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

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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.

Synonyms Top

No known synonyms.

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Biogenic Salvia species synthesized silver nanoparticles with catalytic, sensing, antimicrobial, and antioxidant properties Ihsan S, Gul H, Jamila N, Khan N, Ullah R, Bari A, Nee TW, Hwang JH, Masood R Heliyon 06-Feb-2024
PMCID:PMC10875438
doi:10.1016/j.heliyon.2024.e25814
PMID:38375246
Reactive oxygen species induced oxidative damage to DNA, lipids, and proteins of antibiotic-resistant bacteria by plant-based silver nanoparticles Ali HM, Karam K, Khan T, Wahab S, Ullah S, Sadiq M 3 Biotech 22-Nov-2023
PMCID:PMC10665289
doi:10.1007/s13205-023-03835-1
PMID:38009163
Solvent based fractional biosynthesis, phytochemical analysis, and biological activity of silver nanoparticles obtained from the extract of Salvia moorcroftiana Khan M, Khan T, Wahab S, Aasim M, Sherazi TA, Zahoor M, Yun SI PLoS One 26-Oct-2023
PMCID:PMC10602276
doi:10.1371/journal.pone.0287080
PMID:37883497
Vegetation diversity pattern during spring season in relation to topographic and edaphic variables in sub-tropical zone Ali H, Muhammad Z, Majeed M, Aziz R, Khan A, Mangrio WM, Abdo HG, Almohamad H, Al Dughairi AA Bot Stud 16-Sep-2023
PMCID:PMC10505133
doi:10.1186/s40529-023-00398-5
PMID:37716923
Spatial distribution of the four invasive plants and their impact on natural communities’ dynamics across the arid and semi-arid environments in northwest Pakistan Khan N, Ullah R, Okla MK, Abdel-Maksoud MA, Saleh IA, Abu-Harirah HA, AlRamadneh TN, AbdElgawad H Front Plant Sci 25-Aug-2023
PMCID:PMC10485558
doi:10.3389/fpls.2023.1207222
PMID:37692447
Allelopathy: an alternative tool for sustainable agriculture Ain Q, Mushtaq W, Shadab M, Siddiqui MB Physiol Mol Biol Plants 24-Apr-2023
PMCID:PMC10172429
doi:10.1007/s12298-023-01305-9
PMID:37187777
Traditional foraging for ecological transition? Wild food ethnobotany among three ethnic groups in the highlands of the eastern Hindukush, North Pakistan Khan AH, Adil M, Aziz MA, Sõukand R, Pieroni A J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064566
doi:10.1186/s13002-023-00581-9
PMID:37004043
Prolonged Repellent Activity of Plant Essential Oils against Dengue Vector, Aedes aegypti Haris A, Azeem M, Abbas MG, Mumtaz M, Mozūratis R, Binyameen M Molecules 31-Jan-2023
PMCID:PMC9919174
doi:10.3390/molecules28031351
PMID:36771017
Herbal Arsenal against Skin Ailments: A Review Supported by In Silico Molecular Docking Studies Singab AN, Mostafa NM, Fawzy IM, Bhatia D, Suryawanshi PT, Kabra A Molecules 21-Sep-2022
PMCID:PMC9572213
doi:10.3390/molecules27196207
PMID:36234737
Amelioration of Scopolamine-Induced Cognitive Dysfunction in Experimental Mice Using the Medicinal Plant Salvia moorcroftiana Wahid F, Jan T, Al-Joufi FA, Ali Shah SW, Nisar M, Zahoor M Brain Sci 07-Jul-2022
PMCID:PMC9320495
doi:10.3390/brainsci12070894
PMID:35884701
Processing of Distillery Stillage to Recover Phenolic Compounds with Ultrasound-Assisted and Microwave-Assisted Extractions Mikucka W, Zielinska M, Bulkowska K, Witonska I Int J Environ Res Public Health 25-Feb-2022
PMCID:PMC8910419
doi:10.3390/ijerph19052709
PMID:35270409
Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES Plants (Basel) 28-Dec-2021
PMCID:PMC8747448
doi:10.3390/plants11010087
PMID:35009089
Exploration of ethnomedicinal plants and their practices in human and livestock healthcare in Haripur District, Khyber Pakhtunkhwa, Pakistan Siddique Z, Shad N, Shah GM, Naeem A, Yali L, Hasnain M, Mahmood A, Sajid M, Idrees M, Khan I J Ethnobiol Ethnomed 08-Sep-2021
PMCID:PMC8424965
doi:10.1186/s13002-021-00480-x
PMID:34496911
Gathered Wild Food Plants among Diverse Religious Groups in Jhelum District, Punjab, Pakistan Majeed M, Bhatti KH, Pieroni A, Sõukand R, Bussmann RW, Khan AM, Chaudhari SK, Aziz MA, Amjad MS Foods 11-Mar-2021
PMCID:PMC7999103
doi:10.3390/foods10030594
PMID:33799901
A high-throughput method for dereplication and assessment of metabolite distribution in Salvia species using LC-MS/MS Ul Haq F, Ali A, Akhtar N, Aziz N, Khan MN, Ahmad M, Musharraf SG J Adv Res 03-Feb-2020
PMCID:PMC7082496
doi:10.1016/j.jare.2020.02.001
PMID:32211205

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

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