Scientific name	Authority	First published in
Syrenia biebersteinii	Andrz. ex DC.	Syst. Nat. 2: 493 (1821)
Syrenia cuspidata	Rchb.	Fl. Germ. Excurs. 2: 689 (1832)
Cuspidaria biebersteinii var. stenocarpa	Rupr.	Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 15(2): 74 1869
Cuspidaria cheiranthoides	Link	Handbuch [Link] 2: 315. 1831
Cuspidaria cuspidata	(M.Bieb.) Takht.	Taxt. An. Fed. Fl. Erevana 132 1946
Acachmena cuspidata	(M.Bieb.) H.P.Fuchs	Taxon 9: 55 (1960)
Cheiranthus bithynicus	Pers.	Syn. Pl. 2: 200 (1806)
Cheiranthus cuspidatus	M.Bieb.	Fl. Taur.-Caucas. 2: 120. 1808
Cheiranthus planifolius	Waldst. & Kit. ex M.Bieb.	Fl. Taur.-Caucas. 3: 443 (1819)
Cheiranthus taraxacifolius	Stephan ex Willd.	Sp. Pl., ed. 4 , 3: 525 (1800)
Cheirinia cuspidata	Link	Enum. Hort. Berol. Alt. 2: 170 (1822)
Crucifera cuspidata	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 6: 74 (1902)
Cuspidaria biebersteinii	Andrz. ex Besser	Enum. 104 (1822).
Cuspidaria stenocarpa	(Rupr.) Rupr.	Fl. Caucasi 75, in textu. 1869
Erysimum brevirostre	Tausch	Flora 19: 408 (1836)
Erysimum chrysanthum	Pančić	Fl. Serbiae 131 (1874), in clavi.
Erysimum cuspidatum	Velen.	Fl. Bulg. (1891) 32.
Erysimum cuspidatum f. brevistylos	Nejcev	God. Sof. Univ. Fiz.-Mat. Fac. 2: 135 1906
Erysimum hieracifolium	Pall.	Tabl. Phys. Topogr. Taur. 54. 1795
Erysimum leptopetalum	K.Koch	Linnaea 19: 52 (1847)
Erysimum rarifolium	K.Koch	Linnaea 19: 52 (1847)
Erysimum tetovense	Rohlena	Repert. Spec. Nov. Regni Veg. 42: 199 (1937)
Syrenopsis cuspidatus	(M.Bieb.) H.P.Fuchs	Acta Bot. Acad. Sci. Hung. 5: 52 1959
Sinapis tetraedra	C.Presl	Delic. Prag. : 19 (1822)
Stylonema bithynicum	Kuntze	Revis. Gen. Pl. 1: 36 (1891)
Syrenia latifolia	Andrz. ex Besser	Enum. Pl. Volh. : 27 (1821)
Syreniopsis cuspidata	(M.Bieb.) H.P.Fuchs	Acta Bot. Acad. Sci. Hung. 5: 52 (1959)

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	qalxanlı sarılıqotu
Bulgarian	островърха боянка
Russian	Акахмена длинноостроконечная
Russian	Желтушник длиннозаострённый
Russian	Желтушник заострённый
Russian	Желтушник щитовидный

Subspecies (abbr. subsp./ssp.) Top

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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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Uzbekistan
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- Eastern Europe
  - Central European Russia
  - Krym
  - Ukraine
- Middle Europe
  - Austria
  - Hungary
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Romania
  - Turkey-in-Europe
  - Yugoslavia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000678646
Tropicos	4100474
KEW	urn:lsid:ipni.org:names:283747-1
The Plant List	kew-2799962
Plantarium	15304
Open Tree Of Life	540616
Observations.org	117669
NCBI Taxonomy	358672
IPNI	283747-1
iNaturalist	483165
GBIF	3048411
EPPO	ERYCU
Elurikkus	730183
USDA GRIN	319011

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

Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece

Musarella CM, Brullo S, del Galdo GG

Plants (Basel)

30-Nov-2020

PMCID:	PMC7760968
doi:	10.3390/plants9121678
PMID:	33266088

A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery

Dehyab AS, Bakar MF, AlOmar MK, Sabran SF

Saudi J Biol Sci

10-Jul-2020

PMCID:	PMC7451596
doi:	10.1016/j.sjbs.2020.07.007
PMID:	32884430

Plant evolution in alkaline magnesium-rich soils: A phylogenetic study of the Mediterranean genus Hormathophylla (Cruciferae: Alysseae) based on nuclear and plastid sequences

Salmerón-Sánchez E, Fuertes-Aguilar J, Španiel S, Pérez-García FJ, Merlo E, Garrido-Becerra JA, Mota J

PLoS One

21-Dec-2018

PMCID:	PMC6303028
doi:	10.1371/journal.pone.0208307
PMID:	30576314

Species concepts in Cercospora: spotting the weeds among the roses

Groenewald JZ, Nakashima C, Nishikawa J, Shin HD, Park JH, Jama AN, Groenewald M, Braun U, Crous PW

Stud Mycol

01-Oct-2012

PMCID:	PMC3713887
doi:	10.3114/sim0012
PMID:	24014899

A new species of Albugo parasitic to Arabidopsis thaliana reveals new evolutionary patterns in white blister rusts (Albuginaceae)

Thines M, Choi YJ, Kemen E, Ploch S, Holub EB, Shin HD, Jones JD

Persoonia

26-May-2009

PMCID:	PMC2789544
doi:	10.3767/003158509X457931
PMID:	20198144

Erysimum glycosides X. Cardenolides of Erysimum cuspidatum

V. A. Maslennikova, R. U. Umarova, N. K. Abubakirov

Springer Science and Business Media LLC

09-Jul-2008

doi:	10.1007/BF00570663

Glucosinolates in Erysimum hieracifolium L.; Three New, Naturally Occurring Glucosinolates.

Anders Kjær, Angelica Schuster, G. E. Miksche, S. Liaaen-Jensen, Aud Lamvik, Erling Sunde, Nils Andreas Sørensen

Danish Chemical Society

19-Jun-2008

doi:	10.3891/ACTA.CHEM.SCAND.24-1631

Glycosides of Erysimum VIII. Cardenolides of Erysimum cuspidatum

R. U. Umarova, V. A. Maslennikova, N. K. Abubakirov

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00567927

3-Hydroxypropylglucosinolate, a new glucosinolate in seeds of Erysimum hieracifolium and Malcolmia maritima

Melvin E. Daxenbichler, Gayland F. Spencer, William P. Schroeder

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(80)85117-X

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(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/BF00570663
3-[(3R,5S,8S,9R,10R,11R,13R,14S,17R)-5,11,14-trihydroxy-10,13-dimethyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	162938872	Click to see CC1C(C(C(C(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)O)O	552.70	unknown	https://doi.org/10.1007/BF00567927
3-[(3S,5S,8S,9R,10R,11R,13R,14S,17R)-5,11,14-trihydroxy-10,13-dimethyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	162938868	Click to see CC1C(C(C(C(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)O)O	552.70	unknown	https://doi.org/10.1007/BF00567927
3-[(3S,5S,8S,9S,10R,11R,13R,14S,17R)-3-[(2S,3S,4R,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,11,14-trihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	162853640	Click to see CC1C(C(C(C(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)O)OC7C(C(C(C(O7)CO)O)O)O	714.80	unknown	https://doi.org/10.1007/BF00570663
3-[3-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,11,14-trihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	162853637	Click to see CC1C(C(C(C(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)O)OC7C(C(C(C(O7)CO)O)O)O	714.80	unknown	https://doi.org/10.1007/BF00570663
Bipindogulomethyloside	3735942	Click to see CC1C(C(C(C(O1)OC2CCC3(C4C(CCC3(C2)O)C5(CCC(C5(CC4O)C)C6=CC(=O)OC6)O)C)O)O)O	552.70	unknown	https://doi.org/10.1007/BF00567927
Cheirotoxin	201886	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O)OC7C(C(C(C(O7)CO)O)O)O	712.80	unknown	https://doi.org/10.1007/BF00570663
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/BF00570663
Glucoerysimoside	16409010	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)OC8C(C(C(C(O8)CO)O)O)O)O)O	858.90	unknown	https://doi.org/10.1007/BF00570663
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-4-methylsulfonyl-N-sulfooxybutanimidothioate	159978098	Click to see CS(=O)(=O)CCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	439.50	unknown	https://doi.org/10.1016/0031-9422(80)85117-X
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-4-[(R)-methylsulfinyl]-N-sulfooxybutanimidothioate	154497820	Click to see CS(=O)CCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	423.50	unknown	https://doi.org/10.1016/0031-9422(80)85117-X
[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-6-[(R)-methylsulfinyl]-N-sulfooxyhexanimidothioate	154497804	Click to see CS(=O)CCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	451.50	unknown	https://doi.org/10.1016/0031-9422(80)85117-X
> Organosulfur compounds / Isothiocyanates
Berteroin	206037	Click to see CSCCCCCN=C=S	175.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631
> Organosulfur compounds / Isothioureas
5-Methylsulfanylpentylthiourea	103691566	Click to see CSCCCCCNC(=S)N	192.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631
> Organosulfur compounds / Sulfonyls / Sulfones
(3R)-1-isothiocyanato-5-methylsulfonylpentan-3-ol	162882532	Click to see CS(=O)(=O)CCC(CCN=C=S)O	223.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631
1-Isothiocyanato-5-methylsulfonylpentan-3-ol	162882531	Click to see CS(=O)(=O)CCC(CCN=C=S)O	223.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631
Cheirolin	10454	Click to see CS(=O)(=O)CCCN=C=S	179.30	unknown	https://doi.org/10.1007/BF00570663
> Organosulfur compounds / Sulfoxides
Alyssin	206035	Click to see CS(=O)CCCCCN=C=S	191.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631
Alyssin, (S)-	51548324	Click to see CS(=O)CCCCCN=C=S	191.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-1631

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Erysimum cuspidatum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top