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Luma chequen

Luma chequen - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe1dad8592194039705
Scientific name Luma chequen
Authority (Molina) A.Gray
First published in U.S. Expl. Exped., Phan. 1: 536 (1854)

Description Top

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Synonyms Top

Scientific name Authority First published in
Luma gayana (Barnéoud) Burret Notizbl. Bot. Gart. Berlin-Dahlem 15: 523. 1941
Myrceugenella chequen (Molina) Kausel Revista Argent. Agron. 9: 43 (1942)
Myrceugenella chequen var. myrtomimeta (Diels) Kausel Lilloa 33: 104 (1971 publ. 1972)
Myrceugenella gayana (Barnéoud) Kausel Revista Argent. Agron. ix. 46 (1942).
Myrceugenella langerfeldtii Kausel Revista Argent. Agron. 11: 324 (1944)
Myrtus chequen O.Berg Linnaea 27(2-3): 146. 1856 [Jan 1856]
Myrtus gayana O.Berg Linnaea 27: 399 (1856)
Myrtus uliginosa Miq. Linnaea 25: 652 (1853)
Myrtus gayana var. major O.Berg Bot. Zeitung (Berlin) 15: 859 (1857)
Myrtus uliginosa f. major Miq. Linnaea 25: 652 1853
Eugenia chekan DC. Prodr. 3: 278 (1828)
Eugenia chequen Molina Sag. Stor. Nat. Chili , ed. 2: 148 (1810)
Eugenia gayana Barnéoud Fl. Chil. 2: 390 (1847)
Eugenia myrtomimeta Diels Bot. Jahrb. Syst. 37: 598 (1906)
Eugenia pulchra O.Berg Linnaea 29: 224 (1858)
Myrtus chequen (Molina) Spreng.

Common names Top

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Language Common/alternative name
Spanish chequen
Spanish arrayan blanco
Spanish arrayan de santiago
Spanish arrayán de santiago
Persian مورد شیلیایی سفید
koi Чекен
kv Чекен
lbe Чекен
mrj Чекен
udm Чекен

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000231083
UNII D925IRN6XS
Tropicos 22102228
KEW urn:lsid:ipni.org:names:597590-1
The Plant List kew-115614
Open Tree Of Life 800353
NCBI Taxonomy 375239
IUCN Red List 131397194
IPNI 597591-1
iNaturalist 716611
GBIF 5420322
Freebase /m/08_2rg
EPPO LUMCH
EOL 5450120
USDA GRIN 409842
Wikipedia Luma_chequen

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
From Nature to Innovation: The Uncharted Potential of Natural Deep Eutectic Solvents Schuh L, Reginato M, Florêncio I, Falcao L, Boron L, Gris EF, Mello V, Báo SN Molecules 18-Nov-2023
PMCID:PMC10675409
doi:10.3390/molecules28227653
PMID:38005377
Evaluation of the antioxidant, anti-inflammatory, and anti-tumoral properties of bioactive compounds extracted from murta berries (Ugni molinae T.) dried by different methods López J, Vega-Gálvez A, Ah-Hen KS, Rodríguez A, Quispe-Fuentes I, Delporte C, Valenzuela-Barra G, Arancibia Y, Zambrano A Front Plant Sci 18-May-2023
PMCID:PMC10234425
doi:10.3389/fpls.2023.1095179
PMID:37275254
Research Progress on the Preparation and Action Mechanism of Natural Deep Eutectic Solvents and Their Application in Food Wu K, Ren J, Wang Q, Nuerjiang M, Xia X, Bian C Foods 05-Nov-2022
PMCID:PMC9655939
doi:10.3390/foods11213528
PMID:36360140
Ultrasound-Assisted Extraction of Anthocyanins Using Natural Deep Eutectic Solvents and Their Incorporation in Edible Films Velásquez P, Bustos D, Montenegro G, Giordano A Molecules 12-Feb-2021
PMCID:PMC7918079
doi:10.3390/molecules26040984
PMID:33673385
Antioxidant Effect of a Polyphenol-Rich Murtilla (Ugni molinae Turcz.) Extract and Its Effect on the Regulation of Metabolism in Refrigerated Boar Sperm Jofré I, Cuevas M, de Castro LS, de Agostini Losano JD, Torres MA, Alvear M, Scheuermann E, Andrade AF, Nichi M, Assumpção ME, Romero F Oxid Med Cell Longev 03-Jun-2019
PMCID:PMC6589320
doi:10.1155/2019/2917513
PMID:31281571
Antioxidant and Vasodilator Activity of Ugni molinae Turcz. (Murtilla) and Its Modulatory Mechanism in Hypotensive Response Jofré I, Pezoa C, Cuevas M, Scheuermann E, Freires IA, Rosalen PL, de Alencar SM, Romero F Oxid Med Cell Longev 04-Sep-2016
PMCID:PMC5027056
doi:10.1155/2016/6513416
PMID:27688827
Foliar Essential Oil Glands of Eucalyptus Subgenus Eucalyptus (Myrtaceae) Are a Rich Source of Flavonoids and Related Non-Volatile Constituents Goodger JQ, Seneratne SL, Nicolle D, Woodrow IE PLoS One 15-Mar-2016
PMCID:PMC4792381
doi:10.1371/journal.pone.0151432
PMID:26977933
Leaf traits in Chilean matorral: sclerophylly within, among, and beyond matorral, and its environmental determinants Read J, Sanson G, Pérez Trautmann MF Ecol Evol 03-Feb-2016
PMCID:PMC4739351
doi:10.1002/ece3.1970
PMID:26865953
Anthocyanin Characterization, Total Phenolic Quantification and Antioxidant Features of Some Chilean Edible Berry Extracts Brito A, Areche C, Sepúlveda B, Kennelly EJ, Simirgiotis MJ Molecules 28-Jul-2014
PMCID:PMC6271127
doi:10.3390/molecules190810936
PMID:25072199
Phylogenetic relationships in Myrceugenia (Myrtaceae) based on plastid and nuclear DNA sequences Murillo-A. J, Ruiz-P. E, Landrum LR, Stuessy TF, Barfuss MH Mol Phylogenet Evol 01-Feb-2012
PMCID:PMC3260418
doi:10.1016/j.ympev.2011.11.021
PMID:22155422
Bioactive Flavanones from Luma chequen Cecilia Labbé, Josep Coll, Joseph D. Connolly, Francesca Faini, Louis J. Farrugia, David S. Rycroft Institute of Organic Chemistry & Biochemistry 27-Jul-2002
doi:10.1135/CCCC20020115
Flavonoids and terpenoids from Luma gayana (Barn.) Burret. Wächter GA, Wangmaneerat A, Caple KM, Montenegro G, Timmermann BN Z Naturforsch C J Biosci 01-Dec-1999
doi:10.1515/ZNC-1999-1220
PMID:10685506

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Clovandiol 76319362 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C 238.37 unknown https://doi.org/10.1515/ZNC-1999-1220
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1515/ZNC-1999-1220
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1515/ZNC-1999-1220
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNC-1999-1220
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNC-1999-1220
> 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/10.1515/ZNC-1999-1220
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1515/ZNC-1999-1220
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1515/ZNC-1999-1220
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2R,12R)-5-hydroxy-6,8,8,10,10-pentamethyl-2-phenyl-12-propan-2-yl-3,12-dihydro-2H-pyrano[2,3-a]xanthene-4,9,11-trione 162967343 Click to see CC1=C(C2=C(C3=C1OC4=C(C3C(C)C)C(=O)C(C(=O)C4(C)C)(C)C)OC(CC2=O)C5=CC=CC=C5)O 488.60 unknown https://doi.org/10.1135/CCCC20020115
(2S,12R)-5-hydroxy-6,8,8,10,10-pentamethyl-2-phenyl-12-propan-2-yl-3,12-dihydro-2H-pyrano[2,3-a]xanthene-4,9,11-trione 162967342 Click to see CC1=C(C2=C(C3=C1OC4=C(C3C(C)C)C(=O)C(C(=O)C4(C)C)(C)C)OC(CC2=O)C5=CC=CC=C5)O 488.60 unknown https://doi.org/10.1135/CCCC20020115
(2S,7aS,11aR,12R)-5,7a-dihydroxy-6,8,8,10,10-pentamethyl-2-phenyl-12-propan-2-yl-2,3,11a,12-tetrahydropyrano[2,3-a]xanthene-4,9,11-trione 162844426 Click to see CC1=C(C2=C(C3=C1OC4(C(C3C(C)C)C(=O)C(C(=O)C4(C)C)(C)C)O)OC(CC2=O)C5=CC=CC=C5)O 506.60 unknown https://doi.org/10.1135/CCCC20020115
5-hydroxy-6,8,8,10,10-pentamethyl-2-phenyl-12-propan-2-yl-3,12-dihydro-2H-pyrano[2,3-a]xanthene-4,9,11-trione 85376106 Click to see CC1=C(C2=C(C3=C1OC4=C(C3C(C)C)C(=O)C(C(=O)C4(C)C)(C)C)OC(CC2=O)C5=CC=CC=C5)O 488.60 unknown https://doi.org/10.1135/CCCC20020115
Lumaflavanone C 11145602 Click to see CC1=C(C2=C(C3=C1OC4(C(C3C(C)C)C(=O)C(C(=O)C4(C)C)(C)C)O)OC(CC2=O)C5=CC=CC=C5)O 506.60 unknown https://doi.org/10.1135/CCCC20020115

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