Page last updated: 2024-11-12

turkesterone

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

Cross-References

ID SourceID
PubMed CID14376672
CHEMBL ID2087140
CHEBI ID191170
SCHEMBL ID140174
MeSH IDM0068822

Synonyms (19)

Synonym
2,3,11,14,20,22,25-heptahydroxycholestenone
(2beta,3beta,5beta,11alpha,22r)-2,3,11,14,20,22,25-heptahydroxycholest-7-en-6-one
turkesterone
CHEBI:191170
(2s,3r,5r,9r,10r,11r,13r,14s,17s)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2r,3r)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1h-cyclopenta[a]phenanthren-6-one
41451-87-0
53e6z3f8zg ,
unii-53e6z3f8zg
CHEMBL2087140
cholest-7-en-6-one, 2,3,11,14,20,22,25-heptahydroxy-, (2.beta.,3.beta.,5.beta.,11.alpha.,22r)-
(2.beta.,3.beta.,5.beta.,11.alpha.,22r)-2,3,11,14,20,22,25-heptahydroxycholest-7-en-6-one
WSBAGDDNVWTLOM-XHZKDPLLSA-N
SCHEMBL140174
AC-35148
AKOS032946018
HY-N2548
CS-0022820
Q27261101
MS-29224

Research Excerpts

Overview

Turkesterone is a phytoecdysteroid possessing an 11alpha-hydroxyl group.

ExcerptReferenceRelevance
"Turkesterone is a phytoecdysteroid possessing an 11alpha-hydroxyl group. "( Synthesis and biological activities of turkesterone 11alpha-acyl derivatives.
Bourne, P; Coll, J; Dhadialla, TS; Dinan, L; Hormann, RE; Lafont, R; Saatov, Z; Tsitsekli, A; Whiting, P, 2003
)
2.03
[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]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID683084Inhibition of human ABCB1 expressed in mouse L5178 cells assessed as 75% inhibition of cell proliferation at compound-doxorubicin ratio of 81.5:1 after 48 hrs by MTT assay2012Journal of medicinal chemistry, Jun-14, Volume: 55, Issue:11
Significant activity of ecdysteroids on the resistance to doxorubicin in mammalian cancer cells expressing the human ABCB1 transporter.
AID683081Inhibition of human ABCB1 expressed in mouse L5178 cells assessed as 50% inhibition of cell proliferation at compound-doxorubicin ratio of 81.5:1 after 48 hrs by MTT assay2012Journal of medicinal chemistry, Jun-14, Volume: 55, Issue:11
Significant activity of ecdysteroids on the resistance to doxorubicin in mammalian cancer cells expressing the human ABCB1 transporter.
AID1293713Cytotoxicity against human HuH7 cells assessed as reduction in cell viability after 72 hrs by MTS assay2016Bioorganic & medicinal chemistry letters, May-01, Volume: 26, Issue:9
Ecdysones from Zoanthus spp. with inhibitory activity against dengue virus 2.
AID683087Inhibition of human ABCB1 expressed in mouse L5178 cells assessed as 95% inhibition of cell proliferation at compound-doxorubicin ratio of 81.5:1 after 48 hrs by MTT assay2012Journal of medicinal chemistry, Jun-14, Volume: 55, Issue:11
Significant activity of ecdysteroids on the resistance to doxorubicin in mammalian cancer cells expressing the human ABCB1 transporter.
AID1293709Antiviral activity against Dengue virus 2 DN454009A infected in human HuH7 cells assessed as inhibition of viral RNA level measured 72 hrs post infection by qRT-PCR method2016Bioorganic & medicinal chemistry letters, May-01, Volume: 26, Issue:9
Ecdysones from Zoanthus spp. with inhibitory activity against dengue virus 2.
AID1293714Selectivity index, ratio of CC50 for human HuH7 cells to EC50 for Dengue virus 2 DN454009A infected in human HuH7 cells2016Bioorganic & medicinal chemistry letters, May-01, Volume: 26, Issue:9
Ecdysones from Zoanthus spp. with inhibitory activity against dengue virus 2.
AID683076Inhibition of human ABCB1 pump expressed in mouse L5178 cells assessed as fluorescence activity ratio at 20 uM for 10 mins by flow cytometry relative to control2012Journal of medicinal chemistry, Jun-14, Volume: 55, Issue:11
Significant activity of ecdysteroids on the resistance to doxorubicin in mammalian cancer cells expressing the human ABCB1 transporter.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (20.00)18.7374
1990's2 (20.00)18.2507
2000's1 (10.00)29.6817
2010's5 (50.00)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: 59.31

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index59.31 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index5.17 (4.65)
Search Engine Demand Index184.62 (26.88)
Search Engine Supply Index3.95 (0.95)

This Compound (59.31)

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]