苯丁酰脲

化合物

苯丁酰脲INN:pheneturide;商品名包括Benuride、Deturid、Pheneturid、Septotence、Trinuride)[1]抗惊厥药[2][3]从概念上讲,它可以作为苯巴比妥的代谢降解产物在体内形成。它被认为已过时,[4]现在很少使用。[5]它在欧洲各国销售,包括波兰西班牙英国[6]苯乙酰脲相比,苯丁酰脲具有相似的抗惊厥活性和毒性。[7][8]因此,它仅在其他毒性较小的药物失败的严重癫痫病例中使用。[8]苯丁酰脲抑制新陈代谢,从而增加其他抗惊厥药(如苯妥英)的水平。[5][6]

苯丁酰脲
臨床資料
AHFS/Drugs.com国际药品名称
ATC碼
识别信息
  • (RS)-N-Carbamoyl-2-phenyl-butanamide
CAS号90-49-3  checkY
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.001.817 編輯維基數據鏈接
化学信息
化学式C11H14N2O2
摩尔质量206.25 g·mol−1
3D模型(JSmol英语JSmol
手性外消旋混合物
  • O=C(N)NC(=O)C(c1ccccc1)CC
  • InChI=1S/C11H14N2O2/c1-2-9(10(14)13-11(12)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H3,12,13,14,15) checkY
  • Key:AJOQSQHYDOFIOX-UHFFFAOYSA-N checkY

参见

参考资料

  1. ^ Muller. European Drug Index: European Drug Registrations, Fourth Edition. CRC Press. 19 June 1998: 998–. ISBN 978-3-7692-2114-5. 
  2. ^ Elks J. The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014: 959–. ISBN 978-1-4757-2085-3. 
  3. ^ Byrne B, Rothchild R. 1H NMR studies of drugs with achiral and chiral lanthanide shift reagents: applications to the anticonvulsant pheneturide. Chirality. 1999, 11 (7): 529–35. PMID 10423278. doi:10.1002/(SICI)1520-636X(1999)11:7<529::AID-CHIR3>3.0.CO;2-K. 
  4. ^ Levy RH. Antiepileptic Drugs. Lippincott Williams & Wilkins. 2002: 210–. ISBN 978-0-7817-2321-3. 
  5. ^ 5.0 5.1 Denham MJ. The Treatment of Medical Problems in the Elderly. Springer Science & Business Media. 6 December 2012: 335–. ISBN 978-94-011-6223-4. 
  6. ^ 6.0 6.1 Vida J. Anticonvulsants. Elsevier. 19 July 2013: 4,42. ISBN 978-0-323-14395-0. 
  7. ^ deStevens G, Zingel V, Leschke C, Hoeprich PD, Schultz RM, Mehrotra PK, Batra S, Bhaduri AP, Saxena AK, Saxena M (编). Progress in Drug Research / Fortschritte der Arzneimittelforschung / Progrès des Recherches Pharmaceutiques. Basel: Birkhäuser. 11 November 2013: 217– [3 September 2016]. ISBN 978-3-0348-7161-7. 
  8. ^ 8.0 8.1 Lancaster R. Pharmacology in Clinical Practice. Elsevier. 22 October 2013: 222–. ISBN 978-1-4831-9294-9.