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Erythroxylum argentinum

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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 UUID64401b8608199198470784
Scientific name Erythroxylum argentinum
Authority O.E.Schulz
First published in Pflanzenr. , IV, 134: 99 (1907)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erythroxylum argentinum var. calophyllum O.E.Schulz Pflanzenr. , IV, 134: 99 (1907)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000679688
Tropicos 12500028
KEW urn:lsid:ipni.org:names:96883-2
The Plant List kew-2801265
Open Tree Of Life 907742
NCBI Taxonomy 113285
IPNI 96883-2
GBIF 7284806
USDA GRIN 15793

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
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993
Quantity and quality of seed dispersal by a large arboreal frugivore in small and large Atlantic forest fragments Chaves ÓM, Bicca-Marques JC, Chapman CA PLoS One 21-Mar-2018
PMCID:PMC5862440
doi:10.1371/journal.pone.0193660
PMID:29561869
Medicinal plants for the treatment of obesity: ethnopharmacological approach and chemical and biological studies de Freitas Junior LM, de Almeida Jr EB Am J Transl Res 15-May-2017
PMCID:PMC5446492
PMID:28559960
Feeding Strategies of Brown Howler Monkeys in Response to Variations in Food Availability Chaves ÓM, Bicca-Marques JC PLoS One 05-Feb-2016
PMCID:PMC4743924
doi:10.1371/journal.pone.0145819
PMID:26848959
Traditional botanical knowledge of artisanal fishers in southern Brazil Baptista MM, Ramos MA, de Albuquerque UP, Coelho-de-Souza G, Ritter MR J Ethnobiol Ethnomed 30-Jul-2013
PMCID:PMC3737040
doi:10.1186/1746-4269-9-54
PMID:23898973
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Alkaloids of some south american erythroxylum species Y.M.A. El-Imam, W.C. Evans, T. Plowman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83028-9
Flavonoids from Erythroxylon argentinum Raúl P.A. Iñigo, Alicia B. Pomilio Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83550-5
Diterpenes from the timber of 20 Erythroxylum species Steven M. Ansell, Karl H. Pegel, David A.H. Taylor Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85235-J
Alkaloids of Erythroxylum (Erythroxylaceae) species from Southern Brazil. Zuanazzi JA, Tremea V, Limberger RP, Sobral M, Henriques AT Biochem Syst Ecol 01-Aug-2001
doi:10.1016/S0305-1978(01)00022-9
PMID:11412954

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
> Alkaloids and derivatives
1-(1-Methylpyrrolidin-2-yl)acetone 94157 Click to see CC(=O)CC1CCCN1C 141.21 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
Cuskhygrine 441070 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
Hygrine 440933 Click to see CC(=O)CC1CCCN1C 141.21 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzoyltropein 10834 Click to see CN1C2CCC1CC(C2)OC(=O)C3=CC=CC=C3 245.32 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
Tropacocaine 637578 Click to see CN1C2CCC1CC(C2)OC(=O)C3=CC=CC=C3 245.32 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4R,9R,10R,13R)-7-hydroxy-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadeca-6,14-dien-8-one 162927607 Click to see CC1(C=C(C(=O)C2(C1CCC34C2CCC(C3)(C=C4)CO)C)O)C 316.40 unknown https://doi.org/10.1016/0031-9422(93)85235-J
(1S,4R,9R,10S,13S)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-one 162941730 Click to see CC1(CCCC2(C1CC(=O)C34C2CCC(C3)(C=C4)C)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
(5,5,9-Trimethyl-13-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methanol 85103571 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)CO)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
(E)-2-[2-[(1R,4aR,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethyl]but-2-ene-1,4-diol 162928107 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(=CCO)CO)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
13-(Hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-8-one 162883873 Click to see CC1(CCC(=O)C2(C1CCC34C2CCC(C3)(C=C4)CO)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethyl]but-2-ene-1,4-diol 72952742 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(=CCO)CO)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
5,5,9,13-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-one 162941729 Click to see CC1(CCCC2(C1CC(=O)C34C2CCC(C3)(C=C4)C)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
7-Hydroxy-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadeca-6,14-dien-8-one 162927606 Click to see CC1(C=C(C(=O)C2(C1CCC34C2CCC(C3)(C=C4)CO)C)O)C 316.40 unknown https://doi.org/10.1016/0031-9422(93)85235-J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1R)-1-[(2S,4aS,4bR,8aS,10aS)-2,4a,8a-trimethyl-8-methylidene-1,3,4,4b,5,6,7,9,10,10a-decahydrophenanthren-2-yl]ethane-1,2-diol 163194552 Click to see CC1(CCC2(C(C1)CCC3(C2CCCC3=C)C)C)C(CO)O 306.50 unknown https://doi.org/10.1016/0031-9422(93)85235-J
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
4-Hydroxy-methylprolin 11499239 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1016/S0305-1978(01)00022-9
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Cyclopiamide C 122218853 Click to see CC(CC(=O)O)N1C(=O)C2=C(C1(C)C)C=C3C=CC=C4C3=C2C(=O)N4 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83028-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)83550-5
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/S0031-9422(00)83550-5

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