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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

Molecular Formula C20H16O5
Molecular Weight 336.338
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Erythrinan alkaloids and isoflavonoids from Erythrina poeppigiana.
2001 Dec
Cytotoxic isoflavones from Erythrina indica.
2001 Dec
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 Sep
Prenylated flavonoids of Erythrina lysistemon grown in Egypt.
2002 Aug
Antischistosomal bioactivity of isoflavonoids from Millettia thonningii (Leguminosae).
2002 Feb
Protein tyrosine phosphatase-1B inhibitory activity of isoprenylated flavonoids isolated from Erythrina mildbraedii.
2006 Nov
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 Oct
Isoflavones from Ficus nymphaefolia.
2007 May
Alpinumisoflavone.
2008 Mar 14
Ethnopharmacological uses of Erythrina senegalensis: a comparison of three areas in Mali, and a link between traditional knowledge and modern biological science.
2008 Mar 5
Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae).
2008 Oct 30
Prenylisoflavonoids from Erythrina senegalensis as novel HIV-1 protease inhibitors.
2009 Feb
Methylalpinumisoflavone inhibits hypoxia-inducible factor-1 (HIF-1) activation by simultaneously targeting multiple pathways.
2009 Feb 27
Diacylglycerol acyltransferase-inhibitory compounds from Erythrina senegalensis.
2009 Jan
Genistein-derivatives from Tetracera scandens stimulate glucose-uptake in L6 myotubes.
2009 Mar
Isoflavonoids from Erythrina poeppigiana: evaluation of their binding affinity for the estrogen receptor.
2009 Sep
Cameroonian medicinal plants: pharmacology and derived natural products.
2010
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 Sep 25
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:54:44 GMT 2023
Edited
by admin
on Fri Dec 15 18:54:44 GMT 2023
Record UNII
6Q33HOF94Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALPINUMISOFLAVONE
Common Name English
5-HYDROXY-3-(4-HYDROXYPHENYL)-8,8-DIMETHYLPYRANO(3,2-G)CHROMEN-4-ONE
Systematic Name English
Code System Code Type Description
FDA UNII
6Q33HOF94Z
Created by admin on Fri Dec 15 18:54:44 GMT 2023 , Edited by admin on Fri Dec 15 18:54:44 GMT 2023
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EPA CompTox
DTXSID00187683
Created by admin on Fri Dec 15 18:54:44 GMT 2023 , Edited by admin on Fri Dec 15 18:54:44 GMT 2023
PRIMARY
CAS
34086-50-5
Created by admin on Fri Dec 15 18:54:44 GMT 2023 , Edited by admin on Fri Dec 15 18:54:44 GMT 2023
PRIMARY
PUBCHEM
5490139
Created by admin on Fri Dec 15 18:54:44 GMT 2023 , Edited by admin on Fri Dec 15 18:54:44 GMT 2023
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WIKIPEDIA
ALPINUMISOFLAVONE
Created by admin on Fri Dec 15 18:54:44 GMT 2023 , Edited by admin on Fri Dec 15 18:54:44 GMT 2023
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