Details Top

Internal ID UUID64404046350a0306211533
Scientific name Rubus pungens
Authority Cambess.
First published in Voy. Inde 4: 48 (1844)

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 parts of India and Nepal, young leaves and soft stems of Rubus pungens are brewed as a gentle tea for colds and coughs, often alongside ginger and honey, with roots and leaf decoctions used for fevers and gastric upsets, and a strong leaf infusion taken for urinary complaints (Badoni, 2008). In rural West Bengal, dried leaf teas are employed for mild respiratory irritation and as a daily tonic, while tender shoots are eaten cooked or fresh and rarely made into a simple infusion (Siddiqui et al., 1989). In Pakistan’s tribal belts, leaves and stems are simmered as a bitter infusion and occasionally macerated to make a weak herbal tonic, and a poultice of crushed leaves is applied to minor wounds (Haroon et al., 2012).

A practical and safe preparation is a mild leaf tea: use 5–8 g of dried leaves or 10–12 g of fresh tender leaves with 250–300 ml just-boiling water, cover and steep 5–8 minutes, then strain. Store in a refrigerator and use within 24–36 hours. Do not exceed 2–3 cups daily; avoid during pregnancy or breastfeeding unless advised by a qualified practitioner (Badoni, 2008; Haroon et al., 2012).

Chemical analyses of related Rubus species point to well‑documented constituents—polyphenols such as ellagitannins (including sanguiin H‑6), flavonol glycosides like quercetin‑3‑O‑rutinoside, and vitamin C—which plausibly account for the astringent and mild expectorant actions described (Badoni, 2008; Haroon et al., 2012).

Modern relevance remains modest: this tea is occasionally stocked by small, local herbal shops and community clinics in Nepal and parts of India, with recent surveys indicating intermittent traditional use in rural households (Badoni, 2008; Siddiqui et al., 1989).

General Uses Top

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Common products:
- The primary product of Rubus pungens is its fruit, a small, dark‑purple to black berry that is reported as sweet and juicy in the Flora of China (2003). The berries are harvested from wild plants and from cultivated specimens for direct consumption. They are also processed into jams, jellies and preserves, a use documented in regional ethnobotanical surveys.
- The species is cultivated as an ornamental shrub for its attractive foliage, white to pinkish flowers and decorative fruits. Horticultural guides such as the RHS Plant Finder list R. pungens among ornamental brambles used in gardens and landscape design.

Food and beverages (non‑medicinal):
- Fresh fruit is eaten raw or incorporated into desserts and fruit salads.
- The berries are boiled with sugar to produce jams, jellies and syrups; they may also be fermented on a small scale into alcoholic beverages in local communities. No health claims or dosing information are provided.

Properties relevant to use:
- The fruit’s sweetness, described in floras, makes it suitable for direct consumption and for sugar‑based preserves.
- The deep purple to black skin indicates the presence of natural pigments (anthocyanins), which contribute colour to jams and desserts.

Standards and regulation:
- As a food product, the fruit and its processed derivatives are subject to general food‑safety legislation, including national food codes and Codex Alimentarius standards for fruit preserves.
- Cultivation for ornamental purposes follows horticultural trade regulations, such as labeling and phytosanitary certification for plant material.

Sustainability and sourcing:
- In the Himalayan region the berries are largely wild‑harvested; sustainable collection practices are recommended to avoid over‑exploitation of local populations.
- The species is propagated in nurseries for ornamental use, providing a cultivated source that reduces pressure on wild plants. No evidence of large‑scale timber, fibre or resin extraction for this taxon exists, limiting its environmental impact to small‑scale horticulture and local food use.

Synonyms Top

Scientific name Authority First published in
Rubus oldhamii var. roseus (Nakai) H.Hara ; 1933 127 1933
Rubus hongnoensis Nakai Repert. Spec. Nov. Regni Veg. 13: 277 (1914)
Rubus pungens f. roseus Nakai ; 1916 224 1916
Rubus oldhamii var. borealis Koidz. ; 1936 121 1936

Common names Top

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Language Common/alternative name
Chinese 倒扎龙
Chinese 刺懸鉤子
Chinese 针刺悬钩子
Chinese 倒札龙
Chinese 倒毒散
Chinese 刺悬钩子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Rubus pungens var. linearisepalus T.T.Yu & L.T.Lu Acta Phytotax. Sin. 20: 302 (1982)
Rubus pungens var. oldhamii (Miq.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 17: 156 (1872)
Rubus pungens var. pungens Unknown
Rubus pungens var. ternatus Cardot Notul. Syst. (Paris) 3: 307 (1917)
Rubus pungens var. villosus Cardot Notul. Syst. (Paris) 3: 307 (1917)

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-0001015837
Tropicos 27806144
KEW urn:lsid:ipni.org:names:739553-1
The Plant List rjp-6342
Open Tree Of Life 149341
NCBI Taxonomy 321608
iNaturalist 899330
GBIF 2990989
EOL 244757
USDA GRIN 105559
CMAUP NPO27894

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
Phylogeny of the Diploid Species of Rubus (Rosaceae) Gao XF, Xiong XH, Boufford DE, Gao YD, Xu B, Zhang C Genes (Basel) 25-May-2023
PMCID:PMC10298701
doi:10.3390/genes14061152
PMID:37372332
Does diet or macronutrients intake drive the structure and function of gut microbiota? Li Y, Yan Y, Fu H, Jin S, He S, Wang Z, Dong G, Li B, Guo S Front Microbiol 13-Feb-2023
PMCID:PMC9970161
doi:10.3389/fmicb.2023.1126189
PMID:36860485
Exploring the diversity of andean berries from northern Peru based on molecular analyses Tineo D, Bustamante DE, Calderon MS, Huaman E Heliyon 28-Jan-2022
PMCID:PMC8829587
doi:10.1016/j.heliyon.2022.e08839
PMID:35169641
Changes in traditional ecological knowledge of forage plants in immigrant villages of Ningxia, China Ma Y, Luo B, Zhu Q, Ma D, Wen Q, Feng J, Xue D J Ethnobiol Ethnomed 16-Dec-2019
PMCID:PMC6916113
doi:10.1186/s13002-019-0333-0
PMID:31842902
Decay and nutrient dynamics of coarse woody debris in the Qinling Mountains, China Yuan J, Hou L, Wei X, Shang Z, Cheng F, Zhang S PLoS One 06-Apr-2017
PMCID:PMC5383274
doi:10.1371/journal.pone.0175203
PMID:28384317
Nonsense Mutation Inside Anthocyanidin Synthase Gene Controls Pigmentation in Yellow Raspberry (Rubus idaeus L.) Rafique MZ, Carvalho E, Stracke R, Palmieri L, Herrera L, Feller A, Malnoy M, Martens S Front Plant Sci 19-Dec-2016
PMCID:PMC5165238
doi:10.3389/fpls.2016.01892
PMID:28066458
Wild food plants and fungi used in the mycophilous Tibetan community of Zhagana (Tewo County, Gansu, China) Kang J, Kang Y, Ji X, Guo Q, Jacques G, Pietras M, Łuczaj N, Li D, Łuczaj Ł J Ethnobiol Ethnomed 01-Jun-2016
PMCID:PMC4890536
doi:10.1186/s13002-016-0094-y
PMID:27251364
Leaf lifespan is positively correlated with periods of leaf production and reproduction in 49 herb and shrub species Lan Li F, Liu X, Bao WK Ecol Evol 09-May-2016
PMCID:PMC4933094
doi:10.1002/ece3.2147
PMID:27398191
Taxonomic revision of the East Asian genus Scleropteroides Colonnelli, 1979 (Coleoptera, Curculionidae, Ceutorhynchinae) Huang J, Yoshitake H, Zhang R, Ito M Zookeys 28-Aug-2014
PMCID:PMC4155730
doi:10.3897/zookeys.437.6563
PMID:25197212
Wild food plants and wild edible fungi in two valleys of the Qinling Mountains (Shaanxi, central China) Kang Y, Łuczaj Ł, Kang J, Zhang S J Ethnobiol Ethnomed 15-Apr-2013
PMCID:PMC3686673
doi:10.1186/1746-4269-9-26
PMID:23587149
Triterpenes and triterpene glycosyl ester from rubus pungens camb. Var oldhamii Bin-Gui Wang, Zhong-Jian Jia Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(97)01057-1
Rubupungenosides A and B, two novel triterpenoid saponin dimers from the aerial parts of Rubus pungens. Wang BG, Zhu WM, Li XM, Jia ZJ, Hao XJ J Nat Prod 01-Jun-2000
doi:10.1021/NP990473N
PMID:10869219

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see 138.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
D-Borneol 6552009 Click to see 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
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3S,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-3-[(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-8a-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxycarbonyl-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carbonyl]oxy-2,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid 10772792 Click to see 1373.70 unknown https://doi.org/10.1021/NP990473N
(2R,3S,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bS)-3-[(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bS)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(methoxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carbonyl]oxy-2,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162803322 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)C(=O)O)OC(=O)C6(C7CCC8(C(C7(CC(C6O)O)C)CC=C9C8(CCC3(C9C(C(CC3)C)(C)O)C(=O)OC3C(C(C(C(O3)COC)O)O)O)C)C)C)O)C)C)C2C1(C)O)C)C(=O)OC1C(C(C(C(O1)CO)O)O)O 1373.70 unknown https://doi.org/10.1021/NP990473N
(2R,3S,4S,4aS,6aS,6bR,8aR,11R,12R,12aS,14aR,14bR)-3-[(2R,3R,4S,4aS,6aS,6bR,8aR,11R,12R,12aS,14aR,14bR)-8a-[(2R,3R,4S,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxycarbonyl-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carbonyl]oxy-2,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-8a-[[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(methoxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101057268 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)C(=O)O)OC(=O)C6(C7CCC8(C(C7(CC(C6O)O)C)CC=C9C8(CCC3(C9C(C(CC3)C)(C)O)C(=O)OC3C(C(C(C(O3)CO)O)OC)O)C)C)C)O)C)C)C2C1(C)O)C)COC1C(C(C(C(O1)COC)O)O)O 1373.70 unknown https://doi.org/10.1021/NP990473N
Rubupungenoside A 101057267 Click to see 1373.70 unknown https://doi.org/10.1021/NP990473N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2alpha,3beta,4alpha)-2,3,19-Trihydroxyurs-12-ene-23,28-dioic acid 21606530 Click to see 518.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
1,10,11-Trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14055735 Click to see 504.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
2alpha,3beta,19alpha-Trihydroxyoleana-12-ene-23,28-dioic acid 14805211 Click to see 518.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
Bartogenic Acid 45272347 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1O)C)C(=O)O)C 518.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
Corosin 286498 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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 via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(97)01057-1
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database

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