Rhodiola kirilowii - Unknown
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Internal ID UUID64405c13c5592682893325
Scientific name Rhodiola kirilowii
Authority (Regel) Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 472 (1859)

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Synonyms Top

Scientific name Authority First published in
Sedum kirilowii Regel Nouv. Mém. Soc. Imp. Naturalistes Moscou 11: 92 (1859)
Sedum kirilowii var. rubrum Praeger J. Roy. Hort. Soc. 46: 37 1921
Sedum kirilowii var. altum Fröd.
Sedum kirilowii var. linifolium Regel & Schmalh.
Rhodiola macrolepis (Franch.) Fu Acta Phytotax. Sin., Addit. 1: 125 (1965)
Rhodiola longicaulis (Praeger) Fu Acta Phytotax. Sin., Addit. 1: 124 (1965)
Rhodiola robusta (Praeger) Fu Acta Phytotax. Sin., Addit. 1: 124 (1965)
Rhodiola kirilowii var. latifolia S.H.Fu Acta Phytotax. Sin. 1: 124 1951
Sedum longicaule Praeger J. Bot. 55: 38 (1917)
Sedum macrolepis Franch. Nouv. Arch. Mus. Hist. Nat. , sér. 2, 8: 241 (1885 publ. 1886)
Sedum robustum Praeger Notes Roy. Bot. Gard. Edinburgh 13: 93 (1921)
Rhodiola kirilowii var. rubra (Praeger) H.Jacobsen Natl. Cact. Succ. J. 28: 5 (1973)

Common names Top

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Language Common/alternative name
Azerbaijani xəttyarpaq rodiola
Swedish smalbladig rosenrot
Chinese 狮子草
Chinese 长茎红景天
Chinese 高壮景天
Chinese 狭叶红景天
Chinese 狭叶红景天(大株红景天)
Chinese 狮子七
Chinese 豌豆七
Chinese 九头狮子七
Chinese 涩疙瘩

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001300617
UNII 8Z350223SE
Tropicos 8903424
KEW urn:lsid:ipni.org:names:274823-1
The Plant List tro-8903424
Open Tree Of Life 311039
Observations.org 130330
NCBI Taxonomy 203008
IPNI 274823-1
GBIF 7334350
Elurikkus 590126
USDA GRIN 429690

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_033675215.1 ASM3367521v1 Chromosome Shaanxi Normal University 2023-11-15 123.0x 623.20 Mb

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
Nutraceuticals as Modulators of Immune Function: A Review of Potential Therapeutic Effects Medoro A, Davinelli S, Colletti A, Di Micoli V, Grandi E, Fogacci F, Scapagnini G, Cicero AF Prev Nutr Food Sci 30-Jun-2023
PMCID:PMC10321448
doi:10.3746/pnf.2023.28.2.89
PMID:37416796
The complete chloroplast genome sequence of Sedum bulbiferum (Crassulaceae) Deng Z, Huang K, Xie P, Xie S, Zhang N, Yin H, Ping M, Wang Y Mitochondrial DNA B Resour 24-May-2023
PMCID:PMC10210845
doi:10.1080/23802359.2022.2160220
PMID:37250209
Efficacy and safety of three species of Rhodiola L. in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis Yu H, Lei T, Su X, Zhang L, Feng Z, Dong M, Hou Z, Guo H, Liu J Front Pharmacol 06-Apr-2023
PMCID:PMC10117638
doi:10.3389/fphar.2023.1139239
PMID:37089935
Cannabidiol as a Modulator of the Development of Alcohol Tolerance in Rats Szulc M, Kujawski R, Pacholak A, Poprawska M, Czora-Poczwardowska K, Geppert B, Mikołajczak PŁ Nutrients 30-Mar-2023
PMCID:PMC10097131
doi:10.3390/nu15071702
PMID:37049542
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
A Concise Profile of Gallic Acid—From Its Natural Sources through Biological Properties and Chemical Methods of Determination Wianowska D, Olszowy-Tomczyk M Molecules 25-Jan-2023
PMCID:PMC9919014
doi:10.3390/molecules28031186
PMID:36770851
Therapeutic potential and molecular mechanisms of salidroside in ischemic diseases Han J, Luo L, Wang Y, Wu S, Kasim V Front Pharmacol 19-Aug-2022
PMCID:PMC9437267
doi:10.3389/fphar.2022.974775
PMID:36060000
Role of ethno-phytomedicine knowledge in healthcare of COVID-19: advances in traditional phytomedicine perspective Nasir Ahmed M, Hughes K Beni Suef Univ J Basic Appl Sci 04-Aug-2022
PMCID:PMC9362587
doi:10.1186/s43088-022-00277-1
PMID:35966214
Plant metabolomics: a new strategy and tool for quality evaluation of Chinese medicinal materials Xiao Q, Mu X, Liu J, Li B, Liu H, Zhang B, Xiao P Chin Med 08-Apr-2022
PMCID:PMC8990502
doi:10.1186/s13020-022-00601-y
PMID:35395803
Herbal Medicines—Are They Effective and Safe during Pregnancy? Sarecka-Hujar B, Szulc-Musioł B Pharmaceutics 12-Jan-2022
PMCID:PMC8802657
doi:10.3390/pharmaceutics14010171
PMID:35057067
Impacts of Commonly Used Edible Plants on the Modulation of Platelet Function Albadawi DA, Ravishankar D, Vallance TM, Patel K, Osborn HM, Vaiyapuri S Int J Mol Sci 06-Jan-2022
PMCID:PMC8775512
doi:10.3390/ijms23020605
PMID:35054793
Optimization of Biomass Accumulation and Production of Phenolic Compounds in Callus Cultures of Rhodiola rosea L. Using Design of Experiments Erst AA, Petruk AA, Erst AS, Krivenko DA, Filinova NV, Maltseva SY, Kulikovskiy MS, Banaev EV Plants (Basel) 02-Jan-2022
PMCID:PMC8747766
doi:10.3390/plants11010124
PMID:35009127
Natural Bioactive Molecules: An Alternative Approach to the Treatment and Control of COVID-19 Islam F, Bibi S, Meem AF, Islam MM, Rahaman MS, Bepary S, Rahman MM, Rahman MM, Elzaki A, Kajoak S, Osman H, ElSamani M, Khandaker MU, Idris AM, Emran TB Int J Mol Sci 23-Nov-2021
PMCID:PMC8658031
doi:10.3390/ijms222312638
PMID:34884440
Application of UHPLC Fingerprints Combined with Chemical Pattern Recognition Analysis in the Differentiation of Six Rhodiola Species Ma D, Wang L, Jin Y, Gu L, Yu X, Xie X, Yin G, Wang J, Bi K, Lu Y, Wang T Molecules 13-Nov-2021
PMCID:PMC8618991
doi:10.3390/molecules26226855
PMID:34833946
Simultaneous Determination of 78 Compounds of Rhodiola rosea Extract by Supercritical CO2-Extraction and HPLC-ESI-MS/MS Spectrometry Zakharenko AM, Razgonova MP, Pikula KS, Golokhvast KS Biochem Res Int 06-Jul-2021
PMCID:PMC8279876
doi:10.1155/2021/9957490
PMID:34306755

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 / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.5246/JCPS.2011.02.019
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile 20979868 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)C#N 259.26 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
Rhodiocyanoside A 6442274 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)C#N 259.26 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,4R)-3,7-dimethylocta-2,6-diene-1,4-diol 26437434 Click to see CC(=CCC(C(=CCO)C)O)C 170.25 unknown https://doi.org/10.1007/BF00599280
3,7-Dimethylocta-2,6-diene-1,4-diol 54206902 Click to see CC(=CCC(C(=CCO)C)O)C 170.25 unknown https://doi.org/10.1007/BF00599280
Rosiridol 22323960 Click to see CC(=CCC(C(=CCO)C)O)C 170.25 unknown https://doi.org/10.1007/BF00599280
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-(4-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 73181367 Click to see CC(=CCC(C(=CCOC1C(C(C(C(O1)CO)O)O)O)C)O)C 332.39 unknown https://doi.org/10.1007/BF00599280
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00599280
https://doi.org/10.5246/JCPS.2011.02.019
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.5246/JCPS.2011.02.019
https://doi.org/10.1007/BF00599280
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00599280
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1007/BF00599280
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 https://doi.org/10.1007/BF00599280
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Disaccharides
2-(Hydroxymethyl)-2-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 72669154 Click to see C1C(C(C(C(O1)(CO)OC2C(OC(C(C2O)O)O)CO)O)O)O 342.30 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
Fru(b2-4)b-Glc 60162291 Click to see C1C(C(C(C(O1)(CO)OC2C(OC(C(C2O)O)O)CO)O)O)O 342.30 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2RS)-Lotaustralin 23638286 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown https://doi.org/10.5246/JCPS.2011.02.019
2(R)-Hydroxy-2-methylbutyronitrile-beta-D-glucopyranoside 4626626 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.5246/JCPS.2011.02.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.3797/SCIPHARM.2007.75.29

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