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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H28O4
Molecular Weight 392.4874
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLABROL

SMILES

CC(C)=CCC1=CC(=CC=C1O)[C@@H]2CC(=O)C3=C(O2)C(CC=C(C)C)=C(O)C=C3

InChI

InChIKey=CUFAXDWQDQQKFF-DEOSSOPVSA-N
InChI=1S/C25H28O4/c1-15(2)5-7-17-13-18(8-11-21(17)26)24-14-23(28)20-10-12-22(27)19(25(20)29-24)9-6-16(3)4/h5-6,8,10-13,24,26-27H,7,9,14H2,1-4H3/t24-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
[Chemical constituents of flavonoids from rhizome of Sophora tonkinensis].
2009 Feb
Inhibitory activity of diacylglycerol acyltransferase by glabrol isolated from the roots of licorice.
2010 Feb
Phenolics from Glycyrrhiza glabra roots and their PPAR-gamma ligand-binding activity.
2010 Jan 15
Name Type Language
GLABROL
Common Name English
4H-1-BENZOPYRAN-4-ONE, 2,3-DIHYDRO-7-HYDROXY-2-(4-HYDROXY-3-(3-METHYL-2-BUTEN-1-YL)PHENYL)-8-(3-METHYL-2-BUTEN-1-YL)-, (2S)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID50975274
Created by admin on Sat Dec 16 08:46:07 GMT 2023 , Edited by admin on Sat Dec 16 08:46:07 GMT 2023
PRIMARY
CAS
59870-65-4
Created by admin on Sat Dec 16 08:46:07 GMT 2023 , Edited by admin on Sat Dec 16 08:46:07 GMT 2023
PRIMARY
PUBCHEM
11596309
Created by admin on Sat Dec 16 08:46:07 GMT 2023 , Edited by admin on Sat Dec 16 08:46:07 GMT 2023
PRIMARY
FDA UNII
E4XEY076JN
Created by admin on Sat Dec 16 08:46:07 GMT 2023 , Edited by admin on Sat Dec 16 08:46:07 GMT 2023
PRIMARY