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Rubus amabilis

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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 UUID6440404333389455843475
Scientific name Rubus amabilis
Authority Focke
First published in Beibl. Bot. Jahrb. Syst. 82: 53 (1905)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English showy blackberry
Chinese 大叶蛇泡簕
Chinese 秀丽莓
Chinese 美丽悬钩子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Rubus amabilis var. aculeatissimus T.T.Yu & L.T.Lu Acta Phytotax. Sin. 20: 301 (1982)
Rubus amabilis var. microcarpus T.T.Yu & L.T.Lu Acta Phytotax. Sin. 20: 301 (1982)

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Qinghai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001015798
Tropicos 27807754
KEW urn:lsid:ipni.org:names:735009-1
The Plant List rjp-6298
Open Tree Of Life 721758
NCBI Taxonomy 616954
IPNI 735009-1
GBIF 2988982
EPPO RUBAB
EOL 300849
USDA GRIN 32257

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
Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC Front Pharmacol 08-Mar-2024
PMCID:PMC10957545
doi:10.3389/fphar.2024.1349725
PMID:38523640
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
Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C Front Pharmacol 12-May-2023
PMCID:PMC10213330
doi:10.3389/fphar.2023.1166178
PMID:37251336
The complete chloroplast genome sequence of Rubus irritans Focke 1910 (Rosaceae) Han Y, Tong L, Zhang Z, Yang S, Yang F Mitochondrial DNA B Resour 26-Jan-2023
PMCID:PMC9888452
doi:10.1080/23802359.2023.2168113
PMID:36733273
The Effects of Antioxidants from Natural Products on Obesity, Dyslipidemia, Diabetes and Their Molecular Signaling Mechanism Khutami C, Sumiwi SA, Khairul Ikram NK, Muchtaridi M Int J Mol Sci 12-Feb-2022
PMCID:PMC8875143
doi:10.3390/ijms23042056
PMID:35216172
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
Synthesis of Zinc Oxide Nanoparticles Using Rubus fairholmianus Root Extract and Their Activity against Pathogenic Bacteria Rajendran NK, George BP, Houreld NN, Abrahamse H Molecules 19-May-2021
PMCID:PMC8161024
doi:10.3390/molecules26103029
PMID:34069558
The complete chloroplast genome sequence of Rubus sachalinensis Lévl Liu Y, Song Q, Kang W, Yang F, Yan W Mitochondrial DNA B Resour 12-May-2021
PMCID:PMC8118508
doi:10.1080/23802359.2021.1926354
PMID:34027073
The complete chloroplast genome sequence of Stephanandra incisa Zhang CP, Xu ZZ, Xie XM, Lu YZ, Li W, Wang KL, Jiang XQ Mitochondrial DNA B Resour 08-Feb-2021
PMCID:PMC7872555
doi:10.1080/23802359.2020.1867012
PMID:33659678
Phytoliths in selected broad-leaved trees in China Ge Y, Lu H, Wang C, Gao X Sci Rep 23-Sep-2020
PMCID:PMC7512002
doi:10.1038/s41598-020-72547-w
PMID:32968165
Screening active components from Rubus amabilis for pancreatic β-cells protection Sun M, Zhu T, Tong J, Caidan R, Wang K, Kai G, Zhang W, Ru L, Pengcuo J, Tong L Pharm Biol 13-Jul-2020
PMCID:PMC7470145
doi:10.1080/13880209.2020.1787467
PMID:32659127
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
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
Pregnane glycoside, lignan glycosides, triterpene glycosyl ester and flavonoid glycosides from Rubus amabilis. Chen C, Qixiu Z, Zhu Q, Jia Z Planta Med 01-Apr-2001
doi:10.1055/S-2001-11996
PMID:11345701

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1055/S-2001-11996
Symplocosin 5351523 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1055/S-2001-11996
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Niga-ichigoside F1 16118969 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/10.1055/S-2001-11996
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/10.1055/S-2001-11996
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
1-[(3S,8R,9S,10R,13S,14S,15S,17S)-15-hydroxy-10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 101103562 Click to see CC(=O)C1CC(C2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)O 494.60 unknown https://doi.org/10.1055/S-2001-11996
1-[15-hydroxy-10,13-dimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone 77181119 Click to see CC(=O)C1CC(C2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)O 494.60 unknown https://doi.org/10.1055/S-2001-11996
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1055/S-2001-11996
2'-O-galloylhyperin 6453359 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2001-11996
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 https://doi.org/10.1055/S-2001-11996
Quercetin 3-(2-galloylglucoside) 13889202 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2001-11996
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1055/S-2001-11996
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1055/S-2001-11996
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2001-11996
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2001-11996

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