Isolicoflavonol

Details

Stereochemistry	ACHIRAL
Molecular Formula	C20H18O6
Molecular Weight	354.3533
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(C)=CCC1=C(O)C=CC(=C1)C2=C(O)C(=O)C3=C(O2)C=C(O)C=C3O

InChI

InChIKey=PGCKDCPTJAQQSQ-UHFFFAOYSA-N

InChI=1S/C20H18O6/c1-10(2)3-4-11-7-12(5-6-14(11)22)20-19(25)18(24)17-15(23)8-13(21)9-16(17)26-20/h3,5-9,21-23,25H,4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C20H18O6
Molecular Weight	354.3533
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 09:55:55 UTC 2023` Edited by `admin` on `Sat Dec 16 09:55:55 UTC 2023`
Record UNII	355E7H7EHH
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Isolicoflavonol

Common Name

English

4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-

Systematic Name

English

3,5,7-Trihydroxy-2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-4H-1-benzopyran-4-one

Systematic Name

English

3,5,7-Trihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one

Systematic Name

English

4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-

Systematic Name

English

Code System Code Type Description

CAS

94805-83-1

Created by admin on Sat Dec 16 09:55:55 UTC 2023 , Edited by admin on Sat Dec 16 09:55:55 UTC 2023

PRIMARY

PUBCHEM

5318585

Created by admin on Sat Dec 16 09:55:55 UTC 2023 , Edited by admin on Sat Dec 16 09:55:55 UTC 2023

PRIMARY

EPA CompTox

DTXSID801317129

Created by admin on Sat Dec 16 09:55:55 UTC 2023 , Edited by admin on Sat Dec 16 09:55:55 UTC 2023

PRIMARY

FDA UNII

355E7H7EHH

Created by admin on Sat Dec 16 09:55:55 UTC 2023 , Edited by admin on Sat Dec 16 09:55:55 UTC 2023

PRIMARY

Related Record Type Details


					42B5YD8F0K

GLYCYRRHIZA URALENSIS ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

ISOLICOFLAVONOL showed antibacterial activity against MSSAs (strains FDA 209P and Smith) and MRSAs(strains K3 and ST 28) (MICs1.56?25 ug/ml). This compound exhibited antimicrobial activity against Micrococcus luteus ATCC 9341 and Bacillus subtilis PCI 219 (MICs3.13?25 ug/ml) but not against Klebsiella pneumoniae PCI 602 and Pseudomonas aeruginosa IFO 3445.

Amount: