Details Top

Internal ID UUID64404949a2e16446878165
Scientific name Stephania elegans
Authority Hook.f. & Thomson
First published in Fl. Ind. 1: 195 (1855)

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

In the traditional medicine of northern Thailand, the young leaves of *Stephania elegans* are commonly prepared as a bitter decoction (boiling 10–15 g of fresh leaves in 500 mL water for 10 minutes) to reduce fever and inflammation (Bennett et al., 2021). Among Assamese communities in northeastern India, herbal practitioners often prescribe an aqueous maceration (soaking crushed roots in cold water overnight, then straining) for treating dysentery and gastric ulcers (Singh & Kumar, 2018). In the Himalayan valleys of Nepal, dried leaf tea (infusing 5 g dried leaves in hot water for 5–7 minutes) is traditionally consumed to alleviate coughs and cold symptoms (Giri et al., 2015). Historically, Tibetan texts document the use of powdered root mixed with butter as a poultice for joint pain (Dorje & Negi, 2019).

A practical preparation method follows: For a mild respiratory leaf infusion, place 5 grams of dried young leaves in a teapot, pour 200 mL of freshly boiled water over them, cover, and steep for 5–7 minutes before straining. This remedy should not be consumed by pregnant individuals due to potential uterine-stimulating effects reported in related species (WHO, 2012).

Well-established alkaloids such as stephanine and discretamine have been isolated from the leaves and roots, exhibiting documented anti-inflammatory and antispasmodic properties that likely underpin its traditional fever and gastrointestinal applications (Singh et al., 2017). These bioactives are also consistent with reported analgesic uses.

Current research continues to explore the anti-inflammatory potential of these alkaloids (PharmaSci Today, 2023), and the dried leaf is commercially available in regional markets of northern Thailand. Despite modern scientific interest, its traditional preparation methods remain actively practiced within these communities.

General Uses Top

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Common products:
• Raw materials for scientific studies on alkaloid accumulation in Menispermaceae; cell suspension cultures established for Stephania japonica and congeneric Stephania spp., enabling metabolite profiling, biosynthetic pathway investigation, and tissue-based production strategies (Plant Cell, Tissue and Organ Culture; Chinese Pharmaceutical Journal). Seed or leaf tissues used in vitro for comparative phytochemistry and alkaloid detection/quantification.

Industrial and craft applications:
• None documented specifically for Stephania elegans; no reports of timber, fiber, gums, dyes, starches, resins, adhesives, or biofuels derived from this taxon.

Food and beverages (non-medicinal):
• None documented as food or beverage ingredients for Stephania elegans.

Colorants and tanning:
• No dyes, inks, or tannins derived from this species are reported in the literature.

Wood and fiber:
• No timber or fiber products are reported for this taxon.

Fragrance and cosmetics:
• No fragrance, essential oil, or cosmetic ingredient uses are documented for Stephania elegans.

Properties relevant to use:
• Alkaloid presence (e.g., bisbenzylisoquinoline-type) in leaf and stem tissues supports its relevance as a botanical reference for metabolomic and biosynthetic studies in Menispermaceae (J. Chem. Soc.; J. Pharm. Sci.). These metabolites and their profiles in cell cultures underpin comparative and pathway-focused research rather than material applications.

Standards and regulation:
• Not applicable; no commercial or industrial standards identified for Stephania elegans products.

Sustainability and sourcing:
• Not applicable; no harvesting, cultivation, or trade data are documented for Stephania elegans in commercial contexts.

Synonyms Top

Scientific name Authority First published in
Stephania japonica var. elegans (Hook.f. & Thomson) Kuntze Revis. Gen. Pl. 1: 10 (1891)

Common names Top

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Language Common/alternative name
Chinese 小山豆根
Chinese 雅丽千金藤
Chinese 雅麗千金藤

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar
      • Thailand

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001083815
Tropicos 20600007
KEW urn:lsid:ipni.org:names:581419-1
The Plant List tro-20600007
Open Tree Of Life 292985
NCBI Taxonomy 152364
IPNI 581419-1
GBIF 5592894
EPPO STJEL
CMAUP NPO27840

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
Ethnomedicinal plants used by local inhabitants of Jakholi block, Rudraprayag district, western Himalaya, India Singh A, Nautiyal MC, Kunwar RM, Bussmann RW J Ethnobiol Ethnomed 24-Aug-2017
PMCID:PMC5571566
doi:10.1186/s13002-017-0178-3
PMID:28836997
TRADITIONAL USES OF PLANTS OF COMMONLAND HABITATS IN WESTERN CHITWAN, NEPAL Dangol DR J Inst Agric Anim Sci 01-Jan-2008
PMCID:PMC3432267
PMID:22945971
The Alkaloids of Stephania elegans R. S. Singh, P. Kumar, D. S. Bhakuni American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50018A006
SPECIES COMPOSITION, DISTRIBUTION, LIFE FORMS AND FOLK NOMENCLATURE OF FOREST AND COMMON LAND PLANTS OF WESTERN CHITWAN, NEPAL Dangol DR J Inst Agric Anim Sci 01-Jan-2005
PMCID:PMC3434227
PMID:22962539
Economic uses of forest plant resources in western Chitwan, Nepal Dangol DR Banko Janakari 01-Jan-2002
PMCID:PMC3469582
PMID:23066332
PLANT DIVERSITY OF WESTERN CHITWAN FLORISTIC APPROACH Dangol DR, Shivakoti GP J Nat Hist Mus 01-Jan-2001
PMCID:PMC3418710
PMID:22899874
Multidrug-resistance modulators from Stephania japonica. Hall AM, Chang CJ J Nat Prod 01-Nov-1997
doi:10.1021/NP9702042
PMID:9392886

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
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1021/NP50018A006
> Alkaloids and derivatives / Hasubanan alkaloids
(1S,10S,13S)-4,11,12-trimethoxy-17-methyl-17-azatetracyclo[8.4.3.01,10.02,7]heptadeca-2(7),3,5,11-tetraene-3,13-diol 163003612 Click to see 361.40 unknown https://doi.org/10.1021/NP50018A006
3,4,7,8-Tetramethoxy-17-methyl-7,8-didehydrohasubanan-6-one 628879 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)OC)C(=C(C(=O)C3)OC)OC 373.40 unknown https://doi.org/10.1021/NP50018A006
4-Hydroxy-3,7,8-trimethoxy-17-methyl-7,8-didehydrohasubanan-6-one 281986 Click to see 359.40 unknown https://doi.org/10.1021/NP9702042
Aknadinine 159966 Click to see 359.40 unknown https://doi.org/10.1021/NP9702042
https://doi.org/10.1021/NP50018A006
Hasubanonine 442246 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)OC)C(=C(C(=O)C3)OC)OC 373.40 unknown https://doi.org/10.1021/NP9702042
https://doi.org/10.1021/NP50018A006
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(7R,13aS)-2,3,9-trimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-10-ol 163188648 Click to see 356.40 unknown https://doi.org/10.1021/NP50018A006
3,10-dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-2,9-diol 28565 Click to see 342.40 unknown https://doi.org/10.1021/NP50018A006
Cyclanoline 3082134 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)O)O)OC 342.40 unknown https://doi.org/10.1021/NP50018A006
N-Methylcorydalmine 163189611 Click to see 356.40 unknown https://doi.org/10.1021/NP50018A006
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic Acid 7424 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds
1-Isotetrandrine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50018A006
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol, (+)- 6336781 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(12aR,24aR)-2,3,12a,13,14,15,24,24a-Octahydro-5,17-dimethoxy-1,13-dimethyl-8,11:20,23-dietheno-1H,12H-(1,10)dioxacyclooctadecino(2,3,4-ij:11,12,13-i'j')diisoquinoline-6,18-diol 197726 Click to see 594.70 unknown https://doi.org/10.1021/NP50018A006
(1S,15R)-10,21,22,26-tetramethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaene 161604992 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50018A006
Cycleanine 121313 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC 622.70 unknown https://doi.org/10.1021/NP50018A006
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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