Page last updated: 2024-11-12

etiprednol dicloacetate

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

Description

etiprednol dicloacetate: a soft corticosteroid [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID9935073
CHEMBL ID2107614
CHEBI ID135783
SCHEMBL ID4097770
MeSH IDM0418269

Synonyms (30)

Synonym
D04100
199331-40-3
etiprednol dicloacetate (usan/inn)
etiprednol dicloacetate
CHEBI:135783
unii-332vld554f
332vld554f ,
etiprednol dicloacetate [usan:inn:ban]
ethyl 17-((dichloroacetyl)oxy)-11beta-hydroxy-3-oxoandrosta-1,4-diene-17beta-carboxylate
androsta-1,4-diene-17-carboxylic acid, 17((dichloroacetyl)oxy)-11-hydroxy-3-oxo-, ethyl ester, (11beta,17alpha)-
bnp-166
bnp166
androsta-1,4-diene-17-carboxylic acid, 17-((dichloroacetyl)oxy)-11-hydroxy-3-oxo-, ethyl ester, (11beta,17alpha)-
ethyl 17-((dichloroacetyl)oxy)-11b-hydroxy-3-oxoandrosta-1,4-diene-17b-carboxylate
CHEMBL2107614
androsta-1,4-diene-17-carboxylic acid, 17-((dichloroacetyl)oxy)-11-hydroxy-3-oxo-, ethyl ester, (11.beta.,17.alpha.)-
etiprednol dicloacetate [mi]
etiprednol dicloacetate [usan]
ethyl 17-[(dichloroacetyl)oxy]-11beta-hydroxy-3-oxoandrosta-1,4-diene-17beta-carboxylate
etiprednol dicloacetate [inn]
etiprednol dicloacetate [who-dd]
DB05442
SCHEMBL4097770
Q27095675
ethyl (8s,9s,10r,11s,13s,14s,17r)-17-(2,2-dichloroacetyl)oxy-11-hydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthrene-17-carboxylate
ethyl (8s,9s,10r,11s,13s,14s,17r)-17-(2,2-dichloroacetoxy)-11-hydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3h-cyclopenta[a]phenanthrene-17-carboxylate
DTXSID401313806
CS-0025328
HY-106215
AKOS040751746

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Based on the results, the No Observable Adverse Effect Level (NOAEL) of BNP-166 soft corticosteroid in rat and dog after 28-day oral administration is 2 mg/kg."( 28-day oral toxicity study with soft corticosteroid BNP-166 in rats and dogs, followed by a 14-day recovery period.
Bodor, N; Czégeni, E; Dereszlay, I; Druga, A; Grósz, M; Howes, J; Kiss, E; Magyar, Z; Miklós, A; Novák, I; Nyitray, M, 2002
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
steroid ester
[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 (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (71.43)29.6817
2010's2 (28.57)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: 12.26

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 Index12.26 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.34 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.26)

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]