LICORICIDIN

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C26H32O5
Molecular Weight	424.5293
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=C(CC=C(C)C)C(O)=CC2=C1C[C@@H](CO2)C3=CC=C(O)C(CC=C(C)C)=C3O

InChI

InChIKey=GBRZTUJCDFSIHM-KRWDZBQOSA-N

InChI=1S/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C26H32O5
Molecular Weight	424.5293
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Reduction of bacterial volatile sulfur compound production by licoricidin and licorisoflavan A from licorice.	2012-03	22368239
Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines.	2000-08-23	10953322

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:10:21 GMT 2025` Edited by `admin` on `Mon Mar 31 22:10:21 GMT 2025`
Record UNII	929XTD20VK
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(+)-LICORICIDIN

Preferred Name

English

LICORICIDIN

Common Name

English

LICORISOFLAVAN B

Common Name

English

7-O-DEMETHYLLICORISOFLAVAN A

Common Name

English

1,3-BENZENEDIOL, 4-((3R)-3,4-DIHYDRO-7-HYDROXY-5-METHOXY-6-(3-METHYL-2-BUTENYL)-2H-1-BENZOPYRAN-3-YL)-2-(3-METHYL-2-BUTENYL)-

Systematic Name

English

Code System Code Type Description

FDA UNII

929XTD20VK

Created by admin on Mon Mar 31 22:10:21 GMT 2025 , Edited by admin on Mon Mar 31 22:10:21 GMT 2025

PRIMARY

CAS

30508-27-1

Created by admin on Mon Mar 31 22:10:21 GMT 2025 , Edited by admin on Mon Mar 31 22:10:21 GMT 2025

PRIMARY

PUBCHEM

480865

Created by admin on Mon Mar 31 22:10:21 GMT 2025 , Edited by admin on Mon Mar 31 22:10:21 GMT 2025

PRIMARY

EPA CompTox

DTXSID30952821

Created by admin on Mon Mar 31 22:10:21 GMT 2025 , Edited by admin on Mon Mar 31 22:10:21 GMT 2025

PRIMARY

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Comments:

LICORICIDIN exhibited antimicrobial activity (MICs 3.13?12.5 mgyml) against MSSAs (strains FDA 209P and Smith) and MRSAs(strains K3 and ST 28).