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Details

Stereochemistry ACHIRAL
Molecular Formula C15H12O
Molecular Weight 208.2552
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CHALCONE

SMILES

O=C(\C=C\C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=DQFBYFPFKXHELB-VAWYXSNFSA-N
InChI=1S/C15H12O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-12H/b12-11+

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein.
2015-02
2-Hydroxychalcone and xanthohumol inhibit invasion of triple negative breast cancer cells.
2013-05-25
Rat α-Fetoprotein binding affinities of a large set of structurally diverse chemicals elucidated the relationships between structures and binding affinities.
2012-11-19
Inhibitory effects of aurentiacin from Syzygium samarangense on lipopolysaccharide-induced inflammatory response in mouse macrophages.
2012-03
Anti-tumor effects by a synthetic chalcone compound is mediated by c-Myc-mediated reactive oxygen species production.
2010-10-06
Chalcone inhibits the activation of NF-kappaB and STAT3 in endothelial cells via endogenous electrophile.
2007-03-20
Synthesis, antimycobacterial activity evaluation, and QSAR studies of chalcone derivatives.
2007-03-15
Study on the substituents' effects of a series of synthetic chalcones against the yeast Candida albicans.
2007-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Metabolism of the alpha,beta-unsaturated ketones, chalcone and trans-4-phenyl-3-buten-2-one, by rat liver microsomes and estrogenic activity of the metabolites.
2005-08
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Antioxidative function and substrate specificity of NAD(P)H-dependent alkenal/one oxidoreductase. A new role for leukotriene B4 12-hydroxydehydrogenase/15-oxoprostaglandin 13-reductase.
2001-11-02
In vitro antifungal evaluation and structure-activity relationships of a new series of chalcone derivatives and synthetic analogues, with inhibitory properties against polymers of the fungal cell wall.
2001-08
Inhibition of HIV activation in latently infected cells by flavonoid compounds.
1996-01-01
Commonly occurring plant flavonoids have estrogenic activity.
1993-07
Aspects of the metabolism of the peripheral vasodilator mecinarone (14C-6809 MD) in rat, dog and man.
1980
Patents
Name Type Language
CHALCONE
MI  
Systematic Name English
NSC-167107
Preferred Name English
NSC-26612
Code English
CINNAMOPHENONE
Systematic Name English
(E)-CHALCONE
Systematic Name English
CHALCONE, (E)-
Systematic Name English
BENZALACETOPHENONE
Systematic Name English
BENZYLIDENEACETOPHENONE
Systematic Name English
CHALCONE [MI]
Common Name English
CHALCONE (E)-FORM [MI]
Common Name English
NSC-4523
Code English
PHENYL (E)-2-PHENYLETHENYL KETONE
Systematic Name English
PHENYL 2-PHENYLVINYL KETONE
Systematic Name English
1,3-DIPHENYL-2-PROPEN-1-ONE
Systematic Name English
PHENYL STYRYL KETONE
Systematic Name English
2-PROPEN-1-ONE, 1,3-DIPHENYL-
Systematic Name English
CHALKONE
Common Name English
PHENYL TRANS-STYRYL KETONE
Systematic Name English
3-PHENYLACRYLOPHENONE
Systematic Name English
PHENYL (E)-STYRYL KETONE
Systematic Name English
2-PROPEN-1-ONE, 1,3-DIPHENYL-, (2E)-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
210-383-8
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
ALTERNATIVE
CHEBI
27618
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
CHEBI
48965
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
PUBCHEM
637760
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
DAILYMED
5S5A2Q39HX
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
NSC
4523
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
CAS
614-47-1
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
NSC
167107
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-330-2
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID20873536
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
RXCUI
2592960
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
CAS
94-41-7
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
MERCK INDEX
m3306
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY Merck Index
NSC
26612
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
WIKIPEDIA
CHALCONE
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
MESH
D002599
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY
FDA UNII
5S5A2Q39HX
Created by admin on Mon Mar 31 19:17:06 GMT 2025 , Edited by admin on Mon Mar 31 19:17:06 GMT 2025
PRIMARY