GLABROL

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

SMILES

CC(C)=CCC1=CC(=CC=C1O)[C@@H]2CC(=O)C3=CC=C(O)C(CC=C(C)C)=C3O2

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

Show entries

Title	Date	PubMed
[Chemical constituents of flavonoids from rhizome of Sophora tonkinensis].	2009 Feb	19445149
Inhibitory activity of diacylglycerol acyltransferase by glabrol isolated from the roots of licorice.	2010 Feb	20195824
Phenolics from Glycyrrhiza glabra roots and their PPAR-gamma ligand-binding activity.	2010 Jan 15	20022509

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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)-

Preferred Name

English

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Code System

Code

Type

Description

EPA CompTox

DTXSID50975274

PRIMARY

CAS

59870-65-4

PRIMARY

PUBCHEM

11596309

PRIMARY

FDA UNII

E4XEY076JN

PRIMARY

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SUBSTANCE RECORD


					E4XEY076JN

GLABROL