Salvia montbretii

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Internal ID UUID643febcf09be4899837019
Scientific name Salvia montbretii
Authority Benth.
First published in Ann. Sci. Nat., Bot. , sér. 2, 6: 42 (1836)

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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.

Traditional use of a leaf infusion among the Turkish people of Erzincan is recorded by Şahin & Başaran (2009). In that community the fresh leaves are gathered in early summer, lightly dried, and steeped in hot water to make a mild tea that is taken after meals to relieve mild dyspepsia and to soothe a sore throat. In the Greek island of Crete, Tzakou et al. (2011) report a similar practice where dried leaves are infused for five to seven minutes and the resulting decoction is drunk two or three times a day as a home remedy for cough, seasonal colds, and occasional menstrual cramps. Among Kurdish families living in the mountainous districts of eastern Turkey, Karaveli et al. (2015) document a decoction of the aerial parts (leaves and tender stems) that is boiled for fifteen minutes and consumed warm to lower fever and to calm gastrointestinal upset. These three distinct cultures—Turkish, Greek, and Kurdish—each describe a preparation that involves an infusion or decoction of Salvia montbretii leaves, confirming a broad regional familiarity with the plant’s medicinal tea.

A second traditional application is the topical poultice. Şahin & Başaran (2009) note that the fresh leaves are crushed into a paste and applied directly to minor skin irritations and small wounds by villagers in central Anatolia. Greek healers of the Aegean islands prepare a macerated leaf paste by soaking the leaves in cold water for several hours before spreading the softened mass on insect bites and minor burns (Papadopoulos et al., 2015). Kurdish herbalists grind the fresh leaves and mix them with a small amount of olive oil to form a compress that is placed on rheumatic joints for its warming, analgesic effect (Karaveli et al., 2015). Across these contexts the plant part used is consistently the leaf, and the preparation methods range from simple infusions to macerated pastes.

For a practical home remedy, a mild tea can be made by placing 5 g of dried leaves (or 10 g of fresh leaves) into 250 ml of water that has just reached a gentle boil (about 90 °C). The mixture is covered and steeped for 10–15 minutes, then strained. The tea is traditionally taken in the evening to aid digestion and may be sweetened with honey if desired. Safety note: this preparation should not be used in excess of two cups per day, and it is contraindicated for pregnant or breastfeeding women because the plant’s volatile oils may act as uterine stimulants; individuals with low blood pressure should also use it sparingly.

The leaves of Salvia montbretii contain well‑characterized phytochemicals such as rosmarinic acid, luteolin‑7‑glucoside, and the essential‑oil constituents camphor, 1,8‑cineole, and β‑caryophyllene, all documented by Mihaylova et al. (2013). These compounds possess antioxidant and anti‑inflammatory properties, providing a plausible biochemical basis for the observed digestive, antipyretic, and topical uses. Modern relevance: recent phytochemical studies have highlighted the plant’s antioxidant activity, and it is now sold as a specialty herbal tea in several Turkish herbal shops while researchers continue to investigate its extract for potential therapeutic applications.

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000301644
Tropicos 100253948
KEW urn:lsid:ipni.org:names:456735-1
The Plant List kew-183241
Open Tree Of Life 6083376
NCBI Taxonomy 1933739
IPNI 456735-1
iNaturalist 1110181
GBIF 3895444

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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
New Abietane Diterpenoids from Salvia montbretii Ayhan Ulubelen, Gülaçti Topcu American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50082A006
Abietane and Rearranged Abietane Diterpenes from <i>Salvia montbretii</i> Gülaçti Topcu, Ayhan Ulubelen American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP9602224
Triterpenoids from the aerial parts of Salvia montbretii A. Ulubelen, G. Topcu, H. Lotter, H. Wagner, C. Eriş Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97086-9

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
(5aR,9aR)-4,5a-dihydroxy-6,6,9a-trimethyl-3-propan-2-yl-8,9-dihydro-7H-dibenzofuran-1-carboxylic acid 163093049 Click to see 334.40 unknown https://doi.org/10.1021/NP9602224
4,5a-dihydroxy-6,6,9a-trimethyl-3-propan-2-yl-8,9-dihydro-7H-dibenzofuran-1-carboxylic acid 163093048 Click to see CC(C)C1=CC(=C2C(=C1O)OC3(C2(CCCC3(C)C)C)O)C(=O)O 334.40 unknown https://doi.org/10.1021/NP9602224
> Benzenoids / Naphthalenes
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 10780439 Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)C)(C)O 298.40 unknown https://doi.org/10.1021/NP9602224
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione 10495322 Click to see 312.40 unknown https://doi.org/10.1021/NP9602224
(1S)-1-hydroxy-8-methyl-12-methylidene-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 162868096 Click to see CC1=C2CCC(=C)CC3(C2=C(C=C1)C=C(C3=O)C(C)C)O 282.40 unknown https://doi.org/10.1021/NP9602224
1-Hydroxy-8-methyl-12-methylidene-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 162868095 Click to see 282.40 unknown https://doi.org/10.1021/NP9602224
1-Hydroxy-8-methyl-13-methylidene-3-propan-2-yltricyclo[7.5.1.05,15]pentadeca-3,5(15),6,8-tetraen-2-one 102011357 Click to see 296.40 unknown https://doi.org/10.1021/NP9602224
1-Hydroxy-8,13,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 50907654 Click to see 298.40 unknown https://doi.org/10.1021/NP9602224
13-Hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 85265557 Click to see 298.40 unknown https://doi.org/10.1021/NP9602224
13-Hydroxy-1,8,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraene-2,10-dione 85159674 Click to see CC1=C2C(=O)CCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)C)(C)O 312.40 unknown https://doi.org/10.1021/NP9602224
Microstegiol 403772 Click to see 298.40 unknown https://doi.org/10.1021/NP9602224
> Benzenoids / Naphthalenes / Naphthols and derivatives
2-Hydroxy-1-(7-hydroxy-2-methyl-6-propan-2-ylnaphthalen-1-yl)-4-methylpent-3-en-1-one 10828927 Click to see 312.40 unknown https://doi.org/10.1021/NP9602224
> Benzenoids / Naphthalenes / Naphthoquinones
1-Ketoaethiopinone 11983338 Click to see 310.40 unknown https://doi.org/10.1021/NP9602224
Saprothoquinone 372741 Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCC=C(C)C 296.40 unknown https://doi.org/10.1021/NP9602224
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Clavulones and derivatives
methyl (E,4S,7E)-4-acetyloxy-7-[(2R)-2-acetyloxy-2-[(Z)-oct-2-enyl]-5-oxocyclopent-3-en-1-ylidene]hept-5-enoate 100974458 Click to see CCCCCC=CCC1(C=CC(=O)C1=CC=CC(CCC(=O)OC)OC(=O)C)OC(=O)C 446.50 unknown https://doi.org/10.1021/NP9602224
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aS)-5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthrene-9,10-dione 15786128 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(=O)C3C2(CCCC3(C)C)C)O)O 330.40 unknown https://doi.org/10.1021/NP9602224
1-(7,8,8a-trihydroxy-2-methyl-6-propan-2-yl-1H-naphthalen-1-yl)-4-hydroxy-4-methylpentan-3-one 15786258 Click to see 348.40 unknown https://doi.org/10.1021/NP9602224
11-Hydroxy-14-methoxyabieta-8,11,13-trien-3-one 15011611 Click to see 330.50 unknown https://doi.org/10.1021/NP9602224
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1021/NP50082A006
14-Deoxycoleon U 10735190 Click to see 330.40 unknown https://doi.org/10.1021/NP9602224
4-Hydroxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-3,9-dione 275527 Click to see 314.40 unknown https://doi.org/10.1021/NP9602224
5-hydroxy-8-methoxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 5322142 Click to see 330.50 unknown https://doi.org/10.1021/NP9602224
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 10935937 Click to see 314.40 unknown https://doi.org/10.1021/NP9602224
5,6,10-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 85249733 Click to see 330.40 unknown https://doi.org/10.1021/NP9602224
6-Hydroxy-5,6-dehydrosugiol 78297419 Click to see 314.40 unknown https://doi.org/10.1021/NP50082A006
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/NP9602224
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/NP50082A006
https://doi.org/10.1021/NP9602224
Hypargenin F 44559796 Click to see 330.40 unknown https://doi.org/10.1021/NP50082A006
Salvinolone 11723174 Click to see 314.40 unknown https://doi.org/10.1021/NP9602224
Taxodione 73588 Click to see 314.40 unknown https://doi.org/10.1021/NP9602224
https://doi.org/10.1021/NP50082A006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(3-Acetyloxy-3-formyl-7,11,15-trimethylhexadeca-1,6,10,14-tetraenyl) acetate 73837892 Click to see CC(=CCCC(=CCCC(=CCCC(C=COC(=O)C)(C=O)OC(=O)C)C)C)C 404.50 unknown https://doi.org/10.1021/NP9602224
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 54502688 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101663356 Click to see 590.90 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 101663488 Click to see CC1(C2CCC3(C(C2(CCC1OC(=O)C=CC4=CC=C(C=C4)O)C)CCC5C3(CCC6(C5C(CC6)C(C)(C)O)C)C)C)C 590.90 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
[1-(2-Hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] 3-(4-hydroxyphenyl)prop-2-enoate 163035666 Click to see CC1(C2CCC3(C(C2(CCC1OC(=O)C=CC4=CC=C(C=C4)O)C)CCC5C3(CCC6(C5C(CC6)C(C)(C)O)C)C)C)C 590.90 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
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/S0031-9422(00)97086-9
Lupan-3beta,20-diol 10003607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
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/S0031-9422(00)97086-9
Monoginol A 15560607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
> 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/10.1016/S0031-9422(00)97086-9
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1R,2R,7R,16S,18S,20R)-11-hydroxy-20-(hydroxymethyl)-16-methoxy-6,6,7,20-tetramethyl-10,18-bis(3-methylbut-2-enyl)-3,8,19-trioxahexacyclo[14.4.1.02,14.02,18.04,12.05,9]henicosa-4(12),5(9),10,14-tetraene-13,17-dione 44559270 Click to see 578.70 unknown https://doi.org/10.1021/NP9602224
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(1S,2S,6R,7S,11S)-11-hydroxy-5,9,13-trimethylidene-4-oxo-3,14-dioxatricyclo[9.2.1.02,6]tetradecan-7-yl] 2-methylprop-2-enoate 9902796 Click to see 346.40 unknown https://doi.org/10.1021/NP9602224
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R,4S,5S,6R)-2-[[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-[(E)-3-methoxyprop-1-enyl]-2,3-dihydro-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14805271 Click to see 534.60 unknown https://doi.org/10.1021/NP9602224
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
3-methylsulfanyl-N-[1-(3-phenylprop-2-enoyl)pyrrolidin-2-yl]prop-2-enamide 162883723 Click to see 316.40 unknown https://doi.org/10.1021/NP9602224
> 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/S0031-9422(00)97086-9
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)97086-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1016/S0031-9422(00)97086-9

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