Rosa agrestis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Rosa agrestis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64403e9bbda4d609899044
Scientific name Rosa agrestis
Authority Savi
First published in Fl. Pis. 1: 475 (1798)

Description Top

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Rosa agrestis, also known as the small-leaved sweet briar or field briar, is a type of wild rose that is native to Europe. It is mostly found in southern Europe, but can occasionally be found as far as the Caucasus. There is some disagreement among sources about whether it can also be found in northern Africa and Anatolia. This species belongs to the subgenus Rosa, section Caninae, and subsection Rubigineae. It is closely related to the sweet briar, but has smaller leaves, white to blush petals, and very little scent from its flowers or leaves. While it can be grown in gardens, most gardeners prefer the sweet briar for its fragrant foliage and pink flowers.

Synonyms Top

Scientific name Authority First published in
Rosa sepium Thuill. Fl. Env. Paris, ed. 2. 252. 1799 [24 Jun 1799]
Rosa hispanica H.Christ ; 1877 844 [448] 1877
Rosa gizellae Borbás Math. Term. Közlem. 16: 486 (1880 publ. 1881)
Rosa arvatica Puget ex Baker Naturalist (Hull) 1: 101 (1864)
Rosa haringiana Fritsch Excursionsfl. Oesterreich : 240 (1922)
Rosa graveolens subsp. nuda (Gren.) Arcang. Compendio della flora italiana ; 1882 227 1882
Rosa agrestis subsp. caryophyllacea E.Schenk
Rosa viscaria subsp. agrestis (Savi) Rouy Flore de France ; 1893 347 1900
Rosa agrestis subsp. pubescens (Rapin ex Reut.) E.Schenk
Rosa graveolens subsp. eriophora (Gren.) Arcang. Compendio della flora italiana ; 1882 227 1882
Rosa elliptica subsp. inodora (Fr.) Schwertschl. Die Rosen des s?dlichen und mittleren Frankenjura; ihr System und ihre phylogenetischen Beziehungen ; 1910 60 1910
Rosa kostrakiewiczii Popek Fragm. Florist. Geobot. 29: 350 (1983 publ. 1986)
Rosa denudata (R.Keller) Klášt. Zprávy Ceskoslov. Bot. Spolecn. Ceskoslov. Akad. Ved 4: 183 (1969)
Rosa gisellae Borb. ex Koehne Deut. Dendrol. (1893) 287. [May 1893]

Common names Top

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Language Common/alternative name
English fieldbriar
Arabic ورد مرجي
Catalan roser agrest
Czech růže polní
Czech růže rolní
Welsh drysïen bêr fanddail
German acker-rose
Finnish vainioruusu
French Églantier agreste
French Églantier des haies
French rosier agreste
Upper Sorbian rólna róža
Dutch kraagroos
Polish róża polna
Swedish Åkerros
Chinese 欧洲野蔷薇

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

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-0000985731
USDA Plants ROAG2
Tropicos 27802416
INPN 117986
Flora of Italy 1960
KEW urn:lsid:ipni.org:names:731498-1
The Plant List rjp-1298
Open Tree Of Life 775482
NCBI Taxonomy 267229
NBN Atlas NBNSYS0000003410
iNaturalist 209444
GBIF 3002394
EPPO ROSAG
EOL 631602
Elurikkus 6895
USDA GRIN 32073
Wikipedia Rosa_agrestis
CMAUP NPO5984

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
Long-Term Monitoring of the Traditional Knowledge of Plant Species Used for Culinary Purposes in the Valencia Region, South-Eastern Spain Belda A, Jordán-Nuñez J, Micó-Vicent B, López-Rodríguez D Plants (Basel) 08-Mar-2024
PMCID:PMC10975046
doi:10.3390/plants13060775
PMID:38592810
Challenges and Future Trends in Atopic Dermatitis Gatmaitan JG, Lee JH Int J Mol Sci 12-Jul-2023
PMCID:PMC10380015
doi:10.3390/ijms241411380
PMID:37511138
Phytochemicals and Regulation of NF-kB in Inflammatory Bowel Diseases: An Overview of In Vitro and In Vivo Effects Laurindo LF, dos Santos AR, de Carvalho AC, Bechara MD, Guiguer EL, Goulart RD, Vargas Sinatora R, Araújo AC, Barbalho SM Metabolites 07-Jan-2023
PMCID:PMC9862976
doi:10.3390/metabo13010096
PMID:36677021
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
Potential Natural Biomolecules Targeting JAK/STAT/SOCS Signaling in the Management of Atopic Dermatitis Kopalli SR, Annamneedi VP, Koppula S Molecules 21-Jul-2022
PMCID:PMC9319717
doi:10.3390/molecules27144660
PMID:35889539
Effect of Traditional Chinese Medicine on the Cardiovascular Diseases Jiang Y, Zhao Q, Li L, Huang S, Yi S, Hu Z Front Pharmacol 21-Mar-2022
PMCID:PMC8978630
doi:10.3389/fphar.2022.806300
PMID:35387325
Antioxidant and Antimicrobial Evaluation and Chemical Investigation of Rosa gallica var. aegyptiaca Leaf Extracts Abdelbaky AS, Mohamed AM, Alharthi SS Molecules 27-Oct-2021
PMCID:PMC8587625
doi:10.3390/molecules26216498
PMID:34770907
Bioactive PI3-kinase/Akt/mTOR Inhibitors in Targeted Lung Cancer Therapy Ghareghomi S, Atabaki V, Abdollahzadeh N, Ahmadian S, Hafez Ghoran S Adv Pharm Bull 09-Oct-2021
PMCID:PMC9871280
doi:10.34172/apb.2023.003
PMID:36721812
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Revisiting cancer hallmarks: insights from the interplay between oxidative stress and non-coding RNAs Zhou L, Zhang Z, Huang Z, Nice E, Zou B, Huang C Mol Biomed 31-Aug-2020
PMCID:PMC8603983
doi:10.1186/s43556-020-00004-1
PMID:35006436
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Astragalin Inhibits Nuclear Factor-κB Signaling in Human Colonic Epithelial Cells and Attenuates Experimental Colitis in Mice Han YM, Koh J, Kim JH, Lee J, Im JP, Kim JS Gut Liver 13-May-2020
PMCID:PMC7817923
doi:10.5009/gnl19268
PMID:32390406
Unraveling Natural Products’ Role in Osteoarthritis Management—An Overview Deligiannidou GE, Papadopoulos RE, Kontogiorgis C, Detsi A, Bezirtzoglou E, Constantinides T Antioxidants (Basel) 23-Apr-2020
PMCID:PMC7222394
doi:10.3390/antiox9040348
PMID:32340224
Competition of Parental Genomes in Plant Hybrids Glombik M, Bačovský V, Hobza R, Kopecký D Front Plant Sci 25-Feb-2020
PMCID:PMC7052263
doi:10.3389/fpls.2020.00200
PMID:32158461
The strong competitive role of 2n pollen in several polyploidy hybridizations in Rosa hybrida Gao SM, Yang MH, Zhang F, Fan LJ, Zhou Y BMC Plant Biol 04-Apr-2019
PMCID:PMC6449914
doi:10.1186/s12870-019-1696-z
PMID:30947683

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol 125 Click to see C1=CC(=CC=C1CO)O 124.14 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 450.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rosavin 9823887 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC=CC3=CC=CC=C3)O)O)O)O)O)O 428.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Bacosterol3-O-beta-D-glucopyranoside 101389367 Click to see CCC(CCC(C)C1CC=CC2CCC3CC(CCC3(C2=CCC1C)C)OC4C(C(C(C(O4)CO)O)O)O)C(C)C 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Bacopaside I 21599442 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 979.10 unknown via CMAUP database
bacopaside II 9876264 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 929.10 unknown via CMAUP database
Bacopaside III 15922618 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)O)C)C)C 847.00 unknown via CMAUP database
Bacopaside IV 10865594 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 767.00 unknown via CMAUP database
Bacopaside N1 11949626 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 797.00 unknown via CMAUP database
Bacopaside N2 21574494 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 797.00 unknown via CMAUP database
Bacopaside V 11072737 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 767.00 unknown via CMAUP database
Bacopaside X 10629555 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)(C)O)C 899.10 unknown via CMAUP database
Bacoside A3 91827005 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)(C)O)C 929.10 unknown via CMAUP database
Bacosine 71312547 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C 456.70 unknown via CMAUP database
Bascopasaponin C 21599443 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 899.10 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
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 / Cucurbitacins
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(7S,8S,9S,10R,13R,14S,16R,17R)-2,7,16-trihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate 16216753 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2C(C=C4C3C=C(C(=O)C4(C)C)O)O)C)C)C)O)O 572.70 unknown via CMAUP database
Cucurbitacin E 5281319 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methyldesmosterol 193567 Click to see CC(CCC(=C(C)C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 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
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Bacosterol 101389368 Click to see CCC(CCC(C)C1CC=CC2CCC3CC(CCC3(C2=CCC1C)C)O)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dimethoxyphenyl)- 16848 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
Ferulic acid glucoside 53978589 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/14786410903075507
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/14786410903075507
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 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 https://doi.org/10.1080/14786410903075507
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/10.1080/14786410903075507
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786410903075507
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786410903075507
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/10.1080/14786410903075507
Quercitrin 5280459 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 https://doi.org/10.1080/14786410903075507
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1080/14786410903075507
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[2,4,6-Trihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-1-propanone 19744872 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)CCC2=CC=C(C=C2)O)O)C 342.40 unknown via CMAUP database

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