Hippeastrum aulicum
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
Suggest a correction!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
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Arabic | نجمة الفارس الأميرية |
| Chinese | 美丽孤挺花 |
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
-
Southern America click to expand
-
Brazil
- Brazil Northeast
- Brazil South
- Brazil Southeast
-
Southern South America
- Paraguay
-
Brazil
Links to other databases Top
Suggest others/fix!| 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)!
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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 / 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |