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Baccharis trimera

Baccharis trimera - 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 UUID643fc71dbacce604598356
Scientific name Baccharis trimera
Authority (Less.) DC.
First published in Prodr. 5: 425 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis trimera var. carqueja DC. Prodr. 7: 282 (1838)
Baccharis genistelloides var. trimera (Less.) Baker Fl. Bras. 6(3): 40 (1882)
Molina trimera Less. Linnaea 6: 141 (1831)

Common names Top

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Language Common/alternative name
gn jaguarete ka'a

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
      • Paraguay
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000011819
Tropicos 2728763
KEW urn:lsid:ipni.org:names:183819-1
The Plant List gcc-111448
Open Tree Of Life 7600230
NCBI Taxonomy 1486033
IPNI 183819-1
iNaturalist 450291
GBIF 3129265
USDA GRIN 429390
CMAUP NPO14588

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
Insights into the Neuroprotective Potential of Epicatechin: Effects against Aβ-Induced Toxicity in Caenorhabditis elegans Ayuda-Durán B, Garzón-García L, González-Manzano S, Santos-Buelga C, González-Paramás AM Antioxidants (Basel) 08-Jan-2024
PMCID:PMC10812808
doi:10.3390/antiox13010079
PMID:38247503
Editorial: Natural products in the treatment of Hyperuricemia, gout and other metabolic disorders Abdulhafiz F, Mohammed A, Chiruvella KK, Korivi M, Reduan MF Front Pharmacol 29-Nov-2023
PMCID:PMC10716440
doi:10.3389/fphar.2023.1333257
PMID:38094886
Bridging the Gap: Exploring the Preclinical Potential of Pereskia grandifolia in Metabolic-Associated Fatty Liver Disease Rodrigues Albuquerque E, Ratti da Silva G, de Abreu Braga F, Pelegrini Silva E, Sposito Negrini K, Rodrigues Fracasso JA, Pires Guarnier L, Jacomassi E, Ribeiro-Paes JT, da Silva Gomes R, Gasparotto Junior A, Lívero FA Evid Based Complement Alternat Med 09-Nov-2023
PMCID:PMC10653969
doi:10.1155/2023/8840427
PMID:38026733
Natural Antioxidants in Obesity and Related Diseases Kim HI, Park J Antioxidants (Basel) 05-Nov-2023
PMCID:PMC10669253
doi:10.3390/antiox12111966
PMID:38001819
Use of medicinal plants during COVID-19 pandemic in Brazil da Silva AM, Horsth AL, Timóteo ÉD, Faria RJ, Bazoni PS, Meira EF, dos Santos JB, da Silva MR Sci Rep 02-Oct-2023
PMCID:PMC10545667
doi:10.1038/s41598-023-43673-y
PMID:37783716
Therapeutic Potential of Natural Products in the Treatment of Schistosomiasis Azevedo CM, Meira CS, da Silva JW, Moura DM, de Oliveira SA, da Costa CJ, Santos ED, Soares MB Molecules 26-Sep-2023
PMCID:PMC10574020
doi:10.3390/molecules28196807
PMID:37836650
Digestion-Related Enzyme Inhibition Potential of Selected Mexican Medicinal Plants (Ludwigia octovalvis (Jacq.) P.H.Raven, Cnidoscolus aconitifolius and Crotalaria longirostrata) Calonico K, De La Rosa-Millan J Foods 22-Sep-2023
PMCID:PMC10572748
doi:10.3390/foods12193529
PMID:37835184
Antibacterial activity of medicinal plants on the management of mastitis in dairy cows: A systematic review Kaseke TB, Chikwambi Z, Gomo C, Mashingaidze AB, Murungweni C Vet Med Sci 19-Sep-2023
PMCID:PMC10650345
doi:10.1002/vms3.1268
PMID:37725398
Special Issue “Ethnopharmacology in Latin America” Alonso-Castro AJ Pharmaceuticals (Basel) 22-Aug-2023
PMCID:PMC10538167
doi:10.3390/ph16091189
PMID:37764997
Stability of Leaf Yerba Mate (Ilex paraguariensis) Metabolite Concentrations over the Time from the Prism of Secondary Sexual Dimorphism Rakocevic M, Maia AD, de Liz MV, Imoski R, Helm CV, Cardozo Junior EL, Wendling I Plants (Basel) 02-Jun-2023
PMCID:PMC10255638
doi:10.3390/plants12112199
PMID:37299178
Pterospartum tridentatum Liqueur Using Spirits Aged with Almond Shells: Chemical Characterization and Phenolic Profile Garcia C, Dias MI, Henriques MH, Barros L, Ramos F Molecules 31-May-2023
PMCID:PMC10254753
doi:10.3390/molecules28114455
PMID:37298931
Strong inhibition of xanthine oxidase and elastase of Baccharis trimera (Less.) DC stem extract and analysis of biologically active constituents Song SY, Lee SH, Bae MS, Park DH, Cho SS Front Pharmacol 25-May-2023
PMCID:PMC10248149
doi:10.3389/fphar.2023.1160330
PMID:37305531
Antimicrobial activity in Asterceae: The selected genera characterization and against multidrug resistance bacteria Gou J, Lu Y, Xie M, Tang X, Chen L, Zhao J, Li G, Wang H Heliyon 31-Mar-2023
PMCID:PMC10161380
doi:10.1016/j.heliyon.2023.e14985
PMID:37151707
Pro-Apoptotic and Anti-Cancer Activity of the Vernonanthura Nudiflora Hydroethanolic Extract Nadir A, Shteinfer-Kuzmine A, Pandey SK, Ortas J, Kerekes D, Shoshan-Barmatz V Cancers (Basel) 06-Mar-2023
PMCID:PMC10000589
doi:10.3390/cancers15051627
PMID:36900417
Potential Pharmacokinetic Interactions of Common Cardiovascular Drugs and Selected European and Latin American Herbal Medicines: A Scoping Review Prieto-Garcia JM, Graham L, Alkhabbaz O, Mazzari AL Plants (Basel) 31-Jan-2023
PMCID:PMC9920503
doi:10.3390/plants12030623
PMID:36771707

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
3-[[(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]methoxy]-3-oxopropanoic acid 162936456 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)OC)CCC=C2COC(=O)CC(=O)O)C 422.60 unknown https://doi.org/10.1016/0031-9422(89)80047-0
3-[[(4aR,5S,6S,7R,8aR)-5-[(3S)-5-acetyloxy-3-(acetyloxymethyl)pentyl]-7-hydroxy-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 163105056 Click to see CC1C(CC2(C(C1(C)CCC(CCOC(=O)C)COC(=O)C)CCC=C2COC(=O)CC(=O)O)C)O 510.60 unknown https://doi.org/10.1016/0031-9422(89)80047-0
3-[[5-[2-(5-Methoxyoxolan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methoxy]-3-oxopropanoic acid 14262621 Click to see CC1CCC2(C(C1(C)CCC3CC(OC3)OC)CCC=C2COC(=O)CC(=O)O)C 422.60 unknown https://doi.org/10.1016/0031-9422(89)80047-0
3-O-[[5-[5-acetyloxy-3-(acetyloxymethyl)pentyl]-7-hydroxy-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl] 1-O-methyl propanedioate 14262683 Click to see CC1C(CC2(C(C1(C)CCC(CCOC(=O)C)COC(=O)C)CCC=C2COC(=O)CC(=O)OC)C)O 524.60 unknown https://doi.org/10.1016/0031-9422(89)80047-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(89)80047-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1055/S-2006-962613
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1055/S-2006-962613
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1055/S-2006-957866
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1055/S-2006-962613
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1055/S-2006-962613
https://doi.org/10.1021/JF9711045
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)00223-5
https://doi.org/10.1016/0031-9422(89)80047-0
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database

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