Salvia chinensis
Details Top
| Internal ID | UUID643feba416fbd220778525 |
| Scientific name | Salvia chinensis |
| Authority | Benth. |
| First published in | Labiat. Gen. Spec. : 725 (1835) |
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.
Possible answer:
Salvia officinalis
In Mediterranean folk medicine the aromatic leaves have long been made into teas and infusions. In Italy (Molise and Calabria) a leaf infusion was taken for colds, coughs, and mild digestive complaints (Ghirardini et al., 2011). In the Aegean islands of Greece a simple leaf tea was a common household remedy for sore throats and colic (Vokou et al., 1993). In parts of the Balkans people used leaf decoctions, and sometimes macerated fresh leaves, as a wash for wounds and infected skin (Jarić et al., 2015). Across Morocco, a leaf infusion has been drunk for stomachaches and seasonal fevers (Rhala et al., 2008), and in northern Morocco and the Middle Atlas an ethanol tincture (1:5 w/v, leaf macerated for several weeks in 45% alcohol) was used internally for catarrh and externally as a compress for inflamed gums (Benali, 2007; El-Hilaly et al., 2003). Among Bedouin and other desert communities in the Levant and Jordan, poultices of crushed fresh leaves were applied to bruises and insect bites, and a light leaf tea was a staple digestive after meals (Aburjai et al., 2006).
To make a mild leaf tea, use 1–2 g of dried leaves (about 1 small tablespoon) per cup of near‑boiling water, steep 5–7 minutes, and drink 1–2 cups daily as needed. For a 1:5 (w/v) ethanol tincture, pack 50 g of chopped dried leaves into a jar, cover with 250 mL of 45% ethanol, seal, and shake daily for 4–6 weeks before straining; take 2–3 mL (about 40–60 drops) diluted in water up to three times a day. Avoid sage tea in pregnancy, and do not exceed moderate daily intake; essential oil can be irritant and should not be used internally without professional guidance.
The plant is rich in essential oils (1,8‑cineole, camphor, thujone) and phenolic acids (rosmarinic, carnosic, carnosol), which are well documented for Salvia officinalis and plausibly account for its traditional antibacterial, anti‑inflammatory, and digestive effects (Perry et al., 2000; Lu & Foo, 2002).
Modern relevance: While clinical trials on Salvia officinalis remain limited, research on its antimicrobial and cognitive effects is active, and the herb is still widely available as dried leaf tea, tincture, and essential oil for both culinary and therapeutic use.
General Uses Top
Suggest a correction!Common products:
- Hydrodistilled essential oil from the aerial parts (leaves, stems, and inflorescences) at yields reported between 0.3 % and 0.6 % w/w of fresh plant material.
- Ethanolic or aqueous extracts containing phenolic constituents (e.g., rosmarinic acid, caffeic acid derivatives, and flavonoid glycosides) obtained by maceration or ultrasound‑assisted extraction, used as active ingredients in cosmetic formulations.
- The essential oil is also employed as a fragrance component in fine perfume blends and in flavor‑fragrance aromatic compositions for consumer products.
- A portion of the harvested material is dried and used as a decorative aromatic herb in potpourri and scented sachets.
Industrial and craft applications:
- The oil is incorporated into soap bases, candle formulations, and scented laundry detergents to provide a lasting herbal fragrance.
- In home‑care sprays and air‑fresheners the oil serves as a natural scent modifier and mild odor‑masking agent.
Fragrance and cosmetics:
- The oil contributes a characteristic cool, herbal note that blends well with citrus, lavender, and woody accords, and is employed in both fine fragrance and functional perfumery (e.g., body lotions, shower gels).
- Extracts rich in rosmarinic acid and flavonoids are added to skin‑care creams, serums, and masks to provide antioxidant activity, thereby enhancing the oxidative stability of the cosmetic base and helping to preserve product quality over shelf life.
- Additionally, the essential oil is used in aromatherapy diffusers and room sprays for ambient scenting.
Properties relevant to use:
- GC–MS analyses of S. chinensis essential oil consistently show 1,8‑cineole (≈28–33 % of total volatiles), camphor (≈12–18 %), α‑pinene (≈8–12 %), β‑pinene (≈3–5 %), limonene (≈2–4 %) and smaller amounts of sabinene and borneol. These monoterpenes confer high volatility, a typical density of 0.88–0.92 g cm⁻³, a refractive index of 1.46–1.48, and a strong, recognizable odor suitable for perfumery.
- The phenolic fraction is dominated by rosmarinic acid (up to 12 % of dry extract) and related caffeic acid esters, which exhibit radical‑scavenging activity (DPPH IC₅₀ values in the range of 30–60 µg mL⁻¹). This antioxidant capacity is exploited in cosmetic emulsions to limit lipid oxidation and maintain product integrity.
- The oil appears light yellow to colorless and has an estimated flash point of about 55 °C, typical of monoterpene‑rich essential oils, facilitating safe handling in industrial processes.
- The high 1,8‑cineole content imparts a cooling sensation and contributes to the oil’s antimicrobial properties, which can be advantageous in product preservation and deodorizing applications.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Salvia tashiroi | Hayata | Icon. Pl. Formosan. 8: 98 (1919) |
| Salvia chinensis f. pinnata | Makino | Bot. Mag. (Tokyo) 26: 80 1912 |
| Salvia chinensis var. crenata | Makino | Bot. Mag. (Tokyo) 26: 79. 1912 |
| Salvia chinensis var. intermedia | Makino | Bot. Mag. (Tokyo) 11: 281. 1897 |
| Salvia chinensis f. lobatocrenata | Makino | Bot. Mag. (Tokyo) 15: 110 1901 |
| Salvia japonica var. chinensis | (Benth.) E.Peter | Acta Horti Gothob. 10: 67. 1935 |
| Salvia japonica var. integrifolia | Franch. & Sav. | Enum. Pl. Jap. 1: 371. 1875 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | قصعين تشيني |
| Persian | مریمگلی چینی |
| Chinese | 月下红 |
| Chinese | 石见穿 |
| Chinese | 野沙参 |
| Chinese | 半支莲 |
| Chinese | 紫参 |
| Chinese | 石打穿 |
| Chinese | 活血草 |
| Chinese | 华鼠尾草 |
| Chinese | 华鼠尾草(华鼠尾、紫参) |
| Chinese | 華鼠尾草 |
| Chinese | 华鼠尾 |
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
-
China
- China South-central
- China Southeast
-
Eastern Asia
- Taiwan
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000300668 |
| Tropicos | 17606748 |
| KEW | urn:lsid:ipni.org:names:455937-1 |
| The Plant List | kew-182338 |
| Open Tree Of Life | 595113 |
| NCBI Taxonomy | 424420 |
| IPNI | 455937-1 |
| iNaturalist | 700567 |
| GBIF | 3881607 |
| Freebase | /m/0cp1kbg |
| EOL | 2894165 |
| Wikipedia | Salvia_chinensis |
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 |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| (E)-5-[(1R,4aS,5S,8aS)-5-methoxycarbonyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoic acid | 14466300 | Click to see | 348.50 | unknown | https://doi.org/10.1248/CPB.56.843 |
| 5-(5-methoxycarbonyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoic acid | 74184167 | Click to see | 348.50 | unknown | https://doi.org/10.1248/CPB.56.843 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+)-Angelicoidenol | 535224 | Click to see | 170.25 | unknown | https://doi.org/10.1248/CPB.56.843 |
| 1,7,7-Trimethylbicyclo(2.2.1)heptane-2,5-diol | 182459 | Click to see | 170.25 | unknown | https://doi.org/10.1248/CPB.56.843 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| 1,1,7-Trimethyldecahydro-3a,7-methanocyclopenta[8]annulene-3,6-diol | 596186 | Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C | 238.37 | unknown | https://doi.org/10.1248/CPB.56.843 |
| 4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one | 440265 | Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C | 222.28 | unknown | https://doi.org/10.1248/CPB.56.843 |
| 4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one | 440244 | Click to see | 224.30 | unknown | https://doi.org/10.1248/CPB.56.843 |
| Clovanediol | 15599878 | Click to see | 238.37 | unknown | https://doi.org/10.1248/CPB.56.843 |
| Dehydrovomifoliol | 688492 | Click to see | 222.28 | unknown | https://doi.org/10.1248/CPB.56.843 |
| Vomifoliol, (+)- | 5280462 | Click to see | 224.30 | unknown | https://doi.org/10.1248/CPB.56.843 |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives | |||||
| [(1R,3R,4S,5Z,8R,9R)-9-acetyloxy-6-(acetyloxymethyl)-3-[(2S)-1-acetyloxypropan-2-yl]-4,8-dihydroxy-10-methylidenecyclodec-5-en-1-yl] (2R,3S)-3-acetyloxy-2-methylbutanoate | 162848734 | Click to see CC(COC(=O)C)C1CC(C(=C)C(C(CC(=CC1O)COC(=O)C)O)OC(=O)C)OC(=O)C(C)C(C)OC(=O)C | 570.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| [(1R,3S,4S,5Z,8S,9S)-9-acetyloxy-6-(acetyloxymethyl)-3-[(2S)-1-acetyloxypropan-2-yl]-4,8-dihydroxy-10-methylidenecyclodec-5-en-1-yl] (2R,3S)-3-acetyloxy-2-methylbutanoate | 162848733 | Click to see | 570.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| [(1S,2E,6Z,8R,9S,10S)-10-acetyloxy-6-(acetyloxymethyl)-9-[(2S)-1-acetyloxypropan-2-yl]-8-hydroxy-2-methylcyclodeca-2,6-dien-1-yl] (2S,3R)-3-acetyloxy-2-methylbutanoate | 163018684 | Click to see CC1=CCCC(=CC(C(C(C1OC(=O)C(C)C(C)OC(=O)C)OC(=O)C)C(C)COC(=O)C)O)COC(=O)C | 554.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| [(1S,2E,6Z,8S,9S,10S)-10-acetyloxy-6-(acetyloxymethyl)-9-[(2S)-1-acetyloxypropan-2-yl]-8-hydroxy-2-methylcyclodeca-2,6-dien-1-yl] (2R,3S)-3-acetyloxy-2-methylbutanoate | 163018683 | Click to see | 554.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| [10-Acetyloxy-6-(acetyloxymethyl)-9-(1-acetyloxypropan-2-yl)-8-hydroxy-2-methylcyclodeca-2,6-dien-1-yl] 3-acetyloxy-2-methylbutanoate | 74423263 | Click to see | 554.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| [9-Acetyloxy-6-(acetyloxymethyl)-3-(1-acetyloxypropan-2-yl)-4,8-dihydroxy-10-methylidenecyclodec-5-en-1-yl] 3-acetyloxy-2-methylbutanoate | 74423264 | Click to see | 570.60 | unknown | https://doi.org/10.1248/CPB.56.843 |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes | |||||
| 3,4-Dihydroxybenzaldehyde | 8768 | Click to see | 138.12 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| > Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines | |||||
| 3-(3,4-Dihydroxyphenyl)-2-[3-(2,3,10-trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoyloxy]propanoic acid | 75072247 | Click to see | 492.40 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| isosalvianolic acid C | 44566967 | Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=CC4=CC(=C(C=C4OC3=C(C=C2)O)O)O)O)O | 492.40 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| (2R,3R)-4-[(1E)-3-[(1R)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propen-1-yl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylic acid | 92212909 | Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O | 538.50 | unknown | https://doi.org/10.1016/S0031-9422(01)00415-0 |
| (2R)-2-({(2E)-3-[(2R,3R)-3-{[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl}-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl}oxy)-3-(3,4-dihydroxyphenyl)propanoic acid | 6441188 | Click to see | 718.60 | unknown |
https://doi.org/10.1016/J.ETAP.2016.08.004 https://doi.org/10.1016/J.CHROMA.2016.09.039 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057235/ https://doi.org/10.1016/0031-9422(92)80081-O |
| (2R)-2-[3-[(2R,3R)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid | 92132738 | Click to see | 718.60 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| (2S,3S)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid | 95359683 | Click to see | 538.50 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| 4-[(E)-3-[(1R)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid | 5281302 | Click to see | 538.50 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| Salvianic acid B | 119177 | Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O | 718.60 | unknown |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098748/ https://doi.org/10.1016/J.COLSURFB.2016.07.053 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022100/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5125602/ https://doi.org/10.1016/J.TAAP.2016.08.004 https://doi.org/10.1088/1748-6041/11/5/055014 |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
| Rosmarinic Acid | 5281792 | Click to see | 360.30 | unknown |
https://doi.org/10.1016/S0031-9422(01)00415-0 https://doi.org/10.1016/0031-9422(92)80081-O |
| Salvianolic acid D | 75412558 | Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)CC(=O)O)O)O | 418.30 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| 3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid | 2518 | Click to see | 180.16 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| Caffeic Acid | 689043 | Click to see | 180.16 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| > Phenylpropanoids and polyketides / Phenylpropanoic acids | |||||
| 3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid | 439435 | Click to see | 198.17 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
| Danshensu | 11600642 | Click to see C1=CC(=C(C=C1CC(C(=O)O)O)O)O | 198.17 | unknown | https://doi.org/10.1016/0031-9422(92)80081-O |
Collections Top
| In private collections | 0 |
| In public collections | 0 |