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Baccharis retusa

Baccharis retusa - 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 UUID643fceb44ad74679768812
Scientific name Baccharis retusa
Authority DC.
First published in Prodr. 5: 412 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Baccharis lacrymans Mart. ex Baker Fl. Bras. 6(3): 94 (1882)
Baccharis affinis Spreng. ex Baker Fl. Bras. 6(3): 94 (1882)
Baccharis ramosissima Gardner London J. Bot. 7: 84 (1848)
Baccharis axillaris Mart. ex Baker Fl. Bras. 6(3): 94 (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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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 Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000083802
Tropicos 2704856
KEW urn:lsid:ipni.org:names:183679-1
The Plant List gcc-40276
Open Tree Of Life 7600155
NCBI Taxonomy 2707522
IPNI 183679-1
iNaturalist 1104556
GBIF 3129911

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Metabolic engineering in Streptomyces albidoflavus for the biosynthesis of the methylated flavonoids sakuranetin, acacetin, and genkwanin Pérez-Valero Á, Ye S, Magadán-Corpas P, Villar CJ, Lombó F Microb Cell Fact 14-Nov-2023
PMCID:PMC10648386
doi:10.1186/s12934-023-02247-3
PMID:37964284
Elucidating the molecular mechanisms of essential oils' insecticidal action using a novel cheminformatics protocol Corrêa EJ, Carvalho FC, de Castro Oliveira JA, Bertolucci SK, Scotti MT, Silveira CH, Guedes FC, Melo JO, de Melo-Minardi RC, de Lima LH Sci Rep 21-Mar-2023
PMCID:PMC10028760
doi:10.1038/s41598-023-29981-3
PMID:36944648
Rice Phytoalexins: Half a Century of Amazing Discoveries; Part I: Distribution, Biosynthesis, Chemical Synthesis, and Biological Activities Valletta A, Iozia LM, Fattorini L, Leonelli F Plants (Basel) 05-Jan-2023
PMCID:PMC9862927
doi:10.3390/plants12020260
PMID:36678973
Unravelling the Therapeutic Potential of Botanicals Against Chronic Obstructive Pulmonary Disease (COPD): Molecular Insights and Future Perspectives Mitra S, Anand U, Ghorai M, Vellingiri B, Jha NK, Behl T, Kumar M, Radha, Shekhawat MS, Proćków J, Dey A Front Pharmacol 11-May-2022
PMCID:PMC9130824
doi:10.3389/fphar.2022.824132
PMID:35645819
Escaping mechanisms of ESKAPE pathogens from antibiotics and their targeting by natural compounds Jadimurthy R, Mayegowda SB, Nayak SC, Mohan CD, Rangappa KS Biotechnol Rep (Amst) 04-Apr-2022
PMCID:PMC9171455
doi:10.1016/j.btre.2022.e00728
PMID:35686013
Plant Terpenoids as Hit Compounds against Trypanosomiasis Durão R, Ramalhete C, Madureira AM, Mendes E, Duarte N Pharmaceuticals (Basel) 10-Mar-2022
PMCID:PMC8951850
doi:10.3390/ph15030340
PMID:35337138
Antimicrobial Diterpenes: Recent Development From Natural Sources Saha P, Rahman FI, Hussain F, Rahman SM, Rahman MM Front Pharmacol 28-Feb-2022
PMCID:PMC8918777
doi:10.3389/fphar.2021.820312
PMID:35295739
The Triprenylated Anthranoid Ferruginin A, a Promising Scaffold for the Development of Novel Antibiotics against Gram-Positive Bacteria Casciaro B, Ghirga F, Cappiello F, Vergine V, Loffredo MR, Cammarone S, Puglisi E, Tortora C, Quaglio D, Mori M, Botta B, Mangoni ML Antibiotics (Basel) 11-Jan-2022
PMCID:PMC8773144
doi:10.3390/antibiotics11010084
PMID:35052961
Polyphenolic Antibacterials for Food Preservation: Review, Challenges, and Current Applications Martinengo P, Arunachalam K, Shi C Foods 15-Oct-2021
PMCID:PMC8536111
doi:10.3390/foods10102469
PMID:34681518
Pharmacologic Activities of Plant-Derived Natural Products on Respiratory Diseases and Inflammations Timalsina D, Pokhrel KP, Bhusal D Biomed Res Int 04-Oct-2021
PMCID:PMC8505070
doi:10.1155/2021/1636816
PMID:34646882
Mexican Oregano (Lippia graveolens Kunth) as Source of Bioactive Compounds: A Review Bautista-Hernández I, Aguilar CN, Martínez-Ávila GC, Torres-León C, Ilina A, Flores-Gallegos AC, Kumar Verma D, Chávez-González ML Molecules 25-Aug-2021
PMCID:PMC8434378
doi:10.3390/molecules26175156
PMID:34500592
New perspectives on natural flavonoids on COVID‐19‐induced lung injuries Santana FP, Thevenard F, Gomes KS, Taguchi L, Câmara NO, Stilhano RS, Ureshino RP, Prado CM, Lago JH Phytother Res 29-Apr-2021
PMCID:PMC8242604
doi:10.1002/ptr.7131
PMID:33928690
The Great Healing Potential Hidden in Plant Preparations of Antioxidant Properties: A Return to Nature? Kiełczykowska M, Musik I Oxid Med Cell Longev 09-Oct-2020
PMCID:PMC7569450
doi:10.1155/2020/8163868
PMID:33101592
Natural product derived phytochemicals in managing acute lung injury by multiple mechanisms He YQ, Zhou CC, Yu LY, Wang L, Deng JL, Tao YL, Zhang F, Chen WS Pharmacol Res 29-Sep-2020
PMCID:PMC7522693
doi:10.1016/j.phrs.2020.105224
PMID:33007416

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
2-(6-Acetyl-5-hydroxy-2,3-dihydrobenzo[d]furan-2-yl)prop-2-enyl acetate 481690 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)COC(=O)C)O 276.28 unknown https://doi.org/10.1016/0031-9422(81)84033-2
2-[(2S)-6-acetyl-5-hydroxy-2,3-dihydro-1-benzofuran-2-yl]prop-2-enal 163034065 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)C=O)O 232.23 unknown https://doi.org/10.1016/0031-9422(81)84033-2
2-[(2S)-6-acetyl-5-hydroxy-2,3-dihydro-1-benzofuran-2-yl]prop-2-enyl acetate 163030891 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)COC(=O)C)O 276.28 unknown https://doi.org/10.1016/0031-9422(81)84033-2
Methyl 2-(6-acetyl-5-hydroxy-2,3-dihydrobenzofuran-2-yl)propenoate 86311147 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)C(=O)OC)O 262.26 unknown https://doi.org/10.1016/0031-9422(81)84033-2
Methyl 2-(6-acetyl-5-hydroxy-2,3-dihydrobenzofuran-2-yl)propenoate 71307313 Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)C(=O)OC)O 262.26 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,5R,9S,10S,13R,15S)-5,9-dimethyl-15-[(E)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 162988871 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown https://doi.org/10.1016/0031-9422(81)85107-2
Kaur-16-en-19-al 529648 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C=O 286.50 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives
2,5,7,10,15,15-Hexamethyl-7-(5-methylhex-4-enyl)-19-oxapentacyclo[14.2.1.01,14.02,11.05,10]nonadecane 162982423 Click to see CC(=CCCCC1(CCC2(C3CCC4C(C5CCC4(C3(CCC2(C1)C)C)O5)(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(81)85107-2
D:B-Friedo-18,19-secolup-19-ene, 3,10-epoxy-, (3beta,10beta)- 550409 Click to see CC(=CCCC1(CCC2(C3CCC4C(C5CCC4(C3(CCC2(C1)C)C)O5)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(81)84033-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(81)85107-2

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