Aristotelia chilensis in Genus Aristotelia

Details Top

Internal ID	UUID64400ab8dad55518447012
Scientific name	Aristotelia chilensis
Authority	Stuntz
First published in	U.S.D.A. Bur. Pl. Industr. Invent. Seeds 31: 85 (1914)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Aristotelia glabra	Miers	Ann. Mag. Nat. Hist. , ser. 4, 2: 44 (1868)
Aristotelia glandulosa	Ruiz & Pav.	Syst. Veg. 125.
Aristotelia lucida	Salisb.	Prodr. Stirp. Chap. Allerton : 345 (1796)
Aristotelia macqui	L'Hér.	Stirp. Nov. : 31 (1786)
Aristotelia macqui var. alpestris	Reiche	Anales Univ. Chile 100: 539 1898
Aristotelia maqui var. andina	Phil.	Linnaea 33(1): 31. 1864 [May 1864]
Aristotelia macqui var. leucocarpa	Dimitri	Colecc. Ci. Inst. Nac. Tecnol. Agropecu 10: 221 1972
Beaumaria macqui	Deless. ex Steud.	Nomencl. Bot. [Steudel], ed. 2. i. 192 (1840).
Aristotelia macqui var. brachystyla	Kurz.

Common names Top

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Filter by language:

Language	Common/alternative name
English	maquei
Spanish	cornus chilensis
Spanish	aristotelia maqui
Spanish	queldron
Spanish	queldrón
Hebrew	תות יין צ'יליאני
Thai	มากี้เบอร์รี่
Chinese	酒果
Chinese	馬基果
Chinese	玛基果

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

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

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000548488
UNII	PSW0238Q5L
USDA Plants	ARCH17
Tropicos	11700096
KEW	urn:lsid:ipni.org:names:19666-2
The Plant List	kew-2652039
Open Tree Of Life	126270
NCBI Taxonomy	138855
IPNI	19666-2
iNaturalist	181593
GBIF	5651082
Freebase	/m/07k5c3c
EPPO	AITCH
EOL	5427657
Calflora (Californian flora)	8551
USDA GRIN	4201
Wikipedia	Aristotelia_chilensis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_008921755.1	MAQUI01	Scaffold	INIA	2019-10-08	30.0x	91.89 Mb

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

A Review of the Functional Characteristics and Applications of Aristotelia chilensis (Maqui Berry), in the Food Industry

García-Milla P, Peñalver R, Nieto G

Foods

09-Mar-2024

PMCID:	PMC10969556
doi:	10.3390/foods13060838
PMID:	38540828

Nanoencapsulation of Maqui (Aristotelia chilensis) Extract in Chitosan–Tripolyphosphate and Chenopodin-Based Systems

Andrade D, Maldonado-Bravo F, Alburquerque A, Pérez C, Gamboa A, Caro N, Díaz-Dosque M, Gotelland M, Abugoch L, Tapia C

Antioxidants (Basel)

23-Feb-2024

PMCID:	PMC10967421
doi:	10.3390/antiox13030273
PMID:	38539807

Phenolic composition and bioactivity of Ribes magellanicum fruits from southern Patagonia

Burgos-Edwards A, Theoduloz C, Miño S, Ghosh D, Shulaev V, Ramírez C, Sánchez-Jardón L, Rozzi R, Schmeda-Hirschmann G

Heliyon

11-Feb-2024

PMCID:	PMC10877167
doi:	10.1016/j.heliyon.2024.e25542
PMID:	38380002

Effects of polyphenolic maqui (Aristotelia chilensis) extract on the inhibition of NLRP3 inflammasome and activation of mast cells in a mouse model of Crohn’s disease-like colitis

Ortiz-Cerda T, Argüelles-Arias F, Macías-García L, Vázquez-Román V, Tapia G, Xie K, García-García MD, Merinero M, García-Montes JM, Alcudia A, Witting PK, De-Miguel M

Front Immunol

12-Jan-2024

PMCID:	PMC10811055
doi:	10.3389/fimmu.2023.1229767
PMID:	38283356

Delphinidins from Maqui Berry (Aristotelia chilensis) ameliorate the subcellular organelle damage induced by blue light exposure in murine photoreceptor-derived cells

Yamazaki K, Ishida K, Otsu W, Muramatsu A, Nakamura S, Yamada W, Tsusaki H, Shimoda H, Hara H, Shimazawa M

BMC Complement Med Ther

02-Jan-2024

PMCID:	PMC10759685
doi:	10.1186/s12906-023-04322-z
PMID:	38167061

Assessment of the Physicochemical, Antioxidant, Microbial, and Sensory Attributes of Yogurt-Style Products Enriched with Probiotic-Fermented Aronia melanocarpa Berry Juice

Plessas S, Mantzourani I, Terpou A, Bekatorou A

Foods

28-Dec-2023

PMCID:	PMC10778934
doi:	10.3390/foods13010111
PMID:	38201137

Microwave Treatment vs. Conventional Pasteurization: The Effect on Phytochemical and Microbiological Quality for Citrus–Maqui Beverages

Salar FJ, Díaz-Morcillo A, Fayos-Fernández J, Monzó-Cabrera J, Sánchez-Bravo P, Domínguez-Perles R, Fernández PS, García-Viguera C, Periago PM

Foods

27-Dec-2023

PMCID:	PMC10778303
doi:	10.3390/foods13010101
PMID:	38201129

Phytophthora : taxonomic and phylogenetic revision of the genus

Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ

Stud Mycol

06-Oct-2023

PMCID:	PMC10825748
doi:	10.3114/sim.2023.106.05
PMID:	38298569

Anti-inflammatory natural products modulate interleukins and their related signaling markers in inflammatory bowel disease: A systematic review

Gandhi GR, Mohana T, Athesh K, Hillary VE, Vasconcelos AB, Farias de Franca MN, Montalvão MM, Ceasar SA, Jothi G, Sridharan G, Gurgel RQ, Xu B

J Pharm Anal

22-Sep-2023

PMCID:	PMC10785269
doi:	10.1016/j.jpha.2023.09.012
PMID:	38223446

Antimicrobial, Antioxidant, and Anti-Inflammatory Properties of Monofloral Honeys from Chile

Poulsen-Silva E, Gordillo-Fuenzalida F, Velásquez P, Llancalahuen FM, Carvajal R, Cabaña-Brunod M, Otero MC

Antioxidants (Basel)

21-Sep-2023

PMCID:	PMC10526086
doi:	10.3390/antiox12091785
PMID:	37760088

Deep learning for Chilean native flora classification: a comparative analysis

Figueroa-Flores C, San-Martin P

Front Plant Sci

11-Sep-2023

PMCID:	PMC10520280
doi:	10.3389/fpls.2023.1211490
PMID:	37767291

Genome-wide survey and characterization of microsatellites in cashew and design of a web-based microsatellite database: CMDB

Savadi S, Muralidhara BM, Venkataravanappa V, Adiga JD

Front Plant Sci

21-Aug-2023

PMCID:	PMC10475544
doi:	10.3389/fpls.2023.1242025
PMID:	37670858

Herbal Extracts of Ginseng and Maqui Berry Show Only Minimal Effects on an In Vitro Model of Early Fracture Repair of Smokers

Rinderknecht H, Mayer A, Histing T, Ehnert S, Nüssler A

Foods

04-Aug-2023

PMCID:	PMC10419284
doi:	10.3390/foods12152960
PMID:	37569229

The Effect of Berry Consumption on Oxidative Stress Biomarkers: A Systematic Review of Randomized Controlled Trials in Humans

Stote KS, Burns G, Mears K, Sweeney M, Blanton C

Antioxidants (Basel)

18-Jul-2023

PMCID:	PMC10376627
doi:	10.3390/antiox12071443
PMID:	37507981

The Role of Anthocyanins in Plant Tolerance to Drought and Salt Stresses

Dabravolski SA, Isayenkov SV

Plants (Basel)

05-Jul-2023

PMCID:	PMC10346810
doi:	10.3390/plants12132558
PMID:	37447119

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
(4,4-Dimethyl-8-methylene-3-azabicyclo[3.3.1]non-2-en-2-yl)(1H-indol-3-yl)methanone	369151	Click to see CC1(C2CCC(=C)C(C2)C(=N1)C(=O)C3=CNC4=CC=CC=C43)C	306.40	unknown	https://doi.org/10.1016/0031-9422(90)85469-V
[(1S,5S)-4,4-dimethyl-8-methylidene-3-azabicyclo[3.3.1]non-2-en-2-yl]-(1H-indol-3-yl)methanone	15816299	Click to see CC1(C2CCC(=C)C(C2)C(=N1)C(=O)C3=CNC4=CC=CC=C43)C	306.40	unknown	https://doi.org/10.1016/0031-9422(90)85469-V
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Hobartine	14636497	Click to see CC1=CCC2CC1C(NC2(C)C)CC3=CNC4=CC=CC=C43	294.40	unknown	https://doi.org/10.2307/4119066
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
[(3S)-2,3-dihydro-1H-indol-3-yl]-[(1R,5R)-4,4,8-trimethyl-3-azabicyclo[3.3.1]nona-2,7-dien-2-yl]methanone	162849310	Click to see CC1=CCC2CC1C(=NC2(C)C)C(=O)C3CNC4=CC=CC=C34	308.40	unknown	https://doi.org/10.1016/0031-9422(90)85469-V
2,3-dihydro-1H-indol-3-yl-(4,4,8-trimethyl-3-azabicyclo[3.3.1]nona-2,7-dien-2-yl)methanone	162849309	Click to see CC1=CCC2CC1C(=NC2(C)C)C(=O)C3CNC4=CC=CC=C34	308.40	unknown	https://doi.org/10.1016/0031-9422(90)85469-V
Aristotelone	323715	Click to see CC1(C2CCC3(C(C2)C(N1)CC34C(=O)C5=CC=CC=C5N4)C)C	310.40	unknown	https://doi.org/10.2307/4119066 https://doi.org/10.1016/S0031-9422(00)88987-6 https://doi.org/10.1076/PHBI.35.3.215.13297 https://doi.org/10.1039/P19800002842
Rdojzoukvjesiv-qacnyomvsa-	11023321	Click to see CC1(C2CCC3(C(C2)C(N1)CC34C(=O)C5=CC=CC=C5N4)C)C	310.40	unknown	https://doi.org/10.1039/P19800002842
Rdojzoukvjesiv-vslccporsa-	11056019	Click to see CC1(C2CCC3(C(C2)C(N1)CC34C(=O)C5=CC=CC=C5N4)C)C	310.40	unknown	https://doi.org/10.1016/S0031-9422(00)88987-6
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(1S,2R,4R,12S,15S,18R)-14,14,18-trimethyl-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-16-one	25085910	Click to see CC1(C2CC3C4N1C5C6=CC=CC=C6NC5(C4)C3(CC2=O)C)C	308.40	unknown	https://doi.org/10.1039/P19800002842 https://doi.org/10.1076/PHBI.35.3.215.13297 https://doi.org/10.2307/4119066
14,14,18-Trimethyl-5,13-diazahexacyclo[13.3.1.02,13.04,12.04,18.06,11]nonadeca-6,8,10-trien-16-one	5925099	Click to see CC1(C2CC3C4N1C5C6=CC=CC=C6NC5(C4)C3(CC2=O)C)C	308.40	unknown	https://doi.org/10.1039/P19800002842
> Organoheterocyclic compounds / Quinolidines
(1R,10R,12R,15S,17S,19R)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2,4,6,8-tetraene-10,19-diol	101600056	Click to see CC1(C2CC3C(N1)CC4(C5=CC=CC=C5N=C4C3(CC2O)C)O)C	326.40	unknown	https://doi.org/10.1039/P19800002842
1,14,14-Trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2,4,6,8-tetraen-10-ol	73098733	Click to see CC1(C2CCC3(C(C2)C(N1)CC4(C3=NC5=CC=CC=C54)O)C)C	310.40	unknown	https://doi.org/10.1076/PHBI.35.3.215.13297
Aristotelinine	430968	Click to see CC1(C2CC3C(N1)CC4(C5=CC=CC=C5N=C4C3(CC2O)C)O)C	326.40	unknown	https://doi.org/10.1039/P19800002842 https://doi.org/10.2307/4119066
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(1R,12R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8-tetraene	11098414	Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)C)C	294.40	unknown	https://doi.org/10.1039/P19800002842 https://doi.org/10.1016/S0031-9422(00)88987-6
(1R,15S,17S)-1,14,14-trimethyl-3,13-diazapentacyclo[13.2.2.02,10.04,9.012,17]nonadeca-2(10),4,6,8,12-pentaen-11-one	10957747	Click to see CC1(C2CCC3(C(C2)C(=N1)C(=O)C4=C3NC5=CC=CC=C54)C)C	306.40	unknown	https://doi.org/10.2307/4119066
Aristoteline	323714	Click to see CC1(C2CCC3(C(C2)C(N1)CC4=C3NC5=CC=CC=C45)C)C	294.40	unknown	https://doi.org/10.2307/4119066 https://doi.org/10.1016/S0031-9422(00)88987-6 https://doi.org/10.1076/PHBI.35.3.215.13297 https://doi.org/10.1039/P19800002842
Aristotelinone	11130638	Click to see CC1(C2CCC3(C(C2)C(N1)C(=O)C4=C3NC5=CC=CC=C54)C)C	308.40	unknown	https://doi.org/10.2307/4119066 https://doi.org/10.1016/0031-9422(90)85469-V https://doi.org/10.1076/PHBI.35.3.215.13297
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1016/0031-9422(93)85383-3

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Aristotelia chilensis

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