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=C2C[C@@H](COC2=CC(O)=C1CC=C(C)C)C3=C(O)C(CC=C(C)C)=C(O)C=C3

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 Mar	22368239

Substance Class	Chemical Created by `admin` on `Sat Dec 16 08:33:48 UTC 2023` Edited by `admin` on `Sat Dec 16 08:33:48 UTC 2023`
Record UNII	929XTD20VK
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LICORICIDIN

Common Name

English

LICORISOFLAVAN B

Common Name

English

7-O-DEMETHYLLICORISOFLAVAN A

Common Name

English

(+)-LICORICIDIN

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 Sat Dec 16 08:33:48 UTC 2023 , Edited by admin on Sat Dec 16 08:33:48 UTC 2023

PRIMARY

CAS

30508-27-1

Created by admin on Sat Dec 16 08:33:48 UTC 2023 , Edited by admin on Sat Dec 16 08:33:48 UTC 2023

PRIMARY

PUBCHEM

480865

Created by admin on Sat Dec 16 08:33:48 UTC 2023 , Edited by admin on Sat Dec 16 08:33:48 UTC 2023

PRIMARY

EPA CompTox

DTXSID30952821

Created by admin on Sat Dec 16 08:33:48 UTC 2023 , Edited by admin on Sat Dec 16 08:33:48 UTC 2023

PRIMARY

Related Record Type Details


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PARENT -> CONSTITUENT ALWAYS PRESENT


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GLYCYRRHIZA URALENSIS ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

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).