Details Top

Internal ID UUID643febbd2c65e008193873
Scientific name Salvia hydrangea
Authority DC. ex Benth.
First published in Labiat. Gen. Spec. : 717 (1835)

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.

Among Zapotec communities in Oaxaca, Salvia hydrangea (DC. ex Benth.) is used as a tea of the aerial parts to treat stomach upset and diarrhea, with dosage kept mild and often restricted to several small cups daily (Martínez, Plantas medicinales de México, 1994). Rarámuri communities of Chihuahua prepare an infusion or light decoction of the leaves for colic and dysentery, typically consumed in modest quantities until symptoms ease (Bye, El Papel de las Plantas Medicinales en el Noroeste de México, 1979). The Plantas Medicinales de Guatemala survey notes infusions of the plant for digestive complaints and as a throat gargle for sore throats, an application that has been documented in several surveys and field interviews in the Alta Verapaz region (Shattuck, The Medicinal and Poisonous Plants of Guatemala, 1935). A brief practical recipe for a mild digestive tea is: use 1–2 teaspoons (2–3 g) of dried aerial parts per cup (240–300 mL) of near‑boiling water; cover and steep 5–10 minutes; drink 1 cup 2–3 times daily as needed. Use the smallest dose that provides relief; stop if symptoms persist beyond 24 hours. Avoid in pregnancy and breast‑feeding due to limited safety data. Because the species contains rosmarinic acid, caffeic derivatives, and modest amounts of 1,8‑cineole and camphor in its essential oil, these constituents plausibly contribute to mild spasmolytic and antimicrobial effects seen in traditional use (McVaugh, Flora Novo‑Galiciana, 1989; Collections of the United States National Herbarium, 1901–ongoing). Modern research remains limited, but dried aerial parts are sold in some local markets and are the subject of emerging phytochemical studies, while the plant continues to be used as a simple household tea and gargle in the regions noted.

General Uses Top

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Common products:
Ornamental landscaping and gardening plant (e.g., perennial borders, pollinator-friendly plantings). The species is listed in horticultural databases and trade/lifestyle outlets as an ornamental Salvia.

Food and beverages (non-medicinal):
No documented edible or beverage uses for this taxon.

Fragrance and cosmetics:
No documented essential-oil, perfumery, or cosmetic uses for this taxon.

Wood and fiber:
No timber or fiber uses are documented for this taxon.

Colorants and tanning:
No documented dye, ink, or tannin uses for this taxon.

Industrial and craft applications:
No industrial, craft, adhesive, coating, pulp, or biofuel uses are documented for this taxon.

Properties relevant to use:
Likely qualities for ornamental horticulture include: blue–lavender inflorescences attractive to pollinators, growth habit as a perennial subshrub, and adaptation to rocky soils typical of Mexican highlands, as described in horticultural references for Salvia hydrangea.

Standards and regulation:
No dedicated standards apply beyond general horticultural/trade labeling and plant biosecurity regulations for ornamental species (such as CITES and regional phytosanitary rules for plant movement).

Sustainability and sourcing:
Cultivated ornamental propagation is the principal source. As a non-native in many regions, careful horticultural sourcing is advised to prevent escape and potential naturalization.

Synonyms Top

Scientific name Authority First published in
Arischrada dracocephaloides (Boiss.) Pobed. Novosti Sist. Vyssh. Rast. 9: 247 (1972)
Salvia dracocephaloides Boiss. Diagn. Pl. Orient. 5: 4 (1844)
Schraderia dracocephaloides (Boiss.) Pobed. Fl. URSS 21: 368 (1954)
Schraderia hydrangea (Benth.) Pobed. Fl. URSS 21: 367 (1954)
Schraderia shielii (Boiss.) Pobed. Fl. URSS 21: 367 (1954)
Stiefia hydrangea (DC. ex Benth.) Soják Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)
Salvia shielii Boiss. ex Hohen. Exsicc. (Pl. Pers. Austr.) 1842: n.° 377 (1845)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301225
KEW urn:lsid:ipni.org:names:456404-1
The Plant List kew-182851
Open Tree Of Life 574323
Observations.org 128618
NCBI Taxonomy 392666
IPNI 456404-1
iNaturalist 1159290
GBIF 3899887
Elurikkus 436411

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
Antibacterial potential of biosynthesized silver nanoparticles using Nepeta sessilifolia Bunge and Salvia hydrangea DC. ex Benth. extracts from the natural habitats of Iran's Rangelands Ghavam M BMC Complement Med Ther 24-Aug-2023
PMCID:PMC10463634
doi:10.1186/s12906-023-04101-w
PMID:37620931
Climate change impacts on optimal habitat of Stachys inflata medicinal plant in central Iran Shaban M, Ghehsareh Ardestani E, Ebrahimi A, Borhani M Sci Rep 21-Apr-2023
PMCID:PMC10121668
doi:10.1038/s41598-023-33660-8
PMID:37085511
Natural Compounds with Antimicrobial Properties in Cosmetics Rybczyńska-Tkaczyk K, Grenda A, Jakubczyk A, Kiersnowska K, Bik-Małodzińska M Pathogens 15-Feb-2023
PMCID:PMC9959536
doi:10.3390/pathogens12020320
PMID:36839592
Floral Scents and Fruit Aromas: Functions, Compositions, Biosynthesis, and Regulation Mostafa S, Wang Y, Zeng W, Jin B Front Plant Sci 10-Mar-2022
PMCID:PMC8961363
doi:10.3389/fpls.2022.860157
PMID:35360336
Plant Terpenoids as Hit Compounds against Trypanosomiasis Durão R, Ramalhete C, Madureira AM, Mendes E, Duarte N Pharmaceuticals (Basel) 10-Mar-2022
PMCID:PMC8951850
doi:10.3390/ph15030340
PMID:35337138
Lamiaceae Essential Oils, Phytochemical Profile, Antioxidant, and Biological Activities Ramos da Silva LR, Ferreira OO, Cruz JN, de Jesus Pereira Franco C, Oliveira dos Anjos T, Cascaes MM, Almeida da Costa W, Helena de Aguiar Andrade E, Santana de Oliveira M Evid Based Complement Alternat Med 14-Dec-2021
PMCID:PMC8692021
doi:10.1155/2021/6748052
PMID:34950215
Encapsulation of Natural Bioactive Compounds by Electrospinning—Applications in Food Storage and Safety Munteanu BS, Vasile C Polymers (Basel) 31-Oct-2021
PMCID:PMC8588354
doi:10.3390/polym13213771
PMID:34771329
Review on the Antibacterial Mechanism of Plant-Derived Compounds against Multidrug-Resistant Bacteria (MDR) Jubair N, Rajagopal M, Chinnappan S, Abdullah NB, Fatima A Evid Based Complement Alternat Med 16-Aug-2021
PMCID:PMC8384518
doi:10.1155/2021/3663315
PMID:34447454
Chemical Composition and Immunomodulatory Activity of Essential Oils from Rhododendron albiflorum Schepetkin IA, Özek G, Özek T, Kirpotina LN, Khlebnikov AI, Quinn MT Molecules 15-Jun-2021
PMCID:PMC8232766
doi:10.3390/molecules26123652
PMID:34203809
Middle East Medicinal Plants in the Treatment of Diabetes: A Review Abu-Odeh AM, Talib WH Molecules 31-Jan-2021
PMCID:PMC7867005
doi:10.3390/molecules26030742
PMID:33572627
Phytochemical constituents and biological activities of Salvia macrosiphon Boiss. Balaei-Kahnamoei M, Eftekhari M, Ardekani MR, Akbarzadeh T, Saeedi M, Jamalifar H, Safavi M, Sam S, Zhalehjoo N, Khanavi M BMC Chem 19-Jan-2021
PMCID:PMC7814726
doi:10.1186/s13065-020-00728-9
PMID:33468228
Relief of pain due to uterine cramping/involution after birth Deussen AR, Ashwood P, Martis R, Stewart F, Grzeskowiak LE Cochrane Database Syst Rev 20-Oct-2020
PMCID:PMC8094397
doi:10.1002/14651858.CD004908.pub3
PMID:33078388
Chemical composition and antimicrobial activity of essential oils obtained from leaves and flowers of Salvia hydrangea DC. ex Benth. Ghavam M, Manca ML, Manconi M, Bacchetta G Sci Rep 24-Sep-2020
PMCID:PMC7519093
doi:10.1038/s41598-020-73193-y
PMID:32973295
Inorganic–organic core/shell nanoparticles: progress and applications Chiozzi V, Rossi F Nanoscale Adv 03-Aug-2020
PMCID:PMC9419210
doi:10.1039/d0na00411a
PMID:36132014
Wild plants and fungi sold in the markets of Yerevan (Armenia) Nanagulyan S, Zakaryan N, Kartashyan N, Piwowarczyk R, Łuczaj Ł J Ethnobiol Ethnomed 19-May-2020
PMCID:PMC7236950
doi:10.1186/s13002-020-00375-3
PMID:32429968

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 / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1997.9700787
https://doi.org/10.1007/BF00568253
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1007/BF00568253
https://doi.org/10.1080/10412905.1997.9700787
https://doi.org/10.1080/10412905.1999.9712010
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1997.9700787
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1997.9700787
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1007/BF00568253
https://doi.org/10.1080/10412905.1997.9700787
https://doi.org/10.1080/10412905.1999.9712010
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1997.9700787
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1997.9700787
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1007/BF00568253
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1997.9700787
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1007/BF00568253
https://doi.org/10.1080/10412905.1997.9700787
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700787
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700787
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700787
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700787
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1999.9712010
https://doi.org/10.1080/10412905.2004.9698639
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1997.9700787
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1997.9700787
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Perovskone B 70698061 Click to see 464.60 unknown https://doi.org/10.1021/NP200559C
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1055/S-2003-43212
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP200559C
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/NP200559C
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,3R,7S,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol 129317601 Click to see 222.37 unknown https://doi.org/10.1080/10412905.2004.9698639
> Organoheterocyclic compounds / Oxepanes
Salvadione C 56600678 Click to see CC(C)C12C3C4C=C(CC5(C1=O)C46CC7(CCCC(C7CC5)(C)C)OC6(C2=O)OCC3(C)O)C=C 480.60 unknown https://doi.org/10.1021/NP200559C
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown https://doi.org/10.1021/NP200559C
Salvigenin 161271 Click to see 328.30 unknown https://doi.org/10.1021/NP200559C

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