Page last updated: 2024-12-07

kryptogenin

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

Description

kryptogenin: from carp bile [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID21117640
CHEMBL ID389341
CHEBI ID81367
MeSH IDM0051927

Synonyms (26)

Synonym
nsc 93751
3-beta,26-dihydroxycholest-5-ene-12,22-dione [french]
(3-beta,25r)-3,26-dihydroxycholest-5-ene-16,22-dione
3beta,26-dihydroxycholest-5-ene-16,22-dione
cholest-5-ene-16,22-dione, 3beta,26-dihydroxy-, (20s,25r)-
cholest-5-ene-16,22-dione, 3,26-dihydroxy-, (3-beta,25r)-
cryptogenine [french]
cholest-5-ene-16,22-dione, 3-beta,26-dihydroxy-, (20s,25r)-
cryptogenin
kryptogenin
CHEMBL389341
chebi:81367 ,
C17891
LMST01010341
16,22-dioxo-25s-methyl-cholest-5-en-3beta-ol
cryptogenine
3-beta,26-dihydroxycholest-5-ene-12,22-dione
bxc9x8b37j ,
unii-bxc9x8b37j
GDKGOXUWEBGZBY-WQTURIIHSA-N
3,26-dihydroxycholest-5-ene-16,22-dione #
cholest-5-ene-16,22-dione, 3,26-dihydroxy-, (3.beta.,25r)-
cholest-5-ene-16,22-dione, 3.beta.,26-dihydroxy-, (20s,25r)-
(3.beta.,25r)-3,26-dihydroxycholest-5-ene-16,22-dione
Q27155304
AKOS040752280
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
cholanoid
[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 (5)

Assay IDTitleYearJournalArticle
AID292677Antitumor activity against HeLa cells at 0.1 uM by MTT assay2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
Synthesis of bisdesmosidic kryptogenyl saponins using the 'random glycosylation' strategy and evaluation of their antitumor activity.
AID292678Antitumor activity against HeLa cells at 10 nM by MTT assay2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
Synthesis of bisdesmosidic kryptogenyl saponins using the 'random glycosylation' strategy and evaluation of their antitumor activity.
AID292676Antitumor activity against HeLa cells at 1 uM by MTT assay2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
Synthesis of bisdesmosidic kryptogenyl saponins using the 'random glycosylation' strategy and evaluation of their antitumor activity.
AID292679Antitumor activity against HeLa cells by MTT assay2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
Synthesis of bisdesmosidic kryptogenyl saponins using the 'random glycosylation' strategy and evaluation of their antitumor activity.
AID292675Antitumor activity against HeLa cells at 10 uM by MTT assay2007Bioorganic & medicinal chemistry letters, Jan-01, Volume: 17, Issue:1
Synthesis of bisdesmosidic kryptogenyl saponins using the 'random glycosylation' strategy and evaluation of their antitumor activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)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]

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]