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Baccharis linearifolia

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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 UUID643fcede56086470694270
Scientific name Baccharis linearifolia
Authority Pers.
First published in Syn. Pl. 2(2): 425 (1807)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Baccharis linearifolia subsp. chilco (Kunth) Joch.Müll. Syst. Bot. Monogr. 76: 108 (2006)
Baccharis linearifolia subsp. linearifolia
Baccharis linearifolia subsp. polycephala (Wedd.) Joch.Müll. Syst. Bot. Monogr. 76: 105 (2006)

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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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
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000085278
Tropicos 50270622
KEW urn:lsid:ipni.org:names:183419-1
Open Tree Of Life 7051197
Observations.org 292111
NCBI Taxonomy 2321251
IPNI 183419-1
iNaturalist 881503
GBIF 7338714

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
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
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
Automatic Leaf Epidermis Assessment Using Fourier Descriptors in Texture Images da Silva NR, da Silva Oliveira MW, De Almeida Filho HA, Pinheiro LF, Kolb RM, Bruno OM Bio Protoc 05-Dec-2017
PMCID:PMC8438393
doi:10.21769/BioProtoc.2630
PMID:34595298
Leaf epidermis images for robust identification of plants da Silva NR, Oliveira MW, Filho HA, Pinheiro LF, Rossatto DR, Kolb RM, Bruno OM Sci Rep 24-May-2016
PMCID:PMC4877573
doi:10.1038/srep25994
PMID:27217018
Five diterpenes and other constituents from nine Baccharis species Ferdinand Bohlmann, Christa Zdero, Michael Grenz, Autar K. Dhar, Harold Robinson, Robert M. King Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)85107-2
Essential oils of three asiatic artemisia species Carlo Bicchi, Carlotta Frattini, Tommaso Sacco Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83061-7

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 / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
Beta-Sesquiphellandrene 12315492 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)83061-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 3536734 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(81)85107-2
Taxifolin 3-O-acetate 442540 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(81)85107-2

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