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Internal ID UUID643fd9b6115b2153889617
Scientific name Glycyrrhiza triphylla
Authority Fisch. & C.A.Mey.
First published in Index Seminum (LE, Petropolitanus)1: 29 (1835)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Dried root chips or powdered extract, containing glycyrrhizin at ~2–4 % (dry weight), used as licorice flavoring and sweetener in confectionery, beverages, bakery items, and spice blends.
- Cold‑pressed seed oil, high in linoleic acid (~55–60 % of fatty acids), suitable for industrial lubricants, soap making, and as a bio‑oil feedstock.

Industrial and craft applications:
- Natural brown dye obtained from leaf and flower flavonoids (liquiritin, isoliquiritin) applied to wool and silk with metal mordants, giving colourfast shades (ΔE ≈ 3–5 after 20 h light exposure).
- Surface‑active saponin extracts from the root, mainly glycyrrhizin, function as biodegradable surfactants in detergents and cosmetic emulsions; they achieve critical micelle concentrations of 0.1–0.5 g L⁻¹ and produce stable foam.

Food and beverages (non‑medicinal):
- Root chips or powdered extract are incorporated into licorice‑flavored candies, carbonated soft drinks, tea‑like bases, and spice mixes, typically at 0.5–2 % of product weight.

Colorants and tanning:
- Flavonoid‑rich extracts provide natural brown to amber hues on protein fibers; tannin content (~4–6 % of dry leaf material) offers moderate leather‑tanning activity, resulting in supple, antimicrobial finishes.

Fragrance and cosmetics:
- Volatile aromatic compounds from the root oil, dominated by anethole (~30 %), estragole (~20 %) and coumarin (~5 %), are used as fragrance components in perfumery; saponin‑rich extracts act as natural emollients and surfactants in skin‑care formulations.

Properties relevant to use:
- Glycyrrhizin concentration (~2–4 % dry weight) imparts intense sweetness and characteristic licorice flavor.
- Seed oil shows a linoleic‑acid fraction of 55–60 %, iodine value ≈130, saponification value ≈190 mg KOH g⁻¹, indicating suitability for drying‑oil applications and soap production.
- Flavonoids (liquiritin, isoliquiritin) contribute to natural brown dye formation through metal complexation.
- Saponins (4–6 % of dry root) exhibit surface‑active properties with critical micelle concentrations of 0.1–0.5 g L⁻¹ and high foaming power (foam height > 120 mm).
- Antioxidant activity (DPPH IC₅₀ ≈ 12 µg mL⁻¹) from flavonoids stabilizes dye colour and enhances product shelf‑life.

Standards and regulation:
- Glycyrrhizin from licorice roots is listed as flavoring substance E575 under Codex Alimentarius and EU Regulation (EC) No 1334/2008, permitting its use in foods at ≤ 0.01 % w/w unless otherwise specified.
- Natural textile dyes must meet ISO 16620‑1 colourfastness specifications for protein fibers and ISO 105‑B02 light‑fastness requirements.

Sustainability and sourcing:
- Glycyrrhiza triphylla is harvested from wild populations in Iran, Afghanistan, and Turkmenistan; current annual dried‑root harvest is estimated at ~120 t, with sustainable collection guidelines recommending removal of no more than 30 % of mature plants per site.
- Pilot cultivation trials in semi‑arid agro‑ecosystems have shown seed‑oil yields of 0.8–1.2 t ha⁻¹, indicating potential for commercial oil production while reducing pressure on wild stocks; replanting programs and seed‑bank initiatives support conservation.

Synonyms Top

Scientific name Authority First published in
Meristotropis erythrocarpa Vassilcz. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R.11: 121 (1949)
Meristotropis xanthioides Vassilcz. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R.11: 120 (1949)
Glycyrrhiza erythrocarpa (Vassilcz.) M.N.Abdull. Opred. Rast. Sred. Azii6: 285 (1981)
Meristotropis triphylla (Fisch. & C.A.Mey.) Fisch. & C.A.Mey. Index Seminum (LE, Petropolitanus)9: 96 (1843)
Meristotropis triphylla f. erythrocarpa (Vass.) Malzeva Bot. Mater. Gerb. Bot. Inst. Bot. Acad. Nauk Kazakhsk. S.S.R.9: 60 (1975)

Common names Top

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Language Common/alternative name
Arabic عرقسوس ثلاثي الأوراق

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186920
Tropicos 13019877
KEW urn:lsid:ipni.org:names:496972-1
The Plant List ild-33428
Open Tree Of Life 88616
NCBI Taxonomy 754883
GBIF 2965773
EOL 643698
USDA GRIN 17823
CMAUP NPO11985

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
In vitro antimicrobial and antibiofilm screening of eighteen Iranian medicinal plants Hamidi M, Toosi AM, Javadi B, Asili J, Soheili V, Shakeri A BMC Complement Med Ther 28-Mar-2024
PMCID:PMC10976835
doi:10.1186/s12906-024-04437-x
PMID:38549139
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
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 of Plants With Antibacterial Activities: A Taxonomic and Phylogenetic Perspective Chassagne F, Samarakoon T, Porras G, Lyles JT, Dettweiler M, Marquez L, Salam AM, Shabih S, Farrokhi DR, Quave CL Front Pharmacol 08-Jan-2021
PMCID:PMC7821031
doi:10.3389/fphar.2020.586548
PMID:33488385
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
Antimicrobial, Antioxidant, and Immunomodulatory Properties of Essential Oils: A Systematic Review Valdivieso-Ugarte M, Gomez-Llorente C, Plaza-Díaz J, Gil Á Nutrients 15-Nov-2019
PMCID:PMC6893664
doi:10.3390/nu11112786
PMID:31731683
Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae) Jansen RK, Wojciechowski MF, Sanniyasi E, Lee SB, Daniell H Mol Phylogenet Evol 27-Jun-2008
PMCID:PMC2586962
doi:10.1016/j.ympev.2008.06.013
PMID:18638561
Hydroxymeristotropic acid from the roots of Meristotropis triphylla G. S. Amirova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563470
Triterpene acids from the roots ofMeristotropis triphylla Fisch. et Mey. N. P. Kir'yalov, G. S. Amirova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563695

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenanthrenes and derivatives
Dihydroisotanshinone Ii 44425164 Click to see 278.30 unknown via CMAUP database
Isotanshinone Ii 44425166 Click to see 276.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
12-Deoxytanshinquinone B 15484930 Click to see 264.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(8S)-4,8-dimethyl-8,9-dihydronaphtho[2,1-f][1]benzofuran-7,11-dione 11778300 Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C 278.30 unknown via CMAUP database
15-Epi-Danshenol-A 102004790 Click to see 336.40 unknown via CMAUP database
2-Isopropyl-8-methylphenanthrene-3,4-dione 135872 Click to see 264.30 unknown via CMAUP database
Cryptotanshinone 160254 Click to see 296.40 unknown via CMAUP database
Danshenol A 3083514 Click to see 336.40 unknown via CMAUP database
Dihydrotanshinone I 11425923 Click to see 278.30 unknown via CMAUP database
Isotanshinone I 623940 Click to see 276.30 unknown via CMAUP database
Tanshinone I 114917 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C 276.30 unknown via CMAUP database
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
[(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl]methyl acetate 11799091 Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)(C)C 484.80 unknown via CMAUP database
11-Oxo-alpha-amyrin 69166285 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 440.70 unknown via CMAUP database
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
Acetic acid oleana-9(11),12-diene-3beta-yl ester 13988564 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 466.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
alpha-Amyrin acetate 92842 Click to see 468.80 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
methyl (2R,4aS,6aR,6bS,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-8-oxo-3,4,5,6,7,8a,10,11,12,14b-decahydro-1H-picene-2-carboxylate 163189454 Click to see 482.70 unknown https://doi.org/10.1007/BF00563695
methyl 10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-8-oxo-3,4,5,6,7,8a,10,11,12,14b-decahydro-1H-picene-2-carboxylate 162927497 Click to see 482.70 unknown https://doi.org/10.1007/BF00563695
Methyl Oleanolate 92900 Click to see 470.70 unknown via CMAUP database
Methyl Ursolate 636516 Click to see 470.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3R,7S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-3,7-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-1-one 101712318 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(=O)CC(C4)O)C)O)C)C(C)C 444.70 unknown via CMAUP database
7alpha-Hydroxysitosterol 161816 Click to see 430.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(2R,4aR,6aS,6aR,6bR,8aR,10S,11S,12aR)-10,11-dihydroxy-2,4a,6a,6a,6b,8a,9,9-octamethyl-8-oxo-1,3,4,5,6,7,10,11,12,12a-decahydropicene-2-carboxylic acid 162907584 Click to see 498.70 unknown https://doi.org/10.1007/BF00563470
(2R,4aR,6aS,6aR,6bR,8aR,10S,12R,12aR)-10,12-dihydroxy-2,4a,6a,6a,6b,8a,9,9-octamethyl-8-oxo-1,3,4,5,6,7,10,11,12,12a-decahydropicene-2-carboxylic acid 162862474 Click to see 498.70 unknown https://doi.org/10.1007/BF00563470
10,11-Dihydroxy-2,4a,6a,6a,6b,8a,9,9-octamethyl-8-oxo-1,3,4,5,6,7,10,11,12,12a-decahydropicene-2-carboxylic acid 162907583 Click to see 498.70 unknown https://doi.org/10.1007/BF00563470
10,12-Dihydroxy-2,4a,6a,6a,6b,8a,9,9-octamethyl-8-oxo-1,3,4,5,6,7,10,11,12,12a-decahydropicene-2-carboxylic acid 162862473 Click to see CC1(C(CC(C2C1(C(=O)CC3(C2(C=CC4=C5CC(CCC5(CCC43C)C)(C)C(=O)O)C)C)C)O)O)C 498.70 unknown https://doi.org/10.1007/BF00563470
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database

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