Naringenin chalcone: Difference between revisions

Naringenin chalcone
Names
	Preferred IUPAC name 2′,4,4′,6′-Tetrahydroxychalcone
	Other names Chalconaringenin; Isosalipurpol
Identifiers
CAS Number	25515-46-2 ; 73692-50-9 (non-specific) ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:15413;
ChemSpider	4444447;
KEGG	C06561;
PubChem CID	5280960;
UNII	YCF6Z24AS2 ;
CompTox Dashboard (EPA)	DTXSID101043553 ;
	InChI InChI=1S/C15H12O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14(15)20/h1-8,16-17,19-20H/b6-3+ Key: YQHMWTPYORBCMF-ZZXKWVIFSA-N;
	SMILES C1=CC(=CC=C1/C=C/C(=O)C2=C(C=C(C=C2O)O)O)O;
Properties
Chemical formula	C15H12O5
Molar mass	272.256 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Revision as of 11:47, 24 November 2023

Naringenin chalcone^[1] is a common chalconoid (or chalcone, not to be confused with the compound chalcone). It is synthesized from 4-coumaroyl-CoA and malonyl-CoA by chalcone synthase (CHS), a key enzyme in the phenylpropanoid pathway. Naringenin chalcone can spontaneously cyclize to naringenin (a flavanone). In plant cells, this process is catalyzed by chalcone isomerase.

About Naringenin chalcone

Naringenin chalcone is an intermediate in flavonol biosynthesis, spontaneously metabolizing into naringenin (NAR) through the action of chalcone isomerase. Naringenin chalcone exhibits anti-inflammatory and antiallergic activities.

References

^ PubChem. "Naringenin chalcone". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-08-27.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] PubChem. "Naringenin chalcone". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-08-27.

[1]

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 '''Naringenin chalcone'''<ref>{{Cite web |last=PubChem |title=Naringenin chalcone |url=https://pubchem.ncbi.nlm.nih.gov/compound/5280960 |access-date=2022-08-27 |website=pubchem.ncbi.nlm.nih.gov |language=en}}</ref> is a common [[chalconoid]] (or chalcone, not to be confused with the compound [[chalcone]]). It is synthesized from [[4-coumaroyl-CoA]] and [[malonyl-CoA]] by [[chalcone synthase]] (CHS), a key enzyme in the [[phenylpropanoid pathway]]. Naringenin chalcone can spontaneously [[Cyclization reaction|cyclize]] to [[naringenin]] (a [[flavanone]]). In plant cells, this process is catalyzed by [[chalcone isomerase]].
+== About Naringenin chalcone ==
+[https://www.medchemexpress.com/naringenin-chalcone.html Naringenin chalcone] is an intermediate in flavonol biosynthesis, spontaneously metabolizing into naringenin (NAR) through the action of chalcone isomerase. Naringenin chalcone exhibits anti-inflammatory and antiallergic activities.
 ==References==