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Allium ursinum

Allium ursinum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Allium ursinum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Allium ursinum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644024d5231de832060730
Scientific name Allium ursinum
Authority L.
First published in Sp. Pl. : 300 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Cepa ursina (L.) Bernh. Syst. Verz. Erf. : 201 (1800)
Hylogeton ursinum (L.) Salisb. Gen. Pl. : 91 (1866)
Moly latifolium (Gilib.) Gray Nat. Arr. Brit. Pl. 2: 180 (1821 publ. 1822)
Ophioscorodon ursinus (L.) Wallr. Sched. Crit. : 130 (1822)
Aglitheis ursina (L.) Raf. Fl. Tellur. 2: 18 (1837)
Allium latifolium Gilib. Exerc. Phyt. 2: 470 (1792)
Allium longipetiolatum St.-Lag. Ann. Soc. Bot. Lyon 7: 119 (1880)
Allium nemorale Salisb. Prodr. Stirp. Chap. Allerton : 235 (1796)
Allium petiolatum Lam. Fl. Franç. 3: 261 (1779)
Allium ucrainicum (Oksner & Kleopow) Bordz. Fl. RSS Ucr. 3: 143 (1950)
Allium ursinoides G.Don ex Sweet Hort. Brit. : 422 (1826)
Allium ursinum subsp. ucrainicum Oksner & Kleopow Sched. Herb. Fl. Ucr. 1(10): 37. 1935 (1935)
Allium ursinum var. ucrainicum (Oksner & Kleopow) Soó Magyar Fl. Veg. 6: 185 (1980)
Allium vincetoxicum Pall. ex Ledeb. Fl. Ross. 4: 186 (1852)
Geboscon ursinum (L.) Raf. Autik. Bot. : 59 (1840)
Nectaroscordum ursinum (L.) Banfi & Galasso Atti Soc. Ital. Sci. Nat. Mus. Civico Storia Nat. Milano 152(2): 88. 2011 [Nov 2011]

Common names Top

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Language Common/alternative name
English ramsons
English wild garlic
English broad-leaved garlic
English buckrams
English ramsons garlic
English ransoms
Spanish ajo de los osos
Spanish ajo de osos
Afrikaans wildeknoffel
ang hramsa
ang hramsa/gw
Arabic ثوم الدببة
Azerbaijani ayısoğanı
ba Айыу йыуаһы
ba Йыуа
Belarusian Цыбуля мядзведжая
Bulgarian Левурда
Bulgarian Див лук
Bulgarian Див чесън
Bulgarian Мечи лук
Bulgarian левурда
Bengali বুনো রসুন
br kignen-an-arzhed
Bosnian medvjeđi luk
bxr Халяар
Catalan all de bruixa
Catalan ramsons
ce Хьонка
ce хьонка
Czech česnek medvědí
Czech lesní česnek
Czech medvědí česnek
Welsh craf y geifr
Welsh cra'r gerddi
Danish rams-løg
Danish ramsløg
German bär-lauch
German bärlauch
German bärenlauch
German hexenzwiebel
German knoblauchspinat
German latschenknofel
German ramsell
German ränsel
German waldknoblauch
German waldlauch
German wilder knoblauch
German wilder lauch
German zigeunerlauch
Greek άγριο σκόρδο
Esperanto ursa ajlo
Estonian karulauk
Basque hartz-baratxuri
Persian سیرخرس
Finnish karhunlaukka
French ail des ours
French ail aux ours
French ail des bois
French ail sauvage
frr baarlook
fy blêdlok
Irish creamh
Swiss German bärlauch
Hebrew שום פרא
Hebrew שום בר
Hindi जंगली लहसुन
Croatian medvjeđi luk
Upper Sorbian pyšny kobołk
Hungarian medvehagyma
Armenian ղանձիլ
Icelandic bjarnarlaukur
Italian aglio orsino
Italian erba orsina
Japanese ラムソン
Georgian ღანძილი
Kazakh Ұсақ торлы жуа
Korean 램슨
ku lûş
Cornish koos kennin
lb heckeknuewelek
lb bärlauch
lb wëlle knuewelek
li daslook
Lithuanian meškinis česnakas
Latvian laksis
Latvian mežloks
Macedonian Мечкин лук
Malayalam അല്ലിയം ഉർസിനം
myv Паксячурька
mzn الرزه
mzn اَلِرزی
mzn الزی
mzn اَلِزی
mzn الرزی
Norwegian Bokmål ramsløk
Norwegian Bokmål ramslauk
Dutch daslook
Dutch wilde knoflook
Norwegian Nynorsk ramslauk
Norwegian Nynorsk bjørnelauk
Norwegian Nynorsk bjørneløk
Norwegian Nynorsk ramsløk
Oriya ଜଂଗଲୀ ରସୁଣ
os Давон
os Дабонæ
os Давæттæ
os Скъуда
Punjabi ਜੰਗਲੀ ਲਸਣ
pcd ail des orses
Polish czosnek niedźwiedzi
Portuguese alho de urso
Portuguese alho dos ursos
Portuguese alho-dos-ursos
Romanian leurdă
Russian Черемша
Russian дикий чеснок
Russian калба
Russian колба
Russian лук медвежий
Russian медвежий лук
Russian черемша
Slovak cesnak medvedí
Slovenian Čemaž
Albanian lerthi
Albanian hurdha e egër
Serbian Сремуш
Serbian allii ursini bulbus recens
Serbian allii ursini herba recens
Serbian Дивљи лук
Serbian Медвеђи лук
Serbian Цремош
Serbian сремуш
Swedish ramslök
Tamil காட்டுப் பூண்டு
Turkish yabanî sarımsak
Turkish ayı sarımsağı
tyv Хылба
Ukrainian Цибуля ведмежа
Ukrainian Ведмежа цибуля
Ukrainian Левурда
Ukrainian Черемша
Urdu لہسن دُب
Urdu bear's garlic
Urdu buckrams
Urdu ramsons
Urdu wood garlic
Urdu ثوم دب
Urdu لہسن دب
vec ajo selvadego
Vietnamese tỏi gấu
Walloon a des oûsses
Walloon såvadje a
Walloon a des tchamps
Chinese 熊葱
Chinese 熊蔥
Chinese 熊蒜
Chinese 野葱
Chinese 野蔥
Chinese 野韭菜

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 at 4°C for 3 weeks, then increase to 20°C.
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
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • North European Russia
      • Northwest European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Sicilia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000757676
UNII 2V5E7HGO8G
USDA Plants ALUR
Tropicos 18400122
INPN 81541
Flora of Italy 6901
KEW urn:lsid:ipni.org:names:529088-1
The Plant List kew-296893
Plantarium 2237
Missouri Botanical Garden 281739
PFAF Allium ursinum
Open Tree Of Life 748364
Observations.org 6355
NCBI Taxonomy 4684
NBN Atlas NBNSYS0000002205
IPNI 529088-1
iNaturalist 56152
GBIF 2857601
Freebase /m/02f63f
EPPO ALLUR
EOL 1085089
Elurikkus 2664
USDA GRIN 2413
Wikipedia Allium_ursinum
CMAUP NPO18707

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
Molecular mechanisms and regulation of recombination frequency and distribution in plants Zou M, Shabala S, Zhao C, Zhou M Theor Appl Genet 21-Mar-2024
PMCID:PMC10957645
doi:10.1007/s00122-024-04590-4
PMID:38512498
Metabolism of Phenolic Compounds and Antioxidant Activity in Different Tissue Parts of Post-Harvest Chive (Allium schoenoprasum L.) Dai X, Jia C, Lu J, Yu Z Antioxidants (Basel) 25-Feb-2024
PMCID:PMC10967344
doi:10.3390/antiox13030279
PMID:38539813
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Inhibition of CYP1A1 Alleviates Colchicine-Induced Hepatotoxicity Huang R, Duan J, Huang W, Cheng Y, Zhu B, Li F Toxins (Basel) 09-Jan-2024
PMCID:PMC10818746
doi:10.3390/toxins16010035
PMID:38251251
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A Plants (Basel) 22-Dec-2023
PMCID:PMC10780445
doi:10.3390/plants13010043
PMID:38202351
Wild Garlic (Allium ursinum) Preparations in the Design of Novel Functional Pasta Filipčev B, Kojić J, Miljanić J, Šimurina O, Stupar A, Škrobot D, Travičić V, Pojić M Foods 05-Dec-2023
PMCID:PMC10742902
doi:10.3390/foods12244376
PMID:38137181
Comparison of Antioxidant and Antiproliferative Effects of Various Forms of Garlic and Ramsons Furdak P, Pieńkowska N, Kapusta I, Bartosz G, Sadowska-Bartosz I Molecules 08-Sep-2023
PMCID:PMC10538172
doi:10.3390/molecules28186512
PMID:37764288
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Asynapsis and meiotic restitution in tomato male meiosis induced by heat stress Schindfessel C, De Storme N, Trinh HK, Geelen D Front Plant Sci 13-Jul-2023
PMCID:PMC10373595
doi:10.3389/fpls.2023.1210092
PMID:37521921
Multidirectional Effects of Red Clover (Trifolium pratense L.) in Support of Menopause Therapy Gościniak A, Szulc P, Zielewicz W, Walkowiak J, Cielecka-Piontek J Molecules 03-Jul-2023
PMCID:PMC10343205
doi:10.3390/molecules28135178
PMID:37446841
Determinants of interspecific variation in season length of perennial herbs Koubek T, Mašková T, Herben T Ann Bot 03-Jul-2023
PMCID:PMC10583191
doi:10.1093/aob/mcad088
PMID:37398990
Chenopodium murale Juice Shows Anti-Fungal Efficacy in Experimental Oral Candidiasis in Immunosuppressed Rats in Relation to Its Chemical Profile El-Newary SA, Abd Elkarim AS, Abdelwahed NA, Omer EA, Elgamal AM, ELsayed WM Molecules 24-May-2023
PMCID:PMC10254659
doi:10.3390/molecules28114304
PMID:37298777
Phenolic Content, Amino Acids, Volatile Compounds, Antioxidant Capacity, and Their Relationship in Wild Garlic (A. ursinum L.) Kovačević TK, Major N, Sivec M, Horvat D, Krpan M, Hruškar M, Ban D, Išić N, Goreta Ban S Foods 24-May-2023
PMCID:PMC10252502
doi:10.3390/foods12112110
PMID:37297354
Techno-Functional Properties of Burgers Fortified by Wild Garlic Extract: A Reconsideration Kurćubić VS, Stajić SB, Miletić NM, Petković MM, Dmitrić MP, Đurović VM, Heinz V, Tomasevic IB Foods 23-May-2023
PMCID:PMC10252940
doi:10.3390/foods12112100
PMID:37297346
Opening up new niche dimensions: The stoichiometry of soil microarthropods in European beech and Norway spruce forests Warnke L, Hertel D, Scheu S, Maraun M Ecol Evol 22-May-2023
PMCID:PMC10202621
doi:10.1002/ece3.10122
PMID:37223311

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids
Arhimachalene 11458355 Click to see CC1CCCC(C2=C1C=CC(=C2)C)(C)C 202.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3',4'-Dimethoxyphenyl)prop-2-enyl isovalerate 6442914 Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C=C1)OC)OC 278.34 unknown via CMAUP database
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Cinnamyl isovalerate 5355855 Click to see CC(C)CC(=O)OCC=CC1=CC=CC=C1 218.29 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(7S,8R)-6-Methylidene-5-oxo-8-(3,4,5-trimethoxyphenyl)-7,8-dihydrobenzo[f][1,3]benzodioxole-7-carboxylic acid 11144085 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(=C)C(=O)C3=CC4=C(C=C23)OCO4)C(=O)O 412.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
3',4',5'-Trimethoxycinnamylisovalerate 6442915 Click to see CC(C)CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC)OC 308.40 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
Nootkatin 238797 Click to see CC(C)C1=CC(=O)C(=CC=C1CC=C(C)C)O 232.32 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
alpha-Duprezianene 101985700 Click to see CC1CCC2C13CCC(C2(C)C)C(=C3)C 204.35 unknown via CMAUP database
beta-Duprezianane 91750164 Click to see CC1CCC2C13CCC(C2(C)C)C(=C)C3 204.35 unknown via CMAUP database
Pseudowiddrene 15409431 Click to see CC1=CCC2(C(=CCCC2(C)C)CC1)C 204.35 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
(5R)-5,6,7,8-Tetrahydro-5beta-(3,4,5-trimethoxyphenyl)-7alpha-(hydroxymethyl)naphtho[2,3-d]-1,3-dioxole-6beta-carboxylic acid methyl ester 101618918 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(CC3=CC4=C(C=C23)OCO4)CO)C(=O)OC 430.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Podophyllinic acid 134632 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(C(C3=CC4=C(C=C23)OCO4)O)CO)C(=O)O 432.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Sesamin 382073 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2R,3S,4S)-2-(1,3-benzodioxol-5-yl)-4-(1,3-benzodioxol-5-ylmethyl)oxolan-3-yl]methanol 11653313 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)CC4=CC5=C(C=C4)OCO5 356.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one 11165431 Click to see COC1=CC(=CC(=C1OC)OC)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4 398.40 unknown via CMAUP database
(3S,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(R)-hydroxy-(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 173676 Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 416.40 unknown via CMAUP database
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown via CMAUP database
Podorhizol 9931715 Click to see COC1=CC(=CC(=C1OC)OC)C(C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O 416.40 unknown via CMAUP database
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown via CMAUP database
Yatein 442835 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
beta-Peltatin A methyl ether 159962 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O 428.40 unknown via CMAUP database
Deoxypicropodophyllotoxin 11711021 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
Epipicropodophyllotoxin acetate 14160031 Click to see CC(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 456.40 unknown via CMAUP database
Picropodophyllin 72435 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2E,4Z)-Deca-2,4-dienyl isovalerate 6436644 Click to see CCCCCC=CC=CCOC(=O)CC(C)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-15-Hydroxylabda-8(20),13-dien-19-oic acid methyl ester 14060410 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 334.50 unknown via CMAUP database
(1R,4abeta)-Decahydro-1beta-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8abeta-tetramethylnaphthalen-2alpha-ol 12306731 Click to see CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C 308.50 unknown via CMAUP database
(1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylic acid 97044524 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)OO)OO4)(C)C(=O)O 366.40 unknown via CMAUP database
15-Hydroperoxy-8alpha,12alpha-epidioxyabieta-13-ene-19-oic acid methyl ester 12149368 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)OO)OO4)(C)C(=O)OC 380.50 unknown via CMAUP database
15-Hydroxy-8alpha,12alpha-epidioxyabieta-13-ene-19-oic acid methyl ester 12149369 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)O)OO4)(C)C(=O)OC 364.50 unknown via CMAUP database
4-Epiabietic acid 6973653 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
4-Epicommunic acid 12303810 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Abietal 443479 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietyl alcohol 443474 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)CO 288.50 unknown via CMAUP database
Dehydroabietal 11694869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C 284.40 unknown via CMAUP database
Isopimaric acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown via CMAUP database
Isopimarinol 15586712 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimaric acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aS,8aS)-4a,8,8-trimethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene-2-carbaldehyde 12444332 Click to see CC1(CCCC2(C13CC3C(=CC2)C=O)C)C 218.33 unknown via CMAUP database
[S,(+)]-2-Methyl-6-p-tolylheptane 101694025 Click to see CC1=CC=C(C=C1)C(C)CCCC(C)C 204.35 unknown via CMAUP database
15,16-Dinor-13-oxolabda-8(17)-ene-19-oic acid methyl ester 11255232 Click to see CC(=O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 306.40 unknown via CMAUP database
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown via CMAUP database
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1R,2R,5S,7R)-2,6,6-Trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane 16213223 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-4-one 12308772 Click to see CC1CC(=O)C2C13CC=C(C(C3)C2(C)C)C 218.33 unknown via CMAUP database
(3R,8abeta)-3alpha,8,8-Trimethyl-6-methylenedecahydro-3aalpha,7alpha-methanoazulene-2-one 21576983 Click to see CC1C(=O)CC2C13CCC(=C)C(C3)C2(C)C 218.33 unknown via CMAUP database
(3R)-3alpha,6,8,8-Tetramethyl-2,3,4,7,8,8abeta-hexahydro-3aalpha,7alpha-methanoazulene-2(1H)-one 21576982 Click to see CC1C(=O)CC2C13CC=C(C(C3)C2(C)C)C 218.33 unknown via CMAUP database
(3R)-3beta,8,8-Trimethyl-6-methylene-3,3a,4,5,6,7,8,8abeta-octahydro-3aalpha,7alpha-methanoazulene-1(2H)-one 12308774 Click to see CC1CC(=O)C2C13CCC(=C)C(C3)C2(C)C 218.33 unknown via CMAUP database
[(1S,2R,5R,6S,7S)-2,6,8-trimethyl-6-tricyclo[5.3.1.01,5]undec-8-enyl]methanol 22211622 Click to see CC1CCC2C13CC=C(C(C3)C2(C)CO)C 220.35 unknown via CMAUP database
3beta-Hydroxycedrene 15215015 Click to see CC1C(CC2C13CC=C(C(C3)C2(C)C)C)O 220.35 unknown via CMAUP database
alpha-Cedrene 6431015 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown via CMAUP database
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown via CMAUP database
Cedrenone 13335685 Click to see CC1CCC2C13CC(C2(C)C)C(=CC3=O)C 218.33 unknown via CMAUP database
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
8-Acetoxyelemol 14138886 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown via CMAUP database
8-Hydroxyelemol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown via CMAUP database
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
3beta-Hydroxyisopimaric acid 102193489 Click to see CC1(CCC2C(=CCC3C2(CCC(C3(C)C(=O)O)O)C)C1)C=C 318.40 unknown via CMAUP database
3beta-Hydroxysandaracopimaric acid 101200911 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)C(=O)O)O)C)C=C 318.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-3-prop-2-enylsulfinylpropanoic acid 121922 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1002/HLCA.19480310140
Isoalliin 5281112 Click to see CC=CS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1021/NP0503350
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
S-Allyl-L-cysteine sulfoxide 15558642 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1055/S-2006-960118
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2R)-2-amino-3-ethylsulfinylpropanoic acid 146416 Click to see CCS(=O)CC(C(=O)O)N 165.21 unknown https://doi.org/10.1021/JF990938F
3-(Allylsulphinyl)-L-alanine 87310 Click to see C=CCS(=O)CC(C(=O)O)N 177.22 unknown https://doi.org/10.1055/S-2006-960118
https://doi.org/10.1021/NP0503350
> Organic acids and derivatives / Thiosulfinic acid esters
Allicin 65036 Click to see C=CCSS(=O)CC=C 162.30 unknown https://doi.org/10.1021/NP0503350
Methanesulfinothioic acid, S-1-propenyl ester 10129986 Click to see CC=CSS(=O)C 136.20 unknown https://doi.org/10.1021/NP0503350
S-1-Propenyl 2-propenesulfinothioate 10558949 Click to see CC=CSS(=O)CC=C 162.30 unknown https://doi.org/10.1021/NP0503350
S-2-Propenyl 1-propenesulfinothioate 58219317 Click to see CC=CS(=O)SCC=C 162.30 unknown https://doi.org/10.1021/NP0503350
S-Methyl 2-propene-1-sulfinothioate 5319504 Click to see CSS(=O)CC=C 136.20 unknown https://doi.org/10.1021/NP0503350
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,5R,7R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 101985389 Click to see CC1CCC2C13CCC(C3)(C(C2(C)C)O)C 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Widdrol 94334 Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(3R)-3alpha,7,7-Trimethyl-5-methylene-3a,4,5,6,7,7abeta-hexahydro-3aalpha,6alpha-ethano-1H-indene-2(3H)-one 21576981 Click to see CC1C(=O)CC2C13CCC(C2(C)C)C(=C)C3 218.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,2R,5R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-one 21576985 Click to see CC1CCC2C13CCC(C3)(C(=O)C2(C)C)C 220.35 unknown via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Diallyl disulfide 16590 Click to see C=CCSSCC=C 146.30 unknown https://doi.org/10.1016/0305-1978(95)00072-0
Methyl-allyl-thiosulfinat 54574849 Click to see COS(=S)CC=C 136.20 unknown https://doi.org/10.1055/S-2006-960118
> Organosulfur compounds / Organic disulfides
Dipropenyldisulfid 171311 Click to see CC=CSSC=CC 146.30 unknown https://doi.org/10.1016/0305-1978(95)00072-0
> Organosulfur compounds / Organic trisulfides
Diallyl trisulfide 16315 Click to see C=CCSSSCC=C 178.30 unknown https://doi.org/10.1021/NP0503350
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
1-(4-Hydroxy-3-methoxyphenyl)deca-1,4-dien-3-one 162986747 Click to see CCCCCC=CC(=O)C=CC1=CC(=C(C=C1)O)OC 274.35 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
https://doi.org/10.1016/0031-9422(95)00574-9
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,6,7-Trihydroxy-2-(2,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 71331302 Click to see C1=C(C(=CC(=C1O)O)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44575467 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(95)00574-9
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/10.1016/0031-9422(95)00574-9
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/10.1016/0031-9422(95)00574-9
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
Kaempferol-3-O-glucorhamnoside 13915496 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(95)00574-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5R,6R)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 10581973 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)OC(=O)C=CC7=CC=C(C=C7)O)C8=CC=C(C=C8)O)CO)O)O)O)O)O 1064.90 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[(2S,3R,4S,5R,6S)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 162935421 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)OC(=O)C=CC7=CC=C(C=C7)O)C8=CC=C(C=C8)O)CO)O)O)O)O)O 1064.90 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[(2S,3R,4S,5S,6R)-2-[3-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162943672 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C7=CC=C(C=C7)O)CO)O)O)O)O)O 932.80 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[(2S,3R,4S,5S,6R)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 10772167 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C7=CC=C(C=C7)O)CO)O)O)O)O)O 932.80 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[(2S,3R,4S,5S,6R)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 10533752 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC=C(C=C6)O)C7=CC=C(C=C7)O)CO)O)O)O)O)O 902.80 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[(2S,3R,4S,5S,6R)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101688813 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C7=CC=C(C=C7)O)CO)O)O)O)O)O 932.80 unknown https://doi.org/10.1016/S0031-9422(96)00663-2
[(2S,3R,4S,5S,6S)-2-[3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 162996159 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC=C(C=C6)O)C7=CC=C(C=C7)O)CO)O)O)O)O)O 902.80 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[2-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74978053 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)OC(=O)C=CC6=CC=C(C=C6)O)C7=CC=C(C=C7)O)CO)O)O)O)O)O 902.80 unknown https://doi.org/10.1016/0031-9422(95)00574-9
[2-[3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74978056 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)OC6C(C(C(C(O6)CO)O)O)O)OC(=O)C=CC7=CC=C(C=C7)O)C8=CC=C(C=C8)O)CO)O)O)O)O)O 1064.90 unknown https://doi.org/10.1016/0031-9422(95)00574-9
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163188096 Click to see CC1C(C(C(C(O1)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)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(95)00574-9
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14583594 Click to see CC1C(C(C(C(O1)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)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(95)00574-9

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