Page last updated: 2024-08-03 01:02:17

turkesterone

Description

Turkesterone : no description available [CHeBI]

Cross-References

ID SourceID
PubMed CID14376672
CHEMBL ID2087140
SCHEMBL ID140174
CHEBI ID191170
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

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.

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
ISSN: 1520-4804
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
ISSN: 1520-4804
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
ISSN: 1464-3405
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
ISSN: 1520-4804
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
ISSN: 1464-3405
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
ISSN: 1464-3405
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
ISSN: 1520-4804
Significant activity of ecdysteroids on the resistance to doxorubicin in mammalian cancer cells expressing the human ABCB1 transporter.

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

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%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
undensteroidestrogen00low000000
epiestriolsteroidestrogen00low000000
lynestrenolsteroid00low000000
veratridinesteroidsodium channel modulator00low000000
norgestrienonesteroidestrogen00low000000
furazabolsteroid00low000000
cortivazolsteroid00low000000
remikirenazaspiro compound;
oxaspiro compound;
steroid
00low000000
3 beta-hydroxy-delta 5-cholenic acidsteroid00low000000
demissidinealkaloid;
organic heteropolycyclic compound;
steroid
00low000000
hippurinoxaspiro compound;
steroid
00low000000
cholesta-5,8-dien-3 beta-olsteroid00low000000
3-hydroxystigmast-5-en-7-onesteroid00low000000
16-androstenesteroid00low000000
allylestrenolsteroid00low000000
epimestrolsteroid00low000000
ajugasterone csteroid00low000000
stigmast-7-enolsteroid00low000000
gestodenesteroidestrogen00low000000
spinasterolsteroid00low000000
fucosterolsteroid00low000000
methylestrenolonesteroidestrogen00low000000
24-ethyl-4-cholesten-3-oneC29-steroid;
steroid
metabolite00low000000
stigmast-4-ene-3,6-dionesteroid00low000000
(10R,13S,17R)-17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-onesteroidestrogen00low000000
(13S)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-onesteroidestrogen00low000000
zanoteronesteroid00low000000
promestrienesteroid00low000000
nivazolsteroid00low000000
(2s,3r,5r,10r,13r,14s,17s)-2,3,14-trihydroxy-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-onesteroid00low000000
3'-hydroxystanozololsteroid00low000000
cevinesteroidinsecticide00low000000
27-norcholestane-3,7,12,24,25-pentolsteroid00low000000
gorgosterolsteroid00low000000
stigmasterol glucosidesteroid00low000000
(8R,9S,13S,14R,17R)-17-ethynyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-3,17-diolsteroidestrogen00low000000
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
verapamilaromatic ether;
nitrile;
polyether;
tertiary amino compound
2012201212.0low000010
ecdysone14alpha-hydroxy steroid;
22-hydroxy steroid;
25-hydroxy steroid;
2beta-hydroxy steroid;
3beta-sterol;
6-oxo steroid;
ecdysteroid
prohormone2012201610.0low000020
ponasterone a14alpha-hydroxy steroid;
20-hydroxy steroid;
22-hydroxy steroid;
2beta-hydroxy steroid;
3beta-hydroxy steroid;
6-oxo steroid;
phytoecdysteroid
2012201610.0low000020
cyasterone14alpha-hydroxy steroid;
20-hydroxy steroid;
21-hydroxy steroid;
2beta-hydroxy steroid;
3beta-hydroxy steroid;
6-oxo steroid;
phytoecdysteroid;
steroid lactone
2012201212.0low000010
muristerone a2012201212.0low000010
ajugasterone csteroid201620168.0high000010
2'-c-methylcytidine201620168.0low000010
ecdysterone14alpha-hydroxy steroid;
20-hydroxy steroid;
22-hydroxy steroid;
25-hydroxy steroid;
2beta-hydroxy steroid;
3beta-sterol;
ecdysteroid;
phytoecdysteroid
animal metabolite;
plant metabolite
2012201610.0low000020
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
glyburidemonochlorobenzenes;
N-sulfonylurea
anti-arrhythmia drug;
EC 2.7.1.33 (pantothenate kinase) inhibitor;
EC 3.6.3.49 (channel-conductance-controlling ATPase) inhibitor;
hypoglycemic agent
1999199925.0low001000
methandrostenoloneorganic molecular entity1985201225.5low010010
ecdysone14alpha-hydroxy steroid;
22-hydroxy steroid;
25-hydroxy steroid;
2beta-hydroxy steroid;
3beta-sterol;
6-oxo steroid;
ecdysteroid
prohormone1984198440.0low010000
dactinomycinactinomycinmutagen1984198440.0low010000
ecdysterone14alpha-hydroxy steroid;
20-hydroxy steroid;
22-hydroxy steroid;
25-hydroxy steroid;
2beta-hydroxy steroid;
3beta-sterol;
ecdysteroid;
phytoecdysteroid
animal metabolite;
plant metabolite
1984201324.1high022130
phytosterols1984201226.0low010010
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Alloxan Diabetes01985199932.0high011000
Anxiety02012201212.0medium000010
Depression02012201212.0medium000010
Diseases, Occupational02012201212.0medium000010
Fibrodysplasia Ossificans Progressiva02013201311.0medium000010
Hyperglycemia02012201212.0medium000010
Hyperglycemia, Postprandial02012201212.0medium000010
Myositis Ossificans02013201311.0medium000010