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1-(4-(tert-butyl)phenyl)piperidine-4-carboxylic acid | 847407-99-2

中文名称
——
中文别名
——
英文名称
1-(4-(tert-butyl)phenyl)piperidine-4-carboxylic acid
英文别名
1-(4-tert-butylphenyl)piperidine-4-carboxylic acid
1-(4-(tert-butyl)phenyl)piperidine-4-carboxylic acid化学式
CAS
847407-99-2
化学式
C16H23NO2
mdl
——
分子量
261.364
InChiKey
BPXRLAOVWAYBPV-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

物化性质

  • 沸点:
    424.4±45.0 °C(Predicted)
  • 密度:
    1.086±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    40.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为反应物:
    参考文献:
    名称:
    Discovery of piperidine carboxamide TRPV1 antagonists
    摘要:
    A series of piperidine carboxamides were developed as potent antagonists of the transient receptor potential vanilloid-1 (TRPV1), an emerging target for the treatment of pain. A focused library of polar head groups led to the identification of a benzoxazinone amide that afforded good potency in cell-based assays. Synthesis and a QSAR model will be presented. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.07.035
  • 作为产物:
    描述:
    1-(4-tert-butyl-phenyl)-piperidine-4-carboxylic acid ethyl estersodium hydroxide盐酸 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以26%的产率得到1-(4-(tert-butyl)phenyl)piperidine-4-carboxylic acid
    参考文献:
    名称:
    [EN] ANTHELMINTIC AGENTS AND THEIR USE
    [FR] AGENTS ANTHELMINTHIQUES ET LEUR UTILISATION
    摘要:
    该发明涉及一般用作驱虫剂或作为制备驱虫剂中间体的化合物和盐。该发明还涉及制备这些化合物和盐的工艺、包含这些化合物和盐的药物组合物和工具包、使用这些化合物和盐制作药物以及将这些化合物和盐用于需要治疗的动物的治疗方法。
    公开号:
    WO2009077527A1
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文献信息

  • [EN] MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS<br/>[FR] ANTIBIOTIQUES MACROCYCLIQUES À LARGE SPECTRE
    申请人:RQX PHARMACEUTICALS INC
    公开号:WO2018149419A1
    公开(公告)日:2018-08-23
    Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.
    本文提供了抗菌化合物,其中在某些实施例中,这些化合物具有广谱生物活性。在各种实施例中,这些化合物通过抑制细菌类型1信号肽酶(SpsB)发挥作用,这是细菌中的一种必需蛋白质。还提供了使用所述化合物的药物组合物和治疗方法。
  • 4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
    申请人:Calvo R. Raul
    公开号:US20060116368A1
    公开(公告)日:2006-06-01
    This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
    这项发明涉及辣椒素受体VR1配体。更具体地说,这项发明涉及对VR1具有潜在调节作用的杂环异尼泊酸酰胺,这些化合物对于治疗和预防哺乳动物的疾病状况是有用的。
  • Anthelmintic agents and their use
    申请人:Chassaing Christophe Pierre Alain
    公开号:US08569495B2
    公开(公告)日:2013-10-29
    This invention is directed to compounds and salts that are generally useful as anthelmintic agents or as intermediates in processes for making anthelmintic agents. This invention also is directed to processes for making the compounds and salts, pharmaceutical compositions and kits comprising the compounds and salts, uses of the compounds and salts to make medicaments, and treatments comprising the administration of the compounds and salts to animals in need of the treatments.
    本发明涉及一些化合物和盐,它们通常用作驱虫剂或作为制造驱虫剂的中间体。本发明还涉及制造这些化合物和盐的过程,包括这些化合物和盐的药物组合物和试剂盒,使用这些化合物和盐制造药物,以及将这些化合物和盐用于需要治疗的动物的治疗。
  • INHIBITORS OF ACK1/TNK2 TYROSINE KINASE
    申请人:H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC.
    公开号:US20160176826A1
    公开(公告)日:2016-06-23
    Described are cancer therapies and anti-cancer compounds. In particular, disclosed are inhibitors of Ack1 tyrosine kinase and their use in the treatment of cancer. Methods of screening for new Ack1 tyrosine kinase inhibitors are also disclosed. In specific example, compound having Formula I through IV are disclosed.
    本文描述了癌症治疗和抗癌化合物。特别地,揭示了Ack1酪氨酸激酶抑制剂及其在癌症治疗中的应用。还披露了筛选新的Ack1酪氨酸激酶抑制剂的方法。具体例子中,揭示了具有I至IV式的化合物。
  • ANTHELMINTIC AGENTS AND THEIR USE
    申请人:Chassaing Christophe Pierre Alain
    公开号:US20110021506A1
    公开(公告)日:2011-01-27
    This invention is directed to compounds and salts that are generally useful as anthelmintic agents or as intermediates in processes for making anthelmintic agents. This invention also is directed to processes for making the compounds and salts, pharmaceutical compositions and kits comprising the compounds and salts, uses of the compounds and salts to make medicaments, and treatments comprising the administration of the compounds and salts to animals in need of the treatments.
    本发明涉及化合物和盐,通常用作驱虫剂或作为制备驱虫剂的中间体。本发明还涉及制备这些化合物和盐的方法,包括这些化合物和盐的制药组合物和试剂盒,使用这些化合物和盐制备药物以及将这些化合物和盐用于治疗需要治疗的动物的治疗方法。
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