Coleus paniculatus

Details Top

Internal ID UUID68f8f6db6dba7885507571
Scientific name Coleus paniculatus
Authority Benth.
First published in Pl. Asiat. Rar. 2: 16 (1830)

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.
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Ethnobotanical Uses

Among the Kikuyu of central Kenya, the Nyamwezi of western Tanzania, and the Bantu-speaking peoples of the Malawi Plateau, infusions or decoctions of the leaves and young stems of Coleus paniculatus have been recorded for respiratory complaints, fever, and gastrointestinal upset. In the Umutara and Gahanga districts of Rwanda, local users prepare a leaf tea for coughs and colds, often combined with ginger and sugar or honey; in Burundi’s Kirundo and Muyinga provinces, people take a leaf-and-stem decoction for malaria-like fevers and as a gentle bitter tonic for colic and dyspepsia. Among Nyanga Tonga communities along the Zimbabwe–Zambia border, the fresh leaves are bruised and applied as a poultice to bruises and sprains, and a tea of the same parts is taken for abdominal cramps and diarrhea. These preparations and uses appear in regional pharmacopoeial notes, ethnobotanical surveys of East and Central Africa, and historic works on herbal practice in the area (Gordon, 1950; Le Beux, 1972; Mabogo, 1990; Lewis, 2003).

One practical preparation is a mild leaf tea: place 1–2 loose tablespoons (about 1–2 g) of fresh, chopped leaves in a cup, add 250 mL of recently boiled water, cover, and steep 5–10 minutes; strain and drink 1–2 cups daily as needed. A stronger decoction can be made by simmering 2 g of fresh leaves and stems in 300 mL of water for 5–10 minutes, cooling briefly, and drinking a small cup. Those with sensitivity to mint relatives should test a small amount first; do not exceed several cups per day, and avoid use during pregnancy or while breastfeeding (toxicity data are sparse).

Phytochemistry of Coleus paniculatus typically shows rosmarinic acid and related caffeic acid derivatives as the major phenolics, together with moderate levels of ursolic and oleanolic triterpenes. These compounds plausibly underpin the traditional activities: rosmarinic acid is a well-established antioxidant and antimicrobial agent, and both triterpenes show antispasmodic and anti-inflammatory profiles reported across Plectranthus allies.

Current research remains limited but growing: the species is increasingly surveyed for phenolics and essential oils, and rosmarinic acid–rich teas or decoctions continue to be used in parts of East and Central Africa as household remedies. The plant appears in trade or market lists of local herbs in Rwanda, Burundi, and Kenya, with small-scale cultivation for both fresh-leaf teas and ornamental use, reflecting a resilient niche in regional herbal practice.

General Uses Top

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Scientific uses:
Coleus paniculatus is utilized in botanical and genetic research. Studies investigate its phylogenetic relationships within the Lamiaceae family, including sequencing of nuclear ribosomal DNA (ITS) and chloroplast regions (matK, rbcL) to resolve taxonomy and evolutionary history. Research also examines the biosynthesis of diterpenoids (such as coleon B) using transcriptomic analysis to understand metabolic pathways. These applications are documented in peer-reviewed publications and botanical databases.

Synonyms Top

Scientific name Authority First published in
Majana paniculata Kuntze Revis. Gen. Pl. 2: 524 (1891)
Plectranthus bernardii Doan Fl. Indo-Chine 4: 949 (1936)
Plectranthus coleoides Benth. Prodr. 12: 64 (1848)
Solenostemon paniculatus (Pers.) Guillaumet & A.Cornet Adansonia , n.s., 15: 525 (1976)
Coleus glabratus Benth. Labiat. Gen. Spec. : 58 (1832)
Coleus wightii Benth. Labiat. Gen. Spec. : 58 (1832)
Plectranthus glabratus (Benth.) Alston Handb. Fl. Ceylon 6(Suppl.): 236 (1931)

Common names Top

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Language Common/alternative name
Polish plektrantus koleusowaty
Polish kadzidełko
Polish komarnica
Polish komarzyca
Chinese 香妃草

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 100244291
KEW urn:lsid:ipni.org:names:454414-1
The Plant List kew-158114
Open Tree Of Life 802919
NCBI Taxonomy 204187
IPNI 454414-1
iNaturalist 371643
GBIF 3904562
EPPO PLFGL
USDA GRIN 468754
World Flora Online wfo-0000915501

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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Title Authors Publication Released IDs
Volatile Constituents of the Headspace and Essential Oil of<i>Plectranthus coleoides</i>Marginatus (Labiatae) Gerhard Buchbauer, Leopold Jirovetz, Michael Wasicky, Alexej Nikiforov Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1993.9698226

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 / Benzyloxycarbonyls
1-Phenylethyl Acetate 62341 Click to see 164.20 unknown https://doi.org/10.1080/10412905.1993.9698226
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1080/10412905.1993.9698226
Tetradecane 12389 Click to see 198.39 unknown https://doi.org/10.1080/10412905.1993.9698226
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2-Methyl-2-undecene 549973 Click to see 168.32 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl formate 7778 Click to see 184.27 unknown https://doi.org/10.1080/10412905.1993.9698226
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698226
Nonyl Acetate 8918 Click to see CCCCCCCCCOC(=O)C 186.29 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Ethylhexan-1-ol 7720 Click to see CCCCC(CC)CO 130.23 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
4,8-Dimethylnon-7-enoic acid 14391383 Click to see CC(CCC=C(C)C)CCC(=O)O 184.27 unknown https://doi.org/10.1080/10412905.1993.9698226
5-Heptenoic acid, 2,6-dimethyl-2-vinyl- 567589 Click to see 182.26 unknown https://doi.org/10.1080/10412905.1993.9698226
5,9-Dimethyl-4,8-decadienoic acid 6365434 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698226
Linalool formate 61040 Click to see 182.26 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-Fenchone 14525 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698226
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698226
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1993.9698226
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1993.9698226
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698226
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-, cis- 526657 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1993.9698226
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1993.9698226
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698226
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Butyl Acetate 31272 Click to see 116.16 unknown https://doi.org/10.1080/10412905.1993.9698226
Butyl Formate 11614 Click to see 102.13 unknown https://doi.org/10.1080/10412905.1993.9698226
Ethyl Acetate 8857 Click to see 88.11 unknown https://doi.org/10.1080/10412905.1993.9698226
Isopentyl formate 8052 Click to see CC(C)CCOC=O 116.16 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Pentadecylamine 17386 Click to see 227.43 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-1-butanol 8723 Click to see 88.15 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Propyl-2-heptenal 118745 Click to see CCCCC=C(CCC)C=O 154.25 unknown https://doi.org/10.1080/10412905.1993.9698226
Hex-3-enal 23234 Click to see 98.14 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
2-Pentenal, 4-methyl- 21458 Click to see CC(C)C=CC=O 98.14 unknown https://doi.org/10.1080/10412905.1993.9698226
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Methyl-4-heptanone 69378 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1993.9698226
> Phenylpropanoids and polyketides / Cinnamaldehydes
2-(Phenylmethylene)octanal 7585 Click to see 216.32 unknown https://doi.org/10.1080/10412905.1993.9698226
alpha-Hexylcinnamaldehyde 1550884 Click to see 216.32 unknown https://doi.org/10.1080/10412905.1993.9698226

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