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Details

Stereochemistry ACHIRAL
Molecular Formula C20H16O5
Molecular Weight 336.338
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALPINUMISOFLAVONE

SMILES

CC1(C)OC2=CC3=C(C(=O)C(=CO3)C4=CC=C(O)C=C4)C(O)=C2C=C1

InChI

InChIKey=RQAMSFTXEFSBPK-UHFFFAOYSA-N
InChI=1S/C20H16O5/c1-20(2)8-7-13-15(25-20)9-16-17(18(13)22)19(23)14(10-24-16)11-3-5-12(21)6-4-11/h3-10,21-22H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
The anticancer potential of flavonoids isolated from the stem bark of Erythrina suberosa through induction of apoptosis and inhibition of STAT signaling pathway in human leukemia HL-60 cells.
2013-09-25
Isoflavone dimers and other bioactive constituents from the figs of Ficus mucuso.
2011-06-24
Lupin pyranoisoflavones inhibiting hyphal development in arbuscular mycorrhizal fungi.
2010-11
Cameroonian medicinal plants: pharmacology and derived natural products.
2010
Isoflavonoids from Erythrina poeppigiana: evaluation of their binding affinity for the estrogen receptor.
2009-09
Genistein-derivatives from Tetracera scandens stimulate glucose-uptake in L6 myotubes.
2009-03
Methylalpinumisoflavone inhibits hypoxia-inducible factor-1 (HIF-1) activation by simultaneously targeting multiple pathways.
2009-02-27
Prenylisoflavonoids from Erythrina senegalensis as novel HIV-1 protease inhibitors.
2009-02
Diacylglycerol acyltransferase-inhibitory compounds from Erythrina senegalensis.
2009-01
Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).
2008-10-30
Alpinumisoflavone.
2008-03-14
Ethnopharmacological uses of Erythrina senegalensis: a comparison of three areas in Mali, and a link between traditional knowledge and modern biological science.
2008-03-05
Isoflavones from Ficus nymphaefolia.
2007-05
Protein tyrosine phosphatase-1B inhibitory activity of isoprenylated flavonoids isolated from Erythrina mildbraedii.
2006-11
Invariom structure refinement, electrostatic potential and toxicity of 4-O-methylalpinumisoflavone, O,O-dimethylalpinumisoflavone and 5-O-methyl-4-O-(3-methylbut-2-en-1-yl)alpinumisoflavone.
2006-10
Monoamine oxidase inhibitory constituents from the fruits of Cudrania tricuspidata.
2005-12
Phospholipase Cgamma1 inhibitory activities of prenylated flavonoids isolated from Erythrina senegalensis.
2005-08
Prenylated flavonoids of Erythrina lysistemon grown in Egypt.
2002-08
Antischistosomal bioactivity of isoflavonoids from Millettia thonningii (Leguminosae).
2002-02
Erythrinan alkaloids and isoflavonoids from Erythrina poeppigiana.
2001-12
Cytotoxic isoflavones from Erythrina indica.
2001-12
Inhibition of Site I mitochondrial electron transport by an extract of the seeds of Millettia thonningii: a potential mechanism for the plant's molluscicidal and schistosome larvicidal activity.
2001-09
Name Type Language
ALPINUMISOFLAVONE
Common Name English
5-HYDROXY-3-(4-HYDROXYPHENYL)-8,8-DIMETHYLPYRANO(3,2-G)CHROMEN-4-ONE
Preferred Name English
Code System Code Type Description
FDA UNII
6Q33HOF94Z
Created by admin on Mon Mar 31 19:25:55 GMT 2025 , Edited by admin on Mon Mar 31 19:25:55 GMT 2025
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EPA CompTox
DTXSID00187683
Created by admin on Mon Mar 31 19:25:55 GMT 2025 , Edited by admin on Mon Mar 31 19:25:55 GMT 2025
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CAS
34086-50-5
Created by admin on Mon Mar 31 19:25:55 GMT 2025 , Edited by admin on Mon Mar 31 19:25:55 GMT 2025
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PUBCHEM
5490139
Created by admin on Mon Mar 31 19:25:55 GMT 2025 , Edited by admin on Mon Mar 31 19:25:55 GMT 2025
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WIKIPEDIA
ALPINUMISOFLAVONE
Created by admin on Mon Mar 31 19:25:55 GMT 2025 , Edited by admin on Mon Mar 31 19:25:55 GMT 2025
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