Page last updated: 2024-11-08

oxypaeoniflora

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

Description

oxypaeoniflora: from Paeonia lactiflora [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
PaeoniagenusA plant genus of the family Paeoniaceae, order Dilleniales, subclass Dilleniidae, class Magnoliopsida. These perennial herbs are up to 2 m (6') tall. Leaves are alternate and are divided into three lobes, each lobe being further divided into three smaller lobes. The large flowers are symmetrical, bisexual, have 5 sepals, 5 petals (sometimes 10), and many stamens.[MeSH]Paeoniaceae[no description available]
Paeonia lactifloraspecies[no description available]Paeoniaceae[no description available]

Cross-References

ID SourceID
PubMed CID21631105
CHEMBL ID4871716
CHEBI ID132789
SCHEMBL ID4087053
MeSH IDM0137375

Synonyms (28)

Synonym
nsc-258310
oxypaeoniflora
[(1ar,2s,3ar,5r,5ar,5bs)-1a-(beta-d-glucopyranosyloxy)-5-hydroxy-2-methyltetrahydro-1h-2,5-methano-3,4-dioxacyclobuta[cd]pentalen-5b(3ah)-yl]methyl 4-hydroxybenzoate
CHEBI:132789
3a7o4nbd5s ,
beta-d-glucopyranoside, tetrahydro-5-hydroxy-5b-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2,5-methano-1h-3,4-dioxacyclobuta(cd)pentalen-1a(2h)-yl, (1ar-(1aalpha,2beta,3aalpha,5alpha,5aalpha,5balpha))-
unii-3a7o4nbd5s
nsc 258310
CS-3645
SCHEMBL4087053
AC-34571
(((1ar)-3a.beta.,5,5a.beta.,5b-tetrahydro-5.beta.-hydroxy-5b.beta.-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2.alpha.,5-methano-3,4-dioxa-1h-cyclobuta(cd)pentalen)-1a.beta.(2h)-yl).beta.-d-glucopyranoside
.beta.-d-glucopyranoside, (1ar,2s,3ar,5r,5ar,5bs)-tetrahydro-5-hydroxy-5b-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2,5-methano-1h-3,4-dioxacyclobuta(cd)pentalen-1a(2h)-yl
((2s,3r,5r,6r,8s)-3-(.beta.-d-glucopyranosyloxy)-6-hydroxy-8-methyl-9,10-dioxatetracyclo(4.3.1.02,5.03,8)dec-2-yl)methyl 4-hydroxybenzoate
j17.727j ,
.beta.-d-glucopyranoside, tetrahydro-5-hydroxy-5b-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2,5-methano-1h-3,4-dioxacyclobuta(cd)pentalen-1a(2h)-yl, (1ar-(1a.alpha.,2.beta.,3a.alpha.,5.alpha.,5a.alpha.,5b.alpha.))-
oxypeoniflorin
HY-N0748
(((1ar)-3abeta,5,5abeta,5b-tetrahydro-5beta-hydroxy-5bbeta-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2alpha,5-methano-3,4-dioxa-1h-cyclobuta(cd)pentalen)-1abeta(2h)-yl)beta-d-glucopyranoside
beta-d-glucopyranoside, (1ar,2s,3ar,5r,5ar,5bs)-tetrahydro-5-hydroxy-5b-(((4-hydroxybenzoyl)oxy)methyl)-2-methyl-2,5-methano-1h-3,4-dioxacyclobuta(cd)pentalen-1a(2h)-yl
((2s,3r,5r,6r,8s)-3-(beta-d-glucopyranosyloxy)-6-hydroxy-8-methyl-9,10-dioxatetracyclo(4.3.1.02,5.03,8)dec-2-yl)methyl 4-hydroxybenzoate
mfcd00869478
Q27256957
MS-29219
beta-d-glucopyranoside, (1ar,2s,3ar,5r,5ar,5bs)-tetrahydro-5-hydroxy-5b-[[(4-hydroxybenzoyl)oxy]methyl]-2-methyl-2,5-methano-1h-3,4-dioxacyclobuta[cd]pentalen-1a(2h)-yl
A873733
CHEMBL4871716
AKOS040756009

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
"To establish a HPLC-MS method and investigate the pharmacokinetic properties of paeoniflorin, albiflorin and oxypaeoniflorin and the pharmacokinetics difference of Radix Paeoniae Rubra and Radix Paeoniae Alba."( Pharmacokinetic properties of paeoniflorin, albiflorin and oxypaeoniflorin after oral gavage of extracts of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.
Duan, K; Feng, C; Kong, D; Liu, M; Shi, X; Wang, Q; Yang, W, 2010
)
0.36
" Main pharmacokinetic parameters were estimated and the total AUC of the three components were compared."( Pharmacokinetic properties of paeoniflorin, albiflorin and oxypaeoniflorin after oral gavage of extracts of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.
Duan, K; Feng, C; Kong, D; Liu, M; Shi, X; Wang, Q; Yang, W, 2010
)
0.36
"The pharmacokinetic parameters of paeoniflorin, albiflorin and oxypaeoniflorin were significantly different."( Pharmacokinetic properties of paeoniflorin, albiflorin and oxypaeoniflorin after oral gavage of extracts of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.
Duan, K; Feng, C; Kong, D; Liu, M; Shi, X; Wang, Q; Yang, W, 2010
)
0.36
"A specific and sensitive HPLC-ESI-MS method was developed for simultaneous determination of paeoniflorin, albiflorin and oxypaeoniflorin in rat plasma and was successfully applied to pharmacokinetic study."( Pharmacokinetic properties of paeoniflorin, albiflorin and oxypaeoniflorin after oral gavage of extracts of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.
Duan, K; Feng, C; Kong, D; Liu, M; Shi, X; Wang, Q; Yang, W, 2010
)
0.36
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[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 (6)

ClassDescription
cyclic acetalAn acetal in the molecule of which the acetal carbon and one or both oxygen atoms thereon are members of a ring.
lactolCyclic hemiacetals formed by intramolecular addition of a hydroxy group to an aldehydic or ketonic carbonyl group. They are thus 1-oxacycloalkan-2-ols or unsaturated analogues.
bridged compoundA polycyclic compound in which two rings have two or more atoms in common.
beta-D-glucosideAny D-glucoside in which the anomeric centre has beta-configuration.
4-hydroxybenzoate esterA benzoate ester that is an ester of 4-hydroxybenzoic acid.
monoterpene glycosideA terpene glycoside in which the terpene moiety is a monoterpenoid.
[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
AID1762120Cytotoxicity against human ER-positive MCF7 cells assessed as increase in cell proliferation at 12.5 to 100 uM incubated for 24 hrs2021Bioorganic & medicinal chemistry letters, 05-15, Volume: 40Estrogenic activity of ethyl gallate and its potential use in hormone replacement therapy.
AID1762125Estrogenic activity at human ER-positive MCF7 cells assessed as increase in cell proliferation at 50 uM incubated for 144 hrs by Soto's E-screen assay2021Bioorganic & medicinal chemistry letters, 05-15, Volume: 40Estrogenic activity of ethyl gallate and its potential use in hormone replacement therapy.
AID1762126Cytotoxicity against human ER-positive MCF7 cells assessed as reduction in cell proliferation at 50 uM incubated for 144 hrs by Soto's E-screen assay2021Bioorganic & medicinal chemistry letters, 05-15, Volume: 40Estrogenic activity of ethyl gallate and its potential use in hormone replacement therapy.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (8.33)18.7374
1990's0 (0.00)18.2507
2000's3 (25.00)29.6817
2010's6 (50.00)24.3611
2020's2 (16.67)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%
Reviews1 (8.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (91.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]