Tybamate is a non-benzodiazepine anxiolytic medication. It is structurally related to meprobamate, but has a different pharmacological profile. Tybamate is a GABAergic drug that acts as a positive allosteric modulator of the GABAA receptor, similar to benzodiazepines. It is also thought to have some anticholinergic properties. Tybamate was initially developed in the 1950s for the treatment of anxiety disorders. However, it is no longer widely prescribed in many countries due to concerns about its potential for abuse and dependence. It is still available in some countries, but its use is generally limited to patients who are not able to tolerate other anxiolytics. Tybamate is typically well-tolerated, but common side effects include drowsiness, dizziness, and headache. Research on tybamate has been limited in recent years, but it continues to be studied as a potential treatment for anxiety disorders and other conditions. Some researchers are exploring the possibility that tybamate could be useful in the treatment of chronic pain, insomnia, and alcohol withdrawal syndrome.'
tybamate: major descriptor (65-84); on-line search CARBAMATES (65-84); Index Medicus search TYBAMATE (65-84)
ID Source | ID |
---|---|
PubMed CID | 20266 |
CHEMBL ID | 2104816 |
CHEBI ID | 135133 |
SCHEMBL ID | 78046 |
MeSH ID | M0262806 |
Synonym |
---|
solacin |
benvil |
2-(hydroxymethyl)-2-methylpentyl butylcarbamate carbamate |
solacen |
tibamax |
tibamato |
carbamic acid, ester with 2-(hydroxymethyl)-2-methylpentyl butylcarbamate |
tybamate |
n-butyl-2-methyl-2-propyl-1,3-propanediol dicarbamate |
idalene |
nsc-172126 |
carbamic acid,3-propanediol butylcarbamate |
4268-36-4 |
nsc172126 |
carbamic acid, 2-(hydroxymethyl)-2-methylpentyl ester carbamate |
2-methyl-2-propyl-1,3-propanediol butylcarbamate carbamate |
tybatran |
effisax |
2-methyl-2-propyltrimethylene butylcarbamate carbamate |
nospan |
carbamic acid, ester with 2-(hydroxymethyl)-2-methylpentyl carbamate |
2-(hydroxymethyl)-2-(methylpentyl) butylcarbamate carbamate |
1, 2-methyl-2-propyl-, butylcarbamate carbamate |
depran |
tibamate |
w 713 |
reposan |
wln: zvo1x3&1&1ovm4 |
carbamic acid, butyl-, 2-[[(aminocarbonyl)oxy]methyl]-2-methylpentyl ester |
2-[(carbamoyloxy)methyl]-2-methylpentyl butylcarbamate |
carbamic acid, butyl-, 2-(((aminocarbonyl)oxy)methyl)-2-methylpentyl ester |
n-n-butyl-2-methyl-2-propyl-1,3-propanediol dicarbamate |
carbamate of 2-(hydroxymethyl)-2-methylpentyl ester of butylcarbamic acid |
hsdb 3410 |
carbamic acid, ester with 2-methyl-2-propyl-1,3-propanediol butylcarbamate |
nsc 172126 |
einecs 224-254-9 |
brn 1970468 |
butylcarbamic acid 2-(((aminocarbonyl)oxy)methyl)-2-methylpentyl ester |
1,3-propanediol, 2-methyl-2-propyl-, butylcarbamate carbamate |
tybamatum [inn-latin] |
tibamato [inn-spanish] |
carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester, carbamate |
carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester carbamate (ester) |
carbamic acid, ester with 2-methyl-2-propyl-1, 3-propanediol butylcarbamate |
carbamic acid, butyl-, 2-(hydroxymethyl)-2-methylpentyl ester carbamate |
[2-(carbamoyloxymethyl)-2-methyl-pentyl] n-butylcarbamate |
carbamic acid, butyl-, ester with 2-(hydroxymethyl)-2-methylpentyl carbamate |
carbamic acid, butyl-, {2-[[(aminocarbonyl)oxy]methyl]-2-methylpentyl} ester |
1, 3-propanediol, 2-methyl-2-propyl-, butylcarbamate carbamate |
tybamate (usan/inn) |
solacen (tn) |
D06260 |
CHEBI:135133 |
[2-(carbamoyloxymethyl)-2-methylpentyl] n-butylcarbamate |
tybamatum |
tybamate [usan:inn:ban:nf] |
unii-3875lll8m8 |
3875lll8m8 , |
w-713 |
CHEMBL2104816 |
tybamate [inn] |
tybamate [who-dd] |
tybamate [mi] |
tybamate [usan] |
tybamate [hsdb] |
SCHEMBL78046 |
PRBORDFJHHAISJ-UHFFFAOYSA-N |
DTXSID7023728 |
Q7859691 |
Class | Description |
---|---|
carbamate ester | Any ester of carbamic acid or its N-substituted derivatives. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 9 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (25.14) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 13 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |