Page last updated: 2024-11-07

e 5324

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

Description

E 5324: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID132377
CHEMBL ID47095
SCHEMBL ID692563
MeSH IDM0238320

Synonyms (16)

Synonym
bdbm50047557
1-butyl-3-{2-[3-(5-ethyl-4-phenyl-imidazol-1-yl)-propoxy]-6-methyl-phenyl}-urea
141799-76-0
e-5324
e 5324
urea, n-butyl-n'-02-03-(((5-ethyl-4-phenyl-1h-imidazol-1-yl)propoxy)-6-methylphenyl)-
n-butyl-n'-(2-(3-(5-ethyl-4-phenyl-1h-imidazol-1-yl)propoxy)-6-methylphenyl)urea
urea, n-butyl-n'-(2-(3-(5-ethyl-4-phenyl-1h-imidazol-1-yl)propoxy)-6-methylphenyl)-
e5324
CHEMBL47095 ,
1-butyl-3-[2-[3-(5-ethyl-4-phenylimidazol-1-yl)propoxy]-6-methylphenyl]urea
SCHEMBL692563
DTXSID20161824
HY-19183
CS-0014924
AKOS040741679
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Acyl-CoA:cholesterol acyltransferase Oryctolagus cuniculus (rabbit)IC50 (µMol)0.08800.00600.98467.6000AID31205
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID177206Tested for hypocholesterolemic activity required to decrease serum total cholesterol1993Journal of medicinal chemistry, May-28, Volume: 36, Issue:11
Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2.
AID31202Inhibition against acyl coenzyme A:cholesterol acyltransferase derived from rabbit aorta homogenate1993Journal of medicinal chemistry, May-28, Volume: 36, Issue:11
Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2.
AID31205Inhibition against acyl coenzyme A:cholesterol acyltransferase derived from rabbit intestine microsomes1993Journal of medicinal chemistry, May-28, Volume: 36, Issue:11
Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2.
AID194353Cholesterol lowering activity in rats after a dose of 1 mg/kg once a day for 2 days1993Journal of medicinal chemistry, May-28, Volume: 36, Issue:11
Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's7 (100.00)18.2507
2000's0 (0.00)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: 12.37

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 Index12.37 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.37)

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]