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Tessaria absinthioides

Tessaria absinthioides - 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 UUID643fcc60da607781402298
Scientific name Tessaria absinthioides
Authority (Hook. & Arn.) DC.
First published in Prodr. 5: 457 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis absinthioides Hook. & Arn. Bot. Beechey Voy. : 57 (1832)
Pluchea absinthioides (Hook. & Arn.) H.Rob. & Cuatrec. Phytologia 27: 284 (1973)
Baccharis banksiifolia Bertero Mercurio Chileno 13: 594 (1829)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000062014
Tropicos 2723519
KEW urn:lsid:ipni.org:names:30101017-2
The Plant List gcc-19023
Open Tree Of Life 5739554
NCBI Taxonomy 1548622
IPNI 255282-1
iNaturalist 71230
GBIF 3114905
EPPO TESAB
EOL 6204856

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
Ultra-High-Resolution Liquid Chromatography Coupled with Electrospray Ionization Quadrupole Time-of-Flight Mass Spectrometry Analysis of Tessaria absinthioides (Hook. & Arn.) DC. (Asteraceae) and Antioxidant and Hypocholesterolemic Properties Rey M, Kruse MS, Gómez J, Simirgiotis MJ, Tapia A, Coirini H Antioxidants (Basel) 28-Dec-2023
PMCID:PMC10812689
doi:10.3390/antiox13010050
PMID:38247475
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C Front Pharmacol 12-May-2023
PMCID:PMC10213330
doi:10.3389/fphar.2023.1166178
PMID:37251336
Natural Strategies as Potential Weapons against Bacterial Biofilms Asma ST, Imre K, Morar A, Imre M, Acaroz U, Shah SR, Hussain SZ, Arslan-Acaroz D, Istanbullugil FR, Madani K, Athanassiou C, Atanasoff A, Morar D, Herman V, Zhu K Life (Basel) 17-Oct-2022
PMCID:PMC9604817
doi:10.3390/life12101618
PMID:36295053
Study of Wetland Soils of the Salar de Atacama with Different Azonal Vegetative Formations Reveals Changes in the Microbiota Associated with Hygrophile Plant Type on the Soil Surface Ramos-Tapia I, Nuñez R, Salinas C, Salinas P, Soto J, Paneque M Microbiol Spectr 19-Sep-2022
PMCID:PMC9602281
doi:10.1128/spectrum.00533-22
PMID:36121227
The green chemistry of chalcones: Valuable sources of privileged core structures for drug discovery Marotta L, Rossi S, Ibba R, Brogi S, Calderone V, Butini S, Campiani G, Gemma S Front Chem 12-Sep-2022
PMCID:PMC9511966
doi:10.3389/fchem.2022.988376
PMID:36172001
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Oxonitrogenated Derivatives of Eremophilans and Eudesmans: Antiproliferative and Anti-Trypanosoma cruzi Activity Beer MF, Reta GF, Puerta A, Bivona AE, Alberti AS, Cerny N, Malchiodi EL, Tonn CE, Padrón JM, Sülsen VP, Donadel OJ Molecules 10-May-2022
PMCID:PMC9143450
doi:10.3390/molecules27103067
PMID:35630539
Investigation of bacterial diversity using 16S rRNA sequencing and prediction of its functionalities in Moroccan phosphate mine ecosystem Azaroual SE, Kasmi Y, Aasfar A, El Arroussi H, Zeroual Y, El Kadiri Y, Zrhidri A, Elfahime E, Sefiani A, Meftah Kadmiri I Sci Rep 08-Mar-2022
PMCID:PMC8904503
doi:10.1038/s41598-022-07765-5
PMID:35260670
Editorial: Natural Plant Antioxidants and Cardiovascular Disease Castro C Front Physiol 16-Feb-2022
PMCID:PMC8889139
doi:10.3389/fphys.2022.848497
PMID:35250644
Tessaria absinthioides (Hook. & Arn.) DC. (Asteraceae) Decoction Improves the Hypercholesterolemia and Alters the Expression of LXRs in Rat Liver and Hypothalamus Rey M, Kruse MS, Magrini-Huamán RN, Gómez J, Simirgiotis MJ, Tapia A, Feresin GE, Coirini H Metabolites 27-Aug-2021
PMCID:PMC8467473
doi:10.3390/metabo11090579
PMID:34564396
Antioxidant and Anti-atherogenic Properties of Prosopis strombulifera and Tessaria absinthioides Aqueous Extracts: Modulation of NADPH Oxidase-Derived Reactive Oxygen Species Quesada I, de Paola M, Alvarez MS, Hapon MB, Gamarra-Luques C, Castro C Front Physiol 16-Jul-2021
PMCID:PMC8322988
doi:10.3389/fphys.2021.662833
PMID:34335290
Temporal, spatial and gender-based dietary differences in middle period San Pedro de Atacama, Chile: A model-based approach Pestle WJ, Hubbe M, Torres-Rouff C, Pimentel G PLoS One 25-May-2021
PMCID:PMC8148334
doi:10.1371/journal.pone.0252051
PMID:34032797
Brazilian essential oils as source for the discovery of new anti-COVID-19 drug: a review guided by in silico study Amparo TR, Seibert JB, Silveira BM, Costa FS, Almeida TC, Braga SF, da Silva GN, dos Santos OD, de Souza GH Phytochem Rev 13-Apr-2021
PMCID:PMC8042356
doi:10.1007/s11101-021-09754-4
PMID:33867898
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082

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 / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(2R)-1,2,3,4,6,7,8,8a-Octahydro-8alpha,8aalpha-dimethyl-alpha-methylene-6-oxo-2-naphthaleneacetic acid 14527133 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C(=O)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-(8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid 14527135 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-[(2R,8S,8aR)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 14527136 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-[(2S,8S,8aR)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]prop-2-enyl acetate 163008046 Click to see CC1CCC=C2C1(CC(CC2)C(=C)COC(=O)C)C 262.40 unknown https://doi.org/10.1016/S0031-9422(00)94385-1
Tessaric Acid 14527134 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C(=O)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a,8-Dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid 13819151 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid 496073 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-[(2R,4aS,7S,8aR)-7,8a-dihydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 102065497 Click to see CC12CCC(CC1(C(=C)C(CC2)O)O)C(=C)C(=O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
2-[(4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 137795140 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
3beta,5alpha-Dihydroxycostic acid 13895638 Click to see CC12CCC(CC1(C(=C)C(CC2)O)O)C(=C)C(=O)O 266.33 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
Ilicic acid 11876195 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
methyl 2-[(2S,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 101074441 Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C(=O)OC 248.36 unknown https://doi.org/10.1016/S0031-9422(00)94385-1
Pterodonoic acid 11054003 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1016/S0031-9422(96)00590-0
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
Edeine F 194407 Click to see C1=CC=C(C=C1)C(CN)C(=O)N(C(CN)C(=O)NC(CCCC(C(CC(=O)NC(=O)CNCCCNCCCCN=C(N)N)O)N)C(=O)O)C(=O)CC(N)O 780.90 unknown https://doi.org/10.1016/S0031-9422(96)00590-0

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