Page last updated: 2024-12-10

quercimeritrin

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

Description

quercimeritrin: from Rumex luminiastrum [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

quercetin 7-O-beta-D-glucoside : A quercetin O-glucoside in which a glucosyl residue is attached at position 7 of quercetin via a beta-glycosidic linkage. [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
RumexgenusA plant genus of the family POLYGONACEAE that contains patientosides and other naphthalene glycosides.[MeSH]PolygonaceaeThe only family of the buckwheat order (Polygonales) of dicotyledonous flowering plants. It has 40 genera of herbs, shrubs, and trees.[MeSH]

Cross-References

ID SourceID
PubMed CID5282160
CHEMBL ID248726
CHEBI ID28529
SCHEMBL ID1305182
MeSH IDM0237868

Synonyms (40)

Synonym
AC-2364
quercetin-7-glucoside
CHEBI:28529 ,
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-4-oxo-4h-chromen-7-yl beta-d-glucopyranoside
2-(3,4-dihydroxyphenyl)-7-(beta-d-glucopyranosyloxy)-3,5-dihydroxy-4h-1-benzopyran-4-one
3,5-dihydroxy-2-(3,4-dihydroxyphenyl)-7-(beta-d-glucopyranosyloxy)-4h-1-benzopyran-4-one
4h-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(beta-d-glucopyranosyloxy)-3,5-dihydroxy-
4h-1-benzopyran-4-one, 3,5-dihydroxy-2-(3,4-dihydroxyphenyl)-7-(beta-d-glucopyranosyloxy)-
quercetin 7-o-beta-d-glucoside
quercimeritrin
c.i. 75710
491-50-9
quercimeritroside
nsc-115917
quercetin 7-glucoside
CHEMBL248726
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SCHEMBL1305182
177033m1dl ,
unii-177033m1dl
nsc 115917
quercetin-7-o-|a-d-glucopyranoside
4h-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(.beta.-d-glucopyranosyloxy)-3,5-dihydroxy-
quercimeritrin [mi]
quercetin 7-o-.beta.-glucopyranoside
quercimetrin
quercetin-7-o-beta-d-glucopyranoside
AKOS025401623
quercetin 7-beta-d-glucopyranoside
quercetin 7-o-beta-glucopyranoside
mfcd01762823
quercetin-7-o-d-glucopyranoside
quercetin-7-o-b-d-glucopyranoside
Q23069184
ZB1861
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl)oxy)-4h-chromen-4-one
7-o-ss-d-glucopyranoside
MS-28546
quercetin-7-o--d-glucopyranoside
quercetin-7-o-glucoside 1000 microg/ml in acetone
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
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 (5)

ClassDescription
beta-D-glucosideAny D-glucoside in which the anomeric centre has beta-configuration.
quercetin O-glucosideA quercetin O-glycoside that is an O-glucosylated derivative of quercetin.
monosaccharide derivativeA carbohydrate derivative that is formally obtained from a monosaccharide.
flavonolsAny hydroxyflavone in which is the ring hydrogen at position 3 of the heterocyclic ring is replaced by a hydroxy group.
tetrahydroxyflavoneAny hydroxyflavone carrying four hydroxy substituents.
[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 (9)

Assay IDTitleYearJournalArticle
AID1176148Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated TNFalpha production at 0.4 to 2 uM by ELISA2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
AID310105Antioxidant activity assessed as superoxide radical anion scavenging activity at 0.5 mg/ml by hypoxanthine NBT method2007Bioorganic & medicinal chemistry letters, Nov-15, Volume: 17, Issue:22
A novel flavonoid from Lespedeza virgata (Thunb.) DC.: structural elucidation and antioxidative activity.
AID1176149Inhibition of iNOS protein expression in LPS-stimulated mouse RAW264.7 cells by Western blot analysis2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
AID1176146Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated TNFalpha production at 10 uM by ELISA2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
AID404008Cytotoxicity against human KB cells
AID338974Inhibition of cow milk xanthine oxidase at 50 ug/mL
AID1176142Cytotoxicity against mouse RAW264.7 cells at 50 uM by MTT assay2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
AID1176143Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-stimulated nitric oxide production at 10 uM after 24 hrs by Griess assay2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
AID1176150Inhibition of COX2 protein expression in LPS-stimulated mouse RAW264.7 cells by Western blot analysis2015Bioorganic & medicinal chemistry letters, Jan-15, Volume: 25, Issue:2
Anti-inflammatory components of Chrysanthemum indicum flowers.
[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's1 (11.11)18.2507
2000's1 (11.11)29.6817
2010's6 (66.67)24.3611
2020's1 (11.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.45

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 Index23.45 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index5.35 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.45)

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%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]