Page last updated: 2024-11-11

homocastasterone

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

Description

homocastasterone: putative ecdysteroid antagonist [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5487654
CHEMBL ID488432
SCHEMBL ID20561406
MeSH IDM0191211

Synonyms (15)

Synonym
homocastasterone
stigmastan-6-one, 2,3,22,23-tetrahydroxy-, (2.beta.,3.alpha.,5.alpha.,22r,23r)-
(2r,3s,5s,8s,9s,10r,13s,14s,17r)-17-[(1s,2r,3r,4s)-4-ethyl-2,3-dihydroxy-1,5-dimethyl-hexyl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one
BA793800-32F2-4D3D-A855-8E2AE466F94F
28-homocastasterone
CHEMBL488432
(2r,3s,5s,8s,9s,10r,13s,14s,17r)-17-[(2s,3r,4r,5s)-5-ethyl-3,4-dihydroxy-6-methylheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one
28-homo castasterone
2,3,22,23-tetrahydroxystigmastan-6-one
2,3,22,23-tetrahydroxy-5alpha-stigmastan-6-one
83509-42-6
stigmastan-6-one, 2,3,22,23-tetrahydroxy-, (2alpha,3alpha,5alpha,22r,23r)-
SCHEMBL20561406
(22r,23r,24s)-2a,3a,22,23-tetrahydroxy-24-ethyl-5a-cholestan-6-one
DTXSID101003492

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" For every pair of structurally related compounds, (22R,23R) isomer was found to be significantly more toxic than (22S,23S) isomer."( Toxicity of (22R,23R)-22,23-dihydroxystigmastane derivatives to cultured cancer cells.
Khripach, VA; Mehtiev, AR; Misharin, AY; Timofeev, VP; Tkachev, YV; Zhabinskii, VN, 2010
)
0.36
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID431876Cytotoxicity against human BJ cells after 72 hrs by calcein-AM assay2009Journal of medicinal chemistry, Sep-24, Volume: 52, Issue:18
Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment.
AID344325Cytotoxicity against human MCF7 cells assessed as cell survival after 72 hrs by calcein-AM assay2008Journal of medicinal chemistry, Jul-10, Volume: 51, Issue:13
Brassinosteroids: synthesis and activity of some fluoro analogues.
AID344326Cytotoxicity against human RPMI 8226 cells assessed as cell survival after 72 hrs by calcein-AM assay2008Journal of medicinal chemistry, Jul-10, Volume: 51, Issue:13
Brassinosteroids: synthesis and activity of some fluoro analogues.
AID431874Cytotoxicity against human CEM cells after 72 hrs by calcein-AM assay2009Journal of medicinal chemistry, Sep-24, Volume: 52, Issue:18
Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment.
AID431875Cytotoxicity against human MCF7 cells after 72 hrs by calcein-AM assay2009Journal of medicinal chemistry, Sep-24, Volume: 52, Issue:18
Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment.
AID344327Cytotoxicity against human BJ cells assessed as cell survival after 72 hrs by calcein-AM assay2008Journal of medicinal chemistry, Jul-10, Volume: 51, Issue:13
Brassinosteroids: synthesis and activity of some fluoro analogues.
AID344324Cytotoxicity against human CEM cells assessed as cell survival after 72 hrs by calcein-AM assay2008Journal of medicinal chemistry, Jul-10, Volume: 51, Issue:13
Brassinosteroids: synthesis and activity of some fluoro analogues.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (16.67)18.2507
2000's4 (33.33)29.6817
2010's6 (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]

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%
Other13 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]