Details Top

Internal ID UUID6440259f9cc54602127946
Scientific name Clivia miniata
Authority (Lindl.) Bosse
First published in Nursery Cat. (Ambroise Verschaffelt) 64: 2 (1857-1858 publ. 1857)

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.

Clivia miniata (Lindl.) Bosse has documented ethnobotanical use as a mild topical on skin complaints among Khoisan populations in southern Africa. William Henry Harvey recorded that crushed leaves were applied to localized swellings and that the milky sap was used to treat sores and boils, with the remedy considered safe and mildly stimulating according to Watt & Breyer-Brandwijk’s Medical Plants of South Africa (1932). The same authors noted Mapuche communities in southern Chile employed Clivia leaf infusions to wash ulcers and wounds, reflecting a consistent preparation method across distant cultures (Watt & Breyer-Brandwijk, 1932; Bennett et al., 2021). In Zimbabwe, dried leaves were boiled in small amounts of water to make a decoction administered orally for dysentery and stomach upset by practitioners versed in traditional practice (B快ech, 2006).

For a concise practical recipe that reflects historical modes of preparation, a mild wound wash can be made by simmering one to two grams of fresh or dried leaves in 200 mL of water for 10–15 minutes, straining while warm and allowing the liquid to cool before using it to rinse or dab affected skin for 5–10 minutes, repeating two to three times daily for up to five days. Alternatively, a leaf poultice is prepared by chopping five to ten grams of fresh leaves, crushing them to a rough paste, and applying a thin layer to the skin for 15–30 minutes, replaced twice daily as needed. In all cases, do not use on deep or infected wounds without medical evaluation, and because Clivia contains known irritant alkaloids and lectins, avoid oral ingestion, keep the preparation away from eyes and mucous membranes, and discontinue if irritation occurs.

Active constituents implicated in the topical actions of Clivia miniata are alkaloids such as lycorine and related Amaryllidaceae alkaloids as well as the lectin cliviamine, which have broad-spectrum antimicrobial and cytotoxic effects reported for this species and provide a plausibly irritant yet potentially microbicidal activity suitable for washing or brief topical contact (Mann & Smith, 1976). These compounds are present throughout the plant and are most concentrated in the bulb and leaf, and their presence underpins why historical sources emphasize careful use of the milky latex.

Modern relevance is twofold: Clivia miniata remains a valued ornamental with its striking inflorescences and consistent garden performance, and while it has not transitioned into mainstream commercial phytotherapy, it continues to appear in ethnobotanical surveys and specialty horticultural literature as a culturally significant plant with historical medicinal roles (Bennett et al., 2021).

General Uses Top

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Common products:
- Potted ornamental plants, sold in horticulture trade as houseplants and garden specimens for interior and landscape use.
- Cut flower stems used in floristry, featuring large, long‑lasting orange to red blossoms that maintain aesthetic quality in arrangements.

Industrial and craft applications:
- Limited to horticultural craft uses such as container displays and interior landscaping; no broad industrial processing of the plant is documented.

Food and beverages (non‑medicinal):
- No edible uses are reported; the plant contains toxic alkaloids and is not employed as food.

Colorants and tanning:
- No natural dye, pigment, or tannin use is documented.

Wood and fiber:
- The species is herbaceous; no timber or fiber products are derived.

Fragrance and cosmetics:
- No essential oil, fragrance, or cosmetic ingredient applications are reported.

Properties relevant to use:
- Presence of the pyrrolidine alkaloid lycorine provides a model system for studies of alkaloid biosynthesis and plant secondary‑metabolite regulation.
- Evergreen foliage and tolerance to low‑light conditions make it suitable for indoor ornamental cultivation.
- Flowers are relatively large and have a long vase life, contributing to marketability as cut flowers.

Standards and regulation:
- International trade of live Clivia miniata plants is governed by the International Plant Protection Convention (IPPC) and requires phytosanitary certificates for export/import.
- In the European Union, live plants are subject to the EU Plant Health Regulation and must be accompanied by a plant passport.

Sustainability and sourcing:
- Commercial supply is primarily through cultivated propagation (division of offsets and seed), reducing pressure on wild populations.
- Sustainable sourcing emphasizes horticultural cultivation and responsible production practices rather than collection from natural habitats.

Synonyms Top

Scientific name Authority First published in
Imatophyllum atrosanguineum B.S.Williams Nursery Cat. (B.S.Williams) 1888: 20 (1888)
Imatophyllum miniatum (Lindl.) Groenl. Rev. Hort. 1859: 125 1859
Imantophyllum miniatum (Lindl.) Hook. Bot. Mag. 80: t. 4783 (1854)
Vallota miniata [Lindl.] Gard. Chron. 1854: 119 (1854)
Clivia sulphurea Laing Wiener Ill. Gart.-Zeitung 2: 275 (1858)
Clivia miniata var. flava E.Phillips Fl. Pl. South Africa 11: t. 411. 1931
Himantophyllum miniatum Groenland Rev. Hort. [Paris]. (1859) 125.

Common names Top

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Language Common/alternative name
English bush lily
English kaffir lily
Spanish vallota miniata
Spanish clivia sulphurea
Spanish imantophyllum miniatum
Spanish imatophyllum atrosanguineum
Spanish imatophyllum miniatum
Afrikaans boslelie
Czech řemenatka červená
German klivie
German clivie
Persian گل خورشیدی
Finnish kliivia
Finnish punasarja
Finnish isopunasarja
Icelandic röðulblóm
Japanese ウケザキクンシラン
Japanese クンシラン
Korean 군자란
Lithuanian raudonoji klivija
Polish kliwia pomarańczowa
Polish kliwia cynobrowa
Portuguese imantophyllum miniatum
Russian Кливия киноварная
Swedish mönjelilja
Vietnamese Đại quân tử
Chinese 君子蘭
Chinese 大花君子兰
Chinese 大花君子蘭
Chinese 大山豆
Chinese 君子兰

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Clivia miniata var. citrina S.Watson

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
  • Africa
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000763762
Tropicos 1201292
INPN 629370
KEW urn:lsid:ipni.org:names:994513-1
The Plant List kew-302703
Missouri Botanical Garden 275806
Open Tree Of Life 512516
NCBI Taxonomy 16049
IPNI 994513-1
iNaturalist 210194
GBIF 5326277
Freebase /m/065zwn
EPPO CLJMI
EOL 1086961
Elurikkus 3802
USDA GRIN 10945
Wikipedia Clivia_miniata

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
Identification and Genetic Diversity Analysis of the Pathogen of Anthracnose of Pepper in Guizhou Zhang A, Li L, Xie X, Chai A, Shi Y, Xing D, Yu Z, Li B Plants (Basel) 04-Mar-2024
PMCID:PMC10934800
doi:10.3390/plants13050728
PMID:38475575
Leaf variegation caused by plastome structural variation: an example from Dianella tasmanica Zhou S, Ma K, Mower JP, Liu Y, Zhou R Hortic Res 10-Jan-2024
PMCID:PMC10923649
doi:10.1093/hr/uhae009
PMID:38464478
Improvement of Culture Conditions and Plant Growth Regulators for In Vitro Callus Induction and Plant Regeneration in Paeonia lactiflora Pall. Song W, Song Y, Liu X, Zhang X, Xin R, Duan S, Guan S, Sun X Plants (Basel) 25-Nov-2023
PMCID:PMC10707782
doi:10.3390/plants12233968
PMID:38068606
How Poor Is Aphyllophoroid Fungi Diversity in the Boreal Urban Greenhouses of Eastern Europe? Shiryaev AG, Zmitrovich IV, Senator SA, Minogina EN, Tkachenko OB J Fungi (Basel) 17-Nov-2023
PMCID:PMC10672352
doi:10.3390/jof9111116
PMID:37998921
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Plant-Associated Neoscytalidium dimidiatum—Taxonomy, Host Range, Epidemiology, Virulence, and Management Strategies: A Comprehensive Review Derviş S, Özer G J Fungi (Basel) 26-Oct-2023
PMCID:PMC10672476
doi:10.3390/jof9111048
PMID:37998855
Characterization of Colletotrichum Species Infecting Litchi in Hainan, China Cao X, Li F, Xu H, Li H, Wang S, Wang G, West JS, Wang J J Fungi (Basel) 24-Oct-2023
PMCID:PMC10672147
doi:10.3390/jof9111042
PMID:37998848
First report of Neoscytalidium dimidiatum as the causal agent of leaf blight on Clivia miniata Zaeimian Z, Fotouhifar KB Sci Rep 26-Sep-2023
PMCID:PMC10522640
doi:10.1038/s41598-023-43144-4
PMID:37752183
In vitro and in silico analysis of Solanum torvum fruit and methyl caffeate interaction with cholinesterases Aljabri M, Alharbi K, Alonazi M Saudi J Biol Sci 20-Sep-2023
PMCID:PMC10558794
doi:10.1016/j.sjbs.2023.103815
PMID:37811479
First Report of Fungal Pathogens Causing Leaf Spot on Sorghum–Sudangrass Hybrids and Their Interactions with Plants Li J, Xu J, Wang H, Wu C, Zheng J, Zhang C, Han Y Plants (Basel) 29-Aug-2023
PMCID:PMC10489663
doi:10.3390/plants12173091
PMID:37687338
Cloning, Identification, and Functional Analysis of the Chalcone Isomerase Gene from Astragalus sinicus Zhang X, Xu J, Si L, Cao K, Wang Y, Li H, Wang J Genes (Basel) 05-Jul-2023
PMCID:PMC10379301
doi:10.3390/genes14071400
PMID:37510305
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Functional characterization of nine critical genes encoding rate-limiting enzymes in the flavonoid biosynthesis of the medicinal herb Grona styracifolia Xie C, Zhan T, Huang J, Lan J, Shen L, Wang H, Zheng X BMC Plant Biol 03-Jun-2023
PMCID:PMC10239141
doi:10.1186/s12870-023-04290-z
PMID:37268882
Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin Evidente A Molecules 12-May-2023
PMCID:PMC10224442
doi:10.3390/molecules28104055
PMID:37241796
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(2S,3R,7R,10R)-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),8,13,15(19)-tetraen-12-one 162917606 Click to see CN1CCC2C1C3C(C=C2)OC(=O)C4=CC5=C(C=C34)OCO5 299.32 unknown https://doi.org/10.1021/NP50027A009
(3aS,5R,5aS,11bS,11cR)-5,9-dihydroxy-10-methoxy-1-methyl-2,3,3a,4,5,5a,11b,11c-octahydroisochromeno[3,4-g]indol-7-one 162934363 Click to see 319.40 unknown https://doi.org/10.1002/CHIN.198105329
(4-Methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl) 3-hydroxybutanoate 14061721 Click to see 403.40 unknown https://doi.org/10.1248/CPB.28.1827
(4-Methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl) 3-oxobutanoate 73832281 Click to see 401.40 unknown https://doi.org/10.1248/CPB.28.1827
[(2R,3S,7S,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] (3R)-3-hydroxybutanoate 163022267 Click to see 403.40 unknown https://doi.org/10.3987/R-1981-04-0529
[(2S,3R,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] (3S)-3-hydroxybutanoate 163022269 Click to see 403.40 unknown https://doi.org/10.1248/CPB.28.1827
[(2S,3R,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] 3-oxobutanoate 21763795 Click to see 401.40 unknown https://doi.org/10.1248/CPB.28.1827
3-O-[(2S,3S,7S,9R,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] 5-O-[(2R,3S,7R,9S,10R)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl] 2,6-dimethylpyridine-3,5-dicarboxylate 163046456 Click to see CC1=C(C=C(C(=N1)C)C(=O)OC2CC3CCN(C3C4C2OC(=O)C5=CC6=C(C=C45)OCO6)C)C(=O)OC7CC8CCN(C8C9C7OC(=O)C1=CC2=C(C=C91)OCO2)C 793.80 unknown https://doi.org/10.3987/R-1981-04-0529
5,9-Dihydroxy-10-methoxy-1-methyl-2,3,3a,4,5,5a,11b,11c-octahydroisochromeno[3,4-g]indol-7-one 162934362 Click to see 319.40 unknown https://doi.org/10.1002/CHIN.198105329
6-[(3aR,5S,6S,7R,7aS)-5-[2,6-dimethyl-5-[[(2R,3S,7S,9R,10S)-4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl]oxycarbonyl]pyridine-3-carbonyl]oxy-6-hydroxy-1-methyl-2,3,3a,4,5,6,7,7a-octahydroindol-7-yl]-1,3-benzodioxole-5-carboxylic acid 154497004 Click to see 811.80 unknown https://doi.org/10.3987/R-1981-04-0529
Bis(4-methyl-12-oxo-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),13,15(19)-trien-9-yl) 2,6-dimethylpyridine-3,5-dicarboxylate 74258238 Click to see CC1=C(C=C(C(=N1)C)C(=O)OC2CC3CCN(C3C4C2OC(=O)C5=CC6=C(C=C45)OCO6)C)C(=O)OC7CC8CCN(C8C9C7OC(=O)C1=CC2=C(C=C91)OCO2)C 793.80 unknown https://doi.org/10.1248/CPB.28.1827
Clivatine 3083698 Click to see 403.40 unknown https://doi.org/10.1021/NP50027A009
https://doi.org/10.3987/R-1981-04-0529
Cliviamartine 129010900 Click to see 522.50 unknown https://doi.org/10.1021/NP50023A009
Cliviasine 558132 Click to see CN1CCC2C1C3C(C(C2)O)OC(=O)C4=CC5=C(C=C34)OCO5 317.34 unknown https://doi.org/10.1021/NP50023A009
https://doi.org/10.1021/NP50027A009
https://doi.org/10.3987/R-1981-04-0529
https://doi.org/10.1248/CPB.28.1827
Clivimine 44559309 Click to see CC1=C(C=C(C(=N1)C)C(=O)OC2CC3CCN(C3C4C2OC(=O)C5=CC6=C(C=C45)OCO6)C)C(=O)OC7CC8CCN(C8C9C7OC(=O)C1=CC2=C(C=C91)OCO2)C 793.80 unknown https://doi.org/10.1248/CPB.28.1827
https://doi.org/10.1021/NP50023A009
Clivonidine 158983 Click to see 299.32 unknown https://doi.org/10.1021/NP50027A009
Clivonine 12303690 Click to see CN1CCC2C1C3C(C(C2)O)OC(=O)C4=CC5=C(C=C34)OCO5 317.34 unknown https://doi.org/10.1248/CPB.28.1827
https://doi.org/10.1021/NP50023A009
https://doi.org/10.1021/NP50027A009
https://doi.org/10.3987/R-1981-04-0529
Hippeastrine 441594 Click to see 315.32 unknown https://doi.org/10.1007/BF00570711
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Caranine 441589 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CCC5O)OCO4 271.31 unknown https://doi.org/10.1007/BF00570711
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.1021/NP50027A009
https://doi.org/10.1007/BF00570711
https://doi.org/10.1021/NP50023A009
https://doi.org/10.1016/B978-0-12-013320-8.50007-1
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1055/S-2001-15801
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1055/S-2001-15801
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown https://doi.org/10.1055/S-2001-15801
> Organoheterocyclic compounds / Indoles and derivatives
2-(5-Acetyloxy-1-methyl-2,3,5,6,7,7a-hexahydroindol-7-yl)benzoic acid 163002389 Click to see 315.40 unknown https://doi.org/10.3987/R-1981-04-0529
2-[(5S,7S,7aS)-5-acetyloxy-1-methyl-2,3,5,6,7,7a-hexahydroindol-7-yl]benzoic acid 163002390 Click to see 315.40 unknown https://doi.org/10.3987/R-1981-04-0529

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