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Doniophyton anomalum

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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 UUID643fcf355d178553190075
Scientific name Doniophyton anomalum
Authority (D.Don) Kurtz
First published in Bol. Acad. Nac. Ci. 13: 187, 195. 1893

Description Top

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Synonyms Top

Scientific name Authority First published in
Doniophyton andicola Wedd. Chlor. Andina 1: 8, t. 4 B. (1855)
Chuquiraga anomala D.Don Philos. Mag. Ann. Chem. 11: 392 (1832)
Chuquiraga patagonica Phil. Linnaea 33: 111 (1864)
Doniophyton patagonicum (Phil.) Hieron. 1885
Doniophyton flavescens Suess. Revista Sudamer. Bot. 7: 275 (1943)
Doniophyton patagonicum (Phil.) Cabrera Revista Mus. La Plata, Secc. Bot. 2: 318 (1939)

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000088307
Tropicos 2723026
KEW urn:lsid:ipni.org:names:201936-1
The Plant List gcc-44646
Open Tree Of Life 643724
Observations.org 297303
NCBI Taxonomy 41570
IPNI 201936-1
iNaturalist 978799
GBIF 3139281
Elurikkus 365819
USDA GRIN 14545

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)!
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Title Authors Publication Released IDs
Comparative and phylogenetic analysis based on chloroplast genome of Heteroplexis (Compositae), a protected rare genus Duan N, Deng L, Zhang Y, Shi Y, Liu B BMC Plant Biol 22-Dec-2022
PMCID:PMC9773445
doi:10.1186/s12870-022-04000-1
PMID:36550394
Plastome Diversity and Phylogenomic Relationships in Asteraceae Pascual-Díaz JP, Garcia S, Vitales D Plants (Basel) 08-Dec-2021
PMCID:PMC8705268
doi:10.3390/plants10122699
PMID:34961169
Pseudogenization of the chloroplast threonine (trnT-GGU) gene in the sunflower family (Asteraceae) Abdullah, Mehmood F, Heidari P, Rahim A, Ahmed I, Poczai P Sci Rep 26-Oct-2021
PMCID:PMC8548347
doi:10.1038/s41598-021-00510-4
PMID:34702873
The origin of the bifurcating style in Asteraceae (Compositae) Katinas L, Hernández MP, Arambarri AM, Funk VA Ann Bot 20-Apr-2016
PMCID:PMC4866318
doi:10.1093/aob/mcw033
PMID:27098086
Diterpenes and 5-methyl coumarin derivatives from Gypothamnium pinifolium and Plazia daphnoides C. Zdero, F. Bohlmann, H.M. Niemeyer Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80695-2
Flavonoids of Doniophyton patagonicum (Phil.) Hieron. (Asteraceae). Mendiondo ME, Juárez BE Biochem Syst Ecol 01-Apr-2001
doi:10.1016/S0305-1978(00)00072-7
PMID:11182494

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 / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(88)80695-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0305-1978(00)00072-7
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0305-1978(00)00072-7
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown https://doi.org/10.1016/S0305-1978(00)00072-7
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/10.1016/S0305-1978(00)00072-7

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