Details Top

Internal ID UUID643fdf02b767d455599519
Scientific name Lupinus mutabilis
Authority Sweet
First published in Brit. Fl. Gard.2: t. 130 (1826)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Edible seed (chocho or tarwi), seed flour, seed oil.

Industrial and craft applications:
Research/model organism: a legume reference for nitrogen fixation, nodulation genetics, and comparative Leguminosae genomics; used in studies on symbiotic signaling, mycorrhizal interactions, and seed storage protein expression. Model populations have been developed to support breeding and genomic analyses.

Food and beverages (non-medicinal):
Seeds are consumed after extensive leaching to remove bitter alkaloids; traditional processing includes soaking and boiling, followed by fermentation or drying. Seed flour is used in baking and as a protein supplement; seed oil is edible for cooking and frying. Fermentation uses as a substrate for biomass or protein production are documented in scientific literature.

Colorants and tanning:
No specific colorants or tanning uses are documented for this taxon.

Wood and fiber:
No documented timber or fiber uses.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses are specifically attributed to this species.

Properties relevant to use:
Seeds are protein-rich (≈40–50% protein) and oil-rich (≈16–25% oil). The oil is notable for a relatively high oleic acid content and a favorable unsaturated fatty acid profile. Seeds contain alkaloids (lupinine, sparteine, etc.) that require removal for food uses; breeding has produced low-alkaloid (“sweet”) cultivars. Flour has gluten-like foaming and emulsifying properties useful in baking.

Standards and regulation:
No specific ISO/ASTM/EN standards are identified for chocho seed, flour, or oil. Traditional domestic use as a food legume in Andean countries implies compliance with national food safety and labeling regulations, but no dedicated regulatory standards are recorded in the scientific literature cited.

Sustainability and sourcing:
Grown in Andean highland agroecosystems; recognized as a source of locally adapted, protein-rich seed and for its role in legume crop diversification for sustainable cropping systems. Wild-type forms with bitter alkaloids require specific breeding or selection to produce edible cultivars; agricultural extension in Andean countries emphasizes cultivar choice and seed processing.

Synonyms Top

Scientific name Authority First published in
Lupinus mutabilis var. mutabilis Sweet
Lupinus cruckshanksii Hook. Bot. Mag.58: t. 3056 (1831)
Lupinus mutabilis var. roseus Vargas in C.P.Sm. Spec. Lupinorum: 588 (1948)
Lupinus mutabilis var. cruckshanksii (Hook.) D.Don in Sweet R.Sweet, Brit. Fl. Gard.6: t. 203 (1833)
Lupinus mutabilis f. cruckshanksii (Hook.) Voss Vilm. Blumengärtn. ed. 3, 1: 196 (1896)
Lupinus mutabilis f. variicolor T.Moore Proc. Roy. Hort. Soc. London 1: 319 (1860)

Common names Top

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Language Common/alternative name
English tarwi
Spanish tarhui
Spanish tarwi
Arabic ترمس طفري
ay tarwi
German andenlupine
German chochos
German anden-lupine
Esperanto andena lupeno
Estonian muutlik lupiin
Finnish tuoksulupiini
French tarwi
French lupin changeant
French lupin andin
French chocho
Icelandic andeslúpína
Japanese ザッショクノボリフジ
Lithuanian andinis lubinas
Polish Łubin zmienny
Polish Łubin indyjski
Quechua tarwi
Quechua tawri
Chinese 南美羽扇豆

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-0000213497
USDA Plants LUMU8
Tropicos 13037060
KEW urn:lsid:ipni.org:names:504808-1
The Plant List ild-8563
Open Tree Of Life 324961
NCBI Taxonomy 53232
IPNI 504809-1
iNaturalist 447603
GBIF 2964711
Freebase /m/06lbsf
EPPO LUPMU
EOL 703671
Elurikkus 5580
US Library of Congress sh94000095
USDA GRIN 22844
Wikipedia Lupinus_mutabilis

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
New Analytical Approach to Quinolizidine Alkaloids and Their Assumed Biosynthesis Pathways in Lupin Seeds Namdar D, Mulder PP, Ben-Simchon E, Hacham Y, Basheer L, Cohen O, Sternberg M, Shelef O Toxins (Basel) 21-Mar-2024
PMCID:PMC10974633
doi:10.3390/toxins16030163
PMID:38535829
Field study of parasitic contamination of fruits, vegetables and leafy greens in the Ecuadorian Andes González-Ramírez LC, Djabayan-Djibeyan P, Prato JG, García Ríos CA, Carrero JC, Trelis M, Fuentes MV F1000Res 12-Mar-2024
PMCID:PMC10808852
doi:10.12688/f1000research.132957.1
PMID:38273962
Heavy Metal Bioaccumulation in Peruvian Food and Medicinal Products Tejada-Purizaca TR, Garcia-Chevesich PA, Ticona-Quea J, Martínez G, Martínez K, Morales-Paredes L, Romero-Mariscal G, Arenazas-Rodríguez A, Vanzin G, Sharp JO, McCray JE Foods 29-Feb-2024
PMCID:PMC10931273
doi:10.3390/foods13050762
PMID:38472875
Australian Cool-Season Pulse Seed-Borne Virus Research: 1. Alfalfa and Cucumber Mosaic Viruses and Less Important Viruses Jones RA, Congdon BS Viruses 18-Jan-2024
PMCID:PMC10819373
doi:10.3390/v16010144
PMID:38257844
Evaluation of Phytase Impact on In Vitro Protein and Phosphorus Bioaccessibility of Two Lupin Species for Rainbow Trout (Oncorhynchus mykiss) Azcuy RL, Casaretto ME, Márquez L, Hernández AJ, Morales GA Aquac Nutr 03-Jan-2024
PMCID:PMC10781528
doi:10.1155/2024/2697729
PMID:38213755
Identification and Potential Participation of Lipases in Autophagic Body Degradation in Embryonic Axes of Lupin (Lupinus spp.) Germinating Seeds Wleklik K, Stefaniak S, Nuc K, Pietrowska-Borek M, Borek S Int J Mol Sci 20-Dec-2023
PMCID:PMC10779169
doi:10.3390/ijms25010090
PMID:38203260
Lupin as a Source of Bioactive Antioxidant Compounds for Food Products Estivi L, Brandolini A, Gasparini A, Hidalgo A Molecules 10-Nov-2023
PMCID:PMC10673580
doi:10.3390/molecules28227529
PMID:38005249
Compositional Attributes of Blue Lupin (Lupinus angustifolius) Seeds for Selection of High-Protein Cultivars Roman L, Tsochatzis E, Tarin K, Röndahl EM, Ottosen CO, Corredig M J Agric Food Chem 31-Oct-2023
PMCID:PMC10655177
doi:10.1021/acs.jafc.3c04804
PMID:37906270
Optimization and Characterization of Lupin Protein Isolate Obtained Using Alkaline Solubilization-Isoelectric Precipitation Domínguez R, Bermúdez R, Pateiro M, Lucas-González R, Lorenzo JM Foods 23-Oct-2023
PMCID:PMC10606863
doi:10.3390/foods12203875
PMID:37893768
Unveiling the Evidence for the Use of Pulses in Managing Type 2 Diabetes Mellitus: A Scoping Review Thomas DJ, Shafiee M, Nosworthy MG, Lane G, Ramdath DD, Vatanparast H Nutrients 30-Sep-2023
PMCID:PMC10574713
doi:10.3390/nu15194222
PMID:37836506
Modification of the existing maximum residue levels for mefentrifluconazole in various commodities Bellisai G, Bernasconi G, Carrasco Cabrera L, Castellan I, del Aguila M, Ferreira L, Santonja GG, Greco L, Jarrah S, Leuschner R, Perez JM, Miron I, Nave S, Pedersen R, Reich H, Ruocco S, Santos M, Scarlato AP, Theobald A, Tiramani M, Verani A EFSA J 15-Sep-2023
PMCID:PMC10502649
doi:10.2903/j.efsa.2023.8237
PMID:37719918
Nano-Biofertilizer Formulations for Agriculture: A Systematic Review on Recent Advances and Prospective Applications Garg D, Sridhar K, Stephen Inbaraj B, Chawla P, Tripathi M, Sharma M Bioengineering (Basel) 25-Aug-2023
PMCID:PMC10525541
doi:10.3390/bioengineering10091010
PMID:37760112
Analysis of lncRNAs in Lupinus mutabilis (Tarwi) and Their Potential Role in Drought Response Hidalgo M, Ramos C, Zolla G Noncoding RNA 23-Aug-2023
PMCID:PMC10514842
doi:10.3390/ncrna9050048
PMID:37736894
Product safety aspects of plant molecular farming Buyel JF Front Bioeng Biotechnol 08-Aug-2023
PMCID:PMC10442644
doi:10.3389/fbioe.2023.1238917
PMID:37614627
Sugar Starvation Disrupts Lipid Breakdown by Inducing Autophagy in Embryonic Axes of Lupin (Lupinus spp.) Germinating Seeds Borek S, Stefaniak S, Nuc K, Wojtyla Ł, Ratajczak E, Sitkiewicz E, Malinowska A, Świderska B, Wleklik K, Pietrowska-Borek M Int J Mol Sci 21-Jul-2023
PMCID:PMC10380618
doi:10.3390/ijms241411773
PMID:37511532

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 / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1021/JF00119A003
Monolupin 71056954 Click to see 244.33 unknown https://doi.org/10.1021/JF00119A003
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see 248.36 unknown https://doi.org/10.1021/JF00119A003
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see 248.36 unknown https://doi.org/10.1021/JF00119A003
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see 248.36 unknown https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
https://doi.org/10.1021/JF00119A003
13-Hydroxylupanine 5459919 Click to see 264.36 unknown https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
https://doi.org/10.1021/JF00119A003
17-Oxolupanine 14139904 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3 262.35 unknown https://doi.org/10.1021/JF00119A003
4-Hydroxylupanine 6427216 Click to see 250.38 unknown https://doi.org/10.1021/JF00119A003
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
D-Gluconate 6-phosphate tris(cyclohexylamine) salt 16212687 Click to see 234.38 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
Sparteine 644020 Click to see 234.38 unknown https://doi.org/10.1021/JF00119A003
https://doi.org/10.1111/J.2042-7158.1998.TB04013.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)D-Ido(a1-6)Glc(a1-2b)Psif 132990894 Click to see 666.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Raffinose 439242 Click to see 504.40 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Stachyose 439531 Click to see 666.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-(3,4-Dihydro-5-(2R)-2-piperidinyl-1(2H)-pyridinyl)ethanone 442625 Click to see 208.30 unknown https://doi.org/10.1021/JF00119A003
> Organoheterocyclic compounds / Quinolizidines
(1S,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-5-en-4-one 162886558 Click to see 246.35 unknown https://doi.org/10.1021/JF00119A003
(7S,7aS,14S,14aR)-1,7,7a,8,9,10,11,13,14,14a-Decahydro-7,14-methano-2H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-2-one 6918763 Click to see 246.35 unknown https://doi.org/10.1021/JF00119A003
> Organoheterocyclic compounds / Quinolizidines / Quinolizidinones
(2R,10S)-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecan-6-one 102004777 Click to see C=CCC1C2CC(CN1)C3CCCC(=O)N3C2 234.34 unknown https://doi.org/10.1021/JF00119A003
1,5-Methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one, decahydro-4-(2-propenyl)-, (1S-(1alpha,4alpha,5alpha,11aalpha))- 3080564 Click to see 234.34 unknown https://doi.org/10.1021/JF00119A003
Tetrahydrorhombifoline 15511175 Click to see C=CCCN1CC2CC(C1)C3CCCC(=O)N3C2 248.36 unknown https://doi.org/10.1021/JF00119A003
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/0889-1575(88)90035-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(3-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163049564 Click to see 446.40 unknown https://doi.org/10.1021/JF980386L
5-hydroxy-3-(3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 100954757 Click to see 446.40 unknown https://doi.org/10.1021/JF980386L
5-Hydroxy-3-(3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163049563 Click to see 446.40 unknown https://doi.org/10.1021/JF980386L
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
5,7-Dihydroxy-3-(3-methoxyphenyl)chromen-4-one 9882262 Click to see 284.26 unknown https://doi.org/10.1021/JF980386L

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