Page last updated: 2024-11-06

cyclarbamate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Cyclarbamate is a cyclic carbamate derivative that has been investigated for its potential therapeutic effects. It has been shown to possess anxiolytic, anticonvulsant, and muscle relaxant properties. However, its clinical use has been limited due to concerns about its safety and efficacy. Cyclarbamate is typically synthesized through a multi-step process involving the reaction of an appropriate amine with a cyclic carbonate. Its mechanism of action is not fully understood, but it is believed to act on the central nervous system, potentially modulating the activity of neurotransmitters such as GABA. Research on cyclarbamate has been focused on exploring its potential therapeutic applications and understanding its pharmacological profile. Despite its limitations, cyclarbamate remains an intriguing compound that warrants further investigation.'

cyclarbamate: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID72076
CHEMBL ID2104142
CHEBI ID135553
SCHEMBL ID547006
MeSH IDM0045760

Synonyms (26)

Synonym
5779-54-4
cyclarbamate
CHEBI:135553
[1-(phenylcarbamoyloxymethyl)cyclopentyl]methyl n-phenylcarbamate
cyclopentaphene
CHEMBL2104142
c-1428 ,
cyclarbamatum [inn-latin]
cyclarbamatum
m 906
einecs 227-302-7
ciclarbamato
c 1428
1,1-cyclopentanedimethanol dicarbanilate
unii-779291866j
cyclarbamate [inn:ban:dcf]
779291866j ,
ciclarbamato [inn-spanish]
SCHEMBL547006
cyclarbamate [mi]
cyclarbamate [inn]
cyclarbamat
DTXSID60206480
Q5198119
calmalone; camalon; casmalon; cyclopentaphene
AKOS040751345
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
carbamate esterAny 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]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (87.50)18.7374
1990's0 (0.00)18.2507
2000's1 (12.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.94

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.94 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.14 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]