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Eugenia dysenterica

Eugenia dysenterica - Unknown
Part: Unknown
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 UUID64403a6d35388791884761
Scientific name Eugenia dysenterica
Authority DC.
First published in Prodr. 3: 268 (1828)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myrtus dysenterica Mart. Reise Bras. 2: 571 (1828)
Stenocalyx dysentericus O.Berg Linnaea 27: 314 (1856)

Common names Top

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Language Common/alternative name
German cagaita
Portuguese cagaita
Portuguese cagaiteira

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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 North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000957184
Tropicos 22100530
KEW urn:lsid:ipni.org:names:594325-1
The Plant List kew-75100
Open Tree Of Life 915111
NCBI Taxonomy 866613
IUCN Red List 146076691
IPNI 594325-1
iNaturalist 560898
GBIF 5417055
Freebase /m/0g548k_
EPPO EUEDY
EOL 5450733
USDA GRIN 416557
Wikipedia Eugenia_dysenterica

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
Citizen science data on urban forageable plants: a case study in Brazil Soares FM, Ferreira Pires L, Garcia MC, Coradin L, Ghilardi-Lopes NP, Silva RR, de Carvalho AM, Gavai A, Bouzembrak Y, Maculan BC, Koffler S, Montedo UB, Drucker DP, Santiago R, de Carvalho MC, Lima AC, Gabriel HD, de França SG, de Almeida KR, dos Santos BJ, Saraiva AM GigaByte 21-Feb-2024
PMCID:PMC10905257
doi:10.46471/gigabyte.107
PMID:38434929
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Potential Effects of Essential Oil from Plinia cauliflora (Mart.) Kausel on Leishmania: In Vivo, In Vitro, and In Silico Approaches Holanda VN, Brito TG, de Oliveira JR, da Cunha RX, da Silva AP, da Silva WV, Araújo TF, Tavares JF, dos Santos SG, Figueiredo RC, Lima VL Microorganisms 19-Jan-2024
PMCID:PMC10819817
doi:10.3390/microorganisms12010207
PMID:38276192
β-Caryophyllene Inhibits Endothelial Tube Formation by Modulating the Secretome of Hypoxic Lung Cancer Cells—Possible Role of VEGF Downregulation Wittig F, Koch F, Pannenberg L, Bekeschus S, Ramer R, Hinz B Int J Mol Sci 09-Jan-2024
PMCID:PMC10815222
doi:10.3390/ijms25020810
PMID:38255884
Composition and Anti-Acetylcholinesterase Properties of the Essential Oil of the Ecuadorian Endemic Species Eugenia valvata McVaugh Calva J, Silva M, Morocho V Molecules 15-Dec-2023
PMCID:PMC10746026
doi:10.3390/molecules28248112
PMID:38138598
New Therapeutic Strategies for Obesity and Its Metabolic Sequelae: Brazilian Cerrado as a Unique Biome Monteiro-Alfredo T, Macedo ML, de Picoli Souza K, Matafome P Int J Mol Sci 25-Oct-2023
PMCID:PMC10648839
doi:10.3390/ijms242115588
PMID:37958572
Carbon Storage in Different Compartments in Eucalyptus Stands and Native Cerrado Vegetation Ribeiro FP, Gatto A, de Oliveira AD, Pulrolnik K, Valadão MB, Araújo JB, de Carvalho AM, Ferreira EA Plants (Basel) 24-Jul-2023
PMCID:PMC10386474
doi:10.3390/plants12142751
PMID:37514365
Physicochemical Aspects, Bioactive Compounds, Phenolic Profile and In Vitro Antioxidant Activity of Tropical Red Fruits and Their Blend Paiva YF, de Figueirêdo RM, Queiroz AJ, Amadeu LT, dos Santos FS, dos Reis CG, Carvalho AJ, Lima MD, de Lima AG, Gomes JP, Moura RL, Moura HV, Silva ET Molecules 20-Jun-2023
PMCID:PMC10302636
doi:10.3390/molecules28124866
PMID:37375421
Exploring the Sensory Properties and Preferences of Fruit Wines Based on an Online Survey and Partial Projective Mapping Zhu Y, Su Q, Jiao J, Kelanne N, Kortesniemi M, Xu X, Zhu B, Laaksonen O Foods 29-Apr-2023
PMCID:PMC10178241
doi:10.3390/foods12091844
PMID:37174382
Proanthocyanidins may be potential therapeutic agents for the treatment of carotid atherosclerosis: A review Huang P J Int Med Res 25-Apr-2023
PMCID:PMC10134127
doi:10.1177/03000605231167314
PMID:37096349
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294
Camu Camu (Myrciaria dubia (Kunth) McVaugh): An Amazonian Fruit with Biofunctional Properties–A Review García-Chacón JM, Marín-Loaiza JC, Osorio C ACS Omega 06-Feb-2023
PMCID:PMC9933082
doi:10.1021/acsomega.2c07245
PMID:36816657
Advanced Glycation End-Products and Diabetic Neuropathy of the Retina Oshitari T Int J Mol Sci 02-Feb-2023
PMCID:PMC9917392
doi:10.3390/ijms24032927
PMID:36769249
Optimization of spray-drying parameter for production of better quality orange fleshed sweet potato (Ipomoea batatas L.) powder: Selected physiochemical, morphological, and structural properties Arebo MA, Feyisa JD, Tafa KD, Satheesh N Heliyon 20-Jan-2023
PMCID:PMC9898653
doi:10.1016/j.heliyon.2023.e13078
PMID:36747935
Ammi-visnaga extract; a novel phyto-antiviral agent against bovine rotavirus Harb N, Sarhan AG, El Dougdoug KA, Gomaa HH Virusdisease 04-Jan-2023
PMCID:PMC10050252
doi:10.1007/s13337-022-00803-w
PMID:37009254

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 / Benzene and substituted derivatives / Cumenes
o-Cymene 10703 Click to see CC1=CC=CC=C1C(C)C 134.22 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
(+)-Thujopsene 11401461 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
epi-Cubenol 519857 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
1,4,4-Trimethyltricyclo[5.3.1.02,6]undecan-11-ol 529438 Click to see CC1(CC2C3CCCC(C2C1)(C3O)C)C 208.34 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see C12C3C4C1C5(C2C3=C45)O 118.13 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
> Organoheterocyclic compounds / Epoxides
(1R,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 132587053 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2
Humulene epoxyde 5463721 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1016/S0378-8741(00)00214-2

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