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Lupinus sericeus

Lupinus sericeus - Unknown
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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 UUID643fd78a3564f946466753
Scientific name Lupinus sericeus
Authority Pursh
First published in Fl. Amer. Sept.2: 468 (1813)

Description Top

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Lupinus sericeus, also known as silky lupine or Pursh's silky lupine, is a flowering plant in the legume family native to western North America. It has erect stems covered in silvery or reddish hairs and leaves with lance-shaped leaflets. The flowers are usually purple or blue, but can also be white or yellowish. This plant can be found in a variety of habitats, including forests, woodlands, and grasslands, and is often found in recently burned areas. It is toxic to sheep due to its concentration of quinolizidine alkaloids, but is not harmful to other wild animals such as deer. Other animals, such as bighorn sheep and Columbia ground squirrels, feed on this plant.

Synonyms Top

Scientific name Authority First published in
Lupinus sericeus var. sericeus Pursh

Common names Top

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Language Common/alternative name
English silky lupine

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lupinus sericeus subsp. huffmanii (C.P.Sm.) Fleak & D.B.Dunn Trans. Missouri Acad. Sci.5: 87 (1971)
Lupinus sericeus subsp. huffmannii (C.P.Sm.) Fleak & D.B.Dunn Trans. Missouri Acad. Sci. 5: 87. 1971
Lupinus sericeus subsp. marianus (Rydb.) Fleak & D.B.Dunn Trans. Missouri Acad. Sci.5: 86 (1971)
Lupinus sericeus subsp. sericeus Pursh Unknown

Varieties (abbr. var.) Top

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Name Authority First published in
Lupinus sericeus var. egglestonianus C.P.Sm. Spec. Lupinorum: 104 (1939)
Lupinus sericeus var. flexuosus C.P.Sm. Bull. Torrey Bot. Club51: 307 (1924)
Lupinus sericeus var. maximus Fleak & D.B.Dunn Trans. Missouri Acad. Sci.5: 85 (1971)
Lupinus sericeus var. thompsonianus C.P.Sm. Spec. Lupinorum: 105 (1939)
Lupinus sericeus var. wallowensis C.P.Sm. Spec. Lupinorum: 105 (1939)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Northern America
    • North-central U.S.A.
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000174760
Canadensys 5823
USDA Plants LUSE4
KEW urn:lsid:ipni.org:names:317394-2
The Plant List ild-20857
Open Tree Of Life 810393
NCBI Taxonomy 61075
Nature Serve 2.153040
IPNI 317394-2
iNaturalist 164926
GBIF 2964333
Freebase /m/0hn9xs4
FEIS plants/forb/lupser
EPPO LUPSE
EOL 641027
USDA GRIN 22905
Wikipedia Lupinus_sericeus

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
Power Bars: Mormon Crickets Get Immunity Boost from Eating Grasshoppers Srygley RB, Branson DH Insects 10-Nov-2023
PMCID:PMC10672412
doi:10.3390/insects14110868
PMID:37999067
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649
The First Evidence of Gibberellic Acid’s Ability to Modulate Target Species’ Sensitivity to Honeysuckle (Lonicera maackii) Allelochemicals Barta CÉ, Jenkins BC, Lindstrom DS, Zahnd AK, Székely G Plants (Basel) 23-Feb-2023
PMCID:PMC10005159
doi:10.3390/plants12051014
PMID:36903875
“When the Wild Roses Bloom”: Indigenous Knowledge and Environmental Change in Northwestern North America Turner NJ, Reid AJ Geohealth 01-Nov-2022
PMCID:PMC9665002
doi:10.1029/2022GH000612
PMID:36398276
Mutation of the MYH3 gene causes recessive cleft palate in Limousine cattle Vaiman A, Fritz S, Beauvallet C, Boussaha M, Grohs C, Daniel-Carlier N, Relun A, Boichard D, Vilotte JL, Duchesne A Genet Sel Evol 29-Oct-2022
PMCID:PMC9617432
doi:10.1186/s12711-022-00762-2
PMID:36309651
Highly Resolved Papilionoid Legume Phylogeny Based on Plastid Phylogenomics Choi IS, Cardoso D, de Queiroz LP, de Lima HC, Lee C, Ruhlman TA, Jansen RK, Wojciechowski MF Front Plant Sci 23-Feb-2022
PMCID:PMC8905342
doi:10.3389/fpls.2022.823190
PMID:35283880
Chronosequence and direct observation approaches reveal complementary community dynamics in a novel ecosystem Kulmatiski A, Beard KH PLoS One 18-Mar-2019
PMCID:PMC6422298
doi:10.1371/journal.pone.0207047
PMID:30883554
Multi-omic Analyses of Extensively Decayed Pinus contorta Reveal Expression of a Diverse Array of Lignocellulose-Degrading Enzymes Hori C, Gaskell J, Cullen D, Sabat G, Stewart PE, Lail K, Peng Y, Barry K, Grigoriev IV, Kohler A, Fauchery L, Martin F, Zeiner CA, Bhatnagar JM Appl Environ Microbiol 01-Oct-2018
PMCID:PMC6182905
doi:10.1128/AEM.01133-18
PMID:30097442
A Hypothetical Bottleneck in the Plant Microbiome Newcombe G, Harding A, Ridout M, Busby PE Front Microbiol 31-Jul-2018
PMCID:PMC6080073
doi:10.3389/fmicb.2018.01645
PMID:30108556
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
Community‐level plant–soil feedbacks explain landscape distribution of native and non‐native plants Kulmatiski A Ecol Evol 18-Jan-2018
PMCID:PMC5817120
doi:10.1002/ece3.3649
PMID:29468023
Assessing Greater Sage-Grouse Selection of Brood-Rearing Habitat Using Remotely-Sensed Imagery: Can Readily Available High-Resolution Imagery Be Used to Identify Brood-Rearing Habitat Across a Broad Landscape? Westover M, Baxter J, Baxter R, Day C, Jensen R, Petersen S, Larsen R PLoS One 24-May-2016
PMCID:PMC4878777
doi:10.1371/journal.pone.0156290
PMID:27218829
Abscisic Acid: Hidden Architect of Root System Structure Harris JM Plants (Basel) 11-Aug-2015
PMCID:PMC4844405
doi:10.3390/plants4030548
PMID:27135341
Potential Role of Masting by Introduced Bamboos in Deer Mice (Peromyscus maniculatus) Population Irruptions Holds Public Health Consequences Smith MC, Gomulkiewicz R, Mack RN PLoS One 21-Apr-2015
PMCID:PMC4405191
doi:10.1371/journal.pone.0124419
PMID:25898267
Comparative Phylogenomics Uncovers the Impact of Symbiotic Associations on Host Genome Evolution Delaux PM, Varala K, Edger PP, Coruzzi GM, Pires JC, Ané JM PLoS Genet 17-Jul-2014
PMCID:PMC4102449
doi:10.1371/journal.pgen.1004487
PMID:25032823

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(-)-Sparteine 3966 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1139/V53-025
https://doi.org/10.1021/JA01860A030
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JA01298A063
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JA01298A063
(1R,2R,9S,10R,14S)-14-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 162933370 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(N4C3)O 264.36 unknown https://doi.org/10.1139/V53-025
(1R,2S,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane-8,16-dione 51009885 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCCN4C3=O 262.35 unknown https://doi.org/10.1021/JF00112A048
13-Hydroxylupanine 250873 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1021/JA01875A055
14-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 12305096 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(N4C3)O 264.36 unknown https://doi.org/10.1139/V53-025
17-Oxosparteine 218066 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1021/JF00112A048
9-Hydroxysparteine 91752878 Click to see C1CCN2CC3(CC(C2C1)CN4C3CCCC4)O 250.38 unknown https://doi.org/10.1021/JO01285A024
beta-Isosparteine 168213 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/JF00112A048
Hydroxylupanine 73404 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1021/JA01875A055
Pusilline 6101950 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1021/JA01860A030
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/JF00112A048
https://doi.org/10.1139/V53-025
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0305-1978(82)90034-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0305-1978(82)90034-5
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(82)90034-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497677 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(82)90034-5
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/0305-1978(82)90034-5

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