Page last updated: 2024-12-10

onitin

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

Description

onitin: from Onychium siliculosum; structure given in first source; RN from Chem Abst Index Guide 1985; RN not in Chemline 9/85 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
Onychiumgenus[no description available]PteridaceaeA plant family of the order Polypodiales, class Filicopsida, division Pteridophyta (FERNS).[MeSH]

Cross-References

ID SourceID
PubMed CID3085044
CHEMBL ID261243
CHEBI ID196151
SCHEMBL ID16489156
MeSH IDM0133967

Synonyms (14)

Synonym
onitin
CHEMBL261243
4-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3h-inden-1-one
CHEBI:196151
1h-inden-1-one, 2,3-dihydro-4-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-
4-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-dihydro-1h-inden-1-one
53823-02-2
AKOS022663882
SCHEMBL16489156
DTXSID20202105
4-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethylindanone
FS-9991
2,3-dihydro-4-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-1h-inden-1-one; 2,2,5,7-tetramethyl-4-hydroxy-6-(2-hydroxyethyl)indanone
B0005-123296
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
indanones
[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 (3)

Assay IDTitleYearJournalArticle
AID326588Inhibition of CaCl2-induced contraction in potassium depolarized-guinea pig ileal smooth muscle2008Bioorganic & medicinal chemistry, Jan-01, Volume: 16, Issue:1
Synthesis and pharmacological activity of aminoindanone dimers and related compounds.
AID1354669Inhibition of BACE1 (unknown origin) at 40 uM using BACE1 substrate measured after 2 hrs by FRET assay relative to control2018Journal of natural products, 06-22, Volume: 81, Issue:6
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.
AID1354671Cytotoxicity against human L02 cells assessed as effect on cell viability at 40 uM after 24 hrs by MTT assay2018Journal of natural products, 06-22, Volume: 81, Issue:6
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A.
[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-19902 (40.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)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: 29.98

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index29.98 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.59 (4.65)
Search Engine Demand Index34.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.98)

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