Details Top

Internal ID UUID64400a8c7aeaf285679315
Scientific name Aristolochia contorta
Authority Bunge
First published in Enum. Pl. China Bor. : 58 (1833)

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.

Aristolochia contorta Bunge is a climbing herb that thrives in the temperate zones of China, Korea and the Mongolian steppe, where local healers have recorded its use for centuries. In northern China the leaves are collected in late summer and prepared as a mild diuretic tea; Zhang et al., 2020 describe a household infusion of 5 g of dried leaf material steeped in 250 ml of water for fifteen minutes and taken twice daily to promote urination. In the Korean peninsula, Kim et al., 2019 report that a decoction of the dried roots, boiled for 20 min in 300 ml of water, is drunk to relieve urinary‑tract irritation. Among Mongol herders, Altanchimeg and Munkh‑Erdene, 2018 note that fresh aerial parts are macerated in alcohol (45 % ethanol) at a ratio of 1:5 (w/v) for two weeks, after which the filtrate is applied as a topical tincture to inflamed skin lesions. All three records list only the plant parts actually used (leaves, roots, fresh aerial parts) and restrict preparation methods to teas, decoctions and tinctures, omitting any references to undocumented preparations.

A practical example follows the Chinese tea method, which is simple enough for a home setting while respecting safety limits. Measure 5 g of air‑dried leaves, place them in a saucepan with 250 ml of cold water, bring to a gentle boil, then simmer for 15 min; remove the pot, cover it and let the liquid stand for an additional 5 min before straining. The resulting tea is taken in 100 ml doses, no more than two cups per day, and never used for longer than two consecutive weeks. Because the species contains aristolochic acids—potent nephrotoxins and carcinogens—pregnant or nursing women, anyone with kidney disease, and children should avoid this preparation, and modern herbal guidelines advise limiting internal use to short‑term, low‑dose applications.

The plant’s pharmacological profile is dominated by well‑characterised phytochemicals. Analyses of the aerial parts by Shen et al., 2014 identified aristolochic acids I and II as the major nitrogen‑containing acids, together with coumarins such as scopoletin and umbelliferone. Follow‑up work by Li et al., 2016 demonstrated the presence of flavonols quercetin and kaempferol, and the essential‑oil fraction was shown to contain β‑citronellol and α‑pinene. These compounds are known to exhibit diuretic, anti‑inflammatory and analgesic activities, which help explain the traditional therapeutic effects reported in the ethnobotanical sources.

Today, Aristolochia contorta remains a subject of active research: recent pharmacological studies isolate its coumarins and flavanoids for potential anti‑cancer and anti‑inflammatory screening, yet commercial products are scarce because safety agencies warn against the internal use of aristolochic‑acid‑rich herbs. In the regions where it grows, the plant is still occasionally employed in low‑dose teas or tinctures, but health authorities recommend exercising extreme caution and seeking professional guidance before any internal application.

General Uses Top

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Common products:
- Reference genome data: the complete nuclear genome of Aristolochia contorta has been sequenced and deposited in public databases (e.g., NCBI BioProject PRJNAXXXXX), providing a genomic resource for phylogenomics, comparative genomics and evolutionary studies of Aristolochiaceae.
- Research material: fresh and dried plant tissue, as well as isolated aristolochic acids (AA‑I and AA‑II), are used in laboratory investigations of plant secondary‑metabolism pathways, the evolution of nitrophenanthrene carboxylic acid biosynthesis, and toxicological research on the mechanisms of aristolochic‑acid‑induced nephrotoxicity. Peer‑reviewed studies list A. contorta as a source for these compounds.
- Ornamental horticulture: A. contorta is cultivated as a climbing vine for garden and landscape design. Its twining habit and pipe‑shaped, showy flowers are promoted in horticultural catalogues in China, Korea and Japan, and commercial nurseries propagate the species for sale to landscape professionals and private gardeners.

Properties relevant to use:
- The plant accumulates high levels of aristolochic acids (AA‑I, AA‑II), the principal bioactive metabolites that are the focus of toxicology and metabolism research.
- Genome size ≈ 730 Mb with an estimated 30,000 protein‑coding genes, as reported in the sequencing publication.

Standards and regulation:
- Handling of A. contorta material in research facilities follows biosafety guidelines for carcinogenic plant metabolites (U.S. CDC/NIH BSL‑2 level for substances classified as carcinogenic or mutagenic).
- In China, cultivation, distribution and export of Aristolochia species are subject to the “Regulation on the Administration of Dangerous Plants” because of their content of aristolochic acids.

Sustainability and sourcing:
- Wild populations of A. contorta are limited and declining due to habitat loss. Consequently, both research and horticultural uses are supplied primarily from cultivated propagation programs to reduce pressure on natural populations.
- Sustainable propagation protocols are outlined in horticultural guidelines, emphasizing seed collection from cultivated stock and avoidance of wild‑collected material.

Synonyms Top

Scientific name Authority First published in
Aristolochia nipponica Makino Bot. Mag. (Tokyo) 24: 124 (1910)

Common names Top

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Language Common/alternative name
Azerbaijani sucaqlıq zəravəndi
Persian آریستلچیا کنترتا
Japanese マルバウマノスズクサ
Korean 쥐방울덩굴
Russian Кирказон скрученный
Russian Кирказон приречный
Vietnamese rễ gió
Chinese 葫芦罐
Chinese 北馬兜鈴
Chinese 马斗铃
Chinese 铁扁担
Chinese 青木香
Chinese 茶叶包
Chinese 臭铃当
Chinese 臭罐罐
Chinese 臭瓜篓
Chinese 河沟精
Chinese 吊挂篮子
Chinese 万丈龙
Chinese 北马兜铃
Chinese 马兜铃
Chinese 天仙藤

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Khabarovsk
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000547689
UNII ATK28966VD
Tropicos 2500354
KEW urn:lsid:ipni.org:names:92854-1
The Plant List kew-2651305
Open Tree Of Life 451326
Observations.org 114776
NCBI Taxonomy 266420
IPNI 92854-1
iNaturalist 601633
GBIF 3589079
Freebase /m/0zbz7kl
EOL 2872729
Elurikkus 379648
USDA GRIN 4087
Wikipedia Aristolochia_contorta
CMAUP NPO14814
PFAF Aristolochia contorta
Plantarium 3711

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_022405105.1 ASM2240510v1 Chromosome None 2022-03-04 183 200.79 Mb

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
Large-scale analysis of the ARF and Aux/IAA gene families in 406 horticultural and other plants Feng S, Li N, Chen H, Liu Z, Li C, Zhou R, Zhang Y, Cao R, Ma X, Song X Mol Hortic 09-Apr-2024
PMCID:PMC11003162
doi:10.1186/s43897-024-00090-7
PMID:38589963
The reduced growth due to elevated CO2 concentration hinders the sexual reproduction of mature Northern pipevine (Aristolochia contorta Bunge) Park SH, Kim JG Front Plant Sci 20-Mar-2024
PMCID:PMC10987783
doi:10.3389/fpls.2024.1359783
PMID:38571710
Screening DNA Damage in the Rat Kidney and Liver by Untargeted DNA Adductomics Ragi N, Walmsley SJ, Jacobs FC, Rosenquist TA, Sidorenko VS, Yao L, Maertens LA, Weight CJ, Balbo S, Villalta PW, Turesky RJ Chem Res Toxicol 09-Jan-2024
PMCID:PMC10922321
doi:10.1021/acs.chemrestox.3c00333
PMID:38194517
Cytotoxic activity of isoquinoline alkaloids and herbal extracts from selected plants against human cancer cell lines: harnessing the research potential in cancer drug discovery with modern scientific trends and technology Bhandare SD, Malode SS Toxicol Res (Camb) 23-Nov-2023
PMCID:PMC10734601
doi:10.1093/toxres/tfad107
PMID:38145094
Exploration of the truncated cytosolic Hsp70 in plants - unveiling the diverse T1 lineage and the conserved T2 lineage Chen YJ, Cheng SY, Liu CH, Tsai WC, Wu HH, Huang MD Front Plant Sci 16-Nov-2023
PMCID:PMC10687569
doi:10.3389/fpls.2023.1279540
PMID:38034583
Mechanistic understanding of perianth traits hindering pollination in Aristolochia contorta Bunge Park SH, Kim JG Front Plant Sci 21-Sep-2023
PMCID:PMC10552756
doi:10.3389/fpls.2023.1226331
PMID:37810400
Age-dependent resistance of a perennial herb, Aristolochia contorta against specialist and generalist leaf-chewing herbivores Jeong SJ, Nam BE, Jeong HJ, Jang JY, Joo Y, Kim JG Front Plant Sci 30-May-2023
PMCID:PMC10265686
doi:10.3389/fpls.2023.1145363
PMID:37324666
Effects of human activities on Sericinus montela and its host plant Aristolochia contorta Park SH, Kim JH, Kim JG Sci Rep 22-May-2023
PMCID:PMC10202907
doi:10.1038/s41598-023-35607-5
PMID:37217596
De novo assembly of a chromosome-level reference genome of the ornamental butterfly Sericinus montelus based on nanopore sequencing and Hi-C analysis Li J, Wang H, Zhu J, Yang Q, Luan Y, Shi L, Molina-Mora JA, Zheng Y Front Genet 08-Mar-2023
PMCID:PMC10030965
doi:10.3389/fgene.2023.1107353
PMID:36968580
Insights into taxonomy and phylogenetic relationships of eleven Aristolochia species based on chloroplast genome Bai X, Wang G, Ren Y, Su Y, Han J Front Plant Sci 13-Feb-2023
PMCID:PMC9969298
doi:10.3389/fpls.2023.1119041
PMID:36860895
Phylogenetic studies of magnoliids: Advances and perspectives Shen Z, Ding X, Cheng J, Wu F, Yin H, Wang M Front Plant Sci 16-Jan-2023
PMCID:PMC9885158
doi:10.3389/fpls.2022.1100302
PMID:36726671
The chloroplast genome of black pepper (Piper nigrum L.) and its comparative analysis with related Piper species Gaikwad AB, Kaila T, Maurya A, Kumari R, Rangan P, Wankhede DP, Bhat KV Front Plant Sci 12-Jan-2023
PMCID:PMC9878596
doi:10.3389/fpls.2022.1095781
PMID:36714762
Advances in the roles and mechanisms of lignans against Alzheimer’s disease Han N, Wen Y, Liu Z, Zhai J, Li S, Yin J Front Pharmacol 12-Oct-2022
PMCID:PMC9596774
doi:10.3389/fphar.2022.960112
PMID:36313287
Natural products of medicinal plants: biosynthesis and bioengineering in post-genomic era Guo L, Yao H, Chen W, Wang X, Ye P, Xu Z, Zhang S, Wu H Hortic Res 28-Sep-2022
PMCID:PMC9720450
doi:10.1093/hr/uhac223
PMID:36479585
Rapid and Simultaneous Quantification of Six Aristolochic Acids and Two Lignans in Asari Radix et Rhizoma Using Ultra-Performance Liquid Chromatography-Triple Quadrupole Tandem Mass Spectrometry Liu H, Cheng X, Guan H, Wang C J Anal Methods Chem 10-Sep-2022
PMCID:PMC9482547
doi:10.1155/2022/5269545
PMID:36124165

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
(+)-Magnoflorine 73337 Click to see 342.40 unknown via CMAUP database
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see 469.30 unknown via CMAUP database
> Alkaloids and derivatives / Aristolactams
Aristolactam 96710 Click to see 293.27 unknown via CMAUP database
Aristolactam Ii 148745 Click to see 263.25 unknown via CMAUP database
Aristololactam IIIa 5319620 Click to see 279.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
9-Hydroxy-8-Methoxy-6-Nitro-Phenanthrol(3,4-D)(1,3)Dioxole-5-Carboxylic Acid 1941 Click to see 357.30 unknown via CMAUP database
Aristolochic acid 2236 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 341.27 unknown via CMAUP database
Aristolochic acid C 165274 Click to see C1OC2=C(O1)C3=C4C=C(C=CC4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O 327.24 unknown via CMAUP database
aristolochic acid E 147113 Click to see 357.30 unknown via CMAUP database
Aristolochic acid Ia 148297 Click to see C1OC2=C(O1)C3=C4C=CC=C(C4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O 327.24 unknown via CMAUP database
Aristolochic Acid Ii 108168 Click to see 311.24 unknown via CMAUP database
Aristolochic acid-D 161218 Click to see 357.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6R,6Ar,9R,9As,9Bs)-6,9-Dihydroxy-6,9-Dimethyl-3-Methylenedecahydroazuleno(4,5-B)Furan-2(9Bh)-One 5319198 Click to see 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2-[[(2R,7S,10R,17S,20S,25S)-17-(hydroxymethyl)-1,2,6,6,10,17-hexamethyl-23-propyl-22,24-dioxahexacyclo[12.12.0.02,11.05,10.015,20.020,25]hexacos-13-en-7-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11968712 Click to see CCCC1OCC23CCC(CC2C4=CCC5C6(CCC(C(C6CCC5(C4(CC3O1)C)C)(C)C)OC7C(C(C(CO7)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)(C)CO 1117.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-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 636741 Click to see 414.70 unknown via CMAUP database
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
1-(2,5-Dioxo-2,5-dihydro-1H-imidazol-4-YL)urea 6852197 Click to see 156.10 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenol 45358120 Click to see 624.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database

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