Thiamylal Other names Thiamylal, Thioseconal, Surital AHFS /Drugs.com International Drug Names ATCvet code Legal status
CA : Schedule IV
US : Schedule III
Metabolism Hepatic Elimination half-life 14.3 h (cats)
5-(Pentan-2-yl)-5-(prop-2-en-1-yl)-2-sulfanylidenedihydropyrimidine-4,6(1H ,5H )-dione
CAS Number PubChem CID IUPHAR/BPS DrugBank ChemSpider UNII KEGG ChEBI ChEMBL CompTox Dashboard (EPA ) ECHA InfoCard 100.000.927 Formula C 12 H 18 N 2 O 2 S Molar mass 254.35 g·mol−1 3D model (JSmol )
O=C1NC(=S)NC(=O)C1(C(C)CCC)C\C=C
InChI=1S/C12H18N2O2S/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)
Y Key:XLOMZPUITCYLMJ-UHFFFAOYSA-N
Y
Thiamylal (Surital ) is a barbiturate derivative invented in the 1950s. It has sedative , anticonvulsant , and hypnotic effects, and is used as a strong but short acting sedative. Thiamylal is still in current use, primarily for induction in surgical anaesthesia [1] or as an anticonvulsant to counteract side effects from other anaesthetics.[2] It is the thiobarbiturate analogue of secobarbital .
References [ ]
^ Hsieh MY, Hung GY, Hsieh YL, Chang CY, Hwang B (2005). "Deep sedation with methohexital or thiamylal with midazolam for invasive procedures in children with acute lymphoblastic leukemia". Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi . 46 (5): 294–300. PMID 16640004 .
^ Tsai CJ, Wang HM, Lu IC, Tai CF, Wang LF, Soo LY, Lu DV (February 2007). "Seizure after local anesthesia for nasopharyngeal angiofibroma" . The Kaohsiung Journal of Medical Sciences . 23 (2): 97–100. doi :10.1016/S1607-551X(09)70383-3 . PMID 17339174 .
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