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Xenophyllum poposum

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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 UUID643fd1349a6e2826148274
Scientific name Xenophyllum poposum
Authority (Phil.) V.A.Funk
First published in Novon 7(3): 240 (1997)

Description Top

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Synonyms Top

Scientific name Authority First published in
Werneria lorentziana Hieron. Bot. Jahrb. Syst. 21(3): 364 (1895)
Werneria poposa Phil. Anales Mus. Nac. Santiago de Chile 1891: 40 (1891)

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000111972
Tropicos 50103173
KEW urn:lsid:ipni.org:names:997492-1
The Plant List gcc-7135
Open Tree Of Life 63639
NCBI Taxonomy 462584
IUCN Red List 133163429
IPNI 997492-1
iNaturalist 338222
GBIF 3142276
EOL 5175191

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
Diversity of Culturable Bacteria from Endemic Medicinal Plants of the Highlands of the Province of Parinacota, Chile Moraga D, Latorre K, Muñoz-Torres P, Cárdenas S, Jofré-Quispe A, López-Cepeda J, Bustos L, Balada C, Argaluza MF, González P, Guzmán L Biology (Basel) 27-Jun-2023
PMCID:PMC10376134
doi:10.3390/biology12070920
PMID:37508351
Bio-Actives from Natural Products with Potential Cardioprotective Properties: Isolation, Identification, and Pharmacological Actions of Apigenin, Quercetin, and Silibinin Tomou EM, Papakyriakopoulou P, Skaltsa H, Valsami G, Kadoglou NP Molecules 05-Mar-2023
PMCID:PMC10005323
doi:10.3390/molecules28052387
PMID:36903630
Biogeographical Relationships and Diversity in the Peruvian Flora Reported by Hipólito Ruiz and José Pavón: Vegetation, Uses and Anthropology Arias-Gámez JM, Linares-Perea E, Vicente-Orellana JA, Galán-de-Mera A Biology (Basel) 13-Feb-2023
PMCID:PMC9953382
doi:10.3390/biology12020294
PMID:36829570
Bioprospecting of Helichrysum Species: Chemical Profile, Phytochemical Properties, and Antifungal Efficacy against Botrytis cinerea Matrose NA, Belay ZA, Obikeze K, Mokwena L, Caleb OJ Plants (Basel) 22-Dec-2022
PMCID:PMC9824591
doi:10.3390/plants12010058
PMID:36616185
Chemical Composition, Antipathogenic and Cytotoxic Activity of the Essential Oil Extracted from Amorpha fruticosa Fruits Marinas IC, Oprea E, Buleandra M, Badea IA, Tihauan BM, Marutescu L, Angheloiu M, Matei E, Chifiriuc MC Molecules 24-May-2021
PMCID:PMC8197342
doi:10.3390/molecules26113146
PMID:34074063
Distribution and Transmission of Medicinal Plant Knowledge in the Andean Highlands: A Case Study from Peru and Bolivia Mathez-Stiefel SL, Vandebroek I Evid Based Complement Alternat Med 29-Nov-2011
PMCID:PMC3235884
doi:10.1155/2012/959285
PMID:22203885
Ethnobotany, volatile oils and secretion tissues of werneria poposa from Argentina. Abella L, Cortella AR, Velasco-Negueruela A, Pérez-Alonso MJ Pharm Biol 01-Jan-2000
doi:10.1076/1388-0209(200007)3831-SFT197
PMID:21214462

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Neoisopulegol 6553885 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Isopulegol 24585 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1076/1388-0209(200007)3831-SFT197

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