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3-哌啶甲酸

维基百科,自由的百科全书
3-哌啶甲酸
识别信息
  • piperidine-3-carboxylic acid
CAS号498-95-3
PubChem CID
IUPHAR/BPS
ChemSpider
ChEMBL
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.007.159 編輯維基數據鏈接
化学信息
化学式C6H11NO2
摩尔质量129.16 g·mol−1
3D模型(JSmol英语JSmol
  • C1CC(CNC1)C(=O)O

3-哌啶甲酸是一种有机化合物,化学式为C6H11NO2,它是可溶于水的白色晶体。[1]

合成与性质

3-哌啶甲酸可由烟酸的氢化反应制得。

它和乙醇在酸的催化下进行酯化反应,得到3-哌啶甲酸乙酯。[2]

3-哌啶甲酸是一种Γ-氨基丁酸(GABA)再攝取抑制劑[3],常用于相关研究[4][5]

参考文献

  1. ^ 3-哌啶甲酸页面存档备份,存于互联网档案馆). ChemicalBook. [2019-3-22]
  2. ^ 李运波,唐凤翔,孟春 等. 3-哌啶甲酸及其衍生物的合成与应用研究进展(PDF页面存档备份,存于互联网档案馆)). 有机化学, 2009, 29(7).
  3. ^ Macdonald, R.L. Eadie, Mervyn J.; Vajda, Frank J. E. , 编. Antiepileptic drugs: pharmacology and therapeutics First. [S.l.]: Springer. 2012: 130. ISBN 978-3-642-64244-9. In contrast, prolonged (1 h) exposure to gabapentin enhanced the shunting effect on CAl region excitatory postsynaptic potentials induced by the GABA uptake inhibitor, nipecotic acid, which promotes GABA release. 
  4. ^ Takahashi K, Miyoshi S, Kaneko A, Copenhagen DR. Actions of nipecotic acid and SKF89976A on GABA transporter in cone-driven horizontal cells dissociated from the catfish retina. Jpn. J. Physiol. 1995, 45 (3): 457–73 [2019-03-22]. PMID 7474528. doi:10.2170/jjphysiol.45.457. (原始内容存档于2020-02-02). 
  5. ^ Wahab A, Heinemann U, Albus K. Effects of gamma-aminobutyric acid (GABA) agonists and a GABA uptake inhibitor on pharmacoresistant seizure like events in organotypic hippocampal slice cultures. Epilepsy Research. October 2009, 86 (2-3): 113–23 [2019-03-22]. PMID 19535226. doi:10.1016/j.eplepsyres.2009.05.008. (原始内容存档于2020-02-02).