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Internal ID UUID643fc8161cfe3670842156
Scientific name Baccharis artemisioides
Authority Hook. & Arn.
First published in J. Bot. (Hooker) 3: 41 (1840)

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Synonyms Top

Scientific name Authority First published in
Lanugothamnus artemisioides (Hook. & Arn.) Deble Balduinia 37: 14 (2012)

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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 Northeast
      • Argentina Northwest
      • Argentina South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000019649
Tropicos 2741679
KEW urn:lsid:ipni.org:names:183117-1
The Plant List gcc-1190
Open Tree Of Life 7599846
NCBI Taxonomy 2707380
IPNI 183117-1
iNaturalist 967426
GBIF 3129755

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
Poisoning by Baccharis coridifolia in Early-Weaned Beef Calves: Pathological Study and New Macrocyclic Trichothecene Identification Machado M, Martínez R, Andres S, Sumarah MW, Renaud JB, Armién AG, Barros CS, Riet-Correa F, Menchaca A, Schild CO Toxins (Basel) 01-Dec-2023
PMCID:PMC10747622
doi:10.3390/toxins15120681
PMID:38133185
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 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
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
The structure of bartemidiolide, a clerodane-type diterpene from Baccharis artemisioides Carlos E. Tonn, Oscar S. Giordano, Roberto Bessalle, Felix Frolow, David Lavie Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83127-3
Deoxybartemidiolide, a clerodane-type diterpene from Baccharis artemisioides Carlos E. Tonn, Oscar S. Giordano, Julio Delgado Martín, Victor S. Martín Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97785-9
Macrocyclic trichothecenes in Baccharis coridifolia plants and endophytes and Baccharis artemisioides plants. Rizzo I, Varsavky E, Haidukowski M, Frade H Toxicon 01-May-1997
doi:10.1016/S0041-0101(96)00149-3
PMID:9203300

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 / Sesquiterpenoids / Trichothecenes
(1R,3R,8R,12S,13R,17R,18Z,20Z,24R,25S)-12-hydroxy-17-[(1R)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,22-dione 139596298 Click to see CC1CCOC(C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4)C(C)O 532.60 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
(1R,3R,8R,12Z,17R,18Z,20Z,24R,25S)-17-[(1R)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,22-dione 139595713 Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)O)C 514.60 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
(1R,3R,8R,12Z,18Z,20Z,24R,25S)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,17,22-trione 139595166 Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(=O)C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C 484.50 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
CID 23305159 23305159 Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(=O)C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C 484.50 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
Roridin D 5477986 Click to see CC1=CC2C3(CC1)COC(=O)C4C(O4)(CCOC(C=CC=CC(=O)OC5C3(C6(CO6)C(C5)O2)C)C(C)O)C 530.60 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
Verrucarin A 6326658 Click to see CC1CCOC(=O)C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4 502.60 unknown https://doi.org/10.1016/S0041-0101(96)00149-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4S,5S,5'S,6S,8S,9R,11S)-5'-(furan-3-yl)-4,11-dimethylspiro[10,13-dioxatetracyclo[6.3.2.01,6.09,11]tridecane-5,3'-oxolane]-2',12-dione 13994587 Click to see CC1CCC23C(C14CC(OC4=O)C5=COC=C5)CC(C6C2(O6)C)OC3=O 358.40 unknown https://doi.org/10.1016/0031-9422(88)83127-3
(1R,4S,5S,5'S,6S,8S)-5'-(furan-3-yl)-4,11-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodec-11-ene-5,3'-oxolane]-2',10-dione 163035611 Click to see CC1CCC23C(C14CC(OC4=O)C5=COC=C5)CC(C=C2C)OC3=O 342.40 unknown https://doi.org/10.1016/S0031-9422(00)97785-9
5'-(Furan-3-yl)-4,11-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodec-11-ene-5,3'-oxolane]-2',10-dione 14314611 Click to see CC1CCC23C(C14CC(OC4=O)C5=COC=C5)CC(C=C2C)OC3=O 342.40 unknown https://doi.org/10.1016/S0031-9422(00)97785-9
Bartemidiolide 188871 Click to see CC1CCC23C(C14CC(OC4=O)C5=COC=C5)CC(C6C2(O6)C)OC3=O 358.40 unknown https://doi.org/10.1016/0031-9422(88)83127-3
https://doi.org/10.1016/S0031-9422(00)97785-9

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