Page last updated: 2024-11-13

2',3',4'-trihydroxyflavone

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

Description

2',3',4'-trihydroxyflavone: inhibitor of protein sumoylation; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID22507438
CHEMBL ID3115475
SCHEMBL ID1772778
MeSH IDM000598676

Synonyms (22)

Synonym
CHEMBL3115475
S8696
SCHEMBL1772778
2-d08
144707-18-6
AC-31428
2',3',4'-trihydroxyflavone
AKOS027322100
2-(2,3,4-trihydroxyphenyl)-4h-chromen-4-one
HY-114166
CS-0077855
EX-A3562
BCP18314
2d08;2 d08
AS-16368
mfcd27995567
AMY31051
CCG-267148
D82631
2-(2,3,4-trihydroxyphenyl)-4h-1-benzopyran-4-one
2-(2,3,4-trihydroxyphenyl)chromen-4-one
PD044048
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (8)

Assay IDTitleYearJournalArticle
AID1485948Inhibition of human amyloid beta (1 to 42) aggregation at 100 uM after 48 hrs by transmission electron microscopic analysis2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1485959Inhibition of human amyloid beta (1 to 42) assessed as neuroprotective activity at 2 uM of amyloid beta (1 to 42)-induced toxicity in rat PC12 cells by measuring reduction in cell viability incubated 15 mins prior to amyloid beta (1 to 42) addition measur2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1485945Inhibition of human amyloid beta (1 to 42) assessed as reduction in fibrillisation AUC in cell-free solution at 100 uM measured every 10 mins for 48 hrs by Thioflavin T based fluorescence assay2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1485951Inhibition of human amyloid beta (1 to 42) assessed as neuroprotective activity up to 2 uM of amyloid beta (1 to 42)-induced toxicity in rat PC12 cells by measuring reduction in cell viability at 100 uM incubated 15 mins prior to amyloid beta (1 to 42) ad2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1485949Inhibition of human amyloid beta (1 to 42) aggregation assessed as reduction in fibril formation at 100 uM after 48 hrs by transmission electron microscopic analysis2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1485944Inhibition of human amyloid beta (1 to 42) fibrillisation in cell-free solution at 100 uM measured every 10 mins up to 48 hrs by Thioflavin T based fluorescence assay2017Bioorganic & medicinal chemistry, 07-15, Volume: 25, Issue:14
Structure-activity relationships for flavone interactions with amyloid β reveal a novel anti-aggregatory and neuroprotective effect of 2',3',4'-trihydroxyflavone (2-D08).
AID1070224Inhibition of purified SUMO E1/E2 (unknown origin)-mediated conjugation of His6-SUMO-1 to fluorescent peptide FL-AR at 30 uM after 90 mins by microfluidic electrophoretic mobility shift assay2014Bioorganic & medicinal chemistry letters, Feb-15, Volume: 24, Issue:4
Synthesis of 2',3',4'-trihydroxyflavone (2-D08), an inhibitor of protein sumoylation.
AID1859358Inhibition of His-tagged SUMO1/SUMO E1 /His-tagged Ubc9 (unknown origin)-mediated SUMOylation using FL-AR as substrate incubated for 90 mins in presence of ATP by Western blot analysis2022European journal of medicinal chemistry, Apr-05, Volume: 233Small-molecule inhibitors targeting small ubiquitin-like modifier pathway for the treatment of cancers and other diseases.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (55.56)24.3611
2020's4 (44.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.30

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

MetricThis Compound (vs All)
Research Demand Index12.30 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index4.60 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.30)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (22.22%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (77.78%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]