Page last updated: 2024-12-10

luteolin-7-glucuronide

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

Description

luteolin-7-glucuronide: isolated from Lycopus europaeus L.; active against pregnant mare serum gonadotropin [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

luteolin 7-O-beta-D-glucosiduronic acid : A luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 7-position. [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]

FloraRankFlora DefinitionFamilyFamily Definition
LycopusgenusA plant genus of the family LAMIACEAE that contains rosmarinic acid and isopimarane diterpenoids and has been used in folk medicine for HYPERTHYROIDISM.[MeSH]LamiaceaeThe mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).[MeSH]
Lycopus europaeusspecies[no description available]LamiaceaeThe mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).[MeSH]

Cross-References

ID SourceID
PubMed CID5280601
CHEMBL ID464224
CHEBI ID18128
SCHEMBL ID1279040
MeSH IDM0203212

Synonyms (34)

Synonym
MEGXP0_000794
4h-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(.beta.-d-glucopyranuronosyloxy)-5-hydroxy-
(2s,3s,4s,5r,6s)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-chromen-7-yl]oxy-3,4,5-trihydroxy-tetrahydropyran-2-carboxylic acid
29741-10-4
CHEBI:18128 ,
luteolin 7-o-beta-d-glucuronopyranoside
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-chromen-7-yl beta-d-glucopyranosiduronic acid
luteolin 7-o-beta-d-glucosiduronic acid
cyanidenon-7-o-beta-d-glucuronic acid
luteolin 7-glucuronide
luteolin 7-o-glucuronide
C03515 ,
CHEMBL464224
(2s,3s,4s,5r,6s)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
unii-r4346d0x7p
r4346d0x7p ,
luteolin-7-glucuronide
beta-d-glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-1-benzopyran-7-yl
SCHEMBL1279040
glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-1-benzopyran-7-yl, .beta.-d-
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-1-benzopyran-7-yl .beta.-d-glucopyranosiduronic acid
.beta.-d-glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-1-benzopyran-7-yl
cyanidenon-7-o-.beta.-d-glucuronic acid
luteolin-7-.beta.-d-glucuronide
flavone, 3',4',5,7-tetrahydroxy-, 7-.beta.-d-glucopyranuronoside
luteolin 7-o-beta-d-glucuronide (14)
bdbm226184
AKOS032946035
HY-N1463
CS-0016910
(2s,3s,4s,5r,6s)-6-((2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4h-chromen-7-yl)oxy)-3,4,5-trihydroxytetrahydro-2h-pyran-2-carboxylic acid
luteolin-7-o-glucuronside
MS-28490
DTXSID50952181
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role 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]

Drug Classes (4)

ClassDescription
luteolin O-glucuronosideA glycosyloxyflavone that is an O-glucuronidated derivative of luteolin.
trihydroxyflavoneAny hydroxyflavone carrying three hydroxy groups at unspecified positions.
glycosyloxyflavoneA member of the class of flavones having one or more glycosyl residues attached at unspecified positions.
monosaccharide derivativeA carbohydrate derivative that is formally obtained from a monosaccharide.
[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 (6)

Assay IDTitleYearJournalArticle
AID1460718Neuroprotective activity in human SH-SY5Y cells assessed as reduction in glutamate-induced cytotoxicity at 10 uM relative to untreated control2017Journal of natural products, 04-28, Volume: 80, Issue:4
Neuroprotective Caffeoylquinic Acid Derivatives from the Flowers of Chrysanthemum morifolium.
AID356894Antihyperglycemic activity against streptozotocin-induced diabetic rat assessed as change in plasma glucose at 1 mM/kg, iv2002Journal of natural products, Dec, Volume: 65, Issue:12
Bacopaside III, bacopasaponin G, and bacopasides A, B, and C from Bacopa monniera.
AID1775658Inhibition of LPS induced NO production in mouse RAW264.7 cells measured after 24 hrs by Griess reagent based assay2021Journal of natural products, 03-26, Volume: 84, Issue:3
Sesquiterpenoids from
AID1775659Cytotoxicity against mouse RAW264.7 cells assessed as reduction in cell viability measured after 24 hrs by MTT assay2021Journal of natural products, 03-26, Volume: 84, Issue:3
Sesquiterpenoids from
AID1460719Neuroprotective activity in human SH-SY5Y cells assessed as reduction in hydrogen peroxide-induced cytotoxicity by measuring cell viability level at 10 uM (Rvb = 50.7+/- 2.6%)2017Journal of natural products, 04-28, Volume: 80, Issue:4
Neuroprotective Caffeoylquinic Acid Derivatives from the Flowers of Chrysanthemum morifolium.
AID1460717Neuroprotective activity in human SH-SY5Y cells assessed as reduction in oxygen-glucose deprivation-induced cytotoxicity at 10 uM relative to untreated control2017Journal of natural products, 04-28, Volume: 80, Issue:4
Neuroprotective Caffeoylquinic Acid Derivatives from the Flowers of Chrysanthemum morifolium.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's1 (16.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.68

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 Index28.68 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.92 (4.65)
Search Engine Demand Index40.36 (26.88)
Search Engine Supply Index2.92 (0.95)

This Compound (28.68)

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%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]