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Details

Stereochemistry RACEMIC
Molecular Formula C15H12O2
Molecular Weight 224.2546
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLAVANONE

SMILES

O=C1CC(OC2=CC=CC=C12)C3=CC=CC=C3

InChI

InChIKey=ZONYXWQDUYMKFB-UHFFFAOYSA-N
InChI=1S/C15H12O2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-9,15H,10H2

HIDE SMILES / InChI
Flavanone is the basic chemical skeleton for the class of compounds known as Flavanoids. Flavonoids are naturally occurring secondary plant metabolites. They are mainly found in cereals and herbs. In the western diet, the estimated daily intake of flavonoids is in the range of 20 -50 mg per day. Flavonoids as a class generally have effects on CYP (P450) activity, and therefore may affect drug metabolisms.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P04798
Gene ID: 1543.0
Gene Symbol: CYP1A1
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
The DNA-repair protein AlkB, EGL-9, and leprecan define new families of 2-oxoglutarate- and iron-dependent dioxygenases.
2001
Localization of flavonoid enzymes in Arabidopsis roots.
2001 Jul
8-dimethylallylnaringenin 2'-hydroxylase, the crucial cytochrome P450 mono-oxygenase for lavandulylated flavanone formation in Sophora flavescens cultured cells.
2001 Nov
Comparative genomics and regulatory evolution: conservation and function of the Chs and Apetala3 promoters.
2001 Oct
Coumaronochromones and flavanones from Euchresta formosana roots.
2002 Aug
Enantiomer separation of flavour and fragrance compounds by liquid chromatography using novel urea-covalent bonded methylated beta-cyclodextrins on silica.
2002 Aug 30
Plant defense genes associated with quantitative resistance to potato late blight in Solanum phureja x dihaploid S. tuberosum hybrids.
2002 Jun
Antidiabetic principles of natural medicines. V. Aldose reductase inhibitors from Myrcia multiflora DC. (2): Structures of myrciacitrins III, IV, and V.
2002 Mar
Differential modulation of UDP-glucuronosyltransferase 1A1 (UGT1A1)-catalyzed estradiol-3-glucuronidation by the addition of UGT1A1 substrates and other compounds to human liver microsomes.
2002 Nov
Duplication and adaptive evolution of the chalcone synthase genes of Dendranthema (Asteraceae).
2002 Oct
Arabidopsis UVR8 regulates ultraviolet-B signal transduction and tolerance and contains sequence similarity to human regulator of chromatin condensation 1.
2002 Sep
Plasma concentrations of the flavonoids hesperetin, naringenin and quercetin in human subjects following their habitual diets, and diets high or low in fruit and vegetables.
2002 Sep
Inhibition of [3H]-LSD binding to 5-HT7 receptors by flavonoids from Scutellaria lateriflora.
2003 Apr
Cholinesterase inhibitory constituents from Onosma hispida.
2003 Apr
Enzymatic formation of unnatural novel polyketides from alternate starter and nonphysiological extension substrate by chalcone synthase.
2003 Apr 17
Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins.
2003 Feb
Arabidopsis ICX1 is a negative regulator of several pathways regulating flavonoid biosynthesis genes.
2003 Feb
Recent advances in the biosynthesis and accumulation of anthocyanins.
2003 Jun
Benzophenone synthase and chalcone synthase from Hypericum androsaemum cell cultures: cDNA cloning, functional expression, and site-directed mutagenesis of two polyketide synthases.
2003 Jun
Activity-guided isolation of the chemical constituents of Muntingia calabura using a quinone reductase induction assay.
2003 Jun
Gradual shifts in sites of free-auxin production during leaf-primordium development and their role in vascular differentiation and leaf morphogenesis in Arabidopsis.
2003 Mar
Tracing floral adaptations from ecology to molecules.
2003 Mar
Influence of industrial processing on orange juice flavanone solubility and transformation to chalcones under gastrointestinal conditions.
2003 May 7
Patents

Sample Use Guides

High-flavanone (305 mg) 100% orange juice and an equicaloric low-flavanone (37 mg) orange-flavored cordial (500 mL) were consumed daily for 8 weeks by 37 healthy older adults. The global cognitive function was significantly better after 8 weeks of consumption relative to controls.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
FLAVANONE
Systematic Name English
4-FLAVANONE
Systematic Name English
NSC-50393
Code English
2-PHENYL-4-CHROMANONE
Systematic Name English
(±)-FLAVANONE
Systematic Name English
FLAVANONE, (±)-
Systematic Name English
2,3-DIHYDRO-2-PHENYL-4H-1-BENZOPYRAN-4-ONE
Systematic Name English
DL-FLAVANONE
Common Name English
4H-1-BENZOPYRAN-4-ONE, 2,3-DIHYDRO-2-PHENYL-
Systematic Name English
PROPAFENONE HYDROCHLORIDE IMPURITY H [EP IMPURITY]
Common Name English
Code System Code Type Description
CAS
487-26-3
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
PRIMARY
NSC
50393
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-654-8
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
PRIMARY
CHEBI
5070
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
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FDA UNII
WX22P730FB
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
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PUBCHEM
10251
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
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EPA CompTox
DTXSID9022318
Created by admin on Sat Dec 16 09:05:29 GMT 2023 , Edited by admin on Sat Dec 16 09:05:29 GMT 2023
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