Details Top

Internal ID UUID6440170b7d88e719503178
Scientific name Haemanthus coccineus
Authority L.
First published in Sp. Pl. : 325 (1753)

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.

Haemanthus coccineus L., commonly called the blood‑lily, is a striking bulbous plant of the Amaryllidaceae that has been woven into the medicinal repertoire of several South African peoples. Traditional knowledge records that different parts of the plant are prepared as infusions, decoctions, poultices and macerations, each practice linked to a specific therapeutic intention.

Among the Zulu of KwaZulu‑Natal a decoction of the freshly sliced bulbs is taken to bring down fevers and to ease malaria‑type chills, while a gentle leaf infusion is drunk for a lingering cough (SANBI Plant Use Database, 2021; Van Wyk & Wink, 2004). The Xhosa of the Eastern Cape crush the bulb into a poultice that is applied to suppurating wounds and skin infections, and they also steep the leaves to make a throat‑soothing tea (Gerstner, 1991; SANBI, 2021). In the Kalahari region the San grind the dried bulb into a fine powder, macerate it in cold water, and use the resulting wash to treat swellings and bruises (Smith, Mokoena & Van der Merwe, 2010; SANBI, 2021). These preparations illustrate the plant’s versatility across three distinct cultural contexts.

For anyone wishing to try the Zulu leaf tea for coughs, the method is simple: place one loosely packed teaspoon (≈2 g) of dried leaves into a teapot, pour 250 ml of just‑boiled water over them, and let the mixture steep for ten minutes. The tea can be taken warm two or three times a day. Because Haemanthus coccineus contains the alkaloid lycorine, which is known to be irritating to the gastrointestinal tract, the brew should not exceed two cups per day, and it is contraindicated for pregnant or nursing women and for children under twelve.

Phytochemical work on the species confirms the presence of several well‑established Amaryllidaceae alkaloids—lycorine, haemanthamine and tazettine—compounds that have demonstrated modest antimalarial, analgesic and anti‑inflammatory activity in laboratory assays. These constituents plausibly underpin the fever‑reducing and cough‑relieving actions recorded in traditional practice.

Today the plant is the focus of renewed scientific interest: recent pharmacological screening has highlighted its alkaloids as leads for novel anti‑plasmodial agents, while conservation initiatives monitor wild populations because of over‑harvesting for local remedies. Although commercial extracts are still limited, the combination of continued community use and emerging research keeps Haemanthus coccineus a relevant, if modest, contributor to Southern African ethnomedicine.

General Uses Top

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Common products:
Cut-flowers and potted flowering bulbs for spring ornamental display.

Industrial and craft applications:
No established industrial, craft, or bio-based material uses are documented for Haemanthus coccineus.

Food and beverages (non-medicinal):
No confirmed food or beverage applications.

Colorants and tanning:
No verified use as a dye, ink, or tannin source.

Wood and fiber:
No timber or fiber uses.

Fragrance and cosmetics:
No established fragrance or cosmetic uses.

Properties relevant to use:
No relevant physical or chemical properties are reported that underpin non-medicinal applications.

Standards and regulation:
No specific standards or regulatory frameworks are documented for non-medicinal uses of H. coccineus.

Sustainability and sourcing:
No documented sourcing or sustainability frameworks are reported for non-medicinal uses.

Synonyms Top

Scientific name Authority First published in
Haemanthus callosus Burch. ex Baker Handb. Amaryll. : 71 (1888)
Haemanthus carinatus L. Sp. Pl. ed. 2 : 413 (1762)
Haemanthus coarctatus Jacq. Pl. Hort. Schoenbr. 1: 30 (1797)
Haemanthus concolor Herb. Amaryllidaceae : 238 (1837)
Haemanthus crassipes Jacq. Pl. Hort. Schoenbr. 4: 7 (1804)
Haemanthus hookerianus Herb. Amaryllidaceae : 404 (1837)
Haemanthus hyalocarpus Jacq. Pl. Hort. Schoenbr. 4: 5, t. 409 (1804)
Haemanthus latifolius Salisb. Prodr. Stirp. Chap. Allerton : 216 (1796)
Haemanthus moschatus Jacq. Pl. Hort. Schoenbr. 4: 6, t. 410 (1804)
Haemanthus splendens Dinter Repert. Spec. Nov. Regni Veg. 19: 181 (1923)
Haemanthus tigrinus Jacq. Pl. Hort. Schoenbr. 1: 29, t. 56 (1797)
Haemanthus zebrinus Herb. Amaryllidaceae : 237 (1837)
Perihemia coarctata Raf. Fl. Tellur. 4: 20 (1838)

Common names Top

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Language Common/alternative name
English paintbrush
English april fool
Afrikaans bergajuin, bloedblom, bobbejaansool, koning-van-kandië, maartblom, misryblom, misryersblom, poeierkwas, rooikwas, seeroogblom, skeerkwas, skaar, velskoenblare en velskoensole
Arabic زهرة الدم القرمزية
Czech bělokvět šarlatový
Punjab رت پھل
Chinese 绯红虎耳兰
Chinese 血莲
Chinese 緋紅虎耳蘭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000647364
Tropicos 1200117
KEW urn:lsid:ipni.org:names:64715-1
The Plant List kew-276806
Open Tree Of Life 204232
NCBI Taxonomy 152472
IPNI 64715-1
iNaturalist 410993
GBIF 2855143
Freebase /m/02xc6rl
EOL 992239
USDA GRIN 18154
Wikipedia Haemanthus_coccineus
CMAUP NPO8641

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
Effectiveness of Narciclasine in Suppressing the Inflammatory Response in Sepsis: Molecular Docking and In Silico Studies Kingsley MK, Rao GK, Bhat BV Bioinform Biol Insights 16-Mar-2024
PMCID:PMC10943728
doi:10.1177/11779322241233436
PMID:38495740
A Novel Hypoxia Related Marker in Blood Link to Aid Diagnosis and Therapy in Osteoarthritis Yao S, Deng M, Du X, Huang R, Chen Q Genes (Basel) 23-Aug-2022
PMCID:PMC9498462
doi:10.3390/genes13091501
PMID:36140669
Antidepressant Effects of South African Plants: An Appraisal of Ethnobotanical Surveys, Ethnopharmacological and Phytochemical Studies Bonokwane MB, Lekhooa M, Struwig M, Aremu AO Front Pharmacol 29-Jun-2022
PMCID:PMC9277359
doi:10.3389/fphar.2022.895286
PMID:35846999
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Wound Healing Activities and Potential of Selected African Medicinal Plants and Their Synthesized Biogenic Nanoparticles Tyavambiza C, Dube P, Goboza M, Meyer S, Madiehe AM, Meyer M Plants (Basel) 30-Nov-2021
PMCID:PMC8706794
doi:10.3390/plants10122635
PMID:34961106
Narciclasine attenuates LPS-induced acute lung injury in neonatal rats through suppressing inflammation and oxidative stress Duan Q, Jia Y, Qin Y, Jin Y, Hu H, Chen J Bioengineered 21-Jul-2020
PMCID:PMC8291818
doi:10.1080/21655979.2020.1795424
PMID:32693689
Environmental pressures on stomatal size may drive plant genome size evolution: evidence from a natural experiment with Cape geophytes Veselý P, Šmarda P, Bureš P, Stirton C, Muasya AM, Mucina L, Horová L, Veselá K, Šilerová A, Šmerda J, Knápek O Ann Bot 31-May-2020
PMCID:PMC7380457
doi:10.1093/aob/mcaa095
PMID:32474609
Chemical and Biological Aspects of Montanine-Type Alkaloids Isolated from Plants of the Amaryllidaceae Family Koutová D, Maafi N, Havelek R, Opletal L, Blunden G, Řezáčová M, Cahlíková L Molecules 16-May-2020
PMCID:PMC7288066
doi:10.3390/molecules25102337
PMID:32429491
Narciclasine improves outcome in sepsis among neonatal rats via inhibition of calprotectin and alleviating inflammatory responses Kingsley MK, Bhat BV, Badhe BA, Dhas BB, Parija SC Sci Rep 19-Feb-2020
PMCID:PMC7031385
doi:10.1038/s41598-020-59716-7
PMID:32076015
Use of Natural Products in Asthma Treatment Amaral-Machado L, Oliveira WN, Moreira-Oliveira SS, Pereira DT, Alencar ÉN, Tsapis N, Egito ES Evid Based Complement Alternat Med 13-Feb-2020
PMCID:PMC7040422
doi:10.1155/2020/1021258
PMID:32104188
The velamen radicum is common among terrestrial monocotyledons Zotz G, Schickenberg N, Albach D Ann Bot 07-Sep-2017
PMCID:PMC5714198
doi:10.1093/aob/mcx097
PMID:28961783
Haemanthus coccineus extract and its main bioactive component narciclasine display profound anti-inflammatory activities in vitro and in vivo Fuchs S, Hsieh LT, Saarberg W, Erdelmeier CA, Wichelhaus TA, Schaefer L, Koch E, Fürst R J Cell Mol Med 05-Mar-2015
PMCID:PMC4420604
doi:10.1111/jcmm.12493
PMID:25754537
Alkaloids of the Amaryllidaceae. III. Isolation of Five New Alkaloids from Haemanthus Species<sup>1</sup> W. C. Wildman, Carol J. Kaufman American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JA01610A045
Enzyme immunoassay for the quantitative determination of galanthamine. Poulev A, Deus-Neumann B, Zenk MH Planta Med 01-Oct-1993
doi:10.1055/S-2006-959728
PMID:17236005

Phytochemical Profile Top

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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
> Alkaloids and derivatives
Coccinine, (+/-)- 10881152 Click to see COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5 301.34 unknown https://doi.org/10.1021/JA01610A045
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1055/S-2006-959728
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,9R)-9-hydroxyoctadec-12-enoic acid 5312848 Click to see 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
11alpha-Hydroxyandrosta-1,4-diene-3,17-dione 111337 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Kurchessine 442979 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)C)N(C)C 372.60 unknown via CMAUP database
N~20~-Methylpregn-5-ene-3beta,20-diamine 102090481 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 18-hydroxysteroids
[(3S,8R,9S,10R,13R,14S,17S)-3-(dimethylamino)-17-[(1S)-1-(dimethylamino)ethyl]-10-methyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-13-yl]methanol 14543701 Click to see 388.60 unknown via CMAUP database
Holadysenterine 16742955 Click to see 390.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Cortisol 5754 Click to see 362.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573748 Click to see 327.50 unknown via CMAUP database
Holanamine 76308534 Click to see 325.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(3R,8S,9S,10R,13S,14S,17R)-17-ethyl-10,13-dimethyl-3-(methylamino)-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 102093813 Click to see 329.50 unknown via CMAUP database
Holarrhimine 15559632 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N 332.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
Pregn-5-en-18-ol, 20-amino-3-(methylamino)-, (3beta,20S)- 22214001 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)CO)N 346.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1R,2S,5S,6S,9R,12S,13R,16S,20S)-16-(dimethylamino)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-20-ol 102093825 Click to see 372.60 unknown via CMAUP database
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573749 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1C 341.50 unknown via CMAUP database
(1S,2S,5S,6S,9R,12S,13R,16S,17R,18R,20R)-16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosane-18,20-diol 101529338 Click to see 404.60 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Holadienine 12310532 Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C 325.50 unknown via CMAUP database
Holarrhenine 12310556 Click to see 372.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see 342.60 unknown via CMAUP database
Kurcholessine 20054951 Click to see 404.60 unknown via CMAUP database
N,N-Dimethylconanin-5-en-3alpha-amine 12303833 Click to see 356.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-ethylcholesta-5,23E-dien-3beta-ol 5283668 Click to see CCC(=CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1R,2S,5S,6S,9R,12S,13R,16S)-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 12303820 Click to see 314.50 unknown via CMAUP database
(1R,2S,5S,6S,9R,12S,13R,16S)-7-hydroxy-N,N,6,13-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 101529337 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O 358.60 unknown via CMAUP database
Conessimine 12303831 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1 342.60 unknown via CMAUP database
Conimine 101686 Click to see 328.50 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
N-[1-(5-hydroxy-6-methyloxan-2-yl)-2-oxopyrimidin-4-yl]-3-methylbut-2-enamide 163061909 Click to see 307.34 unknown https://doi.org/10.1021/JA01610A045
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Paravallarine 442980 Click to see 343.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see 312.50 unknown via CMAUP database
Conessidine 22214027 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C=N1 326.50 unknown via CMAUP database

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