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Internal ID UUID643fd7835d05f301597281
Scientific name Lupinus albescens
Authority Hook. & Arn.
First published in Bot. Misc.3: 201 (1833)

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Synonyms Top

Scientific name Authority First published in
Lupinus parodianus C.P.Sm. Spec. Lupinorum: 208 (1940)
Lupinus incanus Graham Edinburgh New Philos. J.1834(Jan.): 178 (1834)

Common names Top

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Language Common/alternative name
Chinese 大叶羽扇豆

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000174682
Tropicos 13036907
KEW urn:lsid:ipni.org:names:504061-1
The Plant List ild-20786
Open Tree Of Life 1015259
NCBI Taxonomy 53214
IPNI 504061-1
GBIF 2964724
EOL 640954
USDA GRIN 465762

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
Plant Growth-Promoting Rhizobacteria Isolated from Degraded Habitat Enhance Drought Tolerance of Acacia (Acacia abyssinica Hochst. ex Benth.) Seedlings Getahun A, Muleta D, Assefa F, Kiros S Int J Microbiol 29-Oct-2020
PMCID:PMC7646561
doi:10.1155/2020/8897998
PMID:33178283
Phylogenetic distribution and evolutionary dynamics of nod and T3SS genes in the genus Bradyrhizobium Teulet A, Gully D, Rouy Z, Camuel A, Koebnik R, Giraud E, Lassalle F Microb Genom 12-Aug-2020
PMCID:PMC7643967
doi:10.1099/mgen.0.000407
PMID:32783800
Importance of Lupinus albescens in agricultural and food-related areas: A review Confortin TC, Todero I, Luft L, Soares JF, Mazutti MA, Zabot GL, Tres MV 3 Biotech 12-Oct-2018
PMCID:PMC6181903
doi:10.1007/s13205-018-1474-x
PMID:30333950
Is Phosphate Solubilization the Forgotten Child of Plant Growth-Promoting Rhizobacteria? Granada CE, Passaglia LM, de Souza EM, Sperotto RA Front Microbiol 03-Sep-2018
PMCID:PMC6129612
doi:10.3389/fmicb.2018.02054
PMID:30233533
Alkaloid Composition of Lupinus albescens (Fabaceae) from South America A. M Planchuelo-Ravelo, M. Wink Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1993-5-602
The genomes of three Bradyrhizobium sp. isolated from root nodules of Lupinus albescens grown in extremely poor soils display important genes for resistance to environmental stress Granada CE, Vargas LK, Sant’Anna FH, Balsanelli E, de Baura VA, de Oliveira Pedrosa F, de Souza EM, Falcon T, Passaglia LM Genet Mol Biol 17-May-2018
PMCID:PMC6082242
doi:10.1590/1678-4685-GMB-2017-0098
PMID:29782030
Phylogeny and Phylogeography of Rhizobial Symbionts Nodulating Legumes of the Tribe Genisteae Stępkowski T, Banasiewicz J, Granada CE, Andrews M, Passaglia LM Genes (Basel) 14-Mar-2018
PMCID:PMC5867884
doi:10.3390/genes9030163
PMID:29538303
Specificity in Legume-Rhizobia Symbioses Andrews M, Andrews ME Int J Mol Sci 26-Mar-2017
PMCID:PMC5412291
doi:10.3390/ijms18040705
PMID:28346361
A Model to Explain Plant Growth Promotion Traits: A Multivariate Analysis of 2,211 Bacterial Isolates da Costa PB, Granada CE, Ambrosini A, Moreira F, de Souza R, dos Passos JF, Arruda L, Passaglia LM PLoS One 26-Dec-2014
PMCID:PMC4277451
doi:10.1371/journal.pone.0116020
PMID:25542031

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
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1515/ZNC-1993-5-602
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1515/ZNC-1993-5-602
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(1R,2R,9R,12S)-12-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridec-5-en-4-one 91747723 Click to see C=CCC1C2CC(CN1)CN3C2CC(=O)C=C3 232.32 unknown https://doi.org/10.1515/ZNC-1993-5-602
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1515/ZNC-1993-5-602
N-Formylalbine 91748400 Click to see C=CCC1C2CC(CN3C2CC(=O)C=C3)CN1C=O 260.33 unknown https://doi.org/10.1515/ZNC-1993-5-602
> Organoheterocyclic compounds / Quinolizidines
13-alpha-Hydroxymultiflorine 15939900 Click to see C1CN2CC3CC(C2CC1O)CN4C3CC(=O)C=C4 262.35 unknown https://doi.org/10.1515/ZNC-1993-5-602
Multiflorine 6918763 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4 246.35 unknown https://doi.org/10.1515/ZNC-1993-5-602

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