U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C15H12O2
Molecular Weight 224.2546
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYCHALCONE

SMILES

OC1=CC=C(\C=C\C(=O)C2=CC=CC=C2)C=C1

InChI

InChIKey=PWWCDTYUYPOAIU-DHZHZOJOSA-N
InChI=1S/C15H12O2/c16-14-9-6-12(7-10-14)8-11-15(17)13-4-2-1-3-5-13/h1-11,16H/b11-8+

HIDE SMILES / InChI
4-Hydroxychalcone is found in herbs and spices. 4-Hydroxychalcone is a constituent of Glycyrrhiza glabra (licorice) roots. 4-hydroxychalcone is a 17beta-hydroxysteroid dehydrogenase inhibitor. 4-hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. Treatment with 40 mg/kg 4HCH reduced systolic hypertension, serum IL-1β, and TNF-α levels and suppressed the activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and renal injury. The impact of 4-Hydroxychalcone on the hyperaldosteronism, inflammation, and kidney injury provides new insights for the future development of therapeutic strategies in resistant hypertension.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: 17beta-hydroxysteroid dehydrogenase
16.0 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003 Oct
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 Aug
Hydroxychalcones exhibit differential effects on XRE transactivation.
2005 Feb 14
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Rat α-Fetoprotein binding affinities of a large set of structurally diverse chemicals elucidated the relationships between structures and binding affinities.
2012 Nov 19
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

Sample Use Guides

The cryptochrome-null mice received high-salt treatment and were treated orally with 4-hydroxychalcone (4HCH) 10 mg/kg, 4HCH 20 mg/kg, and 4HCH 40 mg/kg, respectively.
Route of Administration: Oral
4-hydroxychalcone (22 ug/ml) suppressed several steps of angiogenesis, including endothelial cell proliferation, migration and tube formation without showing any signs of cytotoxicity. 4-hydroxychalcone significantly suppressed both VEGF/TNF-a- and bFGF/TNF-a-induced endothelial tube formation when tested at the concentration of 22 ug/ml in hMVEC.
Name Type Language
4-HYDROXYCHALCONE
Systematic Name English
4-HYDROXYSTYRYL PHENYL KETONE
Systematic Name English
2-PROPEN-1-ONE, 3-(4-HYDROXYPHENYL)-1-PHENYL-
Systematic Name English
2-PROPEN-1-ONE, 3-(4-HYDROXYPHENYL)-1-PHENYL-, (2E)-
Systematic Name English
1-PHENYL-3-(4-HYDROXYPHENYL)-2-PROPEN-1-ONE
Systematic Name English
TRANS-4-HYDROXYCHALCONE
Systematic Name English
(2E)-3-(4-HYDROXYPHENYL)-1-PHENYLPROP-2-EN-1-ONE
Systematic Name English
(E)-3-(4-HYDROXYPHENYL)-1-PHENYL-2-PROPEN-1-ONE
Systematic Name English
CHALCONE, 4-HYDROXY-
Systematic Name English
(E)-4-HYDROXYCHALCONE
Systematic Name English
(4-HYDROXYBENZYLIDENE)ACETOPHENONE
Systematic Name English
3-(4-HYDROXYPHENYL)-1-PHENYL-2-PROPEN-1-ONE
Systematic Name English
NSC-170282
Code English
(4-HYDROXYBENZAL)ACETOPHENONE
Systematic Name English
NSC-60593
Code English
2-PROPEN-1-ONE, 3-(4-HYDROXYPHENYL)-1-PHENYL-, (E)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID3022453
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
CAS
20426-12-4
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
CAS
38239-55-3
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
FDA UNII
JO97Q47VBU
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
NSC
60593
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
NSC
170282
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
CHEBI
34423
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY
PUBCHEM
5282361
Created by admin on Sat Dec 16 05:51:49 GMT 2023 , Edited by admin on Sat Dec 16 05:51:49 GMT 2023
PRIMARY