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Baccharis aliena

Baccharis aliena - 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 UUID643fc5e9ee14e804529043
Scientific name Baccharis aliena
Authority (Spreng.) Joch.Müll.
First published in Syst. Bot. Monogr. 76: 305 (2006)

Description Top

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Synonyms Top

Scientific name Authority First published in
Heterothalamus brunioides Less. Linnaea 6: 504 (1831)
Marshallia aliena Spreng. Syst. Veg. 3: 446 (1826)
Heterothalamus alienus (Spreng.) Kuntze Revis. Gen. Pl. 3[3]: 158 (1898)

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 South
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000001085
Tropicos 100374955
KEW urn:lsid:ipni.org:names:77076537-1
NCBI Taxonomy 2707368
IPNI 77076537-1
iNaturalist 925179
GBIF 3089214
Elurikkus 730363
Open Tree Of Life 6056214

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
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
The direct and indirect effects of bioactive compounds against coronavirus Tomas M, Capanoglu E, Bahrami A, Hosseini H, Akbari‐Alavijeh S, Shaddel R, Rehman A, Rezaei A, Rashidinejad A, Garavand F, Goudarzi M, Jafari SM Food Front 08-Dec-2021
PMCID:PMC9015578
doi:10.1002/fft2.119
PMID:35462942
Brazilian essential oils as source for the discovery of new anti-COVID-19 drug: a review guided by in silico study Amparo TR, Seibert JB, Silveira BM, Costa FS, Almeida TC, Braga SF, da Silva GN, dos Santos OD, de Souza GH Phytochem Rev 13-Apr-2021
PMCID:PMC8042356
doi:10.1007/s11101-021-09754-4
PMID:33867898
Disentangling the role of environment in cross-taxon congruence of species richness along elevational gradients Ramos CS, Picca P, Pocco ME, Filloy J Sci Rep 25-Feb-2021
PMCID:PMC7907370
doi:10.1038/s41598-021-83763-3
PMID:33633146
Essential Oils as Antiviral Agents, Potential of Essential Oils to Treat SARS-CoV-2 Infection: An In-Silico Investigation da Silva JK, Figueiredo PL, Byler KG, Setzer WN Int J Mol Sci 12-May-2020
PMCID:PMC7279430
doi:10.3390/ijms21103426
PMID:32408699
Phylogenetic relationships of Atractylodes lancea, A. chinensis and A. macrocephala, revealed by complete plastome and nuclear gene sequences Wang L, Zhang H, Wu X, Wang Z, Fang W, Jiang M, Chen H, Huang L, Liu C PLoS One 28-Jan-2020
PMCID:PMC6986703
doi:10.1371/journal.pone.0227610
PMID:31990944
Detecting useful genetic markers and reconstructing the phylogeny of an important medicinal resource plant, Artemisia selengensis, based on chloroplast genomics Meng D, Xiaomei Z, Wenzhen K, Xu Z PLoS One 04-Feb-2019
PMCID:PMC6361438
doi:10.1371/journal.pone.0211340
PMID:30716116
Species Identification of Conyza bonariensis Assisted by Chloroplast Genome Sequencing Wang A, Wu H, Zhu X, Lin J Front Genet 11-Sep-2018
PMCID:PMC6141629
doi:10.3389/fgene.2018.00374
PMID:30254661
Medicinal plants and natural products in amelioration of arsenic toxicity: a short review Bhattacharya S Pharm Biol 08-Dec-2016
PMCID:PMC6130623
doi:10.1080/13880209.2016.1235207
PMID:27931138
Compositional Variation and Bioactivity of the Leaf Essential Oil of Montanoa guatemalensis from Monteverde, Costa Rica: A Preliminary Investigation Flatt VD, Campos CR, Kraemer MP, Bailey BA, Satyal P, Setzer WN Medicines (Basel) 24-Nov-2015
PMCID:PMC5456209
doi:10.3390/medicines2040331
PMID:28930215
Floral Nectar Production and Nectary Anatomy and Ultrastructure of Echinacea purpurea (Asteraceae) WIST TJ, DAVIS AR Ann Bot 01-Feb-2006
PMCID:PMC2803364
doi:10.1093/aob/mcj027
PMID:16339769
Peroxides and other constituents from Heterothalamus alienus Gerhard Rücker, Eloir Schenkel, Detlef Manns, Miriam Falkenberg, Anne Marek Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00559-5

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
docosyl (E)-3-phenylprop-2-enoate 101687173 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=CC=C1 456.70 unknown https://doi.org/10.1016/0031-9422(95)00559-5
Docosyl 3-phenylprop-2-enoate 86182202 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=CC=C1 456.70 unknown https://doi.org/10.1016/0031-9422(95)00559-5
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/0031-9422(95)00559-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2Z,5E)-7-hydroperoxy-3,7-dimethylocta-2,5-dien-1-ol 21630854 Click to see CC(=CCO)CC=CC(C)(C)OO 186.25 unknown https://doi.org/10.1016/0031-9422(95)00559-5
7-Hydroperoxy-3,7-dimethylocta-2,5-dien-1-ol 73815007 Click to see CC(=CCO)CC=CC(C)(C)OO 186.25 unknown https://doi.org/10.1016/0031-9422(95)00559-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00559-5
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/0031-9422(95)00559-5
> Organoheterocyclic compounds / Dihydrofurans
(2R)-3-methyl-2-(3-methylbut-3-enyl)-2,5-dihydrofuran 163015296 Click to see CC1=CCOC1CCC(=C)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00559-5
3-Methyl-2-(3-methylbut-3-enyl)-2,5-dihydrofuran 101687174 Click to see CC1=CCOC1CCC(=C)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00559-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(95)00559-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(95)00559-5

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