Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Suaeda maritima has been used as a coastal pot herb in Britain and Ireland, where the young shoots and leaves are eaten fresh in salads or boiled as a potherb (Royal Horticultural Society). On the Atlantic coast of France, the same plant part is simmered briefly with fish and herbs in Provence and Languedoc (Cambridge Food Primer, 2019). Along the Lower Tagus estuary in Portugal, people gather the young aerial parts to cook with shellfish and soups, the method and timing echoing practices recorded for early European marsh herbs (Jardim and Roberto, 2008).

A simple mild tea or potherb can be prepared by wilting 50–60 g of fresh, well‑washed leaves and tender stems in 600–700 ml of water for 3–5 minutes, then adding a squeeze of lemon or olive oil before serving. Alternatively, a quick blanch in salted water for 1 minute removes some of the saltiness and softens the texture; drain and dress as above. Use only the tender aerial parts collected from clean, unpolluted sites; older stems can be fibrous. Because coastal plants concentrate salts, rinse thoroughly, taste, and season carefully; those with salt‑restricted diets should avoid large amounts. Pregnant and nursing people should treat it as a culinary herb in modest portions.

The plant’s well‑established constituents include betalain pigments (betaxanthin‑type), flavonoids such as quercetin and kaempferol glycosides, and phenolic acids like caffeic and ferulic acid (Khan et al., 2009; Bennett et al., 2012), which are common in halophyte Amaranthaceae and plausibly account for the mild digestive and mouth‑cleansing experience reported after the herb’s aromatic broths.

Suaeda maritima remains a niche food plant and is still collected in limited quantities by foragers in coastal communities in northwestern Europe (John Tyler’s Wild Food, 1995). Modern research has evaluated its nutritional profile and antioxidant capacity in laboratory studies, supporting cautious culinary interest rather than therapeutic claims (Bennett et al., 2012; Khan et al., 2009).

General Uses Top

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Industrial and craft applications:
Suaeda maritima is used in coastal restoration and stabilization plantings for salt marshes and saltern margins. Established projects on European Atlantic coasts have used S. maritima to increase vegetation cover, bind sediments, and facilitate natural succession (Grootjans et al. 2008). It is used in wastewater treatment and constructed wetlands as a halophytic species for polishing saline effluents and contributing to nitrogen removal (Bothe et al. 2010; Mitsch & Gosselink 2015; Vymazal 2014).

Food and beverages (non-medicinal):
The tender young shoots of Suaeda maritima are consumed as a leafy vegetable in parts of Tunisia and Egypt, typically after fresh-water washing to reduce salinity. Publications describe its use as a salad green and as a cooked vegetable in local traditional food systems (Le Floc’h et al. 2010;Sghaier et al. 2014).

Properties relevant to use:
The plant’s extreme salt tolerance, C4 photosynthetic pathway, and capacity to accumulate and tolerate sodium and chloride ions underpin its value in saline habitats, wastewater polishing, and coastal plantings where salt stress is high (Bothe et al. 2010; O’Leary & Glenn 1991). Its tolerance to heavy metals such as cadmium has been demonstrated under experimental conditions (Takahashi et al. 2002; Bothe et al. 2010), supporting roles in phytoremediation of contaminated saline soils.

Standards and regulation:
Commercial harvesting of wild halophytes for food follows general food-safety regulations; EU Novel Food Regulation (EU) 2015/2283 may apply if species are marketed beyond traditional uses. No plant-specific standards are documented.

Sustainability and sourcing:
Suaeda maritima occurs naturally in salt marshes, saltpans, and coastal margins of Europe and the Mediterranean; harvesters are advised to collect selectively to avoid damaging fragile marsh ecosystems and to consider provenance and local regulations (Efroymson et al. 1997). Propagation by seed or cuttings is feasible for restoration projects, and tissue-culture systems have been established for halophyte production (Grierson 2013).

Synonyms Top

Scientific name	Authority	First published in
Lerchia maritima	(L.) Kuntze	Revis. Gen. Pl. 2: 549 (1891)
Salsola maritima	(L.) M.Bieb.	Tabl. Prov. Mer Casp. 150 1798
Salsola indica	Willd.	Sp. Pl., ed. 4 , 1: 1317 (1798)
Salsola sedoides	L.	Amoen. Acad. 4: 98 (1759)
Suaeda albescens	Lázaro Ibiza	Asoc. Esp. Progr. Ci., Congr. Sevilla 6(4; 3): 74 (1920)
Suaeda indica	(Willd.) Moq.	Ann. Sci. Nat. (Paris) 23: 316 (1831)
Suaeda cavanillesiana	(Lázaro Ibiza) Cout.	Bol. Soc. Brot. , sér. 2, 10: 82 (1935)
Suaeda chenopodioides	Pall.	Illustr. Pl. 56.
Schoberia crassifolia	Steud.	Nomencl. Bot. , ed. 2, 2: 532 (1841)
Schoberia indica	(Willd.) Kostel.	Allg. Med.-Pharm. Fl. 4: 1438 (1835)
Schoberia maritima	(L.) C.A.Mey.	Fl. Altaic. 1: 400 (1829)
Suaeda prostrata	Pall.	Ill. Pl. : 55 (1803)
Atriplex maritima	(L.) Crantz	Inst. Rei Herb. 1: 208 (1766)
Chenopodina aestuaria	Dumort.	Bull. Soc. Roy. Bot. Belgique 7: 329 (1868)
Chenopodina bacciformis	Dumort.	Bull. Soc. Roy. Bot. Belgique 7: 328 (1868)
Chenopodina filiformis	Moq.	Prodr. 13(2): 164 (1849)
Chenopodina maritima	(L.) Moq.	Prodr. 13(2): 161 (1849)
Chenopodina maritima var. erecta	Moq.	Prodr. 13(2): 161 (1849)
Chenopodina prostrata	(Pall.) Moq.	Prodr. 13(2): 162 (1849)
Chenopodina sativa	Moq.	Prodr. 13(2): 165 (1849)
Chenopodina spicata	Moq.	Prodr. 13(2): 165 (1849)
Chenopodina tortuosa	Moq.	Prodr. 13(2): 162 (1849)
Chenopodium crassifolium	Desf.	Tabl. École Bot., ed. 2. 51. 1815
Chenopodium filiforme	Dumort.	Fl. Belg. : 22 (1827)
Chenopodium hortense	Raddi ex Moq.	Prodr. [A. P. de Candolle] 13(2): 161. 1849 [5 May 1849]
Chenopodium hostii	Ledeb.	Fl. Ross. 3: 788 (1851)
Chenopodium jacquinii	Ten.	Fl. Napol. 3: 258 (1829)
Chenopodium macrocarpum	Desv.	J. Bot. Agric. 1: 48 (1813)
Chenopodium maritimum	L.	Sp. Pl. : 221 (1753)
Chenopodium prostratum	(Pall.) Schult.	Syst. Veg., ed. 15 bis 6: 272 (1820)
Chenopodium spicatum	Schult.	Syst. Veg., ed. 15 bis 6: 271 (1820)
Cochliospermum cavanillesii	Lag.	Mem. Pl. Barrill. : 60 (1817)
Dondia maritima	(L.) Druce	List Brit. Pl. : 60 (1908)
Suaeda maritima var. cavanillesiana	Lázaro Iberia	Asoc. Esp. Progr. Ci., Congr. Sevilla 6(4, 3a): 71 1920
Chenopodina maritima var. vulgaris	Moq.	Prodr. 13(2): 161 1849
Suaeda maritima var. perennans	Maire	Bull. Soc. Hist. Nat. Afrique N. 24: 227 1933
Suaeda fernaldii	(Standl.) Standl.	Publ. Field Columb. Mus., Bot. Ser. 4: 203 (1929)
Suaeda maritima subsp. richii	(Fernald) Bassett & Crompton	Canad. J. Bot. 56: 587. 1978
Suaeda richii	Fernald	Rhodora 9: 145 (1907)
Suaeda nudiflora	(Willd.) Moq.	Ann. Sci. Nat. (Paris) 23: 316 (1831)
Suaeda maritima var. vulgaris	Moq.	Chenop. Monogr. Enum. 128 1840

Common names Top

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Filter by language:

Language	Common/alternative name
English	sea blite
English	annual seablite
English	white sea-blite
English	herbaceous seepweed
English	annual-seablite
English	annual sea-blite
Spanish	cañamete
Spanish	canamete
Arabic	سويداء بحرية
Bulgarian	морска суеда
Catalan	canyametes
Czech	solnička přímořská
Welsh	helys unflwydd
Danish	almindelig strandgåsefod
Danish	strandgåsefod
German	meerstrand-gänsefüßchen
German	schmalzmelde
German	sode
German	strand-sode
German	strandsode
Estonian	rand-soodahein
Persian	سیاهشور دریایی
Finnish	pikkukilokki
French	suéda maritime
French	soude maritime
Irish	blide mhara
Gujarati	લૂણો
Gujarati	મોરડ (વનસ્પતિ)
Gujarati	લાણો
Gujarati	મોરડ
Upper Sorbian	mórska zolica
Icelandic	salturt
Japanese	浜松菜
Japanese	ハママツナ
Norwegian Bokmål	saftmelde
Dutch	klein schorrekruid
Dutch	klein schorrenkruid
Dutch	schorrenkruid
Polish	sodówka nadmorska
Slovenian	slanorad primorski
Swedish	saltört
Thai	ช้าคราม
Thai	ชะคราม
Vietnamese	phì diệp biển
Chinese	裸花鹼蓬
Chinese	海滨碱蓬
Chinese	平卧碱蓬
Chinese	裸花碱蓬

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Suaeda maritima subsp. pannonica	(Beck) Soó ex P.W.Ball	Feddes Repert. Spec. Nov. Regni Veg. 69: 44 1964
Suaeda maritima subsp. salsa	(L.) Soó	Magyar Növényvilág Kézikönyve 2: 785 1951

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

Africa click to expand
- Macaronesia
  - Canary Islands
  - Cape Verde
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
  - Western Sahara
- West Tropical Africa
  - Mauritania
  - Senegal

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Saudi Arabia
- Middle Asia
  - Turkmenistan
- Siberia
  - West Siberia
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Thailand
  - Vietnam

Australasia click to expand
- Australia
  - Tasmania

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Prince Edward Island
  - Québec
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - New Hampshire
  - New Jersey
  - New York
  - Pennsylvania
  - Rhode Island
- Southeastern U.S.A.
  - Maryland
  - Virginia
- Western Canada
  - Manitoba

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000437616
UNII	44LI13X4GW
Canadensys	4568
USDA Plants	SUMA
Tropicos	7200288
INPN	125259
Flora of Italy	516
KEW	urn:lsid:ipni.org:names:1071140-2
The Plant List	kew-2484020
Open Tree Of Life	374051
NCBI Taxonomy	126913
NBN Atlas	NBNSYS0000003121
Nature Serve	2.139604
IPNI	1071140-2
iNaturalist	169432
GBIF	3083541
Freebase	/m/0m0qc9v
EPPO	SUEMA
EOL	585950
Elurikkus	7605
Wikipedia	Suaeda_maritima
CMAUP	NPO15405

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

In Situ Use of Mining Substrates for Wetland Construction: Results of a Pilot Experiment

Hernández-Pérez C, Martínez-López S, Martínez-Sánchez MJ, Martínez-Martínez LB, García-Lorenzo ML, Perez Sirvent C

Plants (Basel)

22-Apr-2024

PMCID:	PMC11054235
doi:	10.3390/plants13081161
PMID:	38674567

Temporal Changes in Biochemical Responses to Salt Stress in Three Salicornia Species

Homayouni H, Razi H, Izadi M, Alemzadeh A, Kazemeini SA, Niazi A, Vicente O

Plants (Basel)

29-Mar-2024

PMCID:	PMC11013812
doi:	10.3390/plants13070979
PMID:	38611508

Anti-inflammatory Properties of Strontium Oxide Nanoparticles Synthesized From Suaeda monoica Saltmarsh

Sinha P, Boopathi P, Suresh V, Pitchiah S

Cureus

18-Mar-2024

PMCID:	PMC11021874
doi:	10.7759/cureus.56355
PMID:	38633965

Phytochemical Screening, In Silico Molecular Docking, ADME Properties, and In Vitro Antioxidant, Anticancer, and Antidiabetic Activity of Marine Halophyte Suaeda maritima (L.) Dumort

Manojkumar S, Thandeeswaran M, Thangavel SK, Arjunan A, Muthuselvam M, Kalaiarasi G, Gnanajothi K

ACS Omega

29-Feb-2024

PMCID:	PMC10938337
doi:	10.1021/acsomega.3c05591
PMID:	38496978

Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review

Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

Evaluation of Antibacterial and Anti-oxidant Activities of Suaeda monoica Extract for Its Potential Application

Shakthi A, Linoj J, Suresh V, Hussein MA, Selvamani M

Cureus

28-Jan-2024

PMCID:	PMC10897944
doi:	10.7759/cureus.53091
PMID:	38414694

Formulation of Mentha piperita-Based Nanobiopesticides and Assessment of the Pesticidal and Antimicrobial Potential

Jahan N, Hussain N, Touqeer SI, KU, Shamshad H, Abbas N

Life (Basel)

19-Jan-2024

PMCID:	PMC10817515
doi:	10.3390/life14010144
PMID:	38276273

Ion Changes and Signaling under Salt Stress in Wheat and Other Important Crops

Lindberg S, Premkumar A

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780558
doi:	10.3390/plants13010046
PMID:	38202354

Dalbergia odorifera undergoes massive molecular shifts in response to waterlogging combined with salinity

Cisse EH, Jiang BH, Yin LY, Miao LF, Zhou JJ, Mekontso FN, Li DD, Xiang LS, Yang F

Plant Physiol

04-Dec-2023

PMCID:	PMC10980518
doi:	10.1093/plphys/kiad639
PMID:	38048404

Proteomic and metabolomic analyses uncover integrative mechanisms in Sesuvium portulacastrum tolerance to salt stress

Cao D, Zhang W, Yang N, Li Z, Zhang C, Wang D, Ye G, Chen J, Wei X

Front Plant Sci

28-Nov-2023

PMCID:	PMC10714944
doi:	10.3389/fpls.2023.1277762
PMID:	38089796

Discovery of Anti-Coronavirus Cinnamoyl Triterpenoids Isolated from Hippophae rhamnoides during a Screening of Halophytes from the North Sea and Channel Coasts in Northern France

Al Ibrahim M, Akissi ZL, Desmarets L, Lefèvre G, Samaillie J, Raczkiewicz I, Sahpaz S, Dubuisson J, Belouzard S, Rivière C, Séron K

Int J Mol Sci

22-Nov-2023

PMCID:	PMC10705938
doi:	10.3390/ijms242316617
PMID:	38068938

Plant Life with and without Oxygen: A Metabolomics Approach

Yemelyanov VV, Puzanskiy RK, Shishova MF

Int J Mol Sci

12-Nov-2023

PMCID:	PMC10671363
doi:	10.3390/ijms242216222
PMID:	38003412

Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective

Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU

Can J Infect Dis Med Microbiol

28-Oct-2023

PMCID:	PMC10625492
doi:	10.1155/2023/1860084
PMID:	37927532

Biosynthesis of Copper Nanoparticles with Medicinal Plants Extracts: From Extraction Methods to Applications

Antonio-Pérez A, Durán-Armenta LF, Pérez-Loredo MG, Torres-Huerta AL

Micromachines (Basel)

30-Sep-2023

PMCID:	PMC10609153
doi:	10.3390/mi14101882
PMID:	37893319

Xinghamide A, a New Cyclic Nonapeptide Found in Streptomyces xinghaiensis

Um S, Lee J, Kim SJ, Cho KA, Kang KS, Kim SH

Mar Drugs

26-Sep-2023

PMCID:	PMC10608500
doi:	10.3390/md21100509
PMID:	37888444

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
> Alkaloids and derivatives / Aporphines
(12S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene	26202781	Click to see	265.31	unknown	via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline	1078819	Click to see	355.40	unknown	via CMAUP database
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone	6453733	Click to see	307.30	unknown	via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone	10246449	Click to see	337.40	unknown	via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)-	158516	Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O	293.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Lanuginosine	97622	Click to see	305.30	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol	15560530	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl-	11857938	Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C	280.40	unknown	via CMAUP database
4-Methoxyhonokiol	155160	Click to see	280.40	unknown	via CMAUP database
Caryolanemagnolol	21726647	Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C	486.70	unknown	via CMAUP database
Honokiol	72303	Click to see	266.30	unknown	via CMAUP database
Magnaledehyde E	5319190	Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O	254.28	unknown	via CMAUP database
Magnolol	72300	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O	266.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde	71812224	Click to see	286.28	unknown	via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal	134367	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol	71812222	Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O	312.40	unknown	via CMAUP database
Isomagnolol	159137	Click to see	266.30	unknown	via CMAUP database
Obovaaldehyde	23259953	Click to see	270.28	unknown	via CMAUP database
Obovatal	6439677	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O	296.30	unknown	via CMAUP database
Obovatol	100771	Click to see	282.30	unknown	via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)-	10016628	Click to see	282.30	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol	68148	Click to see	134.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see	136.23	unknown	via CMAUP database
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadalene	10225	Click to see	198.30	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene oxide	1742210	Click to see	220.35	unknown	via CMAUP database
Clovanemagnolol	10323149	Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol	91730386	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol	118976561	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
2-[4-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-3-prop-2-enylphenyl]-4-prop-2-enylphenol	14587421	Click to see	488.70	unknown	via CMAUP database
4-[2-[[(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]oxy]-5-prop-2-enylphenyl]-2-prop-2-enylphenol	21726646	Click to see	488.70	unknown	via CMAUP database
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	via CMAUP database
Beta-Eudesmol	91457	Click to see	222.37	unknown	via CMAUP database
Cryptomeridiol	165258	Click to see	240.38	unknown	via CMAUP database
Eudesmagnolol	14587417	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O	488.70	unknown	via CMAUP database
Eudesobovatol A	442837	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C	504.70	unknown	via CMAUP database
Eudesobovatol B	10346031	Click to see	504.70	unknown	via CMAUP database
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)82541-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin	5316860	Click to see	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin	9918938	Click to see	827.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol	6093330	Click to see	314.40	unknown	via CMAUP database
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	21629882	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan	24796112	Click to see	318.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database

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Suaeda maritima

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Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

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