Azorella trisecta

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Internal ID UUID68f9057c1edac780311133
Scientific name Azorella trisecta
Authority (H.Wolff) Mart.Fernández & C.I.Calviño
First published in Darwiniana n.s., 7(2): 303. 2019

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Synonyms Top

Scientific name Authority First published in
Mulinum crassifolium Phil. Fl. Atacam. : 24 (1860)
Azorella atacamensis G.M.Plunkett & A.N.Nicolas Brittonia 69: 48 (2016)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
KEW urn:lsid:ipni.org:names:60473300-2
Open Tree Of Life 3887138
NCBI Taxonomy 1277843
IPNI 60473300-2
iNaturalist 797087
GBIF 9539071
Wikipedia Azorella_atacamensis
World Flora Online wfo-1000020537

Genomes (via NCBI) Top

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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
Pathogen-associated gene discovery workflows for novel antivirulence therapeutic development Lau WY, Taylor PK, Brinkman FS, Lee AH eBioMedicine 09-Jan-2023
PMCID:PMC9843249
doi:10.1016/j.ebiom.2022.104429
PMID:36628845
Antimicrobial Properties of Chilean Native Plants: Future Aspects in Their Application in the Food Industry Otero MC, Fuentes JA, Atala C, Cuadros-Orellana S, Fuentes C, Gordillo-Fuenzalida F Foods 15-Jun-2022
PMCID:PMC9222376
doi:10.3390/foods11121763
PMID:35741959
Activity of Semi-Synthetic Mulinanes against MDR, Pre-XDR, and XDR Strains of Mycobacterium tuberculosis Martínez-González MA, Peña-Rodríguez LM, Uc-Cachón AH, Bórquez J, Simirgiotis MJ, Barrios-García HB, Hernández-Pando R, Loyola LA, Areche C, Dzul-Beh AD, Barrios-Payán JA, Mata-Espinosa D, Escalante-Erosa F, García-Sosa K, Molina-Salinas GM Metabolites 16-Dec-2021
PMCID:PMC8703773
doi:10.3390/metabo11120876
PMID:34940634
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Topical Collection “Pharmacology of Medicinal Plants” Romano B, Lucariello G, Capasso R Biomolecules 14-Jan-2021
PMCID:PMC7828774
doi:10.3390/biom11010101
PMID:33466709
Tackling Pseudomonas aeruginosa Virulence by Mulinane-Like Diterpenoids from Azorella atacamensis Azuama OC, Ortiz S, Quirós-Guerrero L, Bouffartigues E, Tortuel D, Maillot O, Feuilloley M, Cornelis P, Lesouhaitier O, Grougnet R, Boutefnouchet S, Wolfender JL, Chevalier S, Tahrioui A Biomolecules 02-Dec-2020
PMCID:PMC7761567
doi:10.3390/biom10121626
PMID:33276611
Mulinane- and Azorellane-Type Diterpenoids: A Systematic Review of Their Biosynthesis, Chemistry, and Pharmacology Dzul-Beh AD, Uc-Cachón AH, Bórquez J, Loyola LA, Peña-Rodríguez LM, Molina-Salinas GM Biomolecules 17-Sep-2020
PMCID:PMC7565077
doi:10.3390/biom10091333
PMID:32957713
Mulinum crassifolium Phil; Two New Mulinanes, Gastroprotective Activity and Metabolomic Analysis by UHPLC-Orbitrap Mass Spectrometry Areche C, Fernandez-Burgos R, Cano de Terrones T, Simirgiotis M, García-Beltrán O, Borquez J, Sepulveda B Molecules 28-Apr-2019
PMCID:PMC6539732
doi:10.3390/molecules24091673
PMID:31035428
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
Nitrogen cycling in an extreme hyperarid environment inferred from δ15N analyses of plants, soils and herbivore diet Díaz FP, Frugone M, Gutiérrez RA, Latorre C Sci Rep 09-Mar-2016
PMCID:PMC4783660
doi:10.1038/srep22226
PMID:26956399
Further Mulinane and Azorellane Diterpenoids Isolated from Mulinum crassifolium and Azorella compacta Bórquez J, Ardiles A, Loyola LA, Peña-Rodriguez LM, Molina-Salinas GM, Vallejos J, Collado IG, Simirgiotis MJ Molecules 28-Mar-2014
PMCID:PMC6271538
doi:10.3390/molecules19043898
PMID:24686578
17-Acet­oxy­mulinic acid Brito I, Bórquez J, Albanez J, Bolte M, Peña-Rodríguez LM Acta Crystallogr Sect E Struct Rep Online 28-Aug-2010
PMCID:PMC3007890
doi:10.1107/S1600536810032952
PMID:21588773
Methyl 5a-acetoxy­methyl-3-isopropyl-8-methyl-1,2,3,3a,4,5,5a,6,7,10,10a,10b-dodeca­hydro-7,10-endo-epidioxy­cylohepta­[e]indene-3a-carboxyl­ate Brito I, Bórquez J, Loyola LA, Cárdenas A, López-Rodríguez M Acta Crystallogr Sect E Struct Rep Online 07-Jun-2008
PMCID:PMC2961694
doi:10.1107/S1600536808016474
PMID:21202848
Bacterial Community Structure in the Hyperarid Core of the Atacama Desert, Chile Drees KP, Neilson JW, Betancourt JL, Quade J, Henderson DA, Pryor BM, Maier RM Appl Environ Microbiol 06-Oct-2006
PMCID:PMC1694221
doi:10.1128/AEM.01305-06
PMID:17028238

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 / Valparane and mulinane diterpenoids
Mulinolic acid 10018937 Click to see 320.50 unknown https://doi.org/10.1016/0031-9422(96)00159-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
17-Acetoxymulinic acid 139079852 Click to see 785.00 unknown https://doi.org/10.1016/0031-9422(90)85372-M
> Organic oxygen compounds / Organic oxides / Organic peroxides / Dialkyl peroxides
Mulinic acid 139078344 Click to see 668.90 unknown https://doi.org/10.1016/S0040-4020(01)87848-0
https://doi.org/10.1021/NP50077A028
> Organoheterocyclic compounds / Epoxides
5,9-Dimethyl-13-propan-2-yl-3,6-dioxapentacyclo[7.7.0.02,4.05,7.012,16]hexadecane-12-carboxylic acid 163192446 Click to see 334.40 unknown https://doi.org/10.1016/S0040-4020(01)87848-0
> Organoheterocyclic compounds / Oxanes
(1S,4S,5R,8S,9S,12R)-12-methyl-5-propan-2-yl-13-oxatetracyclo[10.2.2.01,9.04,8]hexadec-10-ene-4-carboxylic acid 101260442 Click to see CC(C)C1CCC2C1(CCC34C2C=CC(CC3)(OC4)C)C(=O)O 318.40 unknown https://doi.org/10.1021/NP50077A028

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