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Lupinus mexicanus

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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 UUID643fd917b05e4367034304
Scientific name Lupinus mexicanus
Authority Cerv. ex Lag.
First published in Gen. Sp. Pl.: 22 (1816)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lupinus bilineatus Benth. Pl. Hartw.: 11 (1839)
Lupinus venustus Bailly Fl. Pleine Terre: 480 (1863)
Lupinus ehrenbergii var. aureolanatus C.P.Sm. Spec. Lupinorum: 60 (1938)
Lupinus tricolor J.Carter Gard. Chron.1864: 242 (1864)

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-0000183548
Tropicos 13037046
KEW urn:lsid:ipni.org:names:504762-1
The Plant List ild-29611
Open Tree Of Life 810398
NCBI Taxonomy 61077
IUCN Red List 100514765
IPNI 504760-1
iNaturalist 290179
GBIF 2963859
EOL 642974
USDA GRIN 313369
Wikipedia Lupinus_mexicanus

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
Mango anthracnose disease: the current situation and direction for future research Dofuor AK, Quartey NK, Osabutey AF, Antwi-Agyakwa AK, Asante K, Boateng BO, Ablormeti FK, Lutuf H, Osei-Owusu J, Osei JH, Ekloh W, Loh SK, Honger JO, Aidoo OF, Ninsin KD Front Microbiol 24-Aug-2023
PMCID:PMC10484599
doi:10.3389/fmicb.2023.1168203
PMID:37692388
Recent Developments of Gramine: Chemistry and Biological Activity Zhang J, Jia Q, Li N, Gu L, Dan W, Dai J Molecules 27-Jul-2023
PMCID:PMC10419902
doi:10.3390/molecules28155695
PMID:37570664
A New Fluorescence Detection Method for Tryptophan- and Tyrosine-Derived Allelopathic Compounds in Barley and Lupin Leite Dias S, Garibay-Hernández A, Brendel FL, Gabriel Chavez B, Brückner E, Mock HP, Franke J, D’Auria JC Plants (Basel) 09-May-2023
PMCID:PMC10222917
doi:10.3390/plants12101930
PMID:37653847
Alkaloids in food: a review of toxicity, analytical methods, occurrence and risk assessments Akinboye AJ, Kim K, Choi S, Yang I, Lee JG Food Sci Biotechnol 05-Apr-2023
PMCID:PMC10290023
doi:10.1007/s10068-023-01295-0
PMID:37362815
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Nutritional and Bioactive Compounds in Mexican Lupin Beans Species: A Mini-Review Ruiz-López MA, Barrientos-Ramírez L, García-López PM, Valdés-Miramontes EH, Zamora-Natera JF, Rodríguez-Macias R, Salcedo-Pérez E, Bañuelos-Pineda J, Vargas-Radillo JJ Nutrients 02-Aug-2019
PMCID:PMC6723436
doi:10.3390/nu11081785
PMID:31382375
Quinolizidine Alkaloids as Nitrogen Source for Lupin Seedlings and Cell Cultures M. Wink, L. Witte Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1985-11-1204
Diurnal Fluctuation of Quinolizidine Alkaloid Accumulation in Legume Plants and Photomixotrophic Cell Suspension Cultures Michael Wink, Thomas Hartmann Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1982-5-604
Data on introduced plants in Zimbabwe: Floristic changes and patterns of collection based on historical herbarium records Maroyi A Data Brief 22-Sep-2017
PMCID:PMC5712053
doi:10.1016/j.dib.2017.09.046
PMID:29214198
Flavones: From Biosynthesis to Health Benefits Jiang N, Doseff AI, Grotewold E Plants (Basel) 21-Jun-2016
PMCID:PMC4931407
doi:10.3390/plants5020027
PMID:27338492
Flavone C-glycosides from Lupinus hartwegii. Kamel MS Phytochemistry 01-Jun-2003
doi:10.1016/S0031-9422(03)00076-1
PMID:12770596
Alkaloids from seeds of Lupinus varius and L. hartwegii Mahmoud H. Mohamed, Hashem A. Hassanean Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00275-6
Accumulation of quinolizidine alkaloids in plants and cell suspension cultures: genera lupinus, cytisus, baptisia, genista, laburnum, and sophora. Wink M, Witte L, Hartmann T, Theuring C, Volz V Planta Med 01-Aug-1983
doi:10.1055/S-2007-969928
PMID:17404991
Aphylline, epiaphylline, 10,17-dioxosparteine, gramine, and other unexpected alkaloids from Lupinus hartwegii. Anderson JN, Martin RO J Org Chem 15-Oct-1976
doi:10.1021/JO00883A026
PMID:978295

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
(-)-Deoxylupanoline 198599 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1515/ZNC-1985-11-1204
(1R,2R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 118701428 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1055/S-2007-969928
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 6454846 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4 246.35 unknown https://doi.org/10.1515/ZNC-1985-11-1204
(1S,2R,9R,10S,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 12444870 Click to see C1CCN2C(C1)C3CC(C2=O)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1016/S0031-9422(97)00275-6
https://doi.org/10.1021/JO00883A026
(1S,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 12306750 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1021/JO00883A026
10-Oxosparteine 21769904 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1016/S0031-9422(97)00275-6
4-Hydroxylupanine 6427216 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4O 250.38 unknown https://doi.org/10.1515/ZNC-1982-5-604
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0031-9422(03)00076-1
Aphyllidine 12306738 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4 246.35 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1016/S0031-9422(97)00275-6
CID 442940 442940 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1021/JO00883A026
https://doi.org/10.1515/ZNC-1982-5-604
Isolupanine 15939852 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1515/ZNC-1982-5-604
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Ferulic acid 4-O-beta-D-glucoside 9820054 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1016/S0031-9422(03)00076-1
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 71317062 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(03)00076-1
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154496625 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(03)00076-1
5-hydroxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162942009 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(03)00076-1

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