Coleus sylvestris

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Internal ID UUID68f90ac9960af118527798
Scientific name Coleus sylvestris
Authority (Gürke) A.J.Paton & Phillipson
First published in PhytoKeys 129: 103 (2019)

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.

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

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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)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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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)!

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 / 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

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