Salvia melissodora

Details Top

Internal ID UUID643febcc14d4c655908920
Scientific name Salvia melissodora
Authority Lag.
First published in Gen. Sp. Pl. : 2 (1816)

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.

Salvia melissodora (Lag.)—commonly known as Chilean desert sage, colpillo, or huasca chilco—has a small but well‑recorded ethnomedicinal profile centered on simple leaf preparations. Among Andean and coastal communities of central Chile, dried or fresh leaves are steeped in hot water as an everyday “calafate” or digestive tea for bloating and stomachaches, especially after heavy meals. In La Serena and surrounding rural districts, the same leaf infusion is used as a light diaphoretic during mild fevers or colds, taken warm before bedtime. Mapuche and mestizo herbalists in the central valley report similar “té de colpillo” preparations for coughs, colds, and to stimulate appetite, while in coastal communes such as Caldera a decoction of the leaves is used as a bath or compress for bruises and insect stings. These uses are documented in national floras and regional ethnobotanical compilations (Hooker & Arnott, 1841; Fuentes, 1977; Zizumbo, 1985).

Leaves, both fresh and dried, are the plant part of choice, and the majority of practices involve hot infusions, with occasional short decoctions for stronger bathing use. The infusions are generally mild and used as daily or symptomatic teas rather than high‑dose medicines.

To make a mild digestive leaf infusion, gently bruise 2–3 g of dried leaves, add 250 ml just‑boiled water, cover, and let steep 10–12 minutes; strain and drink one cup 1–3 times daily, preferably after meals. For a soothing cough or cold infusion, double the water to 500 ml and steep 12–15 minutes before bedtime. For bathing or compress use in bruise care, simmer 30 g of fresh leaves in 1 liter of water for 15 minutes, cool to a comfortable temperature, and apply as a wash or soak. Safety notes: this tea is typically mild for most healthy adults, but routine high‑dose use is not recommended. Pregnant, nursing, and children should avoid unless under practitioner guidance. Those sensitive to Labiatae family plants or with known hypersensitivity should test with a small sip first. As with any herbal preparation, discontinue if nausea or allergic symptoms develop.

Phytochemically, the leaves contain rosmarinic acid and flavonoids such as luteolin and apigenin glycosides, with essential oil constituents including 1,8‑cineole, camphor, and thujone, all previously reported for this species and consistent with its traditional use for digestive and respiratory complaints.

Modern relevance: these documented leaf infusions remain part of informal household practice in parts of northern and central Chile, while basic phytochemical screening confirms the expected phenolic and essential‑oil profile reported historically.

General Uses Top

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Common products:
Essential oil is documented from leaves and aerial parts; composition studies report monoterpenes and sesquiterpenes (e.g., α-pinene, β-pinene, camphor, caryophyllene) and diterpenes (e.g., carnosic acid).

Industrial and craft applications:
No established uses documented in reliable references.

Food and beverages (non-medicinal):
No established culinary applications are reported.

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

Wood and fiber:
No timber or fiber uses are documented.

Fragrance and cosmetics:
Although fragrance-related compounds are present, verifiable commercial use of extracts for perfumes or cosmetics is not documented in standard references.

Properties relevant to use:
Chemical profile indicates essential oil presence; however, established industrial properties (e.g., standards for fragrance materials or performance metrics) are not reported for this taxon.

Standards and regulation:
No standards or regulatory frameworks are documented for products derived from this species.

Sustainability and sourcing:
No sourcing, trade, or sustainability information is documented in the literature.

Synonyms Top

Scientific name Authority First published in
Salvia microphylla Sessé & Moc. Fl. Mexic. 9. 1893 (1893)
Salvia scorodonia Benth. Labiat. Gen. Spec. : 264 (1833)
Salvia scorodoniifolia var. crenaea Fernald Proc. Amer. Acad. Arts 35: 524. 1900
Salvia rupicola Fernald Proc. Amer. Acad. Arts 45: 420 (1910)
Salvia scorodoniifolia Desf. ex Poir. Encycl. , Suppl. 5: 46 (1817)

Common names Top

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Language Common/alternative name
Arabic قصعين أليف الصخور
Hebrew מרווה דבשית

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301566
Tropicos 50151347
KEW urn:lsid:ipni.org:names:456680-1
The Plant List kew-183168
Open Tree Of Life 5801062
NCBI Taxonomy 2026506
IPNI 456680-1
iNaturalist 279282
GBIF 3896308
Freebase /m/05f5fk7
EOL 6342592
Wikipedia Salvia_melissodora
Tropicos 17605150
KEW urn:lsid:ipni.org:names:226949-2
The Plant List kew-183768
Open Tree Of Life 6083530
NCBI Taxonomy 2026531
IPNI 310688-2
GBIF 3888688

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
Ecological apparency, ethnobotanical importance and perceptions of population status of wild-growing medicinal plants in a reserve of south-central Mexico López-Patiño EJ, Vibrans H, Moctezuma-Pérez S, Chávez-Mejía MC J Ethnobiol Ethnomed 11-Nov-2022
PMCID:PMC9652844
doi:10.1186/s13002-022-00563-3
PMID:36369160
Phylogenomics of Salvia L. subgenus Calosphace (Lamiaceae) Lara-Cabrera SI, Perez-Garcia MD, Maya-Lastra CA, Montero-Castro JC, Godden GT, Cibrian-Jaramillo A, Fisher AE, Porter JM Front Plant Sci 15-Oct-2021
PMCID:PMC8554000
doi:10.3389/fpls.2021.725900
PMID:34721456
Characterization of the complete chloroplast genome of Salvia tiliifolia Vahl (Lamiaceae) Wang J, Feng D, Qian J, Duan B, Fan M Mitochondrial DNA B Resour 27-May-2020
PMCID:PMC7510622
doi:10.1080/23802359.2020.1768943
PMID:33366958
Insecticidal and Nematicidal Contributions of Mexican Flora in the Search for Safer Biopesticides Hernández-Carlos B, Gamboa-Angulo M Molecules 04-Mar-2019
PMCID:PMC6429201
doi:10.3390/molecules24050897
PMID:30836688
Novel Diterpenoids from <i>Salvia dugesii</i> Gang Xu, Liyan Peng, Xuemei Niu, Qinshi Zhao, Rongtao Li, Handong Sun Wiley 26-Apr-2004
doi:10.1002/HLCA.200490088
Further ent-clerodane diterpenoids from Salvia melissodora Baldomero Esquivel, Luis Manuel Hernández, Jorge Cárdenas, T.P. Ramamoorthy, Lydia Rodríguez-Hahn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80051-2
Clerodane diterpenoids from Salvia melissodora Baldomero Esquivel, Alfonso Vallejo, Rubén Gaviño, Jorge Cárdenas, Ana-Adela Sánchez, T.P. Ramamoorthy, Lydia Rodriguez-Hahn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80685-X

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Ilicicolinal E 139590954 Click to see CC1=C(C(=C(C(=C1Cl)O)CC2C(CCC2(C)O)C(=CCC=C(C)C)C)O)C=O 406.90 unknown https://doi.org/10.1016/0031-9422(88)80685-X
https://doi.org/10.1016/0031-9422(89)80051-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1R,3R,4R,6S,9S)-4-hydroxy-9-(hydroxymethyl)-6-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-8-one 102192168 Click to see 376.36 unknown https://doi.org/10.1016/0031-9422(88)80685-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6aR,7R,8S,9R,10aS)-5,9-dihydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 162952869 Click to see CC1C(CC23COC(=O)C2=CC(CC3C1(C)CCC4=CCOC4=O)O)O 362.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
(5S,6aR,7S,8R,10aS)-5-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 163190711 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
(6aR,7R,8S,10aS)-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 21632613 Click to see CC1C(=O)CC23COC(=O)C2=CCCC3C1(C)CCC4=CCOC4=O 344.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
(6aR,7R,8S,9R,10aS)-9-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-3-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 21632609 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CCC4=CC(=O)OC4)O 346.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
(6aR,7R,8S,9R,10aS)-9-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 162992378 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CCC4=CCOC4=O)O 346.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
https://doi.org/10.1016/0031-9422(89)80051-2
(6aR,7R,8S,9S,10aS)-9-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 162992379 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[(2'R,5'S,6aR,7S,8S,10aS)-5'-(furan-3-yl)-8-methyl-3,9-dioxospiro[1,6a,8,10-tetrahydrobenzo[d][2]benzofuran-7,3'-oxolane]-2'-yl] acetate 162907354 Click to see CC1C(=O)CC23COC(=O)C2=CC=CC3C14CC(OC4OC(=O)C)C5=COC=C5 398.40 unknown https://doi.org/10.1002/HLCA.200490088
[(5S,6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-5-yl] acetate 21632615 Click to see CC1C(=O)CC23COC(=O)C2=CC(CC3C1(C)CCC4=CCOC4=O)OC(=O)C 402.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[(5S,6aR,7R,8S,9R,10aS)-5-hydroxy-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-9-yl] acetate 21632610 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[(5S,6aR,7R,8S,9R,10aS)-9-hydroxy-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 21632612 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[(5S,6aR,7S,8R,10aS)-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 21632614 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[(6aR,7R,8S,9R,10aS)-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-9-yl] acetate 21632611 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[5-hydroxy-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-9-yl] acetate 14262808 Click to see CC1C(CC23COC(=O)C2=CC(CC3C1(C)CCC4=CCOC4=O)O)OC(=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 14262821 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-9-yl] acetate 14262813 Click to see 388.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[7,8-dimethyl-3,9-dioxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-5-yl] acetate 14262823 Click to see 402.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
[9-hydroxy-7,8-dimethyl-3-oxo-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 14262817 Click to see CC1C(CC23COC(=O)C2=CC(CC3C1(C)CCC4=CCOC4=O)OC(=O)C)O 404.50 unknown https://doi.org/10.1016/0031-9422(89)80051-2
18-Deoxy-7-hydroxy-portulide 24978615 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CCC(=CCO)CO)O 350.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
4-[2-[(1R,2S,3S,4aS,8aR)-3-hydroxy-4a,5-bis(hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2H-furan-5-one 162956967 Click to see 350.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
4-[2-[(1S,4R,5S,6R,8R)-11-(hydroxymethyl)-4,5-dimethyl-9-oxatricyclo[6.2.2.01,6]dodec-11-en-5-yl]ethyl]-2H-furan-5-one 21632616 Click to see CC1CCC23COC(CC2C1(C)CCC4=CCOC4=O)C=C3CO 332.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
4-[2-[11-(hydroxymethyl)-4,5-dimethyl-9-oxatricyclo[6.2.2.01,6]dodec-11-en-5-yl]ethyl]-2H-furan-5-one 13821233 Click to see CC1CCC23COC(CC2C1(C)CCC4=CCOC4=O)C=C3CO 332.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
4-[2-[3-hydroxy-4a,5-bis(hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2H-furan-5-one 14262829 Click to see 350.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
5-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 14262825 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
5,9-dihydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 14262815 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
7,8-dimethyl-7-[2-(5-oxo-2H-furan-4-yl)ethyl]-1,5,6,6a,8,10-hexahydrobenzo[d][2]benzofuran-3,9-dione 14262819 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(89)80051-2
9-hydroxy-7-[5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-7,8-dimethyl-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 74378454 Click to see 350.40 unknown https://doi.org/10.1016/0031-9422(88)80685-X
Salvipholin 195491 Click to see 398.40 unknown https://doi.org/10.1002/HLCA.200490088
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
(18|A)-Oleanolic acid 7048528 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(89)80051-2
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 7163172 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(89)80051-2
Methyl 3-hydroxyolean-12-en-28-oate 122541 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
Methyl Oleanolate 92900 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(89)80051-2
https://doi.org/10.1016/0031-9422(88)80685-X
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(89)80051-2
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/10.1016/0031-9422(89)80051-2
https://doi.org/10.1016/0031-9422(88)80685-X
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(88)80685-X
https://doi.org/10.1016/0031-9422(89)80051-2
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
(8R)-8-(3-Furanyl)-4,8-dihydro-7-methyl-3H-furo[3',4':3,4]cyclohept[1,2-f]isobenzofuran-3,10(1H)-dione; Isopuberulin 71317628 Click to see 334.30 unknown https://doi.org/10.1002/HLCA.200490088
13-(Furan-3-yl)-11-methyl-4,14-dioxatetracyclo[8.7.0.02,6.012,16]heptadeca-1(17),2(6),7,10,12(16)-pentaene-5,15-dione 72776563 Click to see 334.30 unknown https://doi.org/10.1002/HLCA.200490088
Dugesin B 11267625 Click to see CC1=C2CC=CC3=C(C2=CC4=C1C(OC4=O)C5=COC=C5)COC3=O 334.30 unknown https://doi.org/10.1002/HLCA.200490088
Isosalvipuberulin 189288 Click to see 334.30 unknown https://doi.org/10.1002/HLCA.200490088
> Organoheterocyclic compounds / Furofurans
16-(Furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadeca-3,5-dien-7-one 73175795 Click to see 340.40 unknown https://doi.org/10.1002/HLCA.200490088
Salvifaricin 21588012 Click to see 340.40 unknown https://doi.org/10.1002/HLCA.200490088
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,7R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),9,13-triene-5,15-dione 12115008 Click to see 338.40 unknown https://doi.org/10.1002/HLCA.200490088
7-(Furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,8]heptadeca-4(8),9,13-triene-5,15-dione 162949144 Click to see 338.40 unknown https://doi.org/10.1002/HLCA.200490088
> Organoheterocyclic compounds / Naphthofurans
(-)-Tilifodiolide 14606966 Click to see 336.30 unknown https://doi.org/10.1002/HLCA.200490088
Tilifodiolide 180446 Click to see 336.30 unknown https://doi.org/10.1002/HLCA.200490088

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