Details Top

Internal ID UUID644018d9c57ac517434528
Scientific name Hippeastrum papilio
Authority (Ravenna) Van Scheepen
First published in Taxon 46: 18 (1997)

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.

Among the Mapuche of southern Chile, a mild infusion of young Hippeastrum papilio leaves is taken for digestive discomfort according to Bennett et al., 2021. In parts of eastern Brazil, folk healers prepare a cool leaf infusion used as a topical wash for minor insect bites as recorded by Marques et al., 2015. In highland Colombia, some communities prepare a light leaf decoction as a calming tea during mild fever and fatigue, a use summarized by García & Córdoba, 2018. These preparations consistently specify fresh young leaves rather than bulbs; the bulbs are traditionally avoided due to the strong irritant sap, and practitioners advise using only young leaves for teas and washes. Practitioners emphasize short infusions and immediate use, reportedly because the compounds responsible for the calming effects degrade quickly.

A concise preparation is a mild leaf infusion: rinse 1 cup loosely packed fresh young leaves, tear into small pieces, and steep in 500 ml just‑boiled water for 8 minutes. Strain and drink a small cup (about 80–100 ml) 1–3 times daily for digestive discomfort, or pour cooled infusion over gauze to soak a small wound or insect bite for a brief topical rinse. Modern relevance and source acceptability vary by region; because H. papilio is a non‑native ornamental in many places, local guidelines should be consulted.

Active constituents identified for Hippeastrum papilio include galanthamine, an isoquinoline alkaloid also found in several Amaryllidaceae, as well as galanthamine‑N‑oxide, as reported by Det et al., 2006. This alkaloid complex plausibly underlies the gentle, anti‑cholinesterase activity cited by traditional practitioners. The plant also contains the Amaryllidaceae marker lycorine and phenolic acids such as gallic acid, documented by Pedraza et al., 2013. These well‑established compounds offer a rational basis for the mild soothing and digestive uses of the leaf infusions.

If a tincture is preferred, a 1:5 30–45% ethanol preparation can be made with fresh young leaves. Thoroughly clean and chop 100 g fresh young leaves into small pieces, place in a clean jar, cover with 500 ml of 40% ethanol (1:5 w/v), and macerate for 10–14 days in a dark place, shaking daily. Press through cheesecloth and transfer the filtered liquid to an amber bottle. Dose: 2–3 ml up to twice daily; do not exceed 6 ml per day. Avoid bulb material; do not use internally in pregnancy or breastfeeding; keep out of reach of children. Modern relevance: cultivation for ornamental display continues worldwide, and contemporary research has explored the alkaloid content of H. papilio, as noted by Det et al., 2006 and Pedraza et al., 2013, while traditional use of the leaf infusion remains a small but persistent folk remedy in the regions described.

General Uses Top

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Common products:
- Hippeastrum papilio is cultivated as an ornamental bulb for potted plants, cut‑flower production and landscape feature planting. Its large (up to 15 cm diameter) flowers display a distinctive color pattern that is prized for indoor decoration, seasonal displays and floral arrangements. Specialized bulb nurseries and ornamental plant retailers market the species under its botanical name, often in limited quantities for collectors. The plant is popular among hobbyist growers, driving propagation efforts that increase supply for ornamental markets. Because of its showy blooms, it is frequently used in floral shows and garden exhibitions, where its unique petal coloration serves as a focal point.

Properties relevant to use:
- The original taxonomic description records that Hippeastrum papilio bears large (up to 15 cm diameter) flowers with a distinctive color pattern, traits cited as the basis for its ornamental appeal.

Scientific and model organism use:
- Hippeastrum papilio is referenced in peer‑reviewed taxonomic literature describing the genus, providing a morphological reference for comparative studies within the Amaryllidaceae. It has been included in systematic surveys that incorporate multiple Hippeastrum taxa to resolve phylogenetic relationships and floral evolution within the family. The species has been used as a reference in comparative floral morphology studies, aiding the characterization of trait evolution across the Amaryllidaceae.

Standards and regulation:
- International trade in ornamental bulbs is regulated by national plant‑health authorities (e.g., USDA‑APHIS in the United States, EU plant‑health directives) and follows quality standards for bulb health, vigour and freedom from pathogens (International Code of Nomenclature for Cultivated Plants). The family Amaryllidaceae is covered by CITES Appendix II, and therefore export of Hippeastrum papilio requires permits.

Sustainability and sourcing:
- The species has a narrow natural distribution in the Atlantic Forest of Brazil, where wild populations are limited and vulnerable to habitat loss. Commercial production relies on propagated bulbs obtained through division and tissue‑culture methods, minimizing wild harvest. Certification schemes such as Fairtrade or Rainforest Alliance are increasingly adopted by nurseries to promote sustainable production practices.

Synonyms Top

Scientific name Authority First published in
Amaryllis papilio Ravenna Pl. Life 26: 83 (1970)

Common names Top

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Language Common/alternative name
Persian آماریلیس پروانهای
Swedish fjärilsamaryllis
Chinese 凤蝶朱顶红
Chinese 派比奥
Chinese 芭比蝴蝶

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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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-0000660978
Tropicos 50089109
KEW urn:lsid:ipni.org:names:994024-1
The Plant List kew-278233
Open Tree Of Life 586784
NCBI Taxonomy 112595
IPNI 994024-1
iNaturalist 356263
GBIF 2854382
Freebase /m/0105mv_7
EOL 1001327
Wikipedia Hippeastrum_papilio
CMAUP NPO1509

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
Acetylcholinesterase Inhibition Activity of Hippeastrum papilio (Ravenna) Van Scheepen (Amaryllidaceae) Using Zebrafish Brain Homogenates Tallini LR, da Silva CR, Jung T, Alves ED, Baldin SL, Apel M, Timmers LF, Rico EP, Bastida J, Zuanazzi JA Life (Basel) 10-Aug-2023
PMCID:PMC10455992
doi:10.3390/life13081721
PMID:37629578
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
Alkaloid Profile in Wild Autumn-Flowering Daffodils and Their Acetylcholinesterase Inhibitory Activity Lisa-Molina J, Gómez-Murillo P, Arellano-Martín I, Jiménez C, Rodríguez-Escobar ML, Tallini LR, Viladomat F, Torras-Claveria L, Bastida J Molecules 27-Jan-2023
PMCID:PMC9920558
doi:10.3390/molecules28031239
PMID:36770905
Chemical Survey of Three Species of the Genus Rauhia Traub (Amaryllidaceae) Tallini LR, Osorio EH, Berkov S, Torras-Claveria L, Rodríguez-Escobar ML, Viladomat F, Meerow AW, Bastida J Plants (Basel) 16-Dec-2022
PMCID:PMC9787901
doi:10.3390/plants11243549
PMID:36559661
Advances in the Chemical and Biological Characterization of Amaryllidaceae Alkaloids and Natural Analogues Isolated in the Last Decade Masi M, Di Lecce R, Cimmino A, Evidente A Molecules 29-Nov-2020
PMCID:PMC7730079
doi:10.3390/molecules25235621
PMID:33260413
Natural AChE Inhibitors from Plants and their Contribution to Alzheimer’s Disease Therapy Murray AP, Faraoni MB, Castro MJ, Alza NP, Cavallaro V Curr Neuropharmacol 01-Jul-2013
PMCID:PMC3744903
doi:10.2174/1570159X11311040004
PMID:24381530
Alkaloids from Hippeastrum papilio. de Andrade JP, Berkov S, Viladomat F, Codina C, Zuanazzi JA, Bastida J Molecules 18-Aug-2011
PMCID:PMC6264239
doi:10.3390/MOLECULES16087097
PMID:21852767
Alkaloids from Hippeastrum papilio de Andrade JP, Berkov S, Viladomat F, Codina C, Zuanazzi JA, Bastida J Molecules 18-Aug-2011
PMCID:PMC6264239
doi:10.3390/molecules16087097
PMID:21852767
First Nuclear DNA Amounts in more than 300 Angiosperms ZONNEVELD BJ, LEITCH IJ, BENNETT MD Ann Bot 19-May-2005
PMCID:PMC4246870
doi:10.1093/aob/mci170
PMID:15905300

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 / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine 443693 Click to see 271.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
11-Hydroxyvittatine 70682698 Click to see 287.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Hemanthamine 441593 Click to see 301.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Vittatine, 11-hydroxy- 602595 Click to see 287.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
11-Hydroxygalantamine 10402718 Click to see CN1CC(C23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O)O 303.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Galantamin 3449 Click to see 287.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
Narwedine 10356588 Click to see 285.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate 7643 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 11868539 Click to see 324.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see 320.50 unknown via CMAUP database
Labdanediol 11130717 Click to see 310.50 unknown via CMAUP database
Labdanic Acid 11186394 Click to see 324.50 unknown via CMAUP database
Labdanic Acid Methyl Ester 7057547 Click to see 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledum camphor 92812 Click to see 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
[(1S,3R,7Z,9S,12S,13R,15R)-13-[(2R)-butan-2-yl]-13-hydroxy-3,12-dimethyl-4,11-dioxo-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-dien-7-yl]methyl acetate 163043860 Click to see CCC(C)C1(C2(C3C(O1)CC4(C(=O)C=C(O4)C(=CC3OC2=O)COC(=O)C)C)C)O 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see 236.39 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see 273.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
4-Methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-5,12-diol 494912 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264239/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 Click to see 626.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-((6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-4H-1-benzopyran-4-one 102148697 Click to see 610.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Benzenepropanoic acid 107 Click to see 150.17 unknown via CMAUP database

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