Clinical data | |
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Other names | Thiamylal, Thioseconal, Surital |
AHFS/ Drugs.com | International Drug Names |
ATCvet code | |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Metabolism | Hepatic |
Elimination half-life | 14.3 h (cats) |
Identifiers | |
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CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.000.927 |
Chemical and physical data | |
Formula | C12H18N2O2S |
Molar mass | 254.35 g·mol−1 |
3D model ( JSmol) | |
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(verify) |
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 [2] or as an anticonvulsant to counteract side effects from other anaesthetics. [3] It is the thiobarbiturate analogue of secobarbital.
Clinical data | |
---|---|
Other names | Thiamylal, Thioseconal, Surital |
AHFS/ Drugs.com | International Drug Names |
ATCvet code | |
Legal status | |
Legal status |
|
Pharmacokinetic data | |
Metabolism | Hepatic |
Elimination half-life | 14.3 h (cats) |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.000.927 |
Chemical and physical data | |
Formula | C12H18N2O2S |
Molar mass | 254.35 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(verify) |
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 [2] or as an anticonvulsant to counteract side effects from other anaesthetics. [3] It is the thiobarbiturate analogue of secobarbital.