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Baccharis darwinii

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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 UUID643fcc7f15ef1273944732
Scientific name Baccharis darwinii
Authority Hook. & Arn.
First published in J. Bot. (Hooker) 3: 39 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis grossedentata Heering Jahrb. Hamburg. Wiss. Anst. 31, Beiheft 3: 73 (1915)
Baccharis angulata Griseb. Abh. Königl. Ges. Wiss. Göttingen 24: 180 (1879)
Neomolina darwinii Hook. & Arn. Candollea 48: 212. 1993
Baccharis angulata var. andina Hieron. Bol. Acad. Nac. Ci. 4(1): 34 (1881)
Baccharis ulicina var. subintegrifolia Kuntze Revis. Gen. Pl. 3[3]: 135 (1898)
Neomolina darwinii (Hook. & Arn.) F.H.Hellw. Candollea 48(1): 212 (1993): (1993)
Baccharis heterothalmoides Britton Bull. Torrey Bot. Club 19(1): 4 (1892)

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
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Argentina South
      • Chile South
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000063440
Tropicos 2733177
KEW urn:lsid:ipni.org:names:305101-2
The Plant List gcc-20407
Open Tree Of Life 7599908
NCBI Taxonomy 2707406
IPNI 305101-2
iNaturalist 882109
GBIF 3129943

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
Baccharis Species Essential Oils: Repellency and Toxicity against Yellow Fever Mosquitoes and Imported Fire Ants Ali A, Shah FM, Manfron J, Monteiro LM, de Almeida VP, Raman V, Khan IA J Xenobiot 27-Oct-2023
PMCID:PMC10660731
doi:10.3390/jox13040041
PMID:37987442
Disentangling the last 1,000 years of human–environment interactions along the eastern side of the southern Andes (34–52°S lat.) Nanavati W, Whitlock C, de Porras ME, Gil A, Navarro D, Neme G Proc Natl Acad Sci U S A 22-Feb-2022
PMCID:PMC8892505
doi:10.1073/pnas.2119813119
PMID:35193983
Zuccagnia punctata Cav. Essential Oil into Poly(ε-caprolactone) Matrices as a Sustainable and Environmentally Friendly Strategy Biorepellent against Triatoma infestans (Klug) (Hemiptera, Reduviidae) López S, Tapia A, Zygadlo J, Stariolo R, Abraham GA, Cortez Tornello PR Molecules 02-Jul-2021
PMCID:PMC8271999
doi:10.3390/molecules26134056
PMID:34279396
Anti-Fungal Efficacy and Mechanisms of Flavonoids Al Aboody MS, Mickymaray S Antibiotics (Basel) 26-Jan-2020
PMCID:PMC7168129
doi:10.3390/antibiotics9020045
PMID:31991883
Dermatophyte Resistance to Antifungal Drugs: Mechanisms and Prospectus Martinez-Rossi NM, Bitencourt TA, Peres NT, Lang EA, Gomes EV, Quaresemin NR, Martins MP, Lopes L, Rossi A Front Microbiol 29-May-2018
PMCID:PMC5986900
doi:10.3389/fmicb.2018.01108
PMID:29896175
Antifungal activity of extracts and prenylated coumarins isolated from Baccharis darwinii Hook & Arn. (Asteraceae). Kurdelas RR, Lima B, Tapia A, Feresin GE, Gonzalez Sierra M, Rodríguez MV, Zacchino S, Enriz RD, Freile ML Molecules 13-Jul-2010
PMCID:PMC6257657
doi:10.3390/MOLECULES15074898
PMID:20657398
Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) Kurdelas RR, Lima B, Tapia A, Egly Feresin G, Gonzalez Sierra M, Rodríguez MV, Zacchino S, Enriz RD, Freile ML Molecules 13-Jul-2010
PMCID:PMC6257657
doi:10.3390/molecules15074898
PMID:20657398
Diterpene glycosides and other constituents from argentinian baccharis species C. Zdero, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83754-1
Clerodane and labdane diterpenoids from Baccharis species Ferdinand Bohlmann, Shanta Banerjee, Jasmin Jakupovic, Michael Grenz, Laxmi N. Misra, Guillermo Schmeda-Hirschmann, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80758-X

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 / Diterpenoids / Colensane and clerodane diterpenoids
[(4aR,5S,6R,8aR)-5-[2-[(3R,5R)-5-methoxyoxolan-3-yl]ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 162951810 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)OC)CCC=C2COC(=O)C)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
[5-[2-(5-Methoxyoxolan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 162951809 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)OC)CCC=C2COC(=O)C)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
(3R,4S)-3-ethenyl-3-methyl-6-propan-2-ylidene-4-prop-1-en-2-ylcyclohexene 53310786 Click to see CC(=C1CC(C(C=C1)(C)C=C)C(=C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
3-Ethenyl-3-methyl-6-propan-2-ylidene-4-prop-1-en-2-ylcyclohexene 76006796 Click to see CC(=C1CC(C(C=C1)(C)C=C)C(=C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80758-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
2H-1-Benzopyran-2-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]- 400073 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
7-(3,7-Dimethyl-5-oxoocta-2,6-dienoxy)chromen-2-one 72730526 Click to see CC(=CC(=O)CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 312.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
7-(5-Hydroxy-3,7-dimethylocta-2,6-dienyloxy)-chromen-2-one 72730525 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
7-[(2E,5R)-5-hydroxy-3,7-dimethylocta-2,6-dienoxy]chromen-2-one 25763648 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
https://doi.org/10.1016/S0031-9422(00)83754-1
7-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienoxy]chromen-2-one 14376450 Click to see CC(=CC(=O)CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 312.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
Anisocoumarin H 14376449 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
Auraptene 1550607 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C 298.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257657/
https://doi.org/10.1016/S0031-9422(00)83754-1
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-(3,7-Dimethyl-6-oxooct-2-enoxy)chromen-2-one 163000554 Click to see CC(C)C(=O)CCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C 314.40 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
7-[(E)-3,7-dimethyl-6-oxooct-2-enoxy]chromen-2-one 13965511 Click to see CC(C)C(=O)CCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C 314.40 unknown https://doi.org/10.1016/S0031-9422(00)83754-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(00)80758-X

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