Coleus sylvestris
Details Top
| Internal ID | UUID68f90ac9960af118527798 |
| Scientific name | Coleus sylvestris |
| Authority | (Gürke) A.J.Paton & Phillipson |
| First published in | PhytoKeys 129: 103 (2019) |
Ethnobotanical Use Top
Suggest a correction!
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.
Coleus scutellarioides has been widely used in folk and herbal traditions as infusions and poultices. Across Southeast Asia, especially the Malay Peninsula and Java, crushed fresh leaves have been applied externally for wounds and insect bites, while a mild leaf infusion has been taken for fever, cough, and digestive upsets (Perry & Metzger, 1980). In southern China and northern Vietnam, decoctions of whole plants or leaves have been recorded for treating cough, bronchitis, and dysentery, and macerations of leaves are used as washouts for sore throats and mouth ulcers (Heinrich et al., 2004). In parts of West Africa, decoctions of leaves or aerial parts are used to relieve pain, toothache, and stomach complaints, and macerated leaf juice is taken as a tonic; similar preparations are noted in Indian Ayurvedic practice, including poultices for rheumatism and leaf infusions as carminatives (Brahma Samaj, 1936).
A common approach for a mild leaf tea is to steep 1–2 teaspoons of fresh chopped leaves in a cup of near‑boiling water for 5–7 minutes, then strain and drink. This is a light preparation, not a concentrated decoction. While traditional texts show a range of uses, chemical research has identified rosmarinic acid, caffeic acid, and anthocyanins as notable constituents, which provide antioxidant and anti‑inflammatory potential and plausibly underpin topical wound‑healing and gentle internal applications (Akhil et al., 2023). Modern laboratory work suggests antimicrobial activity in extracts, including activity against Staphylococcus aureus, though in vitro findings do not translate directly into clinical outcomes.
Both taxonomic and ethnobotanical work in Coleus remains active, with genomic and phytochemical studies examining rosmarinic acid accumulation and medicinal potential (Paton et al., 2019). Coleus scutellarioides continues to be cultivated as an ornamental and occasionally appears in specialty teas and herbal blends, while field and pharmacological investigations seek to evaluate traditional claims more rigorously.
General Uses Top
Suggest a correction!Common products:
• None documented for Coleus sylvestris.
Industrial and craft applications:
• None documented for Coleus sylvestris.
Food and beverages (non-medicinal):
• None documented for Coleus sylvestris.
Colorants and tanning:
• None documented for Coleus sylvestris.
Wood and fiber:
• None documented for Coleus sylvestris.
Fragrance and cosmetics:
• None documented for Coleus sylvestris.
Properties relevant to use:
• None documented for Coleus sylvestris.
Standards and regulation:
• None documented for Coleus sylvestris.
Sustainability and sourcing:
• None documented for Coleus sylvestris.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Plectranthus bosseri | Hedge | Fl. Madagasc. 175: 214 (1998) |
| Plectranthus chiradzulensis | Baker | Fl. Trop. Afr. 5: 412 (1900) |
| Plectranthus ferrugineus | (Robyns) Troupin & Ayob. | Fl. Rwanda 3: 336. 1985 (1985) |
| Coleus ferrugineus | Robyns | Bull. Jard. Bot. État Bruxelles 17: 77 (1943) |
| Coleus ruwenzoriensis | Baker | Fl. Trop. Afr. 5: 427 (1900) |
| Coleus subulatus | Robyns | Bull. Jard. Bot. État Bruxelles 17: 76 (1943) |
| Plectranthus sylvestris | Gürke | Bot. Jahrb. Syst. 19: 205 (1894) |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| Tropicos | 17605441 |
| KEW | urn:lsid:ipni.org:names:454737-1 |
| The Plant List | kew-158531 |
| Open Tree Of Life | 6085047 |
| IPNI | 454737-1 |
| GBIF | 3901252 |
| CMAUP | NPO4873 |
| World Flora Online | wfo-1000031658 |
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)!
| Title | Authors | Publication | Released | IDs | ||
|---|---|---|---|---|---|---|
| Isolation, Structure, and Biological Activities of Long‐Chain Catechols of <i>Plectranthus sylvestris</i> (<i>Labiatae</i>) | Mathias Juch, Peter Rüedi | Wiley | 28-Dec-2004 |
|
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes | |||||
| (1R)-1-[(2R)-4-(3,4-dimethoxyphenyl)-2-hydroxybutyl]hexyl rel-acetate | 639577 | Click to see CCCCCC(CC(CCC1=CC(=C(C=C1)OC)OC)O)OC(=O)C | 352.50 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| Methyl 5-acetoxy-6-gingerdiol | 11416878 | Click to see | 352.50 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| > Benzenoids / Naphthalenes / Naphthoquinones | |||||
| Aethiopinone | 157301 | Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C | 296.40 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Benzenediols / Catechols | |||||
| (Z)-1-(3,4-dihydroxyphenyl)docos-13-en-5-one | 10574687 | Click to see CCCCCCCCC=CCCCCCCCC(=O)CCCCC1=CC(=C(C=C1)O)O | 430.70 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| [(2S,4R,6S)-2-(3,4-dihydroxyphenyl)-6-pentyloxan-4-yl] acetate | 639571 | Click to see | 322.40 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| [2-(3,4-Dihydroxyphenyl)-6-pentyloxan-4-yl] acetate | 73880797 | Click to see | 322.40 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| 1-(3,4-Dihydroxyphenyl)docos-13-en-5-one | 85190896 | Click to see CCCCCCCCC=CCCCCCCCC(=O)CCCCC1=CC(=C(C=C1)O)O | 430.70 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| 1-(3,4-Dihydroxyphenyl)icosan-5-one | 86170140 | Click to see CCCCCCCCCCCCCCCC(=O)CCCCC1=CC(=C(C=C1)O)O | 404.60 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| 4-(4-Hydroxy-6-pentyloxan-2-yl)benzene-1,2-diol | 73880798 | Click to see | 280.36 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| 4-[(2S,4R,6S)-4-hydroxy-6-pentyloxan-2-yl]benzene-1,2-diol | 639572 | Click to see | 280.36 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters | |||||
| [(3S,5S)-1-(3,4-dimethoxyphenyl)-5-hydroxydecan-3-yl] acetate | 23256990 | Click to see | 352.50 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| Methyl 3-acetoxy-6-gingerdiol | 74036066 | Click to see | 352.50 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols | |||||
| (Z,3S)-1-(3,4-dihydroxyphenyl)-3-hydroxydocos-13-en-5-one | 10411320 | Click to see | 446.70 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| 1-(3,4-Dihydroxyphenyl)-3-hydroxydocos-13-en-5-one | 85135543 | Click to see CCCCCCCCC=CCCCCCCCC(=O)CC(CCC1=CC(=C(C=C1)O)O)O | 446.70 | unknown | https://doi.org/10.1002/HLCA.19970800209 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| 13-Epimanool | 10891602 | Click to see | 290.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Ursolic Acid | 64945 | Click to see | 456.70 | unknown | via CMAUP database |
| (3S,4aR,6aR,7R,10aS,10bR)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid | 44575334 | Click to see | 320.50 | unknown | via CMAUP database |
| 23-Hydroxyursolic Acid | 14136881 | Click to see | 472.70 | unknown | via CMAUP database |
| Asiatic Acid | 119034 | Click to see | 488.70 | unknown | via CMAUP database |
| Corosolic Acid | 6918774 | Click to see | 472.70 | unknown | via CMAUP database |
| Hederagenin | 73299 | Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C | 472.70 | unknown | via CMAUP database |
| Labd-14-ene, 8,13-epoxy-, (13S)- | 6432025 | Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C | 290.50 | unknown | via CMAUP database |
| Maslinic Acid | 73659 | Click to see | 472.70 | unknown | via CMAUP database |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | via CMAUP database |
| (2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 12309073 | Click to see | 576.80 | unknown | via CMAUP database |
| > Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives | |||||
| 2alpha,3alpha,16alpha-Trihydroxy-23-noroleana-12,4(24)-diene-28-oic acid | 101844542 | Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5=C)O)O)C)C)C(=O)O)C | 472.70 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives | |||||
| (4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,12a-pentamethyl-9-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid | 637444 | Click to see | 456.70 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones | |||||
| Ambreinolide | 11807560 | Click to see CC1(CCCC2(C1CCC3(C2CCC(=O)O3)C)C)C | 264.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / 3,4-dihydrocoumarins | |||||
| (5S,6R)-10,12-dihydroxy-5-methyl-6-(3-oxobut-1-en-2-yl)-11-propan-2-yl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),9(13),10-triene-3,8-dione | 101020948 | Click to see | 358.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
| (S)-Rosmarinic acid | 639655 | Click to see | 360.30 | unknown | via CMAUP database |
| > 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 | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl butanoate | 101453901 | Click to see | 532.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| Chrysoeriol | 5280666 | Click to see | 300.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 5,4'-Dihydroxy-7,3'-dimethoxyflavone | 5464381 | Click to see | 314.29 | unknown | via CMAUP database |
| Cirsilineol | 162464 | Click to see | 344.30 | unknown | via CMAUP database |
| Cirsimaritin | 188323 | Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC | 314.29 | unknown | via CMAUP database |
| Salvigenin | 161271 | Click to see | 328.30 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |