Page last updated: 2024-12-08

epimestrol

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

Description

Epimestrol: A synthetic steroid with estrogenic activity. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID244809
CHEMBL ID2106236
CHEBI ID34738
SCHEMBL ID554257
MeSH IDM0007581

Synonyms (36)

Synonym
nsc 55975
epimestrol
estra-1,5(10)-triene-16,17-diol, 3-methoxy-, (16.alpha.,17.alpha.)-
org 817
stimovul
estra-1,5(10)-triene-16.alpha.,17.alpha.-diol, 3-methoxy-
nsc-55975
7004-98-0
3-methoxy-17-epiestriol
3-methoxyestra-1,5(10)-triene-16.alpha.,17.alpha.-diol
D04021
epimestrol (usan/inn)
3-methoxyestra-1,3,5(10)-triene-16alpha,17alpha-diol
einecs 230-278-0
epimestrol [usan:inn:ban]
epimestrolum [inn-latin]
estra-1,3,5(10)-triene-16,17-diol, 3-methoxy-, (16alpha,17alpha)-
epimestrolo [dcit]
estra-1,3,5(10)-triene-16alpha,17alpha-diol, 3-methoxy-
(8r,9s,13s,14s,16r,17s)-3-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-16,17-diol
CHEMBL2106236
org-817
chebi:34738 ,
epimestrolo
epimestrolum
7ive3sdz38 ,
unii-7ive3sdz38
epimestrol [mart.]
epimestrol [usan]
epimestrol [inn]
epimestrol [who-dd]
epimestrol [mi]
SCHEMBL554257
Q5383041
DB13386
DTXSID90859807

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The hormonal dosage highlighted a clear increase in Gonadotropins and Estradiol levels."( Bromocryptin and epimestrol in MAP-negative secondary amenorrheas.
Polatti, F, 1981
)
0.6
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
steroidAny of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene.
[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 (35)

TimeframeStudies, This Drug (%)All Drugs %
pre-199034 (97.14)18.7374
1990's1 (2.86)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: 21.99

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.

MetricThis Compound (vs All)
Research Demand Index21.99 (24.57)
Research Supply Index3.91 (2.92)
Research Growth Index4.26 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.99)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials6 (13.95%)5.53%
Reviews3 (6.98%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other34 (79.07%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]