Salvia aegyptiaca

Details Top

Internal ID UUID643feb8f2312d110960471
Scientific name Salvia aegyptiaca
Authority L.
First published in Sp. Pl. : 23 (1753)

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 the Bedouin of the Sinai Peninsula, dried leaves of Salvia aegyptiaca are infused in hot water and drunk as a mild tea to relieve cough and cold symptoms (Al‑Masri et al., 2018). In the Balochistan province of Pakistan, rural healers simmer dried aerial parts for fifteen minutes to make a decoction taken after meals for dyspepsia and abdominal discomfort (Khan et al., 2020). Omani traditional healers in the Al‑Batinah region crush fresh leaves and stems and apply the moist mass as a poultice to minor wounds, a practice documented by Al‑Farisi et al., 2019. Ethiopian practitioners in Sidama traditionally macerate the aerial parts in a water‑alcohol mixture for two weeks, filtering the liquid into a fever‑reducing tincture, as reported by Mekonnen and Kebede, 2019. These three cultures and the reported plant parts (leaves, aerial parts, fresh stems) demonstrate a clear pattern of using infusions, decoctions and macerations.

A practical way to prepare a classic mild tea is to use 1 g of dried Salvia aegyptiaca leaves per 200 mL of freshly boiled water, cover and steep for 5–10 minutes, then strain. The resulting infusion can be taken up to three times a day for the temporary relief of cough or cold. Safety note: the plant contains α‑thujone, a mild neurotoxin, so pregnant women and individuals with epilepsy should avoid using it, and the total daily intake should not exceed the dose suggested in the reference monograph (Al‑Masri et al., 2018).

Chemical analyses of the species have consistently identified an essential‑oil fraction rich in 1,8‑cineole (eucalyptol), camphor and α‑thujone, together with flavonoids such as luteolin‑7‑O‑glucoside and apigenin, and phenolic acids like rosmarinic acid and caffeic acid (Ghanem et al., 2015; Al‑Masri et al., 2018). These constituents provide plausible mechanisms for the expectorant, anti‑inflammatory and antimicrobial actions reported in the ethnobotanical surveys.

Modern relevance is evident in the growing body of in‑vitro studies confirming the antibacterial and antioxidant activity of the essential oil and rosmarinic‑acid‑rich extracts, and in the increasing commercial availability of Salvia aegyptiaca leaf tea as a herbal supplement. While clinical trials are still limited, ongoing research and continued traditional use in the regions described above suggest that this modest sage will remain a useful part of both ethnobotanical practice and contemporary phytotherapy.

General Uses Top

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Common products:
• Seed oil (limited non-medicinal technical or food applications reported); essential oil and extracts from aerial parts used as fragrance components; leaves occasionally employed as a flavoring or tea substitute (non-medicinal, food/beverage contexts).

Industrial and craft applications:
• Essential oils and extracts from leaves/flowering tops are incorporated into fragrance matrices; leaf/seed extracts are used as natural flavoring agents; triterpenoids isolated from the plant are employed as chemical standards in fragrance/flavor analytical chemistry.

Food and beverages (non-medicinal):
• Leaves used as an herbal seasoning or tea substitute (non-medicinal beverage); leaf/seed extracts serve as natural flavoring ingredients in food products.

Colorants and tanning:
• No documented tannin, dye, or ink uses reported for the taxon.

Wood and fiber:
• No documented timber, pulp, bast fiber, or cordage uses reported for the taxon.

Fragrance and cosmetics:
• Leaf/flowering-top essential oils and extracts incorporated into fragrance compositions; leaf/seed extracts used as flavor/fragrance ingredients; triterpenoid phytochemicals (e.g., oleanolic and ursolic acids) are referenced as natural product standards and quality markers in fragrance/flavor chemistry.

Properties relevant to use:
• Essential oil composition characterized by monoterpenes and sesquiterpenes (e.g., camphor, 1,8-cineole, α-pinene) suitable for fragrance applications; presence of oleanolic and ursolic acids facilitates standardization and authentication as natural product markers.

Standards and regulation:
• No distinct ISO/ASTM/EN standards are identified for this taxon’s materials; food and fragrance uses must comply with general national/international regulations for natural flavoring and fragrance materials (e.g., FEMA GRAS or equivalent regional authorities, and good manufacturing practice requirements).

Sustainability and sourcing:
• Wild collection in arid regions raises habitat and overharvest concerns; sourcing from cultivated material where possible is recommended to reduce pressure on wild populations.

Synonyms Top

Scientific name Authority First published in
Melissa perennis Forssk. Fl. Aegypt.-Arab. : 108 (1775)
Salvia arida Salisb. Prodr. Stirp. Chap. Allerton : 73 (1796)
Salvia gabrieli Rech.f. Bot. Jahrb. Syst. 71: 538 (1941)
Salvia pumila Benth. Labiat. Gen. Spec. : 726 (1835)
Thymus hirtus Viv. Fl. Libyc. Spec. : 30 (1824)
Thymus syrticus Spreng. Syst. Veg. 2: 697 (1825)
Salvia aegyptiaca var. intermedia E.Peter Repert. Spec. Nov. Regni Veg. 39: 182. 1936
Salvia aegyptiaca var. pumila (Benth.) Asch. & Schweinf. ex I.Löw Sitzungsber. Kaiserl. Akad. Wiss., Phil. Hist. Cl. 161(3): 28 (1909)
Salvia aegyptiaca var. glandulosissima Bornm. & Kneuck. Allg. Bot. Z. Syst. 22: 4 (1916)
Salvia aegyptiaca f. colorata Maire Bull. Soc. Hist. Nat. Afrique N. 23: 205 (1932)
Salvia aegyptiaca f. albiflora Sauvage Mém. Off. Nat. Anti-Acridien 2: 34 (1947)
Pleudia aegyptiaca (L.) M.Will, N.Schmalz & Class.-Bockh. Turkish J. Bot. 39: 701 (2015)

Common names Top

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Language Common/alternative name
Arabic قصعين مصري
Arabic شجرة الغزال
Arabic بشارى
Arabic رعلة
Persian مریمگلی مصری
Finnish egyptinsalvia
French sauge égyptienne
Pashto ملنگيان

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Africa
    • Macaronesia
      • Canary Islands
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Mali
      • Mauritania
      • Niger
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Palestine
      • Sinai
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300188
Tropicos 17600564
KEW urn:lsid:ipni.org:names:455578-1
The Plant List kew-181899
Open Tree Of Life 626525
NCBI Taxonomy 392645
IPNI 455578-1
iNaturalist 467538
GBIF 3886367
Freebase /m/0j249lg
EOL 6341516
USDA GRIN 32901
Wikipedia Salvia_aegyptiaca

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
Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula Alrajhi K, Bibi S, Abu-Dieyeh M Saudi J Biol Sci 25-Dec-2023
PMCID:PMC10805673
doi:10.1016/j.sjbs.2023.103911
PMID:38268781
Road Impact on Plant Colonization in the Arid Timanfaya National Park Bernardos M, Cornejo NS, Torres Hassan AD, Cabrera R, Arévalo JR Plants (Basel) 13-Oct-2023
PMCID:PMC10610428
doi:10.3390/plants12203568
PMID:37896031
LC-MS metabolomics profiling of Salvia aegyptiaca L. and S. lanigera Poir. with the antimicrobial properties of their extracts Nasr A, Yosuf I, Turki Z, Abozeid A BMC Plant Biol 26-Jun-2023
PMCID:PMC10291801
doi:10.1186/s12870-023-04341-5
PMID:37365525
Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia Al-Ghamdi AA, Al-Sagheer NA Plants (Basel) 22-Mar-2023
PMCID:PMC10058344
doi:10.3390/plants12061402
PMID:36987090
The variability of phenolic constituents and antioxidant properties among wild populations of Ziziphora clinopodioides Lam Taheri A, Ganjeali A, Arefi-Oskouie A, Çirak C, Cheniany M Physiol Mol Biol Plants 30-Jan-2023
PMCID:PMC9981857
doi:10.1007/s12298-023-01283-y
PMID:36875730
Diversity of Useful Plants in Cabo Verde Islands: A Biogeographic and Conservation Perspective Duarte MC, Gomes I, Catarino S, Brilhante M, Gomes S, Rendall A, Moreno Â, Fortes AR, Ferreira VS, Baptista I, Dinis H, Romeiras MM Plants (Basel) 15-May-2022
PMCID:PMC9144021
doi:10.3390/plants11101313
PMID:35631738
A Review on the Ethnopharmacology and Phytochemistry of the Neotropical Sages (Salvia Subgenus Calosphace; Lamiaceae) Emphasizing Mexican Species Ortiz-Mendoza N, Aguirre-Hernández E, Fragoso-Martínez I, González-Trujano ME, Basurto-Peña FA, Martínez-Gordillo MJ Front Pharmacol 19-Apr-2022
PMCID:PMC9061990
doi:10.3389/fphar.2022.867892
PMID:35517814
Assessment of the Transfer of Trace Metals to Spontaneous Plants on Abandoned Pyrrhotite Mine: Potential Application for Phytostabilization of Phosphate Wastes El Berkaoui M, El Adnani M, Hakkou R, Ouhammou A, Bendaou N, Smouni A Plants (Basel) 11-Jan-2022
PMCID:PMC8777678
doi:10.3390/plants11020179
PMID:35050067
Biodiversity of arbuscular mycorrhizal fungi in plant roots and rhizosphere soil from different arid land environment of Qatar Alrajhei K, Saleh I, Abu‐Dieyeh MH Plant Direct 09-Jan-2022
PMCID:PMC8743365
doi:10.1002/pld3.369
PMID:35028492
The Essential Oil-Bearing Plants in the United Arab Emirates (UAE): An Overview Shahin SM, Jaleel A, Alyafei MA Molecules 27-Oct-2021
PMCID:PMC8587291
doi:10.3390/molecules26216486
PMID:34770890
A Review on Medicinal Plants Used in the Management of Headache in Africa Frimpong EK, Asong JA, Aremu AO Plants (Basel) 28-Sep-2021
PMCID:PMC8539318
doi:10.3390/plants10102038
PMID:34685845
Impacts of Anthropogenic Disturbance on Vegetation Dynamics: A Case Study of Wadi Hagul, Eastern Desert, Egypt Bedair R, Ibrahim AA, Alyamani AA, Aloufi S, Ramadan S Plants (Basel) 14-Sep-2021
PMCID:PMC8466335
doi:10.3390/plants10091906
PMID:34579436
Phytochemicals and Antioxidant Activity in Oat-Buckwheat Dough and Cookies with Added Spices or Herbs Starowicz M, Arpaci S, Topolska J, Wronkowska M Molecules 14-Apr-2021
PMCID:PMC8070670
doi:10.3390/molecules26082267
PMID:33919764
Ethnobotanical Study on Plant Used by Semi-Nomad Descendants’ Community in Ouled Dabbeb—Southern Tunisia Karous O, Ben Haj Jilani I, Ghrabi-Gammar Z Plants (Basel) 28-Mar-2021
PMCID:PMC8066878
doi:10.3390/plants10040642
PMID:33800664
Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA Saudi J Biol Sci 04-Mar-2021
PMCID:PMC8176062
doi:10.1016/j.sjbs.2021.02.076
PMID:34121869

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 / Anthracenes / Anthraquinones
1,4-Anthracenedione, 5,6,7,8-tetrahydro-2-hydroxy-3-[(1R)-2-hydroxy-1-methylethyl]-5,5,9-trimethyl- 389887 Click to see 328.40 unknown https://doi.org/10.1021/JO00278A021
3,6,10,10-Tetramethyl-2,3,7,8,9,10-hexahydroanthra[1,2-b]furan-4,5-dione 358230 Click to see 310.40 unknown https://doi.org/10.1021/JO00278A021
Agyptenone A 366408 Click to see CC1COC2=C1C(=O)C(=O)C3=C(C4=C(C=C32)C(CCC4)(C)C)C 310.40 unknown https://doi.org/10.1021/JO00278A021
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[(1S,3R,5R,6aS,7R,8R,10aS)-1,3-diacetyloxy-7,8-dimethyl-7-(3-methylidenepent-4-enyl)-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] (2R)-2-methylbutanoate 162902517 Click to see 502.60 unknown https://doi.org/10.1021/JO00278A021
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
1,5,6,6-tetramethyl-2,7,8,9-tetrahydro-1H-naphtho[1,2-g][1]benzofuran-10,11-dione 78385278 Click to see 310.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
6-Methylcryptotanshinone 5319568 Click to see 310.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1002/CHIN.200431151
(4aS,6aR,6aS,6bR,8aR,10S,12aS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 15226483 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see 454.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
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/10.1002/CHIN.200431151
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
https://doi.org/10.1002/CHIN.200431151
> 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/S0031-9422(02)00283-2
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
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/10.1002/CHIN.200431151
https://doi.org/10.1016/S0031-9422(02)00283-2
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/10.1016/S0031-9422(02)00283-2
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/S0031-9422(02)00283-2
Sitoindoside I 9832350 Click to see 815.30 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
https://doi.org/10.1002/CHIN.200431151
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
> Organoheterocyclic compounds / Naphthofurans
(3R,4'R)-4',5,6,6-tetramethylspiro[8,9-dihydro-7H-benzo[g][2]benzofuran-3,2'-oxolane]-1-one 5319567 Click to see CC1CC2(C3=C(C4=C(C(=C3)C)C(CCC4)(C)C)C(=O)O2)OC1 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
(3S,4'R)-4',5,6,6-tetramethylspiro[8,9-dihydro-7H-benzo[g][2]benzofuran-3,2'-oxolane]-1-one 162966636 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
(3S,4'S)-4',5,6,6-tetramethylspiro[8,9-dihydro-7H-benzo[g][2]benzofuran-3,2'-oxolane]-1-one 162966637 Click to see CC1CC2(C3=C(C4=C(C(=C3)C)C(CCC4)(C)C)C(=O)O2)OC1 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
4',5,6,6-tetramethylspiro[8,9-dihydro-7H-benzo[g][2]benzofuran-3,2'-oxolane]-1-one 78385277 Click to see CC1CC2(C3=C(C4=C(C(=C3)C)C(CCC4)(C)C)C(=O)O2)OC1 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
6-Methylcryptoacetalide 5319566 Click to see CC1CC2(C3=C(C4=C(C(=C3)C)C(CCC4)(C)C)C(=O)O2)OC1 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
Methylumbelliferone 10748 Click to see 176.17 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 162154303 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone 10020367 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(02)00283-2
Gonzalitosin I 5272653 Click to see 328.30 unknown https://doi.org/10.1016/S0031-9422(02)00283-2

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