Scientific name	Authority	First published in
Cochlearia alpina	Sweet	Hort. Brit. : 22 (1826)
Cochlearia atlantica	Pobed.	Novosti Sist. Vyssh. Rast. 1968, 131 (1968).
Cochlearia flagrans	Gilib.	Fl. Lit. Inch. ii. 51. 1782
Cochlearia kamtschatica	Schlecht. ex DC.	Prodr. 1: 173 (1824)
Cochlearia linnaei	Griewank ex Asch.	Fl. Brandenburg 1: 54 (1860)
Cochlearia officinalis var. typica	G.Andersson & H.Hesselman	Bih. Kongl. Svenska Vetensk.-Akad. Handl. 26(3; 1): 36 (1900)
Cochlearia polymorpha	Syme	Engl. Bot. , ed. 3, 1: 184 (1863)
Cochlearia renifolia	Stokes	Bot. Mat. Med. 3: 435 (1812)
Cochlearia rotundifolia	Gray	Nat. Arr. Brit. Pl. ii. 695.
Cochlearia vulgaris	Bubani	Fl. Pyren. 3: 195 (1901)
Crucifera cochlearia	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 6: 56 (1902)
Crucifera cochlearia var. officinalis	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 6: 56 (1902)
Draba cochlearioides	Langsd. ex DC.	Syst. Nat. 2: 363 (1821)
Eutrema rossii	Spreng.	Syst. Veg. 2: 880 (1825)
Cochlearia officinalis var. vidassiana	Rouy & Foucaud	Fl. France 2: 200 (1895)
Cochlearia officinalis var. maritima	Gren. & Godr.	Fl. France 1: 128 (1848)
Cochlearia officinalis var. gallicica	Pau	Mem. Real Soc. Esp. Hist. Nat. 2: 513 (1904)

Common names Top

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Filter by language:

Language	Common/alternative name
English	spoonwort
English	scurvy-grass
English	common scurvygrass
Spanish	yerba de cucharas
Spanish	cuchareta
Spanish	crucifera cochlearia
Spanish	coclearia oficinal
Spanish	coclèaria
Spanish	cochlearia vulgaris
Spanish	cochlearia scotica
Spanish	cochlearia pyrenaica subsp. alpina
Spanish	cochlearia groenlandica
Spanish	cochlearia rotundifolia
Spanish	cochlearia atlantica
Spanish	hierba de cucharas
Spanish	coclearia
Spanish	cochlearia groenlandica subsp scotica
Spanish	cochlearia groenlandica subsp. scotica
Spanish	cochlearia islandica
Spanish	cochlearia officinalis subsp scotica
Spanish	cochlearia officinalis subsp. scotica
Arabic	تودري
Catalan	cranson officinal
Catalan	herbe aux cuillères
Catalan	herba de la cullera
Czech	lžičník lékařský
Welsh	llwylys cyffredin
Danish	læge-kokleare
German	echtes löffelkraut
German	bitterkresse
German	cranson officinal
German	herbe aux cuillères
German	löffelblättchen
German	löffelkresse
German	skorbutkraut
Esperanto	skorbutherbo
Estonian	ürt-merisalat
Finnish	rohtokuirimo
Finnish	ruijankuirimo
French	cochléaire officinale
French	cranson officinal
French	herbe aux cuillères
French	cochleaire officinale
frr	greens saloot
frr	skorbükskrüüs
Upper Sorbian	lěkarski chrěn
Icelandic	skarfakál
Japanese	トモシリソウ
Lithuanian	cranson officinal
Lithuanian	herbe aux cuillères
Norwegian Bokmål	skjørbuksurt
Dutch	echt lepelblad
Dutch	echt en engels lepelblad
Norwegian Nynorsk	skjørbuksurt
Polish	warzucha lekarska
Serbo-Croatian	kašikara
Serbian	Кашикара
Swedish	skörbjuggsört
Swedish	herbe aux cuillères
Swedish	cranson officinal
Turkish	kaşık otu
Ukrainian	Ложечниця лікарська
Chinese	辣根菜
Chinese	岩荠

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Cochlearia officinalis subsp. integrifolia	(Hartm.) Nordal & Stabb.	Nordic J. Bot. 10: 261 (1990)
Cochlearia officinalis subsp. norvegica	Nordal & Stabb.	Nordic J. Bot. 10: 261 (1990)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Antarctica click to expand
- Subantarctic Islands
  - Falkland Islands

Asia-temperate click to expand
- Russian Far East
  - Khabarovsk

Europe click to expand
- Eastern Europe
  - Baltic States
  - North European Russia
- Middle Europe
  - Belgium
  - Czechoslovakia
  - Germany
  - Netherlands
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Italy
- Southwestern Europe
  - France
  - Spain

Southern America click to expand
- Southern South America
  - Argentina South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000613801
UNII	2CU75HPQ9P
USDA Plants	COOF4
Tropicos	4100415
INPN	92052
KEW	urn:lsid:ipni.org:names:281469-1
The Plant List	kew-2729901
PFAF	Cochlearia officinalis
Open Tree Of Life	177734
Observations.org	136401
NCBI Taxonomy	270110
NBN Atlas	NHMSYS0000457397
IPNI	281469-1
iNaturalist	55838
GBIF	5373276
Freebase	/m/02rt2kl
EPPO	CCLOF
EOL	584102
Elurikkus	3862
Calflora (Californian flora)	10538
USDA GRIN	11010
Wikipedia	Cochlearia_officinalis
CMAUP	NPO11511

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_900406305.1	ASM90040630v1	Scaffold	MAX PLANCK INSTITUTE FOR PLANT BREEDING RESEARCH	2019-06-14	52.0x	156.85 Mb

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

The interaction of salinity and light regime modulates photosynthetic pigment content in edible halophytes in greenhouse and indoor farming

Fitzner M, Schreiner M, Baldermann S

Front Plant Sci

04-Apr-2023

PMCID:	PMC10110887
doi:	10.3389/fpls.2023.1105162
PMID:	37082347

Water Content of Plant Tissues: So Simple That Almost Forgotten?

Ievinsh G

Plants (Basel)

08-Mar-2023

PMCID:	PMC10058729
doi:	10.3390/plants12061238
PMID:	36986926

CaSPDS, a Spermidine Synthase Gene from Pepper (Capsicum annuum L.), Plays an Important Role in Response to Cold Stress

Zhang J, Xie M, Yu G, Wang D, Xu Z, Liang L, Xiao J, Xie Y, Tang Y, Sun G, Sun B, Huang Z, Lai Y, Li H

Int J Mol Sci

06-Mar-2023

PMCID:	PMC10003509
doi:	10.3390/ijms24055013
PMID:	36902443

Type of Anion Largely Determines Salinity Tolerance in Four Rumex Species

Landorfa-Svalbe Z, Andersone-Ozola U, Ievinsh G

Plants (Basel)

24-Dec-2022

PMCID:	PMC9823408
doi:	10.3390/plants12010092
PMID:	36616221

Acylsugar protection of Nicotiana benthamiana confers mortality and transgenerational fitness costs in Spodoptera litura

Wang R, Gao B, Zhang Q, Zhang Z, Li Y, Yang Q, Zhang M, Li W, Luo C

Front Plant Sci

02-Sep-2022

PMCID:	PMC9478178
doi:	10.3389/fpls.2022.993279
PMID:	36119595

Fruity, Sticky, Stinky, Spicy, Bitter, Addictive, and Deadly: Evolutionary Signatures of Metabolic Complexity in the Solanaceae

Fiesel PD, Parks HM, Last RL, Barry CS

Nat Prod Rep

20-Jul-2022

PMCID:	PMC9308699
doi:	10.1039/d2np00003b
PMID:	35332352

Diverse in Local, Overlapping in Official Medical Botany: Critical Analysis of Medicinal Plant Records from the Historic Regions of Livonia and Courland in Northeast Europe, 1829–1895

Prakofjewa J, Anegg M, Kalle R, Simanova A, Prūse B, Pieroni A, Sõukand R

Plants (Basel)

13-Apr-2022

PMCID:	PMC9032843
doi:	10.3390/plants11081065
PMID:	35448792

Evolutionary footprints of a cold relic in a rapidly warming world

Wolf E, Gaquerel E, Scharmann M, Yant L, Koch MA

eLife

21-Dec-2021

PMCID:	PMC8741218
doi:	10.7554/eLife.71572
PMID:	34930524

lepidium-like, a Naturally Occurring Mutant of Capsella bursa-pastoris, and Its Implications on the Evolution of Petal Loss in Cruciferae

Klepikova AV, Shnayder ED, Kasianov AS, Remizowa MV, Sokoloff DD, Penin AA

Front Plant Sci

25-Nov-2021

PMCID:	PMC8656458
doi:	10.3389/fpls.2021.714711
PMID:	34899769

Vitamin C in East-Greenland traditional nutrition: a reanalysis of the Høygaard nutritional data (1936-1937)

Mullie P, Deliens T, Clarys P

Int J Circumpolar Health

07-Jul-2021

PMCID:	PMC8266228
doi:	10.1080/22423982.2021.1951471
PMID:	34232845

Genetic resources of vegetable crops: from breeding non-traditional crops to functional food

Fotev YV, Artemyeva AM, Zvereva OA

Vavilovskii Zhurnal Genet Selektsii

01-Jul-2021

PMCID:	PMC8765771
doi:	10.18699/VJ21.049
PMID:	35088016

Reports on Greenlandic and Faroese medicine from an eighteenth-century medical book

Porro A, Falconi B, Lorusso L, Franchini AF

Int J Circumpolar Health

18-May-2021

PMCID:	PMC8143637
doi:	10.1080/22423982.2021.1914968
PMID:	34002681

A Structural View on the Stereospecificity of Plant Borneol‐Type Dehydrogenases

Chánique AM, Dimos N, Drienovská I, Calderini E, Pantín MP, Helmer CP, Hofer M, Sieber V, Parra LP, Loll B, Kourist R

ChemCatChem

10-Mar-2021

PMCID:	PMC8261865
doi:	10.1002/cctc.202100110
PMID:	34262629

When everything changes at once: finding a new normal after genome duplication

Bomblies K

Proc Biol Sci

18-Nov-2020

PMCID:	PMC7739491
doi:	10.1098/rspb.2020.2154
PMID:	33203329

A Brassica napus Reductase Gene Dissected by Associative Transcriptomics Enhances Plant Adaption to Freezing Stress

Huang Y, Hussain MA, Luo D, Xu H, Zeng C, Havlickova L, Bancroft I, Tian Z, Zhang X, Cheng Y, Zou X, Lu G, Lv Y

Front Plant Sci

26-Jun-2020

PMCID:	PMC7333310
doi:	10.3389/fpls.2020.00971
PMID:	32676095

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
Chavicine	1548912	Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	285.34	unknown	via CMAUP database
Isochavicine	1548914	Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	285.34	unknown	via CMAUP database
Isopiperine	1548913	Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	285.34	unknown	via CMAUP database
Piperidine, 1-(5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl)-	4840	Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	285.34	unknown	via CMAUP database
Piperine	638024	Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	285.34	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(e)-4-(3,4-Dimethoxy-phenyl)but-3-en-1-yl palmitate	21668972	Click to see CCCCCCCCCCCCCCCC(=O)OCCC=CC1=CC(=C(C=C1)OC)OC	446.70	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3R,3aS,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole	7059611	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
(2R)-3alpha-(3,4-Dimethoxybenzyl)-4beta-[(1,3-benzodioxole-5-yl)methyl]tetrahydrofuran-2beta-ol	102317093	Click to see COC1=C(C=C(C=C1)CC2C(COC2O)CC3=CC4=C(C=C3)OCO4)OC	372.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triol	5280656	Click to see C1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O	296.31	unknown	via CMAUP database
Piperchabaoside A	44521560	Click to see C1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O	458.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,12Z)-N-(2-methylpropyl)octadeca-2,4,12-trienamide	25221579	Click to see CCCCCC=CCCCCCCC=CC=CC(=O)NCC(C)C	333.60	unknown	via CMAUP database
(2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide	73355665	Click to see CCCCCC=CCCC=CC=CC(=O)NCC(C)C	277.40	unknown	via CMAUP database
2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)-	6443006	Click to see CCCCCCCC=CC=CC(=O)NCC(C)C	251.41	unknown	via CMAUP database
2,4-Hexadecadienamide, N-(2-methylpropyl)-, (E,E)-	6442402	Click to see CCCCCCCCCCCC=CC=CC(=O)NCC(C)C	307.50	unknown	via CMAUP database
2,4,14-Eicosatrienoic acid isobutylamide	10338645	Click to see CCCCCC=CCCCCCCCCC=CC=CC(=O)NCC(C)C	361.60	unknown	via CMAUP database
N-Isobutyl-(2E,4E)-tetradecadienamide	10731388	Click to see CCCCCCCCCC=CC=CC(=O)NCC(C)C	279.50	unknown	via CMAUP database
Pellitorine	5318516	Click to see CCCCCC=CC=CC(=O)NCC(C)C	223.35	unknown	via CMAUP database
Pipericine	9974234	Click to see CCCCCCCCCCCCCC=CC=CC(=O)NCC(C)C	335.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
Piperchabaoside B	44521607	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OCC=CC2=CC=CC=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	602.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid amides / Secondary carboxylic acid amides
Chabamide K	53243800	Click to see CCCCCC1C=CC(C(C1CCCCC)C=CC(=O)NCC(C)C)C(=O)NCC(C)C	446.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(2E,4E)-1-Isopentylamino-5-(1,3-benzodioxole-5-yl)-2,4-pentadiene-1-one	45482110	Click to see CC(C)CCNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2	287.35	unknown	via CMAUP database
(2E,8E)-9-(1,3-benzodioxol-5-yl)-N-[(2R)-2-methylbutyl]nona-2,8-dienamide	44521561	Click to see CCC(C)CNC(=O)C=CCCCCC=CC1=CC2=C(C=C1)OCO2	343.50	unknown	via CMAUP database
13-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)trideca-2,4,12-trienamide	179663	Click to see CC(C)CNC(=O)C=CC=CCCCCCCC=CC1=CC2=C(C=C1)OCO2	383.50	unknown	via CMAUP database
15-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)pentadeca-2,4,14-trienamide	85102874	Click to see CC(C)CNC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	411.60	unknown	via CMAUP database
4,5-Dihydropiperlonguminine	12682184	Click to see CC(C)CNC(=O)C=CCCC1=CC2=C(C=C1)OCO2	275.34	unknown	via CMAUP database
5-[(1E)-dodec-1-en-1-yl]-2H-1,3-benzodioxole	9922008	Click to see CCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	288.40	unknown	via CMAUP database
5alpha,6beta-Bis(piperidinocarbonyl)-4beta-[(E)-2-(1,3-benzodioxole-5-yl)ethenyl]-3beta-(1,3-benzodioxole-5-yl)cyclohexene	10438004	Click to see C1CCN(CC1)C(=O)C2C=CC(C(C2C(=O)N3CCCCC3)C=CC4=CC5=C(C=C4)OCO5)C6=CC7=C(C=C6)OCO7	570.70	unknown	via CMAUP database
Brachystamide B	10047263	Click to see CC(C)CNC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2	411.60	unknown	via CMAUP database
Chabamide F	102480093	Click to see C1CCN(C1)C(=O)C2C=CC(C(C2C(=O)N3CCCC3)C=CC4=CC5=C(C=C4)OCO5)C6=CC7=C(C=C6)OCO7	542.60	unknown	via CMAUP database
Chabamide G	102480094	Click to see C1CCN(C1)C(=O)C2C=CC(C(C2C=CC3=CC4=C(C=C3)OCO4)C(=O)N5CCCC5)C6=CC7=C(C=C6)OCO7	542.60	unknown	via CMAUP database
Chabamide H	53242461	Click to see CC(C)CNC(=O)C1C(C=CC(C1C2=CC3=C(C=C2)OCO3)C(=O)N4CCCCC4)C5=CC6=C(C=C5)OCO6	532.60	unknown	via CMAUP database
CID 96931	96931	Click to see CC(C)CNC(=O)C=CC1=CC2=C(C=C1)OCO2	247.29	unknown	via CMAUP database
Dehydropipernonaline	6439947	Click to see C1CCN(CC1)C(=O)C=CC=CCCC=CC2=CC3=C(C=C2)OCO3	339.40	unknown	via CMAUP database
Guineensine	6442405	Click to see CC(C)CNC(=O)C=CC=CCCCCCCC=CC1=CC2=C(C=C1)OCO2	383.50	unknown	via CMAUP database
Ilepcimide	641115	Click to see C1CCN(CC1)C(=O)C=CC2=CC3=C(C=C2)OCO3	259.30	unknown	via CMAUP database
Methyl piperate	9921021	Click to see COC(=O)C=CC=CC1=CC2=C(C=C1)OCO2	232.23	unknown	via CMAUP database
Piperanine	5320618	Click to see C1CCN(CC1)C(=O)C=CCCC2=CC3=C(C=C2)OCO3	287.35	unknown	via CMAUP database
Piperchabamide B	44453655	Click to see C1CCN(CC1)C(=O)C=CCCCCCCC=CC2=CC3=C(C=C2)OCO3	369.50	unknown	via CMAUP database
Piperchabamide C	44454018	Click to see C1CCN(CC1)C(=O)C=CC=CCCCCCCC=CC2=CC3=C(C=C2)OCO3	395.50	unknown	via CMAUP database
Piperchabamide D	16041827	Click to see CC(C)CNC(=O)C=CCCCCCCC=CC1=CC2=C(C=C1)OCO2	357.50	unknown	via CMAUP database
Pipercide	5372162	Click to see CC(C)CNC(=O)C=CC=CCCCCC=CC1=CC2=C(C=C1)OCO2	355.50	unknown	via CMAUP database
Piperlonguminine	5320621	Click to see CC(C)CNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2	273.33	unknown	via CMAUP database
Pipernonaline	9974595	Click to see C1CCN(CC1)C(=O)C=CCCCCC=CC2=CC3=C(C=C2)OCO3	341.40	unknown	via CMAUP database
Piperolein B	21580213	Click to see C1CCN(CC1)C(=O)CCCCCCC=CC2=CC3=C(C=C2)OCO3	343.50	unknown	via CMAUP database
Piperonal	8438	Click to see C1OC2=C(O1)C=C(C=C2)C=O	150.13	unknown	via CMAUP database
Piperundecalidine	44453654	Click to see C1CCN(CC1)C(=O)C=CC=CCCCCC=CC2=CC3=C(C=C2)OCO3	367.50	unknown	via CMAUP database
Piperyline	636537	Click to see C1CCN(C1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3	271.31	unknown	via CMAUP database
Retrofractamide A	11012859	Click to see CC(C)CNC(=O)C=CC=CCCC=CC1=CC2=C(C=C1)OCO2	327.40	unknown	via CMAUP database
Retrofractamide C	25255091	Click to see CC(C)CNC(=O)C=CCCCCC=CC1=CC2=C(C=C1)OCO2	329.40	unknown	via CMAUP database
Sylvatine	90472536	Click to see CC(C)CCCC=CCCCCNC(=O)C=CC=CC1=CC2=C(C=C1)OCO2	383.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines
1-(3-phenylpropanoyl)-5,6-dihydropyridin-2(1H)-one	44453778	Click to see C1CN(C(=O)C=C1)C(=O)CCC2=CC=CC=C2	229.27	unknown	via CMAUP database
> Organosulfur compounds / Isothiocyanates
[S,(+)]-2-Isothiocyanatobutane	737359	Click to see CCC(C)N=C=S	115.20	unknown	https://doi.org/10.1002/ARDP.18992370508 https://doi.org/10.1002/ARDP.19032410906
sec-Butyl isothiocyanate	78151	Click to see CCC(C)N=C=S	115.20	unknown	https://doi.org/10.1002/ARDP.19032410906 https://doi.org/10.1002/ARDP.18992370508
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
Piperidine, 1-(1-oxo-3-phenyl-2-propenyl)-	223147	Click to see C1CCN(CC1)C(=O)C=CC2=CC=CC=C2	215.29	unknown	via CMAUP database
Piperlongumine	637858	Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O	317.34	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3-methoxy-cinnamate	16830	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O	208.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Chabamide I	53242460	Click to see CC(C)CNC(=O)C1C(C=CC(C1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C(=O)N6CCCCC6	532.60	unknown	via CMAUP database

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Cochlearia officinalis

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