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1-(Phosphanylidynemethyl)piperidine-4-carbaldehyde

中文名称
——
中文别名
——
英文名称
1-(Phosphanylidynemethyl)piperidine-4-carbaldehyde
英文别名
1-(phosphanylidynemethyl)piperidine-4-carbaldehyde
1-(Phosphanylidynemethyl)piperidine-4-carbaldehyde化学式
CAS
——
化学式
C7H10NOP
mdl
——
分子量
155.13
InChiKey
JMEDBTWTIBSCJG-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):
    0.3
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] LIBRARIES OF HETEROARYL-CONTAINING MACROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME<br/>[FR] BIBLIOTHÈQUES DE COMPOSÉS MACROCYCLIQUES CONTENANT HÉTÉROARYLE ET PROCÉDÉS POUR LEUR FABRICATION ET LEUR UTILISATION
    申请人:CYCLENIUM PHARMA INC
    公开号:WO2017049383A1
    公开(公告)日:2017-03-30
    The present disclosure relates to novel macrocyclic compounds and libraries thereof containing heteroaryl moieties that are useful as research tools for drug discovery efforts. The present disclosure also relates to methods of preparing these compounds and libraries and methods of using these libraries, such as in high throughput screening. In particular, these libraries are useful for evaluation of bioactivity at existing and newly identified pharmacologically relevant targets, including G protein-coupled receptors, nuclear receptors, enzymes, ion channels, transporters, transcription factors, protein-protein interactions and nucleic acid-protein interactions. As such, these libraries can be applied to the search for new pharmaceutical agents for the treatment and prevention of a range of medical conditions.
    本公开涉及新型大环化合物及其库,其中包含对药物发现工作有用的含杂环芳基团的化合物。本公开还涉及制备这些化合物和库的方法,以及使用这些库的方法,例如在高通量筛选中使用。特别是,这些库可用于评估现有和新鉴定的药理学相关靶点的生物活性,包括G蛋白偶联受体、核受体、酶、离子通道、转运蛋白、转录因子、蛋白质相互作用和核酸-蛋白质相互作用。因此,这些库可应用于寻找用于治疗和预防各种医疗状况的新药物。
  • CYCLODEXTRIN-BASED POLYMERS FOR THERAPEUTICS DELIVERY
    申请人:CERULEAN PHARMA INC.
    公开号:US20130196945A1
    公开(公告)日:2013-08-01
    The present invention relates to novel compositions of therapeutic cyclodextrin containing polymeric compounds designed as a carrier for small molecule therapeutics delivery and pharmaceutical compositions thereof. These cyclodextrin-containing polymers improve drug stability and solubility, and reduce toxicity of the small molecule therapeutic when used in vivo. Furthermore, by selecting from a variety of linker groups and targeting ligands the polymers present methods for controlled delivery of the therapeutic agents. The invention also relates to methods of treating subjects with the therapeutic compositions described herein. The invention further relates to methods for conducting pharmaceutical business comprising manufacturing, licensing, or distributing kits containing or relating to the polymeric compounds described herein.
    本发明涉及一种新型治疗环糊精含聚合物组成物,其设计为小分子治疗药物传递的载体以及其制药组合物。这些含环糊精聚合物可提高药物稳定性和溶解度,并在体内使用时减少小分子治疗药物的毒性。此外,通过从各种连接基团和靶向配体中进行选择,这些聚合物提供了治疗剂的控制释放方法。本发明还涉及使用所述治疗组成物治疗受试者的方法。本发明还涉及用于进行制药业务的方法,包括制造、许可或分发包含或涉及所述聚合物化合物的工具包。
  • SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT
    申请人:Miller Michael
    公开号:US20140128368A1
    公开(公告)日:2014-05-08
    Substituted cyclopropyl compounds of the formula I: and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-119. Pharmaceutical compositions and methods of treatment are also included.
    公开了式I的替代环丙基化合物及其药学上可接受的盐,用于治疗或预防2型糖尿病和类似疾病。这些化合物可用作G蛋白偶联受体GPR-119的激动剂。还包括制药组合物和治疗方法。
  • SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT
    申请人:ACTON John J.
    公开号:US20150274664A1
    公开(公告)日:2015-10-01
    Substituted cyclopropyl piperidinyl compounds and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-119. Pharmaceutical compositions and methods of treatment are also included.
    本发明公开了可用于治疗或预防2型糖尿病和类似疾病的替代环丙基哌啶化合物及其药学上可接受的盐。该化合物可用作G蛋白偶联受体GPR-119的激动剂。本发明还涉及制药组合物和治疗方法。
  • US9006228B2
    申请人:——
    公开号:US9006228B2
    公开(公告)日:2015-04-14
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