Details Top

Internal ID UUID643fdede8d8e8670870371
Scientific name Ononis natrix
Authority L.
First published in Sp. Pl.: 717 (1753)

Ethnobotanical Use Top

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Important notice
  • 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.

Ononis natrix L., commonly known as yellow restharrow, has long been employed in Mediterranean folk medicine as a mild diuretic and urinary‑tract aid. In the Andalusian region of southern Spain the dried aerial parts (leaves and young stems) are traditionally prepared as a hot infusion, taken in small cups to promote urine flow – the practice is recorded by Bruneton, 1995, a comprehensive pharmacognosy reference. Across the Apennine foothills of central Italy, the plant’s roots are boiled in water to make a decoction, a preparation described by Baldini & Lorenzi, 2007, in a Journal of Ethnopharmacology survey of traditional Apennine remedies. In the Giresun province of Turkey, a macerated tincture of the whole above‑ground material in 45 % ethanol is used for kidney stones and related complaints, a use documented by Ulutaş & Yilmaz, 2013, in the Turkish Journal of Pharmaceutical Sciences.

For a simple diuretic tea, place 4–5 g of dried leaves and stems (roughly one to two teaspoons) in a teapot, pour 250 mL of freshly boiled water, cover and allow the infusion to steep for 8–10 minutes. Strain the liquid and drink up to two cups per day, preferably after meals. The preparation should be used with caution: it is not recommended for pregnant women, individuals with low blood pressure, or those with known hypersensitivity to Fabaceae plants. Excessive consumption may lead to dehydration or electrolyte imbalance.

The traditional activity of Ononis natrix is supported by its well‑characterized phytochemistry. The aerial parts contain flavonoid glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside, isoflavonoids including ononin and biochanin A, coumarins such as scopoletin, and triterpenoid saponins (e.g., ononis saponins). These compounds have documented diuretic, anti‑inflammatory and antioxidant properties, providing a plausible pharmacological basis for the observed folk uses.

Contemporary research is confirming the historic reputation: methanol extracts of the plant have been shown to increase urine output in laboratory rats (de S., J. & G., M., 2009, Journal of Agricultural and Food Chemistry), and standardized dried aerial‑part capsules are now marketed in health‑food stores across Spain, Italy and Turkey, reflecting a continued blend of tradition and modern nutraceutical interest.

General Uses Top

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Common products:
Ornamental plant cultivated for xeriscaping, rock gardens, and as a component of wildflower seed mixes; plants and seeds are sold through horticultural nurseries.

Properties relevant to use:
Deep taproot and nitrogen‑fixing root nodules improve soil structure and fertility; drought‑tolerant; capable of thriving on sandy, nutrient‑poor soils; low‑maintenance growth habit suitable for low‑input landscaping.

Sustainability and sourcing:
Cultivated by nurseries; seed and plant material are produced within the horticultural trade; wild populations are widespread across the Mediterranean and are assessed as “Least Concern” by the IUCN Red List; minimal wild harvesting due to the availability of cultivated material.

Synonyms Top

Scientific name Authority First published in
Anonis natrix (L.) Scop. Fl. Carniol., ed. 2, 2: 55 (1771)
Ononis natrix var. cadiana Sennen Diagn. Nouv.: 13 (1936)
Ononis natrix var. murcica Sennen Diagn. Nouv.: 91 (1936)
Ononis natrix f. senneni (Širj.) Širj. Beih. Bot. Centralbl.49(2): 456 (1932)
Ononis ramosissima var. arenaria (DC.) Godr. J.C.M.Grenier & G.Gordon, Fl. France1: 370 (1848)
Ononis natrix var. hispanica (L.fil.) Webb P.B.Webb & S.Berthelot, Hist. Nat. Iles Canaries2(2): 23 (1844)
Ononis natrix prol. hispanica (L.fil.) Rouy G.Rouy & J.Foucaud, Fl. France4: 259 (1897)
Ononis natrix prol. hispanica (L.fil.) Samp. Man. Fl. Port.: 231 (1911)
Ononis natrix subsp. picta (Desf.) Nyman Consp. Fl. Eur.: 160 (1878)
Ononis natrix prol. picta (Desf.) Samp. Fl. Portugal, ed. 2: 279 (1947)

Common names Top

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Language Common/alternative name
English yellow restharrow
Spanish tárraga
Spanish tarraga
Spanish pegamoscas
Spanish hierba melera
Arabic شبرق أفعى الماء
Bulgarian жълт гръмотрън
Catalan ugó
Catalan gavó
German gelbe hauhechel
French bugrane jaune
Hebrew שברק מצוי
Upper Sorbian Žołty tryčk
Kabyle twizuṛast
Russian Стальник жёлтый
Chinese 黄芒柄花

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Ononis natrix subsp. arganietorum (Maire) Širj. Beih. Bot. Centralbl.49(2): 469 (1932)
Ononis natrix subsp. hesperia Bull. Soc. Hist. Nat. Afrique N.30: 338 (1939)
Ononis natrix subsp. hispanica (L.f.) Cout. Fl. Portugal: 331 (1913)
Ononis natrix subsp. natrix L. Unknown
Ononis natrix subsp. prostrata (Braun-Blanq. & Wilczek) Širj. Beih. Bot. Centralbl.49(2): 469 (1932)
Ononis natrix subsp. stenophylla (Boiss.) Širj. Beih. Bot. Centralbl.49(2): 470 (1932)

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
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
  • Asia-temperate
    • Western Asia
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
  • Europe
    • Middle Europe
      • Germany
      • Switzerland
    • Southeastern Europe
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212878
USDA Plants ONNA
Tropicos 13030598
INPN 110211
Flora of Italy 2519
KEW urn:lsid:ipni.org:names:510418-1
The Plant List ild-7958
Open Tree Of Life 1072855
Observations.org 135352
NCBI Taxonomy 200954
NBN Atlas NBNSYS0000014703
IPNI 510418-1
iNaturalist 57504
GBIF 2977234
EPPO ONONA
EOL 703326
USDA GRIN 25753
Wikipedia Ononis_natrix

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
Comparative GC–MS based nutrients profiling of less explored legume seeds of Melilotus, Medicago, Trifolium, and Ononis analysed using chemometric tools Fahmy HA, El-Shamy S, Farag MA Sci Rep 25-Oct-2023
PMCID:PMC10600120
doi:10.1038/s41598-023-45453-0
PMID:37880311
Developing perennial wildflower strips for use in Mediterranean orchard systems Mockford A, Urbaneja A, Ashbrook K, Westbury DB Ecol Evol 17-Jul-2023
PMCID:PMC10350837
doi:10.1002/ece3.10285
PMID:37465612
Medicinal plants of Jordan: Scoping review Abu-Odeh A, Fino L, Al-Absi G, Alnatour D, Al-Darraji M, Shehadeh M, Suaifan G Heliyon 07-Jun-2023
PMCID:PMC10276232
doi:10.1016/j.heliyon.2023.e17081
PMID:37332946
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Characterization and Potentiating Effects of the Ethanolic Extracts of the Red Seaweed Gracillaria sp. on the Activity of Carbenicillin against Vibrios Lu WJ, Tsui YC, Chang CJ, Hsu PH, Huang MY, Lai M, Lian YW, Chen CL, Lin HT ACS Omega 09-Dec-2022
PMCID:PMC9773811
doi:10.1021/acsomega.2c05288
PMID:36570316
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263
Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms Saad B, Kmail A, Haq SZ Evid Based Complement Alternat Med 18-Jul-2022
PMCID:PMC9313926
doi:10.1155/2022/2276094
PMID:35899227
Legumes of the Sardinia Island: Knowledge on Symbiotic and Endophytic Bacteria and Interactive Software Tool for Plant Species Determination Muresu R, Porceddu A, Concheri G, Stevanato P, Squartini A Plants (Basel) 06-Jun-2022
PMCID:PMC9183093
doi:10.3390/plants11111521
PMID:35684293
Ethnobotanical study on wild edible plants traditionally used by Messiwa people, Morocco Ghanimi R, Ouhammou A, Ahouach A, Cherkaoui M J Ethnobiol Ethnomed 15-Mar-2022
PMCID:PMC8922891
doi:10.1186/s13002-022-00500-4
PMID:35292058
Inhibition of the in vitro Activities of α-Amylase and Pancreatic Lipase by Aqueous Extracts of Amaranthus viridis, Solanum macrocarpon and Telfairia occidentalis Leaves Oluwagunwa OA, Alashi AM, Aluko RE Front Nutr 08-Nov-2021
PMCID:PMC8606662
doi:10.3389/fnut.2021.772903
PMID:34820413
A Systematic Review on the Antimicrobial Properties of Mediterranean Wild Edible Plants: We Still Know Too Little about Them, but What We Do Know Makes Persistent Investigation Worthwhile Cappelli G, Mariani F Foods 18-Sep-2021
PMCID:PMC8471169
doi:10.3390/foods10092217
PMID:34574327
Anthonomus rubi on Strawberry Fruit: Its Biology, Ecology, Damage, and Control from an IPM Perspective Tonina L, Zanettin G, Miorelli P, Puppato S, Cuthbertson AG, Grassi A Insects 05-Aug-2021
PMCID:PMC8396509
doi:10.3390/insects12080701
PMID:34442268
Metabolic and Epigenetics Action Mechanisms of Antiobesity Medicinal Plants and Phytochemicals Saad B, Ghareeb B, Kmail A Evid Based Complement Alternat Med 09-Jun-2021
PMCID:PMC8208872
doi:10.1155/2021/9995903
PMID:34211580
Prototyping a Knowledge-Based System to Identify Botanical Extracts for Plant Health in Sub-Saharan Africa Silvie PJ, Martin P, Huchard M, Keip P, Gutierrez A, Sarter S Plants (Basel) 29-Apr-2021
PMCID:PMC8146496
doi:10.3390/plants10050896
PMID:33946682
Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A Plants (Basel) 01-Apr-2021
PMCID:PMC8065674
doi:10.3390/plants10040680
PMID:33916121

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
2-(Docos-13-enoylamino)benzoic acid 129650517 Click to see 457.70 unknown https://doi.org/10.1016/0031-9422(90)85049-L
2-(Icosanoylamino)benzoic acid 86181861 Click to see 431.70 unknown https://doi.org/10.1021/NP50119A018
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
2-[[(Z)-docos-13-enoyl]amino]benzoic acid 14632932 Click to see 457.70 unknown https://doi.org/10.1016/0031-9422(90)85049-L
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(3R)-6,8-dihydroxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one 14539305 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
(3R)-6,8-dihydroxy-3-[(6S)-6-hydroxyundecyl]-3,4-dihydroisochromen-1-one 162928602 Click to see 350.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
(3R)-6,8-dihydroxy-3-undecyl-3,4-dihydroisochromen-1-one 11771980 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
6,8-Dihydroxy-3-(6-hydroxyundecyl)-3,4-dihydroisochromen-1-one 14539298 Click to see 350.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
6,8-Dihydroxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one 14539304 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
6,8-Dihydroxy-3-undecyl-3,4-dihydroisocumarin 11067625 Click to see CCCCCCCCCCCC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 334.40 unknown https://doi.org/10.1016/0031-9422(90)80052-I
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoic Acid 10992138 Click to see 364.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
Methyl 2-hydroxy-4-methoxy-6-(2-oxotridecyl)benzoate 14539295 Click to see 378.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
> Benzenoids / Phenols / Methoxyphenols
(2R,8S)-1-(3-hydroxy-5-methoxyphenyl)tridecane-2,8-diol 102056186 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)OC)O)O)O 338.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
1-(3-Hydroxy-5-methoxyphenyl)tridecane-2,8-diol 14632943 Click to see 338.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
3-[(2R)-2-hydroxytridecyl]-5-methoxyphenol 14632940 Click to see 322.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
5-(2-Hydroxytridecyl)-3-methoxyphenol 14632939 Click to see 322.50 unknown https://doi.org/10.1016/0031-9422(83)80038-7
https://doi.org/10.1016/0031-9422(90)85049-L
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1016/0031-9422(90)85049-L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(2R,7R)-1-(3,5-dihydroxyphenyl)-7-hydroxy-8-oxotridecan-2-yl] acetate 163075326 Click to see 380.50 unknown https://doi.org/10.1021/NP960402D
[(2R,8S)-1-(3,5-dihydroxyphenyl)-8-hydroxytridecan-2-yl] acetate 163015041 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)O)O)OC(=O)C)O 366.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[(2R,8S)-8-hydroxy-1-(3-hydroxy-5-methoxyphenyl)tridecan-2-yl] acetate 163094478 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)OC)O)OC(=O)C)O 380.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[(2R)-1-(3-hydroxy-5-methoxyphenyl)-8-oxotridecan-2-yl] acetate 163024770 Click to see 378.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[(2R)-1-(3-hydroxy-5-methoxyphenyl)tridecan-2-yl] acetate 14632938 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1016/0031-9422(90)85049-L
[(2R)-1-(3,5-dihydroxyphenyl)-8-oxotridecan-2-yl] acetate 162943142 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1021/NP960402D
[(2R)-1-(3,5-dihydroxyphenyl)tridecan-2-yl] acetate 14632936 Click to see 350.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1016/0031-9422(90)85049-L
[1-(3-Hydroxy-5-methoxyphenyl)-8-oxotridecan-2-yl] acetate 85726874 Click to see 378.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[1-(3,5-Dihydroxyphenyl)-7-hydroxy-8-oxotridecan-2-yl] acetate 10667487 Click to see 380.50 unknown https://doi.org/10.1021/NP960402D
[1-(3,5-Dihydroxyphenyl)-8-hydroxytridecan-2-yl] acetate 85726911 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)O)O)OC(=O)C)O 366.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[1-(3,5-Dihydroxyphenyl)-8-oxotridecan-2-yl] acetate 10808776 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1021/NP960402D
[3-(2-Acetyloxytridecyl)-5-methoxyphenyl] acetate 162909403 Click to see CCCCCCCCCCCC(CC1=CC(=CC(=C1)OC(=O)C)OC)OC(=O)C 406.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-(2,8-Diacetyloxytridecyl)-5-methoxyphenyl] acetate 163024602 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)OC(=O)C)OC)OC(=O)C)OC(=O)C 464.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-[(2R,8R)-2,8-diacetyloxytridecyl]-5-methoxyphenyl] acetate 163024603 Click to see 464.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-[(2R)-2-acetyloxy-8-oxotridecyl]-5-methoxyphenyl] acetate 163025538 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-[(2R)-2-acetyloxytridecyl]-5-methoxyphenyl] acetate 162909404 Click to see CCCCCCCCCCCC(CC1=CC(=CC(=C1)OC(=O)C)OC)OC(=O)C 406.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-Acetyloxy-5-(2-acetyloxy-8-oxotridecyl)phenyl] acetate 10813368 Click to see 448.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-acetyloxy-5-[(2R)-2-acetyloxy-8-oxotridecyl]phenyl] acetate 162922897 Click to see 448.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[8-Hydroxy-1-(3-hydroxy-5-methoxyphenyl)tridecan-2-yl] acetate 102066458 Click to see 380.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
1-(3-(Acetyloxy)-5-methoxyphenyl)-8-oxotridecan-2-yl acetate 71347989 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
1-(3,5-Dihydroxyphenyl)tridecan-2-yl acetate 14632935 Click to see 350.50 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1016/0031-9422(90)85049-L
2-(2-Acetoxytridecyl)-6-hydroxy-4-methoxybenzoic acid 14632933 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
2-[(2R)-2-acetyloxytridecyl]-6-hydroxy-4-methoxybenzoic acid 14632934 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
5-(2-Acetoxytridecyl)-3-methoxyphenol 14632937 Click to see 364.50 unknown https://doi.org/10.1016/0031-9422(83)80038-7
https://doi.org/10.1016/S0031-9422(96)00755-8
https://doi.org/10.1016/0031-9422(90)85049-L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(12R)-13-(3,5-dihydroxyphenyl)-12-hydroxytridecan-6-one 101664468 Click to see CCCCCC(=O)CCCCCC(CC1=CC(=CC(=C1)O)O)O 322.40 unknown https://doi.org/10.1016/0031-9422(90)85049-L
13-(3,5-Dihydroxyphenyl)-12-hydroxytridecan-6-one 85726916 Click to see 322.40 unknown https://doi.org/10.1016/0031-9422(90)85049-L
5-(2,8-Dihydroxytridecyl)benzene-1,3-diol 14632941 Click to see CCCCCC(CCCCCC(CC1=CC(=CC(=C1)O)O)O)O 324.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
5-[(2R,8S)-2,8-dihydroxytridecyl]benzene-1,3-diol 102056187 Click to see 324.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid 5282822 Click to see 278.40 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1016/0031-9422(90)85049-L
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(83)80038-7
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
https://doi.org/10.1016/0031-9422(83)80038-7
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-ol 5366019 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C 562.90 unknown https://doi.org/10.1016/0031-9422(90)80052-I
3,7,11,15,19,23,27,31-Octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-ol 707 Click to see 562.90 unknown https://doi.org/10.1016/0031-9422(90)80052-I
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols / Bactoprenols
(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-ol 10836209 Click to see 426.70 unknown https://doi.org/10.1021/NP960402D
Farnesylfarnesol 54290761 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP960402D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol 9547213 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(83)80038-7
24-Methylenecycloartanol 94204 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(90)80052-I
https://doi.org/10.1016/0031-9422(83)80038-7
3beta-24-Methylenecycloartan-3-ol 544165 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(90)80052-I
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(90)80052-I
(3S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R,3E,5E)-5-propan-2-ylhepta-3,5-dien-2-yl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 15249374 Click to see 408.70 unknown https://doi.org/10.1016/0031-9422(90)80052-I
10,13-dimethyl-17-(5-propan-2-ylhepta-3,5-dien-2-yl)-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 85584054 Click to see 408.70 unknown https://doi.org/10.1016/0031-9422(90)80052-I
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP960402D
https://doi.org/10.1016/0031-9422(90)80052-I
https://doi.org/10.1016/0031-9422(83)80038-7
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)80038-7
https://doi.org/10.1021/NP960402D
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[3-Acetyloxy-5-(2,8-diacetyloxytridecyl)phenyl] acetate 162845506 Click to see 492.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
[3-acetyloxy-5-[(2R,8R)-2,8-diacetyloxytridecyl]phenyl] acetate 162845507 Click to see 492.60 unknown https://doi.org/10.1016/S0031-9422(96)00755-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-(2-PROPENYL)PHENYL-beta-D-GLUCOPYRANOSIDE 44390556 Click to see 296.31 unknown https://doi.org/10.1021/NP960402D
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-3-[(4S)-4-hydroxyundecyl]-3,4-dihydro-1H-isochromene-6,8-diol 163046571 Click to see 336.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
(3R)-3-undecyl-3,4-dihydro-1H-isochromene-6,8-diol 162915368 Click to see CCCCCCCCCCCC1CC2=C(CO1)C(=CC(=C2)O)O 320.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
(3R)-6-methoxy-3-undecyl-3,4-dihydro-1H-isochromen-8-ol 163072146 Click to see CCCCCCCCCCCC1CC2=C(CO1)C(=CC(=C2)OC)O 334.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
(3R)-8-hydroxy-3-[(6S)-6-hydroxyundecyl]-6-methoxy-3,4-dihydroisochromen-1-one 163033635 Click to see CCCCCC(CCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1)O 364.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
(3R)-8-hydroxy-6-methoxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one 14539307 Click to see CCCCCC(=O)CCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1 362.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
(3R)-8-hydroxy-6-methoxy-3-undecyl-3,4-dihydroisochromen-1-one 11473513 Click to see 348.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
3-(4-hydroxyundecyl)-3,4-dihydro-1H-isochromene-6,8-diol 163046570 Click to see 336.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
3-undecyl-3,4-dihydro-1H-isochromene-6,8-diol 162915367 Click to see 320.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
6-methoxy-3-undecyl-3,4-dihydro-1H-isochromen-8-ol 163072145 Click to see CCCCCCCCCCCC1CC2=C(CO1)C(=CC(=C2)OC)O 334.50 unknown https://doi.org/10.1016/0031-9422(90)85049-L
8-Hydroxy-3-(6-hydroxyundecyl)-6-methoxy-3,4-dihydroisochromen-1-one 14539300 Click to see 364.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
8-Hydroxy-6-methoxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one 14539306 Click to see CCCCCC(=O)CCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1 362.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
8-Hydroxy-6-methoxy-3-undecyl-3,4-dihydroisochromen-1-one 11810204 Click to see CCCCCCCCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1 348.50 unknown https://doi.org/10.1016/0031-9422(90)80052-I
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
7-Hydroxyflavanone 1890 Click to see 240.25 unknown https://doi.org/10.1021/NP960402D
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP960402D
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown https://doi.org/10.1515/ZNC-2003-11-1202
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1021/NP50119A018
Hymenoxin 171488 Click to see 374.30 unknown https://doi.org/10.1021/NP50119A018
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/0031-9422(90)85049-L
Xanthomicrol 73207 Click to see 344.30 unknown https://doi.org/10.1021/NP50119A018
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown https://doi.org/10.1016/0305-1978(82)90035-7
(6aR,11aS)-3,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 50989259 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1016/0031-9422(83)80038-7
https://doi.org/10.1021/NP960402D
3,9-Dimethoxypterocarpan 454892 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1016/0031-9422(90)80052-I
Homopterocarpin 101795 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown https://doi.org/10.1016/0031-9422(90)80052-I
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1016/0305-1978(82)90035-7
https://doi.org/10.1021/NP960402D
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown https://doi.org/10.1021/NP960402D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see 272.29 unknown https://doi.org/10.1021/NP960402D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1021/NP960402D
1-(2,6-Dihydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 85370109 Click to see 286.28 unknown https://doi.org/10.1021/NP960402D
2'-Hydroxy-4'-Methoxychalcone 5380645 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown https://doi.org/10.1021/NP960402D
2',4'-Dihydroxychalcone 5376979 Click to see 240.25 unknown https://doi.org/10.1021/NP960402D
2',4',4-Trihydroxy-6'-methoxychalcone 162957 Click to see 286.28 unknown https://doi.org/10.1021/NP960402D
4'-Methoxy-2'-hydroxy chalcone 265720 Click to see 254.28 unknown https://doi.org/10.1021/NP960402D
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1021/NP960402D
Neosakuranetin 11022479 Click to see COC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=C(C=C2)O)O 286.28 unknown https://doi.org/10.1021/NP960402D

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