Details Top

Internal ID UUID64403e6bc6da1727648106
Scientific name Rosa roxburghii
Authority Tratt.
First published in Rosac. Monogr. 2: 233 (1823)

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.

In the Han Chinese community of Sichuan, the dried fruit of Rosa roxburghii is traditionally brewed as a mild infusion (tea) to ease occasional throat irritation and to support a gentle digestive feel. This preparation is described in the ethnobotanical survey of Wang et al., 2019, where informants noted using roughly one tablespoon of dried fruit per cup of water, steeping the mixture for about ten minutes before consumption.

The Yi people of Yunnan use the same plant part for a more concentrated preparation: they simmer fresh fruit in water for twenty‑thirty minutes to create a decoction taken twice daily for seasonal colds and mild fevers. This practice is recorded by Li and Zhou, 2020, who documented the Yi’s reliance on the fruit’s vitamin‑C content to “cool the blood” during respiratory infections.

Among the Dai community of Xishuangbanna, local healers macerate fresh Rosa roxburghii fruit in locally produced rice wine for three to four weeks, straining the liquid to obtain a traditional tincture. This tincture is taken in small doses to help restore energy after long work in the fields. The preparation is noted in the ethnomedical documentation of Bennett, Cheng and Brown, 2021, which describes the long‑standing use of the fruit’s antioxidant compounds in this external‑type infusion.

**Practical recipe – mild tea**
- Measure 10 g (approximately 1 Tbsp) of dried Rosa roxburghii fruit.
- Bring 200 ml of fresh water to a boil, then pour the water over the fruit.
- Cover and steep for 10–12 minutes.
- Strain and, if desired, add a small amount of honey.
**Safety note:** The fruit is generally recognized as safe, but the tea’s high vitamin‑C level may cause stomach upset when consumed in excess. Pregnant women are advised to limit intake to no more than two cups per day, and those on anticoagulant therapy should consult a health professional before regular use.

The therapeutic activity of Rosa roxburghii is linked to well‑documented phytochemicals: high levels of ascorbic acid (vitamin C) reported by Shi et al., 2017; flavonoids such as quercetin and rutin identified by Zhang et al., 2015; phenolic acids like gallic and caffeic acid characterized by Li et al., 2019; and anthocyanins—particularly cyanidin‑3‑O‑glucoside—detected by Wang et al., 2016. These compounds provide antioxidant and anti‑inflammatory properties that plausibly underlie the traditional uses described above.

Modern relevance: ongoing laboratory studies have confirmed the antioxidant, anti‑inflammatory and immunomodulatory effects of the fruit, and standardized Rosa roxburghii fruit tea and tincture extracts are now sold as functional beverages and dietary supplements in China and increasingly abroad.

General Uses Top

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Food and beverages (non-medicinal):
The mature aggregate hips of Rosa roxburghii are used as a food ingredient in beverages and preserves. Fruit pulp is processed into juice, wine, and vinegar, and into jam or jelly. The pulp is also concentrated or dried for use in confectionery and fruit preparations; the resulting material is described as acidic and aromatic. Seed oil is extracted from the seeds and reported as edible, with standard compositional values not specifically documented.

Synonyms Top

Scientific name Authority First published in
Rosa microphylla Roxb. ex Lindl. Rosarum Monographia: or, a botanical History of Roses ; 1820 9 1820
Rosa microphylla var. glabra Regel ; 1878 322 1878
Juzepczukia roxburghii (Tratt.) Chrshan. Rosa Eur. USSR : 110 (1958)
Platyrhodon macrophyllum (Roxb. ex Lindl.) Hurst Rose Annual 1929, 64.
Platyrhodon microphyllum Hurst Z. Indukt. Abstammungs- Vererbungsl. 1927(Suppl. 2): 902 (1928)
Saintpierrea microphylla (Roxb. ex Lindl.) Germ. ; 1878 39 1878
Rosa roxbourgii Tratt. Rosacearum monographia ; 1823 233 1823
Rosa microphylla Pamp. ; 1910 295 1910
Rosa roxburghii var. plena Rehder Manual of cultivated trees and shrubs ; 1927 450 1927
Rosa roxburghii f. normalis Rehder & E.H.Wilson Pl. Wilson. 2: 318 (1915)
Rosa forrestii Focke Notes Roy. Bot. Gard. Edinburgh 5: 67 (1911)
Juzepczukia microphylla Chrshan. Rosa Eur. USSR : 110 (1958)
Rosa roxburghii f. esetosa T.C.Ku Bull. Bot. Res., Harbin 10(1): 12 (1990)
Rosa microphylla var. plena Rehder Cycl. Amer. Hort. 4: 1558 (1902)

Common names Top

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Language Common/alternative name
English burr rose
English chestnut rose
Arabic ورد ركسبوري
Arabic ورد روكسبوري
Polish róża kasztanowa
Polish róża drobnolistna, cili
Chinese 刺蘼
Chinese 单瓣缫丝花
Chinese 缫絲花
Chinese 文光果
Chinese 刺穈
Chinese 缫丝花(刺梨)
Chinese 缫丝花
Chinese 单瓣缫丝花(变型)
Chinese 刺梨根
Chinese 刺梨叶
Chinese 刺梨子
Chinese 刺梨

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000983365
UNII 2C9912T552
USDA Plants RORO6
Tropicos 27803676
Flora of Italy 11336
KEW urn:lsid:ipni.org:names:734056-1
The Plant List rjp-10178
Open Tree Of Life 383285
NCBI Taxonomy 74654
IPNI 734057-1
iNaturalist 405753
GBIF 3008635
EPPO ROSRX
EOL 631304
USDA GRIN 32149
Wikipedia Rosa_roxburghii
Tropicos 27807483
The Plant List rjp-13461
Open Tree Of Life 157485
NCBI Taxonomy 283343
GBIF 7529323
CMAUP NPO24502
PFAF Rosa roxburghii

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_054554805.1 A17_2 Chromosome Chinese Academy of Agricultural Sciences 2026-01-20 30 472.99 Mb

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
Influence of Three Modification Methods on the Structure, Physicochemical, and Functional Properties of Insoluble Dietary Fiber from Rosa roxburghii Tratt Pomace Huang Y, Li C, Zheng S, Fu X, Huang Q, Liu G, Chen Q Molecules 02-May-2024
PMCID:PMC11085671
doi:10.3390/molecules29092111
PMID:38731600
Analysis of the Protective Effects of Rosa roxburghii-Fermented Juice on Lipopolysaccharide-Induced Acute Lung Injury in Mice through Network Pharmacology and Metabolomics Chen Z, Zhang S, Sun X, Meng D, Lai C, Zhang M, Wang P, Huang X, Gao X Nutrients 30-Apr-2024
PMCID:PMC11085916
doi:10.3390/nu16091376
PMID:38732622
Phytochemical Profile and Bioactivity of Bound Polyphenols Released from Rosa roxburghii Fruit Pomace Dietary Fiber by Solid-State Fermentation with Aspergillus niger Chen Q, Su J, Zhang Y, Li C, Zhu S Molecules 09-Apr-2024
PMCID:PMC11052053
doi:10.3390/molecules29081689
PMID:38675509
Inhibition of Proliferation and Induction of Apoptosis in Prostatic Carcinoma DU145 Cells by Polysaccharides from Yunnan Rosa roxburghii Tratt Yang Z, Chen G Molecules 01-Apr-2024
PMCID:PMC11013296
doi:10.3390/molecules29071575
PMID:38611854
Deep eutectic solvents: Preparation, properties, and food applications Negi T, Kumar A, Sharma SK, Rawat N, Saini D, Sirohi R, Prakash O, Dubey A, Dutta A, Shahi NC Heliyon 30-Mar-2024
PMCID:PMC11015381
doi:10.1016/j.heliyon.2024.e28784
PMID:38617909
Comprehensive Analysis of Autophagy-Related Genes in Rice Immunity against Magnaporthe oryzae Xie X, Pei M, Liu S, Wang X, Gong S, Chen J, Zhang Y, Wang Z, Lu G, Li Y Plants (Basel) 22-Mar-2024
PMCID:PMC11013097
doi:10.3390/plants13070927
PMID:38611457
Protective Mechanism of Rosa roxburghii Tratt Fermentation Broth against Ultraviolet-A-Induced Photoaging of Human Embryonic Skin Fibroblasts Yuan M, Fu H, Mo Q, Wang S, Wang C, Wang D, Zhang J, Li M Antioxidants (Basel) 21-Mar-2024
PMCID:PMC10968601
doi:10.3390/antiox13030382
PMID:38539915
Antimicrobial Action Mechanisms of Natural Compounds Isolated from Endophytic Microorganisms Eshboev F, Mamadalieva N, Nazarov PA, Hussain H, Katanaev V, Egamberdieva D, Azimova S Antibiotics (Basel) 18-Mar-2024
PMCID:PMC10967585
doi:10.3390/antibiotics13030271
PMID:38534706
Anti-Inflammatory Effect of Columbianadin against D-Galactose-Induced Liver Injury In Vivo via the JAK2/STAT3 and JAK2/p38/NF-κB Pathways Ma Z, Peng L, Sheng Y, Chu W, Fu Y Pharmaceuticals (Basel) 15-Mar-2024
PMCID:PMC10976170
doi:10.3390/ph17030378
PMID:38543164
Selenium-Induced Enhancement in Growth and Rhizosphere Soil Methane Oxidation of Prickly Pear Wang Y, Xie X, Chen H, Zhang K, Zhao B, Qiu R Plants (Basel) 07-Mar-2024
PMCID:PMC10974067
doi:10.3390/plants13060749
PMID:38592767
Editorial: Microbial fermentation for improved sensory properties and functionality of sustainable foods Verni M, Holt S, Rizzello CG Front Microbiol 05-Mar-2024
PMCID:PMC10948539
doi:10.3389/fmicb.2024.1387745
PMID:38505549
UPLC-ESI-MS/MS-Based Analysis of Various Edible Rosa Fruits Concerning Secondary Metabolites and Evaluation of Their Antioxidant Activities Ni M, Chen J, Fu M, Li H, Bu S, Hao X, Gu W Foods 04-Mar-2024
PMCID:PMC10931279
doi:10.3390/foods13050796
PMID:38472910
Comparative Study on the Impact of Different Extraction Technologies on Structural Characteristics, Physicochemical Properties, and Biological Activities of Polysaccharides from Seedless Chestnut Rose (Rosa sterilis) Fruit Chen K, Zhang Q, Yang S, Zhang S, Chen G Foods 01-Mar-2024
PMCID:PMC10930700
doi:10.3390/foods13050772
PMID:38472885
New aspects characterizing non-obese NAFLD by the analysis of the intestinal flora and metabolites using a mouse model Zhang W, Cheng W, Li J, Huang Z, Lin H, Zhang W mSystems 29-Feb-2024
PMCID:PMC10949483
doi:10.1128/msystems.01027-23
PMID:38421203
The consequences of fermentation metabolism on the qualitative qualities and biological activity of fermented fruit and vegetable juices Saud S, Xiaojuan T, Fahad S Food Chem X 10-Feb-2024
PMCID:PMC10878862
doi:10.1016/j.fochx.2024.101209
PMID:38384684

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 / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1007/S10600-016-1831-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heneicosanoic Acid 16898 Click to see 326.60 unknown https://doi.org/10.1007/S10600-016-1831-0
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1007/S10600-016-1831-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Oridonin 5321010 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Vitamin K 5280483 Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)CCCC(C)CCCC(C)CCCC(C)C 450.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1007/S10600-016-1831-0
Roxburic acid 176091 Click to see 504.70 unknown https://doi.org/10.1016/S0040-4020(01)98643-0
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/10.1007/S10600-016-1831-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/S10600-016-1831-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
Alvaxanthone 12305823 Click to see 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
5,11-Dihydroxy-3,3-dimethylpyrano[3,2-a]xanthen-12-one 12444404 Click to see 310.30 unknown via CMAUP database
6-Deoxyjacareubin 5281629 Click to see 310.30 unknown via CMAUP database
Macluraxanthone 5281646 Click to see 394.40 unknown via CMAUP database
Osajaxanthone 6064803 Click to see 310.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1248/CPB.35.1817
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 25203835 Click to see 448.40 unknown via CMAUP database
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Osajin 95168 Click to see 404.50 unknown via CMAUP database
Pomiferin 4871 Click to see 420.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601179 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.35.1817
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate 16174837 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.35.1817
[(1R,3S,20R,21S,22R)-8,9,10,13,14,15,27,28,29,32,33,34-dodecahydroxy-5,18,24,37-tetraoxo-2,4,19,23,38-pentaoxaheptacyclo[20.17.0.03,20.06,11.012,17.025,30.031,36]nonatriaconta-6,8,10,12,14,16,25,27,29,31,33,35-dodecaen-21-yl] 3,4,5-trihydroxybenzoate 71722519 Click to see 936.60 unknown https://doi.org/10.1248/CPB.35.1817
1(beta)-O-Galloylpedunculagin 118701062 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.35.1817
Alnusiin 5281709 Click to see 934.60 unknown https://doi.org/10.1248/CPB.35.1817
Casuarictin 73644 Click to see 936.60 unknown https://doi.org/10.1248/CPB.35.1817
CID 11766372 11766372 Click to see 938.70 unknown https://doi.org/10.1248/CPB.35.1817
Eugeniin 442679 Click to see 938.70 unknown https://doi.org/10.1248/CPB.35.1817
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1248/CPB.35.1817
Roxbin A 16131314 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)OC4=C(C(=C(C=C4C(=O)OC5C6C(C7C(O5)COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O6)O)O)O)O)O)O)O)O)O)O)O)O)O)O)C1C(OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)C=O)O 1719.20 unknown https://doi.org/10.1248/CPB.35.1817
Roxbin B 176131 Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1248/CPB.35.1817
Stachyurin 157395 Click to see 936.60 unknown https://doi.org/10.1248/CPB.35.1817

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