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Salvia nutans

Salvia nutans - Unknown
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643febd324bd7711762791
Scientific name Salvia nutans
Authority L.
First published in Sp. Pl. : 27 (1753)

Description Top

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Salvia nutans, also known as nodding sage, is a type of plant belonging to the Lamiaceae family. It is originally found in Central and Eastern Europe, the Caucasus, and potentially Siberia. However, it has also been brought to North America as a garden plant and can now be found growing in the wild.

Synonyms Top

Scientific name Authority First published in
Salvia acutifolia Lam. Tabl. Encycl. 1: 68 (1791)
Salvia betonicifolia Etl. Salv. : 48 (1777)
Salvia cernua Czernj. ex Des.-Shost. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 8: 154 (1940)
Salvia cremenecensis Besser Enum. Pl. : 40 (1821)
Salvia grandiflora Hornem. Hort. Bot. Hafn. 1: 27 (1813)
Salvia hastata Etl. Salv. : 48 (1777)
Salvia pendula Sessé & Moc. Naturaleza (Mexico City) ser. 2, 2, app. 9. 1893 Fl. Mex
Salvia pilosa Cav. Elench. Pl. Horti Matr. : 32 (1803)
Salvia praemontana Klokov Fl. RSS Ukr. 9: 655 (1960)
Salvia pseudopendula Schur Enum. Pl. Transsilv. : 961 (1866)
Salvia ruthenica Weinm. Bull. Soc. Imp. Naturalistes Moscou 7: 55 (1837)
Sclarea nutans (L.) Soják Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)
Salvia pendula var. betonicifolia (Etl.) Nyman Consp. Fl. Eur. 570. 1881
Salvia nutans subsp. ruthenica (Weinm.) Nyman Consp. Fl. Eur. 570. 1881 (1881)

Common names Top

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Language Common/alternative name
English nodding sage
Bulgarian наведен конски босилек
German nickender salbei
Estonian longus salvei
Hungarian kónya zsálya
Hungarian bókoló zsálya
Russian Шалфей поникающий
Ukrainian Шавлія поникла

Subspecies (abbr. subsp./ssp.) Top

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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
  • Europe
    • Eastern Europe
      • Belarus
      • East European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Hungary
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Romania
      • Turkey-in-Europe
  • Northern America
    • North-central U.S.A.
      • Minnesota
    • Northeastern U.S.A.
      • New York

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301729
USDA Plants SANU5
Tropicos 17600302
KEW urn:lsid:ipni.org:names:456804-1
The Plant List kew-183320
Open Tree Of Life 3882809
Observations.org 136058
NCBI Taxonomy 1933741
Nature Serve 2.152945
IPNI 456804-1
iNaturalist 168388
GBIF 2926984
EPPO SALNU
EOL 485079
Elurikkus 7048
Wikipedia Salvia_nutans

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
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
Assessment of Genetic Diversity and Population Structure of the Endangered Astragalus exscapus subsp. transsilvanicus through DNA-Based Molecular Markers Szabo K, Pamfil D, Bădărău AS, Hârţa M Plants (Basel) 11-Dec-2021
PMCID:PMC8707493
doi:10.3390/plants10122732
PMID:34961203
Improving the Knowledge on Distribution, Food Preferences and DNA Barcoding of Natura 2000 Protected Species Paracossulus thrips (Lepidoptera, Cossidae) in Romania Iacob GM, Craioveanu C, Hula V, Aurelian VM, Beldean M, Sitar C Insects 03-Dec-2021
PMCID:PMC8703911
doi:10.3390/insects12121087
PMID:34940175
Local-scale impact of wind energy farms on rare, endemic, and threatened plant species Urziceanu M, Anastasiu P, Rozylowicz L, Sesan TE PeerJ 19-May-2021
PMCID:PMC8140595
doi:10.7717/peerj.11390
PMID:34055481
Development of 18 microsatellite markers for Salvia pratensis Krak K, Vít P, Douda J, Mandák B Appl Plant Sci 22-Jan-2020
PMCID:PMC6976894
doi:10.1002/aps3.11316
PMID:31993258
A higher‐level classification of the Pannonian and western Pontic steppe grasslands (Central and Eastern Europe) Willner W, Kuzemko A, Dengler J, Chytrý M, Bauer N, Becker T, Biţă‐Nicolae C, Botta‐Dukát Z, Čarni A, Csiky J, Igić R, Kącki Z, Korotchenko I, Kropf M, Krstivojević‐Ćuk M, Krstonošić D, Rédei T, Ruprecht E, Schratt‐Ehrendorfer L, Semenishchenkov Y, Stančić Z, Vashenyak Y, Vynokurov D, Janišová M Appl Veg Sci 16-Sep-2016
PMCID:PMC5348766
doi:10.1111/avsc.12265
PMID:28356815
A study of the flavonoids ofSalvia nutans E. V. Gella, L. I. Prokosheva Springer Science and Business Media LLC 07-Jan-2005
doi:10.1007/BF00941703
12-Deoxy-6,7-dehydroroyleanone, 12-deoxy-6-hydroxy-6,7-dehydroroyleanone and 12-deoxy-7,7-dimethoxy-6-ketoroyleanone from Salvia nutans roots Gábor Nagy, Gábor Günther, Imre Máthé, Gerald Blunden, Ming-he Yang, Trevor A Crabb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00135-1

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see CCCCCCCCC(C)C 156.31 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bS,8aS,10S)-10-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 14609850 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C 316.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
(4bS,8aS)-10,10-dimethoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,4,9-trione 15478909 Click to see CC(C)C1=CC(=O)C2=C(C1=O)C(C(=O)C3C2(CCCC3(C)C)C)(OC)OC 374.50 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione 15478907 Click to see CC(C)C1=CC(=O)C2=C(C1=O)C=CC3C2(CCCC3(C)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
10-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione 14609849 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C 316.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
10,10-Dimethoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,4,9-trione 162873138 Click to see CC(C)C1=CC(=O)C2=C(C1=O)C(C(=O)C3C2(CCCC3(C)C)C)(OC)OC 374.50 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione 162949124 Click to see CC(C)C1=CC(=O)C2=C(C1=O)C=CC3C2(CCCC3(C)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
> 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)00135-1
> 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)00135-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,7aS)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4,4a,5,7a-tetrahydro-3H-cyclopenta[c]pyran-1-one 49788109 Click to see C1COC(=O)C2C1CC=C2COC3C(C(C(C(O3)CO)O)O)O 330.33 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
[(1S,2S,4R,8R,10S)-12-(acetyloxymethyl)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-11-en-10-yl] (E)-2-methylbut-2-enoate 101620868 Click to see CC=C(C)C(=O)OC1CC(C(=O)CCC2(C(O2)C3C1=C(C(=O)O3)COC(=O)C)C)C 420.50 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid 163059045 Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O 786.80 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3aR,4R,5R,9aR,9bS)-5-acetyloxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162926507 Click to see CC1C(O1)(C)C(=O)OC2C3C(C4C(=CC(=O)C4=C(C2OC(=O)C)C)C)OC(=O)C3=C 416.40 unknown https://doi.org/10.1016/S0031-9422(99)00135-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00941703
> 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 https://doi.org/10.1007/BF00941703
> Phenylpropanoids and polyketides / Macrolides and analogues
[(3S,4S,5R,8S,10R,12S,15Z,20R,22S,23S,24R)-24-[(E,4R)-4-acetyloxy-2-methylhept-1-enyl]-4,8,12,20,22-pentahydroxy-3,5,15,23-tetramethyl-2-oxo-1-oxacyclotetracos-15-en-10-yl] acetate 102064352 Click to see CCCC(CC(=CC1C(C(CC(CCCC=C(CCC(CC(CC(CCC(C(C(C(=O)O1)C)O)C)O)OC(=O)C)O)C)O)O)C)C)OC(=O)C 712.90 unknown https://doi.org/10.1016/S0031-9422(99)00135-1

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