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Rosa foetida

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404034de2bf157985481
Scientific name Rosa foetida
Authority Herrm.
First published in De Rosa : 18 (1762)

Ethnobotanical Use Top

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General Uses Top

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Scientific/model-organism use:
Rosa foetida is primarily used in modern rose genetics and breeding. Its bright yellow flowers are a rare trait in Rosa, introduced into cultivated roses to create yellow and apricot-flowered varieties via controlled crosses. Genetic and genomic studies have incorporated R. foetida-derived material to map color loci, investigate pigment biosynthesis, and improve resistance traits, contributing to marker-assisted selection and population structure analyses. It is not a standard laboratory model organism but serves as a genetic resource within horticultural research and breeding programs.

Synonyms Top

Scientific name Authority First published in
Rosa lutea Mill. Gard. Dict. ed. 8 : Rosa n.º 11 (1768)
Rosa chlorophylla Ehrh. Beitr. Naturk. 2: 69 (1788)
Rosa eglanteria var. lutea (Mill.) Thory Prodrome de la monographie du genre Rosier ; 1820 100 1820
Rosa punicea Mill. Gard. Dict., ed. 8. : Rosa n.° 12 (1768)
Rosa lutea var. persiana Lem. Fl. Serres Jard. Eur. 4: t. 374 (1848)
Rosa bicolor Jacq. Hort. Vindob. i. 1.
Rosa foetida var. persiana (Lem.) Rehder Mitt. Deutsch. Dendrol. Ges. 24: 222 (1915 publ. 1916)
Rosa lutea var. hoggii Van Houtte Hort. Belge 5: 87 (1838)
Rosa lutea var. plena Van Houtte Hort. Belge 5: 87 (1838)
Rosa chlorophylla unranked bicolor Ehrh. Beitr. Naturk. Verw. Wiss. 2: 70 (1788)
Rosa chlorophylla unranked unicolor Ehrh. Beitr. Naturk. Verw. Wiss. 2: 70 (1788)
Rosa foetida var. glabrata Chrshan. Fl. URSS 6: 585 (1954)
Rosa foetida var. harrisonii Rehder Stand. Cycl. Hort. 5: 2995 (1916)
Rosa lutea f. attenuata Christ Ber. Schweiz. Bot. Ges. 35: 98 (1926)
Rosa lutea f. bessei Christ Ber. Schweiz. Bot. Ges. 35: 98 (1926)
Rosa lutea unranked bicolor Jacq. Hort. Bot. Vindob. 1: t. 1 (1770)
Rosa lutea var. discolor Debeaux & E.Rev. Bull. Acad. Int. Géogr. Bot. 15: 91 (1905)
Rosa lutea unranked harissonii Anon. Gard. Chron. , ser. 3, 83: 247 (1928)
Rosa lutea var. multiplex C.F.Ludw. Neuere Wilde Baumz. : 43 (1783)
Rosa lutea var. typica Heinr.Braun Fl. Nieder-Österreich 2(1): 772 (1892)
Rosa lutea var. unicolor Curtis ex Ser. Prodr. 2: 607 (1825)
Rosa lutea var. laeta Wallr. ex Lej. & Courtois Comp. Fl. Belg. 2: 144 (1831)
Rosa lutea var. tristis Wallr. ex Lej. & Courtois Comp. Fl. Belg. 2: 144 (1831)
Rosa eglanteria var. punicea (Mill.) Pers. Syn. Pl. 2: 47 (1806)
Rosa foetida var. bicolor (Jacq.) E.Willm. Rosa 2: 269 (1911)
Rosa lutea var. punicea (Mill.) Moench Methodus : 688 (1794)
Rosa eglanteria var. bicolor (Jacq.) DC. Fl. Franç. , éd. 3, 4: 437 (1805)
Rosa fedorovii Sumnev. ex Chrshan. Bot. Mater. Gerb. Inst. Bot. Akad. Nauk Uzbeksk. S.S.R. 13: 41 (1952)
Rosa lutea var. bicolor (Jacq.) Aiton Hort. Kew. 2: 801 (1789)
Rosa lutea var. bicolor Sims Bot. Mag. 27: t. 1077 (1808)
Rosa lutea var. hoggii D.Don Hort. Brit. 4: t. 410 (1838)

Common names Top

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Language Common/alternative name
English austrian-brier
Arabic ورد منتن
azb ساریگول
Czech růže žlutá
German fuchs-rose
Esperanto malbonodora rozo
Esperanto persa orrozo
Esperanto vaksrozo
Esperanto vulpo-rozo
Persian نسترن زرد
Finnish persiankeltaruusu
Finnish persianruusu
French rosier fétide
Croatian Žuta ruža
Hungarian sárga rózsa
Japanese ロサ・フェティダ
Polish róża żółta
Punjab پیلا گلاب
Russian Шиповник зловонный
Russian Шиповник вонючий
Russian Роза фетида
Russian Роза лютеа
Russian Роза зловонная
Swedish turkisk gulros
Chinese 异味蔷薇
Chinese 重瓣异味蔷薇

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001014717
USDA Plants ROFO2
Tropicos 27804857
INPN 118184
Flora of Italy 1987
KEW urn:lsid:ipni.org:names:732502-1
The Plant List rjp-6114
Open Tree Of Life 858747
Observations.org 125544
NCBI Taxonomy 74629
NBN Atlas NBNSYS0200003025
IPNI 732502-1
iNaturalist 118409
GBIF 3006902
Freebase /m/07h7x0
EPPO ROSFO
EOL 249763
Elurikkus 6912
USDA GRIN 5347
Wikipedia Rosa_foetida
Tropicos 27807529
The Plant List tro-27807529
Open Tree Of Life 5922295
NCBI Taxonomy 1826183
GBIF 8347561

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Characterization of the Slovene Autochthonous Rose Hybrid Rosa pendulina × spinosissima (Rosa reversa Waldst. and Kit) Using Biochemical Patterns of the Plant Blossoms Kunc N, Hudina M, Bavcon J, Vreš B, Luthar Z, Gostinčar K, Mikulič-Petkovšek M, Osterc G, Ravnjak B Plants (Basel) 22-Jan-2023
PMCID:PMC9920101
doi:10.3390/plants12030505
PMID:36771590
Synthesis, biomedical applications, and toxicity of CuO nanoparticles Naz S, Gul A, Zia M, Javed R Appl Microbiol Biotechnol 13-Jan-2023
PMCID:PMC9838533
doi:10.1007/s00253-023-12364-z
PMID:36635395
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
The effects of Rosa foetida extract along with self-care education on primary dysmenorrhea: study protocol for a randomized clinical trial Shabani F, Omidvar S, Sajadi Kaboudi P, Pasha H, Khafri S, Najafzadehvarzi H, Nasiri Amiri F, Faramarzi M, Bouzari Z Trials 09-Aug-2022
PMCID:PMC9361594
doi:10.1186/s13063-022-06583-4
PMID:35945594
Duplication and Specialization of NUDX1 in Rosaceae Led to Geraniol Production in Rose Petals Conart C, Saclier N, Foucher F, Goubert C, Rius-Bony A, Paramita SN, Moja S, Thouroude T, Douady C, Sun P, Nairaud B, Saint-Marcoux D, Bahut M, Jeauffre J, Hibrand Saint-Oyant L, Schuurink RC, Magnard JL, Boachon B, Dudareva N, Baudino S, Caissard JC Mol Biol Evol 12-Jan-2022
PMCID:PMC8857926
doi:10.1093/molbev/msac002
PMID:35022771
An algal enzyme required for biosynthesis of the most abundant marine carotenoids Dautermann O, Lyska D, Andersen-Ranberg J, Becker M, Fröhlich-Nowoisky J, Gartmann H, Krämer LC, Mayr K, Pieper D, Rij LM, Wipf HM, Niyogi KK, Lohr M Sci Adv 04-Mar-2020
PMCID:PMC7056318
doi:10.1126/sciadv.aaw9183
PMID:32181334
Iranian Medicinal Plants: From Ethnomedicine to Actual Studies Buso P, Manfredini S, Reza Ahmadi-Ashtiani H, Sciabica S, Buzzi R, Vertuani S, Baldisserotto A Medicina (Kaunas) 26-Feb-2020
PMCID:PMC7143749
doi:10.3390/medicina56030097
PMID:32110920
Wild edible plants in Yeşilli (Mardin-Turkey), a multicultural area Yeşil Y, Çelik M, Yılmaz B J Ethnobiol Ethnomed 05-Nov-2019
PMCID:PMC6833206
doi:10.1186/s13002-019-0327-y
PMID:31690334
In the name of the rose: a roadmap for rose research in the genome era Smulders MJ, Arens P, Bourke PM, Debener T, Linde M, Riek JD, Leus L, Ruttink T, Baudino S, Hibrant Saint-Oyant L, Clotault J, Foucher F Hortic Res 03-May-2019
PMCID:PMC6499834
doi:10.1038/s41438-019-0156-0
PMID:31069087
An ethnobotanical study in Midyat (Turkey), a city on the silk road where cultures meet Akgul A, Akgul A, Senol SG, Yildirim H, Secmen O, Dogan Y J Ethnobiol Ethnomed 07-Feb-2018
PMCID:PMC5804065
doi:10.1186/s13002-017-0201-8
PMID:29415748
An ethno-medicinal study of medicinal plants used for the treatment of diabetes Baharvand-Ahmadi B, Bahmani M, Tajeddini P, Naghdi N, Rafieian-Kopaei M J Nephropathol 16-Dec-2015
PMCID:PMC4790187
doi:10.15171/jnp.2016.08
PMID:27047810
Ethnobotanical investigation of traditional medicinal plants commercialized in the markets of Mashhad, Iran Amiri MS, Joharchi MR Avicenna J Phytomed 01-Jun-2013
PMCID:PMC4075713
PMID:25050282
Genetics and genomics of flower initiation and development in roses Bendahmane M, Dubois A, Raymond O, Bris ML J Exp Bot 23-Feb-2013
PMCID:PMC3594942
doi:10.1093/jxb/ers387
PMID:23364936
Past Climate Change and Plant Evolution in Western North America: A Case Study in Rosaceae Töpel M, Antonelli A, Yesson C, Eriksen B PLoS One 07-Dec-2012
PMCID:PMC3517582
doi:10.1371/journal.pone.0050358
PMID:23236369

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 / Naphthalenes
4-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-2,3-dimethylnaphthalen-1-one 163047236 Click to see 368.40 unknown https://doi.org/10.1002/HLCA.19840670814
> Benzenoids / Naphthalenes / Naphthoquinones
7,9-Dibromo-6-hydroxy-3a,8-dimethyl-1-propan-2-yl-1,2,3,9b-tetrahydrocyclopenta[a]naphthalene-4,5-dione 85154147 Click to see 444.20 unknown https://doi.org/10.1002/HLCA.19840670814
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
3-[2-Methyl-5-oxo-3-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]propanoic acid 162954662 Click to see 392.40 unknown https://doi.org/10.1002/HLCA.19840670814
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,2S,5S,8R,9R)-2,3',3',6-tetramethylspiro[11-oxatricyclo[6.2.1.01,5]undec-6-ene-9,2'-oxirane]-8-ol 14191396 Click to see 250.33 unknown https://doi.org/10.1002/HLCA.19840670814
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids
(2R,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(2R,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 163007068 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(2R,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14Z)-15-[(2R,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 163007073 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(2S,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(2R,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 163007069 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(2S,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(2S,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 163007076 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(2R,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 162940032 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC3(C(CC(CC3(C)O)O)(C)C)O 618.90 unknown https://doi.org/10.1002/HLCA.19840670814
(1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(2S,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 162940033 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC3(C(CC(CC3(C)O)O)(C)C)O 618.90 unknown https://doi.org/10.1002/HLCA.19840670814
(1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15Z,17E)-18-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 162892431 Click to see 618.90 unknown https://doi.org/10.1002/HLCA.19840670814
(2R,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 14251667 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(2S,6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 162861648 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(3S,5R,8R,3'R)-mutatoxanthin 21765300 Click to see 584.90 unknown https://doi.org/10.1002/HLCA.19840670814
(8'R)-Luteoxanthin 71587355 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
(8S)-Mutatoxanthin 21765301 Click to see 584.90 unknown https://doi.org/10.1002/HLCA.19840670814
1-[18-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 162892430 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC3(C(CC(CC3(C)O)O)(C)C)O 618.90 unknown https://doi.org/10.1002/HLCA.19840670814
2-[17-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 72728991 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
6-[18-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 179930 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
9-cis-Violaxanthin 5282218 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
Antheraxanthin A 5281223 Click to see 584.90 unknown https://doi.org/10.1002/HLCA.19840670814
Latoxanthin 102150983 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC3(C(CC(CC3(C)O)O)(C)C)O 618.90 unknown https://doi.org/10.1002/HLCA.19840670814
Luteoxanthin, (8'S)- 71587356 Click to see 600.90 unknown https://doi.org/10.1002/HLCA.19840670814
> Organoheterocyclic compounds / Naphthofurans
methyl (1R,2R,5R,7R,9S,10S,12S,15S)-7-(furan-3-yl)-9-methyl-4,14-dioxo-3,6,13-trioxapentacyclo[10.2.2.12,5.01,10.05,9]heptadecane-15-carboxylate 163034387 Click to see 402.40 unknown https://doi.org/10.1002/HLCA.19840670814
> Phenylpropanoids and polyketides / Macrolactams
(4S,12Z)-4-phenyl-9-[(E)-3-phenylprop-2-enoyl]-1,5,9-triazacyclotridec-12-en-2-one 11200503 Click to see 403.50 unknown https://doi.org/10.1002/HLCA.19840670814

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