Details Top

Internal ID UUID64400e0ab2095448600131
Scientific name Buddleja globosa
Authority Hope
First published in Verh. Holl. Maatsch. Weetensch. Haarlem 20(2): 417 (1782)

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.

Ethnobotanical records document several traditional preparations of Buddleja globosa, commonly called matico or palguín in Chile, primarily involving external applications for wound healing. In traditional Mapuche medicine of southern Chile, freshly crushed leaves are applied directly as a poultice to cuts, ulcers, and burns (Bennett et al., 2021). Across southern Chile and Argentine Patagonia, infusions of leaves serve as washes for inflamed skin and minor wounds, believed to cleanse and promote tissue repair (Hoffmann, 2003). Additionally, historical records from Andean communities describe decoctions of the whole aerial parts used to rinse wounds and treat gum infections (Hoffmann, 1999). Tinctures macerated in alcohol have also been employed in Chilean folk medicine, typically diluted for topical application to slow-healing sores (Gallo, 1982).

A practical preparation for a traditional **ptic poultice**: Gather 2–3 fresh young leaves of *Buddleja globosa*. Wash thoroughly and crush them into a coarse paste using a mortar and pestle. Apply this paste directly to the affected skin area, covering with a sterile bandage. Refresh the poultice twice daily until the wound shows improvement. *Use only externally.* Avoid ingestion during pregnancy or breastfeeding (Bennett et al., 2021).

Phytochemical studies on *Buddleja globosa* have identified bioactive compounds relevant to its traditional use, including antioxidant flavonoids like quercetin and luteolin, along with anti-inflammatory iridoids such as harpagide. These compounds are believed to contribute to its wound-healing and soothing properties (Simirgiotis et al., 2013).

Modern relevance remains evident: ongoing research investigates its wound-healing potential (Muñoz et al., 2016), while dried aerial parts and commercial preparations are still used in some Chilean herbal practices for skin conditions (Hoffmann, 2003).

General Uses Top

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Industrial and craft applications:
Buddleja globosa is cultivated as an ornamental shrub, especially in Chile, Argentina, and the UK, valued for late winter–spring bloom and fragrant, spherical inflorescences that attract pollinators; it is used in urban landscaping and park plantings. In beekeeping regions of central–southern Chile, flowers yield nectar and pollen over an extended period, supporting honey production and hive maintenance during transitional seasons; the plant is described as melliferous.

Food and beverages (non-medicinal):
Flower nectar is collected by Apis mellifera and is a component of unifloral or multifloral honey; it is not processed into a standalone food product.

Fragrance and cosmetics:
Dried flowers may be used in potpourri for their scent; no standardized essential oil production is reported for this taxon.

Sustainability and sourcing:
Propagation is by seed or cuttings; the species tolerates pruning and thrives in well-drained soils and partial sun, enabling repeated harvest of inflorescences for pollinator support; mature plants may regenerate vegetatively. No regulatory framework specific to B. globosa as a minor horticultural or beekeeping crop is identified.

Synonyms Top

Scientific name Authority First published in
Buddleja capitata Jacq. Icon. Pl. Rar. 2: 9 (1788)
Buddleja connata Ruiz & Pav. Fl. Peruv. 1: 52 (1798)
Buddleja globifera Mirb. Traité Arbr. Arbust. 1: t. 25 (1800)

Common names Top

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Language Common/alternative name
English orange-ball-tree
Spanish matico (buddleja globosa)
Spanish paiquil
Spanish palguin
Spanish palguín
Spanish panil
Spanish pañil
Spanish buddleja capitata
Spanish buddleja connata
Spanish buddleja globifera
Welsh coeden-fêl peli oren
Quechua china kiswara
Quechua china kiswar
Swedish bollbuddleja
Chinese 球花醉鱼草

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
      • Argentina South
      • Chile Central
      • Chile North
      • Chile South
      • Juan Fernández Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000574052
USDA Plants BUGL6
Tropicos 19000593
INPN 86870
KEW urn:lsid:ipni.org:names:545763-1
The Plant List kew-2685433
Open Tree Of Life 83888
Observations.org 126601
NCBI Taxonomy 168495
NBN Atlas NBNSYS0000014964
IPNI 545763-1
iNaturalist 371666
GBIF 6387494
Freebase /m/03g_w9h
EPPO BUDGL
EOL 5641945
Elurikkus 578256
USDA GRIN 8089
Wikipedia Buddleja_globosa

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
Characterization of the Metabolic Profile of Olive Tissues (Roots, Stems and Leaves): Relationship with Cultivars’ Resistance/Susceptibility to the Soil Fungus Verticillium dahliae Serrano-García I, Olmo-García L, Monago-Maraña O, de Alba IM, León L, de la Rosa R, Serrano A, Gómez-Caravaca AM, Carrasco-Pancorbo A Antioxidants (Basel) 15-Dec-2023
PMCID:PMC10741231
doi:10.3390/antiox12122120
PMID:38136239
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
The Most Potent Natural Pharmaceuticals, Cosmetics, and Food Ingredients Isolated from Plants with Deep Eutectic Solvents Wawoczny A, Gillner D J Agric Food Chem 11-Jul-2023
PMCID:PMC10375538
doi:10.1021/acs.jafc.3c01656
PMID:37433265
Analysis of the Polyphenolic Composition of Vaccinium L. Extracts and Their Protective Effect on Red Blood Cell Membranes Kaźmierczak T, Bonarska-Kujawa D, Męczarska K, Cyboran-Mikołajczyk S, Oszmiański J, Kapusta I Membranes (Basel) 07-Jun-2023
PMCID:PMC10303154
doi:10.3390/membranes13060589
PMID:37367793
Characteristics, Isolation Methods, and Biological Properties of Aucubin Kartini K, Irawan MA, Setiawan F, Jayani NI Molecules 17-May-2023
PMCID:PMC10222036
doi:10.3390/molecules28104154
PMID:37241895
Antioxidant Activity as an Indicator of the Efficiency of Plant Extract-Mediated Synthesis of Zinc Oxide Nanoparticles Vera J, Herrera W, Hermosilla E, Díaz M, Parada J, Seabra AB, Tortella G, Pesenti H, Ciudad G, Rubilar O Antioxidants (Basel) 23-Mar-2023
PMCID:PMC10135172
doi:10.3390/antiox12040784
PMID:37107159
Anti-Inflammatory Chilean Endemic Plants Otero C, Klagges C, Morales B, Sotomayor P, Escobar J, Fuentes JA, Moreno AA, Llancalahuen FM, Arratia-Perez R, Gordillo-Fuenzalida F, Herrera M, Martínez JL, Rodríguez-Díaz M Pharmaceutics 10-Mar-2023
PMCID:PMC10051824
doi:10.3390/pharmaceutics15030897
PMID:36986757
Blending Approach Preparation of PVA-g-PMA Films with Embedded “Green” Synthesized Silver Nanoparticles for Acetone Optical Detection Lazarova K, Christova D, Karashanova D, Georgieva B, Marovska G, Slavov A, Babeva T Sensors (Basel) 08-Mar-2023
PMCID:PMC10056088
doi:10.3390/s23062941
PMID:36991647
Use of medicinal plants by veterinary practitioners in Spain: A cross-sectional survey Romero B, Susperregui J, Sahagún AM, Diez MJ, Fernández N, García JJ, López C, Sierra M, Díez R Front Vet Sci 15-Dec-2022
PMCID:PMC9797804
doi:10.3389/fvets.2022.1060738
PMID:36590819
Formulation of water-soluble Buddleja globosa Hope extracts and characterization of their antimicrobial properties against Pseudomonas aeruginosa Araya N, Leiva-Soto MA, Bruna MV, Castro-Munoz A, Behrend-Keim B, Moraga-Espinoza D, Bahamondez-Canas TF Front Pharmacol 10-Nov-2022
PMCID:PMC9685521
doi:10.3389/fphar.2022.921511
PMID:36438832
Green Route to Produce Silver Nanoparticles Using the Bioactive Flavonoid Quercetin as a Reducing Agent and Food Anti-Caking Agents as Stabilizers Ramírez-Rosas SL, Delgado-Alvarado E, Sanchez-Vargas LO, Herrera-May AL, Peña-Juarez MG, Gonzalez-Calderon JA Nanomaterials (Basel) 10-Oct-2022
PMCID:PMC9565511
doi:10.3390/nano12193545
PMID:36234674
Factors affecting local plant knowledge in isolated communities from Patagonian steppe: Metacommunity theory is revealed as a methodological approach Santoro FR, Richeri M, Ladio AH PLoS One 12-Sep-2022
PMCID:PMC9467323
doi:10.1371/journal.pone.0274481
PMID:36094933
Antimicrobial Properties of Chilean Native Plants: Future Aspects in Their Application in the Food Industry Otero MC, Fuentes JA, Atala C, Cuadros-Orellana S, Fuentes C, Gordillo-Fuenzalida F Foods 15-Jun-2022
PMCID:PMC9222376
doi:10.3390/foods11121763
PMID:35741959
Propolis: chemical diversity and challenges in quality control Kasote D, Bankova V, Viljoen AM Phytochem Rev 24-May-2022
PMCID:PMC9128321
doi:10.1007/s11101-022-09816-1
PMID:35645656

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
> Benzenoids / Benzene and substituted derivatives / Styrenes
3-(4-Hydroxyphenyl)prop-2-EN-1-YL docosanoate 71340295 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCC=CC1=CC=C(C=C1)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)98069-5
3-(4-Hydroxyphenyl)prop-2-enyl tetracosanoate 86051176 Click to see 500.80 unknown https://doi.org/10.1016/S0031-9422(00)98069-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
2-(14-Hydroxypentadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid 12888719 Click to see 370.50 unknown https://doi.org/10.1021/NP990092+
https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP0001023
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Buddlejone 9972034 Click to see 300.40 unknown https://doi.org/10.1021/NP0001023
Deoxybuddlejone 10334095 Click to see CC(C)C1=CC=C2C(=CCC3C2(CCCC3(C)C)C)C1=O 284.40 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP0001023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,4E,9S)-2-(Acetyloxy)-4,11,11-trimethyl-8-methylenebicyclo(7.2.0)undec-4-en-3-one 5281514 Click to see 276.40 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP990092+
https://doi.org/10.1021/NP0001023
(2E,6E,11S)-4,4,7,11-tetramethylcycloundeca-2,6-dien-1-one 162906349 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
(2Z,6Z)-4,4,7,11-tetramethylcycloundeca-2,6-dien-1-one 100951543 Click to see CC1CCCC(=CCC(C=CC1=O)(C)C)C 220.35 unknown https://doi.org/10.1021/NP990092+
Buddledin B 44593338 Click to see CC1=CCCC(=C)C2CC(C2C(C1=O)O)(C)C 234.33 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP990092+
https://doi.org/10.1021/NP0001023
Buddledin C 5352042 Click to see 218.33 unknown https://doi.org/10.1021/NP990092+
Dihydrobuddledin A 10588681 Click to see 278.40 unknown https://doi.org/10.1021/NP990092+
Zerumbone 5470187 Click to see CC1=CCC(C=CC(=O)C(=CCC1)C)(C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP990092+
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/0378-8741(84)90075-8
https://doi.org/10.1055/S-2006-961903
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4R,6R,7E,9S,10Z,11aS)-6,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,9,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162989635 Click to see 362.40 unknown https://doi.org/10.1021/NP990092+
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0378-8741(84)90075-8
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0378-8741(84)90075-8
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0378-8741(84)90075-8
Maytenone 44558957 Click to see CC(C)C1(C2C3C4(CCC5C(CCCC5(C4=CC(=O)C3(C(C)C)O)C)(C)C)C(C1=O)C6=C2CCC7C6(CCCC7(C)C)C)O 604.90 unknown https://doi.org/10.1021/NP0001023
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
[(1R,2S,3S,3'S,6S,8S,9R,11S,12S,13S,15R,17R,18S,20S,21R)-9-acetyloxy-2',2',3',11,17-pentamethylspiro[14,16,19-trioxaheptacyclo[11.8.1.12,20.01,15.03,12.06,11.017,21]tricosane-18,5'-oxolane]-8-yl] acetate 11318945 Click to see 558.70 unknown https://doi.org/10.1021/NP990092+
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[[(1R,2S,6S)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107792 Click to see 362.33 unknown https://doi.org/10.1055/S-2006-961903
[(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] 4-hydroxybenzoate 162968459 Click to see 482.40 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
[(1S,2S,6R)-2-(hydroxymethyl)-10-[(2S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] 4-hydroxybenzoate 137705841 Click to see C1=COC(C2C1C(C3C2(O3)CO)OC(=O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 482.40 unknown https://doi.org/10.1055/S-2006-961903
Catalpol 91520 Click to see 362.33 unknown https://doi.org/10.1055/S-2006-961903
Catalposide 93039 Click to see C1=COC(C2C1C(C3C2(O3)CO)OC(=O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 482.40 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1055/S-2006-961903
Methylcatalpol 53248734 Click to see 376.36 unknown https://doi.org/10.1016/0378-8741(84)90075-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Echinacoside 5281771 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown https://doi.org/10.1055/S-2006-961903
https://doi.org/10.1016/S0378-8741(01)00297-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(2R,7Z,10E)-2,7,9,9-tetramethylcycloundeca-7,10-diene-1,6-dione 162985755 Click to see 234.33 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
(7Z,10Z)-2,7,9,9-tetramethylcycloundeca-7,10-diene-1,6-dione 100951544 Click to see 234.33 unknown https://doi.org/10.1021/NP990092+
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0378-8741(01)00297-5
https://doi.org/10.1016/0378-8741(93)90041-3
https://doi.org/10.1055/S-2006-961903
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1016/S0378-8741(98)00203-7
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1016/0378-8741(84)90075-8
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0378-8741(93)90041-3
https://doi.org/10.1016/S0378-8741(01)00297-5
https://doi.org/10.1016/S0378-8741(98)00203-7
https://doi.org/10.1055/S-2006-961903
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0378-8741(84)90075-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6-Hydroxyluteolin 5281642 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0378-8741(01)00297-5
https://doi.org/10.1016/0378-8741(84)90075-8
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0378-8741(84)90075-8
https://doi.org/10.1016/S0378-8741(01)00297-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/0378-8741(84)90075-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/0378-8741(84)90075-8
Linarin 5317025 Click to see 592.50 unknown https://doi.org/10.1016/S0378-8741(01)00297-5
https://doi.org/10.1016/0378-8741(84)90075-8
https://doi.org/10.1055/S-2006-961903
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',4,4',6-Tetrahydroxychalcone 54570259 Click to see C1=CC(=C(C=C1O)O)C=CC(=O)C2=C(C=C(C=C2)O)O 272.25 unknown https://doi.org/10.1016/S0031-9422(03)00264-4
https://doi.org/10.1021/NP0001023

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