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Baccharis calvescens

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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 UUID643fc971cf45f595046287
Scientific name Baccharis calvescens
Authority DC.
First published in Prodr. 5: 413 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis oleifolia Gardner London J. Bot. 7: 86. 1848
Baccharis disticha Sch.Bip. ex Baker Fl. Bras. 6(3): 53 (1882)
Baccharis calvescens f. rufidula Heering Jahrb. Hamburg. Wiss. Anst. 31(3): 146 (1915)
Baccharis calvescens f. ferruginea Heering Jahrb. Hamburg. Wiss. Anst. 31(3): 146 (1915)
Baccharis calvescens f. glutinosa Heering Jahrb. Hamburg. Wiss. Anst. 31(3): 146 (1915)
Baccharis oleifolia Mart. ex Colla Herb. Pedem. iii. 318 (1834)
Baccharis flocculosa Mart. ex Baker Fl. Bras. 6(3): 53 (1882)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000030508
Tropicos 2704648
KEW urn:lsid:ipni.org:names:183174-1
The Plant List gcc-129495
Open Tree Of Life 7599875
NCBI Taxonomy 2707393
IPNI 183174-1
GBIF 3129516

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
Insecticidal and oviposition deterrent effects of essential oils of Baccharis spp. and histological assessment against Drosophila suzukii (Diptera: Drosophilidae) de Souza MT, de Souza MT, Bernardi D, de Melo DJ, Zarbin PH, Zawadneak MA Sci Rep 17-Feb-2021
PMCID:PMC7889903
doi:10.1038/s41598-021-83557-7
PMID:33597617
Methacrylate: An alternative fixing agent for identifying the botanical origin of propolis Teixeira ÉW, Message D, Meira RM Appl Plant Sci 08-Dec-2019
PMCID:PMC6923709
doi:10.1002/aps3.11309
PMID:31890355
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
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

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 / Acetophenones
(6-Acetyl-5-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-3-yl) acetate 163018088 Click to see CC(=C)C1C(C2=CC(=C(C=C2O1)C(=O)C)O)OC(=O)C 276.28 unknown https://doi.org/10.1016/0031-9422(81)85107-2
[(2R,3S)-6-acetyl-5-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-3-yl] acetate 163018089 Click to see CC(=C)C1C(C2=CC(=C(C=C2O1)C(=O)C)O)OC(=O)C 276.28 unknown https://doi.org/10.1016/0031-9422(81)85107-2
1-(5-Hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-6-yl)ethanone 14887260 Click to see CC(=C)C1CC2=CC(=C(C=C2O1)C(=O)C)O 218.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2
1-[(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone 12414274 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2
1-[(2S)-2,3-Dihydro-5-hydroxy-2-(1-methylethenyl)-6-benzofuranyl]ethanone 131397201 Click to see CC(=C)C1CC2=CC(=C(C=C2O1)C(=O)C)O 218.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2
Ethanone, 1-[2,3-dihydro-2-(1-methylethenyl)-5-benzofuranyl]- 317196 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 202.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Decene-4,6-diynoic acid, methyl ester, (Z)- 643924 Click to see CCCC#CC#CC=CC(=O)OC 176.21 unknown https://doi.org/10.1016/0031-9422(81)85107-2
Methyl-dec-2-en-4,6-diynoate 96905 Click to see CCCC#CC#CC=CC(=O)OC 176.21 unknown https://doi.org/10.1016/0031-9422(81)85107-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Methyl 9-hydroxyoctadec-11-enoate 163074698 Click to see CCCCCCC=CCC(CCCCCCCC(=O)OC)O 312.50 unknown https://doi.org/10.1016/0031-9422(81)85107-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-[2-(Furan-3-YL)ethyl]-8A-(hydroxymethyl)-5,6-dimethyl-3,4,4A,6,7,8-hexahydronaphthalene-1-carboxylic acid 12310371 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)CO 332.40 unknown https://doi.org/10.1016/0031-9422(81)85107-2
Hautriwaic acid 12310372 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C(=O)O)CO 332.40 unknown https://doi.org/10.1016/0031-9422(81)85107-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4-Hydroxy-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 2-methylbut-2-enoate 163024184 Click to see CC=C(C)C(=O)OC1CCC(C2C1(CC=C(C2)C(C)C)C)(C)O 320.50 unknown https://doi.org/10.1016/0031-9422(81)85107-2
[(1R,4S,4aR,8aR)-4-hydroxy-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (Z)-2-methylbut-2-enoate 163024185 Click to see CC=C(C)C(=O)OC1CCC(C2C1(CC=C(C2)C(C)C)C)(C)O 320.50 unknown https://doi.org/10.1016/0031-9422(81)85107-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(2,2-Dimethylchromen-6-yl)ethanone 177040 Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C 202.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2

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