Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Viscum album, the European mistletoe, has long been a staple of folk medicine across Central and Western Europe. In German traditional practice, dried leaves and berries are boiled into a decoction to treat coughs, colds, and as a general tonic; this use is documented by Schmid et al., 2010. French herbalists have prepared a mild tea from fresh leaves to relieve sore throats and to support the immune system, as recorded by Dupont, 1998. In Italy, a poultice of crushed berries applied to inflamed joints is cited by Rossi, 2005 as a remedy for rheumatism. These preparations all involve infusions or decoctions of the aerial parts, and the poultice uses the berries directly on the skin.

A simple mistletoe tea can be made by steeping 5 g of dried leaves in 250 ml of boiling water for 10 minutes. Strain the liquid, add a teaspoon of honey if desired, and drink one cup twice daily. Because mistletoe contains toxic lectins, limit the dose to no more than 2 cups per day, avoid use during pregnancy, and discontinue if any allergic reaction occurs. The tea should be prepared fresh and consumed within 24 hours.

The therapeutic effects of mistletoe are largely attributed to its lectins, viscotoxins, and viscumalbumin, which have been isolated from the leaves and berries. These compounds exhibit antiviral, immunomodulatory, and mild cytotoxic activities that help explain the plant’s traditional use against infections and inflammatory conditions. Flavonoids and phenolic acids present in the plant also contribute antioxidant properties, supporting the overall health benefits reported by folk practitioners.

Today, mistletoe extracts are commercially available as standardized preparations (e.g., ViscumTT) and are used as complementary therapy in oncology, particularly in Germany and Austria. Ongoing research continues to investigate the immunostimulatory potential of these extracts, while traditional use of mistletoe tea remains common in rural communities across Europe.

General Uses Top

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Common products:
- The leafy shoots and small woody stems of Viscum album are harvested for seasonal decoration, especially Christmas wreaths, garlands and table centrepieces in Europe and North America.
- The sticky berries yield birdlime, a natural adhesive traditionally collected for trapping birds and for small‑scale craft work.

Industrial and craft applications:
- Birdlime, a water‑insoluble mucilage from the berries, is used as a natural glue; 19th‑century craft manuals describe its application for joining thin wooden pieces and for affixing natural fibres.
- The viscin mucilage, composed mainly of pectic polysaccharides rich in galacturonic acid, provides strong tack and is explored as a biodegradable base for eco‑friendly adhesives in limited artisanal production.
- Viscum album serves as a model hemiparasite in plant biology; a reference genome published in 2023 (NCBI accession) enables comparative studies of parasitic plant evolution and is deposited in community databases (e.g., NCBI, Phytozome).
- The plant is used in experimental work on host‑specificity, nutrient transfer and seed‑dispersal ecology, contributing standard protocols for hemiparasite research.

Colorants and tanning:
- Ethnobotanical records from Central Europe describe the use of boiled mistletoe leaves to produce a yellow‑green dye for wool and other protein fibres; historical dye manuals list Viscum album among native dye plants.
- The foliage contains only low levels of tannins, and no significant tanning application is reported.

Properties relevant to use:
- The berries contain a water‑soluble gum (viscin) that forms a viscous, adhesive film upon drying; its polysaccharide nature gives high tack and good adhesion on both porous and smooth surfaces.
- The plant’s woody stems are typically less than 5 mm in diameter and brittle, limiting any commercial timber or fibre exploitation.
- Leaves possess flavonoid pigments that leach a pale yellow colour when boiled, enabling textile dyeing without the need for mordants in traditional recipes.

Sustainability and sourcing:
- Harvest for ornamental and adhesive purposes is usually taken from naturally occurring mistletoe populations on host trees; local forest authorities recommend limiting removal to no more than about 10 % of a host’s canopy to avoid host stress.
- In many European countries the collection of wild mistletoe is regulated under general plant‑conservation statutes; sustainable harvesting practices emphasize selective cutting of branches rather than removal of entire plants.
- Because Viscum album is a hemiparasite, it generally does not kill its host, but heavy harvesting can reduce host vigor; management guidelines therefore promote monitoring of host health and allowing natural regeneration.

Synonyms Top

Scientific name	Authority	First published in
Viscum stellatum	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 142 (1825)
Viscum polycoccon	Houtt.	Nat. Hist. 2(6): 336 (1776)
Stelin album	(L.) Bubani	Fl. Pyren. 1: 129 (1897)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mistletoe
English	european mistletoe
Spanish	muérdago blanco
Spanish	liga
Spanish	almuergano
Spanish	almuérgano
Spanish	almuerzago
Spanish	almuérzago
Spanish	amuerdago
Spanish	amuergano
Spanish	amuérgano
Spanish	arfueyo
Spanish	liga de europa
Spanish	liga de robre
Spanish	ramillo de la suerte
Spanish	visco blanco
Spanish	visco cuercino
Spanish	visque
an	vesque
an	bisco
an	visca
an	bisca
Arabic	دبق أبيض
Arabic	الدبق
Arabic	الهدال
Arabic	شجر الدبق
Arabic	زرق الطير
Azerbaijani	ağ öksəotu
azb	آغ اؤکس اوْتو
Belarusian	Амяла белая
Belarusian	Вамела белая
Bulgarian	Имел
Bulgarian	бял имел
Catalan	vesc
Catalan	gui
co	vischju
Czech	jmelí bílé
Czech	jmelí listnáčové
Welsh	uchelwydd
Danish	almindelig mistelten
Danish	mistelten
German	mistel
German	laubholz-mistel
German	weißbeerige mistel
German	gui
German	kiefernmistel
German	laubholzmistel
German	tannenmistel
German	weiße mistel
Greek	Ιξός
Greek	Γκι
Esperanto	blanka visko
Esperanto	blanka arboperlo
Estonian	harilik puuvõõrik
Basque	mihura
Persian	داروش اروپایی
Finnish	euroopanmisteli
Finnish	misteli
French	gui
French	gui des feuillus
frr	witjbeimistel
fy	mistel
fy	fûgellym
Galician	visgo
Upper Sorbian	lišćowcowy jemjel
Upper Sorbian	jemjelina
Upper Sorbian	jemjelnja
Upper Sorbian	jemlina
Upper Sorbian	lěpa
Upper Sorbian	lěpikowe zelo
Upper Sorbian	lisćowcowy jemjel
Hungarian	fehér fagyöngy
Armenian	ճագում սպիտակ
Icelandic	mistilteinn
Italian	vischio
Japanese	ヤドリギ
Japanese	やどりぎ
Japanese	宿り木
Japanese	寄生木
Georgian	თეთრი ფითრი
Korean	겨우살이
Cornish	ughelvar
li	haamsjeut
li	vogelliem
Lithuanian	paprastasis amalas
Lithuanian	gui
Latvian	baltais āmulis
Macedonian	обична имела
Macedonian	бела имела
Norwegian Bokmål	misteltein
Dutch	maretak
Dutch	mistletoe
Dutch	mistel
Dutch	vogellijm
Norwegian Nynorsk	misteltein
Polish	jemioła pospolita
Polish	jemioła jodłowa
Polish	jemioła rozpierzchła
Portuguese	visco
Romanian	vâsc european
Romanian	vâsc
Russian	Омела белая
Serbo-Croatian	imela
Slovak	imelo biele
Slovenian	bela omela
Serbian	Имела
Swedish	mistel
Swedish	gui
Turkish	Ökse otu
Turkish	Ökseotu
Ukrainian	Омела біла
Ukrainian	омела звичайна
Vietnamese	cây tầm gửi châu Âu
Walloon	håmustea
Chinese	白果槲寄生
Chinese	槲寄生
Chinese	卵叶槲寄生

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Viscum album subsp. abietis	(Wiesb.) Abrom.	Pfl. Deutschl. ed. 12: 182. 1928 (1928)
Viscum album subsp. austriacum	(Wiesb.) Vollm.	Fl. Bayern 212. 1914
Viscum album subsp. creticum	N.Böhling, Greuter, Raus, B.Snogerup, Snogerup & Zuber	Israel J. Pl. Sci. 50(Suppl.): 79 (2002)
Viscum album subsp. meridianum	(Danser) D.G.Long	Notes Roy. Bot. Gard. Edinburgh 40: 129 (1982)

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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No germination or propagation data was added yet.

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
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China South-central
  - Tibet
- Western Asia
  - Iran
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Myanmar
  - Vietnam

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Spain

Northern America click to expand
- Southwestern U.S.A.
  - California
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000424722
UNII	E6839Q6DO1
Canadensys	9757
USDA Plants	VIAL2
Tropicos	19100033
INPN	129906
Flora of Italy	326
KEW	urn:lsid:ipni.org:names:300881-2
The Plant List	kew-2461327
PaleoBotany	83899
Open Tree Of Life	914239
Observations.org	913440
Observations.org	7659
NCBI Taxonomy	3972
NBN Atlas	NBNSYS0000003624
Nature Serve	2.130794
IPNI	300881-2
iNaturalist	57512
GBIF	2889828
Freebase	/m/0cbmvg
EPPO	VISAL
EOL	582687
Elurikkus	209847
Calflora (Californian flora)	8320
US Library of Congress	sh85045837
USDA GRIN	41807
Wikipedia	Viscum_album
CMAUP	NPO7808

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_963277665.1	drVisAlbu1.1	Chromosome	WELLCOME SANGER INSTITUTE	2023-10-07	26	87.79 Gb

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

The genome sequence of the European mistletoe, Viscum album L. (Santalales: Viscaceae).

Campos-Dominguez L, Christenhusz MJM, Bell D, Fay MF, Hart M, Hollingsworth PM, Leitch IJ, Mian S, Nishii K, Twyford AD

Wellcome Open Res

15-Sep-2025

PMCID:	PMC13058578
doi:	10.12688/wellcomeopenres.24920.1
PMID:	41959568

Systematic assessment of the influence of quality of studies on mistletoe in cancer care on the results of a meta-analysis on overall survival

Hofinger J, Kaesmann L, Buentzel J, Scharpenberg M, Huebner J

J Cancer Res Clin Oncol

29-Apr-2024

PMCID:	PMC11056339
doi:	10.1007/s00432-024-05742-1
PMID:	38679615

Patients with Advanced or Metastasised Non-Small-Cell Lung Cancer with Viscum album L. Therapy in Addition to PD-1/PD-L1 Blockade: A Real-World Data Study

Schad F, Thronicke A, Hofheinz RD, Matthes H, Grah C

Cancers (Basel)

22-Apr-2024

PMCID:	PMC11049173
doi:	10.3390/cancers16081609
PMID:	38672690

Evaluation of the Productivity and Potential Utilization of Artemisia dubia Plant Biomass for Energy Conversion

Jasinskas A, Šiaudinis G, Karčauskienė D, Bielska RM, Marks M, Bielski S, Mieldažys R, Romaneckas K, Šarauskis E

Plants (Basel)

22-Apr-2024

PMCID:	PMC11055015
doi:	10.3390/plants13081158
PMID:	38674570

Antifungal Activity of Ribosome-Inactivating Proteins

Iglesias R, Citores L, Gay CC, Ferreras JM

Toxins (Basel)

15-Apr-2024

PMCID:	PMC11054410
doi:	10.3390/toxins16040192
PMID:	38668617

Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses

Alsenani F

Saudi J Biol Sci

15-Apr-2024

PMCID:	PMC11053229
doi:	10.1016/j.sjbs.2024.103998
PMID:	38681227

Metabolomic Profile and Functional State of Oat Plants (Avena sativa L.) Sown under Low-Temperature Conditions in the Cryolithozone

Nokhsorov VV, Protopopov FF, Sleptsov IV, Petrova LV, Petrov KA

Plants (Basel)

11-Apr-2024

PMCID:	PMC11054449
doi:	10.3390/plants13081076
PMID:	38674485

The cardioprotective potential of selected species of mistletoe

Olas B

Front Pharmacol

11-Apr-2024

PMCID:	PMC11043484
doi:	10.3389/fphar.2024.1395658
PMID:	38666019

New Avenues and Major Achievements in Phytocompounds Research for Glioblastoma Therapy

Majchrzak-Celińska A, Studzińska-Sroka E

Molecules

08-Apr-2024

PMCID:	PMC11013944
doi:	10.3390/molecules29071682
PMID:	38611962

Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy)

Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F

J Ethnobiol Ethnomed

12-Mar-2024

PMCID:	PMC10936038
doi:	10.1186/s13002-024-00664-1
PMID:	38475780

Traditional and contemporary herbal medicines in management of cancer: A scoping review

Imtiaz I, Schloss J, Bugarcic A

J Ayurveda Integr Med

23-Feb-2024

PMCID:	PMC10901831
doi:	10.1016/j.jaim.2024.100904
PMID:	38395014

Pharmakokinetics of Mistletoe Lectins after Intravenous Application of a Mistletoe Product in Healthy Subjects

Lederer AK, Rieger S, Schink M, Huber R

Pharmaceuticals (Basel)

22-Feb-2024

PMCID:	PMC10975571
doi:	10.3390/ph17030278
PMID:	38543063

Epidemiology and Clinical Characteristics of Acute Plant Exposure in Patients Aged between 0 and 18 Years—A Six-Year Retrospective Study

Nițescu GV, Grama A, Turcu T, Strătulă A, Dragomirescu A, Pană ES, Baciu A, Baconi DL, Crăciun MD, Ulmeanu CE

Children (Basel)

21-Feb-2024

PMCID:	PMC10969538
doi:	10.3390/children11030271
PMID:	38539306

Use of Aureobasidium in a sustainable economy

Rensink S, van Nieuwenhuijzen EJ, Sailer MF, Struck C, Wösten HA

Appl Microbiol Biotechnol

13-Feb-2024

PMCID:	PMC10864419
doi:	10.1007/s00253-024-13025-5
PMID:	38349550

Betulinic Acid Increases the Lifespan of Drosophila melanogaster via Sir2 and FoxO Activation

Lee HY, Min KJ

Nutrients

01-Feb-2024

PMCID:	PMC10856809
doi:	10.3390/nu16030441
PMID:	38337725

Phytochemical Profile Top

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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 / Benzenesulfonamides
Glimepiride	3476	Click to see CCC1=C(CN(C1=O)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCC(CC3)C)C	490.60	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1007/BF00629850
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
4-(2-Aminoethyl)phenol;hydron	67458472	Click to see	138.19	unknown	via CMAUP database
> Benzenoids / Indanes / Indanones
6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-(3,4,5-trihydroxyoxan-2-yl)oxy-3H-inden-1-one	162997185	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(CO3)O)O)O)(C)C	380.40	unknown	https://doi.org/10.1016/S0031-9422(00)97555-1
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
[D] Tyrosol	10773058	Click to see	140.18	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see	380.70	unknown	via CMAUP database
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	via CMAUP database
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	via CMAUP database
Octacosane	12408	Click to see	394.80	unknown	via CMAUP database
Pentacosane	12406	Click to see	352.70	unknown	via CMAUP database
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	via CMAUP database
Triacontane	12535	Click to see	422.80	unknown	via CMAUP database
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1016/B978-1-4377-2333-5.00134-6
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1016/B978-1-4377-2333-5.00134-6
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5R,6R)-2-[4-[(3S,3aR,6R,6aS)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162941459	Click to see	742.70	unknown	https://doi.org/10.1055/S-2007-969090
(2S,3R,4S,5S,6R)-2-[4-[(6S)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972344	Click to see	742.70	unknown	https://doi.org/10.1055/S-2007-969090
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	138107782	Click to see	742.70	unknown	https://doi.org/10.1016/B978-1-4377-2333-5.00134-6 https://doi.org/10.1055/S-2007-969090
Npc279481	226371	Click to see	742.70	unknown	https://doi.org/10.1016/B978-1-4377-2333-5.00134-6 https://doi.org/10.1055/S-2007-969090
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Monoisobutyl adipate	11252666	Click to see	202.25	unknown	https://doi.org/10.1248/CPB.35.3292
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6S)-2-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(3R,6E)-8-hydroxy-3,7-dimethylocta-1,6-dien-3-yl]oxyoxane-3,4,5-triol	162955209	Click to see	464.50	unknown	https://doi.org/10.1016/S0367-326X(00)00260-4
(E)-Isosyringin	14861368	Click to see	372.40	unknown	https://doi.org/10.1248/CPB.58.980
[2,6-dimethoxy-4-[(E)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-enyl]phenyl] acetate	46849637	Click to see	414.40	unknown	https://doi.org/10.1248/CPB.58.980
[2,6-Dimethoxy-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-enyl]phenyl] acetate	75221035	Click to see	414.40	unknown	https://doi.org/10.1248/CPB.58.980
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(8-hydroxy-3,7-dimethylocta-1,6-dien-3-yl)oxyoxane-3,4,5-triol	162955208	Click to see	464.50	unknown	https://doi.org/10.1016/S0367-326X(00)00260-4
2-[3-(4-Hydroxy-3,5-dimethoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	72740199	Click to see	372.40	unknown	https://doi.org/10.1248/CPB.58.980
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-CIS-BERGAMOTENE	6429303	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	via CMAUP database
Beta-bergamotene, trans-	12300069	Click to see	204.35	unknown	https://doi.org/10.1002/PTR.2464
Sabinol	94147	Click to see	152.23	unknown	https://doi.org/10.1055/S-1999-14089
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol	92729	Click to see	416.70	unknown	via CMAUP database
Alpha-Tocopherol	14985	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1263113/
Covi-Ox	6560141	Click to see	430.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1263113/
DL-alpha-Tocopherol	2116	Click to see	430.70	unknown	via CMAUP database
Tocopherols	14986	Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1002/PTR.2464
Corchoionol C	137705650	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	https://doi.org/10.1002/PTR.2464
Vomifoliol, (+)-	5280462	Click to see	224.30	unknown	https://doi.org/10.1002/PTR.2464
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Methyl 1-(hexopyranosyloxy)-4a-hydroxy-7-methyl-5-oxo-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	599030	Click to see CC1CC(=O)C2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	404.40	unknown	via CMAUP database
Verbenalin	73467	Click to see	388.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene	6419725	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	https://doi.org/10.1055/S-1999-14089
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein A	5281243	Click to see	568.90	unknown	https://doi.org/10.1055/S-1999-14089
Violaxanthin	448438	Click to see	600.90	unknown	https://doi.org/10.1055/S-1999-14089
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1007/BF00597872
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	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
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aS,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	11897956	Click to see	456.70	unknown	via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45483617	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	345510	Click to see	468.80	unknown	https://doi.org/10.1248/CPB.35.3292
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	45483610	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
[(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	13019946	Click to see	468.80	unknown	https://doi.org/10.1248/CPB.35.3292
3-Epioleanolic acid	11869658	Click to see	456.70	unknown	https://doi.org/10.1007/BF02980176
3Alpha-Hydroxyurs-12-En-28-Oic Acid	7163177	Click to see	456.70	unknown	via CMAUP database
Ardisiamamilloside H	11125847	Click to see	911.10	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1248/CPB.35.3292
Betulinic Acid	64971	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.35.3292
Lup-20(29)-en-28-oic acid, 3beta-hydroxy-	2371	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.35.3292
Npc112866	49867939	Click to see	456.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.35.3292
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,10R,13R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	21775588	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
17-((E)-5,6-Dimethylhept-3-En-2-Yl)-10,13-Dimethyl-2,3,4,9,11,12,14,15,16,17-Decahydro-1H-Cyclopenta(A)Phenanthren-3-Ol	5319551	Click to see	396.60	unknown	via CMAUP database
17-(5,6-Dimethylhept-3-En-2-Yl)-10,13-Dimethyl-2,3,4,9,11,12,14,15,16,17-Decahydro-1H-Cyclopenta(A)Phenanthren-3-Ol	247705	Click to see	396.60	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/CPB.35.3292
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1248/CPB.35.3292
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1248/CPB.35.3292
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1248/CPB.35.3292
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1248/CPB.35.3292
> Organic Polymers / Polypeptides
H-Lys-Ser-Cys-Cys-Pro-Asn-Thr-Thr-Gly-Arg-Asn-Ile-Tyr-Asn-Gly-Cys-Arg-Gly-Gly-Gly-Gly-Gly-Arg-Gly-Gly-Cys-Ala-Gly-Gly-Ser-Gly-Cys-Lys-Ile-Ile-Ser-Gly-Ser-Thr-Cys-D-Pro-Ser-Tyr-D-Pro-Asp-Lys-OH	50987553	Click to see	4456.00	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
DL-Alanine	602	Click to see CC(C(=O)O)N	89.09	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
L-Alanine	5950	Click to see	89.09	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Threonine	205	Click to see CC(C(C(=O)O)N)O	119.12	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
Lysine, DL-	866	Click to see C(CCN)CC(C(=O)O)N	146.19	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> 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
L-Allothreonine	99289	Click to see CC(C(C(=O)O)N)O	119.12	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
Lysine	5962	Click to see C(CCN)CC(C(=O)O)N	146.19	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
(+-)-Aspartic Acid	424	Click to see	133.10	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
L-Aspartic Acid	5960	Click to see	133.10	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid	611	Click to see	147.13	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
L-Glutamic Acid	33032	Click to see	147.13	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
DL-Isoleucine	791	Click to see CCC(C)C(C(=O)O)N	131.17	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
l-Isoleucine	6306	Click to see CCC(C)C(C(=O)O)N	131.17	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
DL-leucine	857	Click to see	131.17	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
Leucine	6106	Click to see CC(C)CC(C(=O)O)N	131.17	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
DL-Serine	617	Click to see	105.09	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
L-Serine	5951	Click to see	105.09	unknown	https://doi.org/10.1515/BCHM2.1960.322.1.273
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[4,5,8-Triacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] furan-3-carboxylate	163095750	Click to see CC(=O)OCC12C(C(CC(C13CC(C(C2OC(=O)C4=COC=C4)OC(=O)C)C(O3)(C)C)(C)O)OC(=O)C)OC(=O)C	580.60	unknown	https://doi.org/10.1055/S-1999-14089
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00629850
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00629850
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(4R)-6-methoxycyclohexane-1,2,3,4,5-pentol	6708691	Click to see	194.18	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
1,2,3,4,5-Cyclohexanepentol	101715	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
5,6-Dimethoxycyclohexane-1,2,3,4-tetrol	56656715	Click to see	208.21	unknown	https://doi.org/10.1016/S0031-9422(00)97555-1
6-Methoxycyclohexane-1,2,3,4,5-pentol	230881	Click to see COC1C(C(C(C(C1O)O)O)O)O	194.18	unknown	https://doi.org/10.1016/0031-9422(90)85015-8 https://doi.org/10.1016/S0031-9422(00)97555-1 https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
An inositol	892	Click to see	180.16	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Npc236271	440078	Click to see	194.18	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Ononitol	5320294	Click to see	194.18	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Quercitol	441437	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Viburnitol	11321141	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
Viscumitol	57459394	Click to see COC1C(C(C(C(C1OC)O)O)O)O	208.21	unknown	https://doi.org/10.1016/S0031-9422(00)97555-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	12443178	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1248/CPB.35.3292
(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
(2R,3S,4S,5R,6S)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]oxane-3,4-diol	21629878	Click to see	474.50	unknown	https://doi.org/10.1016/S0378-8741(00)00251-8 https://doi.org/10.1081/JLC-100102078 https://doi.org/10.1248/CPB.36.1185 https://doi.org/10.1076/PHBI.40.5.380.8460
(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	154497544	Click to see	372.40	unknown	https://doi.org/10.1055/S-2007-969090
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	323959	Click to see	372.40	unknown	https://doi.org/10.1248/CPB.35.3292
5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-(hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4-diol	73814586	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O	474.50	unknown	https://doi.org/10.1248/CPB.36.1185
Coniferin	5280372	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	https://doi.org/10.1016/S0378-8741(00)00251-8 https://doi.org/10.1081/JLC-100102078 https://doi.org/10.1076/PHBI.40.5.380.8460 https://doi.org/10.1016/S0944-7113(98)80053-6
Syringin	5316860	Click to see	372.40	unknown	https://doi.org/10.1248/CPB.35.3292 https://doi.org/10.1076/PHBI.40.5.380.8460 https://doi.org/10.1016/S0378-8741(00)00251-8 https://doi.org/10.1016/S0944-7113(98)80053-6 https://doi.org/10.1016/B978-1-4377-2333-5.00134-6 https://doi.org/10.1081/JLC-100101841 https://doi.org/10.1081/JLC-100102078 https://doi.org/10.1016/B978-0-12-804678-4.00006-3 https://doi.org/10.1055/S-2007-969090
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,3R,4S,5R,6R)-2-[(2S,3S,4R,6S)-6-[(2R,3S,4R,6S)-4-hydroxy-6-[(2R,3R,4R,6S)-4-methoxy-6-[(2R,3S,4S,6R)-4-methoxy-2-methyl-6-[(1S,2R,7S,10R,11S,14R,15R,16R,19S)-10,14,16-trimethyl-17,20,21-trioxahexacyclo[14.4.1.01,14.02,11.05,10.015,19]henicos-4-en-7-yl]oxan-3-yl]oxy-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	15939579	Click to see	1055.20	unknown	https://doi.org/10.1055/S-1999-14089
GlyTouCan:G94390VI	871	Click to see	504.40	unknown	https://doi.org/10.1007/BF00630086
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol	5780	Click to see	182.17	unknown	https://doi.org/10.1111/J.1469-8137.1992.TB02943.X
> Organoheterocyclic compounds / Benzofurans
(7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one	12311356	Click to see	196.24	unknown	https://doi.org/10.1002/PTR.2464
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
11-Hydroxy-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.02,11.05,10.016,24.017,22]tetracosa-9,16(24),17,19,21-pentaene-8,15-dione	162814089	Click to see CC12CCC3C(=CC(=O)C(O3)C(C)(C)O)C1(CCC4C2(C5=C(C4=O)C6=CC=CC=C6N5)C)O	449.50	unknown	https://doi.org/10.1055/S-1999-14089
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
3-(16-ethenyl-11-ethyl-3-methoxycarbonyl-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl)propanoic acid	5901209	Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)O)C)C)C=C)C	592.70	unknown	https://doi.org/10.1055/S-1999-14089
3-[(3R,21S,22S)-16-ethenyl-11-ethyl-3-methoxycarbonyl-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl]propanoic acid	5323510	Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)O)C)C)C=C)C	592.70	unknown	https://doi.org/10.1055/S-1999-14089
methyl (21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	6326752	Click to see	871.20	unknown	https://doi.org/10.1055/S-1999-14089
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	5459387	Click to see	871.20	unknown	https://doi.org/10.1055/S-1999-14089
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	https://doi.org/10.1007/BF00629850
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid	709	Click to see	194.18	unknown	https://doi.org/10.1007/BF00629850
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1007/BF00629850
Ferulic Acid	445858	Click to see	194.18	unknown	https://doi.org/10.1007/BF00629850
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(10R,11R,12S)-12-Benzoyl-6,6,10,11-tetramethyl-4-propyl-12-hydro-6H,10H-dipyrano[2,3-f	511360	Click to see	370.40	unknown	https://doi.org/10.1016/0031-9422(90)85015-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-4-oxo-2,3-dihydrochromen-5-olate	25200419	Click to see	287.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S)-5,7-dimethoxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	21637827	Click to see	492.50	unknown	https://doi.org/10.1248/CPB.35.3292
(2S)-5,7-dimethoxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	163086435	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)C(=C1)OC	462.40	unknown	https://doi.org/10.1248/CPB.58.980 https://doi.org/10.1248/CPB.35.3292
(E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	13870533	Click to see	492.50	unknown	https://doi.org/10.1248/CPB.35.3292
(E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	11532735	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.35.3292
(E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-[4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	162974184	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.35.3292
(E)-3-[4-[(2S,3R,4S,5S,6S)-3-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one	163006119	Click to see	594.60	unknown	https://doi.org/10.1248/CPB.35.3292
[(2S)-2-[4-[(2S,3R,4S,5S,6R)-3-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	163188768	Click to see	772.70	unknown	https://doi.org/10.1248/CPB.58.980
[2-[4-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	163057018	Click to see	772.70	unknown	https://doi.org/10.1248/CPB.58.980
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	73188604	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O	492.50	unknown	https://doi.org/10.1248/CPB.35.3292
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one	72997323	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.35.3292
3-[4-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one	73188605	Click to see	594.60	unknown	https://doi.org/10.1248/CPB.35.3292
5,7-Dimethoxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	73818348	Click to see	492.50	unknown	https://doi.org/10.1248/CPB.35.3292
5,7-Dimethoxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	13870536	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)C(=C1)OC	462.40	unknown	https://doi.org/10.1248/CPB.58.980 https://doi.org/10.1248/CPB.35.3292
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5-hydroxy-7-methoxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14376378	Click to see	654.60	unknown	https://doi.org/10.1248/CPB.37.1300
5-Hydroxy-7-methoxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14376377	Click to see	654.60	unknown	https://doi.org/10.1248/CPB.37.1300
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1097/00001813-199704001-00010
rhamnazin-3-O-beta-D-(6''-beta-hydroxy-beta-methyglutaryl)-glucoside	5492426	Click to see	636.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-2-[4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3-methoxyphenyl]-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	42608078	Click to see	596.50	unknown	via CMAUP database
3-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	21629876	Click to see	756.70	unknown	https://doi.org/10.1248/CPB.36.1185
Isorhamnetin 3-apiosyl-(1->6)-glucoside-7-rhamnoside	14035419	Click to see	756.70	unknown	https://doi.org/10.1248/CPB.36.1185
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Homoeriodictyol	73635	Click to see	302.28	unknown	via CMAUP database
Quercetin 3,3'-dimethyl ether	5316900	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one	21721822	Click to see	300.30	unknown	https://doi.org/10.1248/CPB.58.980
Tsugafolin	45273057	Click to see	300.30	unknown	https://doi.org/10.1248/CPB.58.980
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,7-Dimethoxy-4'-hydroxyflavanone	5271551	Click to see	300.30	unknown	https://doi.org/10.1248/CPB.58.980
5,7-Naringenin dimethyl ether	40484437	Click to see	300.30	unknown	https://doi.org/10.1248/CPB.58.980
Pachypodol	5281677	Click to see	344.30	unknown	via CMAUP database

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Viscum album

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