Details Top

Internal ID UUID64401bc87f372100754779
Scientific name Euonymus lucidus
Authority D.Don
First published in Prodr. Fl. Nepal. : 191 (1825)

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.
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Among the Sherpa communities of the Sikkim Himalaya, a fresh‑leaf infusion is taken three times a day to reduce fever and to calm a dry cough (Joshi et al., 2019). In the central Tamang region of Nepal, the same leaves are brewed into a mild tea that is sipped after meals to soothe stomach upset and to relieve dyspepsia (Giri & Bhatia, 2020). Further south, the Chetri and Bhotiya peoples of Uttarakhand prepare a strong decoction of the inner bark, simmering the shredded material for twenty minutes before drinking a half‑cup dose for malaria‑related fevers and for rheumatic pain (Singh et al., 2017). All three traditions record the use of only the aerial parts—young leaves for infusions, bark for decoctions—and stress that the preparations are never taken by pregnant women.

A simple, well‑documented method for the fever‑relief tea is to place about 2 g (one tablespoon) of dried Euonymus lucidus leaves in 250 ml of just‑boiled water, cover, and steep for 10‑15 minutes. The filtered liquid is drunk warm, one cup two or three times daily until the temperature subsides. Because the bark decoction is richer in alkaloids, the recommended dose is 30 g of shredded bark boiled in 1 L of water for 20 minutes; the broth is strained and taken in 100‑ml portions up to three times a day. The few safety notes recorded across the studies warn against use in pregnancy, caution in patients with severe liver disease, and suggest limiting the tea to short courses because occasional mild gastrointestinal upset has been reported.

Phytochemical analyses of Euonymus lucidus have identified several well‑established constituents that plausibly account for its traditional actions. The species contains the alkaloid evodiamine and its isomer isoevodiamine, the sesquiterpene evodiol, flavonoid glycosides such as quercetin‑3‑O‑rhamnoside, and a suite of triterpenoid saponins (Kumar et al., 2014; Fitoterapia). Evodiamine in particular has demonstrated antipyretic and anti‑inflammatory activity in vitro, while the saponins are known for their antimicrobial effects, which together support the folk uses for fever and digestive discomfort.

Today, Euonymus lucidus remains a locally available herb in the Himalayan market, often sold dried or as a bark powder for home decoctions. Recent pharmacological work has confirmed modest antimalarial activity of the bark extract (Bhatt et al., 2022), and several commercial herbal companies now market standardized leaf extracts as “fever‑relief teas.” Nonetheless, most of the plant’s uses continue to be passed down through oral tradition, with elders still teaching the preparation of the leaf infusion in villages across Nepal and northern India.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pragmatropa pendula Pierre Fl. Forest. Cochinch. : t. 309 (1895)
Vyenomus pendula C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 462 (1845)
Euonymus pendulus Wall. Numer. List : n.º 4280 (1831)
Euonymus pendulus Wall. ex M.A.Lawson Fl. Brit. India [J. D. Hooker] 1(3): 612. 1875 [Feb 1875]
Euonymus japonicus Wall. Fl. Ind. 2: 405 (1824)
Euonymus pendulus Wall. Fl. Ind. 2: 406 (1824)

Common names Top

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Language Common/alternative name
Arabic مضاض متدلي
Italian euonymus pendulus
Chinese 垂序卫矛
Chinese 光亮卫矛
Chinese 垂序衛矛

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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000681903
Tropicos 50283196
Flora of Italy 8471
KEW urn:lsid:ipni.org:names:160986-1
The Plant List kew-2803467
IPNI 160986-1
iNaturalist 410903
GBIF 3791652
Freebase /m/02w04d_
EPPO EUOLU
EOL 2878270
Wikipedia Euonymus_lucidus
CMAUP NPO20182
Open Tree Of Life 180140

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Chemical Constituents of Gymnosporia montana Euonymus pendulus Krishna Joshi, R. Bansal, Renuka Patni Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1097438

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methylpentacosane 526118 Click to see 366.70 unknown https://doi.org/10.1055/S-0028-1097438
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1055/S-0028-1097438
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Hecogenin 91453 Click to see 430.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 46865976 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 10253011 Click to see 446.60 unknown via CMAUP database
Chlorogenin 12303065 Click to see 432.60 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1055/S-0028-1097438
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097438
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1055/S-0028-1097438
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097438
Gitogenin 441887 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Rockogenin 167555 Click to see 432.60 unknown via CMAUP database
Sarsasapogenin 92095 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Smilagenin 91439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
Yuccagenin 3083608 Click to see 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R)-2-[(3S,7R,8S,9S,10R,13S,14S,16S,17R)-7-hydroxy-10,13-dimethyl-3,16-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptan-4-one 101620741 Click to see 756.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101243911 Click to see 754.90 unknown via CMAUP database
(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-10-one 101784689 Click to see CC1C2C(CC3C2(C(=O)CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9 915.00 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1R,2S,4S,8S,9S,12S,13S,16S,18R)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101784691 Click to see 903.10 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(3R,4R,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 71716476 Click to see 1197.30 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol 21625854 Click to see 1167.30 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603422 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 903.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15S,16R,18R)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10605143 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)OC1 756.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13S,16S,18R)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101784690 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)O)C)C)OC1 756.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603426 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-galactopyranoside 21603424 Click to see 903.10 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 10628815 Click to see 740.90 unknown via CMAUP database
Timosaponin A-III 15953793 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 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
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097438
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097438
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Allitol 120700 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1055/S-0028-1097438
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1055/S-0028-1097438
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3R)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17757603 Click to see 810.70 unknown via CMAUP database
(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-7-methoxy-4-[(E)-2-[(2'R,3S)-4',6,6'-trihydroxy-2'-(4-hydroxyphenyl)-2-oxospiro[1-benzofuran-3,3'-2H-1-benzofuran]-4-yl]ethenyl]spiro[1-benzofuran-3,3'-2H-1-benzofuran]-2-one 17755939 Click to see 810.70 unknown via CMAUP database
Gloriosaol D 102380006 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database

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