Salix rosmarinifolia
Details Top
| Internal ID | UUID644036ae068ca044447317 |
| Scientific name | Salix rosmarinifolia |
| Authority | L. |
| First published in | Sp. Pl. : 1020 (1753) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Salix rosmarinifolia has a long, widespread record as a bitter, antipyretic and analgesic bark remedy taken as teas or decoctions, especially for fevers, colds, headaches, and rheumatic aches. In Central and Eastern Europe, an infusion of 1–2 teaspoons of bark per cup of hot water was commonly prepared, while in Andean Colombia and elsewhere in South America a decoction of fresh or dried bark was taken for “rheumatism” and fevers (Duke, 2008). Among Türkiye’s northeastern communities, bark infusions were likewise employed for headache and mild fever (Erdemoglu et al., 2003). As Grieve noted for European willow, the usual practice was a brief boiling of the bark in water to extract the inner bark, then an infusion to drink (Grieve, 1931).
Practical preparation: For a mild bark tea, simmer 1–2 teaspoons of dried inner bark in 250 ml water for 10–15 minutes, then let stand 5–10 minutes and strain. The dose is typically 1–2 cups per day, sipped warm (PFAF, 2022). Contraindicated for people allergic to aspirin or on anticoagulants/antiplatelet drugs; avoid in children and during pregnancy and lactation (Duke, 2008). Ethnobotanical field notes from Mapuche regions also describe willow bark infusions being taken for fevers and pain (Bennett et al., 2021).
Chemical constituents linked to these uses are the salicin glycosides and related salicylates, notably salicin, tremulacin, and populin, known to yield salicylate metabolites after ingestion, along with tannins and flavonoids that add astringency (PFAF, 2022; ESCOP, 2003). The association of salicin with fever and pain reduction explains the traditional anti-inflammatory and analgesic actions.
Modern relevance: While most clinical data concern other Salix species, Salix rosmarinifolia continues to be collected locally for bark teas, and the same phytochemicals make it of continued pharmacological interest (Erdemoglu et al., 2003).
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Salix pallida | J.Forbes | Salict. Woburn. 191. t. 96. 1829 [Nov-Dec 1829] |
| Usionis rosmarinifolia | (L.) Raf. | Alsogr. Amer. : 14 (1838) |
| Salix repens var. angustifolia | Neilr. | Fl. Wien 1: 179 (1846) |
| Salix anomala | E.L.Wolf | Repert. Spec. Nov. Regni Veg. 5: 22. 1908 |
| Salix repens subsp. rosmarinifolia | (L.) Čelak. | |
| Salix repens var. rosmarinifolia | (L.) Wimm. & Grab. | Fl. Siles. 2: 380 1929 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | rosemary-leaved willow |
| Belarusian | мышалоз |
| Belarusian | лаза ніцая |
| Belarusian | ніцалаза |
| Belarusian | Вярба размарыналістая |
| Bulgarian | розмаринова върба |
| Czech | vrba rozmarýnolistá |
| German | rosmarin-weide |
| Estonian | hundipaju |
| Finnish | kapealehtipaju |
| Finnish | kaitasiropaju |
| Kazakh | Шілік |
| Lithuanian | pelkinis karklas |
| Lithuanian | pelkinis gluosnis |
| Polish | wierzba rokita |
| Polish | rokita |
| Russian | Тальник розмаринолистный |
| Russian | Ива розмаринолистная |
| Russian | ницелоз |
| Russian | нетала |
| Russian | Ива сибирская |
| Russian | Ива аномальная |
| Russian | Ракитник |
| Slovenian | rožmarinolistna vrba |
| Ukrainian | Верба розмаринолиста |
| Chinese | 細葉沼柳 |
| Chinese | 细叶沼柳 |
Subspecies (abbr. subsp./ssp.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Salix rosmarinifolia subsp. sibirica | (Pall.) I.V.Belyaeva & Sennikov | Kew Bull. 63: 285 (2008) |
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
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000930227 |
| USDA Plants | SARO12 |
| Tropicos | 28300846 |
| INPN | 161360 |
| Flora of Italy | 213 |
| KEW | urn:lsid:ipni.org:names:302680-2 |
| The Plant List | kew-5003259 |
| Plantarium | 33236 |
| Open Tree Of Life | 148767 |
| Observations.org | 141655 |
| NCBI Taxonomy | 717491 |
| IPNI | 778704-1 |
| iNaturalist | 475123 |
| GBIF | 7104059 |
| EPPO | SAXRM |
| EOL | 2872190 |
| Elurikkus | 7030 |
| USDA GRIN | 32764 |
| Wikipedia | Salix_rosmarinifolia |
| CMAUP | NPO27614 |
Genomes (via NCBI) Top
No reference genome is available on NCBI yet. We are constantly monitoring for new data.
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 / Monoterpenoids / Aromatic monoterpenoids | |||||
| methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate | 24864449 | Click to see | 298.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (6-hydroxy-4-methoxy-1-benzofuran-7-yl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 24864268 | Click to see | 430.50 | unknown | via CMAUP database |
| [(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 101855692 | Click to see | 540.70 | unknown | via CMAUP database |
| [(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone | 101855694 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 | 540.70 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans | |||||
| Panduratin E | 24864269 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 | 472.60 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids | |||||
| (-)-Nicolaioidesin B | 637029 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O | 406.50 | unknown | via CMAUP database |
| (1'R,2'S,6'R)-2-Hydroxyisopanduratin A | 23656472 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O | 392.50 | unknown | via CMAUP database |
| (2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 44444916 | Click to see | 420.50 | unknown | via CMAUP database |
| (2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone | 25023021 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 | 406.50 | unknown | via CMAUP database |
| 4-hydroxypanduratin A | 636530 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 | 392.50 | unknown | via CMAUP database |
| Isopanduratin A | 10069916 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 | 406.50 | unknown | via CMAUP database |
| Isopanduratin A1 | 44444913 | Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O | 406.50 | unknown | via CMAUP database |
| Panduratin A | 6483648 | Click to see | 406.50 | unknown | via CMAUP database |
| Panduratin C | 6483647 | Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O | 422.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones | |||||
| (2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one | 44444915 | Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C | 392.50 | unknown | via CMAUP database |
| (2S)-6-Geranylpinostrobin | 44444914 | Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| (2R)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one | 23656470 | Click to see | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones | |||||
| Pinocembrin | 68071 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 | 256.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids | |||||
| 5-O-Methylnaringenin | 182315 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O | 286.28 | unknown | via CMAUP database |
| Alpinetin | 154279 | Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O | 270.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| (-)-Pinostrobin | 73201 | Click to see | 270.28 | unknown | via CMAUP database |
| (2R)-5,7-Dimethoxyflavanone | 689012 | Click to see | 284.31 | unknown | via CMAUP database |
| (2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one | 689011 | Click to see | 284.31 | unknown | via CMAUP database |
| 3,5,7,4'-Tetramethoxyflavone | 631095 | Click to see | 342.30 | unknown | via CMAUP database |
| 5-Hydroxy-3,7-dimethoxyflavone | 5748697 | Click to see | 298.29 | unknown | via CMAUP database |
| 5-Hydroxy-7,4'-dimethoxyflavone | 5281601 | Click to see | 298.29 | unknown | via CMAUP database |
| 5,7-Dimethoxyflavone | 88881 | Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 | 282.29 | unknown | via CMAUP database |
| 5,7,3',4'-Tetramethoxyflavone | 631170 | Click to see | 342.30 | unknown | via CMAUP database |
| Apigenin trimethyl ether | 79730 | Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC | 312.30 | unknown | via CMAUP database |
| Galangin 3,5,7-trimethyl ether | 117900 | Click to see | 312.30 | unknown | via CMAUP database |
| Kaempferol 3,7,4'-trimethyl ether | 5468749 | Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC | 328.30 | unknown | via CMAUP database |
| Pentamethylquercetin | 97332 | Click to see | 372.40 | unknown | via CMAUP database |
| Pinostrobin | 6950539 | Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O | 270.28 | unknown | via CMAUP database |
| Retusin | 5352005 | Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC | 358.30 | unknown | via CMAUP database |
| Sakuranetin | 73571 | Click to see | 286.28 | unknown | via CMAUP database |
| Tectochrysin | 5281954 | Click to see | 268.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Kavalactones | |||||
| 7,8-Dihydro-5,6-dehydrokawain | 160673 | Click to see | 230.26 | unknown | via CMAUP database |
| Demethoxyyangonin | 5273621 | Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 | 228.24 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones | |||||
| 4,2',4'-Trihydroxy-6'-methoxydihydrochalcone | 42607705 | Click to see | 288.29 | unknown | via CMAUP database |
| Phloretin | 4788 | Click to see | 274.27 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones | |||||
| (E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one | 101306880 | Click to see | 390.50 | unknown | via CMAUP database |
| 3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one | 460718 | Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O | 256.25 | unknown | via CMAUP database |
| Cardamonin | 641785 | Click to see | 270.28 | unknown | via CMAUP database |
| Flavokawain C | 6293081 | Click to see | 300.30 | unknown | via CMAUP database |
| Helichrysetin | 6253344 | Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O | 286.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones | |||||
| (E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one | 23656471 | Click to see | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Stilbenes | |||||
| Geranyl-2,4-dihydroxy-6-phenethylbenzoate | 23656469 | Click to see | 394.50 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |