Scientific name	Authority	First published in
Buphthalmum gussonii	Pasq.	Not. Bot.: 2 (1878)
Buphthalmum salicifolium subsp. grandiflorum	(L.) Ces.	Ces. in Cattaneo, Not. Nat. Civ. Lombardia 1. 1844. 302 1844
Buphthalmum salicinum	H.J.Coste	H. J. Coste, Fl. Descr. France 2. 1903. 355 1903
Buphthalmum salicifolium var. alpicola	Beck

Common names Top

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Filter by language:

Language	Common/alternative name
English	yellow oxeye daisy
English	ox-eye
Arabic	ربد صفصافي الورق
Czech	volovec vrbolistý
German	rindsauge
German	weidenblatt-rindsauge
German	weidenblättriges ochsenauge
German	ochsenauge
Finnish	häränkukka
French	buphtalme à feuilles de saule
Croatian	Žuti volujac
Hungarian	fűzlevelű ökörszem
Italian	asteroide salicina
Dutch	wilgkoeienoog
Polish	kołotocznik wierzbolistny
Slovak	volovec vŕbolistý
Slovenian	vrbovolistni primožek
Swedish	ljusöga
Chinese	黃牛眼菊
Chinese	黄牛眼菊
Chinese	牛眼菊

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Buphthalmum salicifolium subsp. flexile	(Bertol.) Garbari	197 1971
Buphthalmum salicifolium subsp. salicifolium

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

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

Asia-tropical click to expand
- Malesia
  - Jawa

Europe click to expand
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Switzerland
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Italy
  - Yugoslavia
- Southwestern Europe
  - France

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000082220
USDA Plants	BUSA7
Tropicos	2701962
INPN	87009
Flora of Italy	5533
KEW	urn:lsid:ipni.org:names:186459-1
The Plant List	gcc-38742
Open Tree Of Life	434009
Observations.org	142280
NCBI Taxonomy	56523
NBN Atlas	NBNSYS0000014191
IPNI	186459-1
iNaturalist	357176
GBIF	5391074
Freebase	/m/0fm1sy
EPPO	BPTSA
EOL	6260003
USDA GRIN	8151
Wikipedia	Buphthalmum_salicifolium
CMAUP	NPO8

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

Polyphenols of the Inuleae-Inulinae and Their Biological Activities: A Review

Malarz J, Michalska K, Stojakowska A

Molecules

27-Apr-2024

PMCID:	PMC11085778
doi:	10.3390/molecules29092014
PMID:	38731504

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

No species loss, but pronounced species turnover in grasslands in the Northern Alps over 25 years

Schwaiger H, Lenzer B, Essl F

Appl Veg Sci

18-Dec-2022

PMCID:	PMC10107162
doi:	10.1111/avsc.12700
PMID:	37082134

Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe)

Ilić T, Kuzmanović N, Vukojičić S, Lakušić D

Plants (Basel)

22-Nov-2022

PMCID:	PMC9741231
doi:	10.3390/plants11233194
PMID:	36501234

Differentiation of natural scrub communities of the Cotoneastro-Amelanchieretum group in Central Europe

Świerkosz K, Reczyńska K

PLoS One

12-Apr-2022

PMCID:	PMC9004749
doi:	10.1371/journal.pone.0266868
PMID:	35413069

Constituents of Xerolekia speciosissima (L.) Anderb. (Inuleae), and Anti-Inflammatory Activity of 7,10-Diisobutyryloxy-8,9-epoxythymyl Isobutyrate

Kłeczek N, Malarz J, Gierlikowska B, Kiss AK, Stojakowska A

Molecules

23-Oct-2020

PMCID:	PMC7660698
doi:	10.3390/molecules25214913
PMID:	33114240

Functional Diversity and Invasive Species Influence Soil Fertility in Experimental Grasslands

Teixeira LH, Yannelli FA, Ganade G, Kollmann J

Plants (Basel)

01-Jan-2020

PMCID:	PMC7020219
doi:	10.3390/plants9010053
PMID:	31906387

Dormancy and endosperm presence influence the ex situ conservation potential in central European calcareous grassland plants

Tausch S, Leipold M, Reisch C, Poschlod P

AoB Plants

25-Jun-2019

PMCID:	PMC6735842
doi:	10.1093/aobpla/plz035
PMID:	31528324

A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens

Frey D, Moretti M

Data Brief

23-May-2019

PMCID:	PMC6545399
doi:	10.1016/j.dib.2019.103982
PMID:	31194048

Carpesium divaricatum Sieb. & Zucc. Revisited: Newly Identified Constituents from Aerial Parts of the Plant and Their Possible Contribution to the Biological Activity of the Plant

Kłeczek N, Michalak B, Malarz J, Kiss AK, Stojakowska A

Molecules

24-Apr-2019

PMCID:	PMC6514683
doi:	10.3390/molecules24081614
PMID:	31022860

Ecological differentiation, speciation, and rarity: How do they match in Tephroseris longifolia agg. (Asteraceae)?

Janišová M, Skokanová K, Hlásny T

Ecol Evol

31-Jan-2018

PMCID:	PMC5838062
doi:	10.1002/ece3.3770
PMID:	29531667

Traits and climate are associated with first flowering day in herbaceous species along elevational gradients

Bucher SF, König P, Menzel A, Migliavacca M, Ewald J, Römermann C

Ecol Evol

20-Dec-2017

PMCID:	PMC5773311
doi:	10.1002/ece3.3720
PMID:	29375786

A higher‐level classification of the Pannonian and western Pontic steppe grasslands (Central and Eastern Europe)

Willner W, Kuzemko A, Dengler J, Chytrý M, Bauer N, Becker T, Biţă‐Nicolae C, Botta‐Dukát Z, Čarni A, Csiky J, Igić R, Kącki Z, Korotchenko I, Kropf M, Krstivojević‐Ćuk M, Krstonošić D, Rédei T, Ruprecht E, Schratt‐Ehrendorfer L, Semenishchenkov Y, Stančić Z, Vashenyak Y, Vynokurov D, Janišová M

Appl Veg Sci

16-Sep-2016

PMCID:	PMC5348766
doi:	10.1111/avsc.12265
PMID:	28356815

Are obligatory apomicts invested in the pollen tube transmitting tissue? Comparison of the micropyle ultrastructure between sexual and apomictic dandelions (Asteraceae, Lactuceae)

Płachno BJ, Świątek P, Kozieradzka-Kiszkurno M, Majeský Ľ, Marciniuk J, Stolarczyk P

Protoplasma

05-Feb-2015

PMCID:	PMC4561075
doi:	10.1007/s00709-015-0765-x
PMID:	25652809

A DNA Barcoding Approach to Characterize Pollen Collected by Honeybees

Galimberti A, De Mattia F, Bruni I, Scaccabarozzi D, Sandionigi A, Barbuto M, Casiraghi M, Labra M

PLoS One

08-Oct-2014

PMCID:	PMC4190116
doi:	10.1371/journal.pone.0109363
PMID:	25296114

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 / Phenol esters
[2-[(2R)-2-(acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylpropanoate	163022762	Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C)OC(=O)C(C)C	292.33	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[2-[2-(Acetyloxymethyl)oxiran-2-yl]-5-methylphenyl] 2-methylpropanoate	14427473	Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C)OC(=O)C(C)C	292.33	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne	5322029	Click to see CC#CC#CC#CC=CC=CC=C	166.22	unknown	https://doi.org/10.1002/CBER.19711040336
1-Tridecene-3,5,7,9,11-pentayne	441552	Click to see CC#CC#CC#CC#CC#CC=C	162.19	unknown	https://doi.org/10.1002/CBER.19711040336
Trideca-1,3,5-trien-7,9,11-triyne	528756	Click to see CC#CC#CC#CC=CC=CC=C	166.22	unknown	https://doi.org/10.1002/CBER.19711040336
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,10-Trimethyl-2,6,9,11-dodecatetraene	442368	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	https://doi.org/10.1002/CBER.19711040336
4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one	440265	Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C	222.28	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	https://doi.org/10.1002/CBER.19711040336
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Dehydrovomifoliol	688492	Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C	222.28	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3,5-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-4-hydroxy-1-(2-methylpropanoyloxy)cyclohexane-1-carboxylic acid	162893089	Click to see CC(C)C(=O)OC1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)C(=O)O	586.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-[[(2R)-5-heptyl-2,7-dihydroxy-4-oxo-3H-chromen-2-yl]methyl]-4,6-dihydroxybenzoic acid	162961282	Click to see CCCCCCCC1=C2C(=O)CC(OC2=CC(=C1)O)(CC3=C(C(=CC(=C3)O)O)C(=O)O)O	444.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Organoheterocyclic compounds / Bi- and oligothiophenes
(5'-(But-3-en-1-yn-1-yl)-[2,2'-bithiophen]-5-yl)methanol	24066914	Click to see C=CC#CC1=CC=C(S1)C2=CC=C(S2)CO	246.40	unknown	https://doi.org/10.1002/CBER.19650980329
[5-(5-But-3-en-1-ynylthiophen-2-yl)thiophen-2-yl]methyl acetate	5315563	Click to see CC(=O)OCC1=CC=C(S1)C2=CC=C(S2)C#CC=C	288.40	unknown	https://doi.org/10.1002/CBER.19650980329
2,2'-Bithiophene, 5-(3-buten-1-ynyl)-5'-methyl-	3083681	Click to see CC1=CC=C(S1)C2=CC=C(S2)C#CC=C	230.40	unknown	https://doi.org/10.1002/CBER.19650980329
> Organosulfur compounds / Thioethers / Thioenol ethers
(3E,5E,7Z)-7-methylsulfanyltrideca-1,3,5,7-tetraen-9,11-diyne	101416374	Click to see CC#CC#CC=C(C=CC=CC=C)SC	214.33	unknown	https://doi.org/10.1002/CBER.19711040336
7-Methylsulfanyltrideca-1,3,5,7-tetraen-9,11-diyne	162977268	Click to see CC#CC#CC=C(C=CC=CC=C)SC	214.33	unknown	https://doi.org/10.1002/CBER.19711040336
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S)-5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	162906021	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
5,7-Dihydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	74819388	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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/S0031-9422(99)00082-5
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	11968829	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14134315	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
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/S0031-9422(99)00082-5
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/S0031-9422(99)00082-5
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/S0031-9422(99)00082-5
Isorhamnetin 3-galactoside	13245586	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
isorhamnetin 3-O-glucoside	5318645	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6-methoxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 2-methylpropanoate	10076594	Click to see CC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2R)-2-methylbutanoate	162982184	Click to see CCC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-methylbutanoate	100982655	Click to see CC(C)CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[6-[2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-6-methoxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 2-methylpropanoate	74978500	Click to see CC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[6-[2-(3,4-Dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 2-methylbutanoate	162982183	Click to see CCC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[6-[2-(3,4-Dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 2-methylpropanoate	74978497	Click to see CC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	550.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
[6-[2-(3,4-Dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-methylbutanoate	162897573	Click to see CC(C)CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
3,5,6-Trihydroxy-2-(3,4-dihydroxyphenyl)-7-(6-O-isobutyryl-beta-D-glucopyranosyloxy)-4H-1-benzopyran-4-one	100982656	Click to see CC(C)C(=O)OCC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O)O	550.50	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
6-Hydroxykaempferol 7-alloside	14825511	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)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
6-Hydroxykaempferol 7-O-\|A-glucopyranoside	5318240	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)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Eriodictyol-7-O-glucoside	13254473	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=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/S0031-9422(99)00082-5
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=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/S0031-9422(99)00082-5
Miscanthoside	13254471	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Patuletin 7-glucoside	14157911	Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5
Patulitrin	5320435	Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00082-5

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Buphthalmum salicifolium

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