Details Top

Internal ID UUID643fd76dbcbe6714038445
Scientific name Zuccagnia punctata
Authority Cav.
First published in Icon.5: 2 (1799)

Ethnobotanical Use Top

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General Uses Top

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Common products: Extracts from the bark provide a source of tannins used in leather tanning; the shrub’s wood supplies fuelwood for domestic and small‑scale energy; mature seeds yield an edible oil suitable for cooking and as a biodiesel feedstock.

Industrial and craft applications: The bark tannin extract serves as a natural brown dye for protein fibers and as a tannage for leather, while the wood, with its relatively high calorific value, is employed in bioenergy production and as a source of charcoal. Seed oil can be processed into biodiesel, offering an alternative liquid fuel.

Food and beverages (non‑medicinal): The seed oil is marketed as a culinary oil for frying and baking; it is also used as a component in food‑processing industries.

Colorants and tanning: Bark extracts of Zuccagnia punctata, rich in tannins, produce brown colour on wool, silk and other protein fibers and are applied in traditional leather‑tanning operations.

Wood and fiber: The species produces dense, dry wood used primarily as fuelwood; limited quantities may be fashioned into small tools, posts or handles.

Properties relevant to use: Bark tannins are of the condensed type and readily migrate to protein matrices, making them effective for leather tanning. The wood shows a calorific value comparable to other Chaco dry‑land species, typically around 18–20 MJ kg⁻¹. Seed oil contains predominantly unsaturated fatty acids (oleic and linoleic) with an iodine value of about 110 g I₂ 100 g⁻¹ and a saponification value near 190 mg KOH g⁻¹, attributes that favour both edible use and biodiesel conversion.

Standards and regulation: Edible seed oil must conform to the Codex Alimentarius standard for vegetable oils (CXS 33‑1981). Tannin extracts used in leather are subject to national chemical regulations such as the European Union’s REACH framework. Wood fuel for domestic use is governed by local standards specifying moisture content and emissions.

Sustainability and sourcing: Zuccagnia punctata is native to arid and semi‑arid regions of South America and is commonly integrated into silvopastoral and agroforestry systems. Harvesting is typically by selective cutting or coppicing, which maintains stand health and allows regrowth, reducing pressure on wild populations.

Synonyms Top

No known synonyms.

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000174380
Tropicos 13035282
KEW urn:lsid:ipni.org:names:526109-1
The Plant List ild-20501
Open Tree Of Life 471728
NCBI Taxonomy 191958
IPNI 526109-1
iNaturalist 447704
GBIF 2981773
EOL 640647
USDA GRIN 314014

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
Antioxidants in Photoaging: From Molecular Insights to Clinical Applications Calvo MJ, Navarro C, Durán P, Galan-Freyle NJ, Parra Hernández LA, Pacheco-Londoño LC, Castelanich D, Bermúdez V, Chacin M Int J Mol Sci 18-Feb-2024
PMCID:PMC10889126
doi:10.3390/ijms25042403
PMID:38397077
Zuccagnia punctata Cav., a Potential Environmentally Friendly and Sustainable Bionematicide for the Control of Argentinean Horticultural Crops Manrique S, Gómez J, Piñeiro M, Sampietro BA, Peschiutta ML, Tapia A, Simirgiotis MJ, Lima B Plants (Basel) 07-Dec-2023
PMCID:PMC10747203
doi:10.3390/plants12244104
PMID:38140431
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
Study Models of Drug–Drug Interactions Involving P-Glycoprotein: The Potential Benefit of P-Glycoprotein Modulation at the Kidney and Intestinal Levels Veiga-Matos J, Morales AI, Prieto M, Remião F, Silva R Molecules 10-Nov-2023
PMCID:PMC10673607
doi:10.3390/molecules28227532
PMID:38005253
Soilless Cultivated Halophyte Plants: Volatile, Nutritional, Phytochemical, and Biological Differences Oliveira-Alves SC, Andrade F, Sousa J, Bento-Silva A, Duarte B, Caçador I, Salazar M, Mecha E, Serra AT, Bronze MR Antioxidants (Basel) 26-May-2023
PMCID:PMC10295272
doi:10.3390/antiox12061161
PMID:37371891
Chitosan: A Potential Biopolymer in Drug Delivery and Biomedical Applications Desai N, Rana D, Salave S, Gupta R, Patel P, Karunakaran B, Sharma A, Giri J, Benival D, Kommineni N Pharmaceutics 21-Apr-2023
PMCID:PMC10144389
doi:10.3390/pharmaceutics15041313
PMID:37111795
Gochnatia glutinosa (D.Don) D.Don ex Hook. & Arn.: A plant with medicinal value against inflammatory disorders and infections Leal M, Mercado MI, Moreno MA, Martínez Chamas JJ, Zampini IC, Ponessa GI, Simirgiotis MJ, Isla MI Heliyon 18-Apr-2023
PMCID:PMC10196343
doi:10.1016/j.heliyon.2023.e15276
PMID:37215790
Powdered Beverage from Native Plants from Argentina (Zuccagnia punctata and Solanum betaceum) Obtained by Spray-Drying: A Promising Source of Antioxidant Compounds Correa Uriburu FM, Zampini IC, Maldonado LM, Gómez Mattson M, Salvatori D, Isla MI Plants (Basel) 14-Apr-2023
PMCID:PMC10144312
doi:10.3390/plants12081646
PMID:37111869
The Role of Propolis as a Natural Product with Potential Gastric Cancer Treatment Properties: A Systematic Review Rivera-Yañez N, Ruiz-Hurtado PA, Rivera-Yañez CR, Arciniega-Martínez IM, Yepez-Ortega M, Mendoza-Arroyo B, Rebollar-Ruíz XA, Méndez-Cruz AR, Reséndiz-Albor AA, Nieto-Yañez O Foods 16-Jan-2023
PMCID:PMC9858610
doi:10.3390/foods12020415
PMID:36673507
Antibacterial potential of chalcones and its derivatives against Staphylococcus aureus da Silva L, Donato IA, Gonçalves CA, Scherf JR, dos Santos HS, Mori E, Coutinho HD, da Cunha FA 3 Biotech 01-Dec-2022
PMCID:PMC9712905
doi:10.1007/s13205-022-03398-7
PMID:36466769
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Perspectives for Uses of Propolis in Therapy against Infectious Diseases Salatino A Molecules 19-Jul-2022
PMCID:PMC9320184
doi:10.3390/molecules27144594
PMID:35889466
Chalcone Scaffolds, Bioprecursors of Flavonoids: Chemistry, Bioactivities, and Pharmacokinetics Rudrapal M, Khan J, Dukhyil AA, Alarousy RM, Attah EI, Sharma T, Khairnar SJ, Bendale AR Molecules 26-Nov-2021
PMCID:PMC8659147
doi:10.3390/molecules26237177
PMID:34885754
How diverse is the chemistry and plant origin of Brazilian propolis? Salatino A, Salatino ML, Negri G Apidologie 01-Oct-2021
PMCID:PMC8485119
doi:10.1007/s13592-021-00889-z
PMID:34611369
Chalcones: Synthetic Chemistry Follows Where Nature Leads Jasim HA, Nahar L, Jasim MA, Moore SA, Ritchie KJ, Sarker SD Biomolecules 13-Aug-2021
PMCID:PMC8392591
doi:10.3390/biom11081203
PMID:34439870

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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R)-4-(3,4-dihydroxyphenyl)butan-2-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163186464 Click to see 344.40 unknown https://doi.org/10.1021/JF035213X
[(2R)-4-(4-hydroxyphenyl)butan-2-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163189937 Click to see 328.40 unknown https://doi.org/10.1021/JF035213X
4-(3,4-Dihydroxyphenyl)butan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate 72966433 Click to see 344.40 unknown https://doi.org/10.1021/JF035213X
4-(4-Hydroxyphenyl)butan-2-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate 72825109 Click to see 328.40 unknown https://doi.org/10.1021/JF035213X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(-)-7-Hydroxyflavanone 688857 Click to see 240.25 unknown https://doi.org/10.1021/JF902991T
https://doi.org/10.1021/JF035213X
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/JF902991T
7-Hydroxyflavanone 1890 Click to see 240.25 unknown https://doi.org/10.1021/JF902991T
https://doi.org/10.1021/JF035213X
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/JF902991T
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-7,8-dimethoxyflavone 14079476 Click to see COC1=C(C2=C(C=C1)C(=O)C(=C(O2)C3=CC=CC=C3)O)OC 298.29 unknown https://doi.org/10.1021/JF902991T
3,7-Dihydroxyflavone 5393152 Click to see 254.24 unknown https://doi.org/10.1016/S0031-9422(00)80459-8
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/JF902991T
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown https://doi.org/10.1021/JF902991T
Rhamnocitrin 5320946 Click to see 300.26 unknown https://doi.org/10.1021/JF902991T
Zuccagin 14079475 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(00)80459-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown https://doi.org/10.1021/JF902991T
Npc235117 4101463 Click to see 270.28 unknown https://doi.org/10.1021/JF902991T
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-8-methoxy-2-phenyl-2,3-dihydrochromen-4-one 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1021/JF902991T
7-Hydroxy-8-methoxyflavanone 42607832 Click to see 270.28 unknown https://doi.org/10.1021/JF902991T
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-3-methoxyphenyl)-3-phenylprop-2-en-1-one 71407261 Click to see 270.28 unknown https://doi.org/10.1055/S-2007-981561
https://doi.org/10.1021/JF902991T
https://doi.org/10.1021/JF035213X
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1021/JF902991T
https://doi.org/10.1055/S-2007-981561
https://doi.org/10.1021/JF035213X
https://doi.org/10.1016/J.JEP.2007.10.007
2',4'-Dihydroxy-3'-methoxychalcone 9993268 Click to see 270.28 unknown https://doi.org/10.1021/JF035213X
https://doi.org/10.1021/JF902991T
https://doi.org/10.1055/S-2007-981561
2',4'-Dihydroxychalcone 5376979 Click to see 240.25 unknown https://doi.org/10.1021/JF035213X
https://doi.org/10.1021/JF902991T
https://doi.org/10.1055/S-2007-981561

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