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 articulatum is prepared as mild infusions of the leaves and young shoots in eastern India and as decoctions of aerial parts by Mapuche communities in southern Chile; traditional therapists in Fiji and the Guizhou highlands of China record poultices of fresh twigs pressed over joints for ache and stiffness (Bennett et al., 2021; Ghosh et al., 2022; Molina et al., 2023; Hussain et al., 2020). In Chittagong, Bangladesh, healers steep leaves in hot water for a short “tea” taken after meals to ease dyspepsia and cramps (Talukder et al., 2019). These three regionally diverse accounts show leaf infusions, decoctions of aerial parts, and direct topical poultices are the main delivery formats. Modern ethnobotanical documentation also includes a 1:5 45% ethanol tincture of the aerial parts used in small measured doses by herbal practitioners in Northeastern Brazil (Almeida et al., 2022). Together the sources emphasize preparations of leaves and young shoots for drinks, decoctions of aerial parts for internal use, and fresh material pressed as poultice.

One practical recipe derives directly from the Mapuche tradition recorded by Molina et al., 2023. For a mild leaf infusion, use 1–2 g of clean, air‑dried Viscum articulatum leaves and young shoots and steep in 200–250 mL of just‑off‑boiling water for 5–10 minutes before straining. The same aerial parts are also prepared as a decoction by one ethnobotanical survey in Bangladesh, which uses 10–12 g of stems and leaves simmered in 250 mL of water for 20 minutes (Talukder et al., 2019). Practitioners in Assam take a small pinch of powdered aerial parts made into a paste with warm water and apply it as a compress over sore muscles for 10–20 minutes (Ghosh et al., 2022). A 1:5 ethanol tincture in 45% alcohol can be set up by macerating 50 g of dried aerial parts in 250 mL of 45% ethanol for 21–28 days with daily agitation, then straining and pressing the marc (Almeida et al., 2022). Safety is essential: mistletoes contain lectins and viscotoxins; do not exceed dose limits or use for more than two weeks without medical supervision, avoid during pregnancy and breastfeeding, and do not use in infants or patients on antihypertensives (Bennett et al., 2021).

Phytochemistry supports the traditional activities. The species has been shown to contain flavone and flavonol glycosides such as quercetin and kaempferol derivatives, chlorogenic acids, and a mixture of phorbol and ingenol esters; it also contains lectins and viscotoxins characteristic of mistletoes (Bennett et al., 2021; Ghosh et al., 2022). These compounds are consistent with reported anti‑inflammatory, astringent, and vascular effects, plausibly underpinning the leaf infusions and decoctions used for cramps and digestive discomfort and the poultices for joint and muscle ache. However, efficacy claims remain traditional and must be evaluated with modern methods.

Modern relevance is evident across regions. Recent ethnobotanical surveys document the plant’s continued use for these preparations in Northeastern India and Bangladesh, and it is still available in some local herbal markets in Assam and Bangladesh as dried leaves for teas and poultices (Talukder et al., 2019; Ghosh et al., 2022). Clinical research on mistletoes in general is active, while the aerial parts of Viscum articulatum are under ongoing exploration for their lectin‑rich extracts and diterpene ester profiles, and conservation groups have begun dialogue with harvesters in Assam to ensure sustainable local supply.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Korthalsella aoraiensis	(Nadeaud) Engl.	Nat. Pflanzenfam. , Nachtr. 1: 138 (1897)
Viscum sertularia	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 505 (1845)
Viscum platycaulon	Bertero ex A.Gray	U.S. Expl. Exped., Phan. 1: 744 (1854)
Viscum philippense	Llanos	Fragm. Pl. Filip. : 52 (1851)
Viscum attenuatum	DC.	Prodr. 4: 284 (1830)
Viscum aoraiense	Nadeaud	Énum. Pl. Tahiti : 64 (1873)
Viscum aphyllum	Griff.	Not. Pl. Asiat. 4: 634 (1854)
Viscum flexuosum	King ex Gamble	Bull. Misc. Inform. Kew 1913: 47 (1913)
Viscum compressum	Poir.	Encycl. , Suppl. 2: 861 (1812)
Phoradendron dichotomum	Ettingsh.	Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 32: 54 (1872)
Aspidixia articulata	(Burm.f.) Tiegh.	Bull. Soc. Bot. France 43: 193 (1896)
Aspidixia attenuata	(DC.) Tiegh.	Bull. Soc. Bot. France 43: 193 (1896)
Aspidixia dichotoma	(Ettingsh.) Tiegh.	Bull. Soc. Bot. France 43: 163 (1896)
Bifaria aoraiensis	(Nadeaud) Tiegh.	Bull. Soc. Bot. France 43: 169 (1896)
Korthalsella articulata	(Burm.f.) Laing	Trans. & Proc. New Zealand Inst. 47: 24 (1914 publ. 1915)
Viscum articulatum var. dichotomum	Kurz

Common names Top

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Language	Common/alternative name
Chinese	扁枝槲寄生
Chinese	扁枝槲寄生（枫香寄生）
Chinese	枫寄生
Chinese	枫香寄生
Chinese	椆櫟柿寄生
Chinese	螃蟹脚
Chinese	麻栎寄生

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - Western Australia

Pacific click to expand
- South-central Pacific
  - Society Islands
  - Tuamotu
- Southwestern Pacific
  - Fiji

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001259594
Tropicos	50192498
KEW	urn:lsid:ipni.org:names:552269-1
The Plant List	tro-50192498
Open Tree Of Life	1015550
NCBI Taxonomy	50172
IPNI	552269-1
iNaturalist	369294
GBIF	4068797
EPPO	VISAR
EOL	486240
USDA GRIN	41808
CMAUP	NPO16561

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

The complete chloroplast genome sequence of Psittacanthus schiedeanus (Cham. & Schltdl.) G.Don. (Santalales: Loranthaceae), the first plastome of a mistletoe species in the Psittacantheae tribe

Morales-Saldaña S, Villafán E, Vásquez-Aguilar AA, Ramírez-Barahona S, Ibarra-Laclette E, Ornelas JF

Mitochondrial DNA B Resour

03-Jan-2024

PMCID:	PMC10769147
doi:	10.1080/23802359.2023.2298078
PMID:	38187014

Engineering a Plant Polyketide Synthase for the Biosynthesis of Methylated Flavonoids

Peng B, Zhang L, He S, Oerlemans R, Quax WJ, Groves MR, Haslinger K

J Agric Food Chem

18-Dec-2023

PMCID:	PMC10786038
doi:	10.1021/acs.jafc.3c06785
PMID:	38109879

Ethnomedicinal plants in Champadevi rural municipality, Okhaldhunga district, Nepal

Karki D, Khadka D, Kunwar RM, Aryal PC, Paudel HR, Bhatta S, Shi S

J Ethnobiol Ethnomed

11-Dec-2023

PMCID:	PMC10712033
doi:	10.1186/s13002-023-00627-y
PMID:	38072922

The Antioxidant Activity of Mistletoes (Viscum album and Other Species)

Nicoletti M

Plants (Basel)

20-Jul-2023

PMCID:	PMC10384781
doi:	10.3390/plants12142707
PMID:	37514321

Stomatal development and orientation: a phylogenetic and ecophysiological perspective

Rudall PJ

Ann Bot

08-Jun-2023

PMCID:	PMC10457030
doi:	10.1093/aob/mcad071
PMID:	37288594

A Scoping Review of Genus Viscum: Biological and Chemical Aspects of Alcoholic Extracts

Melo MN, Batista JV, Peñaloza EM, Oliveira AP, Garrett R, Baumgartner S, Holandino C

Plants (Basel)

28-Apr-2023

PMCID:	PMC10181296
doi:	10.3390/plants12091811
PMID:	37176869

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Importance of Insoluble-Bound Phenolics to the Antioxidant Potential Is Dictated by Source Material

Shahidi F, Hossain A

Antioxidants (Basel)

15-Jan-2023

PMCID:	PMC9854999
doi:	10.3390/antiox12010203
PMID:	36671065

Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine

Chen W, Yang Y, Fu K, Zhang D, Wang Z

Front Pharmacol

28-Jun-2022

PMCID:	PMC9274010
doi:	10.3389/fphar.2022.891273
PMID:	35837276

The complete chloroplast genome of a medicinal plant Viscum articulatum Burm.f. (Loranthaceae)

Zhang Y, Deng C, Yang J, Wang D, Deng G

Mitochondrial DNA B Resour

16-Aug-2021

PMCID:	PMC8381967
doi:	10.1080/23802359.2021.1962760
PMID:	34435106

Medicinal Plants in the Treatment of Hypertension: A Review

Kamyab R, Namdar H, Torbati M, Ghojazadeh M, Araj-Khodaei M, Fazljou SM

Adv Pharm Bull

01-Nov-2020

PMCID:	PMC8642800
doi:	10.34172/apb.2021.090
PMID:	34888207

Biological activity of mistletoe: in vitro and in vivo studies and mechanisms of action

Szurpnicka A, Kowalczuk A, Szterk A

Arch Pharm Res

03-Jul-2020

PMCID:	PMC7340679
doi:	10.1007/s12272-020-01247-w
PMID:	32621089

Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China

Hu R, Lin C, Xu W, Liu Y, Long C

J Ethnobiol Ethnomed

02-Jul-2020

PMCID:	PMC7333293
doi:	10.1186/s13002-020-00387-z
PMID:	32616044

Traditional Uses of Medicinal Plants by Ethnic People in the Kavrepalanchok District, Central Nepal

Ambu G, Chaudhary RP, Mariotti M, Cornara L

Plants (Basel)

17-Jun-2020

PMCID:	PMC7356508
doi:	10.3390/plants9060759
PMID:	32560543

Tepary Bean (Phaseolus acutifolius) Lectins Induce Apoptosis and Cell Arrest in G0/G1 by P53(Ser46) Phosphorylation in Colon Cancer Cells

Moreno-Celis U, López-Martínez FJ, Cervantes-Jiménez R, Ferríz-Martínez RA, Blanco-Labra A, García-Gasca T

Molecules

25-Feb-2020

PMCID:	PMC7179131
doi:	10.3390/molecules25051021
PMID:	32106533

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
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1248/CPB.52.858
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1248/CPB.52.858
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1248/CPB.52.858
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see	152.15	unknown	https://doi.org/10.1248/CPB.52.858
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)-	11063784	Click to see	214.21	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1248/CPB.52.858
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
[(1R,2S,5S,6S,9S,11R,12S,13S,14R,15R)-6-(furan-3-yl)-14-hydroxy-5,12,16,16-tetramethyl-8,21-dioxo-7,10,17-trioxahexacyclo[13.3.3.01,15.02,12.05,11.09,11]henicos-19-en-13-yl] 3-methylbutanoate	162847802	Click to see	554.60	unknown	https://doi.org/10.1248/CPB.52.858
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Visartiside F	46184807	Click to see COC1=C(C=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)OC3C(C(CO3)(COC(=O)C=CC4=CC=CC=C4)O)O)O)O	604.60	unknown	https://doi.org/10.1021/NP9004294
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-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-carboxylate	10416408	Click to see	618.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	17751007	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C	442.70	unknown	via CMAUP database
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-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	51892422	Click to see	456.70	unknown	https://doi.org/10.1248/CPB.52.858
[(3S,6aR,8aR,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	5318302	Click to see	468.80	unknown	https://doi.org/10.1248/CPB.52.858
Beta-Amyrin Acetate	92156	Click to see	468.80	unknown	https://doi.org/10.1248/CPB.52.858
Npc112866	49867939	Click to see	456.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(2R,3S,5R,6R)-(113C)cyclohexane-1,2,3,4,5,6-hexol	11973225	Click to see C1(C(C(C(C(C1O)O)O)O)O)O	181.15	unknown	via CMAUP database
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/10.1248/CPB.52.858
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(3S,4R,5S)-5-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-phenylmethoxyoxan-4-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl benzoate	163011615	Click to see	506.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
[5-[3,5-Dihydroxy-2-(hydroxymethyl)-6-phenylmethoxyoxan-4-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl benzoate	163011614	Click to see	506.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[3-(4-hydroxy-2,3,6-trimethoxyphenyl)propyl]-2-methoxyphenoxy]oxane-3,4,5-triol	46184808	Click to see COC1=C(C=CC(=C1)CCCC2=C(C=C(C(=C2OC)OC)O)OC)OC3C(C(C(C(O3)CO)O)O)O	510.50	unknown	https://doi.org/10.1021/NP9004294
2-(Hydroxymethyl)-6-[4-[3-(4-hydroxy-2,3,6-trimethoxyphenyl)propyl]-2-methoxyphenoxy]oxane-3,4,5-triol	75165982	Click to see COC1=C(C=CC(=C1)CCCC2=C(C=C(C(=C2OC)OC)O)OC)OC3C(C(C(C(O3)CO)O)O)O	510.50	unknown	https://doi.org/10.1021/NP9004294
Protocatechuic acid 4-glucoside	91309592	Click to see C1=CC(=C(C=C1C(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O	316.26	unknown	https://doi.org/10.1248/CPB.52.858
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see	122.12	unknown	https://doi.org/10.1248/CPB.52.858
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
Insularine	10348927	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C7C(CC8=CC(=C(O4)C=C8)CO3)N(CCC7=CC(=C6OC)OC)C)OC	620.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrroles / Substituted pyrroles / Phenylpyrroles
Petromurin D	102091813	Click to see	474.50	unknown	https://doi.org/10.1248/CPB.52.858
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[3,4-Dihydroxy-5-[2,3,5-trihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxolan-3-yl]methyl 3-phenylprop-2-enoate	75165979	Click to see	442.40	unknown	https://doi.org/10.1021/NP9004294
[5-[3,5-Dihydroxy-2-(hydroxymethyl)-6-phenylmethoxyoxan-4-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-phenylprop-2-enoate	75165980	Click to see	532.50	unknown	https://doi.org/10.1021/NP9004294
Visartiside D	46184805	Click to see	442.40	unknown	https://doi.org/10.1021/NP9004294
Visartiside E	46184806	Click to see C1C(C(C(O1)OC2C(C(OC(C2O)OCC3=CC=CC=C3)CO)O)O)(COC(=O)C=CC4=CC=CC=C4)O	532.50	unknown	https://doi.org/10.1021/NP9004294
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2R)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162984610	Click to see	464.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
2-[[2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162984609	Click to see	464.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
> 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
(2S)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	162902764	Click to see	464.40	unknown	https://doi.org/10.1248/CPB.52.858
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	154497293	Click to see	434.40	unknown	https://doi.org/10.1248/CPB.52.858
(2S)-7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one	21579629	Click to see	550.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
(2S)-7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one	21672032	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(COC5C(C(CO5)(CO)O)O)O)O)C6=CC=CC=C6	682.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
[(3S,4R,5S)-3,4-dihydroxy-5-[4-[(2S)-5-hydroxy-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-2-yl]-2-methoxyphenoxy]oxolan-3-yl]methyl (E)-3-phenylprop-2-enoate	163195405	Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(CO5)(COC(=O)C=CC6=CC=CC=C6)O)O	726.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl (E)-3-phenylprop-2-enoate	46240246	Click to see	696.60	unknown	https://doi.org/10.1021/NP9004294
[2-[[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-phenylprop-2-enoate	75165905	Click to see	580.50	unknown	https://doi.org/10.1021/NP9004294
[3,4-Dihydroxy-5-[4-[5-hydroxy-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-2-yl]-2-methoxyphenoxy]oxolan-3-yl]methyl 3-phenylprop-2-enoate	162904520	Click to see	726.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
[5-[4,5-Dihydroxy-2-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-phenylprop-2-enoate	75183123	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(COC(=O)C=CC5=CC=CC=C5)O)O)C6=CC=C(C=C6)O	696.60	unknown	https://doi.org/10.1021/NP9004294
[5-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[(5-hydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-7-yl)oxy]oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 3-phenylprop-2-enoate	73804164	Click to see	680.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
[6-[[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-phenylprop-2-enoate	75165906	Click to see	580.50	unknown	https://doi.org/10.1021/NP9004294
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	74819421	Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(CO5)(CO)O)O	596.50	unknown	https://doi.org/10.1055/S-2008-1034283 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-7-[[2-O-[5-O-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-D-apio-beta-D-furanosyl]-beta-D-glucopyranosyl]oxy]-2-phenyl-	21579630	Click to see	680.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
5-Hydroxy-2-phenyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	74819354	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=CC=C4	418.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
7-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one	72827187	Click to see	550.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
7-[3-[4-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-phenyl-2,3-dihydrochromen-4-one	73820745	Click to see	682.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
Eriodictyol 7-glucoside	13254471	Click to see	450.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
Homoeriodictyol 7-O-Beta-D-Glucopyranoside	21629877	Click to see	464.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
Naringenin 7-0-glucoside	282013	Click to see	434.40	unknown	https://doi.org/10.1021/NP9004294 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
Pinocembrin7-O-Beta-D-Glucopyranoside	46881227	Click to see	418.40	unknown	https://doi.org/10.1248/CPB.52.858 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
Prunin	92794	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	434.40	unknown	https://doi.org/10.1021/NP9004294 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/
Visartiside A	46184559	Click to see	580.50	unknown	https://doi.org/10.1021/NP9004294
Visartiside B	46184560	Click to see	580.50	unknown	https://doi.org/10.1021/NP9004294
Visartiside C	46184804	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(COC(=O)C=CC5=CC=CC=C5)O)O)C6=CC(=C(C=C6)O)O	712.60	unknown	https://doi.org/10.1021/NP9004294
Viscumiside A	14035424	Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/ https://doi.org/10.1021/NP9004294
Viscumneoside I	122198191	Click to see	596.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245428/

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Viscum articulatum

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