Allium victorialis - Unknown
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Details Top

Internal ID UUID644024d61b669034040357
Scientific name Allium victorialis
Authority L.
First published in Sp. Pl. : 295 (1753)

Description Top

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Allium victorialis, also known as victory onion, Alpine leek, and Alpine broad-leaf allium, is a perennial wild onion found in mountainous regions of Europe and parts of Asia. It can reach a height of 30-45 cm and has broad, elliptical or lanceolate leaves. The flowers are whitish green. Some sources consider certain populations in East Asia and Alaska to be a subspecies, while others recognize them as a distinct species called Allium ochotense. The plant has been used as a medicinal and fetish plant in the past and was also consumed by the Ainu people in northern Japan. Its name, "victorialis," comes from its use as an amulet for protection against impure spirits by Bohemian miners.

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]

Common names Top

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Language Common/alternative name
English alpine leek
English victory onion
English alpine broad-leaf allium
Spanish geboscon triphylum
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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
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-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • 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

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.
Title Authors Publication Released IDs
Hepatoprotective Effect of Allium ochotense Extracts on Chronic Alcohol-Induced Fatty Liver and Hepatic Inflammation in C57BL/6 Mice Go MJ, Kim JM, Lee HL, Kim TY, Kim JH, Lee HS, Kim IY, Sim SJ, Heo HJ Int J Mol Sci 20-Mar-2024
PMCID:PMC10970900
doi:10.3390/ijms25063496
PMID:38542468
Authentication of Allium ulleungense, A. microdictyon and A. ochotense based on super-barcoding of plastid genome and 45S nrDNA Lee M, Lee HY, Kang JS, Lee H, Park KJ, Park JY, Yang TJ PLoS One 20-Nov-2023
PMCID:PMC10659177
doi:10.1371/journal.pone.0294457
PMID:37983242
Beware of accidental ingestion of Colchicum autumnale mistaken for Allium victorialis Nara T, Nakae H, Irie Y, Kameyama K, Okuyama M Acute Med Surg 30-May-2023
PMCID:PMC10227730
doi:10.1002/ams2.854
PMID:37261376
New insights into the phylogenetic relationships among wild onions (Allium, Amaryllidaceae), with special emphasis on the subgenera Anguinum and Rhizirideum, as revealed by plastomes Yang J, Kim SH, Gil HY, Choi HJ, Kim SC Front Plant Sci 21-Mar-2023
PMCID:PMC10070991
doi:10.3389/fpls.2023.1124277
PMID:37025138
Carotenoid and Tocopherol Profiling in 18 Korean Traditional Green Leafy Vegetables by LC-SIM-MS Ko EY, Lee JH, Sivanesan I, Choi MJ, Keum YS, Saini RK Foods 19-Mar-2023
PMCID:PMC10048374
doi:10.3390/foods12061312
PMID:36981238
Bio-Actives from Natural Products with Potential Cardioprotective Properties: Isolation, Identification, and Pharmacological Actions of Apigenin, Quercetin, and Silibinin Tomou EM, Papakyriakopoulou P, Skaltsa H, Valsami G, Kadoglou NP Molecules 05-Mar-2023
PMCID:PMC10005323
doi:10.3390/molecules28052387
PMID:36903630
Natural Bioactive Substances in Fruits of Aronia melanocarpa (Michx.) Elliott Exposed to Combined Light-Type, Chitosan Oligosaccharide, and Spent Mushroom Residue Treatments Duan Y, Wei X, Zhao W, Li J, Yang G, Zhou S, Zhou C, Zhang L, Li P, Hou S, Shi D, Liu C, Guo B Plants (Basel) 30-Jan-2023
PMCID:PMC9919629
doi:10.3390/plants12030604
PMID:36771688
In situ occurrence and protection of crop wild relatives in Italian sites of natura 2000 network: Insights from a data-driven approach Raggi L, Zucchini C, Gigante D, Negri V Front Plant Sci 22-Dec-2022
PMCID:PMC9814127
doi:10.3389/fpls.2022.1080615
PMID:36618609
Bioactive extracts and association with C and N in Eleutherococcus senticosus subjected to chitosan nanoparticles in contrasting light spectra Guo S, Wang H, Sui Y, Liu X, Tan L PLoS One 01-Dec-2022
PMCID:PMC9714952
doi:10.1371/journal.pone.0277233
PMID:36454898
Forage quality and physiological performance of mowed alfalfa (Medicago sativa L.) subjected to combined light quality and drought He C, Zhao Y, Wang Y, Cai J, Gao J, Zhang J Front Plant Sci 22-Nov-2022
PMCID:PMC9723141
doi:10.3389/fpls.2022.1047294
PMID:36483958
Leek Yellow Stripe Virus Can Adjust for Host Adaptation by Trimming the N-Terminal Domain to Allow the P1 Protein to Function as an RNA Silencing Suppressor Sasaki J, Kawakubo S, Kim H, Kim OK, Yamashita K, Shimura H, Masuta C Plant Pathol J 01-Aug-2022
PMCID:PMC9372110
doi:10.5423/PPJ.FT.06.2022.0077
PMID:35953058
The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae Danquah CA, Minkah PA, Agana TA, Moyo P, Ofori M, Doe P, Rali S, Osei Duah Junior I, Amankwah KB, Somuah SO, Nugbemado IN, Maharaj VJ, Bhakta S, Gibbons S Molecules 13-Jul-2022
PMCID:PMC9316996
doi:10.3390/molecules27144475
PMID:35889346
Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine Chen W, Yang Y, Fu K, Zhang D, Wang Z Front Pharmacol 28-Jun-2022
PMCID:PMC9274010
doi:10.3389/fphar.2022.891273
PMID:35837276
Chemistry and bioactivities of natural steroidal alkaloids Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD Nat Prod Bioprospect 15-Jun-2022
PMCID:PMC9198197
doi:10.1007/s13659-022-00345-0
PMID:35701630
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116

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 / Phenethylamines
4-(2-Aminoethyl)phenol;hydron 67458472 Click to see [H+].C1=CC(=CC=C1CCN)O 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
2,6-Dideuterio-4-(2-hydroxyethyl)phenol 10773058 Click to see C1=CC(=CC=C1CCO)O 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 CC(=CCCC(=CCOC=O)C)C 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 C1CCC(CC1)CCCCCCCCCCCCCCCCCCCCCCO 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 CC(=O)OCC(C1(CCC2C(=C1)CCC3C2(CC(=O)CC3(C)CO)C)C)O 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 CC(=C)C(CC=C(C)C=C)O 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 CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 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 CC(C)C12CC=C(C1C2)C=O 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)-1-Isopropenyl-4-methyl-3-cyclohexene-1beta-ol 16059268 Click to see CC1=CCC(CC1)(C(=C)C)O 152.23 unknown via CMAUP database
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)- 11469649 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 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 CC(=C)C1CCC(=C)C(C1)O 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Calamenene 11298625 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown via CMAUP database
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
beta-(Z)-Elemenone 22211636 Click to see CC(=C1CC(C(CC1=O)(C)C=C)C(=C)C)C 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
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene 10899740 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
(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 CC1CCC2C1C3C(C3(C)C)CCC2(C)O 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 CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
Palustrol (Ledum) 9794494 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 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 CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 7163172 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1080/10286020.2011.619183
beta-Sitosterol acetate 5354503 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1080/10286020.2011.619183
Olean-12-en-3beta-ol 225689 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
Stigmast-5-en-3-yl acetate 521199 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1080/10286020.2011.619183
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 222284 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 C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)COC3(C(C(C(O3)CO)O)O)CO)O)O)O)O 504.40 unknown via CMAUP database
Einecs 222-991-0 107452 Click to see C(C1C(C(C(O1)(CO)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O 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-methylene-1,7-octadien-3-one 93231 Click to see CC(=C)C(=O)CCC(=C)C=C 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 C1C=CCO1 70.09 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
cis-Isoascaridole 6430795 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-(4-Methyl-1,4-pentadienyl)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 CC1CCC2(C(C1=O)O2)C(C)C 168.23 unknown via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Allyl methyl disulfide 62434 Click to see CSSCC=C 120.20 unknown via CMAUP database
Allyl methyl sulfide 66282 Click to see CSCC=C 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
Allyl methyl trisulfide 61926 Click to see CSSSCC=C 152.30 unknown via CMAUP database
Methyl trans-1-propenyl trisulfide 5352690 Click to see CC=CSSSC 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 COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 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 CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C=C(O2)C3=C(C=C(C=C3)O)OC 468.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 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 C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O)O)O 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 C1=CC(=CC=C1C=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 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 C1=CC(=CC=C1C=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)O)CO)O)O)O 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 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 https://doi.org/10.1016/J.BMCL.2012.10.043
Kaempferol 3,4'-diglucoside 14730437 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)OC5C(C(C(C(O5)CO)O)O)O 610.50 unknown https://doi.org/10.1016/J.BMCL.2012.10.043
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.BMCL.2012.10.043
Quercetin 3-(6''-p-hydroxybenzoylgalactoside) 91666354 Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 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
[(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 COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=C(C4=O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)O)O)CO)O)O)O 786.70 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-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 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)O)CO)O)O)O 756.70 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] 3-(4-hydroxyphenyl)prop-2-enoate 162965960 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
7-(beta-D-Glucopyranosyloxy)-2-[4-(beta-D-glucopyranosyloxy)phenyl]-5-hydroxy-3-[[2-O-[(2E)-3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propen-1-yl]-beta-D-glucopyranosyl]oxy]-4H-1-benzopyran-4-one 21626414 Click to see COC1=C(C=CC(=C1)C=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 948.80 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 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 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 COC1=C(C=CC(=C1)C=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)O)CO)O)O)O 786.70 unknown https://doi.org/10.1016/J.BMCL.2012.10.043
Allivictoside H 71459649 Click to see COC1=C(C=CC(=C1)C=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)O)CO)O)O)O 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 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)OC6C(C(C(C(O6)CO)O)O)O 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 COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O 374.30 unknown via CMAUP database
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown via CMAUP database

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