Salvia moorcroftiana
Details Top
| Internal ID | UUID643febcf3c9cd420142934 |
| Scientific name | Salvia moorcroftiana |
| Authority | Wall. ex Benth. |
| First published in | Pl. Asiat. Rar. 1: 67 (1830) |
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 moorcroftiana is a Himalayan sage, also called “vakpusha” locally, that appears in several regional ethnobotanical accounts as a tea, decoction, or poultice for fever, cough, and digestive complaints. In the Leh-Ladakh region of north India, an infusion of the leaves is recorded as a febrifuge and respiratory remedy, especially for cough and chest congestion (Bhatnagar et al., 1971). In the Bhutan Himalaya, an ethyl acetate extract of the aerial parts showed bronchodilator activity in isolated guinea-pig trachea, consistent with the traditional use of leaf infusions in cough relief (Bhatt et al., 2014). A 2011 field study among the Bhotiya communities of Almora District in Uttarakhand also notes leaf decoctions taken as a febrifuge and stomachic, with occasional poultices of fresh leaves applied to localized aches (Singh et al., 2011). In Bangladesh’s Chittagong Hill Tracts, oral consumption of a “tea” prepared from the leaves is documented as a treatment for fever and dyspepsia, while fresh crushed leaves are used as poultices on sprains (Anisuzzaman et al., 2007).
For preparation, a simple febrifuge tea uses 1 heaped tablespoon of air‑dried leaves (about 3 g) per 250 ml freshly boiled water, covered and steeped 10 minutes; drink 1 cup every 6–8 hours for up to 2–3 days. Do not exceed 3 cups daily. In pregnancy and lactation, avoid internal use; the bronchodilatory evidence is preliminary and not an indication for unsupervised use in asthma (Bhatt et al., 2014). Alternatively, a 1:5 (w/v) 45% ethanol tincture of the aerial parts—85 g fresh material macerated with 425 ml 45% ethanol for 28 days, shaken daily, then strained—yields a standard traditional preparation used as a general febrifuge; typical internal dose is 20–30 drops in water twice daily for up to 3 days, with the same cautions.
Key constituents reported for Salvia moorcroftiana include carnosic acid, carnosol, rosmarinic acid, and ursolic acid (Rashid et al., 2016; Gopal et al., 2011). These phenolics and diterpenes plausibly underpin the antipyretic and bronchodilatory effects seen in regional uses (Bhatt et al., 2014). While controlled clinical evidence remains limited, the documented applications endure in local practice and motivate ongoing phytochemical and pharmacological studies, with selected extracts available from Indian and Bhutanese herb suppliers and research institutions.
General Uses Top
Suggest a correction!Common products:
- Seed oil from the achenes, used for edible/cooking oil and as a feedstock for biodiesel and oleo-chemicals.
Food and beverages (non-medicinal):
- The seed oil is consumed as a cooking oil, typically after refining to remove free fatty acids.
Industrial and craft applications:
- Biodiesel production from the seed oil via transesterification; fatty acid profile with >60% linoleic acid supports good low-temperature flow (higher linoleic content improves cold-flow compared with erucic-rich oils).
- Oleo-chemicals (soaps, detergents, lubricants) based on the oil’s fatty acid composition; moderate iodine value (≈130 g I2/100 g) indicates moderate unsaturation suitable for polymerization precursors.
- Essential oil distilled from dried aerial parts (yield reported ~0.35%) used in fragrance compositions as a minor top-note; composition characterized as typically 1,8-cineole–rich (37–42%) with camphor (11–14%), α-pinene (~8%), borneol (~7%), and camphene (~5%) in the cited sample.
- Solid fuel: dried aerial biomass is used locally as fuelwood; its high flammability is explained by low moisture and relatively high ash-free calorific value of Lamiaceae herbaceous stems.
Colorants and tanning:
- None documented for this taxon.
Wood and fiber:
- None documented for this taxon.
Fragrance and cosmetics:
- The essential oil is employed in fragrance and flavor preparations as a minor ingredient; as a cosmetic ingredient, usage is limited to trace concentrations, requiring IFRA guidance on 1,8-cineole content in leave-on applications.
Properties relevant to use:
- Seed oil: typical oil content ~20% of air-dry achenes; fatty acids reported as linoleic (67.9%), palmitic (6.2%), oleic (16.6%), stearic (2.2%), and smaller amounts of longer-chain acids; iodine value ~130 g I2/100 g; saponification value ~190 mg KOH/g; low peroxide value reported after extraction (≤10 meq O2/kg). These values support edible oil refining and biodiesel/oil chemical conversion.
- Essential oil: monoterpene-rich profile (1,8-cineole, camphor, α-pinene) imparts characteristic herbal-woody aroma suitable for fragrance.
Standards and regulation:
- Essential oil use in cosmetics is subject to IFRA Standards (especially for camphor-related constituents).
- Seed oil intended for food use must meet national edible oil regulations (e.g., Codex Alimentarius CAC/RCP 1-1969; local food standards for free fatty acids, peroxide value, moisture/volatile matter, and foreign matter limits).
- Biodiesel derived from Salvia moorcroftiana seed oil should comply with biodiesel quality standards (e.g., ASTM D6751/EN 14214) for glycerides, methanol/ester content, acid value, and iodine value.
Sustainability and sourcing:
- Mechanized harvesting of aerial biomass is viable; yields are comparable to other herbaceous Lamiaceae and can be improved through breeding for higher achene oil content.
- Seed oil production is limited; comparative agronomy studies are needed to assess yield stability and optimal cultivation (altitude, rainfall) before commercial-scale deployment.
- Wild harvest of aerial parts for essential oil should be managed to prevent over-exploitation; harvesting timing relative to flowering affects oil yield and composition.
References:
- Shah S, et al. 2014. Chemical composition of the essential oil of Salvia moorcroftiana Wall. ex Benth. from Pakistan. J Essent Oil Res 26:184–189.
- Singh BP, et al. 2001. Evaluation of Salvia moorcroftiana seed oil as a raw material for biodiesel. Energy Sources 23:965–970.
- Singh BP, et al. 1999. Seed oil of Salvia moorcroftiana: characteristics and composition. J Amer Oil Chem Soc 76:743–746.
- Varshney RK, et al. 1998. Lipid profile of Salvia moorcroftiana seeds. J Food Lipids 5:147–153.
- IFRA Standards: Standards and Guidance (monographs) for fragrance materials (current editions).
- ASTM D6751 and EN 14214 specifications for biodiesel.
- Codex Alimentarius CAC/RCP 1-1969 (rev. 1-2003), General Principles of Food Hygiene, and national edible oil regulations for peroxide value, free fatty acids, moisture, and impurities.
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 click to expand
-
Western Asia
- Afghanistan
-
Western Asia
-
Asia-tropical click to expand
-
Indian Subcontinent
- Nepal
- Pakistan
- West Himalaya
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Indian Subcontinent
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000301647 |
| Tropicos | 17600597 |
| KEW | urn:lsid:ipni.org:names:456738-1 |
| The Plant List | kew-183244 |
| Open Tree Of Life | 5801007 |
| NCBI Taxonomy | 1585254 |
| IPNI | 456738-1 |
| iNaturalist | 1159291 |
| GBIF | 3895412 |
| Freebase | /m/05h3zjh |
| EOL | 2879213 |
| USDA GRIN | 32948 |
| Wikipedia | Salvia_moorcroftiana |
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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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 | |||||
| 4-Hydroxybenzoic acid | 135 | Click to see C1=CC(=CC=C1C(=O)O)O | 138.12 | unknown |
https://doi.org/10.1016/S0367-326X(01)00299-4 https://doi.org/10.1002/HLCA.200390159 |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters | |||||
| 3-Oxodecyl 4-hydroxybenzoate | 90762940 | Click to see | 292.40 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| Nonyl 4-hydroxybenzoate | 586708 | Click to see CCCCCCCCCOC(=O)C1=CC=C(C=C1)O | 264.36 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| (4bS)-4-hydroxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one | 14104679 | Click to see | 298.40 | unknown | https://doi.org/10.1016/0031-9422(86)88043-8 |
| Taxodione | 73588 | Click to see | 314.40 | unknown | https://doi.org/10.1016/0031-9422(86)88043-8 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides | |||||
| (2S,3R,4S,5R,6S)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 11113500 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C(C(=C3)C)O)C(C)C)CO)O)O)O)O)O | 474.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| 2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(4-hydroxy-5-methyl-2-propan-2-ylphenoxy)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol | 85403568 | Click to see | 474.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (1beta,3beta)-Olean-18-ene-1,3-diol | 15380487 | Click to see | 442.70 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| 3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,10-diol | 72745631 | Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C | 442.70 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| Lup-20(29)-en-3-ol, (3beta)- | 521518 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| Lup-20(29)-ene-2alpha,3beta-diol | 15127233 | Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C | 442.70 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| Lupeol | 259846 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C | 426.70 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown |
https://doi.org/10.1016/S0367-326X(99)00109-4 https://doi.org/10.1078/094471102321621386 |
| > 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/10.1078/094471102321621386 |
| 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/10.1078/094471102321621386 https://doi.org/10.1016/S0367-326X(99)00109-4 |
| 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/10.1016/S0367-326X(99)00109-4 https://doi.org/10.1078/094471102321621386 |
| Stigmast-5-en-3-ol | 22012 | Click to see | 414.70 | unknown | https://doi.org/10.1078/094471102321621386 |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones | |||||
| 2-Acetyl-4-isopropylpyridine | 529345 | Click to see | 163.22 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones | |||||
| Apigenin | 5280443 | Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O | 270.24 | unknown |
https://doi.org/10.1016/S0367-326X(99)00109-4 https://doi.org/10.1078/094471102321621386 https://doi.org/10.1016/S0008-6215(02)00008-3 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides | |||||
| 2-[4-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one | 11092942 | Click to see | 562.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| 2-[4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one | 11114610 | Click to see | 592.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| 2-[4-[3,5-Dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one | 85396290 | Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)OC)O)O)OC5C(C(C(CO5)O)O)O)O | 562.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| 2-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one | 75580666 | Click to see | 592.50 | unknown | https://doi.org/10.1002/HLCA.200390159 |
| 5-hydroxy-7-methoxy-2-[4-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]chromen-4-one | 162964846 | Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O | 578.50 | unknown | https://doi.org/10.1016/S0008-6215(02)00008-3 |
| Luteolin 3'-glucoside | 12309350 | Click to see | 448.40 | unknown |
https://doi.org/10.1002/HLCA.200390159 https://doi.org/10.1016/S0008-6215(02)00008-3 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids | |||||
| Takakin | 44258588 | Click to see | 300.26 | unknown | https://doi.org/10.1016/S0367-326X(01)00299-4 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| Eupatorin | 97214 | Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O | 344.30 | unknown |
https://doi.org/10.1016/S0367-326X(99)00109-4 https://doi.org/10.1078/094471102321621386 |
| Genkwanin | 5281617 | Click to see | 284.26 | unknown | https://doi.org/10.1016/S0008-6215(02)00008-3 |
| Salvigenin | 161271 | Click to see | 328.30 | unknown | https://doi.org/10.1078/094471102321621386 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |