Salvia verticillata - Unknown
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Internal ID UUID643fec0142079788947319
Scientific name Salvia verticillata
Authority L.
First published in Sp. Pl. : 26 (1753)

Description Top

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Salvia verticillata, also known as lilac sage or whorled clary, is a perennial herb found in central Europe, western Asia, and naturalized in northern Europe and North America. It was first identified by Carl Linnaeus in 1753. This plant has a leafy base of mid-green leaves covered in hairs, with stems that can reach up to 3 feet in height. Its small lavender flowers grow in tight whorls, with lime-green and purple calyces. The name verticillata comes from the whorls that grow in a spiral pattern. A popular cultivar, 'Purple Rain', was introduced in the 1990s and is known for its showy and long-lasting blooms, growing up to 2 feet tall.

Synonyms Top

Scientific name Authority First published in
Horminum verticillatum Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Sphacopsis verticillata Briq. Lab. Alp. Mar. : 184 (1891)
Salvia verticillata f. natronata Simonk. Term. Közl. 32: 266 1900
Salvia verticillata var. parvifolia K.Koch Linnaea 21: 660. 1849
Covola verticillata Medik. Philos. Bot. 2: 67 (1791)
Hemisphace verticillata Opiz Seznam : 50 (1852)

Common names Top

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Language Common/alternative name
English whorled clary
Belarusian шалфей мутоўчаты
Czech šalvěj přeslenitá
Welsh clari troellennog
German quirl-salbei
German quirlblütiger salbei
German quirlblütige salbei
Estonian männassalvei
Persian سالویای بنفش
Finnish kiehkurasalvia
French sauge verticillée
Croatian pršljenasta kadulja
Upper Sorbian mutličkata želbija
Georgian დაჯირა
Norwegian Bokmål kranssalvie
Dutch kranssalie
Norwegian Nynorsk kranssalvie
Polish szałwia okręgowa
Russian Шалфей мутовчатый
Slovak šalvia praslenatá
Swedish kranssalvia
Turkish helezonik ada çayı
Ukrainian Шавлія кільчаста
Chinese 轮生鼠尾草
Chinese 轮叶鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Salvia verticillata subsp. amasiaca (Freyn & Bornm.) Bornm. Bull. Herb. Boissier , sér. 2, 8: 110 (1908)
Salvia verticillata subsp. verticillata Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • Krasnoyarsk
    • Western Asia
      • Iran
      • Iraq
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Great Britain
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Massachusetts
      • New Jersey
      • New York
      • Pennsylvania
      • Vermont
    • Southeastern U.S.A.
      • Delaware
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302602
Canadensys 6451
USDA Plants SAVE5
Tropicos 17600313
INPN 120703
KEW urn:lsid:ipni.org:names:457502-1
The Plant List kew-184133
Missouri Botanical Garden 281428
Open Tree Of Life 499328
Observations.org 2730
NCBI Taxonomy 49220
NBN Atlas NBNSYS0000004219
Nature Serve 2.143630
IPNI 457502-1
iNaturalist 128689
GBIF 2926995
Freebase /m/02q_pp3
EPPO SALVE
EOL 579418
Elurikkus 7051
USDA GRIN 32976
Wikipedia Salvia_verticillata

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
Green Synthesis of Novel Silver Nanoparticles Using Salvia blepharophylla and Salvia greggii: Antioxidant and Antidiabetic Potential and Effect on Foodborne Bacterial Pathogens Geremew A, Gonzalles J III, Peace E, Woldesenbet S, Reeves S, Brooks N Jr, Carson L Int J Mol Sci 11-Jan-2024
PMCID:PMC10815671
doi:10.3390/ijms25020904
PMID:38255978
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Accumulation of Polyphenols and Associated Gene Expression in Hairy Roots of Salvia viridis Exposed to Methyl Jasmonate Grzegorczyk-Karolak I, Krzemińska M, Grąbkowska R, Gomulski J, Żekanowski C, Gaweda-Walerych K Int J Mol Sci 07-Jan-2024
PMCID:PMC10815010
doi:10.3390/ijms25020764
PMID:38255839
Natural Compounds of Salvia L. Genus and Molecular Mechanism of Their Biological Activity Zhumaliyeva G, Zhussupova A, Zhusupova GE, Błońska-Sikora E, Cerreto A, Omirbekova N, Zhunusbayeva Z, Gemejiyeva N, Ramazanova M, Wrzosek M, Ross SA Biomedicines 27-Nov-2023
PMCID:PMC10740457
doi:10.3390/biomedicines11123151
PMID:38137372
In vitro Antimicrobial Activity of Some Extracts of Salvia spp Harvested from the Oltenia Flora Using Different Solvents BĂLĂȘOIU RM, BIȚĂ A, STĂNCIULESCU EC, BĂLĂȘOIU M, BEJENARU C, BEJENARU LE, PISOSCHI CG Curr Health Sci J 30-Sep-2023
PMCID:PMC10832872
doi:10.12865/CHSJ.49.03.12
PMID:38314220
Recent advances towards natural plants as potential inhibitors of SARS-Cov-2 targets He Z, Yuan J, Zhang Y, Li R, Mo M, Wang Y, Ti H Pharm Biol 22-Aug-2023
PMCID:PMC10446791
doi:10.1080/13880209.2023.2241518
PMID:37605622
Chemical Profile and Bioactivity Evaluation of Salvia Species from Eastern Europe Luca SV, Skalicka-Woźniak K, Mihai CT, Gradinaru AC, Mandici A, Ciocarlan N, Miron A, Aprotosoaie AC Antioxidants (Basel) 28-Jul-2023
PMCID:PMC10451821
doi:10.3390/antiox12081514
PMID:37627509
Nontarget catches of traps with chemical lures may refer to the flower‐visitation, probable pollination, and feeding of bush crickets (Ensifera: Tettigoniidae) Nagy A, Ősz A, Tóth M, Rácz IA, Kovács S, Szanyi S Ecol Evol 04-Jul-2023
PMCID:PMC10319520
doi:10.1002/ece3.10249
PMID:37415641
Antimicrobial activity of phytofabricated silver nanoparticles using Carica papaya L. against Gram-negative bacteria Arsene MM, Viktorovna PI, Alla M, Mariya M, Davares AK, Carime BZ, Anatolievna GO, Vyacheslavovna YN, Vladimirovna ZA, Andreevna SL, Aleksandrovna VE, Alekseevich BL, Nikolaïevna BM, Parfait K, Andrey V Vet World 13-Jun-2023
PMCID:PMC10421558
doi:10.14202/vetworld.2023.1301-1311
PMID:37577189
Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M BMC Complement Med Ther 03-Jun-2023
PMCID:PMC10239571
doi:10.1186/s12906-023-04004-w
PMID:37270541
Chrysoeriol Improves In Vitro Porcine Embryo Development by Reducing Oxidative Stress and Autophagy Wang CR, Ji HW, He SY, Liu RP, Wang XQ, Wang J, Huang CM, Xu YN, Li YH, Kim NH Vet Sci 10-Feb-2023
PMCID:PMC9958645
doi:10.3390/vetsci10020143
PMID:36851447
Green Synthesis of Silver Nanoparticles Using Salvia verticillata and Filipendula ulmaria Extracts: Optimization of Synthesis, Biological Activities, and Catalytic Properties Mihailović V, Srećković N, Nedić ZP, Dimitrijević S, Matić M, Obradović A, Selaković D, Rosić G, Katanić Stanković JS Molecules 13-Jan-2023
PMCID:PMC9861472
doi:10.3390/molecules28020808
PMID:36677866
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
An Ethnobotanical study of medicinal plants in Taşköprü (Kastamonu–Turkey) Senkardes I, Dogan A, Emre G Front Pharmacol 20-Oct-2022
PMCID:PMC9630845
doi:10.3389/fphar.2022.984065
PMID:36339567
Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy Van Doan H, Soltani M, Leitão A, Shafiei S, Asadi S, Lymbery AJ, Ringø E Animals (Basel) 16-Sep-2022
PMCID:PMC9495100
doi:10.3390/ani12182443
PMID:36139303

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)CO)(CCC6C5(CC(C(C6(C)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)(C)C)OC8C(C(C(C(O8)C)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)O)O)O 1237.30 unknown https://doi.org/10.1016/S0031-9422(99)00343-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP50036A047
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP50036A047
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP50036A047
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP50036A047
Virgatic acid 14489125 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP50036A047
> 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/10.1021/NP50036A047
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/10.1021/NP50036A047
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/10.1021/NP50036A047
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/10.1021/NP50036A047
> Organoheterocyclic compounds / Benzodioxoles
Sesamolin 101746 Click to see C1C2C(COC2OC3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 370.40 unknown https://doi.org/10.1016/0305-1978(85)90071-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP50036A047
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
6,7-dimethoxy-2-(4-methoxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162873866 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC4C(C(C(C(O4)CO)O)O)O 490.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 https://doi.org/10.1021/NP50036A047
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/NP50036A047

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