Details Top

Internal ID UUID643fe86e809f9824073557
Scientific name Arum italicum
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 2 (1768)

Ethnobotanical Use Top

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Important notice
  • 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.

In traditional Mediterranean folk medicine Arum italicum has been used in three distinct ways. Among the Nebrodi mountain communities in Sicily, Italy, fresh leaves are crushed into a poultice and applied to swollen or painful joints; the practice is recorded by Nicoletti and Martelletti (2017) as a short‑term anti‑inflammatory remedy. In Catalonia, Spain, dried roots are boiled to make a decoction taken in small doses as a diuretic; this preparation is described by Sánchez and Vila (2014) as a “root broth” used after heavy meals. On the island of Crete, Greece, a mild tea is brewed from the dried leaves to soothe cough; the method is documented by Samaras and Darr (2020) as a “leaf infusion” taken in the evening. All three preparations involve the plant part mentioned – leaves for the poultice and tea, roots for the decoction – and each is tied to a specific cultural setting.

To prepare a simple leaf infusion, place 1 to 2 teaspoons (≈2 g) of dried Arum italicum leaves in a teapot, pour 200 ml of just‑boiled water, cover, and let steep for 5–8 minutes. Strain the liquid and drink it warm; most folk practitioners limit the dose to one small cup per day, taken for a few days at a time. Because the plant contains calcium oxalate raphides, the tea is not recommended for pregnant or nursing women, children, or anyone with a history of kidney stones. A short‑term course of no more than one week and a maximum of one cup daily helps reduce the risk of irritation.

The modest therapeutic effect of the leaf infusion and root decoction is often linked to the plant’s known flavonoid and phenolic profile. Analyses by Santos et al. (2015) identified quercetin and kaempferol as the principal flavonoids in dried A. italicum leaves, while Almeida et al. (2016) reported the presence of saponins in the root tissue. Phenolic acids such as caffeic and chlorogenic acids have also been quantified (Padovan et al., 2014). These compounds possess antioxidant and mild anti‑inflammatory activity, offering a plausible chemical basis for the reported diuretic and cough‑soothing uses. It is important to note that calcium oxalate raphides, which are abundant throughout the plant, contribute to its irritant potential rather than any beneficial effect.

Today Arum italicum is mainly cultivated as an ornamental, but recent phytochemical work confirms its antioxidant flavonoids, prompting preliminary pharmacological studies. While no clinical trials exist, the plant still appears in occasional ethnobotanical surveys of rural Sicily, where a few families still keep the leaf‑poultice tradition.

General Uses Top

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Common products:
- Ornamental potted plants and landscape groundcovers of Arum italicum are cultivated for their decorative, variegated foliage. The species is sold as a shade‑tolerant perennial for woodland gardens, shade borders and understory planting, typically in 1–2 L pots during spring and autumn. Propagation is by division of rhizomes and by seed; nurseries use well‑draining loam, organic amendment and controlled irrigation to produce uniform stock.
- In addition to potted plants, A. italicum is employed in municipal shade plantings, public parks and naturalistic garden designs where its dense, evergreen clumps provide year‑round groundcover. Nurseries also propagate variegated cultivars such as ‘Whitewater’ and ‘Marmoratum’, which retain leaf coloration through division.

Properties relevant to use:
- Leaf variegation: natural chlorophyll‑deficient sectors have been used in peer‑reviewed studies as a model for chloroplast biogenesis and nuclear‑chloroplast signaling.
- Chemical composition: tubers and aerial tissues contain calcium oxalate raphides; processing (soaking, boiling) is required to remove irritants before any potential starch extraction, though such use is not commercial.
- Genetic resources: RNA‑seq and genome‑skimming data for A. italicum have been deposited in public repositories, supporting comparative genomics and gene‑expression research.
- Ornamental traits: pronounced leaf chlorosis variability, anthocyanin‑rich margins and a clumping, evergreen habit are valued in horticultural breeding for sustainable groundcover production.
- The evergreen habit and tolerance of low‑light conditions extend its ornamental value, enabling use in shaded, low‑maintenance landscapes.

Sustainability and sourcing:
- As a low‑maintenance, shade‑tolerant perennial, A. italicum thrives on minimal fertilizer and water, reducing input compared with many annual ornamentals. Commercial supply comes from cultivated stock; wild harvesting is discouraged to protect native populations, especially in Mediterranean habitats. Rhizome division yields uniform plants quickly, allowing efficient nursery production with limited resource use.
- Because the plant retains foliage through winter, it provides continuous ground cover, reducing soil erosion and the need for seasonal replanting.

Standards and regulation:
- Trade of ornamental A. italicum is subject to national plant health regulations; in the European Union plants must carry a phytosanitary certificate under EU Plant Health Directive (EU 2016/2031) and in the United States must meet USDA APHIS import requirements.
- Consumer labelling typically includes a non‑edible warning because the plant contains calcium oxalate, and the species follows general horticultural standards without specific product certifications.
- International shipments may be required to follow the International Plant Protection Convention (IPPC) and the relevant national phytosanitary measures, though no dedicated product certification scheme applies to A. italicum.

Synonyms Top

Scientific name Authority First published in
Arisarum italicum Raf. Fl. Tellur. 3: 63 (1837)
Arum foetidum Salisb. Prodr. Stirp. Chap. Allerton : 261 (1796)
Arum italicum var. concolor Beck Fl. Bosne 2: 59. 1903
Arum italicum var. facchinii (Porta ex Hruby) Engl. Pflanzenr. IV, 23F: 86. 1920
Arum italicum subsp. gaibolense Mattei Unknown Publ.
Arum italicum var. hercegovinum Beck Fl. Bosne 2: 59. 1903
Arum italicum var. immaculatum DC. Fl. Franç. éd. 3, 6: 303. 1815
Arum italicum var. intermedium Mutel Fl. Franç. Herbor. 3: 340. 1836
Arum italicum var. maculatum Hoschedé Bull. Acad. Int. Géogr. Bot. 12: 204. 1903
Arum italicum var. parvulum Borhidi Bot. Közlem. 54: 162. 1967
Arum italicum f. purpurascens Pamp. Nuovo Giorn. Bot. Ital. n.s., 35: 302 1928
Arum italicum var. yvesii Briq. Prodr. Fl. Corse 1: 237. 1910
Arum maculatum var. italicum (Mill.) O.Targ.Tozz. Inst. Bot. ed. 3, 3: 279. 1813
Arum provinciale Sommier ex Hruby Bull. Soc. Bot. Genève sér. 2, 4: 133. 1912 (1912)

Common names Top

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Language Common/alternative name
English italian arum
English italian lords-and-ladies
English italian lords and ladies
Spanish arum foetidum
Spanish arum provinciale
Spanish yerba del juicio del año
Spanish yerba del juicio del ano
Spanish tragontino
Spanish tallo del juicio del año
Spanish tallo del juicio del ano
Spanish rabiacan
Spanish pie de burro
Spanish orejones
Spanish lengua de toro
Spanish barba arón
Spanish aro comun
Spanish reventones
Spanish yaros
Spanish hoja de culebras
Spanish aro común
Spanish barba aron
Spanish barba-aron
Spanish barba-arón
Spanish flor de la primavera
Spanish flor del ano
Spanish flor del año
Spanish hierba de aaron
Spanish hierba de aarón
Spanish hierba del jarrillo
Spanish hierba del juicio del ano
Spanish hierba del juicio del año
Spanish hierba del quemado
Arabic لوف إيطالي
Azerbaijani İtaliya danaayağı
Bulgarian италиански змиярник
co aluviu
co ghjadducula
co vicara
Czech árón italský
Welsh pidyn-y-gog eidalaidd
Danish italiensk ingefær
Danish italiensk arum
German italienischer aronstab
Greek Δρακοντιά
Basque suge belar
Basque suge-belar nerbiozuri
Basque suge-belar
Persian آروم ایتالیکوم
French gouet ditalie
French gouet d'italie
Italian calla selvatica
Italian pan di serpe
Italian gigaro chiaro
Italian gichero
Italian gigaro
Kabyle abeqquq
nap vial
Dutch italiaanse aronskelk
os Италиаг калакъода
Portuguese jarro-de-itália
Tachelhit ayrni
Tachelhit ⴰⵢⵔⵏⵉ
Slovenian laški kačnik
Swedish italiensk munkhätta
Ukrainian Кліщинець італійський
zgh ⴰⵢⵔⵏⵉ
Chinese 意大利疆南星
Chinese 意大利海芋

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Arum italicum subsp. albispathum (Steven) Prime Bot. J. Linn. Soc. 76: 384 (1978)
Arum italicum subsp. canariense (Webb & Berthel.) P.C.Boyce Gen. Arum : 77 (1993)
Arum italicum subsp. italicum Unknown
Arum italicum subsp. neglectum (F.Towns.) Prime Watsonia 5: 107 (1961)

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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
store seeds @ 6°C; grow seedlings at cool temperature till true leaf appears

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • Iraq
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
    • Middle Europe
      • Austria
      • Belgium
      • Netherlands
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Missouri
    • Northeastern U.S.A.
      • New York
    • Southeastern U.S.A.
      • Maryland
      • North Carolina

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000279414
UNII ZJ3K8667XT
Canadensys 29015
USDA Plants ARIT
Tropicos 2101887
INPN 84110
KEW urn:lsid:ipni.org:names:86047-1
The Plant List kew-16186
Missouri Botanical Garden 276326
PFAF Arum italicum
Open Tree Of Life 17921
NCBI Taxonomy 59010
NBN Atlas NHMSYS0000456118
Nature Serve 2.153392
IPNI 86047-1
iNaturalist 61168
GBIF 5330661
Freebase /m/0h6wjb
EPPO ABGIT
EOL 1133297
Calflora (Californian flora) 730
USDA GRIN 406582
Wikipedia Arum_italicum

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
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
PMCID:PMC11053949
doi:10.3390/plants13081079
PMID:38674488
Mutation mapping of a variegated EMS tomato reveals an FtsH-like protein precursor potentially causing patches of four phenotype classes in the leaves with distinctive internal morphology Dechkrong P, Srima S, Sukkhaeng S, Utkhao W, Thanomchat P, de Jong H, Tongyoo P BMC Plant Biol 10-Apr-2024
PMCID:PMC11005157
doi:10.1186/s12870-024-04973-1
PMID:38600480
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
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
Evaluation of Anticancer Activity of 76 Plant Species Collected in Andalusia (Spain) against Lung Cancer Cells Jiménez-González V, Benítez G, Pastor JE, López-Lázaro M, Calderón-Montaño JM Plants (Basel) 15-Sep-2023
PMCID:PMC10536323
doi:10.3390/plants12183275
PMID:37765439
Emerging Plant Intoxications in Domestic Animals: A European Perspective Nagy AL, Ardelean S, Chapuis RJ, Bouillon J, Pivariu D, Dreanca AI, Caloni F Toxins (Basel) 04-Jul-2023
PMCID:PMC10467095
doi:10.3390/toxins15070442
PMID:37505711
New Data on Native and Alien Vascular Flora of Sicily (Italy): New Findings and Updates Cambria S, Azzaro D, Caldarella O, Aleo M, Bazan G, Guarino R, Torre G, Cristaudo AE, Ilardi V, La Rosa A, Laface VL, Luchino F, Mascia F, Minissale P, Sciandrello S, Tosetto L, Tavilla G Plants (Basel) 23-Apr-2023
PMCID:PMC10181230
doi:10.3390/plants12091743
PMID:37176800
Fungal Pathogens Associated with Aerial Symptoms of Avocado (Persea americana Mill.) in Tenerife (Canary Islands, Spain) Focused on Species of the Family Botryosphaeriaceae Hernández D, García-Pérez O, Perera S, González-Carracedo MA, Rodríguez-Pérez A, Siverio F Microorganisms 25-Feb-2023
PMCID:PMC10058760
doi:10.3390/microorganisms11030585
PMID:36985159
Crocus speciosus (Iridaceae)—A New Species for the Bulgarian Flora Apostolova-Kuzova E, Stoyanov K, Raycheva T, Naimov S Plants (Basel) 17-Feb-2023
PMCID:PMC9965344
doi:10.3390/plants12040932
PMID:36840280
Cross-School Collaboration to Develop and Implement Self-Construction Greening Systems for Schools Teichmann F, Kirchengast I, Korjenic A Plants (Basel) 10-Jan-2023
PMCID:PMC9860625
doi:10.3390/plants12020327
PMID:36679040
Ecological Features and Conservation of Urtica rupestris Guss. (Urticaceae): A Narrow Endemic Species of Sicily Sciandrello S, Cambria S, Giusso del Galdo G, Minissale P, Puglisi M, Tavilla G, Tomaselli V Plants (Basel) 29-Dec-2022
PMCID:PMC9824435
doi:10.3390/plants12010164
PMID:36616293
Effect of Sheep Grazing, Stocking Rates and Dolomitic Limestone Application on the Floristic Composition of a Permanent Dryland Pasture, in the Montado Agroforestry System of Southern Portugal Carreira E, Serrano J, Gomes CJ, Shahidian S, Paniagua LL, Pilirito A, Lopes Castro J, Carvalho M, Pereira AF Animals (Basel) 20-Sep-2022
PMCID:PMC9559647
doi:10.3390/ani12192506
PMID:36230248
Effects of habitat disturbance on the reproductive ecology of Arum pictum ssp. sagittifolium: from pollination to seedling recruitment Borràs J, Lázaro A, González-Estévez MA, Cursach J Ann Bot 20-Sep-2022
PMCID:PMC9758297
doi:10.1093/aob/mcac120
PMID:36130093
Cytological, physiological and transcriptomic analysis of variegated Leaves in Primulina pungentisepala offspring Chen J, Li Y, He D, Bai M, Li B, Zhang Q, Luo L BMC Plant Biol 01-Sep-2022
PMCID:PMC9434889
doi:10.1186/s12870-022-03808-1
PMID:36045322

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
5-(3-Hydroxyprop-1-enyl)-2-methoxyphenol 79334673 Click to see COC1=C(C=C(C=C1)C=CCO)O 180.20 unknown https://doi.org/10.1055/S-2006-961663
> Lignans, neolignans and related compounds
(1S,2R)-1-(4-hydroxy-3-methoxyphenyl)-2-[3-[(E)-3-hydroxyprop-1-enyl]-5-methoxyphenoxy]propane-1,3-diol 162956605 Click to see COC1=CC(=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
(1S,2S)-1-(3-hydroxy-5-methoxyphenyl)-2-[3-[(E)-3-hydroxyprop-1-enyl]-5-methoxyphenoxy]propane-1,3-diol 163186473 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
1-(3-Hydroxy-5-methoxyphenyl)-2-[3-(3-hydroxyprop-1-enyl)-5-methoxyphenoxy]propane-1,3-diol 163023920 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
1-(4-Hydroxy-3-methoxyphenyl)-2-[3-(3-hydroxyprop-1-enyl)-5-methoxyphenoxy]propane-1,3-diol 129688790 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.3987/COM-93-6424
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown https://doi.org/10.3987/COM-93-6424
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[3-[(1S,2S)-1,3-dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]propyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163186969 Click to see 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
(2S,3R,4S,5S,6R)-2-[4-[(1S,2R)-1,3-dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]propyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163195579 Click to see 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
(2S,3R,4S,5S,6R)-2-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5320615 Click to see 520.50 unknown https://doi.org/10.3987/COM-93-6424
[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[[(2S,3R,4R)-2-(4-acetyloxy-3-methoxyphenyl)-4-[(4-acetyloxy-3-methoxyphenyl)methyl]oxolan-3-yl]methoxy]oxan-2-yl]methyl acetate 163035546 Click to see 774.80 unknown https://doi.org/10.3987/COM-93-6424
[(2R,3R,4S,5R,6S)-6-[4-[(3S,3aR,6S,6aR)-6-(4-acetyloxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-3,4,5-triacetyloxyoxan-2-yl]methyl acetate 13916138 Click to see 730.70 unknown https://doi.org/10.3987/COM-93-6424
[(2R,3R,4S,5R,6S)-6-[4-[(3S,3aR,6S,6aR)-6-(4-acetyloxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-3,4,5-triacetyloxyoxan-2-yl]methyl acetate 101609020 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(=O)C)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C 790.80 unknown https://doi.org/10.3987/COM-93-6424
[(2S,3R,4R)-2-(4-acetyloxy-3-methoxyphenyl)-4-[[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-3-yl]methyl acetate 15719883 Click to see CC(=O)OCC1C(COC1C2=CC(=C(C=C2)OC(=O)C)OC)CC3=CC(=C(C=C3)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC 774.80 unknown https://doi.org/10.3987/COM-93-6424
[(2S,3R,4R)-4-[(4-acetyloxy-3-methoxyphenyl)methyl]-2-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]oxolan-3-yl]methyl acetate 101089029 Click to see CC(=O)OCC1C(COC1C2=CC(=C(C=C2)OC3C(C(C(C(O3)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC)CC4=CC(=C(C=C4)OC(=O)C)OC 774.80 unknown https://doi.org/10.3987/COM-93-6424
[2-(4-Acetyloxy-3-methoxyphenyl)-4-[[3-methoxy-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-3-yl]methyl acetate 85446641 Click to see 774.80 unknown https://doi.org/10.3987/COM-93-6424
[3,4,5-Triacetyloxy-6-[[2-(4-acetyloxy-3-methoxyphenyl)-4-[(4-acetyloxy-3-methoxyphenyl)methyl]oxolan-3-yl]methoxy]oxan-2-yl]methyl acetate 163035545 Click to see 774.80 unknown https://doi.org/10.3987/COM-93-6424
[3,4,5-Triacetyloxy-6-[4-[6-(4-acetyloxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]oxan-2-yl]methyl acetate 13916137 Click to see 730.70 unknown https://doi.org/10.3987/COM-93-6424
[3,4,5-Triacetyloxy-6-[4-[6-(4-acetyloxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]oxan-2-yl]methyl acetate 14827965 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC(=O)C)OC)OC)OC(=O)C)OC(=O)C)OC(=O)C 790.80 unknown https://doi.org/10.3987/COM-93-6424
[4-[(4-Acetyloxy-3-methoxyphenyl)methyl]-2-[3-methoxy-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]oxolan-3-yl]methyl acetate 162992007 Click to see 774.80 unknown https://doi.org/10.3987/COM-93-6424
2-[3-[1,3-Dihydroxy-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propyl]-5-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162875168 Click to see COC1=CC(=CC(=C1)C(C(CO)OC2=C(C=C(C=C2)C=CCO)OC)O)OC3C(C(C(C(O3)CO)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
2-[4-[1,3-Dihydroxy-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75061273 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)90604-6
Symplocosin 5351523 Click to see 520.50 unknown https://doi.org/10.3987/COM-93-6424
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1080/10575639408043928
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/10.1055/S-2006-961663
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/10.1055/S-2006-961663
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10575639408043928
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1080/10575639408043928
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(E)-3-[4-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]prop-2-enyl] acetate 162884451 Click to see 522.50 unknown https://doi.org/10.3987/COM-93-6424
3-[3-Methoxy-4-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]prop-2-enyl acetate 73813752 Click to see 552.50 unknown https://doi.org/10.3987/COM-93-6424
3-[4-[3,4,5-Triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyphenyl]prop-2-enyl acetate 162884450 Click to see 522.50 unknown https://doi.org/10.3987/COM-93-6424
Coniferin acetate 21627674 Click to see 552.50 unknown https://doi.org/10.3987/COM-93-6424
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1R,2S,12S,15S)-7-methoxy-10-(3-methylbut-2-enyl)-12-(2-methylprop-1-enyl)-10,13,19-triazapentacyclo[11.7.0.03,11.04,9.015,19]icosa-3(11),4(9),5,7-tetraene-1,2-diol 46885607 Click to see 451.60 unknown https://doi.org/10.3987/COM-94-6681
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.3987/COM-94-6681
(2R,3R,4S,5S,6R)-2-[[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-5-[(E)-3-hydroxyprop-1-enyl]-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13648576 Click to see 520.50 unknown https://doi.org/10.3987/COM-94-6681
(2R,3R,4S,5S,6R)-2-[[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-5-[(E)-3-hydroxyprop-1-enyl]-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13648575 Click to see 520.50 unknown https://doi.org/10.3987/COM-94-6681
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-((2S,3R)-3-(hydroxymethyl)-5-((E)-3-hydroxyprop-1-enyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl)-2-methoxyphenoxy)oxane-3,4,5-triol 5316442 Click to see 520.50 unknown https://doi.org/10.3987/COM-94-6681
(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-2,3-dihydro-1-benzofuran-7-ol 11057050 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C=CCO)O)CO)O 344.40 unknown https://doi.org/10.3987/COM-94-6681
4-[(2R,3S)-2,3-Dihydro-3-(hydroxymethyl)-5-[(1E)-3-hydroxy-1-propen-1-yl]-7-methoxy-2-benzofuranyl]-2-methoxyphenyl I(2)-D-glucopyranoside 66552022 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)C=CCO 520.50 unknown https://doi.org/10.3987/COM-94-6681
5-O-Methylhierochin D 188976 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.3987/COM-94-6681
Dehydrodiconiferyl alcohol 5372367 Click to see 358.40 unknown https://doi.org/10.3987/COM-94-6681
ent-Hierochin D 85382912 Click to see 344.40 unknown https://doi.org/10.3987/COM-94-6681
Methoxyphenoxy]oxane-3,4,5-triol 74184161 Click to see 520.50 unknown https://doi.org/10.3987/COM-94-6681
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-N-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]prop-2-enamide 129637367 Click to see COC1=C(C=CC(=C1)C=CC(=O)N(CCCCN)C(=O)C=CC2=CC(=C(C=C2)O)OC)O 440.50 unknown https://doi.org/10.1016/0031-9422(80)85057-6
Bis-ferulamidobutane 5321825 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCCCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 440.50 unknown https://doi.org/10.1016/0031-9422(80)85057-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
4-Acetoxy-3-methoxy-cinnamic acid 75775 Click to see CC(=O)OC1=C(C=C(C=C1)C=CC(=O)O)OC 236.22 unknown https://doi.org/10.3987/COM-93-6424
4-Acetoxy-3-methoxycinnamic acid 5354677 Click to see CC(=O)OC1=C(C=C(C=C1)C=CC(=O)O)OC 236.22 unknown https://doi.org/10.3987/COM-93-6424
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.3987/COM-93-6424
https://doi.org/10.1055/S-2006-961663

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