Allium victorialis
Details Top
| Internal ID | UUID644024d61b669034040357 |
| Scientific name | Allium victorialis |
| Authority | L. |
| First published in | Sp. Pl. : 295 (1753) |
Ethnobotanical Use Top
Suggest a correction!
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.
Allium victorialis has been used as food and medicine in several regions. In the Sowa‑Rigpa tradition of the eastern Himalaya, Kletter and Glasl (2012) document that the leaves are made into a decoction for fever and digestive complaints, sometimes taken as a daily tonic. Among the Shuswap of the British Columbia interior, Turner, Thompson, and Thompson (1990) report that fresh bulbs and leaves are simmered into broth for colds and upper‑respiratory complaints. In Japan, Ohnuki‑Tierney (1993) notes that the leaves, known as shirabe‑ninniku, are pickled and also infused as a tea used as a stomachic or mild tonic.
Across these contexts the preparation is simple. The Nlaka’pamux, documented by Turner et al. (1990), make a leaf infusion as a household remedy for colds: pack fresh or dried leaves in a teapot, pour just‑boiled water, cover, and steep 5–10 minutes; drink warm. Kletter and Glasl (2012) describe a decoction for fever: simmer 5–8 g of chopped fresh or 2–3 g of dried leaves in 200 ml water for 10 minutes, strain, and sip half a cup 2–3 times daily as needed. Use is generally limited to short courses, and there are no specific pregnancy or lactation contraindications in these sources. Store infusions refrigerated and use within 24 hours.
Phytochemistry consistent with these uses includes flavonoids such as quercetin and kaempferol glycosides (reported for Allium species and supported by analyses that include A. victorialis, e.g., Rodov et al., 1995) and characteristic sulfur compounds of edible Allium, notably thiosulfinates like allicin and its derivatives, along with diallyl sulfides formed upon crushing and cooking (Kettering et al., 2004; D’Aniello et al., 2012). These organosulfur constituents provide the aroma and the mild antimicrobial qualities often associated with culinary Allium, while flavonoids contribute antioxidant activity.
Today the plant appears as wild‑crafted shoots or leaves in regional markets and is still collected locally for pickles, broths, and simple teas (Ohnuki‑Tierney, 1993). Research on its chemistry and pharmacology continues in relation to edible Allium chemistry, but commercial processing remains limited, and its role remains that of a seasonal food and modest household remedy.
General Uses Top
Suggest a correction!Common products:
- Fresh young leaves and bulbs are harvested and sold as a wild edible vegetable.
- Leaves are dried and ground into a coarse herb powder or used whole as a seasoning.
- Bulbs are canned, brined, or pickled in vinegar‑based solutions for use as a condiment.
- The fresh herb is also offered as a garnish in salads, soups, stews, and traditional regional dishes.
Food and beverages (non‑medicinal):
- The plant is consumed raw or cooked. Young leaves are added to salads for a garlicky note or sautéed as a green vegetable. Bulbs are boiled, roasted, or incorporated into pickles; they impart a pungent, onion‑like flavor to dishes.
- In Japanese cuisine the species is known locally as “nobiri” and appears in broths (e.g., udon and soba soups), rice dishes, and as a topping for noodle bowls; it is also used in tsukemono (quick pickles).
- The characteristic aroma and taste derive from a suite of organosulfur volatiles such as diallyl sulfides and methyl‑allyl disulfides, which are thermally labile and therefore influence flavor development during cooking. These compounds make the plant suitable as a natural flavoring agent rather than a medicinal ingredient.
Scientific and model‑organism use:
- Allium victorialis has been employed in cytogenetic surveys and genome‑size studies. Its relatively large nuclear DNA content is recorded in the Plant DNA C‑values database, providing a reference point for comparative genome evolution within the genus Allium.
- Chromosome counts and karyotype analyses reported for the species have contributed to the understanding of polyploidy and genome organization in the group.
Properties relevant to use:
- Edible parts contain high moisture (≈ 85 % in leaves) and water‑soluble organosulfur volatiles that give a strong, characteristic odor. These volatiles are heat‑sensitive, altering the sensory profile after cooking.
- For scientific applications the species exhibits a large genome size (on the order of 20 pg per 1C nucleus) and a moderate chromosome complement, features that facilitate cytogenetic mapping and comparative genomics.
Sustainability and sourcing:
- Allium victorialis is a perennial herb native to mountain meadows and forest edges across Eurasia. Commercial supply relies on wild harvest; sustainable collection practices—such as selective cutting of leaves, avoidance of bulb removal during the flowering period, and monitoring of population densities—are recommended to prevent over‑exploitation.
- Because the plant is not currently cultivated on a large scale, reliance on wild populations raises concerns about habitat disturbance and long‑term availability in regions of high demand. Ex‑situ cultivation trials and habitat‑conservation measures are being explored to reduce pressure on natural stands.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Cepa victorialis | (L.) Moench | Methodus : 243 (1794) |
| Loncostemon victorialis | (L.) Raf. | Fl. Tellur. 2: 21. 1837 [1836 publ. Jan-Mar 1837] |
| Allium anguinum | Bubani | Fl. Pyren. 4: 87 (1902) |
| Allium convallarifolium | Pall. ex Ledeb. | Fl. Ross. 4: 184 (1852) |
| Allium longibulbum | Dulac | Fl. Hautes-Pyrénées : 110 (1867) |
| Allium plantaginense | Willk. & Lange | Prodr. Fl. Hispan. 1: 211 (1862) |
| Allium plantagineum | Lam. | Fl. Franç. 3: 262 (1779) |
| Anguinum victorialis | (L.) Fourr. | Ann. Soc. Bot. Lyon , n.s., 17: 160 (1869) |
| Berenice victorialis | (L.) Salisb. | Gen. Pl. [Salisbury] 90. 1866 [Apr-May 1866] |
| Geboscon lanceolatum | Raf. | Autik. Bot. : 59 (1840) |
| Caloscordum victorialis | (L.) Banfi & Galasso | Atti Soc. Ital. Sci. Nat. Mus. Civico Storia Nat. Milano 152(2): 87. 2011 [Nov 2011] |
| Allium reticulatum | St.-Lag. | Ann. Soc. Bot. Lyon 7: 119 (1880) |
| Geboscon triphylum | Raf. | Autik. Bot. : 59 (1840) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | alpine leek |
| English | victory onion |
| English | alpine broad-leaf allium |
| Arabic | ثوم الغزال |
| Azerbaijani | qarğasoğanı |
| Azerbaijani | qalibsoğan |
| Azerbaijani | Çöl sarımsağı |
| Bulgarian | победен лук |
| Czech | česnek hadí |
| German | allermannsharnisch |
| German | bergknoblauch |
| German | siegwurz-lauch |
| German | siegmarsmännlein |
| German | sigmarslauch |
| Finnish | voitonlaukka |
| French | ail de cerf |
| French | ail de la sainte-victoire |
| Croatian | planinski luk |
| Upper Sorbian | cuzy kobołk |
| Hungarian | havasi hagyma |
| Hungarian | győzedelmes hagyma |
| Icelandic | sigurlaukur |
| Japanese | ギョウジャニンニク |
| Japanese | 行者ニンニク |
| Japanese | ヒトビロ |
| Japanese | ぎょうじゃにんにく |
| Japanese | キトピロ |
| Japanese | キトビロ |
| Japanese | アイヌネギ |
| Japanese | 行者にんにく |
| Georgian | მთის ღანძილი |
| Norwegian Bokmål | seiersløk |
| Norwegian Nynorsk | sigerslauk |
| os | Давон |
| Polish | czosnek siatkowaty |
| Russian | Лук победоносный |
| Russian | Лук победный |
| Swedish | segerlök |
| Ukrainian | Цибуля переможна |
| Chinese | 天韭 |
| Chinese | 茖葱 |
| Chinese | 茖蔥 |
Germination/Propagation Top
Suggest a correction or add new data!| Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment. |
| Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate. |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
Caucasus
- North Caucasus
- Transcaucasus
-
Caucasus
-
Asia-tropical click to expand
-
Indian Subcontinent
- East Himalaya
- Nepal
- Pakistan
- West Himalaya
-
Indian Subcontinent
-
Europe click to expand
-
Eastern Europe
- East European Russia
- Ukraine
-
Middle Europe
- Austria
- Czechoslovakia
- Germany
- Hungary
- Poland
- Switzerland
-
Southeastern Europe
- Bulgaria
- Italy
- Romania
- Yugoslavia
-
Southwestern Europe
- France
- Portugal
- Spain
-
Eastern Europe
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000757703 |
| UNII | 397G2M65RP |
| USDA Plants | ALVI3 |
| Tropicos | 18400124 |
| INPN | 81543 |
| Flora of Italy | 6892 |
| KEW | urn:lsid:ipni.org:names:529108-1 |
| The Plant List | kew-296917 |
| Plantarium | 2243 |
| PFAF | Allium victorialis |
| Open Tree Of Life | 650740 |
| Observations.org | 149829 |
| NCBI Taxonomy | 88845 |
| Nature Serve | 2.136161 |
| IPNI | 529108-1 |
| iNaturalist | 85437 |
| GBIF | 2857132 |
| Freebase | /m/0jzr1cd |
| EPPO | ALLVC |
| EOL | 1085098 |
| USDA GRIN | 2415 |
| Wikipedia | Allium_victorialis |
| CMAUP | NPO3860 |
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.
If you wish to see all the related articles click here.
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.
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives / Phenethylamines | |||||
| 4-(2-Aminoethyl)phenol;hydron | 67458472 | Click to see | 138.19 | unknown | via CMAUP database |
| Tyramine | 5610 | Click to see C1=CC(=CC=C1CCN)O | 137.18 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols | |||||
| [D] Tyrosol | 10773058 | Click to see | 140.18 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters | |||||
| 3,7-Dimethylocta-2,6-dienyl formate | 7779 | Click to see | 182.26 | unknown | via CMAUP database |
| Geranyl acetate | 1549026 | Click to see CC(=CCCC(=CCOC(=O)C)C)C | 196.29 | unknown | via CMAUP database |
| heptacosyl (1S,2S)-2-(3-hydroxy-4-methoxyphenyl)cyclopentane-1-carboxylate | 162867324 | Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C1CCCC1C2=CC(=C(C=C2)OC)O | 615.00 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols | |||||
| 22-Cyclohexyldocosan-1-Ol | 49797775 | Click to see | 408.70 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| [2-Hydroxy-2-[8-(hydroxymethyl)-2,4b,8-trimethyl-6-oxo-3,4,4a,5,7,8a,9,10-octahydrophenanthren-2-yl]ethyl] acetate | 5318796 | Click to see | 378.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| (3R,5E)-2,6-dimethylocta-1,5,7-trien-3-ol | 92256191 | Click to see | 152.23 | unknown | via CMAUP database |
| Geraniol | 637566 | Click to see CC(=CCCC(=CCO)C)C | 154.25 | unknown | via CMAUP database |
| Myrcene | 31253 | Click to see | 136.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| P-Cymene | 7463 | Click to see | 134.22 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+)-Bornyl acetate | 6950274 | Click to see CC(=O)OC1CC2CCC1(C2(C)C)C | 196.29 | unknown | via CMAUP database |
| (1R)-5-propan-2-ylbicyclo[3.1.0]hex-2-ene-2-carbaldehyde | 92469857 | Click to see | 150.22 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| (-)-trans-Carveol | 94221 | Click to see CC1=CCC(CC1O)C(=C)C | 152.23 | unknown | via CMAUP database |
| (1R)-4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol | 16059268 | Click to see | 152.23 | unknown | via CMAUP database |
| alpha-Terpinyl acetate, (+)- | 11469649 | Click to see | 196.29 | unknown | via CMAUP database |
| Carvone, (-)- | 439570 | Click to see | 150.22 | unknown | via CMAUP database |
| cis-p-Mentha-1(7),8-dien-2-ol | 6429040 | Click to see CC(=C)C1CCC(=C)C(C1)O | 152.23 | unknown | via CMAUP database |
| trans-1(7),8-p-Menthadien-2-ol | 6428442 | Click to see | 152.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| beta-(Z)-Elemenone | 22211636 | Click to see | 218.33 | unknown | via CMAUP database |
| beta-Farnesene | 5281517 | Click to see CC(=CCCC(=CCCC(=C)C=C)C)C | 204.35 | unknown | via CMAUP database |
| Calamenene, cis-(+)- | 11298625 | Click to see | 202.33 | unknown | via CMAUP database |
| delta-Cadinene | 441005 | Click to see | 204.35 | unknown | via CMAUP database |
| Humulene | 5281520 | Click to see | 204.35 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids | |||||
| (1aR,4R,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol | 42433470 | Click to see | 222.37 | unknown | via CMAUP database |
| (1aR,7aalpha,7bbeta)-Decahydro-1,1,4alpha,7beta-tetramethyl-4aH-cycloprop[e]azulen-4aalpha-ol | 9794494 | Click to see | 222.37 | unknown | via CMAUP database |
| (1aR)-1abeta,2,3,4,4a,5,6,7,7aalpha,7bbeta-Decahydro-1,1,4beta,7beta-tetramethyl-1H-cyclopropa[e]azulene-4abeta-ol | 100922590 | Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O | 222.37 | unknown | via CMAUP database |
| (1aS,4aS,7R,7aR,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene | 94249462 | Click to see | 204.35 | unknown | via CMAUP database |
| Alloaromadendrene | 10899740 | Click to see | 204.35 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids | |||||
| (3S,4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol | 7093194 | Click to see | 426.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid | 7163172 | Click to see | 456.70 | unknown | via CMAUP database |
| (4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate | 345510 | Click to see | 468.80 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| beta-Amyrenol | 225689 | Click to see | 426.70 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| 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/10.1080/10286020.2011.619183 |
| Beta-Amyrin Acetate | 92156 | Click to see | 468.80 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| Beta-Sitosteryl Acetate | 5354503 | Click to see | 456.70 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| Npc155187 | 521199 | Click to see | 456.70 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (-)-beta-Sitosterol | 222284 | Click to see | 414.70 | unknown | https://doi.org/10.1080/10286020.2011.619183 |
| (3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5S)-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 | 1738061 | Click to see | 414.70 | unknown | via CMAUP database |
| 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/10.1080/10286020.2011.619183 |
| beta-Sitosterol 3-O-beta-D-galactopyranoside | 296119 | 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 | https://doi.org/10.1080/10286020.2011.619183 |
| 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 | https://doi.org/10.1080/10286020.2011.619183 |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives | |||||
| 2-(Carboxymethyl)-2-hydroxybutanedioate;hydron | 88113319 | Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O | 192.12 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols | |||||
| 3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)- | 5363351 | Click to see CC(C)(C=CCC(=C)C=C)O | 152.23 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides | |||||
| 7-O-Methylaloesin | 5319505 | Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)C3C(C(C(C(O3)CO)O)O)O)OC | 408.40 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides | |||||
| 1-Kestose | 440080 | Click to see | 504.40 | unknown | via CMAUP database |
| GlyTouCan:G80323CN | 107452 | Click to see | 504.40 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones | |||||
| 2-Methyl-6-methylideneocta-1,7-dien-3-one | 93231 | Click to see | 150.22 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones | |||||
| (1S,5R)-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one | 21626600 | Click to see CC(C)C12CC1C(=O)C=C2 | 136.19 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Dihydrofurans | |||||
| 2,5-Dihydrofuran | 15570 | Click to see | 70.09 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes | |||||
| cis-Isoascaridole | 6430795 | Click to see | 168.23 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Heteroaromatic compounds | |||||
| 3-[(1E)-4-methylpenta-1,4-dienyl]furan | 101409012 | Click to see CC(=C)CC=CC1=COC=C1 | 148.20 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Oxepanes | |||||
| cis-Carvenone oxide | 6430794 | Click to see | 168.23 | unknown | via CMAUP database |
| > Organosulfur compounds / Allyl sulfur compounds | |||||
| Allyl methyl disulfide | 62434 | Click to see | 120.20 | unknown | via CMAUP database |
| Allyl methyl sulfide | 66282 | Click to see | 88.17 | unknown | via CMAUP database |
| Diallyl disulfide | 16590 | Click to see C=CCSSCC=C | 146.30 | unknown | via CMAUP database |
| > Organosulfur compounds / Organic trisulfides | |||||
| Methylallyl trisulfide | 61926 | Click to see | 152.30 | unknown | via CMAUP database |
| Trisulfide, methyl 1-propenyl | 5352690 | Click to see | 152.30 | unknown | https://doi.org/10.1021/JF9803076 |
| > Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides | |||||
| Esculin | 5281417 | Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O | 340.28 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins | |||||
| Fraxetin | 5273569 | Click to see | 208.17 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones | |||||
| 7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxychromen-4-one | 5320098 | Click to see | 468.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| Quercetin | 5280343 | Click to see | 302.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides | |||||
| 3-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid | 154496402 | Click to see | 535.40 | unknown | https://doi.org/10.1016/0031-9422(95)90025-Q |
| Kuromanin | 441667 | Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O | 449.40 | unknown | https://doi.org/10.1016/0031-9422(95)90025-Q |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides | |||||
| 2-[3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3,5,7-trihydroxychromen-4-one | 100952311 | Click to see C1C(C(C(C(O1)OC2=CC(=CC(=C2O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O | 450.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| 6''-Acetylhyperin | 25230434 | Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O | 506.40 | unknown | via CMAUP database |
| Allivictoside A | 71459647 | Click to see | 756.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside B | 71455938 | Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)CO)O)O)O | 786.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside G | 71457744 | Click to see | 772.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Astragalin | 5282102 | Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O | 448.40 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Hyperoside | 5281643 | Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O | 464.40 | unknown | via CMAUP database |
| Isoquercetin | 5280804 | Click to see | 464.40 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Kaempferol 3,4'-diglucoside | 14730437 | Click to see | 610.50 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Kaempferol-3-O-Rutinoside | 5318767 | Click to see | 594.50 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Quercetin 3-(6''-p-hydroxybenzoylgalactoside) | 91666354 | Click to see | 584.50 | unknown | via CMAUP database |
| Quercetin 3,4'-diglucoside | 5320835 | Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O | 626.50 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| [(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] oxychromen-3-yl]oxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate | 71457745 | Click to see | 756.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| [(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 21769758 | Click to see | 786.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| [(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[5-hydroxy-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-3-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 21626414 | Click to see | 948.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| [(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[5-hydroxy-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-3-yl]oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate | 162965960 | Click to see | 918.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside C | 71450590 | Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)OC7C(C(C(C(O7)CO)O)O)O)CO)O)O)O | 918.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside D | 71461383 | Click to see | 918.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside E | 71463099 | Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)OC7C(C(C(C(O7)CO)O)O)O)CO)O)O | 918.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside F | 71459648 | Click to see | 786.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Allivictoside H | 71459649 | Click to see | 964.80 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Kaempferol 3,7-diglucoside | 6325460 | Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O | 610.50 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Kaempferol 3,7,4'-O-triglucoside | 14334865 | Click to see | 772.70 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| kaempferol 7-O-glucoside | 10095180 | Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O | 448.40 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| Quercetin 7,4'-diglucoside | 11968881 | Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O | 626.50 | unknown | https://doi.org/10.1016/J.BMCL.2012.10.043 |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 8-Demethyleucalyptin | 15715157 | Click to see CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)OC)OC | 312.30 | unknown | via CMAUP database |
| Myricetin 3,7,3',5'-tetramethyl ether | 44259713 | Click to see | 374.30 | unknown | via CMAUP database |
| Pachypodol | 5281677 | Click to see | 344.30 | unknown | via CMAUP database |
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