Page last updated: 2024-12-08

irisflorentin

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

Description

irisflorentin: bioactive substance isolated from Rhizoma Belamcandae; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID170569
CHEMBL ID487216
CHEBI ID81410
MeSH IDM0571935

Synonyms (26)

Synonym
irisflorentin
41743-73-1
C17958
chebi:81410 ,
CHEMBL487216
5,3',4',5'-tetramethoxy-6,7-methylenedioxyisoflavone
LMPK12050419
9-methoxy-7-(3,4,5-trimethoxyphenyl)-[1,3]dioxolo[4,5-g]chromen-8-one
9-methoxy-7-(3,4,5-trimethoxyphenyl)-8h-1,3-dioxolo(4,5-g)(1)benzopyran-8-one
8h-1,3-dioxolo(4,5-g)(1)benzopyran-8-one, 9-methoxy-7-(3,4,5-trimethoxyphenyl)-
S9053
FT-0688295
AKOS015896764
AC-34062
Q-100469
9-methoxy-7-(3,4,5-trimethoxyphenyl)-8h-1,3-dioxolo[4,5-g][1]benzopyran-8-one
DTXSID60194575
9-methoxy-7-(3,4,5-trimethoxyphenyl)-8h-[1,3]dioxolo[4,5-g]chromen-8-one
Q27155343
mfcd02183467
HY-N0268
CS-0008287
CCG-268476
AS-56483
irisfloretin
I1063

Research Excerpts

Overview

Irisflorentin is an isoflavone component derived from the roots of Belamcanda chinensis (L.) DC.

ExcerptReferenceRelevance
"Irisflorentin is an isoflavone component derived from the roots of Belamcanda chinensis (L.) DC. "( Irisflorentin modifies properties of mouse bone marrow-derived dendritic cells and reduces the allergic contact hypersensitivity responses.
Chan, TM; Chen, YM; Chiu, SC; Fu, RH; Ho, YC; Hung, HS; Lin, HL; Lin, SZ; Liu, SP; Shyu, WC; Tsai, CH; Tsai, CW; Tsai, RT; Wang, YC, 2015
)
3.3

Pharmacokinetics

ExcerptReferenceRelevance
" This method was successfully applied to a pharmacokinetic study of the three isoflavones after oral administration of Rhizoma Belamcandae extract to rats."( Simultaneous determination of tectorigenin, irigenin and irisflorentin in rat plasma and urine by UHPLC-MS/MS: application to pharmacokinetics.
Gu, Y; Wang, R; Wang, XJ; Yang, WJ; Zhang, WD, 2011
)
0.61

Compound-Compound Interactions

ExcerptReferenceRelevance
" The metabolites were identified by ultra-high performance liquid chromatography combined with quadrupole/orbitrap tandem mass spectrometry."( Characterization of the metabolites of irisflorentin by using ultra-high performance liquid chromatography combined with quadrupole/orbitrap tandem mass spectrometry.
Qiao, GX; Zhang, X; Zhao, GF; Zhao, SF, 2021
)
0.89
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
4'-methoxyisoflavonesAny methoxyisoflavone which has a methoxy group at the 4-position of the phenyl substituent.
[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 (5)

Assay IDTitleYearJournalArticle
AID377457Estrogenic activity in human T47D cells assessed as drug level causing stimulation of cell proliferation equivalent to 10 pM estradiol by alamar blue assay2005Journal of natural products, Mar, Volume: 68, Issue:3
Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines.
AID377458Estrogenic activity in human T47D cells assessed as drug level causing stimulation of cell proliferation equivalent to 100 pM estradiol by alamar blue assay2005Journal of natural products, Mar, Volume: 68, Issue:3
Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines.
AID377456Estrogenic activity in human MCF7 cells assessed as drug level causing stimulation of cell proliferation equivalent to 100 pM estradiol by alamar blue assay2005Journal of natural products, Mar, Volume: 68, Issue:3
Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines.
AID377455Estrogenic activity in human MCF7 cells assessed as drug level causing stimulation of cell proliferation equivalent to 10 pM estradiol by alamar blue assay2005Journal of natural products, Mar, Volume: 68, Issue:3
Phenolic constituents of the rhizomes of the Thai medicinal plant Belamcanda chinensis with proliferative activity for two breast cancer cell lines.
AID338974Inhibition of cow milk xanthine oxidase at 50 ug/mL
[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's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's4 (66.67)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: 22.22

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 Index22.22 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index5.12 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.22)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (12.50%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (87.50%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]