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Details

Stereochemistry ACHIRAL
Molecular Formula C16H12O6
Molecular Weight 300.2629
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRATENSEIN

SMILES

COC1=CC=C(C=C1O)C2=COC3=C(C2=O)C(O)=CC(O)=C3

InChI

InChIKey=FPIOBTBNRZPWJW-UHFFFAOYSA-N
InChI=1S/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Flavonoids and isoflavonoids from Sophorae Flos improve glucose uptake in vitro.
2010-01
Characterization of the isoflavone pratensein as a novel transcriptional up-regulator of scavenger receptor class B type I in HepG2 cells.
2009-07
Protective effect of isoflavones from Trifolium pratense on dopaminergic neurons.
2008-10
Identification of upregulators of human ATP-binding cassette transporter A1 via high-throughput screening of a synthetic and natural compound library.
2008-08
NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis.
2008-01
Identification of novel human high-density lipoprotein receptor Up-regulators using a cell-based high-throughput screening assay.
2007-03
Isoflavone profiles of red clovers and their distribution in different parts harvested at different growing stages.
2006-08-09
Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus.
2006-07
Determination of isoflavones in dietary supplements containing soy, Red Clover and kudzu: extraction followed by basic or acid hydrolysis.
2006-02-24
Determination of isoflavones in red clover and related species by high-performance liquid chromatography combined with ultraviolet and mass spectrometric detection.
2003-10-24
Patents

Patents

Name Type Language
3',5,7-TRIHYDROXY-4'-METHOXYISOFLAVONE
Preferred Name English
PRATENSEIN
MI  
Common Name English
PRATENSEIN [MI]
Common Name English
5,7-DIHYDROXY-3-(3-HYDROXY-4-METHOXYPHENYL)-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
PRATENSEIN
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID60177388
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
CHEBI
61323
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
FDA UNII
D2CF8CJ6AP
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
CHEBI
8359
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
CAS
2284-31-3
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
PUBCHEM
5281803
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY
MERCK INDEX
m9104
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY Merck Index
MESH
C543998
Created by admin on Mon Mar 31 19:29:01 GMT 2025 , Edited by admin on Mon Mar 31 19:29:01 GMT 2025
PRIMARY