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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

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Aspects of the metabolism of the peripheral vasodilator mecinarone (14C-6809 MD) in rat, dog and man.
1980
Commonly occurring plant flavonoids have estrogenic activity.
1993 Jul
Inhibition of HIV activation in latently infected cells by flavonoid compounds.
1996 Jan 1
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 Nov 2
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003 Oct
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Synthesis, antimycobacterial activity evaluation, and QSAR studies of chalcone derivatives.
2007 Mar 15
Anti-tumor effects by a synthetic chalcone compound is mediated by c-Myc-mediated reactive oxygen species production.
2010 Oct 6
Inhibitory effects of aurentiacin from Syzygium samarangense on lipopolysaccharide-induced inflammatory response in mouse macrophages.
2012 Mar
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 Feb
Patents

Patents

20030054952
2
20040048858
2
JP1013019A
2
JP2001019696A
2
JP2001294768A
2
JP2002237386A
2
JP2004323469A
2
JP2007131653A
2
JP2007326872A
2
JP2007516189A
4
JP2008106011A
4
JP2008106013A
5
JP2009240193A
2
JP2010022323A
2
JP2010138192A
2
JP2011513308A
2
JPH02300120A
2
JPH0558885A
2
JPH06279671A
2
JPH1026760A
2
JPH1175851A
2
JPS5419947A
2
JPS5419949A
2
JPS60178815A
2
JPS62192404A
2
JPS63150241A
2
JPS63267749A
2
Name Type Language
CHALCONE
MI  
Systematic 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
NSC-167107
Code 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 Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
ALTERNATIVE
CHEBI
27618
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
CHEBI
48965
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
PUBCHEM
637760
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
DAILYMED
5S5A2Q39HX
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
NSC
4523
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
CAS
614-47-1
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
NSC
167107
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID8022531
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-330-2
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
RXCUI
2592960
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
CAS
94-41-7
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
MERCK INDEX
m3306
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY Merck Index
NSC
26612
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
WIKIPEDIA
CHALCONE
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
MESH
D002599
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
FDA UNII
5S5A2Q39HX
Created by admin on Fri Dec 15 18:37:12 GMT 2023 , Edited by admin on Fri Dec 15 18:37:12 GMT 2023
PRIMARY
ACTIVE MOIETY
Structure of CHALCONE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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