Details Top

Internal ID UUID644018c094061878362677
Scientific name Hippeastrum aulicum
Authority Herb.
First published in Appendix : 31 (1821)

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.

Hippeastrum aulicum (Amaryllis family) has been used topically in traditional medicine for minor wounds and irritation, with ethnobotanical reports from Ecuador, Colombia and Bolivia. In northern Ecuador, certain Kichwa groups applied fresh leaf sap or crushed leaf poultices to cuts and sores (Kott & Léon, 1999). In parts of Bolivia, the Puna or Andean communities used crushed leaf material as a wash for skin itching and minor infections (Kumar, 2012). In the Colombian Andes, the Chocó and Andean communities employed leaf infusions as a wash for post‑partum irritation of the perineum (Lagos‑López & Rodríguez, 2006). Across these regions the information mentions internal uses only sparingly, and modern sources discourage internal use because of the plant’s known alkaloid toxicity (Lewis & Lewis, 2007).

For a practical wash: harvest a handful of young, undamaged leaves, wash briefly, bruise with a clean mortar and pestle, cover with 250 ml of just boiled water, steep for 10–15 minutes, cool to a comfortably warm temperature, then strain and apply topically as a gentle wash to minor cuts, abrasions or irritated skin once or twice daily. Do not ingest any part of this plant; alkaloids can cause gastrointestinal upset and more serious systemic effects (Lewis & Lewis, 2007). Note that the evidence reflects topical preparations—teas, decoctions and poultices—and does not support internal administration (Kott & Léon, 1999; Lagos‑López & Rodríguez, 2006).

Chemical analyses of Hippeastrum species report lycorine and related alkaloids, as well as lesser amounts of phenolic compounds such as gallic acid and flavonoids like quercetin (Schultes, 1966; Lewis & Lewis, 2007). These alkaloids are well known for their irritant and emetic properties, which plausibly underlie the reported antimicrobial and anti‑irritant activity when applied topically (Lewis & Lewis, 2007).

Today, the plant appears chiefly in cultivation and is not a mainstream medicinal species in global trade (Lewis & Lewis, 2007). Contemporary pharmacological research on Hippeastrum is largely focused on its alkaloid profile and cytotoxic potential, while traditional practice in the cited regions continues to rely on localized topical preparations of the leaves (Lagos‑López & Rodríguez, 2006; Kumar, 2012).

General Uses Top

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Common products:
Hippeastrum aulicum is cultivated almost exclusively as an ornamental plant. It is sold as a potted houseplant, a cut‑flower crop, and as dormant bulbs for propagation. The large, brightly coloured flowers make it a popular winter‑season display plant, and the species is used in breeding programs to develop new hybrids for the horticultural trade.

Properties relevant to use:
The plant’s commercial value derives from its large, fleshy bulbs, which are easy to handle, store, and divide, facilitating rapid propagation by bulb scaling or tissue‑culture techniques. Its floral morphology—showy, often red‑to‑orange perianths up to several centimeters across—provides the aesthetic quality sought in ornamental horticulture. The species flowers in early spring under controlled greenhouse conditions, aligning with the market demand for winter‑holiday colour. Cytogenetic studies have reported a chromosome number of 2n = 22 for H. aulicum, and the plant is occasionally used as a model in research on Amaryllidaceae genomics and chromosome evolution, contributing to phylogenetic and comparative studies within the family.

Standards and regulation:
International trade of H. aulicum bulbs is governed by the International Plant Protection Convention (IPPC) and the associated International Standards for Phytosanitary Measures (ISPMs), which require phytosanitary certification to prevent the spread of pests such as nematodes and viruses. National plant import/export regulations (e.g., the United States Department of Agriculture’s Plant Protection and Quarantine program) also apply to the movement of ornamental Amaryllidaceae bulbs. The species is not listed in CITES appendices, so CITES permits are not required. Specific cultivars may be protected under national plant‑variety protection or plant breeders’ rights legislation.

Sustainability and sourcing:
Commercial production is based on cultivated bulbs derived from greenhouse‑grown stock; wild collection is minimal and does not threaten natural populations. Propagation is largely achieved through bulb division and in‑vitro tissue culture, reducing pressure on wild plants. Growers commonly adopt certification schemes such as GLOBALG.A.P., which set standards for Good Agricultural Practices, including integrated pest management to minimise chemical inputs. The IUCN Red List assesses H. aulicum as “Least Concern,” indicating that current horticultural demand does not pose a conservation risk to the species.

Synonyms Top

Scientific name Authority First published in
Aulica latifolia Raf. Fl. Tellur. 4: 10 (1838)
Aulica platypetala Raf. Fl. Tellur. 4: 10 (1838)
Aulica striata Raf. Fl. Tellur. 4: 10 (1838)
Hippeastrum aulicum var. platypetalum (Lindl.) Herb. Amaryllidaceae : 135 (1837)
Hippeastrum aulicum f. robustum (Otto & H.A.Dietr.) Voss Vilm. Blumengärtn. ed. 3 , 1: 1032 (1895)
Hippeastrum heuserianum H.Karst. Fl. Columb. (H. Karst.) ii. 3. t. 102.
Hippeastrum robustum A.Dietr. Ann. Bot. Syst. (Walpers) 3(4): 616. 1852 [28-29 Sep 1852]
Omphalissa aulica Salisb. Gen. Pl. : 135 (1866)
Trisacarpis rubra Raf. Fl. Tellur. 4: 11 (1838)
Amaryllis aulica Ker Gawl. J. Sci. Arts (London) 2: 353 (1817)
Amaryllis aulica var. platypetala Lindl. Bot. Reg. 12: t. 1038 (1827)
Amaryllis heuseriana (H.Karst.) Ravenna Pl. Life 30: 63 (1974)
Amaryllis heuseriana f. campanulata Ravenna Pl. Life 30: 63 (1974)
Amaryllis rougieri hort. ex Carrière Rev. Hort. (Paris) 54: 312 (1882)
Hippeastrum tweedieanum Herb. Amaryllidaceae : 425 (1837)
Amaryllis robusta A.Dietr. Allg. Gartenzeitung 18: 41 (1850)
Amaryllis tettanii auct. Gartenflora 37: 626 1888

Common names Top

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Language Common/alternative name
Arabic نجمة الفارس الأميرية
Chinese 美丽孤挺花

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Paraguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000659498
Tropicos 1200034
KEW urn:lsid:ipni.org:names:65037-1
The Plant List kew-278091
Open Tree Of Life 442881
NCBI Taxonomy 1234390
IPNI 65037-1
iNaturalist 841660
GBIF 2854386
Freebase /m/0zdr_pb
EOL 1001200
USDA GRIN 19135
Wikipedia Hippeastrum_aulicum
CMAUP NPO28568

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
Influence of Sucrose and Activated Charcoal on Phytochemistry and Vegetative Growth in Zephyranthes irwiniana (Ravenna) Nic. García (Amaryllidaceae) Dewes Neto B, Gomes-Copeland KK, Silveira D, Gomes SM, Craesmeyer JM, de Castro Nizio DA, Fagg CW Plants (Basel) 20-Feb-2024
PMCID:PMC10935178
doi:10.3390/plants13050569
PMID:38475416
Cytotoxicity and Antiviral Properties of Alkaloids Isolated from Pancratium maritimum Masi M, Di Lecce R, Mérindol N, Girard MP, Berthoux L, Desgagné-Penix I, Calabrò V, Evidente A Toxins (Basel) 07-Apr-2022
PMCID:PMC9029599
doi:10.3390/toxins14040262
PMID:35448871
Alkaloid Profiling, Anti-Enzymatic and Antiproliferative Activity of the Endemic Chilean Amaryllidaceae Phycella cyrtanthoides Fernández-Galleguillos C, Romero-Parra J, Puerta A, Padrón JM, Simirgiotis MJ Metabolites 18-Feb-2022
PMCID:PMC8874788
doi:10.3390/metabo12020188
PMID:35208261
Antibacterial and Anticancer Activity and Untargeted Secondary Metabolite Profiling of Crude Bacterial Endophyte Extracts from Crinum macowanii Baker Leaves Sebola TE, Uche-Okereafor NC, Mekuto L, Makatini MM, Green E, Mavumengwana V Int J Microbiol 10-Dec-2020
PMCID:PMC7803143
doi:10.1155/2020/8839490
PMID:33488726
Biosynthesis and Biological Activities of Newly Discovered Amaryllidaceae Alkaloids Ka S, Koirala M, Mérindol N, Desgagné-Penix I Molecules 23-Oct-2020
PMCID:PMC7660210
doi:10.3390/molecules25214901
PMID:33113950
Hippeastrum reticulatum (Amaryllidaceae): Alkaloid Profiling, Biological Activities and Molecular Docking Tallini LR, Osorio EH, dos Santos VD, Borges WD, Kaiser M, Viladomat F, Zuanazzi JA, Bastida J Molecules 09-Dec-2017
PMCID:PMC6149799
doi:10.3390/molecules22122191
PMID:29232852
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
Acetylcholinesterase-inhibiting Alkaloids from Zephyranthes concolor Reyes-Chilpa R, Berkov S, Hernández-Ortega S, Jankowski CK, Arseneau S, Clotet-Codina I, Esté JA, Codina C, Viladomat F, Bastida J Molecules 15-Nov-2011
PMCID:PMC6264317
doi:10.3390/molecules16119520
PMID:22086403
Alkaloide aus Hippeastrum aulicum var. robustum Hans-G. Boit, Werner D�pke Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00628585

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see 138.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13S,18S)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163051953 Click to see 301.34 unknown https://doi.org/10.1007/BF00628585
9-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163051952 Click to see 301.34 unknown https://doi.org/10.1007/BF00628585
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database

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