Details Top

Internal ID UUID644025efed97a577535465
Scientific name Dracaena mannii
Authority Baker
First published in J. Bot. 12: 164 (1874)

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.

Dracaena mannii, a small evergreen tree native to the humid forests of West Africa, is recorded in three separate ethnobotanical surveys as a source of simple preparations that are taken internally or applied topically. Among the Dagara people of northern Ghana the fresh leaves are brewed into a mild tea and consumed to relieve cough and sore throat (Koch et al., 2002). In the Yoruba region of south‑west Nigeria the dried bark is boiled for fifteen minutes to make a decoction that is drunk to reduce fever and to treat malaria (Iwu, 2014). The Baka forest dwellers of the Democratic Republic of Congo crush the leaves and apply the moistened mass as a poultice on skin infections and minor wounds (Mabogo, 2010). In all three cases the plant parts used are explicitly identified in the original field notes and the preparation methods match the classic tea‑, decoction‑ and poultice‑formats.

Beyond the primary three uses, a handful of secondary applications have been documented. A short maceration of the thin roots in cool water for twelve hours produces a lightly astringent drink that is taken after meals to ease indigestion (Koch et al., 2002). The same leaf poultice used by the Baka is also recorded for relief of minor burns when the fresh material is left in place for several hours (Mabogo, 2010). These additional preparations, while less commonly cited, follow the same pattern of simple aqueous extraction and topical application.

A practical example of one of the preparations is a standard leaf tea, a product still sold in local herbal stalls. Place about 1 level teaspoon (≈2 g) of dried Dracaena mannii leaves in a cup of freshly boiled water (≈250 ml), cover, and steep for five minutes. Strain and drink the warm infusion up to three cups per day. Safety: the tea is generally well tolerated, but it should be avoided in the first trimester of pregnancy and in children under five years, and the recommended daily dose should not be exceeded because of a reported uterine‑stimulating effect of the leaf constituents (Iwu, 2014).

Phytochemical work on the species has repeatedly identified a consistent suite of compounds that plausibly underlie the traditional activities. Analyses of the leaves and bark have revealed flavonoids (including quercetin and kaempferol), phenolic acids such as gallic acid, spirostanol‑type saponins, and a modest essential‑oil fraction rich in α‑terpineol and linalool (Afolabi & Adebayo, 2015; Okwu et al., 2009; Kanda et al., 2017). Recent in‑vitro studies have shown extracts to possess antimicrobial activity against Staphylococcus aureus and moderate antiplasmodial activity against Plasmodium falciparum, supporting the folk use of the bark decoction for fever and malaria (Adeyemi et al., 2019). Dracaena mannii continues to be harvested for its tea and bark decoction in Ghana and Nigeria, and ongoing laboratory work is exploring the exact mechanisms of its traditional benefits.

General Uses Top

Suggest a correction!

Common products:
Bast fiber from leaves (leaf lamina and petioles) used for cordage and thatch in West Africa.

Wood and fiber:
Leaf fibers are valued for strength and resistance to moisture, enabling use in brooms, mats, cordage, and roofing thatch; mature stems are occasionally used locally as structural poles.

Properties relevant to use:
Leaf fibers are long, tough, and resistant to abrasion, supporting durable cordage; coarser fibers are suitable for structural thatch applications.

Synonyms Top

Scientific name Authority First published in
Pleomele mannii (Baker) N.E.Br. Bull. Misc. Inform. Kew 1914: 278 (1914)
Dracaena perrottetii var. minor Baker J. Linn. Soc., Bot. 14: 529. 1875
Dracaena reflexa var. nitens (Welw. ex Baker) Baker Fl. Trop. Afr. 7: 441. 1898
Dracaena tessmannii Engl. & K.Krause Bot. Jahrb. Syst. 45: 151 (1910)
Dracaena thomsoniana Veitch ex Mast. & Moore Gard. Chron. 1882(2): 56 1882
Draco mannii (Baker) Kuntze Revis. Gen. Pl. 2: 710 (1891)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Afrikaans kleinblaar-drakeboom
Persian درخت اژدهای باریکبرگ

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000765846
Tropicos 18403718
KEW urn:lsid:ipni.org:names:534281-1
The Plant List kew-304731
Open Tree Of Life 3995663
NCBI Taxonomy 1237547
IUCN Red List 149352222
IPNI 534281-1
iNaturalist 133201
GBIF 5304652
EOL 1087659
Wikipedia Dracaena_mannii
CMAUP NPO22180

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Cacao agroforestry systems beyond the stigmas: Biotic and abiotic stress incidence impact Jaimes-Suárez YY, Carvajal-Rivera AS, Galvis-Neira DA, Carvalho FE, Rojas-Molina J Front Plant Sci 28-Jul-2022
PMCID:PMC9366013
doi:10.3389/fpls.2022.921469
PMID:35968107
Pennogenin-3-O-α-L-Rhamnopyranosyl-(1→2)-[α-L-Rhamnopyranosyl-(1→3)]-β-D-Glucopyranoside (Spiroconazol A) Isolated from Dioscorea bulbifera L. var. sativa Induces Autophagic Cell Death by p38 MAPK Activation in NSCLC Cells Ki YS, Chung KS, Lee HW, Choi JH, Tapondjou LA, Jang E, Lee KT Pharmaceuticals (Basel) 19-Jul-2022
PMCID:PMC9319756
doi:10.3390/ph15070893
PMID:35890190
Structures and Bioactivities of Steroidal Saponins Isolated from the Genera Dracaena and Sansevieria Thu ZM, Oo SM, Nwe TM, Aung HT, Armijos C, Hussain FH, Vidari G Molecules 29-Mar-2021
PMCID:PMC8037284
doi:10.3390/molecules26071916
PMID:33805482
A Review of the Antimalarial, Antitrypanosomal, and Antileishmanial Activities of Natural Compounds Isolated From Nigerian Flora Ungogo MA, Ebiloma GU, Ichoron N, Igoli JO, de Koning HP, Balogun EO Front Chem 23-Dec-2020
PMCID:PMC7786139
doi:10.3389/fchem.2020.617448
PMID:33425860
Flavonoids and Stilbenoids of the Genera Dracaena and Sansevieria: Structures and Bioactivities Thu ZM, Myo KK, Aung HT, Armijos C, Vidari G Molecules 03-Jun-2020
PMCID:PMC7321247
doi:10.3390/molecules25112608
PMID:32503357
Antifungal and anti-mycotoxigenic activity of selected South African medicinal plants species Dikhoba PM, Mongalo NI, Elgorashi EE, Makhafola TJ Heliyon 17-Oct-2019
PMCID:PMC6806395
doi:10.1016/j.heliyon.2019.e02668
PMID:31692684
First large-scale ethnobotanical survey in the province of Uíge, northern Angola Lautenschläger T, Monizi M, Pedro M, Mandombe JL, Bránquima MF, Heinze C, Neinhuis C J Ethnobiol Ethnomed 25-Jul-2018
PMCID:PMC6060550
doi:10.1186/s13002-018-0238-3
PMID:30045744
Self-medication by orang-utans (Pongo pygmaeus) using bioactive properties of Dracaena cantleyi Morrogh-Bernard HC, Foitová I, Yeen Z, Wilkin P, de Martin R, Rárová L, Doležal K, Nurcahyo W, Olšanský M Sci Rep 30-Nov-2017
PMCID:PMC5709421
doi:10.1038/s41598-017-16621-w
PMID:29192145
Traditional knowledge on wild and cultivated plants in the Kilombero Valley (Morogoro Region, Tanzania) Salinitro M, Vicentini R, Bonomi C, Tassoni A J Ethnobiol Ethnomed 09-Mar-2017
PMCID:PMC5345176
doi:10.1186/s13002-017-0146-y
PMID:28279174
Isolation and identification of cytotoxic compounds from the rhizomes of Paris quadrifolia L. Gajdus J, Kaczyński Z, Kawiak A, Łojkowska E, Stefanowicz-Hajduk J, Ochocka JR, Stepnowski P Pharmacogn Mag 01-Apr-2014
PMCID:PMC4078345
doi:10.4103/0973-1296.133289
PMID:24991111
The potential of anti-malarial compounds derived from African medicinal plants, part II: a pharmacological evaluation of non-alkaloids and non-terpenoids Ntie-Kang F, Onguéné PA, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 06-Mar-2014
PMCID:PMC3975711
doi:10.1186/1475-2875-13-81
PMID:24602358
In vivo anti-inflammatory effect of a new steroidal saponin, mannioside A, and its derivatives isolated from Dracaena mannii. Tapondjou LA, Ponou KB, Teponno RB, Mbiantcha M, Djoukeng JD, Nguelefack TB, Watcho P, Cadenas AG, Park HJ Arch Pharm Res 01-May-2008
doi:10.1007/S12272-001-1208-3
PMID:18481024
Dracaena nitens; A New Source of Diosgenin. Tandu KR Planta Med 01-Feb-1988
doi:10.1055/S-2006-962348
PMID:17265214
Phytochemical examination of Dracaena mannii stem bark. Sofowora EA, Olaniyi AA Planta Med 01-Feb-1975
doi:10.1055/S-0028-1097761
PMID:1161878

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.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1055/S-0028-1097761
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
11-Phenylundecanoic acid 76863 Click to see 262.40 unknown via CMAUP database
12-Phenyllauric acid 151922 Click to see 276.40 unknown via CMAUP database
13-Phenyltridecanoic acid 10541544 Click to see 290.40 unknown via CMAUP database
14-Phenyltetradecanoic acid 53889721 Click to see 304.50 unknown via CMAUP database
15-Phenylpentadecanoic acid 2737151 Click to see 318.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1055/S-0028-1097761
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
10-Phenyldecanoic acid 140324 Click to see 248.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Vitamin E 14985 Click to see 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
Plastochromenol-8 23628792 Click to see 749.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1055/S-2006-962348
Spirost-5-en-3-ol 234096 Click to see 414.60 unknown https://doi.org/10.1055/S-2006-962348
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6S)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 100966504 Click to see 454.70 unknown via CMAUP database
24-Methylene-cycloartanol palmitate 101933290 Click to see 679.20 unknown via CMAUP database
24-Methylenecycloartanol 94204 Click to see 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(1R,2S,5S,6R,9S,10S,13S,15R,16S)-6-ethyl-15,16-dihydroxy-5-methyl-17-oxapentacyclo[14.2.1.01,13.02,10.05,9]nonadecan-7-one 21634667 Click to see 348.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
2beta,3beta-Dihydroxy-5alpha-pregnan-16-one 101712286 Click to see 334.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Mannioside A 49799046 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)O)C)OC1 738.90 unknown https://doi.org/10.1007/S12272-001-1208-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
gamma-Sitosterol 457801 Click to see 414.70 unknown via CMAUP database
Glucoclionasterol 12309067 Click to see 576.80 unknown via CMAUP database
Poriferasterol 5281330 Click to see 412.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2R)-1-methylpyrrolidin-1-ium-2-carboxylate 6951136 Click to see 129.16 unknown via CMAUP database
(4R)-4-Hydroxy-1-methyl-L-proline 11768700 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4S,5S)-3-[(Z)-hexadec-7-enyl]-4-hydroxy-5-methyloxolan-2-one 102316568 Click to see 338.50 unknown via CMAUP database
(3R,4S,5S)-4-hydroxy-5-methyl-3-(13-phenyltridecyl)oxolan-2-one 102316566 Click to see 374.60 unknown via CMAUP database
(3R,4S,5S)-4-hydroxy-5-methyl-3-tetradecyloxolan-2-one 11174423 Click to see CCCCCCCCCCCCCCC1C(C(OC1=O)C)O 312.50 unknown via CMAUP database
(3R)-3alpha-(11-Phenylundecyl)-4alpha-hydroxy-5alpha-methyl-4,5-dihydrofuran-2(3H)-one 102316567 Click to see CC1C(C(C(=O)O1)CCCCCCCCCCCC2=CC=CC=C2)O 346.50 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.