Scientific name	Authority	First published in
Lupinus hirsutus	L.	Sp. Pl.: 721 (1753)
Lupinus pilosus f. albus	Voss	Vilm. Blumengärtn. ed. 3, 1: 195 (1896)
Lupinus pilosus f. coeruleus	Voss	Vilm. Blumengärtn. ed. 3, 1: 195 (1896)

Common names Top

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Filter by language:

Language	Common/alternative name
English	blue lupine
Arabic	ترمس شعري
Hebrew	תורמוס ההרים
Portuguese	tremoço-de-flor-azul
Chinese	柔毛羽扇豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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

Africa click to expand
- East Tropical Africa
  - Tanzania
  - Uganda
- Southern Africa
  - Cape Provinces

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Nepal
  - Pakistan

Australasia click to expand
- Australia
  - New South Wales

Europe click to expand
- Eastern Europe
  - Central European Russia
- Southeastern Europe
  - Albania
  - Greece
  - Kriti
  - Turkey-in-Europe

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000185679
USDA Plants	LUPI9
INPN	717789
KEW	urn:lsid:ipni.org:names:504920-1
The Plant List	ild-31979
Open Tree Of Life	902815
Observations.org	138681
NCBI Taxonomy	53237
IUCN Red List	19379279
IPNI	504920-1
iNaturalist	489458
GBIF	2964596
Freebase	/m/0yxzbrp
EPPO	LUPVO
EOL	703673
Elurikkus	730891
USDA GRIN	22853
Wikipedia	Lupinus_pilosus

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

Valorization of Local Legumes and Nuts as Key Components of the Mediterranean Diet

Hernández-López I, Ortiz-Solà J, Alamprese C, Barros L, Shelef O, Basheer L, Rivera A, Abadias M, Aguiló-Aguayo I

Foods

29-Nov-2022

PMCID:	PMC9740325
doi:	10.3390/foods11233858
PMID:	36496665

Calcium/calmodulin-mediated microbial symbiotic interactions in plants

Yuan P, Luo F, Gleason C, Poovaiah BW

Front Plant Sci

18-Oct-2022

PMCID:	PMC9623113
doi:	10.3389/fpls.2022.984909
PMID:	36330252

Adaptive Mechanisms Make Lupin a Choice Crop for Acidic Soils Affected by Aluminum Toxicity

Quiñones MA, Lucas MM, Pueyo JJ

Front Plant Sci

05-Jan-2022

PMCID:	PMC8766672
doi:	10.3389/fpls.2021.810692
PMID:	35069669

Host Specificity and Preliminary Impact of Lepidapion argentatum (Coleoptera, Brentidae), a Biocontrol Candidate for French Broom (Genista monspessulana, Fabaceae)

Kerdellant E, Thomann T, Sheppard A, Sforza RF

Insects

31-Jul-2021

PMCID:	PMC8396517
doi:	10.3390/insects12080691
PMID:	34442257

The Doctrine of Signatures in Israel—Revision and Spatiotemporal Patterns

Dafni A, Aqil Khatib S, Benítez G

Plants (Basel)

01-Jul-2021

PMCID:	PMC8309186
doi:	10.3390/plants10071346
PMID:	34371549

Herbal Medicine Used in the Treatment of Human Diseases in the Rif, Northern Morocco

Chaachouay N, Douira A, Zidane L

Arab J Sci Eng

07-Apr-2021

PMCID:	PMC8024440
doi:	10.1007/s13369-021-05501-1
PMID:	33842189

The Puzzling Fate of a Lupin Chromosome Revealed by Reciprocal Oligo-FISH and BAC-FISH Mapping

Bielski W, Książkiewicz M, Šimoníková D, Hřibová E, Susek K, Naganowska B

Genes (Basel)

10-Dec-2020

PMCID:	PMC7764521
doi:	10.3390/genes11121489
PMID:	33322080

Strength and size of phosphorus-rich patches determine the foraging strategy of Neyraudia reynaudiana

Cai L, Wang Y, Tigabu M, Hou X, Wu P, Zhou C, Ma X

BMC Plant Biol

07-Dec-2020

PMCID:	PMC7720531
doi:	10.1186/s12870-020-02738-0
PMID:	33287710

Chromatographic Fingerprinting of the Old World Lupins Seed Alkaloids: A Supplemental Tool in Species Discrimination

Święcicki W, Czepiel K, Wilczura P, Barzyk P, Kaczmarek Z, Kroc M

Plants (Basel)

27-Nov-2019

PMCID:	PMC6963311
doi:	10.3390/plants8120548
PMID:	31783673

Ethnobotanical and ethnopharmacological studies of medicinal and aromatic plants used in the treatment of metabolic diseases in the Moroccan Rif

Chaachouay N, Benkhnigue O, Fadli M, El Ibaoui H, Zidane L

Heliyon

01-Nov-2019

PMCID:	PMC6838988
doi:	10.1016/j.heliyon.2019.e02191
PMID:	31720440

Impact of Chromosomal Rearrangements on the Interpretation of Lupin Karyotype Evolution

Susek K, Bielski W, Czyż KB, Hasterok R, Jackson SA, Wolko B, Naganowska B

Genes (Basel)

01-Apr-2019

PMCID:	PMC6523792
doi:	10.3390/genes10040259
PMID:	30939837

Light induces petal color change in Quisqualis indica (Combretaceae)

Yan J, Wang M, Zhang L

Plant Divers

24-Nov-2017

PMCID:	PMC6091926
doi:	10.1016/j.pld.2017.11.004
PMID:	30159538

The Role of the Plasma Membrane H+-ATPase in Plant Responses to Aluminum Toxicity

Zhang J, Wei J, Li D, Kong X, Rengel Z, Chen L, Yang Y, Cui X, Chen Q

Front Plant Sci

17-Oct-2017

PMCID:	PMC5651043
doi:	10.3389/fpls.2017.01757
PMID:	29089951

The dead seed coat functions as a long-term storage for active hydrolytic enzymes

Raviv B, Aghajanyan L, Granot G, Makover V, Frenkel O, Gutterman Y, Grafi G

PLoS One

11-Jul-2017

PMCID:	PMC5507414
doi:	10.1371/journal.pone.0181102
PMID:	28700755

Phytochemical Profile Top

Add a new one!

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 / Anagyrine-type alkaloids
Anagyrin	71056954	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O	244.33	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
(+)-Epilupinine acetate N-oxide	163184632	Click to see CC(=O)OCC1CCC[N+]2(C1CCCC2)[O-]	227.30	unknown	https://doi.org/10.1021/NP50074A020
[(1S,5R,9aR)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl]methanol	163190146	Click to see C1CC[N+]2(CCCC(C2C1)CO)[O-]	185.26	unknown	https://doi.org/10.1021/NP50074A020
[(1S,5R,9aR)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl]methyl acetate	163195235	Click to see CC(=O)OCC1CCC[N+]2(C1CCCC2)[O-]	227.30	unknown	https://doi.org/10.1021/NP50074A020
[(1S,9aR)-5-oxido-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-5-ium-1-yl]methanol	15144020	Click to see C1CC[N+]2(CCCC(C2C1)CO)[O-]	185.26	unknown	https://doi.org/10.1021/NP50074A020
1-Epilupinine	92767	Click to see C1CCN2CCCC(C2C1)CO	169.26	unknown	https://doi.org/10.1016/0305-1978(96)00034-8 https://doi.org/10.1139/V55-157 https://doi.org/10.1021/NP50074A020 https://doi.org/10.3987/COM-91-5716 https://doi.org/10.1016/0031-9422(90)85361-I https://doi.org/10.1248/BPB.16.1182
Lupinine	91461	Click to see C1CCN2CCCC(C2C1)CO	169.26	unknown	https://doi.org/10.1016/0031-9422(92)80112-R
Octahydro-2H-quinolizin-1-ylmethanol	297272	Click to see C1CCN2CCCC(C2C1)CO	169.26	unknown	https://doi.org/10.1139/V55-157 https://doi.org/10.1016/0031-9422(90)85361-I
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(-)-Sparteine sulfate	6452127	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4	234.38	unknown	https://doi.org/10.1071/CH9570177
(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/10.1016/0305-1978(96)00034-8
13alpha-Hydroxyspartein-2-one	5459919	Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O	264.36	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V	16212687	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4	234.38	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
alpha-Isolupanine	119201	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
Sparteine	644020	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4	234.38	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[3-methoxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	163185758	Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)OC)O)O)O	491.60	unknown	https://doi.org/10.1016/0031-9422(94)85108-5
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[3-methoxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	162948588	Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)OC)O)O)O	491.60	unknown	https://doi.org/10.1016/0031-9422(94)85108-5
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	163188805	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	101589361	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[4-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	162938616	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (Z)-3-[3-methoxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	163186856	Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)OC)O)O)O	491.60	unknown	https://doi.org/10.1016/0031-9422(94)85108-5
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (Z)-3-[3-methoxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	162948587	Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)OC)O)O)O	491.60	unknown	https://doi.org/10.1016/0031-9422(94)85108-5
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (Z)-3-[4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	163188804	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (Z)-3-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoate	101589362	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-[3-methoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]prop-2-enoate	162948584	Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)OC)O)O)O	491.60	unknown	https://doi.org/10.1016/0031-9422(94)85108-5
2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-[4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]prop-2-enoate	162938614	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=CC(=O)OCC3CCCN4C3CCCC4)O)O)O	461.50	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine	442625	Click to see CC(=O)N1CCCC(=C1)C2CCCCN2	208.30	unknown	https://doi.org/10.1016/0031-9422(90)85361-I https://doi.org/10.1016/0305-1978(96)00034-8
Pyridine, 1-acetyl-1,2,3,4-tetrahydro-5-(2-piperidinyl)-	108191	Click to see CC(=O)N1CCCC(=C1)C2CCCCN2	208.30	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
> 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 C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4	246.35	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
(1S,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,5-dien-4-one	163050009	Click to see C1CCN2CC3CC(C2C1)CN4C3=CC(=O)C=C4	244.33	unknown	https://doi.org/10.1021/NP50074A020
[(1R,2S,4S,9R,10R)-12-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-13-en-4-yl] (E)-2-methylbut-2-enoate	162880353	Click to see CC=C(C)C(=O)OC1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4	344.40	unknown	https://doi.org/10.1021/NP50074A020
13-alpha-Hydroxymultiflorine	15939900	Click to see C1CN2CC3CC(C2CC1O)CN4C3CC(=O)C=C4	262.35	unknown	https://doi.org/10.1016/0305-1978(96)00034-8
15-oxido-7-aza-15-azoniatetracyclo[7.7.1.02,7.010,15]heptadec-5-en-4-one	73201075	Click to see C1CC[N+]2(CC3CC(C2C1)CN4C3CC(=O)C=C4)[O-]	262.35	unknown	https://doi.org/10.3987/COM-91-5716
Multiflorine	6918763	Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4	246.35	unknown	https://doi.org/10.1021/NP50074A020 https://doi.org/10.3987/COM-91-5716 https://doi.org/10.1016/0031-9422(90)85361-I https://doi.org/10.1248/BPB.16.1182 https://doi.org/10.1016/0305-1978(96)00034-8
Multiflorine N-oxide	163184630	Click to see C1CC[N+]2(CC3CC(C2C1)CN4C3CC(=O)C=C4)[O-]	262.35	unknown	https://doi.org/10.3987/COM-91-5716
NoName_4034	119038	Click to see C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4	246.35	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
> Organoheterocyclic compounds / Quinolizines
quinolizidine N-oxide	101412417	Click to see C1CC[N+]2(CCCCC2C1)[O-]	155.24	unknown	https://doi.org/10.1021/NP50074A020
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-(4-acetyloxyphenyl)prop-2-enoate	163003836	Click to see CC(=O)OC1=CC=C(C=C1)C=CC(=O)OCC2CCCN3C2CCCC3	357.40	unknown	https://doi.org/10.1021/NP50074A020
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	20979974	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2CCCN3C2CCCC3)O	345.40	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
3-(4-Hydroxy-3-methoxy-phenyl)-acrylic acid octahydro-quinolizin-1-ylmethyl ester	643006	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2CCCN3C2CCCC3)O	345.40	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
Feruloyllupinine	6430132	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2CCCN3C2CCCC3)O	345.40	unknown	https://doi.org/10.1016/0031-9422(92)80112-R
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	14274648	Click to see C1CCN2CCCC(C2C1)COC(=O)C=CC3=CC=C(C=C3)O	315.40	unknown	https://doi.org/10.1016/0031-9422(92)80112-R https://doi.org/10.1016/0031-9422(90)85361-I
[(1S,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate	14274647	Click to see C1CCN2CCCC(C2C1)COC(=O)C=CC3=CC=C(C=C3)O	315.40	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-(4-hydroxyphenyl)prop-2-enoate	78409539	Click to see C1CCN2CCCC(C2C1)COC(=O)C=CC3=CC=C(C=C3)O	315.40	unknown	https://doi.org/10.1016/0031-9422(90)85361-I
p-Coumaroyllupinine	91748140	Click to see C1CCN2CCCC(C2C1)COC(=O)C=CC3=CC=C(C=C3)O	315.40	unknown	https://doi.org/10.1016/0031-9422(92)80112-R
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
6,8-Diprenylgenistein	480783	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C	406.50	unknown	https://doi.org/10.1021/NP50071A031
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
2',4'-Dihydroxy-5,7-dimethoxyisoflavone	14756217	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O	314.29	unknown	https://doi.org/10.1021/NP50071A031

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Lupinus pilosus

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