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).

General Uses Top

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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

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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

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Name Authority First published in
Salix rosmarinifolia subsp. sibirica (Pall.) I.V.Belyaeva & Sennikov Kew Bull. 63: 285 (2008)

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

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Links to other databases Top

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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

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Scientific Literature Top

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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

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