Talbutal

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Talbutal
Talbutal.svg
Systematic (IUPAC) name
(RS)-5-allyl-5-sec-butylpyrimidine-2,4,6(1H,3H,5H)-trione
Clinical data
Legal status
Identifiers
CAS Number 115-44-6 YesY
ATC code N05CA07 (WHO)
PubChem CID: 8275
DrugBank DB00306 YesY
ChemSpider 7976 YesY
UNII 4YIR8202AX YesY
ChEMBL CHEMBL1200802 N
Synonyms 5-(1-methylpropyl)-5-(2-propenyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
Chemical data
Formula C11H16N2O3
Molecular mass 224.256 g/mol
  • O=C1NC(=O)NC(=O)C1(C(C)CC)C\C=C
  • InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16) YesY
  • Key:BJVVMKUXKQHWJK-UHFFFAOYSA-N YesY
 NYesY (what is this?)  (verify)

Talbutal (Lotusate) is a barbiturate with a short to intermediate duration of action. It is a structural isomer of butalbital. Talbutal is a schedule III drug in the U.S.

Pharmacology

Talbutal is a short to intermediate-acting barbiturate. Barbiturates act as nonselective depressants of the central nervous system (CNS), capable of producing all levels of CNS mood alteration from excitation to mild sedation, hypnosis, and deep coma. In sufficiently high therapeutic doses, barbiturates induce anesthesia.[1]

Mechanism of action

Talbutal binds at a distinct binding site associated with a Cl ionopore at the GABAA receptor, increasing the duration of time for which the Cl ionopore is open. The post-synaptic inhibitory effect of GABA in the thalamus is, therefore, prolonged.

Toxicity

Symptoms of acute barbiturate poisoning include drowsiness, confusion, coma, respiratory depression, hypotension,[1] and shock.

References

<templatestyles src="Reflist/styles.css" />

Cite error: Invalid <references> tag; parameter "group" is allowed only.

Use <references />, or <references group="..." />



<templatestyles src="Asbox/styles.css"></templatestyles>

  1. 1.0 1.1 Lua error in package.lua at line 80: module 'strict' not found.