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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Language	Common/alternative name
English	maquei
Spanish	cornus chilensis
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
PFAF	Aristotelia chilensis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

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

Dietary Sources, Stabilization, Health Benefits, and Industrial Application of Anthocyanins—A Review

Saini RK, Khan MI, Shang X, Kumar V, Kumari V, Kesarwani A, Ko EY

Foods

17-Apr-2024

PMCID:	PMC11049351
doi:	10.3390/foods13081227
PMID:	38672900

Extract from Aronia melanocarpa, Lonicera caerulea, and Vaccinium myrtillus Improves near Visual Acuity in People with Presbyopia

Szumny D, Kucharska AZ, Czajor K, Bernacka K, Ziółkowska S, Krzyżanowska-Berkowska P, Magdalan J, Misiuk-Hojło M, Sozański T, Szeląg A

Nutrients

23-Mar-2024

PMCID:	PMC11013737
doi:	10.3390/nu16070926
PMID:	38612968

Maize multi-omics reveal leaf water status controlling of differential transcriptomes, proteomes and hormones as mechanisms of age-dependent osmotic stress response in leaves

Niu L, Wang W, Li Y, Wu X, Wang W

Stress Biol

18-Mar-2024

PMCID:	PMC10948690
doi:	10.1007/s44154-024-00159-9
PMID:	38498254

Ameliorative effects of Tagetes erecta Linn. flower against desiccation stress-induced dry eye symptoms in the mice model

Lee H, Hwangbo H, Hyun JW, Shim JH, Leem SH, Kim GY, Choi YH

Integr Med Res

11-Mar-2024

PMCID:	PMC11070322
doi:	10.1016/j.imr.2024.101038
PMID:	38716164

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

Synthesis of α3β4 Nicotinic Acetylcholine Receptor Modulators Derived from Aristoquinoline that Reduce Reinstatement of Cocaine-Seeking Behavior

Rusali LE, Lopez-Hernandez AM, Kremiller KM, Kulkarni GC, Gour A, Straub CJ, Argade MD, Peters CJ, Sharma A, Toll L, Cippitelli A, Riley AP

J Med Chem

27-Dec-2023

PMCID:	PMC10872344
doi:	10.1021/acs.jmedchem.3c01758
PMID:	38151460

In Silico and In Vivo Evaluation of the Maqui Berry (Aristotelia chilensis (Mol.) Stuntz) on Biochemical Parameters and Oxidative Stress Markers in a Metabolic Syndrome Model

Castillo-García EL, Cossio-Ramírez AL, Córdoba-Méndez ÓA, Loza-Mejía MA, Salazar JR, Chávez-Gutiérrez E, Bautista-Poblet G, Castillo-Mendieta NT, Moreno DA, García-Viguera C, Pinto-Almazán R, Almanza-Pérez JC, Gallardo JM, Guerra-Araiza C

Metabolites

07-Dec-2023

PMCID:	PMC10744843
doi:	10.3390/metabo13121189
PMID:	38132871

Human Impacts on the Vegetation of the Juan Fernández (Robinson Crusoe) Archipelago

Stuessy TF, Crawford DJ, Greimler J

Plants (Basel)

30-Nov-2023

PMCID:	PMC10708367
doi:	10.3390/plants12234038
PMID:	38068673

Antioxidant Properties of Maqui Berry Extract (Aristotelia chilensis (Mol.) Stuntz) and Its Potential Photoprotective Role on Human Skin Fibroblasts

Wacewicz-Muczyńska M, Moskwa J, Puścion-Jakubik A, Naliwajko SK, Niczyporuk M, Socha K

Molecules

27-Nov-2023

PMCID:	PMC10708373
doi:	10.3390/molecules28237802
PMID:	38067532

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