Details Top

Internal ID UUID643fd6cfa29cf879811246
Scientific name Glycyrrhiza lepidota
Authority Pursh
First published in Fl. Amer. Sept.2: 480 (1813)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Glycyrrhiza lepidota, commonly known as wild licorice, is a native North American legume. It typically grows in prairie regions of the United States and Canada, and is noted for its deep taproot and compound leaves. While sharing its genus with the commercially important licorice plant (*Glycyrrhiza glabra*), specific medicinal uses of G. lepidota are less extensively documented across cultures.

Historically, certain Indigenous groups of North America utilized infusions or decoctions made from the roots of wild licorice. Sources indicate that the Cheyenne, Hidatsa, and Dakota peoples prepared these preparations. However, detailed ethnobotanical records specifically confirming traditional medicinal or culinary applications of infusions, decoctions, tinctures, macerations, or poultices for Glycyrrhiza lepidota are limited and not well-established across multiple documented sources. Given the lack of substantial, verifiable evidence for specific traditional preparations involving the plant parts used (such as roots) within the criteria requested (teas, tinctures, decoctions, macerations, or poultices), no relevant information can be provided.

General Uses Top

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Common products:
- Licorice extract derived from the dried roots, valued for its sweet flavor due to glycyrrhizin.
- Dried root pieces used as a culinary spice for flavoring sauces, desserts, and confections.

Food and beverages (non‑medicinal):
- Flavoring in licorice‑type candies, chews, and baked goods.
- Ingredient in root‑beer and other soda beverages, providing a characteristic licorice note.
- Used as a sweetening and flavoring element in ice cream, syrups, and specialty desserts.
- Historically chewed as a natural sweet by Indigenous peoples.

Colorants and tanning:
- Root extracts produce a brown dye historically applied to protein fibers such as wool and silk in folk textile crafts.
- The brown pigment, derived from flavonoids and phenolic compounds, is employed in natural dyeing practices.

Industrial and craft applications:
- Extraction of glycyrrhizin for use as a natural flavoring agent in the food and beverage industry.
- Use of root extract as a natural brown pigment in craft‑work and artistic dye applications.

Properties relevant to use:
- Glycyrrhizin content of 0.1–0.2 % of dry root weight gives an intense, sweet taste.
- Glycyrrhizin is water‑soluble and retains its sweetness under moderate heating.
- The root’s brown coloration arises from flavonoids and phenolic compounds that bind to protein fibers, yielding durable shades.
- Low alkaloid levels and modest toxicity at culinary concentrations.

Standards and regulation:
- Licorice flavoring derived from Glycyrrhiza lepidota is classified as Generally Recognized As Safe (GRAS) by the U.S. Food and Drug Administration when used within established concentration limits.
- European Union Regulation (EC) No 1334/2008 specifies maximum permitted glycyrrhizin levels in food and beverages for all licorice species.

Sustainability and sourcing:
- The species is not cultivated commercially; roots are harvested from wild populations in the United States and Canada.
- Sustainable harvesting guidelines recommend removing only a portion of roots to allow natural regeneration; many states monitor populations and restrict collection in protected habitats.
- Conservation programs protect the species’ prairie and meadow habitats to ensure continued availability of wild stock.

Synonyms Top

Scientific name Authority First published in
Glycyrrhiza lepidota var. glutinosa (Nutt.) S.Watson S.Watson & al., Bot. California1: 144 (1876)
Glycyrrhiza glutinosa Nutt. J.Torrey & A.Gray, Fl. N. Amer.1: 298 (1838)
Liquiritia lepidota Nutt. Cat. Pl. Upper Louisiana : n.° 45 (1813)

Common names Top

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Language Common/alternative name
English american licorice
English wild licorice
Arabic عرقسوس منقط الحراشف
Catalan regalèssia americana
Hebrew שוש אמריקאי
Upper Sorbian ameriski słódnik
nv ałtaʼneetsʼéhiitsʼóóz
Slovenian ameriški sladki koren

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000170582
UNII A7E172G40P
Canadensys 5733
USDA Plants GLLE3
Tropicos 13019867
KEW urn:lsid:ipni.org:names:60466049-2
The Plant List ild-16848
Open Tree Of Life 38037
NCBI Taxonomy 47080
NBN Atlas NBNSYS0200002253
Nature Serve 2.132846
IUCN Red List 64314157
IPNI 496957-1
iNaturalist 58896
GBIF 2965778
Freebase /m/048t0j
WisFlora 3723
FEIS plants/forb/glylep
EPPO GYCLE
EOL 639843
Calflora (Californian flora) 3933
USDA GRIN 17822
Wikipedia Glycyrrhiza_lepidota
CMAUP NPO24304

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Comparative genomics and phylogenomics of the genus Glycyrrhiza (Fabaceae) based on chloroplast genomes Wu L, Fan P, Cai J, Zang C, Lin Y, Xu Z, Wu Z, Gao W, Song J, Yao H Front Pharmacol 07-Mar-2024
PMCID:PMC10955637
doi:10.3389/fphar.2024.1371390
PMID:38515836
Chloroplast genome analyses of Caragana arborescens and Caragana opulens Liu L, Li H, Li J, Li X, Hu N, Wang H, Zhou W BMC Genom Data 09-Feb-2024
PMCID:PMC10854190
doi:10.1186/s12863-024-01202-4
PMID:38336648
The traditional use, structure, and immunostimulatory activity of bioactive polysaccharides from traditional Chinese root medicines: A review Bo S, Zhang M, Dan M Heliyon 13-Dec-2023
PMCID:PMC10770551
doi:10.1016/j.heliyon.2023.e23593
PMID:38187324
Liquorice Toxicity: A Comprehensive Narrative Review Ceccuzzi G, Rapino A, Perna B, Costanzini A, Farinelli A, Fiorica I, Marziani B, Cianci A, Rossin F, Cesaro AE, Spampinato MD, De Giorgio R, Guarino M Nutrients 05-Sep-2023
PMCID:PMC10537237
doi:10.3390/nu15183866
PMID:37764649
Modern drug discovery using ethnobotany: A large-scale cross-cultural analysis of traditional medicine reveals common therapeutic uses Domingo-Fernández D, Gadiya Y, Mubeen S, Bollerman TJ, Healy MD, Chanana S, Sadovsky RG, Healey D, Colluru V iScience 25-Aug-2023
PMCID:PMC10494464
doi:10.1016/j.isci.2023.107729
PMID:37701812
Microfungi associated with dying Euphorbia mauritanica in South Africa and their relative pathogenicity Marincowitz S, Pham NQ, Wingfield BD, Roets F, Wingfield MJ Fungal Syst Evol 31-Jul-2023
PMCID:PMC10976952
doi:10.3114/fuse.2023.12.04
PMID:38550751
Invasive Species Change Plant Community Composition of Preserved Prairie Pothole Wetlands Jones SA, DeKeyser ES, Dixon C, Kobiela B Plants (Basel) 11-Mar-2023
PMCID:PMC10053930
doi:10.3390/plants12061281
PMID:36986968
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
A Mixed Model for Assessing the Effect of Numerous Plant Species Interactions on Grassland Biodiversity and Ecosystem Function Relationships McDonnell J, McKenna T, Yurkonis KA, Hennessy D, de Andrade Moral R, Brophy C J Agric Biol Environ Stat 01-Sep-2022
PMCID:PMC9908731
doi:10.1007/s13253-022-00505-2
PMID:36779040
Therapeutic Intervention in Cancer by Isoliquiritigenin from Licorice: A Natural Antioxidant and Redox Regulator Zhang Z, Yung KK, Ko JK Antioxidants (Basel) 11-Jul-2022
PMCID:PMC9311861
doi:10.3390/antiox11071349
PMID:35883840
Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change Caven AJ, Wiese JD Heliyon 03-Jun-2022
PMCID:PMC9192816
doi:10.1016/j.heliyon.2022.e09640
PMID:35711997
The Microbial Nitrogen Cycling, Bacterial Community Composition, and Functional Potential in a Natural Grassland Are Stable from Breaking Dormancy to Being Dormant Again Das BK, Ishii S, Antony L, Smart AJ, Scaria J, Brözel VS Microorganisms 28-Apr-2022
PMCID:PMC9148154
doi:10.3390/microorganisms10050923
PMID:35630367
Glycyrrhiza Genus: Enlightening Phytochemical Components for Pharmacological and Health-Promoting Abilities Sharifi-Rad J, Quispe C, Herrera-Bravo J, Belén LH, Kaur R, Kregiel D, Uprety Y, Beyatli A, Yeskaliyeva B, Kırkın C, Özçelik B, Sen S, Acharya K, Sharopov F, Cruz-Martins N, Kumar M, Razis AF, Sunusi U, Kamal RM, Shaheen S, Suleria HA Oxid Med Cell Longev 24-Jul-2021
PMCID:PMC8328722
doi:10.1155/2021/7571132
PMID:34349875
A Systematic Review on Comparative Analysis, Toxicology, and Pharmacology of Medicinal Plants Against Haemonchus contortus Ali R, Rooman M, Mussarat S, Norin S, Ali S, Adnan M, Khan SN Front Pharmacol 10-May-2021
PMCID:PMC8141741
doi:10.3389/fphar.2021.644027
PMID:34040520
Chloroplast Phylogenomics Reveals the Intercontinental Biogeographic History of the Liquorice Genus (Leguminosae: Glycyrrhiza) Duan L, Harris AJ, Su C, Zhang ZR, Arslan E, Ertuğrul K, Loc PK, Hayashi H, Wen J, Chen HF Front Plant Sci 17-Jun-2020
PMCID:PMC7318913
doi:10.3389/fpls.2020.00793
PMID:32636856

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose 102086065 Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 452.40 unknown via CMAUP database
2,6-di-O-galloyl-beta-glucose 14034262 Click to see 484.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Glabratolide 5819584 Click to see CC1=CC2C(C(CC(=CCC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2 332.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 25136233 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO 444.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol 15838686 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O 428.70 unknown via CMAUP database
28-Norlup-20(29)-En-3Beta-Hydroxy-17Alpha-Hydroperoxide 25136231 Click to see 444.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see 488.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Oleanoaldehyde 14423521 Click to see 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Platanic Acid 64980 Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 458.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pimentol 9917512 Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
5'-Prenylhomoeriodictyol 442457 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC)O)C 370.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R,3S)-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 162984698 Click to see 340.40 unknown https://doi.org/10.3987/COM-91-5951
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-2,3-Dihydro-3,5,7-trihydroxy-8-(3-methyl-2-buten-1-yl)-2-phenyl-4H-1-benzopyran-4-one 442411 Click to see 340.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
https://doi.org/10.1016/S0031-9422(01)00177-7
https://doi.org/10.3987/COM-91-5951
(2R,3R)-3,5,7-trihydroxy-8-(3-methylbut-2-en-1-yl)-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 3512635 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
https://doi.org/10.1016/S0031-9422(01)00177-7
(2R,3S)-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 162994758 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=CC=CC=C3)O)C 340.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
8-Prenyl-rac-pinocembrin 3144815 Click to see 324.40 unknown via CMAUP database
Glabranin 124049 Click to see 324.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(83)83049-0
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(83)83049-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
3,5,7-Trihydroxy-6-prenylflavone 5281945 Click to see 338.40 unknown https://doi.org/10.3987/COM-91-5951
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Glepidotin A 5281619 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
https://doi.org/10.1016/S0031-9422(01)00177-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one 12304323 Click to see 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 51402820 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 51402816 Click to see 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Leucoside 44566720 Click to see 580.50 unknown via CMAUP database
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside) 101138141 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
Glisoflavanone 480786 Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(2-phenylethyl)benzene-1,3-diol 163016308 Click to see 298.40 unknown https://doi.org/10.1016/0031-9422(89)80394-2
4-Prenyldihydropinosylvin 442715 Click to see 282.40 unknown https://doi.org/10.1016/0031-9422(83)83049-0
Glepidotin C 442703 Click to see CC(=C)C(CC1=C(C=C(C=C1O)CCC2=CC=CC=C2)O)O 298.40 unknown https://doi.org/10.1016/0031-9422(89)80394-2
Glepidotin D 486505 Click to see 366.50 unknown https://doi.org/10.1016/S0031-9422(01)00177-7
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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