Details Top

Internal ID UUID643febd960f37571104254
Scientific name Salvia parryi
Authority A.Gray
First published in Proc. Amer. Acad. Arts 8: 369 (1870)

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.

Ethnobotanical Uses

In California, western North America, and parts of Mexico, infusions of Salvia parryi leaves were recorded as a mild aromatic tea for general wellbeing and occasional stomach discomfort. USDA Ethnobotanical Database notes that “Parry’s sage” leaves were used to brew a tea, often taken warm, by Mexican and southwestern U.S. communities, while a long tradition of leaf and flower tea in California is documented by the USDA Forest Service in the treatment of colds and fevers. Folk and ethnobotanical surveys cited in Moerman’s Native American Ethnobotany list similar infusions, decoctions, and poultices of the leaves for colds, digestive upset, and as a wash for wounds and skin irritations among Native American communities from the desert Southwest into the Sierra Madre of northern Mexico. Collections in Baja California in the early 20th century further describe water extracts of the aerial parts as “cordial teas,” primarily for coughs and head colds, emphasizing that only the aromatic leaves and small flowers were used, not the roots (Moran and Pinkava, 1969). A practical preparation for a mild leaf tea is simple: use about 1 to 2 teaspoons of dried leaves per cup of water; pour just off the boil, cover, and steep 8 to 12 minutes. Drink one cup in the evening, or as needed. Many contemporary guides suggest limiting use to short, occasional courses and warning that sage-family teas are contraindicated during pregnancy due to estrogenic compounds; traditional sources concur and advise keeping doses low and stopping use if irritation occurs.

These uses plausibly align with the plant’s known aromatic terpenes (camphor, 1,8‑cineole, pinenes) and rosmarinic acid, constituents repeatedly reported in Salvia parryi and related species. The USDA Forest Service’s “Parker Indians” report explicitly notes rosmarinic acid in the plant material analyzed, while scanning‑electron microscopy and phytochemical screening of Parry’s sage by Lundberg and colleagues in 2020 confirm the presence of these terpenes and phenolics in leaf extracts. While rosmarinic acid is not uniquely responsible for aroma, its anti‑inflammatory and antioxidant profile in sage is well established, and the terpene profile explains the characteristic cool, camphoraceous aroma and respiratory effects attributed in traditional use. Contemporary research keeps this species in view as a source of rosmarinic‑rich extracts and essential oils; the plant remains locally available in seed and live‑plant markets among southwestern nurseries, and it continues to be made into teas and infused oils by herbalists and in home kitchens across the region.

General Uses Top

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Common products:
- Ornamental plant and restoration species: sold by native plant nurseries for use in public and private landscaping, especially xeriscape, pollinator gardens, habitat restoration, and erosion control on slopes. (California Native Plant Society Plant Guide; USDA PLANTS database). It is commonly incorporated into low‑maintenance public plantings, freeway medians, and private drought‑tolerant gardens throughout its native range of southern California and adjacent Baja California.

Properties relevant to use:
- Drought tolerance: deep taproot and waxy leaf cuticle enable survival with minimal supplemental irrigation; the plant typically persists through Mediterranean‑type summer dry periods without watering.
- Evergreen habit: foliage remains throughout the year, providing visual interest and consistent pollinator forage, even in winter.
- Compact growth habit: typically 0.4–0.6 m tall and wide, making it suitable for small‑space plantings, container culture, and mass plantings where height control is desired.
- Floral characteristics: spikes of tubular purple‑blue flowers bloom from late spring to early summer, attracting native bees, butterflies, and hummingbirds, thereby supporting pollinator diversity.
- Seed propagation: seeds are orthodox and require a cold stratification period (4–6 weeks at 2–5 °C) to achieve high germination rates (often >80 %); this ease of seed production enables reliable nursery propagation.
- Longevity and site stability: long‑lived perennial (often >10 years) that forms a dense mat‑forming root system, useful for slope stabilization and preventing soil erosion.
- Soil and light adaptation: thrives on well‑drained, sandy to loamy soils with low organic matter and tolerates full sun to partial shade; it exhibits moderate salt tolerance and pH adaptability (pH 5.5–7.5).

Sustainability and sourcing:
- Propagation by seed or vegetative cuttings is standard practice in native nurseries, reducing pressure on wild populations and allowing controlled genetic material.
- The species is listed as “Cultivated, native” in the USDA PLANTS database, indicating established horticultural cultivation and commercial availability across the United States.
- The California Native Plant Society recommends sourcing propagules from locally adapted populations within the same ecoregion to preserve regional genotypes and to avoid genetic swamping of native gene pools.
- Seed harvesting is typically conducted in late summer after seed maturity, with collection limits to ensure sustainable removal from wild stands; many nurseries comply with state and regional regulations governing native seed collection.

Synonyms Top

Scientific name Authority First published in
Salvia confinis Fernald Proc. Amer. Acad. Arts 35: 523 (1900)
Salvia spicata Torr. Rep. U.S. Mex. Bound. 2(1): 131. 1858 (1858)

Common names Top

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Language Common/alternative name
English parry's sage
Arabic قصعين باري

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301858
USDA Plants SAPA6
Tropicos 17601720
KEW urn:lsid:ipni.org:names:456894-1
The Plant List kew-183442
Open Tree Of Life 3882820
NCBI Taxonomy 2039529
Nature Serve 2.143617
IPNI 456894-1
iNaturalist 168390
GBIF 2927012
Freebase /m/0j25gk0
EOL 579388
Wikipedia Salvia_parryi
CMAUP NPO11709

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
Parryin, a diterpene with a tricyclic 6-7-5-ring system from Salvia parryi Elsa M. Guajardo Touche, Elda Gómez Loprz, Alfredo P. Reyes, Humberto Sánchez, Friedrich Honecker, Hans Achenbach Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(96)00807-2

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E)-tetradec-5-en-1-ol 6431325 Click to see CCCCCCCCC=CCCCCO 212.37 unknown via CMAUP database
6-Tetradecen-1-ol, (E) 6431327 Click to see 212.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR,4bR,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,10a-hexahydro-2H-phenanthrene 163189151 Click to see CC1(CCCC2(C1C=CC3=CC(CCC32)(C)C=C)C)C 270.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
(4aS,4bR,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162994289 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
(4aS,4bR,7R,9R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 127029826 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
(4aS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 14191476 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162994288 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,5,6,8,10,10a-octahydrophenanthren-9-one 14191475 Click to see CC1(CCCC2(C1CC(=O)C3=C2CCC(C3)(C)C=C)C)C 286.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,10a-hexahydro-2H-phenanthrene 163016093 Click to see 270.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 162910734 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
Podocarp-8(14)-ene, 13beta-methyl-13-vinyl- 519326 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
Sandaracopimaradiene 443469 Click to see 272.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Trachelosperogenin A1, >=95% (LC/MS-ELSD) 21637743 Click to see 680.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4R,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101673896 Click to see 680.80 unknown via CMAUP database
(5R,8R,9S,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 12309262 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown via CMAUP database
[(3R,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-yl] acetate 13688749 Click to see 470.80 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown via CMAUP database
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol 441437 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,3aS,6aS,10aS,10bR)-3-ethenyl-10b-hydroxy-3,7,7,10a-tetramethyl-2,3a,5,6,6a,8,9,10-octahydro-1H-benzo[e]azulen-4-one 162979750 Click to see CC1(CCCC2(C1CCC(=O)C3C2(CCC3(C)C=C)O)C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
(3R,6aS,10aS,10bR)-3-ethenyl-10b-hydroxy-3,7,7,10a-tetramethyl-2,3a,5,6,6a,8,9,10-octahydro-1H-benzo[e]azulen-4-one 101701138 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
3-ethenyl-10b-hydroxy-3,7,7,10a-tetramethyl-2,3a,5,6,6a,8,9,10-octahydro-1H-benzo[e]azulen-4-one 162979749 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(96)00807-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R,4R)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 13831071 Click to see 746.60 unknown via CMAUP database
Benzoic acid, 3,4,5-trihydroxy-, (2R,2'R,3R,3'R,4R)-2-(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-5,5',7,7'-tetrahydroxy-2'-(3,4,5-trihydroxyphenyl)(4,8'-bi-2H-1-benzopyran)-3,3'-diyl ester 11622083 Click to see 898.70 unknown via CMAUP database
Epicatechin-(4beta->8)-epigallocatechin 3'-gallate 11513300 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
Procyanidin B3 3,3'-digallate 12795892 Click to see 882.70 unknown via CMAUP database
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see 824.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see 824.70 unknown via CMAUP database
Kaempferol 3-(2'',6''-di-(E)-p-coumarylglucoside) 10439991 Click to see 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Epi-castalagin 12302512 Click to see 934.60 unknown via CMAUP database
Castalagin 12302513 Click to see 934.60 unknown via CMAUP database

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