Rubus xanthocarpus is a type of flowering plant that belongs to the raspberry genus Rubus and the Rosaceae family. It is originally found in central and southern China, but has also been introduced to Poland and the former Czechoslovakia. This plant is widely available from commercial suppliers. Its fruit, which are orange-yellow in color, are edible and have a similar taste to raspberries. They can be consumed raw or used to make preserves or wine.

Synonyms Top

Scientific name	Authority	First published in
Rubus spinipes	Hemsl.	J. Linn. Soc., Bot. 29: 306 (1892)
Rubus potaninii	Regel	; 1892 108 1892
Rubus sitiens	Focke	Biblioth. Bot. 17(Heft 72.1): 117 (29). 1910

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	عوسج أصفر
Czech	ostružiník žlutoplodý
Danish	guldbær
German	goldbeere
Swedish	guldhallon
Chinese	地梅子
Chinese	地莓子
Chinese	黄果悬钩子
Chinese	泡儿刺
Chinese	莓子刺
Chinese	黄莓子

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-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast

Europe click to expand
- Middle Europe
  - Czechoslovakia
  - Poland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001017827
USDA Plants	RUXA2
Tropicos	27807864
KEW	urn:lsid:ipni.org:names:741293-1
The Plant List	rjp-8571
Open Tree Of Life	3907075
Observations.org	151528
NCBI Taxonomy	2761762
IPNI	741293-1
iNaturalist	829095
GBIF	2989336
EPPO	RUBXA
EOL	231156
Elurikkus	215310
USDA GRIN	32492
Wikipedia	Rubus_xanthocarpus
CMAUP	NPO28344

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

Characteristics and phylogenetic analysis of the complete chloroplast genome of Rubus chingii Hu 1925 from the family Rosaceae

Li Y, Qiu Y, Yang M, Yin Y, Li M, Zhang Y

Mitochondrial DNA B Resour

20-Nov-2023

PMCID:	PMC10986437
doi:	10.1080/23802359.2023.2268220
PMID:	38566881

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

Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities

Desmiaty Y, Hanafi M, Saputri FC, Elya B, Rifai EA, Syahdi RR

Sci Rep

14-Oct-2021

PMCID:	PMC8516952
doi:	10.1038/s41598-021-99970-x
PMID:	34650166

Diversity, knowledge, and valuation of plants used as fermentation starters for traditional glutinous rice wine by Dong communities in Southeast Guizhou, China

He J, Zhang R, Lei Q, Chen G, Li K, Ahmed S, Long C

J Ethnobiol Ethnomed

27-Apr-2019

PMCID:	PMC6486954
doi:	10.1186/s13002-019-0299-y
PMID:	31029145

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

Ethnobotany of wild plants used for starting fermented beverages in Shui communities of southwest China

Hong L, Zhuo J, Lei Q, Zhou J, Ahmed S, Wang C, Long Y, Li F, Long C

J Ethnobiol Ethnomed

28-May-2015

PMCID:	PMC4458060
doi:	10.1186/s13002-015-0028-0
PMID:	26017691

Wild food plants used by the Tibetans of Gongba Valley (Zhouqu county, Gansu, China)

Kang Y, Łuczaj Ł, Kang J, Wang F, Hou J, Guo Q

J Ethnobiol Ethnomed

06-Feb-2014

PMCID:	PMC3933068
doi:	10.1186/1746-4269-10-20
PMID:	24502461

Pentacyclic triterpenoids from Rubus xanthocarpus

Bao-Zhi Li, Bin-Gui Wang, Zhong-Jian Jia

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(98)00161-7

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-14-oxo-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	102480386	Click to see CC1CCC2(CCC3=C(C2C1C)C(=O)CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	780.90	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6bR,8aR,10S,12aR,14bS)-2,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate	21625902	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)O	751.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9-formyl-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	53463457	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	664.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
24-epi-Pinfaensin	11802541	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	664.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
4-Epi-niga-ichigoside	134693040	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	666.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
4-O-methyl 8a-O-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,3R,4R,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-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-4,8a-dicarboxylate	23259300	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	694.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
4-O-methyl 8a-O-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 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-4,8a-dicarboxylate	74037098	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	694.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
Quercilicoside A	14055729	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	666.80	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4S,5R,8R,10S,13R,14R,17R,18R)-10-hydroxy-5,9,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one	102480384	Click to see CC1(CCC23CCC4C5(CCC6C(C(CCC6(C5CCC4(C2C1)OC3=O)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
(1S,2R,4S,4aS,6aR,6aR,6bR,8aR,12aR,14bS)-4-hydroxy-1,2,6b,9,9,12a-hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid	102480385	Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C(=O)O)C(=O)O)O	500.70	unknown	via CMAUP database
dimethyl (2R,3R,4R,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-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-4,8a-dicarboxylate	162877831	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)O)O)C)C)C2C1(C)O)C)C(=O)OC	546.70	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
Dimethyl 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-4,8a-dicarboxylate	14707017	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)O)O)C)C)C2C1(C)O)C)C(=O)OC	546.70	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
Jacarandic acid	13653335	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(98)00161-7
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-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-carboxylate	101624723	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC	518.70	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
Methyl 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-carboxylate	73813138	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC	518.70	unknown	https://doi.org/10.1016/S0031-9422(98)00161-7
Quinovic acid	120678	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O	486.70	unknown	via CMAUP database
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(98)00161-7
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid	12314810	Click to see CC1(CCC2(CCC3=C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C(=O)O)C	442.70	unknown	via CMAUP database
3beta-Hydroxy-27-norolean-13-en-28-oic acid ethyl ester	101682287	Click to see CCOC(=O)C12CCC3=C(C1CC(CC2)(C)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C	470.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid	7067333	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
> Organoheterocyclic compounds / Indolizidines
Mitraphylline	94160	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
Uncarine A	188999	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	46936193	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one	15939939	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one	5318763	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	via CMAUP database
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
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Neohesperidin	442439	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O	610.60	unknown	via CMAUP database

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Rubus xanthocarpus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top