liquiritin (Q3242316)

(R)-2,3-Dihydro-7-hydroxy-2-[4-(beta-D-glucopyranosyloxy)phenyl]-4H-1-benzopyran-4-one

Liquiritin (English)

8 October 2016

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₁H₂₂O₉

1 reference

Liquiritin (English)

8 October 2016

C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O

1 reference

Liquiritin (English)

8 October 2016

C1[C@H](OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

1 reference

Blockade of the dioxin pathway by herbal medicine Formula Bupleuri Minor: identification of active entities for suppression of AhR activation.

Liquiritin (English)

8 October 2016

9 references

High-performance liquid chromatographic analysis of licorice extracts

Experimental pharmacokinetics of biologically active plant phenolic compounds. II. Pharmacokinetics of likviritin in the rat

Determinatin of nine flavonoids and coumarins in licorice root by high-performance liquid chromatography

Chemical studies of Chinese licorice-roots. I. Elucidation of five new flavonoid constituents from the roots of Glycyrrhiza glabra L. collected in Xinjiang

Phenolic constituents of licorice. IV. Correlation of phenolic constituents and licorice specimens from various sources, and inhibitory effects of licorice extracts on xanthine oxidase and monoamine oxidase

[Quantitative determination of constituents in various licorice roots by means of high performance liquid chromatography]

Quality control of traditional chinese drugs by high performance liquid chromatography.

Über das Flavanon-Glucosid in Glycyrrhiza glabra L. var. glandulifera, Regel et Herder

Artemisia capillaris

1 reference

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris

Glycyrrhiza aspera

1 reference

[Quantitative determination of constituents in various licorice roots by means of high performance liquid chromatography]

Glycyrrhiza inflata

7 references

Effects of flavonoids isolated from licorice roots (Glycyrrhiza inflata Bat.) On degranulation in human polymorphonuclear neutrophils

Effects of flavonoids from licorice roots (Glycyrrhiza inflata Bat.) On arachidonic acid metabolism and aggregation in human platelets

Determinatin of nine flavonoids and coumarins in licorice root by high-performance liquid chromatography

Apioglycyrrhizin and araboglycyrrhizin, two new sweet oleanene-type triterpene oligoglycosides from the root of Glycyrrhiza inflata.

Saponin and sapogenol. XLIX. On the constituents of the roots of Glycyrrhiza inflata Batalin from Xinjiang, China. Characterization of two sweet oleanane-type triterpene oligoglycosides, apioglycyrrhizin and araboglycyrrhizin

Phenolic constituents of licorice. IV. Correlation of phenolic constituents and licorice specimens from various sources, and inhibitory effects of licorice extracts on xanthine oxidase and monoamine oxidase

[Quantitative determination of constituents in various licorice roots by means of high performance liquid chromatography]

Glycyrrhiza uralensis

14 references

Antitussive principles of Glycyrrhizae radix, a main component of the Kampo preparations Bakumondo-to (Mai-men-dong-tang).

Determinatin of nine flavonoids and coumarins in licorice root by high-performance liquid chromatography

Flavonoid glycosides of the roots of Glycyrrhiza uralensis

Saponin and sapogenol. L. On the constituents of the roots of Glycyrrhiza uralensis Fischer from Xinjiang, China. Chemical structures of licorice-saponin L3 and isoliquiritin apioside

Saponin and sapogenol. XLVII. On the constituents of the roots of Glycyrrhiza uralensis Fischer from northeastern China. (1). Licorice-saponins A3, B2, and C2

Phenolic constituents of licorice. VIII. Structures of glicophenone and glicoisoflavanone, and effects of licorice phenolics on methicillin-resistant Staphylococcus aureus

A novel biflavonoid from roots of Glycyrrhiza uralensis cultivated in China

Phenolic constituents of licorice. IV. Correlation of phenolic constituents and licorice specimens from various sources, and inhibitory effects of licorice extracts on xanthine oxidase and monoamine oxidase

[Quantitative determination of constituents in various licorice roots by means of high performance liquid chromatography]

Chemical Investigation of the Crude Drugs Stored in Shosoin for over Twelve Hundred Years

Effect of genotype and environment on five bioactive components of cultivated licorice (Glycyrrhiza uralensis) populations in northern China

Pharmacokinetic and pharmacodynamic profiles of the antitussive principles of Glycyrrhizae radix (licorice), a main component of the Kampo preparation Bakumondo-to (Mai-men-dong-tang).

Inhibition of neuraminidase activity by polyphenol compounds isolated from the roots of Glycyrrhiza uralensis

A Novel Biflavonoid from Roots of Glycyrrhiza uralensis Cultivated in China.

Tetradium glabrifolium

1 reference

Constituents of Leaves of Tetradium Glabrifolium

Polygonum aviculare

1 reference

Flavonoid composition of the herb Polygonum aviculare

Portulaca oleracea

1 reference

A rapid extraction and analysis method for the simultaneous determination of 26 bioflavonoids in Portulaca oleracea L

Commons category

Liquiritin

0 references

Identifiers

InChI

InChI=1S/C21H22O9/c22-9-17-18(25)19(26)20(27)21(30-17)28-12-4-1-10(2-5-12)15-8-14(24)13-6-3-11(23)7-16(13)29-15/h1-7,15,17-23,25-27H,8-9H2/t15-,17+,18+,19-,20+,21+/m0/s1

1 reference

Liquiritin (English)

8 October 2016

2 references

Liquiritin (English)

8 October 2016

ChEBI release 2020-09-01

2 references

liquiritin (English)

8 October 2016

https://commonchemistry.cas.org/detail?cas_rn=551-15-5

10 April 2021

1 reference

Liquiritin (English)

8 October 2016

2 references

English

title

Liquiritin (English)

retrieved

8 October 2016

Reaxys registry number

61653

1 reference

liquiritin (English)

8 October 2016

mapping relation type

2 references

English

title

liquiritin (English)

retrieved

8 October 2016

International Chemical Identifier

InChI

InChI=1S/C21H22O9/c22-9-17-18(25)19(26)20(27)21(30-17)28-12-4-1-10(2-5-12)15-8-14(24)13-6-3-11(23)7-16(13)29-15/h1-7,15,17-23,25-27H,8-9H2/t15-,17+,18+,19-,20+,21+/m0/s1

1 reference

LIQUIRITIN (English)

8 October 2016

2 references

inferred from InChIKey

MSBNK-Univ_Toyama-TY000139

1 reference

MassBank accession ID

0 references

MSBNK-Univ_Toyama-TY000140

0 references

SPLASH

splash10-0a4i-0090000000-5d8899e4eac7a9a20ad9

0 references

splash10-0a4i-0090000000-be8a596c2731ba92bc72

0 references

splash10-0a4i-0090000000-e0ef2b922828538142d6

0 references

DSSTox substance ID

DTXSID40203619

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

2 references

Global Substance Registration System

UNII

T0O79T74CD

English

title

LIQUIRITIN (English)

retrieved

8 October 2016

0 references

1 reference