Details Top

Internal ID UUID64404d8c17350602697414
Scientific name Zanthoxylum coco
Authority Gillies ex Hook. & Arn.
First published in Bot. Misc. 3: 168 (1833)

Ethnobotanical Use Top

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Synonyms Top

Scientific name Authority First published in
Zanthoxylum stipitatum Engl. Fl. Bras. 12(2): 161 (1874)
Fagara coco Engl. Nat. Pflanzenfam. [Engler & Prantl] iii. IV. 117.

Common names Top

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Language Common/alternative name
Spanish cochucho
Spanish cura tura
Spanish cura turá
Spanish curá turá
Spanish sauco hediondo
Spanish sauco oloroso
Chinese 梗花椒

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001133181
Tropicos 28101456
KEW urn:lsid:ipni.org:names:775658-1
The Plant List tro-28101456
Open Tree Of Life 5747726
NCBI Taxonomy 2099532
IUCN Red List 158461856
IPNI 775658-1
iNaturalist 887202
GBIF 3832175
Freebase /m/02rhq_x
USDA GRIN 42189
Wikipedia Zanthoxylum_coco

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
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Innovative Bioactive Nanofibrous Materials Combining Medicinal and Aromatic Plant Extracts and Electrospinning Method Stoyanova N, Nachev N, Spasova M Membranes (Basel) 21-Oct-2023
PMCID:PMC10608671
doi:10.3390/membranes13100840
PMID:37888012
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
Phylobioactive hotspots in plant resources used to treat Chagas disease Salm A, Krishnan SR, Collu M, Danton O, Hamburger M, Leonti M, Almanza G, Gertsch J iScience 15-Mar-2021
PMCID:PMC8040286
doi:10.1016/j.isci.2021.102310
PMID:33870129
Synthetic Lethal Activity of Benzophenanthridine Alkaloids From Zanthoxylum coco Against BRCA1-Deficient Cancer Cells García IA, Pansa MF, Pacciaroni AD, García ME, Gonzalez ML, Oberti JC, Bocco JL, Carpinella MC, Barboza GE, Nicotra VE, Soria G Front Pharmacol 03-Dec-2020
PMCID:PMC7793782
doi:10.3389/fphar.2020.593845
PMID:33424604
Unprecedented plant species loss after a decade in fragmented subtropical Chaco Serrano forests Aguilar R, Calviño A, Ashworth L, Aguirre-Acosta N, Carbone LM, Albrieu-Llinás G, Nolasco M, Ghilardi A, Cagnolo L PLoS One 28-Nov-2018
PMCID:PMC6261552
doi:10.1371/journal.pone.0206738
PMID:30485340
In Vitro Anti-Cholinesterase and Antioxidant Activity of Extracts of Moringa oleifera Plants from Rivers State, Niger Delta, Nigeria Nwidu LL, Elmorsy E, Aprioku JS, Siminialayi I, Carter WG Medicines (Basel) 05-Jul-2018
PMCID:PMC6164601
doi:10.3390/medicines5030071
PMID:29976887
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Parrots as key multilinkers in ecosystem structure and functioning Blanco G, Hiraldo F, Rojas A, Dénes FV, Tella JL Ecol Evol 04-Sep-2015
PMCID:PMC4588639
doi:10.1002/ece3.1663
PMID:26445664
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
The Role of Small Woodland Remnants on Ground Dwelling Insect Conservation in Chaco Serrano, Central Argentina Moreno ML, Fernández MG, Molina SI, Valladares G J Insect Sci 13-May-2013
PMCID:PMC3738104
doi:10.1673/031.013.4001
PMID:23902409
Fagara coco Gill. (Zanthoxylum coco Gill.) Shakhnoza S. Azimova, Anna I. Glushenkova Springer London 05-Jan-2012
doi:10.1007/978-0-85729-323-7_2697
Medicinal plants used for traditional veterinary in the Sierras de Córdoba (Argentina): An ethnobotanical comparison with human medicinal uses Martínez GJ, Luján MC J Ethnobiol Ethnomed 04-Aug-2011
PMCID:PMC3163512
doi:10.1186/1746-4269-7-23
PMID:21816043
Effect of plant extracts on Alzheimer's disease: An insight into therapeutic avenues Obulesu M, Rao DM J Neurosci Rural Pract 01-Jan-2011
PMCID:PMC3122981
doi:10.4103/0976-3147.80102
PMID:21716802
Aurapten and Flindersine From Zanthoxylum coco Miguel A. Muñoz, René Torres, Bruce K. Cassels American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50021A023

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 / Protopine alkaloids
2,3-Dimethoxy-6-methyl-5,7,8,15-tetrahydro-[1,3]dioxolo[4',5':4,5]benzo[1,2-g]benzo[c]azecin-14(6H)-one 15559220 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC(=C(C=C4C1)OC)OC)OCO3 369.40 unknown https://doi.org/10.1021/JA01171A072
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Auraptene 1550607 Click to see 298.40 unknown https://doi.org/10.1007/978-0-85729-323-7_2697
https://doi.org/10.1021/NP50021A023
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8S,9R,10R,13S,14S,17S)-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] acetate 162869063 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(71)85016-1
Npc155187 521199 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(71)85016-1
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/0031-9422(71)85016-1
https://doi.org/10.1021/NP50021A023
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C 227.26 unknown https://doi.org/10.1007/978-0-85729-323-7_2697
https://doi.org/10.1021/NP50021A023

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