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

Description Top

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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
Vietnamese rễ gió
Chinese 茶叶包
Chinese 北馬兜鈴
Chinese 马斗铃
Chinese 铁扁担
Chinese 葫芦罐
Chinese 青木香
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

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 2022-03-04 183.0x 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
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
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
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
Systematic palynology in Korean Piperales with special focus on its exine surface ornamentation and orbicule morphology Oak MK, Yang S, Choi G, Song JH Sci Rep 09-Mar-2022
PMCID:PMC8907175
doi:10.1038/s41598-022-08105-3
PMID:35264735
Chromosome-level genome assembly of Aristolochia contorta provides insights into the biosynthesis of benzylisoquinoline alkaloids and aristolochic acids Cui X, Meng F, Pan X, Qiu X, Zhang S, Li C, Lu S Hortic Res 11-Feb-2022
PMCID:PMC8973263
doi:10.1093/hr/uhac005
PMID:35147168
Revisiting traditional Chinese materia medica from European historical collections and perspective for current use Jia Y, Wang M, van Andel T J Tradit Complement Med 23-Nov-2021
PMCID:PMC9072815
doi:10.1016/j.jtcme.2021.11.001
PMID:35528475
Complete Plastome of Three Korean Asarum (Aristolochiaceae): Confirmation Tripartite Structure within Korean Asarum and Comparative Analyses Yoo MJ, Jin DP, Lee HO, Lim CE Plants (Basel) 29-Sep-2021
PMCID:PMC8540983
doi:10.3390/plants10102056
PMID:34685866

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
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 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I 469.30 unknown via CMAUP database
> Alkaloids and derivatives / Aristolactams
Aristolactam II 148745 Click to see C1OC2=C(O1)C3=C4C(=C2)C(=O)NC4=CC5=CC=CC=C53 263.25 unknown via CMAUP database
Aristololactam 96710 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC5=C3OCO5 293.27 unknown via CMAUP database
Aristololactam IIIa 5319620 Click to see C1OC2=C(O1)C3=C4C=C(C=CC4=CC5=C3C(=C2)C(=O)N5)O 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 COC1=CC(=CC(=C1O)OC)C(=O)O 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 COC1=C(C=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 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 d 161218 Click to see COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O 357.30 unknown via CMAUP database
Aristolochic acid E 147113 Click to see COC1=C(C2=CC(=C3C(=CC4=C(C3=C2C=C1)OCO4)C(=O)O)[N+](=O)[O-])O 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 C1OC2=C(O1)C3=C(C(=C2)C(=O)O)C(=CC4=CC=CC=C43)[N+](=O)[O-] 311.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Magnograndiolide 5319198 Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O 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 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 C1(=O)C(=NC(=O)N1)NC(=O)N 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 CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)OC)O)OC)OC 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 C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database

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