Scientific name	Authority	First published in
Helleboraster viridis	Moench	Methodus : 236 (1794)
Helleborus angustifolius	Host	Fl. Austriaca 2: 90 (1831)
Helleborus brevicaulis	Jord. & Fourr.	Ann. Soc. Linn. Lyon , n.s., 16: 325 (1868)
Helleborus pallidus	Host	Fl. Austriaca 2: 90 (1831)
Helleborus personati	Masclef	Rev. Gén. Bot. 1: 606 (1889)
Helleborus vaginatus	Kit. ex Steud.	Nomencl. Bot. , ed. 2, 1: 746 (1840)
Helleborus viridiflorus	Stokes	Bot. Mat. Med. 3: 274 (1812)

Common names Top

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Filter by language:

Language	Common/alternative name
English	green hellebore
Spanish	vedegambre de jardines
Spanish	vedegambre verde
Spanish	helleborus vaginatus
Spanish	helleborus personati
Spanish	helleborus pallidus
Spanish	helleborus brevicaulis
Spanish	helleboraster viridis
Spanish	heleboro negro
Spanish	helleborus occidentalis
Spanish	eléboro verde
Spanish	heléboro negro
Spanish	helleborus viridiflorus
Spanish	barredero
Spanish	helleborus angustifolius
Spanish	elebor
Spanish	eleboro verde
Arabic	خربق أخضر
Bulgarian	зелен кукуряк
Catalan	el·lèbor verd
Czech	čemeřice zelená
Welsh	crafanc-yr-arth werdd
Danish	grøn nyserod
German	grüne nieswurz
Basque	otsababa eme
Finnish	viherjouluruusu
French	ellébore vert
French	hellébore vert
Upper Sorbian	zelena čemjerca
Hungarian	zöld hunyor
Armenian	Ղանձլամեր կանաչ
Italian	elleboro verde
Japanese	アサギフユボタン
Cornish	kraban an ors glas
Dutch	helleborus viridis subsp. occidentalis
Dutch	wrangwortel
Polish	ciemiernik zielony
Russian	морозник зелёный
Russian	Морозник зелёный
Slovak	Čemernica zelená
Swedish	grön julros
Turkish	yeşil çöpleme
Walloon	yebe di feu
Chinese	绿铁筷子

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Helleborus viridis subsp. abruzzicus	(M.Thomsen, McLewin & B.Mathew) Bartolucci, F.Conti & Peruzzi	Inform. Bot. Ital. 45: 106 (2013)
Helleborus viridis subsp. liguricus	(M.Thomsen, McLewin & B.Mathew) Bartolucci, F.Conti & Peruzzi	Inform. Bot. Ital. 45: 106 (2013)
Helleborus viridis subsp. occidentalis	(Reut.) Schiffn.	Bot. Jahrb. Syst. 11: 118. 1889 (1889)

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!

Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

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.

dry storage impairs germination

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Eastern Europe
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Italy
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - West Virginia
- Southeastern U.S.A.
  - Maryland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000719221
UNII	DEU35I458S
USDA Plants	HEVI
Tropicos	27100406
INPN	101202
Flora of Italy	9603
KEW	urn:lsid:ipni.org:names:711386-1
The Plant List	kew-2844826
PFAF	Helleborus viridis
Open Tree Of Life	948053
Observations.org	2555
NCBI Taxonomy	171903
NBN Atlas	NBNSYS0000002694
Nature Serve	2.142005
IPNI	711386-1
iNaturalist	163661
GBIF	3033108
Freebase	/m/012r1wsc
EPPO	HLLVI
EOL	595621
USDA GRIN	18835
Wikipedia	Helleborus_viridis
CMAUP	NPO16256

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

Fruit Photosynthesis: More to Know about Where, How and Why

Garrido A, Conde A, Serôdio J, De Vos RC, Cunha A

Plants (Basel)

21-Jun-2023

PMCID:	PMC10347175
doi:	10.3390/plants12132393
PMID:	37446953

The vessel wall thickness–vessel diameter relationship across woody angiosperms

Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME

Am J Bot

12-Jun-2022

PMCID:	PMC9328290
doi:	10.1002/ajb2.1854
PMID:	35435252

Photosynthetic contribution and characteristics of cucumber stems and petioles

Sun W, Ma N, Huang H, Wei J, Ma S, Liu H, Zhang S, Zhang Z, Sui X, Li X

BMC Plant Biol

06-Oct-2021

PMCID:	PMC8493697
doi:	10.1186/s12870-021-03233-w
PMID:	34615487

Exchange of medicinal plant information in California missions

McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL

J Ethnobiol Ethnomed

15-Jun-2020

PMCID:	PMC7296748
doi:	10.1186/s13002-020-00388-y
PMID:	32539795

Herbal fertility treatments used in North America from colonial times to 1900, and their potential for improving the success rate of assisted reproductive technology

Lans C, Taylor-Swanson L, Westfall R

Reprod Biomed Soc Online

12-Apr-2018

PMCID:	PMC6047296
doi:	10.1016/j.rbms.2018.03.001
PMID:	30023440

The photosynthetic and structural differences between leaves and siliques of Brassica napus exposed to potassium deficiency

Lu Z, Pan Y, Hu W, Cong R, Ren T, Guo S, Lu J

BMC Plant Biol

11-Dec-2017

PMCID:	PMC5725657
doi:	10.1186/s12870-017-1201-5
PMID:	29228924

The bear in Eurasian plant names: motivations and models

Kolosova V, Svanberg I, Kalle R, Strecker L, Özkan AM, Pieroni A, Cianfaglione K, Molnár Z, Papp N, Łuczaj Ł, Dimitrova D, Šeškauskaitė D, Roper J, Hajdari A, Sõukand R

J Ethnobiol Ethnomed

21-Feb-2017

PMCID:	PMC5320662
doi:	10.1186/s13002-016-0132-9
PMID:	28222790

Beyond food and medicine, but necessary for life, too: other folk plant uses in several territories of Catalonia and the Balearic Islands

Gras A, Garnatje T, Bonet MÀ, Carrió E, Mayans M, Parada M, Rigat M, Vallès J

J Ethnobiol Ethnomed

17-Jun-2016

PMCID:	PMC4912702
doi:	10.1186/s13002-016-0097-8
PMID:	27316670

Detecting Fragmentation Extinction Thresholds for Forest Understory Plant Species in Peninsular Spain

Rueda M, Moreno Saiz JC, Morales-Castilla I, Albuquerque FS, Ferrero M, Rodríguez MÁ

PLoS One

15-May-2015

PMCID:	PMC4433258
doi:	10.1371/journal.pone.0126424
PMID:	25978329

Photosynthesis in reproductive structures: costs and benefits

Raven JA, Griffiths H

J Exp Bot

20-Feb-2015

PMCID:	PMC4669558
doi:	10.1093/jxb/erv009
PMID:	25871648

Contributions of Nonleaf Organs to the Yield of Cotton Grown with Different Water Supply

Zhan D, Yang Y, Hu Y, Zhang Y, Luo H, Zhang W

ScientificWorldJournal

01-Jun-2014

PMCID:	PMC4058802
doi:	10.1155/2014/602747
PMID:	24982968

Medical Ethnobotany in Europe: From Field Ethnography to a More Culturally Sensitive Evidence-Based CAM?

Quave CL, Pardo-de-Santayana M, Pieroni A

Evid Based Complement Alternat Med

30-Jul-2012

PMCID:	PMC3413992
doi:	10.1155/2012/156846
PMID:	22899952

Plant identification credibility in ethnobotany: a closer look at Polish ethnographic studies

Łuczaj ŁJ

J Ethnobiol Ethnomed

17-Dec-2010

PMCID:	PMC3022638
doi:	10.1186/1746-4269-6-36
PMID:	21167056

Marcescent corollas as functional structures: effects on the fecundity of two insect-pollinated plants

Herrera CM

Ann Bot

01-Aug-2010

PMCID:	PMC2944983
doi:	10.1093/aob/mcq160
PMID:	20870656

Saponins in aerial parts of Helleborus viridis L.

Anna Stochmal, Angela Perrone, Sonia Piacente, Wieslaw Oleszek

Elsevier BV

26-Apr-2010

doi:	10.1016/J.PHYTOL.2010.04.005

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-dimethoxybenzoate	370912	Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2	272.29	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D	10905866	Click to see CC1=C2CC(C3(C(CCCC3(C2=CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5	418.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid	5192	Click to see C(CCCCC(=O)O)CCCC(=O)O	202.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698321	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	572.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10531102	Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	570.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	6479669	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C	464.60	unknown	via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	10951647	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)COC(=O)C6=CC=CC=C6	540.60	unknown	via CMAUP database
Isovouacapenol A	636673	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	420.50	unknown	via CMAUP database
Isovouacapenol B	11812203	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3(C)O)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	438.60	unknown	via CMAUP database
Isovouacapenol C	3009285	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	438.60	unknown	via CMAUP database
Pulcharrin G	11750983	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)O)O)(C)C)C	438.60	unknown	via CMAUP database
Pulcherrimin F	11375664	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)C	510.60	unknown	via CMAUP database
Pulcherrin D	54597502	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(CC2OC(=O)C)O)(C)C)C	360.50	unknown	via CMAUP database
Pulcherrin E	54597503	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)O)O)(C)C)C	376.50	unknown	via CMAUP database
Pulcherrin F	54597504	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C)O)(C)C)C	376.50	unknown	via CMAUP database
Pulcherrin H	54597566	Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O	422.60	unknown	via CMAUP database
Pulcherrin I	54597567	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5	422.60	unknown	via CMAUP database
Pulcherrin J	54597568	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C=CC5=CC=CC=C5	448.60	unknown	via CMAUP database
Pulcherrin K	53388795	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C=O)C	452.50	unknown	via CMAUP database
Pulcherrin L	53388797	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O	438.60	unknown	via CMAUP database
Pulcherrin M	54597569	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5	452.50	unknown	via CMAUP database
Pulcherrin O	53388938	Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1(C(C(CC4)OC(=O)C5=CC=CC=C5)(C)C)O)C)O	540.60	unknown	via CMAUP database
Vouacapen-5alpha-ol	73354918	Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol	40467768	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	42433495	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	7067459	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
7-Hydroxycadalene	608115	Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O	214.30	unknown	via CMAUP database
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol	16046185	Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.3109/13880209009082817
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10627788	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)OC(=O)C)C	630.70	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11157932	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)OC(=O)C6=CC=CC=C6)C	630.70	unknown	via CMAUP database
(8beta,10beta,14alpha)-6beta,7beta-Bis(benzoyloxy)-3beta,5alpha-dihydroxy-12,16-epoxycassa-12,15-dien-19-oic acid	10698605	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)O)C	588.60	unknown	via CMAUP database
Pulcherrin N	53388796	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6	572.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
Pulcherrin P	53388939	Click to see CC(=O)OCC1(C(CCC2(C1(C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)OC(=O)C)O)O)C)OC(=O)C5=CC=CC=C5)C	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(3S,5S,10S,13R,14S,17R)-3-[(2R,4R,5R)-3,4-dihydroxy-6-methyl-5-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	131676378	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=COC(=O)C=C6)C)C=O)O)O)OC7C(C(C(C(O7)CO)O)O)O	724.80	unknown	https://doi.org/10.3109/13880209009082817
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-13-methyl-17-(6-oxopyran-3-yl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde	44584382	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=COC(=O)C=C6)C)C=O)O)O)O	562.60	unknown	https://doi.org/10.3109/13880209009082817
3-[(6-Deoxyhexopyranosyl)oxy]-5,14-dihydroxy-19-oxobufa-20,22-dienolide	30097	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=COC(=O)C=C6)C)C=O)O)O)O	562.60	unknown	https://doi.org/10.3109/13880209009082817
Gellebrigenin	16070014	Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)O)C=O)O	416.50	unknown	https://doi.org/10.3109/13880209009082817
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4R,5R,6S)-2-[(2R)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,16S)-16-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-methyloxane-3,4,5-triol	162900957	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)O	1065.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18R)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	163013983	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	921.10	unknown	https://doi.org/10.1016/J.PHYTOL.2010.04.005
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	163013982	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	921.10	unknown	https://doi.org/10.1016/J.PHYTOL.2010.04.005
(2S,3S,4R,5R,6S)-2-[(2S)-4-[(1S,2S,4S,6R,7S,8R,9R,12S,13S,16R)-16-[(2S,3S,4R,5S,6S)-4-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-methyloxane-3,4,5-triol	162934871	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)OC	1079.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
[(2R,3R,4S,5R,6R)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate	162994449	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)COC(=O)C)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1123.20	unknown	https://doi.org/10.1016/J.PHYTOL.2010.04.005
[(2R,3R,4S,5R,6S)-6-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-4-yl]oxy-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate	162932732	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)O	1107.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
[(2S,3S,4R,5S,6R)-6-[(2S,3S,4R,5S,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9R,12S,13S,16R)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-4-yl]oxy-3,5-dihydroxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate	163042561	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)OC	1121.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
[6-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate	162994448	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)COC(=O)C)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1123.20	unknown	https://doi.org/10.1016/J.PHYTOL.2010.04.005
[6-[3,5-Dihydroxy-2-(hydroxymethyl)-6-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-4-yl]oxy-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate	162932731	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)O	1107.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
[6-[3,5-Dihydroxy-2-(hydroxymethyl)-6-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-4-yl]oxy-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate	73803903	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)OC	1121.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
2-(Hydroxymethyl)-6-[[3,4,5-trihydroxy-6-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	75032158	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	921.10	unknown	https://doi.org/10.1016/J.PHYTOL.2010.04.005
2-[4-[16-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-methyloxane-3,4,5-triol	162900956	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)O	1065.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
2-[4-[16-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-methyloxane-3,4,5-triol	73803904	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)C)O)O)O)OC	1079.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Neocaesalpin E	11450901	Click to see CC1C2CCC3(C(CCCC3(C2CC4(C1=CC(=O)O4)OC)C)(C)C)O	348.50	unknown	via CMAUP database
Neocaesalpin F	11386164	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	484.60	unknown	via CMAUP database
Neocaesalpin G	11295185	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C	510.60	unknown	via CMAUP database
Pulcherrin Q	53388940	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C	436.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-3-[[2-O-[2-O-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]-alpha-L-arabinopyranosyl]-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-4H-1-benzopyran-4-one	21579173	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)O	758.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	14825575	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
5,7-Dihydroxy-2-(3,4-dihydroxyphenyl)-3-(2-O-alpha-L-arabinopyranosyl-beta-D-galactopyranosyloxy)-4H-1-benzopyran-4-one	21579174	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R)-2-[(2S,3S,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-7-[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163194117	Click to see C1C(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)O)CO)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)O)O)O	920.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
[2-[2-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	73803905	Click to see C1C(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)O)CO)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)O)O)O	920.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
2-(3,4-Dihydroxyphenyl)-3-[[2-O-[2-O-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]-alpha-L-arabinopyranosyl]-beta-D-galactopyranosyl]oxy]-5-hydroxy-7-(beta-D-glucopyranosyloxy)-4H-1-benzopyran-4-one	21579172	Click to see C1C(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)O)CO)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)O)O)O	920.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	101151128	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.013
Quercimeritrin	5282160	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)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone	10336604	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC4=C(C=C3)OCO4)C(=C1)OC	328.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-	11681403	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4	326.30	unknown	via CMAUP database
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one	44260091	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O	340.30	unknown	via CMAUP database
6-Methoxypulcherrimin	44260092	Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O)OC	370.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-(2,4-Dimethoxybenzylidene)-7-hydroxychroman-4-one	101356812	Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC	312.30	unknown	via CMAUP database
(3E)-3-(4-Methoxybenzylidene)-7-methoxychroman-4-one	6507117	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)OC	296.30	unknown	via CMAUP database
(3E)-3-[(3,4-dimethoxyphenyl)methylidene]-7-methoxychromen-4-one	5783568	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC(=C(C=C3)OC)OC)CO2	326.30	unknown	via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one	16082056	Click to see COC1=CC(=CC(=C1OC)OC)C=C2COC3=C(C2=O)C=CC(=C3)O	342.30	unknown	via CMAUP database
3-(4-Hydroxybenzylidene)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one	14079440	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC=C(C=C3)O)CO2	282.29	unknown	via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one	18778791	Click to see C1C(=CC2=CC3=C(C=C2)OCO3)C(=O)C4=C(O1)C=C(C=C4)O	296.27	unknown	via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one	101489712	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2	310.30	unknown	via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-6,7-dimethoxy-2,3-dihydro-4H-1-benzopyran-4-one	44475180	Click to see COC1=C(C=C(C=C1)C=C2COC3=CC(=C(C=C3C2=O)OC)OC)O	342.30	unknown	via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one	13846662	Click to see COC1=C(C=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)O	298.29	unknown	via CMAUP database
Bonducellin	14079439	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
Isobonducellin	10423880	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one	51533159	Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC(=C3)O	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone	10337542	Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O	344.40	unknown	via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone	6537040	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database

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Helleborus viridis

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