    Compounds of Formula (I), their preparation and use in preventing or treating bacterial infections are disclosed.
    公式(I)化合物的制备和在预防或治疗细菌感染中的用途被披露。
  • KRAS MUTANT PROTEIN INHIBITORS
    申请人:Jacobio Pharmaceuticals Co., Ltd.
    公开号:US20210094919A1
    公开(公告)日:2021-04-01
    The invention relates to a KRAS mutant protein inhibitor, a composition containing the inhibitor and the use thereof.
    这项发明涉及一种KRAS突变蛋白抑制剂,包含该抑制剂的组合物以及其用途。
  • Cytisine and Acetylcholine Analogs and Methods of Treating Mood Disorders
    申请人:Picciotto Marina
    公开号:US20090318491A1
    公开(公告)日:2009-12-24
    The present invention relates to compounds which are derivatives of cytisine or acetylcholine which exhibit activity as agonists, partial agonists or antagonists of nicotinic acetylcholine receptors and may be used in modulating these receptors and in treating mood disorders in patients in need of therapy.
    本发明涉及一种衍生自细胞毒素或乙酰胆碱的化合物,其表现为尼古丁乙酰胆碱受体的激动剂、部分激动剂或拮抗剂,并可用于调节这些受体和治疗需要治疗的情绪障碍患者。
  • Methods and compositions of treating a flaviviridae family viral infection
    申请人:Einav Shirit
    公开号:US20100015093A1
    公开(公告)日:2010-01-21
    Briefly described, embodiments of this disclosure include compounds, pharmaceutical compositions, methods of treating a host infected with a virus from the Flaviviridae family of viruses, methods of inhibiting HCV replication in a host, methods of inhibiting the binding of NS4B polypeptide to the 3′UTR of HCV negative strand RNA in a host, methods of treating liver fibrosis in a host, and the like.
    简要概述,本公开的实施例包括化合物、药物组合物、治疗感染黄病毒科病毒的宿主的方法、抑制宿主中HCV复制的方法、抑制NS4B多肽与HCV负链RNA的3′UTR结合的方法、治疗宿主肝纤维化的方法等。
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