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Showing content from https://en.wikipedia.org/wiki/Hexethal below:

Hexethal - Wikipedia

From Wikipedia, the free encyclopedia

Chemical compound

Pharmaceutical compound

Hexethal Other names Sodium 5-ethyl-5-hexylbarbiturate, Ortal, Hebaral ATC code

none

CA: Schedule IV

sodium 5-ethyl-5-hexyl-4,6-dioxo-1H-pyrimidin-2-olate

144-00-3^Y

PubChem CID

8941

8597^Y

ATA79U054W

CompTox Dashboard (EPA)

DTXSID00162591

Formula C₁₂H₁₉N₂NaO₃ Molar mass 262.285 g·mol⁻¹ 3D model (JSmol)

Interactive image

[Na+].O=C1/N=C(/[O-])NC(=O)C1(CCCCCC)CC

InChI=1S/C12H20N2O3.Na/c1-3-5-6-7-8-12(4-2)9(15)13-11(17)14-10(12)16;/h3-8H2,1-2H3,(H2,13,14,15,16,17);/q;+1/p-1
^Y
Key:HXUAXLUDTCGASZ-UHFFFAOYSA-M
^Y

(verify)

Hexethal (Ortal) is a barbiturate derivative invented in the 1940s. It has sedative, anxiolytic, muscle relaxant, and anticonvulsant properties, and was used primarily as an anaesthetic in veterinary medicine.^[1]

Hexethal is considered similar in effects to pentobarbital, with a very fast onset of action but short duration of effects.

^ Butler TC (October 1950). "The rate of penetration of barbituric acid derivatives into the brain". The Journal of Pharmacology and Experimental Therapeutics. 100 (2): 219–26. PMID 14784958.

v
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GABA_A receptor positive modulators Alcohols

Benzodiazepines

Kava constituents

Neuroactive steroids

Nonbenzodiazepines

Piperidinediones

Pyrazolopyridines

Volatiles/gases

Others/unsorted

Unsorted benzodiazepine site positive modulators: α-Pinene
MRK-409 (MK-0343)
TCS-1105
TCS-1205

See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators

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