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2-(Piperid-4-yl)-propionsaeure | 90205-09-7

中文名称
——
中文别名
——
英文名称
2-(Piperid-4-yl)-propionsaeure
英文别名
2-piperidin-1-ium-4-ylpropanoate
2-(Piperid-4-yl)-propionsaeure化学式
CAS
90205-09-7
化学式
C8H15NO2
mdl
MFCD11899359
分子量
157.213
InChiKey
ZSFHGXOMOOJAGZ-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

  • 熔点:
    275-277 °C
  • 沸点:
    290.7±13.0 °C(Predicted)
  • 密度:
    1.053±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.875
  • 拓扑面积:
    56.7
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] HIGHLY SELECTIVE NOVEL AMIDATION METHOD<br/>[FR] PROCÉDÉ D'UNE NOUVELLE AMIDATION TRÈS SÉLECTIVE
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2005121133A1
    公开(公告)日:2005-12-22
    The present invention provides an industrial production method with a short process having a high yield of an aliphatic cyclic carboxamide having carboxyl group, which comprises reacting functional group-selectively using an inexpensive condensing agent without protecting the carboxyl group by esterification, that is, reacting carboxylic acid anhydride obtained by reacting carboxylic acid and tertiary carboxylic acid halide with aliphatic cyclic secondary amine having carboxyl group.
    本发明提供了一种工业生产方法,该方法具有短流程、高产率,用于制备含有羧基的脂肪族环状酰胺,其特点在于使用廉价的缩合剂对功能团进行选择性反应,而不通过酯化保护羧基,即通过将由羧酸与叔羧酸卤化物反应得到的羧酸酐与含有羧基的脂肪族环状仲胺进行反应。
  • SUBSTITUTED THIAZOLIDINEDIONE INDAZOLES, INDOLES AND BENZOTRIAZOLES AS ESTROGEN-RELATED RECEPTOR-a MODULATORS
    申请人:Bignan Gilles
    公开号:US20110294780A1
    公开(公告)日:2011-12-01
    The present invention relates to compounds of Formula (I), methods for preparing these compounds, compositions, intermediates and derivatives thereof and for treating a condition including but not limited to ankylosing spondylitis, artherosclerosis, arthritis (such as rheumatoid arthritis, infectious arthritis, childhood arthritis, psoriatic arthritis, reactive arthritis), bone-related diseases (including those related to bone formation), breast cancer (including those unresponsive to anti-estrogen therapy), cardiovascular disorders, cartilage-related disease (such as cartilage injury/loss, cartilage degeneration, and those related to cartilage formation), chondrodysplasia, chondrosarcoma, chronic back injury, chronic bronchitis, chronic inflammatory airway disease, chronic obstructive pulmonary disease, diabetes, disorders of energy homeostasis, gout, pseudogout, lipid disorders, metabolic syndrome, multiple myeloma, obesity, osteoarthritis, osteogenesis imperfecta, osteolytic bone metastasis, osteomalacia, osteoporosis, Paget's disease, periodontal disease, polymyalgia rheumatica, Reiter's syndrome, repetitive stress injury, hyperglycemia, elevated blood glucose level, and insulin resistance.
    本发明涉及式(I)的化合物,制备这些化合物的方法,组合物,中间体及其衍生物,并用于治疗包括但不限于强直性脊柱炎,动脉粥样硬化,关节炎(如类风湿关节炎,感染性关节炎,儿童关节炎,屑病性关节炎,反应性关节炎),与骨相关的疾病(包括与骨形成有关的疾病),乳腺癌(包括对抗雌激素治疗无效的癌症),心血管疾病,软骨相关疾病(如软骨损伤/丧失,软骨退化以及与软骨形成有关的疾病),软骨发育不良,软骨肉瘤,慢性腰部损伤,慢性支气管炎,慢性炎症性气道疾病,慢性阻塞性肺疾病,糖尿病,能量稳态紊乱,痛风,假性痛风,脂质紊乱,代谢综合征,多发性骨髓瘤,肥胖,骨关节炎,遗传性骨发育不全,骨溶解性骨转移,软骨软化症,骨质疏松症,帕森病,牙周病,多肌痛风,Reiter综合征,重复性应激损伤,高血糖,血糖平升高和胰岛素抵抗等病症的方法。
  • [EN] GLYCINE METABOLISM MODULATORS AND USES THEREOF<br/>[FR] MODULATEURS DU MÉTABOLISME DE LA GLYCINE ET LEURS UTILISATIONS
    申请人:AGENCY SCIENCE TECH & RES
    公开号:WO2018021977A1
    公开(公告)日:2018-02-01
    The present invention relates to a compound of general formula (I) and/or its solvates, hydrates and pharmaceutically acceptable salts, which are modulators of glycine metabolism. The present invention also relates to the methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of disorders/conditions/diseases involving, relating to or associated with glycine metabolism or a pathway where glycine decarboxylase (GLDC, or glycine cleavage system) plays a role. In a preferred embodiment the disorders/conditions/disease is cancer, inflammatory conditions, Alzheimer's disease, metabolic disorders and CNS disorders.
    本发明涉及一般式(I)的化合物及/或其溶剂合物、合物和药学上可接受的盐,这些化合物是甘酸代谢调节剂。本发明还涉及其制备方法、含有这些化合物的药物组合物以及这些化合物在治疗涉及或与甘酸代谢或甘酸脱羧酶(GLDC,或甘酸裂解系统)发挥作用的病症/疾病/疾病的用途。在一个首选实施例中,疾病/疾病是癌症、炎症性疾病、阿尔茨海默病、代谢性疾病和中枢神经系统疾病。
  • [EN] COMPOUNDS THAT ARE S1P MODULATING AGENTS AND/OR ATX MODULATING AGENTS<br/>[FR] COMPOSÉS ÉTANT DES AGENTS DE MODULATION DE S1P ET/OU DES AGENTS DE MODULATION D'ATX
    申请人:BIOGEN IDEC INC
    公开号:WO2014025709A1
    公开(公告)日:2014-02-13
    Compounds of formula (I) can modulate the activity of one or more SIP receptors and/or the activity of autotaxin (ATX).
    式(I)的化合物可以调节一个或多个SIP受体的活性和/或自体稅脂酶(ATX)的活性。
  • Steroid compounds, use of these compounds for the preparation of meiosis-regulating medicaments and method for the preparation of these compounds
    申请人:Schering AG
    公开号:US20020188143A1
    公开(公告)日:2002-12-12
    The present invention relates to steroid compounds of general formula X, which may advantageously be employed to stimulate meiosis in human oocytes, the steroid being specifically characterized by amino nitrogen bonded to C 17 of the steroid skeleton via a spacer A. 1
    本发明涉及通式X的类固醇化合物,这些化合物可优势地用于刺激人卵母细胞的减数分裂,该类固醇化合物的特征在于基氮通过间距A.1与类固醇骨架的C17键合。
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