| Weight | 254.355 g/mol |
|---|---|
| Formula | C12H18N2O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
thiamylal (77-27-0)
Surital · Thiamylal Sodium · Thioquinalbarbitone
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- SITE OF ACTION OF THIAMYLAL SODIUM ON THE MONOSYNAPTIC SPINAL REFLEX PATHWAY IN CATS (Journal of Neurophysiology, 1964)
- Effects of xylazine and acetylpromazine upon induced ventricular fibrillation in dogs anesthetized with thiamylal and halothane. (American Journal of Veterinary Research, 1975)
- Reduction of the Slow Inward Current of Isolated Rat Ventricular Cells by Thiamylal and Halothane (Acta Anaesthesiologica Scandinavica, 1985)
- COMPARISON OF PROPOFOL AND THIAMYLAL FOR INDUCTION AND MAINTENANCE OF ANAESTHESIA FOR OUTPATIENT SURGERY (BJA: British Journal of Anaesthesia, 1988)
- Intravenous propofol vs thiamylal-isoflurane for caesarean section, comparative maternal and neonatal effects (Acta Anaesthesiologica Scandinavica, 1995)
- Clonidine decreases the dose of thiamylal required to induce anesthesia in children (Anesthesia & Analgesia, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Surital
- Thiamylal Sodium
- Thioquinalbarbitone
- Parke Davis Brand of Thiamylal Sodium
-
SMILESCCCC(C)C1(C(=O)NC(=S)NC1=O)CC=C
-
InChIKeyXLOMZPUITCYLMJ-UHFFFAOYSA-N
- Pubchem - thiamylal
- Wikipedia - thiamylal
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 or as an anticonvulsant to counteract side effects from other anaesthetics.
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