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6-乙基-2-吡嗪羧酸 | 13515-09-8

中文名称
6-乙基-2-吡嗪羧酸
中文别名
——
英文名称
6-Ethyl-pyrazincarbonsaeure-2
英文别名
6-ethyl-pyrazine-2-carboxylic acid;6-Ethylpyrazine-2-carboxylic acid
6-乙基-2-吡嗪羧酸化学式
CAS
13515-09-8
化学式
C7H8N2O2
mdl
——
分子量
152.153
InChiKey
YFOUKQXHDANAEL-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:
    112 °C
  • 沸点:
    310.8±42.0 °C(Predicted)
  • 密度:
    1?+-.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:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933990090

文献信息

  • [EN] BICYCLO[3.2.1]OCTYL AMIDE DERIVATIVES AND USES OF SAME<br/>[FR] DÉRIVÉS BICYCLO[3.2.1]OCTYLAMIDE ET LEURS UTILISATIONS
    申请人:LUNDBECK & CO AS H
    公开号:WO2012088365A1
    公开(公告)日:2012-06-28
    The present invention provides bicyclo[3.2.1]octyl amide derivatives of formula (I): wherein L, R1 and R2 are as defined herein, or a pharmaceutically acceptable salt thereof; pharmaceutical compositions and methods using the same.
    本发明提供了公式(I)的双环[3.2.1]辛基酰胺衍生物,其中L、R1和R2如本文所定义,或其药学上可接受的盐;以及使用这些衍生物的药物组合物和方法。
  • OXAZOLINE DERIVATIVES
    申请人:Galley Guido
    公开号:US20110112080A1
    公开(公告)日:2011-05-12
    The invention relates to compounds of formula I wherein the definitions of X, R and R 1 are as defined herein. The compounds of formula I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1. The compounds can be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    该发明涉及公式I中的化合物,其中X、R和R1的定义如本文所述。公式I中的化合物对痕量胺相关受体(TAARs)有良好的亲和力,特别是对TAAR1。这些化合物可用于治疗抑郁症、焦虑障碍、躁郁症、注意力缺陷多动障碍(ADHD)、与压力相关的障碍、精神分裂症等精神障碍、帕金森病等神经疾病、阿尔茨海默病等神经退行性疾病、癫痫、偏头痛、高血压、物质滥用和代谢性障碍,如进食障碍、糖尿病、糖尿病并发症、肥胖、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍以及心血管疾病。
  • OXAZOLINE DERIVATIVES FOR TREATMENT OF CNS DISORDERS.
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2499121B1
    公开(公告)日:2015-10-07
  • BICYCLO[3.2.1]OCTYL AMIDE DERIVATIVES AND USES OF SAME
    申请人:H. Lundbeck A/S
    公开号:EP2654422A1
    公开(公告)日:2013-10-30
  • BICYCLIC HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF THE PAR-2 SIGNALING PATHWAY
    申请人:VERTEX PHARMACEUTICALS INCORPORATED
    公开号:US20180057505A1
    公开(公告)日:2018-03-01
    The compounds of formula I, wherein the variables are as defined herein, and pharmaceutically acceptable salts thereof are useful as inhibitors of the PAR-2 signaling pathway. The compounds of formula I and pharmaceutically acceptable compositions comprising such compounds can be employed for treating various diseases, disorders, and conditions.
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