Details Top

Internal ID UUID64400a94140cb148747407
Scientific name Aristolochia gigantea
Authority Mart.
First published in Nov. Gen. Sp. Pl. (Martius) 1(3): 75, t. 48. 1824 [1 Oct 1824]

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Ornamental vine: Aristolochia gigantea is widely cultivated by nurseries for its large, pipe‑shaped, deep‑maroon to purple flowers and vigorous climbing habit. It is marketed under names such as “giant Dutchman’s pipe” and is sold as a potted or ground‑cover plant for tropical and subtropical gardens.
- Landscape use: The species is employed in vertical greening of walls, trellises, pergolas and arbors, where its fast‑growing, woody stems (up to 10–15 m long) and glossy, heart‑shaped leaves provide dense foliage cover and ornamental value. Its flowers attract butterflies, enhancing ecological interest in designed plantings.
- Floral foliage: Mature branches with full‑sized leaves are occasionally harvested for decorative green arrangements in floristry, complementing cut‑flower designs.

Properties relevant to use:
- Vigorous climbing habit: The plant produces long, flexible stems that readily attach to support structures, enabling rapid coverage of vertical surfaces.
- Ornamental flower morphology: The tubular corolla measures 6–10 cm in length, displaying a pipe‑like shape and a strong fragrance, making it a focal point in garden displays.
- Vegetative propagation: Stem cuttings root readily in warm, humid conditions, allowing commercial nurseries to produce uniform stock without seed‑derived variation.
- Chemical consideration: All Aristolochia species contain aristolochic acids; while this does not affect horticultural utility, it informs regulatory oversight of plant material in many jurisdictions.

Sustainability and sourcing:
- Nursery propagation: Commercial production relies on vegetative cuttings and seed propagation in controlled greenhouse environments, minimizing pressure on wild populations.
- Conservation status: The species is not listed on CITES appendices and is not evaluated on the IUCN Red List, indicating that current horticultural trade does not threaten its wild occurrence.
- Regulatory compliance: Because aristolochic acid–containing plants are subject to import and safety controls (e.g., U.S. FDA regulations on plant material, EU restrictions on substances of concern), commercial suppliers adhere to standard plant quarantine and labeling guidelines to ensure lawful distribution.

Synonyms Top

Scientific name Authority First published in
Howardia gigantea Klotzsch Monatsber. Königl. Preuss. Akad. Wiss. Berlin 1859: 610 (1859)

Common names Top

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Language Common/alternative name
Finnish pelikaanipiippuköynnös
Japanese アリストロキア・ギガンテア
Dutch reuzenpijpbloem
Portuguese mil-homens
Slovenian orjaški podraščec
Chinese 大马兜铃
Chinese 巨花马兜铃
Chinese 大馬兜鈴

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000547827
Tropicos 2500214
KEW urn:lsid:ipni.org:names:60460287-2
The Plant List kew-2651433
Missouri Botanical Garden 276777
Open Tree Of Life 186420
NCBI Taxonomy 12948
IPNI 92960-1
iNaturalist 71036
GBIF 3589283
Freebase /m/026hs6p
Elurikkus 216129
USDA GRIN 4094
Wikipedia Aristolochia_gigantea

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
De novo Assembly and Comparative Analyses of Mitochondrial Genomes in Piperales Yu R, Chen X, Long L, Jost M, Zhao R, Liu L, Mower JP, dePamphilis CW, Wanke S, Jiao Y Genome Biol Evol 10-Mar-2023
PMCID:PMC10036691
doi:10.1093/gbe/evad041
PMID:36896589
Floral Scents of a Deceptive Plant Are Hyperdiverse and Under Population-Specific Phenotypic Selection Gfrerer E, Laina D, Gibernau M, Fuchs R, Happ M, Tolasch T, Trutschnig W, Hörger AC, Comes HP, Dötterl S Front Plant Sci 24-Sep-2021
PMCID:PMC8500232
doi:10.3389/fpls.2021.719092
PMID:34630465
On pollen and airborne virus transmission Dbouk T, Drikakis D Phys Fluids (1994) 22-Jun-2021
PMCID:PMC8320470
doi:10.1063/5.0055845
PMID:34335004
Illuminating Photosynthesis in the Mesophyll of Diverse Leaves Holloway-Phillips M Plant Physiol 27-Jun-2019
PMCID:PMC6752918
doi:10.1104/pp.19.00592
PMID:31253750
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
ESSENTIAL OILS FROM TWO BRAZILIAN VITEX SPECIES S.G. Leitão, E.N. Fonseca, T.C. dos Santos International Society for Horticultural Science (ISHS) 27-Jul-2015
doi:10.17660/ACTAHORTIC.1999.500.11
The betrayed thief – the extraordinary strategy of Aristolochia rotunda to deceive its pollinators Oelschlägel B, Nuss M, von Tschirnhaus M, Pätzold C, Neinhuis C, Dötterl S, Wanke S New Phytol 08-Dec-2014
PMCID:PMC4357391
doi:10.1111/nph.13210
PMID:25488155
Proteomic profiling of γ-ECS overexpressed transgenic Nicotiana in response to drought stress Kumar D, Datta R, Sinha R, Ghosh A, Chattopadhyay S Plant Signal Behav 20-May-2014
PMCID:PMC4203497
doi:10.4161/psb.29246
PMID:25763614
Major trends in stem anatomy and growth forms in the perianth-bearing Piperales, with special focus on Aristolochia Wagner ST, Hesse L, Isnard S, Samain MS, Bolin J, Maass E, Neinhuis C, Rowe NP, Wanke S Ann Bot 02-Apr-2014
PMCID:PMC4030810
doi:10.1093/aob/mcu044
PMID:24694829
Characterization of the basal angiosperm Aristolochia fimbriata: a potential experimental system for genetic studies Bliss BJ, Wanke S, Barakat A, Ayyampalayam S, Wickett N, Wall PK, Jiao Y, Landherr L, Ralph PE, Hu Y, Neinhuis C, Leebens-Mack J, Arumuganathan K, Clifton SW, Maximova SN, Ma H, dePamphilis CW BMC Plant Biol 24-Jan-2013
PMCID:PMC3621149
doi:10.1186/1471-2229-13-13
PMID:23347749
Liana Abundance, Diversity, and Distribution on Barro Colorado Island, Panama Schnitzer SA, Mangan SA, Dalling JW, Baldeck CA, Hubbell SP, Ledo A, Muller-Landau H, Tobin MF, Aguilar S, Brassfield D, Hernandez A, Lao S, Perez R, Valdes O, Yorke SR PLoS One 21-Dec-2012
PMCID:PMC3528767
doi:10.1371/journal.pone.0052114
PMID:23284889
Aristolactams and Alkamides of Aristolochia gigantea. Holzbach JC, Lopes LM Molecules 21-Dec-2010
PMCID:PMC6259121
doi:10.3390/MOLECULES15129462
PMID:21178901
Aristolactams and Alkamides of Aristolochia gigantea Holzbach JC, Lopes LM Molecules 21-Dec-2010
PMCID:PMC6259121
doi:10.3390/molecules15129462
PMID:21178901
Foldable structures and the natural design of pollen grains Katifori E, Alben S, Cerda E, Nelson DR, Dumais J Proc Natl Acad Sci U S A 19-Apr-2010
PMCID:PMC2867878
doi:10.1073/pnas.0911223107
PMID:20404200
From Forgotten Taxon to a Missing Link? The Position of the Genus Verhuellia (Piperaceae) Revealed by Molecules Wanke S, Vanderschaeve L, Mathieu G, Neinhuis C, Goetghebeur P, Samain MS Ann Bot 01-Jun-2007
PMCID:PMC3243581
doi:10.1093/aob/mcm063
PMID:17513306

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 / Aporphines
(+)-Corytuberine 160500 Click to see 327.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(2S,3R,4S,5S,6R)-2-[[(8S,13aR)-2,11-dihydroxy-8-[(4-hydroxyphenyl)methyl]-3-methoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101701149 Click to see 581.60 unknown https://doi.org/10.1016/S0031-9422(96)00835-7
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
4-Hydroxyphenylacetaldehyde 440113 Click to see 136.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
4-Hydroxyphenylpyruvic acid 979 Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O 180.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine 681 Click to see 153.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see 142.28 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Dodecane 8182 Click to see 170.33 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Nonane 8141 Click to see 128.25 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Undecene 13190 Click to see 154.29 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lignans, neolignans and related compounds / Furanoid lignans
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene 86608 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Trans-alpha-Bergamotene 6429302 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Elemene 12309449 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A 9548706 Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.17660/ACTAHORTIC.1999.500.11
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(96)00835-7
Sequoyitol 439990 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(96)00835-7
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1016/S0031-9422(00)97573-3
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Higenamine 440927 Click to see 271.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
(S)-3'-Hydroxy-N-methylcoclaurine 440591 Click to see 315.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
(S)-N-Methylcoclaurine 440584 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
Coclaurine 160487 Click to see 285.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/
Reticuline 439653 Click to see 329.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259121/

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