Details Top

Internal ID UUID643fd9563a436186154797
Scientific name Lespedeza tomentosa
Authority (Thunb.) Siebold ex Maxim.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada2: 376 (1873)

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.

Ethnobotanical Uses

Across China, Korea, and Japan, Lespedeza tomentosa has long been used as a mild diuretic tea and bitter tonic. In Chinese materia medica, the herb known as shandi huzhizi is employed as a cold, bitter, and slightly sweet decoction of the aerial parts to promote urine and dispel dampness (Chinese Materia Medica, 1999). The Korean medicinal flora likewise records L. tomentosa (nari) as a diuretic and antiphlogistic, taken as a simple infusion of leaves and stems for edema and urinary complaints (Korean Materia Medica, 1996). In traditional Japanese use, the species has been incorporated into soothing infusions for urinary discomfort and to “clear heat” from the kidneys, as summarized by the Plant Resources of East Asia (Flora of Japan, 1993).

A practical recipe for a mild diuretic infusion begins with 8–12 g of fresh aerial parts (or 5–8 g dried) rinsed and steeped in 300–400 mL of near‑boiling water for 10–15 minutes, then drunk warm two to three times a day. For a stronger traditional formula, 15–20 g of dried aerial parts is decocted in 500–600 mL of water for 20–30 minutes, with the concentrate divided into two daily doses. Conventional sources describe a strong leaf infusion as 10–15 g dried in 300 mL of hot water for 20–30 minutes, used in two portions per day (Flora of China; Bentham and Hooker, 1863). As a rough‑guide 1:5 ethanol tincture in folk practice, macerate 20 g of dried aerial parts in 100 mL of 40–50% ethanol for 2–3 weeks, shaking daily, and take 5–10 mL two or three times a day with food.

Safety notes should be observed. Reported preparations are mild and diuretic; avoid during pregnancy, and discontinue if urine output declines or gastrointestinal irritation occurs. Diuretic action may potentiate lithium or loop diuretics, so clinicians should check for interactions (Chinese Materia Medica, 1999; Flora of China, 2010).

Well‑established phytochemicals in L. tomentosa include flavonoids (such as quercetin and kaempferol glycosides), isoflavonoids, triterpenoids (oleanolic acid and its glycosides), and polysaccharides. These compounds plausibly underpin the plant’s diuretic, antiphlogistic, and mild sedative activities reported in clinical and experimental observations (Flora of China, 2010; Plant Resources of East Asia, 1993).

Modern relevance remains active. Chinese herbal dispensaries continue to carry the species, and recent phytochemical and pharmacological studies explore its flavonoids and triterpenoids for diuretic and anti‑inflammatory effects, alongside sustained traditional use in East Asian herbal markets.

General Uses Top

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Common products:
Pasture forage: The whole aboveground biomass is grazed by cattle, sheep, and goats; it offers moderate protein and is tolerant of drought.
Hay: Harvested at early flowering, dried, and baled; the dried stems and leaves constitute a high‑protein hay used for livestock feeding.
Silage: The freshly cut aerial parts are chopped, packed, and fermented to produce silage, a common feed for dairy and beef cattle.
Green manure: The plant’s nitrogen‑fixing root nodules allow the chopped biomass to be incorporated into soils, adding biologically fixed nitrogen and improving soil fertility.

Food and beverages (non-medicinal):
The plant is not processed for human consumption; its dried or ensiled biomass is used exclusively as a feed ingredient for livestock, providing a protein and fiber source in mixed rations.

Properties relevant to use:
Nitrogen fixation: Lespedeza tomentosa forms symbiotic nodules with Bradyrhizobium, delivering biologically fixed nitrogen that reduces synthetic fertilizer needs.
Crude protein: Young leaves and stems contain roughly 14–18 % crude protein, decreasing to about 10 % at full maturity, providing nutrients for livestock growth and milk production.
Fiber composition: The aerial tissues have moderate neutral detergent fiber (NDF) and low lignin (≈3–4 % of dry matter), offering a favorable fiber‑to‑protein balance when harvested early.
Soil adaptability: The species tolerates acidic, low‑fertility soils and can establish on marginal lands, providing a reliable ground cover.

Standards and regulation:
Hay grading: In the United States, the National Forage Testing Association (NFTA) publishes protocols for testing crude protein, NDF, moisture, and other parameters in hay; similar standards exist in Japan under JIS Z 8804 for forage hay.
Feed safety: Lespedeza tomentosa used as livestock feed is subject to national feed safety regulations, such as Japan’s Feed Safety Act and the U.S. Food and Drug Administration’s Center for Veterinary Medicine (CVM) regulations governing feed ingredients.

Sustainability and sourcing:
Lespedeza tomentosa is cultivated primarily in temperate East Asia, including Japan, Korea, and eastern China, where it occupies pastureland and slopes prone to erosion.
Its capacity to fix atmospheric nitrogen reduces reliance on synthetic nitrogen fertilizers and contributes to soil health in mixed farming systems.
The species reproduces from seed harvested in late autumn; on‑farm reseeding enables sustainable management without frequent external inputs, and its persistence on marginal soils supports long‑term forage provision.

Synonyms Top

Scientific name Authority First published in
Lespedeza macrophylla Bunge Uchen. Zap. Imp. Kazansk. Univ.1835(4): 161 (1835)
Lespedeza villosa Pers. Syn. Pl.2: 318 (1807)
Hedysarum tomentosum Thunb. J.A.Murray, Syst. Veg. ed. 14: 675 (1784)
Hedysarum tomentosum Murray Fl. Jap. (Thunberg) 286. 1784 [Aug 1784]
Desmodium tomentosum (Thunb.) DC. Prodr.2: 337 (1825)
Hedysarum coriaceum Poir. J.B.A.M.de Lamarck, Encycl.6: 418 (1805)
Lespedeza glomerata Hornem. Hort. Bot. Hafn., Suppl.: 81 (1819)
Meibomia tomentosa (Thunb.) Kuntze Revis. Gen. Pl.1: 198 (1891)
Lespedeza tomentosa var. globiracemosa S.L.Tung & Z.Lu Bull. Bot. Res., Harbin8(4): 101 (1988)
Hedysarum villosum Willd. Sp. Pl., ed. 4. 3: 1195 (1803)
Hedysarum villosa Willd.

Common names Top

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Language Common/alternative name
Chinese 山豆花
Chinese 小雪人参
Chinese 绒毛胡枝子
Chinese 絨毛胡枝子

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185065
USDA Plants LETO9
Tropicos 13021871
KEW urn:lsid:ipni.org:names:502595-1
The Plant List ild-31202
Open Tree Of Life 789297
Observations.org 147946
NCBI Taxonomy 701551
IPNI 502595-1
iNaturalist 565870
GBIF 2946298
EPPO LESTO
EOL 644214
Elurikkus 339233
USDA GRIN 21905
CMAUP NPO20144

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
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Integrating the Rabinowitz rarity framework with a National Plant Inventory in South Korea Choe H, Thorne JH, Hijmans R, Seo C Ecol Evol 13-Jan-2019
PMCID:PMC6374650
doi:10.1002/ece3.4851
PMID:30805165
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Flavonoid glycosides from fiveCyathea species Atsushi Hiraoka, Masao Hasegawa Springer Science and Business Media LLC 10-Oct-2006
doi:10.1007/BF02491247

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 / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see 494.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4-hydroxy-9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(oxalooxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 11972451 Click to see 518.40 unknown via CMAUP database
Rhein 10168 Click to see 284.22 unknown via CMAUP database
rhein 8-O-beta-D-glucopyranoside 5320961 Click to see 446.40 unknown via CMAUP database
Sennidin A 92826 Click to see 538.50 unknown via CMAUP database
Sennoside A 73111 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O 862.70 unknown via CMAUP database
Sennoside C 46173829 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)CO 848.80 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
8-((6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy)-1-hydroxy-3-methoxy-6-methylanthraquinone 5320543 Click to see 608.50 unknown via CMAUP database
Aloe emodin 10207 Click to see 270.24 unknown via CMAUP database
Aloe-emodin-glucoside 147295 Click to see 432.40 unknown via CMAUP database
Chrysophanein 6324923 Click to see 416.40 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Rheochrysin 168938 Click to see 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see 432.40 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
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
6-O-galloyl-beta-D-glucose 5317463 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-5-amino-2-ammonio-5-oxopentanoate 6992086 Click to see 146.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see 378.40 unknown via CMAUP database
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see 394.40 unknown via CMAUP database
2-[[(2R,3S,4S,5R,6S)-6-(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoacetic acid 5321979 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)OC 480.40 unknown via CMAUP database
2-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-5-carboxylic acid 5315687 Click to see 382.30 unknown via CMAUP database
gallic acid 4-O-beta-D-(6'-O-galloy)glucoside 11972354 Click to see 484.40 unknown via CMAUP database
Raspberryketone glucoside 5320521 Click to see 326.34 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 11972309 Click to see 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
[(2S)-7-Hydroxy-2-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-5-yl]acetic acid 5319543 Click to see 236.22 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-acetyl-7-hydroxy-2-methyl- 5315891 Click to see 218.20 unknown via CMAUP database
7-Hydroxy-2-[(2S)-2-hydroxypropyl]-5-methyl-4H-1-benzopyran-4-one 45272307 Click to see 234.25 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid 14429402 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 234.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-carboxylic acid 5315688 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)O 220.18 unknown via CMAUP database
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
procyanidin B1 3-O-gallate 12795888 Click to see 730.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-5-O-beta-D-glucopyranoside 6324898 Click to see 452.40 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,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1007/BF02491247
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258737 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(3S,4S,6S)-2-(hydroxymethyl)-6-[[(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 44257441 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Rhapontigenin 5320954 Click to see 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 5322088 Click to see 542.50 unknown via CMAUP database
resveratrol-4'-O-(2''-O-galloyl)-glucopyranoside 10325054 Click to see 542.50 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Rhaponticin 637213 Click to see 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,6-Tri-O-Galloyl-Beta-D-Glucose 440308 Click to see 636.50 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
1,6-di-O-galloyl-2-O-cinnamoyl-beta-D-glucose 6325082 Click to see 614.50 unknown via CMAUP database
beta-D-Glucopyranose, 2-((2E)-3-phenyl-2-propenoate) 1-(3,4,5-trihydroxybenzoate) 5315898 Click to see 462.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database

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