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Maytenus chubutensis

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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 UUID643ff5c558173763441465
Scientific name Maytenus chubutensis
Authority (Speg.) Lourteig, O'Donell & Sleumer
First published in Natura (Buenos Aires) 1: 208 (1955)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pernettya chubutensis Speg. Revista Fac. Agron. Univ. Nac. La Plata 3: 618. 1897

Common names Top

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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
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000375067
Tropicos 6600542
KEW urn:lsid:ipni.org:names:155482-2
The Plant List kew-2370003
Open Tree Of Life 6092930
NCBI Taxonomy 1825833
IPNI 155482-2
GBIF 3794284
EPPO MYUCH
EOL 6940216

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
Maytenus disticha Extract and an Isolated β-Dihydroagarofuran Induce Mitochondrial Depolarization and Apoptosis in Human Cancer Cells by Increasing Mitochondrial Reactive Oxygen Species González-Chavarría I, Duprat F, Roa FJ, Jara N, Toledo JR, Miranda F, Becerra J, Inostroza A, Kelling A, Schilde U, Heydenreich M, Paz C Biomolecules 29-Feb-2020
PMCID:PMC7175306
doi:10.3390/biom10030377
PMID:32121436
Triterpenoid and Phenolic Compounds from Two Chilean Celastraceae Orlando Muñoz, Antonio González, Angel Ravelo, Ana Estevez Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1999-1-223
Does Nature and Persistence of Substrate at a Mesohabitat Scale Matter for Chironomidae Assemblages? a Study of Two Perennial Mountain Streams in Patagonia, Argentina Epele LB, Miserendino ML, Brand C J Insect Sci 27-May-2012
PMCID:PMC3481470
doi:10.1673/031.012.6801
PMID:22947060
Terpenoids from Maytenus species and assessment of their reversal activity against a multidrug-resistant Leishmania tropica line. Kennedy ML, Llanos GG, Castanys S, Gamarro F, Bazzocchi IL, Jiménez IA Chem Biodivers 01-Dec-2011
doi:10.1002/CBDV.201000356
PMID:22162167
Minor sesquiterpenes from Maytenus chubutensis. González AG, Nuñez MP, Ravelo AG, Luis JG, Jiménez IA, Munoz OM J Nat Prod 01-Mar-1990
doi:10.1021/NP50068A031
PMID:2380720

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 / Phenanthrenes and derivatives
6-Oxopristimerol 11754914 Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C 480.60 unknown https://doi.org/10.1002/CBDV.201000356
methyl (2R,4aS,6aR,6aS,14aS,14bR)-11-hydroxy-10-methoxy-2,4a,6a,6a,9,14a-hexamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 56593433 Click to see CC1=C2C(=CC(=C1OC)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C 494.70 unknown https://doi.org/10.1002/CBDV.201000356
Methyl 10,11-dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 73086832 Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C 480.60 unknown https://doi.org/10.1002/CBDV.201000356
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1R,2R,4R,5S,6S,7S,9S,12R)-4,5,12-triacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162919479 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)CO)OC(=O)C)OC(=O)C 532.60 unknown https://doi.org/10.1021/NP50068A031
> 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/10.1515/ZNC-1999-1-223
Celastrol 122724 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://doi.org/10.1515/ZNC-1999-1-223
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1515/ZNC-1999-1-223
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2R,4R,5S,6S,7R,8R,9S,12S)-4,5,8,12-tetraacetyloxy-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162885790 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C)C(O3)(C)C)OC(=O)C)CO)OC(=O)C)OC(=O)C 590.60 unknown https://doi.org/10.1021/NP50068A031
[(1S,2S,4S,5R,6R,7R,9R,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 163038990 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 574.60 unknown https://doi.org/10.1021/NP50068A031
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1515/ZNC-1999-1-223
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1515/ZNC-1999-1-223

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