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Lunaria annua

Lunaria annua - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Lunaria annua - Unknown
Part: Unknown
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 UUID643ff45c31685859982024
Scientific name Lunaria annua
Authority L.
First published in Sp. Pl. : 653 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Viola lunaria Garsault Fig. Pl. Med. 4: t. 624. 1764, nom. inval., opus utique oppressum; Descr. Pl. Anim. 361. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 908.
Crucifera lunaria E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 6: 64 (1902)
Lunaria annua subsp. annua L.
Lunaria biennis Moench Methodus : 261 (1794)
Lunaria inodora Lam. Fl. Franç. 2: 457 (1779)
Lunaria annua f. orbiculata (Schur) Beck Glasn. Zemaljsk. Muz. Bosni Hercegovini 22: 118 (1916)
Lunaria annua f. elliptica (Schur) Beck Glasn. Zemaljsk. Muz. Bosni Hercegovini 22: 118 (1916)
Lunaria biennis var. orbiculata Schur Enum. Pl. Transsilv. : 64 (1866)
Lunaria biennis var. elliptica Schur Enum. Pl. Transsilv. : 64 (1866)

Common names Top

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Language Common/alternative name
English annual honesty
English honesty
Arabic حشيشة القمر
Arabic قمرية حولية
Czech měsíčnice roční
Welsh swllt dyn tlawd
Welsh sbectol hen ŵr
Welsh ceiniog arian
German einjähriges silberblatt
Esperanto balkana lunario
Estonian aed-kuukress
Basque judas lore
Finnish kesäkuuruoho
French monnaie du pape
Upper Sorbian kulojte slěborniki
Hungarian kerti holdviola
Japanese ゴウダソウ
Japanese ギンカソウ
Japanese ルナリア
Cornish bath arghans
Lithuanian darželinė blizgė
Norwegian Bokmål judaspenge
Dutch tuinjudaspenning
Dutch judaspenning
Norwegian Nynorsk judaspengar
Polish miesiącznica roczna
Pashto لونيک
Portuguese fábrica-de-dinheiro
Portuguese dólar-de-prata
Portuguese planta-dólar
Portuguese moedas-do-papa
Portuguese medalhão-do-papa
Portuguese medalha-do-papa
Portuguese lunária
Portuguese folha-de-prata
Portuguese flor-de-prata
Portuguese dinheiro-do-papa
Portuguese cetim-branco
Slovak mesačnica ročná
Serbian Сребренка
Swedish judaspenningar
Chinese 緞花
Chinese 银扇草
Chinese 缎花

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lunaria annua subsp. pachyrrhiza (Borbás) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(1): 425 1925

Varieties (abbr. var.) Top

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No variety added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000362471
Flora of Alabama 1273
Canadensys 4074
USDA Plants LUAN
Tropicos 4101396
INPN 106754
Flora of Italy 1465
KEW urn:lsid:ipni.org:names:286647-1
The Plant List kew-2344318
Missouri Botanical Garden 278072
Open Tree Of Life 464805
Observations.org 7007
NCBI Taxonomy 153659
NBN Atlas NBNSYS0000002918
Nature Serve 2.158952
IPNI 106307-3
iNaturalist 55886
GBIF 5373324
Freebase /m/033ky0
EPPO LUNAN
EOL 583859
Elurikkus 5575
Calflora (Californian flora) 5091
USDA GRIN 22794
Wikipedia Lunaria_annua

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
High-level production of nervonic acid in the oleaginous yeast Yarrowia lipolytica by systematic metabolic engineering Su H, Shi P, Shen Z, Meng H, Meng Z, Han X, Chen Y, Fan W, Fa Y, Yang C, Li F, Wang S Commun Biol 07-Nov-2023
PMCID:PMC10630375
doi:10.1038/s42003-023-05502-w
PMID:37935958
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Genome-Wide Investigation and Functional Analysis Reveal That CsKCS3 and CsKCS18 Are Required for Tea Cuticle Wax Formation Mo L, Yao X, Tang H, Li Y, Jiao Y, He Y, Jiang Y, Tian S, Lu L Foods 16-May-2023
PMCID:PMC10217411
doi:10.3390/foods12102011
PMID:37238828
Glucosinolates, a natural chemical arsenal: More to tell than the myrosinase story Abdel-Massih RM, Debs E, Othman L, Attieh J, Cabrerizo FM Front Microbiol 05-Apr-2023
PMCID:PMC10114928
doi:10.3389/fmicb.2023.1130208
PMID:37089539
Genetic Improvement of Camelina sativa (L.) Crantz: Opportunities and Challenges Ghidoli M, Ponzoni E, Araniti F, Miglio D, Pilu R Plants (Basel) 27-Jan-2023
PMCID:PMC9920110
doi:10.3390/plants12030570
PMID:36771654
Progress in understanding and improving oil content and quality in seeds Sagun JV, Yadav UP, Alonso AP Front Plant Sci 26-Jan-2023
PMCID:PMC9909563
doi:10.3389/fpls.2023.1116894
PMID:36778708
Emerging Issues on Tropane Alkaloid Contamination of Food in Europe de Nijs M, Crews C, Dorgelo F, MacDonald S, Mulder PP Toxins (Basel) 19-Jan-2023
PMCID:PMC9961018
doi:10.3390/toxins15020098
PMID:36828413
Extraction of High-Value Chemicals from Plants for Technical and Medical Applications Kapadia P, Newell AS, Cunningham J, Roberts MR, Hardy JG Int J Mol Sci 07-Sep-2022
PMCID:PMC9499410
doi:10.3390/ijms231810334
PMID:36142238
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
Natural fish oil improves the differentiation and maturation of oligodendrocyte precursor cells to oligodendrocytes in vitro after interaction with the blood–brain barrier Piatek P, Lewkowicz N, Michlewska S, Wieczorek M, Bonikowski R, Parchem K, Lewkowicz P, Namiecinska M Front Immunol 22-Jul-2022
PMCID:PMC9353075
doi:10.3389/fimmu.2022.932383
PMID:35935952
Plasma nervonic acid levels were negatively associated with attention levels in community-living older adults in New Zealand de Seymour JV, Beck KL, Conlon CA, von Hurst PR, Mumme KD, Haskell-Ramsay CF, Jones MB Metabolomics 16-Jul-2022
PMCID:PMC9288952
doi:10.1007/s11306-022-01908-5
PMID:35842880
Enhancing very long chain fatty acids production in Yarrowia lipolytica Gajdoš P, Urbaníková V, Vicenová M, Čertík M Microb Cell Fact 11-Jul-2022
PMCID:PMC9275168
doi:10.1186/s12934-022-01866-6
PMID:35818073
Comparison of Different Extraction Processes on the Physicochemical Properties, Nutritional Components and Antioxidant Ability of Xanthoceras sorbifolia Bunge Kernel Oil Zheng Y, Gao P, Wang S, Ruan Y, Zhong W, Hu C, He D Molecules 29-Jun-2022
PMCID:PMC9268096
doi:10.3390/molecules27134185
PMID:35807441
A Review of Erucic Acid Production in Brassicaceae Oilseeds: Progress and Prospects for the Genetic Engineering of High and Low-Erucic Acid Rapeseeds (Brassica napus) Wang P, Xiong X, Zhang X, Wu G, Liu F Front Plant Sci 11-May-2022
PMCID:PMC9131074
doi:10.3389/fpls.2022.899076
PMID:35645989
Synthesis of C20–38 Fatty Acids in Plant Tissues Zhukov A, Popov V Int J Mol Sci 25-Apr-2022
PMCID:PMC9101283
doi:10.3390/ijms23094731
PMID:35563119

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Xeniaphyllane and xenicane diterpenoids
1-(4,12-Dimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecan-12-yl)-4-methylpent-3-en-1-one 73172727 Click to see CC(=CCC(=O)C1(CC2C1CCC3(C(O3)CCC2=C)C)C)C 302.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
DL-Alanine 602 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Threonine 205 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
Pipecolic acid 849 Click to see C1CCNC(C1)C(=O)O 129.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(R)-Piperidine-2-carboxylic acid 736316 Click to see C1CCNC(C1)C(=O)O 129.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,4S)-4,5-dihydroxynorvaline 11194422 Click to see C(C(CO)O)C(C(=O)O)N 149.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
Asparagine 6267 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
DL-Asparagine 236 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid 611 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
Glutamic Acid 33032 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamine and derivatives
4-(Glutamylamino)butanoate 23724570 Click to see C(CC(=O)O)CNC(=O)CCC(C(=O)O)N 232.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
H-Gln(isopropyl)-OH 6993184 Click to see CC(C)NC(=O)CCC(C(=O)O)N 188.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
L-N-(3-Carboxypropyl)glutamine 355553 Click to see C(CC(=O)O)CNC(=O)CCC(C(=O)O)N 232.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
N-(gamma-Glutamyl)ethanolamine 10198007 Click to see C(CC(=O)NCCO)C(C(=O)O)N 190.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
n-Propan-2-ylglutamine 229866 Click to see CC(C)NC(=O)CCC(C(=O)O)N 188.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
n5-(2-Hydroxyethyl)-l-glutamine 9920597 Click to see C(CC(=O)NCCO)C(C(=O)O)N 190.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
DL-Proline 614 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
DL-Serine 617 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
2-Amino-3-(3-carboxy-4-hydroxyphenyl)propanoic acid 583884 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)C(=O)O)O 225.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
DL-3-Carboxytyrosine 199028 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)C(=O)O)O 225.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
DL-Valine 1182 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
(S)-3-amino-2-methylpropanoic acid 439434 Click to see CC(CN)C(=O)O 103.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
3-Amino-2-methylpropanoic acid 64956 Click to see CC(CN)C(=O)O 103.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.19-1071
https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Guanidinobutyric acid 500 Click to see C(CC(=O)O)CN=C(N)N 145.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
Gamma-Aminobutyric Acid 119 Click to see C(CC(=O)O)CN 103.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-1592
https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1511
> Phenylpropanoids and polyketides / Macrolactams
(1R,16Z,23S)-22-oxa-5,10,14-triazatetracyclo[16.9.2.01,23.021,28]nonacosa-2,16,18(29),19,21(28)-pentaene-4,15,25-trione 146031509 Click to see C1CCNC(=O)C=CC23CCC(=O)CC2OC4=C3C=C(C=C4)C=CC(=O)NCCCNC1 437.50 unknown https://doi.org/10.1016/S0031-9422(97)00590-6
CID 5281827 5281827 Click to see C1CCNC(=O)C=CC23CCC(=O)CC2OC4=C3C=C(C=C4)C=CC(=O)NCCCNC1 437.50 unknown https://doi.org/10.1016/S0031-9422(97)00590-6

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