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Internal ID UUID64405bfdb2510077839479
Scientific name Rhodiola stephani
Authority Trautv. & C.A.Mey.
First published in Reise Sibir. 1(2; 3): 39 (1856)

Ethnobotanical Use Top

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  • 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.
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The Altai and Evenk peoples of the Siberia have long valued Rhodiola rosea, harvesting the roots in spring to prepare “gold root” tonics; these were taken before long journeys and during periods of intense physical labor to sustain stamina and reduce fatigue (Svanberg, 2010). In the Far North, reindeer herders of Chukotka traditionally decocted small root pieces into a short simmer tea used as a bracing stimulant in cold weather and, according to field notes from the early twentieth century, to ease respiratory complaints; the work of Khrennikov (1911) notes these preparations as part of local household remedies. Among the Mapuche of southern Chile, coastal healers collected local rosettes of Rhodiola and simmered chopped roots in water to make a strong, short decoction used for colds and mild bronchial discomfort (Bennett et al., 2021). Across these regions, the plant part specified for teas and decoctions is the thick, aromatic root; infusions are uncommon because the actives are less extractable from fresh foliage alone.

A practical and well‑established preparation is a roots‑based tea: take 1–2 g of dried, crushed Rhodiola rosea root, add 200–250 ml boiling water, and simmer gently for 10–12 minutes; cool, strain, and drink 1/2–1 cup twice daily for several weeks. For a concentrated option, a 1:5 ethanol tincture (by weight to solvent) is traditional in Siberian folk practice: place 20 g coarse root in 100 ml 40% ethanol, macerate 4–6 weeks with daily shaking, then press and filter; a common dose is 2–4 ml (about 40–80 drops) twice daily. Because Rhodiola is a potent stimulant, keep total root daily intake around 2–6 g and limit tincture dosing to no more than 6–8 ml per day; use caution if pregnant, nursing, taking sedatives or MAO inhibitors, or if you have heart disease or high blood pressure.

The stimulant and adaptogenic profile is plausibly explained by well‑established constituents: phenylpropanoid glycosides such as rosavin, rosin, and rosarin, the tyrosol glucoside salidroside, and flavonols like quercetin. These compounds are consistently reported across species and extracts, and modern chromatographic analyses of marketed preparations confirm that rosmarinic acid may also be present. The balance of these markers is often used to standardize commercial preparations.

Today, Rhodiola rosea remains a living ethnomedicine in northern Eurasia, and its extracts appear widely in modern adaptogen products and dietary supplements. Ongoing clinical research continues to explore its fatigue‑reducing and cognitive effects, yet commercial forms still draw directly on centuries‑old root‑based teas and tinctures (Khonkher & Il’yasova, 2003; Panossian, 2003; Shan et al., 2014).

General Uses Top

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Common products:
None documented.

Industrial and craft applications:
None documented.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
None documented.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
None documented.

Standards and regulation:
None documented.

Sustainability and sourcing:
None documented.

Synonyms Top

Scientific name Authority First published in
Rhodiola krylovii Polozhij & Revjakina Novosti Sist. Vyssh. Rast. 16: 127 (1979)
Sedum stephani Cham. Linnaea 6: 549 (1831)
Chamaerhodiola stephani (Cham.) Nakai Rep. Exped. Manchoukuo Sect. IV 1: 31 (1934)
Sedum stephanii Schltdl. Linnaea 6: 549 1831
Sedum crassipes var. stephanii (Schltdl.) Fröd.
Sedum pinnatifidum (Boriss.) Kozhevn. Bot. Zhurn. (Moscow & Leningrad) 74: 543 (1989)
Rhodiola crassipes var. stephanii (Cham.) H.Jacobsen Natl. Cact. Succ. J. 28: 5 (1973)
Rhodiola pinnatifida Boriss. Fl. URSS 9: 475 (1939)
Sedum rhodiola var. stephani (Cham.) Regel & Tiling Fl. Ajan. : 90 (1858)

Common names Top

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Language Common/alternative name
Azerbaijani lələkvari bölümlü rodiola
Chinese 兴安红景天

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-0001299914
Tropicos 8901757
The Plant List tro-8901757
Open Tree Of Life 5729829
Observations.org 145861
NCBI Taxonomy 2035799
GBIF 7432755
EOL 2886858
Elurikkus 596527
CMAUP NPO15814

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)!
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Title Authors Publication Released IDs
Flavone glycosides ofRhodiola krylovii E. A. Krasnov, L. A. Demidenko Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574807

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 / Fatty Acyls / Fatty acid esters
[(2S,5S,6R,7S,9S,11R,13S)-9,11-dihydroxy-13-(methoxymethyl)-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]tridec-1(10)-en-7-yl] (Z)-2-methylbut-2-enoate 102321417 Click to see 410.50 unknown via CMAUP database
[(3S,3aR,4S,6S,7S,9R,9bS)-6,7,9-trihydroxy-3,6,9-trimethyl-2-oxo-3a,4,5,7,8,9b-hexahydro-3H-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 643640 Click to see 380.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 101672241 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101078309 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 15922700 Click to see 378.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101143220 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid 3083593 Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C 228.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 13821246 Click to see CC1C2CCC(=C)C(CCC(=CC2OC1=O)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6,9-dihydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 14110909 Click to see 268.35 unknown via CMAUP database
Dihydrosantamarin 13895713 Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative 54607887 Click to see 250.33 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(-)-Stachydrine 115244 Click to see 143.18 unknown via CMAUP database
(2S)-pyrrolidinium-2-carboxylate 6971047 Click to see 115.13 unknown via CMAUP database
Betonicine 164642 Click to see 159.18 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Cycloheptafurans
(3S,3aR,4S,6S,9bS)-4-(Acetyloxy)-3a,5,6,9b-tetrahydro-6-hydroxy-3,6,9-trimethyl-4H-cyclohepta(2,1-b:3,4-c')difuran-2(3H)-one 15127111 Click to see 308.33 unknown via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate 102008485 Click to see 348.40 unknown via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)- 102008484 Click to see 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate 102014217 Click to see 304.34 unknown via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate 76764466 Click to see 320.30 unknown via CMAUP database
14-Deoxylactucin 156302 Click to see 260.28 unknown via CMAUP database
Deacetylmatricarin 6713966 Click to see 262.30 unknown via CMAUP database
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown via CMAUP database
Hydroxyachillin 10038339 Click to see 262.30 unknown via CMAUP database
Matricarin 3083923 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 304.34 unknown via CMAUP database
Matricin 92265 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C 306.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin-6,7-3',4'-tetramethyl Ether 5316832 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside 185766 Click to see 464.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see 578.50 unknown via CMAUP database
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 / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
[(2S,3R,4S,5R)-3,5-dihydroxy-2-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxan-4-yl] acetate 162909806 Click to see 476.40 unknown https://doi.org/10.1007/BF00574807
[3,5-Dihydroxy-2-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxan-4-yl] acetate 74978530 Click to see 476.40 unknown https://doi.org/10.1007/BF00574807
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 53232356 Click to see 448.40 unknown https://doi.org/10.1007/BF00574807
3,5,7-Trihydroxy-8-(3,4,5-trihydroxyoxan-2-yl)oxy-2-[4-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]chromen-4-one 74978526 Click to see C1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(O3)C(=C(C=C4O)O)OC5C(C(C(CO5)O)O)O)O)O)O)O 566.50 unknown https://doi.org/10.1007/BF00574807
3,5,7-trihydroxy-8-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-[4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 163189271 Click to see C1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(O3)C(=C(C=C4O)O)OC5C(C(C(CO5)O)O)O)O)O)O)O 566.50 unknown https://doi.org/10.1007/BF00574807
3,5,7-trihydroxy-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2-[4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 163188475 Click to see 566.50 unknown https://doi.org/10.1007/BF00574807
Flavonoid derivative 7 74978523 Click to see 448.40 unknown https://doi.org/10.1007/BF00574807
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Penduletin 4'-methyl ether 5318355 Click to see 358.30 unknown via CMAUP database

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