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Rosa cymosa

Rosa cymosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644040a775446194023564
Scientific name Rosa cymosa
Authority Tratt.
First published in Rosac. Monogr. : 87 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rosa banksiae var. microcarpa (Lindl.) Regel ; 1878 376 1878
Rosa fragariiflora Ser. ex DC. Prodr. [A. P. de Candolle] 2: 601. 1825 [mid Nov 1825]
Rosa fragariifolia Steud. Nomencl. Bot. [Steudel], ed. 2. ii. 468, sphalm.
Rosa sorbifolia Anon. Revue horticole; journal d'horticulture pratique ; 1901 234 1905

Common names Top

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Language Common/alternative name
Arabic ورد سنمي
Persian رز سالخورده
Russian Роза полузонтичная
Chinese 小果蔷薇
Chinese 小果蔷薇叶
Chinese 小果蔷薇果
Chinese 小果蔷薇根
Chinese 小果蔷薇花
Chinese 小果蔷薇茎
Chinese 小果薔薇
Chinese 山木香
Chinese 野蔷薇
Chinese 倒钩竻
Chinese 红荆藤

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001018279
Tropicos 27803785
KEW urn:lsid:ipni.org:names:732228-1
The Plant List rjp-9092
Open Tree Of Life 868176
NCBI Taxonomy 117261
IPNI 732228-1
iNaturalist 639233
GBIF 3005661
Freebase /m/0clj9n
EPPO ROSCY
EOL 235184
USDA GRIN 5327
Wikipedia Rosa_cymosa

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
Determinants of taxonomic, functional, and phylogenetic beta diversity in breeding birds within urban remnant woodlots: Implications for conservation Liu Y, Zhu Y, Wu S, Wang Y, Xie J, Zhang K, Xu Y Ecol Evol 14-May-2024
PMCID:PMC11091548
doi:10.1002/ece3.11426
PMID:38746544
Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China Li K, Tan B, Liao M, Ni J Front Plant Sci 20-Mar-2024
PMCID:PMC10987713
doi:10.3389/fpls.2024.1348182
PMID:38571712
The complete chloroplast genome sequence of Rosa ‘Limoncello’ (Rosales: Rosaceae) Wang J, Xie QL, Feng EY, Liu XF Mitochondrial DNA B Resour 18-Dec-2023
PMCID:PMC10768736
doi:10.1080/23802359.2023.2290854
PMID:38189025
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Companion Plants of Tea: From Ancient to Terrace to Forest Wu H, Long X, Geng Y Plants (Basel) 25-Aug-2023
PMCID:PMC10490072
doi:10.3390/plants12173061
PMID:37687308
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
SMRT Sequencing Technology Was Used to Construct the Batocera horsfieldi (Hope) Transcriptome and Reveal Its Features Wei X, Xu D, Liu Z, Liu Q, Zhuo Z Insects 11-Jul-2023
PMCID:PMC10380457
doi:10.3390/insects14070625
PMID:37504630
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
Naturalization of an alien ancient fruit tree at a fine scale: Community structure and population dynamics of Cydonia oblonga in China Xie Y, Li J, Zhao L, Liu W, Gong Q, Deng M, Zhao M, Huang S Ecol Evol 06-Jan-2023
PMCID:PMC9817190
doi:10.1002/ece3.9703
PMID:36620396
Modulation of Cytoskeleton, Protein Trafficking, and Signaling Pathways by Metabolites from Cucurbitaceae, Ericaceae, and Rosaceae Plant Families Patel A, Rasheed A, Reilly I, Pareek Z, Hansen M, Haque Z, Simon-Fajardo D, Davies C, Tummala A, Reinhardt K, Bustabad A, Shaw M, Robins J, Vera Gomez K, Suphakorn T, Camacho Gemelgo M, Law A, Lin K, Hospedales E, Haley H, Perez Martinez JP, Khan S, DeCanio J, Padgett M, Abramov A, Nanjundan M Pharmaceuticals (Basel) 10-Nov-2022
PMCID:PMC9698530
doi:10.3390/ph15111380
PMID:36355554
Towards a unified theory of plant photosynthesis and hydraulics Joshi J, Stocker BD, Hofhansl F, Zhou S, Dieckmann U, Prentice IC Nat Plants 27-Oct-2022
PMCID:PMC9663302
doi:10.1038/s41477-022-01244-5
PMID:36303010
Study on the relationship between functional characteristics and environmental factors in karst plant communities Wang Y, Zhang L, Chen J, Feng L, Li F, Yu L Ecol Evol 20-Sep-2022
PMCID:PMC9486817
doi:10.1002/ece3.9335
PMID:36188516
Relationship between diversity and stability of a karst plant community Wang Y, Chen J, Zhang L, Feng L, Yan L, Li F, Zhao X, Yu L, Liu N Ecol Evol 26-Aug-2022
PMCID:PMC9412136
doi:10.1002/ece3.9254
PMID:36035266
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
Supramolecular assemblies based on natural small molecules: Union would be effective Hou Y, Zou L, Li Q, Chen M, Ruan H, Sun Z, Xu X, Yang J, Ma G Mater Today Bio 15-Jun-2022
PMCID:PMC9214787
doi:10.1016/j.mtbio.2022.100327
PMID:35757027

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 9982058 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
[3,4,5-Trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 85082218 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 10395827 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C(=C(C(=C4)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(93)85250-U
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 15593127 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C(=C(C(=C4)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(3S)-3-hydroxy-3-(4-hydroxyphenyl)-1-[4-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 162877886 Click to see C1=CC(=CC=C1C(CC(=O)C2=C(C=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Rocymosin B 42607726 Click to see C1=CC(=CC=C1C(CC(=O)C2=C(C=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Tannins / Complex tannins
[(10R,11R)-10-[(14R,15S,19S)-19-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-2,3,4,7,8,9-hexahydroxy-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 101458433 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C3=C(C(=C6O)O)O)C(=O)O4)O)O)O)C7C(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(=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1208.90 unknown https://doi.org/10.1016/0031-9422(93)85250-U
[(10R,11R)-10-[(15S,19S)-19-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-2,3,4,7,8,9-hexahydroxy-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 101651021 Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C3=C(C(=C6O)O)O)C(=O)O4)O)O)O)C7C(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(=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1208.90 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19S)-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 101601178 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/10.1016/0031-9422(93)85250-U
Casuarinin 442673 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/10.1016/0031-9422(93)85250-U
Rugosin D 16129626 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)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 1875.30 unknown https://doi.org/10.1016/0031-9422(93)85250-U

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