Scientific name	Authority	First published in
Pastinaca sphondylium	Calest.	Webbia 1: 244 (1905)
Sphondylium branca	Scop.	Fl. Carniol. , ed. 2, 1: 204 (1771)
Sphondylium vulgare	Gray	Nat. Arr. Brit. Pl. 2: 520 (1821 publ. 1822)
Sphondylium conforme	Moench	Methodus : 83 (1794)
Sphondylium longifolium	Hoffm.	Gen. Pl. Umbell. : 134 (1814)
Sphondylium panaces	Gaertn.	Fruct. Sem. Pl. 1: 86 (1788)
Sphondylium proteiforme	Bubani	Fl. Pyren. 2: 394 (1899)
Selinum sphondylium	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 136 (1904)
Heracleum angustifolium	Jacq.	Enum. Stirp. Vindob. : 45 (1762)
Heracleum angustifolium	M.Bieb.	Fl. Taur.-Caucas. 1: 222 (1808)
Heracleum armoricum	Boreau ex Nyman	Consp. Fl. Eur. : 290 (1879)
Heracleum australe	Hartm.	Sv. Norsk Exc.-Fl. : 39 (1846)
Heracleum chloranthum	Borbás	Fl. Comit. Temesiensis : 57 (1884)
Heracleum elegans	(Crantz) Jacq.	Fl. Austriac. 2: t. 175 (1774)
Heracleum laciniatum	Desf.	Tabl. École Bot. 119. 1804
Heracleum longifolium	Jacq.	Fl. Austriac. 2: 46 (1774)
Heracleum micranthum	Borbás	Magyar Orv. Termész. Nagy Gyül. Tört. Vázl. Munk. 23: 236 (1887)
Heracleum moritzianum	Thell.	Oesterr. Bot. Z. 73: 209 (1924)
Heracleum occidentale	Boreau	Fl. Centre France , ed. 3, 2: 287 (1857)
Heracleum palmatilobum	DC.	Prodr. 4: 192 (1830)
Heracleum panaces	L.	Sp. Pl. : 249 (1753)
Heracleum paniculatum	Lavy	État Général Vég. Orig. : 10 (1830)
Heracleum trachycarpum	Soják	Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1963: 44 (1963)
Heracleum sphondylium var. angustifolium	(Jacq.) C.C.Gmel.	Fl. Bad. 1: 659 (1805)
Heracleum sphondylium var. stenophyllum	Gaudin	Fl. Helv. 2: 318 (1828)

Common names Top

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Filter by language:

Language	Common/alternative name
English	eltrot
English	hogweed
English	common hogweed
English	cow parsnip
Spanish	talaprados
Spanish	zebuoda
Spanish	hierba de hércules
Spanish	hierba de hercules
Spanish	cornases
Spanish	copa garbancera
Spanish	cancuera
Spanish	branca-ursina espuria
Spanish	belleraca
Arabic	هرقلية سفندوليونية
Arabic	اقنثة كاذبة
Arabic	سفندليون
Arabic	هرقلية نافعة
Azerbaijani	adi baldırğan
azb	عادی بالدیرغان
Belarusian	Баршчэўнік звычайны
Bulgarian	сибирски девесил
Catalan	bellerenca
Czech	bolševník obecný
cv	Ахаль пултран
Welsh	efwr
Danish	almindelig bjørneklo
German	gemeiner bärenklau
German	gewöhnliche bärenklau
German	wiesenbärenklau
German	wiesen-bärenklau
Esperanto	ordinara herakleo
Estonian	euroopa karuputk
Basque	urdanaza
Persian	هویج وحشی گاوی
Finnish	euroopanukonputki
Finnish	ukonputki
Finnish	etelänukonputki
French	berce commune - patte dours
French	grande berce
French	berce sphondyle
French	berce commune
Irish	feabhrán
gd	odharan
Croatian	medvjeđi dlan
Hungarian	közönséges medvetalp
Icelandic	hrossahvönn
Italian	panace
Italian	spondilio
Japanese	ホグウィード
Japanese	ハナウド
Japanese	ハナウド属
Lithuanian	lankinis barštis
Macedonian	мечкина шепа
Macedonian	обичен свински коров
Norwegian Bokmål	kystbjørnekjeks
Dutch	gewone berenklauw
Dutch	gewone bereklauw
Norwegian Nynorsk	bjønnkjeks
Norwegian Nynorsk	bjørnekjeks
pcd	bibreulh
pcd	avérdhiés
pcd	beurèies
pcd	grant-bibeu
pcd	churs
pcd	chus
pcd	cornaÿe
pcd	cornue
pcd	crachou
pcd	cralàr
pcd	férnéle
pcd	patroulhe
pcd	pénache
pcd	rafourèis
pcd	tàrte-às-lapins
pcd	chwéles
Polish	barszcz zwyczajny
Russian	Борщевик обыкновенный
Slovak	boľševník borščový
Slovenian	navadni dežen
Serbian	Медвеђа шапа
Swedish	björnloka
Swedish	vit björnloka
Swedish	sibirisk björnloka
Swedish	jätte björnloka
Swedish	jätte björn loka
Swedish	björnfloka
Swedish	björn loka
tt	гади балтырган
Walloon	paxhnåde

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Heracleum sphondylium subsp. algeriense	(Coss. ex Batt. & Trab.) Dobignard	Index Syn. Fl. Afrique N. 2: 100 (2011)
Heracleum sphondylium subsp. alpinum	(L.) Bonnier & Layens	Tabl. Syn. Pl. Vasc. France 128. 1894 (1894)
Heracleum sphondylium subsp. artvinense	(Manden.) P.H.Davis	Fl. Turkey 4: 491 (1972)
Heracleum sphondylium subsp. aurasiacum	(Maire) Dobignard	Index Syn. Fl. Afrique N. 2: 100 (2011)
Heracleum sphondylium subsp. carpaticum	(Porcius) Soó	Acta Bot. Acad. Sci. Hung. 23: 380 (1977 publ. 1978)
Heracleum sphondylium subsp. cyclocarpum	(K.Koch) P.H.Davis	Fl. Turkey 4: 491 (1972)
Heracleum sphondylium subsp. embergeri	Maire	Bull. Soc. Hist. Nat. Afrique N. 25: 359. 1937 (1937)
Heracleum sphondylium subsp. flavescens	(Willd.) Soó	Acta Bot. Acad. Sci. Hung. 18: 175 (1973)
Heracleum sphondylium subsp. granatense	(Boiss.) Masclans	Collect. Bot. (Barcelona) 8: 77. 1972
Heracleum sphondylium subsp. montanum	(Schleich. ex Gaudin) Briq.	Fl. Schweiz , ed. 2, 1: 372 (1905)
Heracleum sphondylium subsp. orsinii	(Guss.) H.Neumayer	Verh. Zool.-Bot. Ges. Wien 72: 169. 1923 (1923)
Heracleum sphondylium subsp. pyrenaicum	(Lam.) Bonnier & Layens	Tabl. Syn. Pl. Vasc. France 128. 1894 (1894)
Heracleum sphondylium subsp. sibiricum	(L.) Simonk.	Enum. Fl. Transsilv. 266 1887
Heracleum sphondylium subsp. suaveolens	(Litard. & Maire) Dobignard	Index Syn. Fl. Afrique N. 2: 100 (2011)
Heracleum sphondylium subsp. ternatum	(Velen.) Brummitt	Feddes Repert. 79: 65. 1968 (1968)
Heracleum sphondylium subsp. transsilvanicum	(Schur) Brummitt	Feddes Repert. 79: 65. 1968 (1968)
Heracleum sphondylium subsp. trifoliolatum	(Blanch.) Kerguélen	Coll. Patrim. Nat. 8: xiii (1993)
Heracleum sphondylium subsp. verticillatum	(Pančić) Brummitt	Feddes Repert. 79: 65. 1968 (1968)

Varieties (abbr. var.) Top

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Name	Authority	First published in
Heracleum sphondylium var. fontqueri	O.Bolòs & Vigo	Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 83 (1974)
Heracleum sphondylium var. rarum	(Gawlowska) Soó	Acta Bot. Acad. Sci. Hung. 16: 371 (1970 publ. 1971)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Name	Authority	First published in
Heracleum sphondylium f. atropurpureum	(F.Malý) Nikolic	Fl. SR Srbije 5: 302 (1973)
Heracleum sphondylium f. dissectum	H.Ohba	J. Jap. Bot. 69: 119 (1994)
Heracleum sphondylium f. rubriflorum	H.Ohba	J. Jap. Bot. 69: 119 (1994)

Germination/Propagation Top

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco

Asia-temperate click to expand
- China
  - Tibet
- Siberia
  - Buryatiya
- Western Asia
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - East 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
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- Eastern Canada
  - Newfoundland
- Northeastern U.S.A.
  - New York
  - Vermont

Southern America click to expand
- Caribbean
  - Haiti

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000720220
UNII	59145H149J
Canadensys	2585
USDA Plants	HESP6
Tropicos	1700138
INPN	101300
Flora of Italy	3642
KEW	urn:lsid:ipni.org:names:843179-1
The Plant List	kew-2846164
Open Tree Of Life	903088
Observations.org	6855
NCBI Taxonomy	40919
NBN Atlas	NBNSYS0000003710
Nature Serve	2.135608
IPNI	843179-1
iNaturalist	163682
GBIF	3034830
Freebase	/m/09nxhs
EPPO	HERSP
EOL	581673
Elurikkus	5054
USDA GRIN	70346
Wikipedia	Heracleum_sphondylium
CMAUP	NPO23289

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

Vasorelaxant and Blood Pressure-Lowering Effects of Cnidium monnieri Fruit Ethanol Extract in Sprague Dawley and Spontaneously Hypertensive Rats

Park J, Shin S, Bu Y, Choi HY, Lee K

Int J Mol Sci

11-Apr-2024

PMCID:	PMC11050430
doi:	10.3390/ijms25084223
PMID:	38673809

Wild Edible Plants Used in Dalmatian Zagora (Croatia)

Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł

Plants (Basel)

11-Apr-2024

PMCID:	PMC11053949
doi:	10.3390/plants13081079
PMID:	38674488

Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential

Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR

Pharmaceutics

25-Mar-2024

PMCID:	PMC11054966
doi:	10.3390/pharmaceutics16040454
PMID:	38675115

Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour

Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J

Ecol Evol

07-Mar-2024

PMCID:	PMC10918743
doi:	10.1002/ece3.11061
PMID:	38455145

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

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

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

Hoverflies of the Timon-David collection (Diptera, Syrphidae)

Nève G, Lair X, Lebard T, Meunier JY, Teste LJ, Séguinel L

Biodivers Data J

19-Feb-2024

PMCID:	PMC10946086
doi:	10.3897/BDJ.12.e117265
PMID:	38501073

Effects of mowing on body size patterns in spider assemblages of mesic meadows

Stański T, Stańska M, Hajdamowicz I, Nicewicz Ł, Hiller A

Ecol Evol

15-Feb-2024

PMCID:	PMC10869948
doi:	10.1002/ece3.10892
PMID:	38371868

Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines

Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW

J Fungi (Basel)

26-Jan-2024

PMCID:	PMC10890244
doi:	10.3390/jof10020105
PMID:	38392777

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

Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization

Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G

Plants (Basel)

26-Dec-2023

PMCID:	PMC10780482
doi:	10.3390/plants13010077
PMID:	38202385

Do Poisonous Plants in Pastures Communicate Their Toxicity? Meta-Study and Evaluation of Poisoning Cases in Central Europe

Aboling S

Animals (Basel)

08-Dec-2023

PMCID:	PMC10740430
doi:	10.3390/ani13243795
PMID:	38136831

LandS: Vegetation modeling based on Ellenberg's ecological indicator values

Rumohr Q, Grimm V, Lennartz G, Schäffer A, Toschki A, Roß-Nickoll M, Hudjetz S

MethodsX

13-Nov-2023

PMCID:	PMC10709510
doi:	10.1016/j.mex.2023.102486
PMID:	38076710

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Natural Products as Mite Control Agents in Animals: A Review

Liao F, Han C, Deng Q, Zhou Z, Bao T, Zhong M, Tao G, Li R, Han B, Qiao Y, Hu Y

Molecules

27-Sep-2023

PMCID:	PMC10574536
doi:	10.3390/molecules28196818
PMID:	37836661

Mediterranean Plants as Potential Source of Biopesticides: An Overview of Current Research and Future Trends

Fragkouli R, Antonopoulou M, Asimakis E, Spyrou A, Kosma C, Zotos A, Tsiamis G, Patakas A, Triantafyllidis V

Metabolites

22-Aug-2023

PMCID:	PMC10535963
doi:	10.3390/metabo13090967
PMID:	37755247

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 / Phenanthrenes and derivatives
Regeol A	10694409	Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC5=C(C(=C(C=C54)O)O)C)C)C)C)(C(C1=O)O)C	440.60	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Isolariciresinol	1023563	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	via CMAUP database
(+)-8-Methoxyisolariciresinol	10249800	Click to see COC1=C(C(=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)OC)O	390.40	unknown	via CMAUP database
(+)-Lyoniresinol	11711453	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO	420.50	unknown	via CMAUP database
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
3-(4-{[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy}-3-methoxyphenyl)propyl b-D-glucopyranoside	21672401	Click to see COC1=C(C=CC(=C1)CCCOC2C(C(C(C(O2)CO)O)O)O)OC(CO)C(C3=CC(=C(C=C3)O)OC)O	540.60	unknown	via CMAUP database
Episyringaresinol 4'-O-beta-D-glncopyranoside	45482321	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC	580.60	unknown	via CMAUP database
Foliachinenoside C	101857083	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)CO)CO	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-(3-methylbut-3-enoxy)-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	53494099	Click to see CC(=C)CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O	380.39	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-(3-methylbutoxy)-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	53494100	Click to see CC(C)CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O	382.40	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(5R)-5-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	101843551	Click to see CC1=C(C(C(CC1)O)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	506.60	unknown	via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2R)-4-[(1S,2S,4R)-2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl]but-3-en-2-yl]oxyoxane-3,4,5-triol	53494103	Click to see CC(C=CC12C(CC(O1)CC2(C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O	388.50	unknown	via CMAUP database
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2R)-4-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxyoxane-3,4,5-triol	101843547	Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O	506.60	unknown	via CMAUP database
(4R)-3-(hydroxymethyl)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	11303786	Click to see CC(CCC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	via CMAUP database
(4R)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	101450243	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C	504.60	unknown	via CMAUP database
(4R)-4-[(3R)-3-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	101450244	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O)(C)C	504.60	unknown	via CMAUP database
(5R)-5-[8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctyl]oxolan-2-one	53493975	Click to see C1CC(=O)OC1CCCCCCCCOC2C(C(C(C(O2)CO)O)O)O	376.40	unknown	via CMAUP database
(Z)-3-Hexenylvicianoside	11560275	Click to see CCC=CCCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O	394.40	unknown	via CMAUP database
3-Methyl-2-buten-1-yl 6-O-I+/--L-arabinopyranosyl-I(2)-D-glucopyranoside	101695746	Click to see CC(=CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C	380.39	unknown	via CMAUP database
Foliasalacioside C	101450245	Click to see CC1=C(C(C(=O)CC1)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	504.60	unknown	via CMAUP database
Foliasalacioside D	101450246	Click to see CC1=C(C(CCC1=O)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O	504.60	unknown	via CMAUP database
Foliasalacioside E2	101843546	Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	506.60	unknown	via CMAUP database
Myrsinionoside D	10384912	Click to see CC1CC(CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O	376.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Octyl Acetate	8164	Click to see CCCCCCCCOC(=O)C	172.26	unknown	https://doi.org/10.1080/14786419.2014.904311
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(2S)-3-hydroxy-2-octadeca-9,12,15-trienoyloxypropyl] octadeca-9,12,15-trienoate	90769662	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCC=CCC=CCC=CCC	612.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-octadeca-9,12,15-trienoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadeca-9,12,15-trienoate	91551905	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	775.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(21R)-Hopa-22(29)-ene-3beta,30-diol	102032092	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5C4(CCC5C(=C)CO)C)C)C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-abscisic acid beta-D-glucopyranosyl ester	46173811	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)C)O)(C)C	426.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2R,4S,5R,6S,7S,9R,12R)-12-acetyloxy-6-(acetyloxymethyl)-7-benzoyloxy-5-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-4-yl] benzoate	11061019	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)O)OC(=O)C5=CC=CC=C5	594.60	unknown	via CMAUP database
Celahin C	10007243	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)O)OC(=O)C	532.60	unknown	via CMAUP database
Salasol A	11092680	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)O	532.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1R,3S,4S)-3,4-dihydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	53494102	Click to see CC(C=CC1(C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O)O	406.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R)-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-3-en-1-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	101843548	Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C)CCC(C)O	506.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1S,4R,5R)-4-[(E,3R)-3,4-dihydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	53494101	Click to see CC1CC(CC(C1C=CC(CO)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O	390.50	unknown	via CMAUP database
Euodionoside G	101450242	Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O	388.50	unknown	via CMAUP database
Foliasalacioside E1	101843545	Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C)CCC(C)O	506.60	unknown	via CMAUP database
Foliasalacioside H	101843550	Click to see CC1CC(CC(C1CCC(C)O)(C)C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	508.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-[(2R)-1-hydroxypropan-2-yl]-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one	101863234	Click to see CC(CO)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	442.70	unknown	via CMAUP database
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-[(2S)-1-hydroxypropan-2-yl]-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one	101863236	Click to see CC(CO)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	442.70	unknown	via CMAUP database
(2R)-2-[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]propanoic acid	101863235	Click to see CC(C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)C(=O)O	456.70	unknown	via CMAUP database
(2S)-2-[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]propanal	91587731	Click to see CC(C=O)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	440.70	unknown	via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,15S,17S)-17-[(5S)-5,6-dimethylhepta-1,6-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,15-diol	101863232	Click to see CC(CCC(=C)C1CC(C2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C(=C)C	456.70	unknown	via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2R,5S)-2-hydroxy-5,6-dimethylhept-6-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	101863231	Click to see CC(CCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C(=C)C	458.80	unknown	via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2S,5S)-2-hydroxy-5,6-dimethylhept-6-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	101863230	Click to see CC(CCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C(=C)C	458.80	unknown	via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	101863233	Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O	458.80	unknown	via CMAUP database
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one	38359273	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	via CMAUP database
(4R,4aR,6R,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-6-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-4H-picene-1,3-dione	101286914	Click to see CC1C(=O)CC(=O)C2C1(CC(C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)O)C	456.70	unknown	via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-4,6a,6b,8a,11,11,14a-heptamethyl-1,3-dioxo-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-4H-picene-4a-carbaldehyde	22217114	Click to see CC1C(=O)CC(=O)C2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C=O	454.70	unknown	via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,10R,11S,12aR,14aS,14bS)-10-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	14466315	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)CO)C)C)C)C)C	458.70	unknown	via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,11S,12aR,14aS,14bS)-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	14108942	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C	442.70	unknown	via CMAUP database
(4R,4aS,6R,6aS,6aS,6bR,8aS,10R,12aR,14aS,14bS)-6,10-dihydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	50924227	Click to see CC1C(=O)CCC2C1(CC(C3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)C)C)O)C	458.70	unknown	via CMAUP database
(4R,4aS,6R,6aS,6aS,6bR,8aS,11R,12aR,14aS,14bS)-6-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	50924380	Click to see CC1C(=O)CCC2C1(CC(C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)O)C	458.70	unknown	via CMAUP database
15alpha-Hydroxyfriedelan-3-one	15038301	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)C)C)O)C)C)C)C	442.70	unknown	via CMAUP database
29-Hydroxyfriedelan-3-one	14108943	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C	442.70	unknown	via CMAUP database
30-Hydroxylup-20(29)-en-3-one	15038289	Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C	440.70	unknown	via CMAUP database
3beta,22beta-Dihydroxyolean-12-en-29-oic acid	21603566	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)O)C)C)C)C	472.70	unknown	via CMAUP database
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	via CMAUP database
beta-Amyrone	12306160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Betulone	10411004	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)CO	440.70	unknown	via CMAUP database
Demethylregelin	44559663	Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C)O)C(=O)O	470.70	unknown	via CMAUP database
Epifriedelin	15559350	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Erythrodiol	101761	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C	442.70	unknown	via CMAUP database
Foliasalacin C	101863237	Click to see CC1(CCC2(CC(C3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)C)C	442.70	unknown	via CMAUP database
Fridel-1-en-3-one	11384730	Click to see CC1C(=O)C=CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	424.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Hennadiol	489919	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C	442.70	unknown	via CMAUP database
Lupan-3beta,20-diol	10003607	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C	444.70	unknown	via CMAUP database
Maytenonic acid	169521	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C	456.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
Orthosphenic acid	20056194	Click to see CC1C23CCC4C(C2CC(C1(OC3)O)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C	488.70	unknown	via CMAUP database
Salasone A	21589703	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(=O)CC5(C4CC(CC5)(C)C)C)CO)C)C)C	456.70	unknown	via CMAUP database
Salasone B	21589704	Click to see CC1C(=O)CCC2C1(CC(C3C2(CCC4(C3(C(=O)CC5(C4CC(CC5)(C)C)C)C)C)C)O)C	456.70	unknown	via CMAUP database
Salasone C	21589705	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)CO)C)O)C)C)C)C	458.70	unknown	via CMAUP database
Salasone D	12068725	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)C)C)O)CO)C)C)C	458.70	unknown	via CMAUP database
Salasone E	12068726	Click to see CC1C(=O)CCC2C1(CC(C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)CO)C)C)O)C	458.70	unknown	via CMAUP database
Salaspermic Acid	44593364	Click to see CC1C23CCC4C(C2CCC1(OC3)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C	472.70	unknown	via CMAUP database
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
Tripterygic Acid A	21672627	Click to see CC1C(CC(C2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)O)C(=O)O	472.70	unknown	via CMAUP database
Triptotriterpenic acid A	21594203	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)O)C)C)C)C	472.70	unknown	via CMAUP database
Ursolic Acid	64945	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
Uvaol	92802	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	via CMAUP database
Wilfolic acid C	44559659	Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C)O	472.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
29-Nor-20-oxolupeol	490365	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	428.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
(2R,4S,4aR,6aS,6aS,14aS,14bS)-4,10,11-trihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,8,13,14,14b-octahydropicene-3,6-dione	11733114	Click to see CC1CC2C3(CCC4(C(=CCC5=C(C(=C(C=C54)O)O)C)C3(C(=O)CC2(C(C1=O)O)C)C)C)C	452.60	unknown	via CMAUP database
(6aS,6bS,8aR,9S,11R,12aS,14aS)-3,9-dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-9,11,12,12a,13,14-hexahydro-8H-picene-2,7,10-trione	11091624	Click to see CC1CC2C3(CCC4(C(=CC=C5C4=CC(=O)C(=C5C)O)C3(C(=O)CC2(C(C1=O)O)C)C)C)C	450.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(3R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3-acetyl-5a,5b,8,8,11a,13b-hexamethyl-2,3,3a,4,5,6,7,7a,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-9-one	52914560	Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C	426.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Tingenin B	73147	Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C	436.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl vicianoside	101714791	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O	416.40	unknown	via CMAUP database
Benzyl beta-d-glucopyranoside	188977	Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O	270.28	unknown	via CMAUP database
Benzyl beta-primeveroside	131248	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	via CMAUP database
Benzyl vicianoside	71511240	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(2,4,6-trimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol	23259943	Click to see COC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC	346.33	unknown	via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	9799599	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-(2-hydroxyethyl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10959332	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CCO	360.36	unknown	via CMAUP database
(E)-3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid	5280550	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CC(=O)O	386.30	unknown	via CMAUP database
2-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]benzoic acid benzyl ester	101857077	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O	552.50	unknown	via CMAUP database
2-Butanone, 4-(3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl)-	181027	Click to see CC(=O)CCC1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	via CMAUP database
2,3-Bis(beta-D-glucopyranosyloxy)benzoic acid benzyl ester	101857078	Click to see C1=CC=C(C=C1)COC(=O)C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	568.50	unknown	via CMAUP database
benzyl 2,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]benzoate	101857079	Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	568.50	unknown	via CMAUP database
Coniferin	5280372	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	via CMAUP database
Dihydrosyringin	71720642	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CCCO	374.40	unknown	via CMAUP database
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
Geoside	25087713	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	458.50	unknown	via CMAUP database
methyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate	21770576	Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	446.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Tingenone	101520	Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C	420.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Triptocalline A	44559634	Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC5=C(C(=O)C(CC54)O)C)C)C)C)(C(C1=O)O)C	442.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin	5281647	Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O	422.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Urolignoside	10602086	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-O-(4-Coumaroyl)-beta-D-glucose	14158117	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	326.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isobergapten	68082	Click to see COC1=C2C=CC(=O)OC2=C3C=COC3=C1	216.19	unknown	https://doi.org/10.1002/JHRC.1240080305 https://doi.org/10.1021/NP50047A020
Pimpinellin	4825	Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC	246.21	unknown	https://doi.org/10.1002/JHRC.1240080305 https://doi.org/10.1021/NP50047A020
Sphondin	108104	Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2	216.19	unknown	https://doi.org/10.1002/JHRC.1240080305 https://doi.org/10.1021/NP50047A020 https://doi.org/10.1016/S0031-9422(00)81503-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
9-Hydroxy-5,6-dihydrofuro[3,2-g]chromen-7-one	29920867	Click to see C1CC(=O)OC2=C1C=C3C=COC3=C2O	204.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Pentosalen	10212	Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C	270.28	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N https://doi.org/10.1007/BF00600845 https://doi.org/10.1016/S0031-9422(00)81503-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N https://doi.org/10.1007/BF00600845 https://doi.org/10.1021/NP50047A020 https://doi.org/10.1002/JHRC.1240080305
Byakangelicin	10211	Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O	334.30	unknown	https://doi.org/10.1007/BF00600845
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin	68079	Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC	246.21	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N https://doi.org/10.1007/BF00600845 https://doi.org/10.1021/NP50047A020 https://doi.org/10.1002/JHRC.1240080305 https://doi.org/10.1007/BF00563460
Methoxsalen	4114	Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2	216.19	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N https://doi.org/10.1007/BF00600845 https://doi.org/10.1007/BF00563460
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin	162350	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	101857081	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)OC)OC7C(C(C(C(O7)C)O)O)O)O)O)O)O)O	932.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Hovetrichoside A	21668725	Click to see COC1=C(C=CC(=C1)C(CO)C(C2=CC(=C(C=C2)O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	482.50	unknown	via CMAUP database

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Heracleum sphondylium

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