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Rubus cochinchinensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440409b5de34912930384
Scientific name Rubus cochinchinensis
Authority Tratt.
First published in Rosac. Monogr. 3: 97 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rubus playfairii Hemsl. J. Linn. Soc., Bot. 23: 235 (1887)

Common names Top

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Language Common/alternative name
Vietnamese ngấy hương
Chinese 越南悬钩子
Chinese 五叶泡
Chinese 五叶泡叶
Chinese 蛇泡筋
Chinese 猫枚筋
Chinese 蛇藨筋
Chinese 鸡足刺

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Rubus cochinchinensis var. glabrescens Cardot Notul. Syst. (Paris) 3: 292 (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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001017951
Tropicos 27808093
KEW urn:lsid:ipni.org:names:735897-1
The Plant List rjp-8725
Open Tree Of Life 538507
Observations.org 507820
NCBI Taxonomy 714648
IPNI 735897-1
iNaturalist 55915
GBIF 2999072
EOL 635833
Elurikkus 350287

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
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Characterization of the complete chloroplast genome sequence of Rubus rufus Focke (Rosaceae) Huang W, Qiao F, Guo W, Wu W Mitochondrial DNA B Resour 30-Sep-2021
PMCID:PMC8491697
doi:10.1080/23802359.2021.1967810
PMID:34621984
Traditions and plant use during pregnancy, childbirth and postpartum recovery by the Kry ethnic group in Lao PDR Lamxay V, de Boer HJ, Björk L J Ethnobiol Ethnomed 10-May-2011
PMCID:PMC3120637
doi:10.1186/1746-4269-7-14
PMID:21569234
Triterpenes from Rubus cochinchinensis Trinh Phuong Lien, Christine Kamperdick, Tran Van Sung, Günter Adam Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00598-6

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2-acetyloxy-3,12-dihydroxy-4,6a,6b,11,12,14b-hexamethyl-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 100958603 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 722.90 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bS)-2-acetyloxy-3,12-dihydroxy-4,6a,6b,11,12,14b-hexamethyl-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 162853854 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 722.90 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
2-Acetyloxy-3,12-dihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[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 73157008 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 722.90 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13653345 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)00598-6
(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 163014055 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 7163172 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72977595 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OCC6C(C(C(C(O6)O)O)O)O 650.80 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 11-acetyloxy-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162844078 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OCC6C(C(C(C(O6)O)O)O)O 692.90 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162887112 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OCC6C(C(C(C(O6)O)O)O)O 650.80 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-11-acetyloxy-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162844079 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OCC6C(C(C(C(O6)O)O)O)O 692.90 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 9870041 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
2-Oxopomolic Acid 44593379 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(98)00598-6
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)00598-6
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)00598-6

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