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Details

Stereochemistry ACHIRAL
Molecular Formula C21H22O5
Molecular Weight 354.3964
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEHYDROGLYASPERIN C

SMILES

COC1=C2C=C(COC2=CC(O)=C1CC=C(C)C)C3=C(O)C=C(O)C=C3

InChI

InChIKey=UACNRZUVCUEUPY-UHFFFAOYSA-N
InChI=1S/C21H22O5/c1-12(2)4-6-16-19(24)10-20-17(21(16)25-3)8-13(11-26-20)15-7-5-14(22)9-18(15)23/h4-5,7-10,22-24H,6,11H2,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A licorice ethanolic extract with peroxisome proliferator-activated receptor-gamma ligand-binding activity affects diabetes in KK-Ay mice, abdominal obesity in diet-induced obese C57BL mice and hypertension in spontaneously hypertensive rats.
2003 Nov
Dehydroglyasperin C isolated from licorice caused Nrf2-mediated induction of detoxifying enzymes.
2010 Feb 10
Neuroprotective effects of dehydroglyasperin C through activation of heme oxygenase-1 in mouse hippocampal cells.
2012 Jun 6
Dehydroglyasperin C, a component of liquorice, attenuates proliferation and migration induced by platelet-derived growth factor in human arterial smooth muscle cells.
2013 Aug 28
Patents
Name Type Language
DEHYDROGLYASPERIN C
Common Name English
1,3-BENZENEDIOL, 4-(7-HYDROXY-5-METHOXY-6-(3-METHYL-2-BUTEN-1-YL)-2H-1-BENZOPYRAN-3-YL)-
Systematic Name English
1,3-BENZENEDIOL, 4-(7-HYDROXY-5-METHOXY-6-(3-METHYL-2-BUTENYL)-2H-1-BENZOPYRAN-3-YL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
480775
Created by admin on Sat Dec 16 08:28:26 GMT 2023 , Edited by admin on Sat Dec 16 08:28:26 GMT 2023
PRIMARY
FDA UNII
80H8MSZ44I
Created by admin on Sat Dec 16 08:28:26 GMT 2023 , Edited by admin on Sat Dec 16 08:28:26 GMT 2023
PRIMARY
CAS
199331-35-6
Created by admin on Sat Dec 16 08:28:26 GMT 2023 , Edited by admin on Sat Dec 16 08:28:26 GMT 2023
PRIMARY