Rubus pungens
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
Suggest a correction!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
Add a new one! Suggest a correction!| 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 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| 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) |
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
Suggest others/fix!| 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)!
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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 / 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |