(Q6557526)

Gene Ontology release 2020-05-02

Rhea release 113

mass

256.074±0 dalton

1 reference

Liquiritigenin (English)

19 October 2016

chemical formula

C₁₅H₁₂O₄

1 reference

Liquiritigenin (English)

20 November 2016

canonical SMILES

C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O

1 reference

Liquiritigenin (English)

20 November 2016

isomeric SMILES

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

1 reference

[Application of supercritical fluid extraction to components of crude drugs and plants. III. Extraction of pigments from lithospermum root and licorice root]

Liquiritigenin (English)

20 November 2016

4 references

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

In vitro and in vivo antiallergic effects of Glycyrrhiza glabra and its components

Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra.

Butea monosperma

1 reference

Bioactive flavonoids of the flowers of Butea monosperma

Baptisia lecontei

1 reference

The identification of twenty-three 5-deoxy- and ten 5-hydroxy-flavonoids from Baptisia lecontei (leguminosae)

Brosimum acutifolium

2 references

Flavonoids from Brosimum acutifolium

Brosimacutins A-I, nine new flavonoids from Brosimum acutifolium.

Centrolobium robustum

1 reference

Diarylheptanoid and other phenolic constituents of Centrolobium species

Clausena excavata

2 references

Alkaloidal and other constituents from the root bark of Clausena excavata

Two coumarins from the root bark of Clausena excavata

Crinum bulbispermum

1 reference

Minor phenolics from Crinum bulbispermum bulbs

Dalbergia ecastaphyllum

1 reference

Flavonoids from Dalbergia ecastophyllum

Dalbergia odorifera

3 references

Three new flavonoids and antiallergic, anti-inflammatory constituents from the heartwood of Dalbergia odorifera.

Liquid chromatography/electrospray ionization mass spectrometry for the characterization of twenty-three flavonoids in the extract of Dalbergia odorifera

Isoflavan and related compounds from Dalbergia odorifera. I.

Dracaena draco

1 reference

Phenolic compounds of Dragon's blood from Dracaena draco

Erythrina fusca

2 references

A New Pterocarpan from Erythrina fusca

Fuscacarpans A-C, new pterocarpans from the stems of Erythrina fusca

Glycyrrhiza pallidiflora

2 references

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

Flavonoids and isoflavonoids of chemotaxonomic significance from Glycyrrhiza pallidiflora (Leguminosae)

Lespedeza cyrtobotrya

1 reference

Melanin synthesis inhibitors from Lespedeza cyrtobotrya

Melilotus altissimus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus dentatus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus elegans

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus infestus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus neapolitanus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus sulcatus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus polonicus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus tauricus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus wolgicus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Onobrychis viciifolia

1 reference

Flavonoid and Isoflavonoid Compounds from Leaves of Sainfoin (Onobrychis vicii folia )

Pancratium maritimum

1 reference

Acetophenones, a chalcone, a chromone and flavonoids from Pancratium maritimum

Peltogyne paniculata

1 reference

(+)-2,3-Trans-pubeschin, the first catechin analogue of peltogynoids from Peltogyne pubescens and P. venosa

Peltogyne venosa

1 reference

(+)-2,3-Trans-pubeschin, the first catechin analogue of peltogynoids from Peltogyne pubescens and P. venosa

Pericopsis elata

1 reference

Phytochemical examination of Pericopsis species

Pericopsis mooniana

1 reference

Phytochemical examination of Pericopsis species

pea

1 reference

Chromatographic analysis of isoflavonoid accumulation in stressed Pisum sativum

Pterocarpus angolensis

1 reference

A novel α-hydroxydihydrochalcone from the heartwood of Pterocarpus angolensis D.C.: absolute configuration, synthesis, photochemical transformations, and conversion into α-methyldeoxybenzoins

Pterocarpus macrocarpus

1 reference

Macrocarposide, a new isoflavanone c-glucoside from Pterocarpus macrocarpus heart wood

Spatholobus suberectus

1 reference

Bioactive constituents of Spatholobus suberectus in regulating tyrosinase-related proteins and mRNA in HEMn cells

Trifolium subterraneum

1 reference

Flavonoids in genotypes of Trifolium subterraneum—I

Umtiza listerana

1 reference

O-(Dihydrobenzofuranyl)-dibenzo-α-pyrones from Umtiza listerana

Acalypha wilkesiana

2 references

Phytochemical and biological studies of Abies species

PHYTOCHEMICAL AND BIOLOGICAL STUDIES ON TWO ACALYPHA SPECIES

Calea platylepis

1 reference

Constituents of Calea platylepis Sch. Bip. ex Baker

Dalbergia louvelii

1 reference

Flavonoids from Dalbergia louvelii and their antiplasmodial activity.

Dalbergia nitidula

1 reference

An isoflavanoid-neoflavonoid and an O-methylated isoflavone from the heartwood of Dalbergia nitidula

Dalbergia parviflora

2 references

Flavonoids from the heartwood of the Thai medicinal plant Dalbergia parviflora and their effects on estrogenic-responsive human breast cancer cells

Bioactive constituents from the stems of Dalbergia parviflora

Dalbergia sissoides

1 reference

Chemical constituents of Dalbergia odorifera

Glycyrrhiza echinata

2 references

NAD(P)H-dependent 6′-deoxychalcone synthase activity in Glycyrrhiza echinata cells induced by yeast extract

Licodione Synthase, a Cytochrome P450 Monooxygenase Catalyzing 2-Hydroxylation of 5-Deoxyflavanone, in Cultured Glycyrrhiza echinata L. Cells

Glycyrrhiza inflata

5 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

Inhibitory effect of chalcones and their derivatives from Glycyrrhiza inflata on protein tyrosine phosphatase 1B.

Screening for bioactive natural products from a 67-compound library of Glycyrrhiza inflata

Glycyrrhiza uralensis

12 references

Phenolics with PPAR-γ Ligand-Binding Activity Obtained from Licorice (Glycyrrhiza uralensis Roots) and Ameliorative Effects of Glycyrin on Genetically Diabetic KK-Ay Mice.

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

Formation of chalcones and isoflavones by callus culture of Glycyrrhiza uralensis with different production patterns.

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

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

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).

Phenolics with PPAR-gamma ligand-binding activity obtained from licorice (Glycyrrhiza uralensis roots) and ameliorative effects of glycyrin on genetically diabetic KK-A(y) mice

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

Antithrombotic phenolic compounds from Glycyrrhiza uralensis

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

Hedysarum polybotrys

1 reference

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Isatis tinctoria

1 reference

Chemical consitituents from root of Isatis indigotica

Luxemburgia octandra

1 reference

Luxenchalcone, a new bichalcone and other constituents from Luxemburgia octandra

Oxytropis trichophysa

1 reference

A chemical study of plants of the Mongolian flora the flavonoids of two species of Oxytropis

Physochlaina physaloides

1 reference

Flavonoids and sterols of Physochlaina physaloides

Platymiscium yucatanum

1 reference

Flavonoids and Isoflavonoids with Antifungal Properties fromPlatymiscium yucatanumHeartwood

Pterocarpus marsupium

4 references

Flavonoid analogues from Pterocarpus species

Constituents of Pterocarpus marsupium

Antihyperlipidemic effect of flavonoids from Pterocarpus marsupium

Structure Elucidation of Pterosupin from Pterocarpus marsupium, the First Naturally Occurring C-Glycosyl-β-hydroxy-dihydrochalcone

Pterocarpus santalinus

1 reference

An isoflavone from Pterocarpus santalinus

Robinia pseudoacacia

1 reference

The Constituents of the Heartwood of Robinia Pseudoacacia

Sesbania rostrata

1 reference

7,4'-Dihydroxyflavanone Is the MajorAzorhizobium nodGene-Inducing Factor Present inSesbania rostrataSeedling Exudate

Sinofranchetia chinensis

1 reference

Inhibition of xanthine oxidase by liquiritigenin and isoliquiritigenin isolated from Sinofranchetia chinensis

Virgilia oroboides

1 reference

Flavonoids and isoflavonoids from the heartwood ofVirgilia oroboides

Xanthorrhoea glauca

1 reference

Xanthorrhoea johnsonii

1 reference

Xanthorrhoea latifolia

1 reference

Xanthorrhoea resinosa

1 reference

Platymiscium floribundum

1 reference

Cytotoxic flavonoids from Platymiscium floribundum

Medicago truncatula

1 reference

Metabolic profiling and systematic identification of flavonoids and isoflavonoids in roots and cell suspension cultures of Medicago truncatula using HPLC-UV-ESI-MS and GC-MS.

Astragalus microcephalus

1 reference

Flavonoids from Astragalus microcephalus

Maackia amurensis

1 reference

Minor polyphenols from Maackia amurensis wood

Melilotus messanensis

1 reference

1 reference

2 references

Flavonoids in the poisonous plant Oxytropis falcata

Flavonoid aglycones of Oxytropis falcata

Calea mediterranea

1 reference

Constituents of Calea platylepis Sch. Bip. ex Baker

Dioscorea nipponica

1 reference

Phenolic derivatives from the rhizomes of Dioscorea nipponica and their anti-neuroinflammatory and neuroprotective activities

Acalypha marginata

2 references

Phytochemical and biological studies of Abies species

PHYTOCHEMICAL AND BIOLOGICAL STUDIES ON TWO ACALYPHA SPECIES

Schnella guianensis

1 reference

Flavonoid and other constituents of Bauhinia manca

Melilotus italicus

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Melilotus neapolitana

1 reference

Notizen: Medicarpin as a Phytoalexin of the Genus Melilotus

Pongamia pinnata

1 reference

Anti-inflammatory Flavanones and Flavanols from the Roots of Pongamia pinnata

Tripterygium wilfordii

1 reference

Isolation and characterization of a glycosyltransferase with specific catalytic activity towards flavonoids from Tripterygium wilfordii

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Sophora

1 reference

Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila

Sophora koreensis

1 reference

Five flavonoid compounds from Echinosophora koreensis

Dermatophyllum gypsophilum

1 reference

Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila

Flemingia prostrata

1 reference

Prenylated flavonoids from Moghania philippinensis

Flemingia macrophylla

1 reference

Prenylated flavonoids from Moghania philippinensis

Propolis

2 references

Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship.

Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition.

Identifiers

InChI

InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2/t14-/m0/s1

1 reference

Liquiritigenin (English)

FURUXTVZLHCCNA-AWEZNQCLSA-N

20 November 2016

InChIKey

2 references

Liquiritigenin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

578-86-9

2 references

Global Substance Registration System

UNII

T194LKP9W6

liquiritigenin (English)

FURUXTVZLHCCNA-AWEZNQCLSA-N

20 November 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=578-86-9

1 reference

(2S)-7-Hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one (English)

20 November 2016

1 reference

Liquiritigenin (English)

20 November 2016

Reaxys registry number

3593780

1 reference

liquiritigenin (English)

19 October 2016

ChEBI ID

28777

mapping relation type

1 reference

LIQUIRTIGENIN (English)

20 November 2016

1 reference

splash10-0a4i-0090010000-4f0e0e7c69cd0563f154

LIQUIRTIGENIN (English)

20 November 2016

1 reference

MassBank accession ID

MSBNK-BS-BS003364

0 references

MSBNK-BS-BS003365

0 references

SPLASH

0 references

splash10-0a4i-0090000000-e0ef2b922828538142d6

0 references

splash10-14io-4940000000-37623183ba063fae1aef

0 references

splash10-01pa-0990000000-b55ccc74a2ff9f8ee58a

0 references

DSSTox substance ID

DTXSID90206493

1 reference

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

DSSTOX compound identifier

0 references

1 reference

1 reference

5-deoxyflavanone (English)

Human Metabolome Database ID

20 November 2016

HMDB0029519

1 reference

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

liquiritigenin (English)

19 October 2016

1 reference

UNII

T194LKP9W6

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

liquiritigenin (English)

20 November 2016

0 references

0 references

1 reference

30 June 2018

0 references

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

1FM7 (English)

19 October 2016

1 reference

1JX1 (English)

19 October 2016

1 reference

1JX0 (English)