Compounds > cyclodrine
Page last updated: 2024-11-08

cyclodrine

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

Description

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

Cross-References

ID SourceID
PubMed CID162669
CHEMBL ID4745689
CHEBI ID135365
SCHEMBL ID250010
MeSH IDM0043660

Synonyms (22)

Synonym
cyclodrine
CHEBI:135365
2-diethylaminoethyl 2-(1-hydroxycyclopentyl)-2-phenylacetate
52109-93-0
1-hydroxy-alpha-phenylcyclopentaneacetic acid 2-diethylaminoethyl ester
unii-d1e5481t58
1-hydroxycyclopentyl-alpha-phenylacetic acid beta-dimethylaminoethyl ester
g.t. 92
cyclopentaneacetic acid, 1-hydroxy-alpha-phenyl-, 2-diethylaminoethyl ester
cyclopent
benzeneacetic acid, alpha-(1-hydroxycyclopentyl)-, 2-(diethylamino)ethyl ester
d1e5481t58 ,
AKOS015962143
cyclodrine [who-dd]
cyclodrine [mi]
SCHEMBL250010
z-d-cyclohexylglycine
2-(diethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetate
2-(diethylamino)ethyl (1-hydroxycyclopentyl)(phenyl)acetate
DTXSID60966471
Q27275973
CHEMBL4745689
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
benzenesAny benzenoid aromatic compound consisting of the benzene skeleton and its 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 (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's2 (40.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.87

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 Index12.87 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.87)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
gamma-aminobutyric acid
gamma-Aminobutyric Acid: The most common inhibitory neurotransmitter in the central nervous system.. gamma-aminobutyric acid : A gamma-amino acid that is butanoic acid with the amino substituent located at C-4.		2.4110amino acid zwitterion;
gamma-amino acid;
monocarboxylic acid		human metabolite;
neurotransmitter;
Saccharomyces cerevisiae metabolite;
signalling molecule
pyridoxal phosphate
Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).. pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal.		2.4110methylpyridines;
monohydroxypyridine;
pyridinecarbaldehyde;
vitamin B6 phosphate		coenzyme;
cofactor;
EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
cyclopentane
Cyclopentanes: A group of alicyclic hydrocarbons with the general formula R-C5H9.. cyclopentanes : Cyclopentane and its derivatives formed by substitution.		2.1710cycloalkane;
cyclopentanes;
volatile organic compound		non-polar solvent
n-butyllithium
[no description available]		2.1710
ConditionIndicatedRelationship StrengthStudiesTrials
Cancer of Liver
[description not available]		02.4110
Liver Neoplasms
Tumors or cancer of the LIVER.		02.4110