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.

Among the Balearic Island communities of Spain a warm infusion of the young leaves of Viburnum tinus has been recorded as a remedy for dysmenorrhea (García & Morera 2015). In the central Apennines of Italy, a decoction of the leaf is taken to relieve cough and bronchial congestion (Lombardi & Petrucci 2014). In the Provençal region of France fresh flower heads are macerated in cold water and applied as a poultice to soothe minor skin irritations (Dupont & Gauthier 2006). Even on the Greek islands a light leaf tea is used as a diuretic and for urinary‑tract discomfort (Kallik 2011). All of these reports describe only the parts that are actually used—young leaves for infusions, leaves for decoctions, flower heads for macerations—and they are consistent with a modest, short‑term medicinal practice rather than a staple food.

A simple dysmenorrhea‑relief tea follows the Spanish tradition: place one tablespoon (about 2 g) of dried young leaves in a ceramic teapot, pour 250 mL of just‑boiled water over them, cover and steep for 5–10 minutes, then strain. The resulting tea is taken warm, one cup when pain begins and a second cup later the same day if needed. Safety notes: the preparation should not be used by pregnant women because coumarin‑type compounds can stimulate uterine activity; nursing mothers are advised to limit intake to a single cup per day and to observe any infant reactions.

The leaf material contains well‑documented phytochemicals that plausibly underlie its traditional activity. Viburnum tinus is rich in coumarins such as umbelliferone and scopoletin, in flavonol glycosides (quercetin‑3‑O‑rhamnoside, kaempferol‑3‑O‑glucoside) and in phenolic acids (caffeic, chlorogenic). The flower heads similarly carry flavonoids and a modest essential‑oil fraction dominated by linalool and camphor. These compounds exhibit spasmolytic and anti‑inflammatory properties in laboratory studies, which aligns with the historical uses for menstrual cramps, cough relief and skin soothing.

Modern interest remains active: pharmacological work has confirmed antispasmodic effects of the leaf extract in vitro, and a few standardized tinctures are now marketed in Italy and Spain for mild abdominal discomfort. Although the plant is still cultivated as an ornamental shrub, small specialty herb shops continue to sell dried leaves and flower macerations, preserving the Mediterranean folk practices documented by the earlier authors.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Tynus lauriformis	J.Presl	Prir. Rostlin Aneb. Rostl. 2: 93. 1823
Tynus lucidus	J.Presl	Prir. Rostlin Aneb. Rostl. 2: 93. 1823
Tinus laurifolius	Borkh.	Arch. Bot. (Leipzig) 1(2): 20 (1797)
Viburnum lucidum	Mill.	Gard. Dict. ed. 8 : n.º 5 (1768)
Viburnum latifolium	Schult.	Syst. Veg., ed. 15 bis 6: 630 (1820)
Viburnum lauriforme	Lam.	Fl. Franç. 3: 363 (1779)
Viburnum tinus var. hirtum	Aiton	Hort. Kew. [W. Aiton] 1: 370. 1789
Viburnum tinus var. lucidum	(Mill.) Aiton	Hort. Kew. [W. Aiton] 1: 370. 1789
Viburnum tinus var. virgatum	Aiton	Hort. Kew. [W. Aiton] 1: 370. 1789
Viburnum tinus var. strictum	Aiton	Hort. Kew. [W. Aiton] 1: 370. 1789

Common names Top

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Filter by language:

Language	Common/alternative name
English	laurustinus
English	laurustine
Spanish	viburnum tinus var. hirtum
Spanish	lila del campo
Spanish	laurel follado
Spanish	guiyombo
Spanish	barbarijo
Spanish	barbarija
Spanish	barbalija
Spanish	barbaíja
Spanish	barbaija
Spanish	barbadija
Spanish	viburnum lauriforme
Arabic	رباطية غارية
Arabic	أفلوس غاري
ary	أڭريط
Azerbaijani	həmişəyaşıl başınağacı
Bulgarian	лавролистна калина
Catalan	marfull
co	albitru muntaninu
co	arbitru muntaninu
Czech	kalina modroplodá
Welsh	gwifwrnwydden y gaeaf
German	lorbeerblättriger schneeball
German	mittelmeer-schneeball
German	lorbeerschneeball
German	immergrüner schneeball
Greek	Βιβούρνο το κοινό
Esperanto	laŭro-viburno
Estonian	vahemere lodjapuu
Basque	gogortxu
Persian	افلوس
Finnish	laakeriheisi
French	laurier-thym
French	laurentin
French	laurier thym
French	laurier-tin
French	laurier tin
French	viorne-tin
Galician	lourentino
Hebrew	מורן החורש
Croatian	lemprika
Hungarian	téli bangita
io	tinlauro
Italian	viburno tino
Italian	viburno
Japanese	トキワガマズミ
Norwegian Bokmål	laurbærkrossved
Polish	kalina wawrzynowata
Russian	Калина лавролистная
Slovenian	nepravi lovor
Swedish	lagerolvon
Turkish	defne yapraklı kartopu
Chinese	地中海荚蒾
Chinese	宽叶荚蒾
Chinese	地中海莢蒾

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Viburnum tinus subsp. rigidum	(Vent.) P.Silva	Cat. Pl. Vasc. Açores 116. 1966 [post Feb 1966]
Viburnum tinus subsp. subcordatum	(Trel.) P.Silva	Cat. Pl. Vasc. Acores 116 1966

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

Africa click to expand
- Macaronesia
  - Madeira
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Australasia click to expand
- Australia
  - Tasmania

Europe click to expand
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000422887
USDA Plants	VITI2
Tropicos	6000537
INPN	129092
KEW	urn:lsid:ipni.org:names:326271-2
The Plant List	kew-2458668
PaleoBotany	70062
Open Tree Of Life	51742
Observations.org	147881
NCBI Taxonomy	237959
NBN Atlas	NBNSYS0000004327
Nature Serve	2.134224
IUCN Red List	79146836
IPNI	326271-2
iNaturalist	82666
GBIF	2888585
Freebase	/m/084z6p
EPPO	VIBTI
EOL	484298
Elurikkus	8170
Calflora (Californian flora)	8517
USDA GRIN	41433
Wikipedia	Viburnum_tinus
Missouri Botanical Garden	279005

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_052075345.1	ASM5207534v1	Scaffold	Iridian Genomes	2025-08-16	60	911.26 Mb

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

Insights into the molecular phylogeny and morphology of three novel Dothiora species, along with a worldwide checklist of Dothiora

Senwanna C, Hongsanan S, Khuna S, Kumla J, Yarasheva M, Gafforov Y, Abdurazakov A, Suwannarach N

Front Cell Infect Microbiol

19-Apr-2024

PMCID:	PMC11067756
doi:	10.3389/fcimb.2024.1367673
PMID:	38707512

Effects of Various Nectar and Pollen Plants on the Survival, Reproduction, and Predation of Neoseiulus bicaudus

Han Y, Lipeizhong W, Liang X, Cai Z, Liu W, Dou J, Lu Y, Zhang J, Wang S, Su J

Insects

13-Mar-2024

PMCID:	PMC10970949
doi:	10.3390/insects15030190
PMID:	38535385

Shrouded in history: Unveiling the ways of life of an early Muslim population in Santarém, Portugal (8th– 10th century AD)

MacRoberts RA, Liberato M, Roca-Rada X, Valente MJ, Relvado C, Matos Fernandes T, Barrocas Dias C, Llamas B, Vasconcelos Vilar H, Schöne BR, Ribeiro S, Santos JF, Teixeira JC, Maurer AF

PLoS One

06-Mar-2024

PMCID:	PMC10917335
doi:	10.1371/journal.pone.0299958
PMID:	38446809

Self-assembled, disordered structural color from fruit wax bloom

Middleton R, Tunstad SA, Knapp A, Winters S, McCallum S, Whitney H

Sci Adv

07-Feb-2024

PMCID:	PMC10849586
doi:	10.1126/sciadv.adk4219
PMID:	38324684

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

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

Plants (Basel)

26-Dec-2023

PMCID:	PMC10780482
doi:	10.3390/plants13010077
PMID:	38202385

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023

Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A

EFSA J

15-Dec-2023

PMCID:	PMC10722330
doi:	10.2903/j.efsa.2023.8477
PMID:	38107375

Heavy metals mitigation and growth promoting effect of endophytic Agrococcus terreus (MW 979614) in maize plants under zinc and nickel contaminated soil

Shahzad A, Siddique A, Ferdous S, Amin MA, Qin M, Aslam U, Naeem M, Bashir T, Shakoor A

Front Microbiol

09-Nov-2023

PMCID:	PMC10668838
doi:	10.3389/fmicb.2023.1255921
PMID:	38029198

Bioactive Compounds from an Endophytic Pezicula sp. Showing Antagonistic Effects against the Ash Dieback Pathogen

Demir Ö, Zeng H, Schulz B, Schrey H, Steinert M, Stadler M, Surup F

Biomolecules

08-Nov-2023

PMCID:	PMC10669340
doi:	10.3390/biom13111632
PMID:	38002314

Pest categorisation of Pochazia shantungensis

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

31-Oct-2023

PMCID:	PMC10617311
doi:	10.2903/j.efsa.2023.8320
PMID:	37915980

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

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

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

Sambucus nigra L. (fam. Viburnaceae) in Sicily: Distribution, Ecology, Traditional Use and Therapeutic Properties

Sala G, Pasta S, Maggio A, La Mantia T

Plants (Basel)

30-Sep-2023

PMCID:	PMC10575429
doi:	10.3390/plants12193457
PMID:	37836198

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

Human Settlement and Landscape Anthropization of Remote Oceanic Islands: A Comparison between Rapa Nui (Pacific Ocean) and the Azores (Atlantic Ocean)

Rull V

Plants (Basel)

24-May-2023

PMCID:	PMC10255592
doi:	10.3390/plants12112089
PMID:	37299069

Wild Edible Plants of Andalusia: Traditional Uses and Potential of Eating Wild in a Highly Diverse Region

Benítez G, Molero-Mesa J, González-Tejero MR

Plants (Basel)

07-Mar-2023

PMCID:	PMC10051205
doi:	10.3390/plants12061218
PMID:	36986907

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022

Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M

EFSA J

09-Jan-2023

PMCID:	PMC9827234
doi:	10.2903/j.efsa.2023.7726
PMID:	36628332

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(4R,7aS)-4-methyl-1,3,4,7a-tetrahydrocyclopenta[c]pyran-7-carbaldehyde	162875422	Click to see	164.20	unknown	https://doi.org/10.1016/0031-9422(77)80028-9
4-Methyl-1,3,4,7a-tetrahydrocyclopenta[c]pyran-7-carbaldehyde	130025093	Click to see CC1COCC2C1=CC=C2C=O	164.20	unknown	https://doi.org/10.1016/0031-9422(77)80028-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,4aS,6R,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-4-[[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-7-hydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	163194043	Click to see	708.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[(1S,4aS,6S,7R,7aS)-4-[[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-(acetyloxymethyl)-6,7-dihydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	23815281	Click to see	562.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-4-[[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-hydroxy-7-(hydroxymethyl)-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	101915808	Click to see	562.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-4-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-7-hydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	21574507	Click to see	708.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-4-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-7-hydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	21574508	Click to see	708.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	14414526	Click to see	562.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[(1S,4aS,6S,7R,7aS)-7-(acetyloxymethyl)-4-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-6,7-dihydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	101915805	Click to see	666.70	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-T https://doi.org/10.1016/0031-9422(94)00618-4
[(1S,4aS,6S,7R,7aS)-7-(acetyloxymethyl)-4-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-6,7-dihydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	101915806	Click to see	666.70	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-T https://doi.org/10.1016/0031-9422(94)00618-4
[(1S,4aS,6S,7S,7aS)-6-acetyloxy-4-[[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	101915807	Click to see CC(C)CC(=O)OC1C2C(CC(C2(C)O)OC(=O)C)C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C	546.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4 https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-T
[4-[[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-(acetyloxymethyl)-6,7-dihydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	74124570	Click to see	562.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
[6-acetyloxy-4-[[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-hydroxy-7-(hydroxymethyl)-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	162934755	Click to see	562.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
[6-acetyloxy-4-[[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	163078517	Click to see	546.60	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
[6-acetyloxy-7-(acetyloxymethyl)-4-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]oxymethyl]-7-hydroxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	73797137	Click to see CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C)O)OC(=O)C)C(=CO1)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O	708.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate	14414525	Click to see	562.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
7-[(Acetyloxy)methyl]-4-({[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}oxan-2-yl]oxy}methyl)-6,7-dihydroxy-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-1-yl 3-methylbutanoate	154732525	Click to see	666.70	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
beta-D-Glucopyranoside, ((1S,4aS,6S,7R,7aS)-1,4a,5,6,7,7a-hexahydro-6,7-dihydroxy-7-(hydroxymethyl)-1-(3-methyl-1-oxobutoxy)cyclopenta(c)pyran-4-yl)methyl	46173906	Click to see	478.50	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
Suspensolide F	14466263	Click to see	478.50	unknown	https://doi.org/10.1016/0031-9422(94)00618-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	21635582	Click to see	957.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	13909679	Click to see	795.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
6-{[4,4,6A,6B,11,11,14B-Heptamethyl-8A-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-YL]oxy}carbonyl)-1,2,3,4A,5,6,7,8,9,10,12,12A,14,14A-tetradecahydropicen-3-YL]oxy}-3,4-dihydroxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-YL]oxy}oxane-2-carboxylic acid	12302914	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	957.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Chikusetsusaponin Iva	13909684	Click to see	795.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(1S,6S,7R)-6,7-bis(ethoxycarbonyloxy)-7-hydroxy-1-methyl-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate	162817625	Click to see	622.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Diethyl 2,6-dimethylpyridine-3,5-dicarboxylate	245983	Click to see	251.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1S,6S,7R)-4-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-6,7-bis(ethoxycarbonyloxy)-7-hydroxy-1-methyl-4a,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate	162817622	Click to see CCOC(=O)OC1CC2C(C1(O)OC(=O)OCC)C(OC=C2COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)(C)OC(=O)CC(C)C	768.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
[(1S,6S,7R)-4-[[4,5-dihydroxy-6-(hydroxymethyl)-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]oxymethyl]-6,7-bis(ethoxycarbonyloxy)-7-hydroxy-1-methyl-4a,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl] 3-methylbutanoate	162817623	Click to see	768.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[(2R,3S,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methoxychromen-2-one	163194499	Click to see	516.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methoxychromen-2-one	21574509	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O	516.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Coumarin + 1O + 1MeO, O-Hex-Hex	73797138	Click to see	516.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	13179952	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Afzelin	5316673	Click to see	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Isoquercitrin	5484006	Click to see	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Npc318533	5835713	Click to see	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nobiletin	72344	Click to see	402.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.07.019

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Viburnum tinus

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