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Erysimum crepidifolium

Erysimum crepidifolium - 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 UUID64401b6a776f7524397989
Scientific name Erysimum crepidifolium
Authority Rchb.
First published in Icon. Fl. Germ. Helv. 1: 8 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cheirinia crepidifolia A.Dietr. Fl. Boruss. 7: 446 (1839)
Crucifera crepidifolia E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 6: 77 (1902)
Erysimum carniolicum Schur Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 10: 143 (1859)
Erysimum cheiranthus J.Presl & C.Presl Fl. Cech. 138.
Erysimum ochroleucum Zaw. ex Niessl in Verh. Naturf. Ver. Bruenn viii. I. (1870) 59.
Erysimum odoratum Baumg. Enum. Stirp. Transsilv. 2: 262. 1816
Erysimum pallens Wallr. Sched. Crit. : 363 (1822)
Erysimum pumilum Schur Oesterr. Bot. Z. 8: 22 (1858)

Common names Top

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Language Common/alternative name
Czech trýzel škardolistý
German bleicher schöterich
Finnish kelttoukonnauris
Upper Sorbian blědy hórnač
Hungarian sziklai repcsény
Swedish blekkårel
Chinese 锈耳糖芥

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Czechoslovakia
      • Germany
      • Hungary
    • Southeastern Europe
      • Bulgaria
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000678637
INPN 990435
KEW urn:lsid:ipni.org:names:283739-1
The Plant List kew-2799954
Open Tree Of Life 3933233
Observations.org 117665
NCBI Taxonomy 761865
IPNI 283739-1
iNaturalist 515329
GBIF 3048522
EPPO ERYCP
EOL 5145758
Elurikkus 356881
Wikipedia Erysimum_crepidifolium

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
Identification of key genes involved in secondary metabolite biosynthesis in Digitalis purpurea Amiri F, Moghadam A, Tahmasebi A, Niazi A PLoS One 09-Mar-2023
PMCID:PMC9997893
doi:10.1371/journal.pone.0277293
PMID:36893121
Differentiation of natural scrub communities of the Cotoneastro-Amelanchieretum group in Central Europe Świerkosz K, Reczyńska K PLoS One 12-Apr-2022
PMCID:PMC9004749
doi:10.1371/journal.pone.0266868
PMID:35413069
Knockout of Arabidopsis thaliana VEP1, Encoding a PRISE (Progesterone 5β-Reductase/Iridoid Synthase-Like Enzyme), Leads to Metabolic Changes in Response to Exogenous Methyl Vinyl Ketone (MVK) Klein J, Ernst M, Christmann A, Tropper M, Leykauf T, Kreis W, Munkert J Metabolites 23-Dec-2021
PMCID:PMC8778713
doi:10.3390/metabo12010011
PMID:35050133
Independent evolution of ancestral and novel defenses in a genus of toxic plants (Erysimum, Brassicaceae) Züst T, Strickler SR, Powell AF, Mabry ME, An H, Mirzaei M, York T, Holland CK, Kumar P, Erb M, Petschenka G, Gómez JM, Perfectti F, Müller C, Pires JC, Mueller LA, Jander G eLife 07-Apr-2020
PMCID:PMC7180059
doi:10.7554/eLife.51712
PMID:32252891
Biosynthetic approach to combine the first steps of cardenolide formation in Saccharomyces cerevisiae Rieck C, Geiger D, Munkert J, Messerschmidt K, Petersen J, Strasser J, Meitinger N, Kreis W Microbiologyopen 22-Aug-2019
PMCID:PMC6925150
doi:10.1002/mbo3.925
PMID:31436030
A multisubstrate reductase from Plantago major: structure-function in the short chain reductase superfamily Fellows R, Russo CM, Silva CS, Lee SG, Jez JM, Chisholm JD, Zubieta C, Nanao MH Sci Rep 04-Oct-2018
PMCID:PMC6172241
doi:10.1038/s41598-018-32967-1
PMID:30287897
Identification and Characterization of the Iridoid Synthase Involved in Oleuropein Biosynthesis in Olive (Olea europaea) Fruits Alagna F, Geu-Flores F, Kries H, Panara F, Baldoni L, O'Connor SE, Osbourn A J Biol Chem 26-Dec-2015
PMCID:PMC4786697
doi:10.1074/jbc.M115.701276
PMID:26709230
Cardiac glycosides of Erysimum crepidifolium I. F. Makarevich, O. I. Klimenko, D. G. Kolesnikov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00567853

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3R,5S,10S,13R,14S,17R)-3-[(2R,5S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 11967805 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O 534.60 unknown https://doi.org/10.1007/BF00567853
(3S,5S,10S,13R,14S,17R)-3-[(2R,5S)-6-[[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 23485 Click to see CC1C(C(CC(O1)O)O)OCC2C(C(C(C(O2)OC3CCC4(C5CCC6(C(CCC6(C5CCC4(C3)O)O)C7=CC(=O)OC7)C)C=O)O)O)O 696.80 unknown https://doi.org/10.1007/BF00567853
3-[(3S,5R,8R,9S,10R,13R,14S,17R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101600421 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O 698.80 unknown https://doi.org/10.1007/BF00567853
Erysimin 12303929 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O 534.60 unknown https://doi.org/10.1007/BF00567853
Erysimoside 12308885 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O 696.80 unknown https://doi.org/10.1007/BF00567853
Glucostrophalloside 49799515 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O)O 712.80 unknown https://doi.org/10.1007/BF00567853

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