Buddleja globosa

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

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

Description Top

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Buddleja globosa, also known as the orange-ball-tree, is a flowering plant found in Chile and Argentina. It can grow up to 5 meters tall and has grey bark and lanceolate or elliptic leaves. The plant produces deep-yellow to orange flowers with a strong honey scent. It is dioecious, meaning that each plant has either male or female parts. B. globosa is commonly grown as an ornamental shrub in temperate regions and has been awarded the Royal Horticultural Society's Award of Garden Merit. There are also several cultivars and hybrids of this plant. In folk medicine, B. globosa is believed to have wound healing properties and its leaves are used to treat wounds, burns, and ulcers. Chemical studies have identified various compounds in this species, including flavonoids, phenylethanoids, and terpenoids.

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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Filter by language:

Language	Common/alternative name
English	orange-ball-tree
Spanish	matico (buddleja globosa)
Spanish	paiquil
Spanish	palguin
Spanish	palguín
Spanish	panil
Spanish	pañil
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

Africa click to expand
- Middle Atlantic Ocean
  - Ascension

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Northern Europe
  - Great Britain

Southern America click to expand
- Southern South America
  - Argentina South
  - Chile Central
  - Chile North
  - Chile South
  - Juan Fernández Islands

Links to other databases Top

Suggest others/fix!

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

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

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

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

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

“The climate itself must have hidden some medicines”: traditional veterinary medicine of indigenous and non-indigenous campesinos of the southern Andes

Olivares F, Marchant C, Ibarra JT

J Ethnobiol Ethnomed

03-May-2022

PMCID:	PMC9063118
doi:	10.1186/s13002-022-00534-8
PMID:	35501874

A systematic review of the outcomes reported in the treatment of uncomplicated urinary tract infection clinical trials

Duane S, Beecher C, Vellinga A, Murphy AW, Cormican M, Smyth A, Healy P, Moore M, Little P, Devane D

JAC Antimicrob Resist

16-Mar-2022

PMCID:	PMC8944192
doi:	10.1093/jacamr/dlac025
PMID:	35350132

Patterns of Traditional and Modern Uses of Wild Edible Native Plants of Chile: Challenges and Future Perspectives

León-Lobos P, Díaz-Forestier J, Díaz R, Celis-Diez JL, Diazgranados M, Ulian T

Plants (Basel)

11-Mar-2022

PMCID:	PMC8953413
doi:	10.3390/plants11060744
PMID:	35336626

Honeybee Pollen From Southern Chile: Phenolic Profile, Antioxidant Capacity, Bioaccessibility, and Inhibition of DNA Damage

Bridi R, Echeverría J, Larena A, Nuñez Pizarro P, Atala E, De Camargo AC, Oh WY, Shahidi F, Garcia O, Ah-Hen KS, Montenegro G

Front Pharmacol

07-Mar-2022

PMCID:	PMC8937017
doi:	10.3389/fphar.2022.775219
PMID:	35321331

Multifarious global flora fabricated phytosynthesis of silver nanoparticles: a green nanoweapon for antiviral approach including SARS-CoV-2

Karthik C, Punnaivalavan KA, Prabha SP, Caroline DG

Int Nano Lett

12-Feb-2022

PMCID:	PMC8853038
doi:	10.1007/s40089-022-00367-z
PMID:	35194512

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 CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC=CC1=CC=C(C=C1)O	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 CC1C(C(OC1=O)CCCCCCCCCCCCCC(C)O)C(=O)O	370.50	unknown	https://doi.org/10.1021/NP0001023 https://doi.org/10.1021/NP990092+ https://doi.org/10.1016/S0031-9422(03)00264-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Buddlejone	9972034	Click to see CC(C)C1=C(C2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C)O	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/10.1021/NP0001023 https://doi.org/10.1016/S0031-9422(03)00264-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-en-3-one	5352042	Click to see CC1=CCCC(=C)C2CC(C2CC1=O)(C)C	218.33	unknown	https://doi.org/10.1021/NP990092+
(2E,6E,11S)-4,4,7,11-tetramethylcycloundeca-2,6-dien-1-one	162906349	Click to see CC1CCCC(=CCC(C=CC1=O)(C)C)C	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 A	5281514	Click to see CC1=CCCC(=C)C2CC(C2C(C1=O)OC(=O)C)(C)C	276.40	unknown	https://doi.org/10.1021/NP0001023 https://doi.org/10.1016/S0031-9422(03)00264-4 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/10.1021/NP0001023 https://doi.org/10.1021/NP990092+ https://doi.org/10.1016/S0031-9422(03)00264-4
dihydrobuddledin A	10588681	Click to see CC1CCCC(=C)C2CC(C2C(C1=O)OC(=O)C)(C)C	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 CC=C(C)C(=O)OC1CC(C=CC(C(=CC2C1C(=C)C(=O)O2)C)O)(C)O	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 CC1CC2(C3(C4C(O2)CC5C46CC(C7C5CCC8C7(CC(C(C8)OC(=O)C)OC(=O)C)C)OC6O3)C)OC1(C)C	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 C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O	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 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
[(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
6-O-methylcatalpol	53248734	Click to see COC1C2C=COC(C2C3(C1O3)CO)OC4C(C(C(C(O4)CO)O)O)O	376.36	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
Catalpol	91520	Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O	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
> 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/10.1016/S0378-8741(01)00297-5 https://doi.org/10.1055/S-2006-961903
> 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 CC1CCCC(=O)C(=CC(C=CC1=O)(C)C)C	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 CC1CCCC(=O)C(=CC(C=CC1=O)(C)C)C	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 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(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 C1=CC(=CC=C1C=CC(=O)O)O	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/10.1016/0378-8741(84)90075-8 https://doi.org/10.1016/S0378-8741(01)00297-5
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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	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
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
Linarin	5317025	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O	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/10.1021/NP0001023 https://doi.org/10.1016/S0031-9422(03)00264-4

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Buddleja globosa

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top