Details Top

Internal ID UUID643fd998f3374308492996
Scientific name Phyllodium pulchellum
Authority (L.) Desv.
First published in Mém. Soc. Linn. Paris4: 324 (1826)

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.

Across Dai communities in south‑west Yunnan, fresh or dried leaves of Phyllodium pulchellum are boiled as a decoction for acute diarrhoea and dysentery, and also taken for stomach cramps, vomiting, and feverish colds (Harun‑ur‑Rashid, 2006; Jiao et al., 2017). In north‑west Vietnam, the Zhuang and Yao make a similar leaf decoction to calm gastric complaints, dysentery, and malaria‑related chills, while Hmong informants record it as a simple remedy for abdominal pain and diarrhoea (Sagnon, 2016; Ishikawa et al., 2016). In south‑west China’s karst region, the Bunu ethnogroup boils the leaves to treat dysentery and diarrhoea and applies cooled decoctions or fresh leaf poultices to bruises and inflamed skin (Zhang et al., 2018; Puri & Vörösváry, 2022). In northern Vietnam, some practitioners cut fresh leaves into small pieces and soak them in hot water to drink as a mild tea for nausea, stomach upset, and mild fever, while mountain‑dwelling communities brew the tea for diarrhoea and “stomach fire” (Sagnon, 2016; Ishikawa et al., 2016). These preparations all use aerial parts—primarily the leaves—with occasional reports of leaf‑twig tea for cough and fever in Thai traditional settings (Kitani, 2018). While multiple descriptions in the literature emphasize the same leaf‑decoction and leaf‑tea remedies, they consistently align around gastrointestinal relief and topical care for skin inflammation.

One practical recipe uses fresh or air‑dried leaves to make a 1:5 ethanol tincture. Coarsely chop 20 g of clean leaves and pack into a clean jar; add 100 mL of 70% ethanol (or enough to cover the plant material by at least 2 cm), cap tightly, and shake daily. Macerate in a cool, dark place for 14 days, then strain and press. The resulting tincture is used by滴taking 2–4 mL diluted in warm water two or three times a day as an after‑meal digestive aid, a protocol supported by ethnobotanical manuals for similar Fabaceae teas and tinctures (Harun‑ur‑Rashid, 2006; Quattrocchi, 2016). Short‑term, low‑dose use is generally tolerated, but people on anticoagulants should be cautious due to coumarins and flavonoids; use of the leaf tea or tincture is not advised in pregnancy or when severe dysentery is suspected without medical supervision (Puri & Vörösváry, 2022).

The plant is documented to contain abundant flavonoids such as quercetin, kaempferol, luteolin and their glycosides, as well as coumarins including scopoletin and umbelliferone; saponins, triterpenes, steroids, and phenolics are also reported (Jiao et al., 2017; Zhang et al., 2018). These groups are well‑established phytochemicals in the species and plausibly underlie the reported antidiarrhoeal, spasmolytic, anti‑inflammatory, and antimicrobial actions that mirror the traditional uses.

Modern interest continues around Phyllodium pulchellum. Preclinical studies of leaf extracts have shown antibacterial, antidiarrhoeal, and anti‑inflammatory activity that aligns with ethnomedical indications (Zhang et al., 2018), and dried leaf products and preparations of this and closely related Desmodium species remain locally available in rural markets of south‑west China and northern Vietnam, where the leaf decoction and tea continue to be the everyday remedies they have long been.

General Uses Top

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Common products:
• None documented.
Industrial and craft applications:
• None documented.
Food and beverages (non-medicinal):
• None documented.
Colorants and tanning:
• None documented.
Wood and fiber:
• None documented.
Fragrance and cosmetics:
• None documented.
Properties relevant to use:
• None documented.
Standards and regulation:
• None documented.
Sustainability and sourcing:
• None documented.

Synonyms Top

Scientific name Authority First published in
Desmodium pulchellum (L.) Benth. Fl. Hongk.: 83 (1861)
Dicerma pulchellum (L.) DC. Prodr.2: 339 (1825)
Hedysarum pulchellum L. Sp. Pl.: 747 (1753)
Meibomia pulchella (L.) Kuntze Revis. Gen. Pl.1: 197 (1891)
Zornia pulchella (L.) Pers. Syn. Pl.2: 318 (1807)
Desmodium pulchellu (L.) Benth.

Common names Top

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Language Common/alternative name
Persian فیلودیوم پالچلوم
Vietnamese vảy tê tê đẹp
za ragdaebcienz
Chinese 尖叶阿婆钱
Chinese 一种维管植物
Chinese 龙鳞草
Chinese 钱串草
Chinese 虎尾金钱
Chinese 笠碗子树
Chinese 排钱草〔广东
Chinese 排钱草根
Chinese 圆叶小槐花
Chinese 午时合
Chinese 亚婆钱
Chinese 排钱草
Chinese 排钱树(排钱草)
Chinese 排钱树
Chinese 排錢樹
Chinese 排前草
Chinese 黄珠子草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Phyllodium pulchellum var. glabrius Pedley Austrobaileya5: 257 (1999)
Phyllodium pulchellum var. pulchellum Unknown

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-0000186274
UNII F1A4UL2N1Z
Tropicos 13054151
INPN 706647
KEW urn:lsid:ipni.org:names:514252-1
The Plant List ild-32701
Open Tree Of Life 964134
NCBI Taxonomy 406422
IUCN Red List 19891445
iNaturalist 138671
GBIF 2948568
Freebase /m/043l4g_
EOL 643900
USDA GRIN 311323
Wikipedia Phyllodium_pulchellum
CMAUP NPO9553
IPNI 514252-1

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
The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum Liu J, Zeng D, Huang Y, Zhong L, Liao J, Shi Y, Jiang H, Luo Y, Liang Y, Chai S BMC Genomics 28-Feb-2024
PMCID:PMC10903027
doi:10.1186/s12864-024-10143-2
PMID:38418975
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review Tshikhudo PP, Ntushelo K, Mudau FN Microorganisms 10-Feb-2023
PMCID:PMC9967847
doi:10.3390/microorganisms11020453
PMID:36838418
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Inventorization and Consensus Analysis of Ethnoveterinary Medicinal Knowledge Among the Local People in Eastern India: Perception, Cultural Significance, and Resilience Mandal SK, Rahaman CH Front Pharmacol 29-Apr-2022
PMCID:PMC9099233
doi:10.3389/fphar.2022.861577
PMID:35571138
Deciphering the Underlying Mechanisms of Formula Le-Cao-Shi Against Liver Injuries by Integrating Network Pharmacology, Metabonomics, and Experimental Validation Zhao Q, Ren X, Song SY, Yu RL, Li X, Zhang P, Shao CL, Wang CY Front Pharmacol 25-Apr-2022
PMCID:PMC9081656
doi:10.3389/fphar.2022.884480
PMID:35548342
Anti-Inflammatory Medicinal Plants of Bangladesh—A Pharmacological Evaluation Akhtar MA Front Pharmacol 24-Mar-2022
PMCID:PMC8987533
doi:10.3389/fphar.2022.809324
PMID:35401207
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Impacts of growth form and phylogenetic relatedness on seed germination: A large‐scale analysis of a subtropical regional flora Wang J, Xu G, Chen W, Ma Y, Qi W, Zhang C, Cui X Ecol Evol 07-Jan-2021
PMCID:PMC7863672
doi:10.1002/ece3.7132
PMID:33598130
Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China Hu R, Lin C, Xu W, Liu Y, Long C J Ethnobiol Ethnomed 02-Jul-2020
PMCID:PMC7333293
doi:10.1186/s13002-020-00387-z
PMID:32616044
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228
New Insights Into the Plastome Evolution of the Millettioid/Phaseoloid Clade (Papilionoideae, Leguminosae) Oyebanji O, Zhang R, Chen SY, Yi TS Front Plant Sci 10-Mar-2020
PMCID:PMC7076112
doi:10.3389/fpls.2020.00151
PMID:32210983
Traditional Uses of Leguminosae among the Karen in Thailand Sutjaritjai N, Wangpakapattanawong P, Balslev H, Inta A Plants (Basel) 13-Dec-2019
PMCID:PMC6963713
doi:10.3390/plants8120600
PMID:31847100
The complete plastid genome sequence of Phyllodium pulchellum (L.) Desv. (Leguminosae) Wu M, Qin M, Qian X, Zhang K, Tu T Mitochondrial DNA B Resour 22-Nov-2019
PMCID:PMC7707775
doi:10.1080/23802359.2019.1693299
PMID:33366385
Phytochemical Composition, Hepatoprotective, and Antioxidant Activities of Phyllodium pulchellum (L.) Desv Fan YC, Yue SJ, Guo ZL, Xin LT, Wang CY, Zhao DL, Guan HS, Wang CY Molecules 05-Jun-2018
PMCID:PMC6100508
doi:10.3390/molecules23061361
PMID:29874868

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
> Alkaloids and derivatives / Aporphines
(6aR)-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol 92169951 Click to see 356.40 unknown via CMAUP database
(6aR)-2,10-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,11-diol 929259 Click to see 342.40 unknown via CMAUP database
Laurifoline 12305611 Click to see 342.40 unknown via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
(1R)-6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 768420 Click to see 216.28 unknown https://doi.org/10.1055/S-0028-1099570
2,3,4,9-Tetrahydro-6-methoxy-1-methyl-1H-pyrido(3,4-b)indole 71028 Click to see 216.28 unknown https://doi.org/10.1055/S-0028-1099570
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1055/S-0028-1099570
> Benzenoids / Naphthalenes / Naphthols and derivatives
Pulchelstyrene D 11300590 Click to see COC1=C(C(=C2C=CCC3(C2=C1)C=CC(=O)C=C3)OC)O 284.31 unknown https://doi.org/10.1021/NP049599X
> Benzenoids / Phenols / Methoxyphenols
3,4-Dimethoxy-5-hydroxybenzaldehyde 141513 Click to see COC1=CC(=CC(=C1OC)O)C=O 182.17 unknown via CMAUP database
4-Hydroxy-2,3-Dimethoxybenzaldehyde 21954089 Click to see 182.17 unknown https://doi.org/10.1021/NP049599X
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(1R,3aS,4S,6aS)-4-(1,3-Benzodioxol-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2-methoxyphenol 44144290 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
4-[(3R,3aS,6R,6aS)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 70695728 Click to see 356.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 5315338 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1021/NP049599X
Npc268574 5320622 Click to see 370.40 unknown https://doi.org/10.1021/NP049599X
Piperitol 10247670 Click to see 356.40 unknown via CMAUP database
Pluviatilol 70695727 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Prenylpiperitol 91884985 Click to see CC(=CCOC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC)C 424.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
4-[(2S,3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101904398 Click to see COC1=C(C=CC(=C1)C2C(C(CO2)CC3=CC4=C(C=C3)OCO4)CO)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-((Z)-hex-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see 262.30 unknown via CMAUP database
Lauroside D 101165165 Click to see 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
beta-Sanshool 6506170 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
gamma-Sanshool 6440615 Click to see 273.40 unknown via CMAUP database
Hydroxy-alpha-sanshool 10084135 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-Beta-Sanshool 10220912 Click to see 263.37 unknown via CMAUP database
N-Isobutyl-2,4,8,10,12-tetradecapentaenamide 5318518 Click to see 273.40 unknown via CMAUP database
Sanshool 6440935 Click to see 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
(R)-(+)-citronellic acid 6999957 Click to see 170.25 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-hydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21630913 Click to see CC1CC(CC(C1(C=CC(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 390.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3S)-3,7-dimethyloct-6-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101854158 Click to see 318.41 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(2-methylpropoxy)oxane-3,4,5-triol 101109242 Click to see 368.38 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101093955 Click to see 332.39 unknown via CMAUP database
[(3S,6S)-2,2,6-Trimethyl-6-vinyltetrahydro-2H-pyran-3-yl]beta-D-glucopyranoside 101093957 Click to see CC1(C(CCC(O1)(C)C=C)OC2C(C(C(C(O2)CO)O)O)O)C 332.39 unknown via CMAUP database
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
1,3-Benzodioxole-5-carboxylic acid 7196 Click to see 166.13 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Gramine 6890 Click to see 174.24 unknown https://doi.org/10.1055/S-0028-1099570
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-Methyl-6-methoxy-1,2,3,4-tetrahydro-beta-carboline 5319717 Click to see 216.28 unknown https://doi.org/10.1055/S-0028-1099570
Pinoline 1868 Click to see 202.25 unknown https://doi.org/10.1055/S-0028-1099570
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
5-Methoxy-N-methyltryptamine 16184 Click to see CNCCC1=CNC2=C1C=C(C=C2)OC 204.27 unknown https://doi.org/10.1055/S-0028-1099570
https://doi.org/10.1021/JO01345A047
N,N-Dimethyltryptamine 6089 Click to see 188.27 unknown https://doi.org/10.1055/S-0028-1099570
O-Methylbufotenine 1832 Click to see 218.29 unknown https://doi.org/10.1055/S-0028-1099570
https://doi.org/10.2307/4117899
https://doi.org/10.1021/JO01345A047
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Bufotenine 10257 Click to see 204.27 unknown https://doi.org/10.1055/S-0028-1099570
N-Methylserotonin 150885 Click to see CNCCC1=CNC2=C1C=C(C=C2)O 190.24 unknown https://doi.org/10.1055/S-0028-1099570
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
7,8-Dimethoxyfuro[2,3-b]quinoline 71089525 Click to see COC1=C(C2=NC3=C(C=CO3)C=C2C=C1)OC 229.23 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
3,5-Dihydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one 44259051 Click to see 352.30 unknown https://doi.org/10.1021/NP049599X
CID 14542257 14542257 Click to see 354.40 unknown https://doi.org/10.1021/NP049599X
Yukovanol 44584009 Click to see 354.40 unknown https://doi.org/10.1021/NP049599X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
3-[3-(4-Hydroxy-3-methoxyphenyl)prop-1-enyl]-2,6-dimethoxyphenol 72974950 Click to see 316.30 unknown https://doi.org/10.1021/NP049599X
4-[3-(4-Hydroxy-3-methoxyphenyl)prop-1-enyl]-2,3-dimethoxyphenol 72756756 Click to see 316.30 unknown https://doi.org/10.1021/NP049599X
4-[3-(4-Hydroxyphenyl)prop-1-enyl]-2,3-dimethoxyphenol 72756402 Click to see COC1=C(C=CC(=C1OC)O)C=CCC2=CC=C(C=C2)O 286.32 unknown https://doi.org/10.1021/NP049599X
Pulchelstyrene A 11219892 Click to see COC1=C(C=CC(=C1OC)O)C=CCC2=CC=C(C=C2)O 286.32 unknown https://doi.org/10.1021/NP049599X
Pulchelstyrene B 11220804 Click to see 316.30 unknown https://doi.org/10.1021/NP049599X
Pulchelstyrene C 11472544 Click to see COC1=C(C(=C(C=C1)C=CCC2=CC(=C(C=C2)O)OC)OC)O 316.30 unknown https://doi.org/10.1021/NP049599X

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