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Aristolochia chilensis

Aristolochia chilensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400a8aa307d301375128
Scientific name Aristolochia chilensis
Authority Bridges ex Lindl.
First published in Edwards's Bot. Reg. 20: t. 1680 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aristolochia setigera Klotzsch Monatsber. Königl. Preuss. Akad. Wiss. Berlin 1859: 617 (1859)
Howardia setigera Klotzsch Monatsb. Akad. Berl. (1859) 617.

Common names Top

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Language Common/alternative name
Spanish oreja de zorro

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
  • Southern America
    • Southern South America
      • Chile Central
      • Chile North

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000547655
KEW urn:lsid:ipni.org:names:330838-2
The Plant List kew-2651275
Open Tree Of Life 111746
NCBI Taxonomy 304180
IPNI 330838-2
iNaturalist 559298
GBIF 3589409
Freebase /m/0jt1lb4
EOL 5103232
USDA GRIN 4085
Wikipedia Aristolochia_chilensis

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
High-throughput sequencing-based analysis of the composition and diversity of the endophyte community in roots of Stellera chamaejasme Zhang JZ, Li XZ, Yin YB, Luo SC, Wang DX, Zheng H, Liu YX Sci Rep 13-Apr-2024
PMCID:PMC11016073
doi:10.1038/s41598-024-59055-x
PMID:38615120
Mode of action, chemistry and defensive efficacy of the osmeterium in the caterpillar Battus polydamas archidamas Palma-Onetto V, Bergmann J, González-Teuber M Sci Rep 24-Apr-2023
PMCID:PMC10126055
doi:10.1038/s41598-023-33390-x
PMID:37095102
Endophytic Fungal Community of Stellera chamaejasme L. and Its Possible Role in Improving Host Plants’ Ecological Flexibility in Degraded Grasslands Tang W, Gong W, Xiao R, Mao W, Zhao L, Song J, Awais M, Ji X, Li H J Fungi (Basel) 12-Apr-2023
PMCID:PMC10146894
doi:10.3390/jof9040465
PMID:37108919
Interaction of Plants and Endophytic Microorganisms: Molecular Aspects, Biological Functions, Community Composition, and Practical Applications Aleynova OA, Kiselev KV Plants (Basel) 06-Feb-2023
PMCID:PMC9958707
doi:10.3390/plants12040714
PMID:36840062
Changes in Diversity and Community Composition of Root Endophytic Fungi Associated with Aristolochia chilensis along an Aridity Gradient in the Atacama Desert Guevara-Araya MJ, Escobedo VM, Palma-Onetto V, González-Teuber M Plants (Basel) 05-Jun-2022
PMCID:PMC9182583
doi:10.3390/plants11111511
PMID:35684284
Molecular identification and characterization of Botrytis cinerea associated to the endemic flora of semi-desert climate in Chile Notte AM, Plaza V, Marambio-Alvarado B, Olivares-Urbina L, Poblete-Morales M, Silva-Moreno E, Castillo L Curr Res Microb Sci 24-Jul-2021
PMCID:PMC8610304
doi:10.1016/j.crmicr.2021.100049
PMID:34841340
Rapid Identification and Simultaneous Quantification of Aristolochic Acids by HPLC-DAD and Confirmations by MS in Aristolochia chilensis Using a Limited Biomass Araya M, García S, González-Teuber M J Anal Methods Chem 06-Jun-2018
PMCID:PMC6011054
doi:10.1155/2018/5036542
PMID:29977642
In-silico screening for anti-Zika virus phytochemicals Byler KG, Ogungbe IV, Setzer WN J Mol Graph Model 28-Aug-2016
PMCID:PMC7185537
doi:10.1016/j.jmgm.2016.08.011
PMID:27588363
Temporal Variation of Aristolochia chilensis Aristolochic Acids during Spring Santander R, Urzúa A, Olguín Á, Sánchez M Molecules 13-Nov-2015
PMCID:PMC6332109
doi:10.3390/molecules201119704
PMID:26580587
Fate of Ingested Aristolactams from Aristolochia chilensis in Battus polydamas archidamas (Lepidoptera: Papilionidae) Urzúa A, Olguín A, Santander R Insects 11-Oct-2013
PMCID:PMC4553502
doi:10.3390/insects4040533
PMID:26462522
Manipulating JNK Signaling with (−)-zuonin A Kaoud TS, Park H, Mitra S, Yan C, Tseng CC, Shi Y, Jose J, Taliaferro JM, Lee K, Ren P, Hong J, Dalby KN ACS Chem Biol 30-Aug-2012
PMCID:PMC6459613
doi:10.1021/cb300261e
PMID:22916726
Aristolochic acids in Aristolochia chilensis and the Aristolochia-FEEDER Battus Archidamas (Lepidoptera) Alejandro Urzúa, Guillermo Salgado, Bruce K. Cassels, Gert Eckhardt Institute of Organic Chemistry & Biochemistry 08-Mar-2011
doi:10.1135/CCCC19831513
The 4-Aryltetralones of Aristolochia chilensis Alejandro Urzúa, Maurice Shamma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50055A017
Aristolodione, a 4,5-Dioxoaporphine from Aristolochia chilensis Alejandro Urzúa, Alan J. Freyer, Maurice Shamma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50050A043
2,5-diaryl-3,4-dimethyltetrahydrofuranoid lignans Alejandro Urzúa, Alan J. Freyer, Maurice Shamma Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81846-4

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
Cepharadione A 94577 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O 305.30 unknown https://doi.org/10.1021/NP50050A043
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
Aristolodione 184116 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)O)C(=O)C1=O 307.30 unknown https://doi.org/10.1021/NP50050A043
> Alkaloids and derivatives / Aristolactams
Aristololactam 96710 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC5=C3OCO5 293.27 unknown https://doi.org/10.1021/NP50055A017
> Alkaloids and derivatives / Proaporphines
Suavedol 442245 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1021/NP50055A017
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
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 https://doi.org/10.1135/CCCC19831513
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[5-(1,3-Benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13844298 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown https://doi.org/10.1016/S0031-9422(00)81846-4
Aristolignin 26213322 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)81846-4
Calopiptin 12302265 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown https://doi.org/10.1016/S0031-9422(00)81846-4
Zuihonin A 338287 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)81846-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 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 https://doi.org/10.1021/NP50055A017

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