Page last updated: 2024-12-08

gitogenin

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

Description

gitogenin: an alpha-glucosidase inhibitor [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID441887
CHEMBL ID1770687
CHEBI ID5363
SCHEMBL ID23524443
MeSH IDM0060417

Synonyms (34)

Synonym
gitogenin
C08899
511-96-6
digin
nsc-147752
CHEMBL1770687
chebi:5363 ,
LMST01080010
(25r)-5alpha-spirostan-2alpha,3beta-diol
unii-60zmy8ih51
nsc 147752
5alpha,22alpha-spirostane-2alpha,3beta-diol
ai3-62266
5alpha-spirostan-2alpha,3beta-diol, (25r)-
spirostan-2,3-diol, (2alpha,3beta,5alpha,25r)-
60zmy8ih51 ,
AKOS016009639
spirostan-2,3-diol, (2a,3b,5a,25r)-
AC-35113
5.alpha.,25d-spirostan-2.alpha.,3.beta.-diol
2.alpha.-hydroxytigogenin
gitogenin [mi]
(2alpha,3|a,5alpha,25r)-spirostan-2,3-diol
digine
SCHEMBL23524443
(25r,s)-5alpha-spirostane-2alpha,3beta-diol
HY-N2574
CS-0022911
Q5880476
mfcd00273328
(1r,2s,4s,5'r,6r,7s,8r,9s,12s,13s,15r,16r,18s)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol
A927966
MS-27723
DTXSID101023656
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
triterpenoidAny terpenoid derived from a triterpene. The term includes compounds in which the C30 skeleton of the parent triterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
[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 (4)

Assay IDTitleYearJournalArticle
AID594707Antifungal activity against Candida albicans ATCC 10231 assessed as reduction in growth after 48 hrs by broth microdilution method relative to control2011Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
Synthesis and antifungal activity of functionalized 2,3-spirostane isomers.
AID594709Antifungal activity against Cryptococcus neoformans ATCC 36556 assessed as reduction in growth after 48 hrs by broth microdilution method relative to control2011Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
Synthesis and antifungal activity of functionalized 2,3-spirostane isomers.
AID594706Antifungal activity against Candida glabrata ATCC 48435 assessed as reduction in growth after 48 hrs by broth microdilution method relative to control2011Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
Synthesis and antifungal activity of functionalized 2,3-spirostane isomers.
AID594708Antifungal activity against Aspergillus fumigatus ATCC 16424 reduction in growth after 48 hrs by broth microdilution method relative to control2011Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
Synthesis and antifungal activity of functionalized 2,3-spirostane isomers.
[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's1 (10.00)18.2507
2000's2 (20.00)29.6817
2010's4 (40.00)24.3611
2020's1 (10.00)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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]