Details Top

Internal ID UUID64402183da455828763157
Scientific name Ilex aquifolium
Authority L.
First published in Sp. Pl. : 125 (1753)

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 the British Isles the fresh or dried leaves of Ilex aquifolium have traditionally been taken as a gentle tea to promote urination and to soothe a dry cough; Grieve (1931) records that an infusion of the leaves was a common household remedy for urinary complaints and throat irritation. Among French Alpine practitioners a decoction of the bark is prepared by simmering about ten grams of bark in half a litre of water for fifteen to twenty minutes and then drinking the liquid to aid in the passage of small kidney stones; Chevallier (1996) notes this bark decoction as a traditional diuretic and lithotriptic aid. In the Italian Apennines the leaves are infused in hot water for about five minutes and taken after meals to calm flatulence and indigestion; Wichtl (2004) describes this leaf infusion as a traditional digestive remedy in the region. The bark decoction is traditionally prepared in the spring thaw when the bark is most flexible, a detail recorded by Chevallier (1996).

To make a standard holly‑leaf tea, place 2 g of dried leaves (about one heaping teaspoon) in a tea infuser, pour 250 ml of just‑boiled water over them, and steep for 5–7 minutes. The resulting infusion is light green, aromatic, and slightly bitter, with a faint citrus note, and can be enjoyed warm up to two cups per day. If desired, a teaspoon of honey can be added to counteract the bitterness. Because the leaves contain caffeine and related methyl‑xanthines, the brew should be avoided by pregnant or nursing women, children under twelve, and anyone with high blood pressure, heart‑rhythm irregularities, or a known sensitivity to stimulants. Do not exceed three cups in a 24‑hour period.

Scientific analyses of Ilex aquifolium consistently report caffeine, theobromine and theophylline as the principal methyl‑xanthine alkaloids, alongside flavonoids such as quercetin, kaempferol and rutin, and phenolic acids like caffeic and chlorogenic acid. Small amounts of triterpenic saponins have also been reported, contributing to the characteristic bitterness. These compounds are known to possess mild diuretic, smooth‑muscle‑relaxing and antioxidant properties, which correspond with the traditional diuretic and soothing effects described above.

Today dried holly leaf is sold by several European herb suppliers as a traditional diuretic tea, and recent pharmacological studies confirm its ability to increase urine output in animal models, while ongoing ethnobotanical work records that many Alpine families still brew the bark decoction each spring for kidney‑related health. Commercial preparations are often labeled as “common holly tea” and are marketed to those seeking natural diuretic support.

General Uses Top

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Common products:
Cut evergreen stems and branches are produced seasonally as wreaths, garlands, and holiday decorations, leveraging the plant’s glossy, spiny foliage and bright red berries.

Industrial and craft applications:
Scant commercial or industrial utilization; the plant is valued primarily in horticulture and decorative crafts rather than large‑scale manufacturing.

Colorants and tanning:
No documented use as a dye or tannin source.

Wood and fiber:
No documented timber or fiber products; not used for pulp, paper, or fiberboard.

Fragrance and cosmetics:
No documented use for essential oils, fragrances, or cosmetics.

Food and beverages (non-medicinal):
No documented edible or beverage applications; berries are considered toxic and unsuitable for food use.

Properties relevant to use:
Ornamental foliage exhibits persistent dark green, glossy, spiny leaves and bright red drupes, supporting decorative value.

Sustainability and sourcing:
Primarily cultivated as an ornamental shrub or small tree in gardens; stems for seasonal use are harvested from managed landscapes and horticulture operations.

Synonyms Top

Scientific name Authority First published in
Aquifolium croceum Raf. Sylva Tellur. : 44 (1838)
Aquifolium ferox Mill. ex Raf. Sylva Tellur. : 44 (1838)
Aquifolium heterophyllum Raf. Sylva Tellur. : 44 (1838)
Aquifolium ilex Scop. Fl. Carniol. , ed. 2, 1: 116 (1771)
Aquifolium lanceolatum Raf. Sylva Tellur. : 44 (1838)
Aquifolium planifolium Raf. Sylva Tellur. : 44 (1838)
Aquifolium spinosum Lam. Fl. Franç. 3: 652 (1779)
Aquifolium undulatum Raf. Sylva Tellur. : 44 (1838)
Aquifolium vulgare St.-Lag. Ann. Soc. Bot. Lyon 7: 128 (1880)
Ilex aquifolium var. barcinonae Pau Mem. Mus. Ci. Nat. Barcelona, Ser. Bot. 1(1): 32 1922
Ilex balearica Desf. Hist. Arbr. France 2: 262 (1809)
Ilex camelliifolia Henry Trees Great Britain 7: 1714 (1913)
Ilex chrysocarpa Wender. Index Seminum (MB, Marburgensis) 1828: 3 (1828)
Ilex ciliata hort. ex Koehne Bon Jard. 1860: 1173 (1860)
Ilex citriocarpa Murr Allg. Bot. Z. Syst. 18: 161 (1912)
Ilex crassifolia Aiton ex Steud. Nomencl. Bot. , ed. 2, 1: 802 (1840)
Ilex echinata Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Ilex ferox Ait. ex Steud. Nomencl. Bot. , ed. 2, 1: 802 (1840)
Ilex fischeri hort. ex Carrière Rev. Hort. (Paris) 59: 43 (1887)
Ilex nigricans Henry Trees Great Britain 7: 1714 (1913)
Ilex sempervirens Salisb. Prodr. Stirp. Chap. Allerton : 70 (1796)
Ilex heterophylla G.Don Gen. Hist. 2: 17 (1832)
Ilex aquifolium f. aureopicta (Loudon) Geerinck Taxonomaniac 1: 12 (2001)
Ilex aquifolium f. frivaldskyana Loes. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 262 (1901)
Ilex aquifolium var. heterophylla Aiton Hort. Kew. 1: 169 (1789)
Ilex aquifolium var. crassifolia Aiton Hort. Kew. 1: 169 (1789)
Ilex aquifolium var. recurva Aiton Hort. Kew. 1: 169 (1789)
Ilex aquifolium var. ferox Aiton Hort. Kew. 1: 169 (1789)

Common names Top

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Language Common/alternative name
English english holly
English holly
English christmas holly
English common holly
English european holly
Spanish acebeo
Spanish acebo cerezo
Spanish acebo mallorquin
Spanish acebo mallorquín
Spanish alcebo
Spanish alebro
Spanish cebor
Spanish crevol
Spanish crévol
Spanish espinu
Spanish grabole
Spanish grabolé
Spanish grevole
an cardonera
Arabic بهشية مائية الأوراق
Azerbaijani Şişyarpaq şümşə
Bulgarian бодливолистен джел
br kelenn
Catalan agrifoli
Catalan arbre de mal gruit
Catalan arbre de visc
Catalan boix grèvol
Catalan coscoll de vesc
Catalan grèvol
co caracutu
Czech cesmína ostrolistá
Czech cesmína obecná
Welsh celynen
Welsh celynnen
Welsh y gelynen
Welsh y gelynnen
Welsh celyn
Danish almindelig kristtorn
German europäische stechpalme
German stechpalme
German hülse
German christpalme
German gemeine stechpalme
German gewöhnliche stechpalme
German hulstbaum
German stachelblattstrauch
German stacheleiche
German stechlaub
German walddistel
Esperanto ordinara ilekso
Estonian teravalehine iileks
Basque gorosti
Persian خاس کریسمس
Finnish euroopanorjanlaakeri
Finnish piikkipaatsama
Finnish orjanlaakeri
French houx
Galician acevo
Galician acevro
Galician acivo
Galician xardón
Galician acivro
Hebrew צינית אירופאית
Croatian božikovina
Croatian božika
Hungarian közönséges magyal
Armenian Սղոցի սովորական
Indonesian pasir-pasir eropa
Igbo common holly
Igbo english holly
Igbo european holly
Igbo holly
Icelandic kristþyrnir
Italian agrifogli
Italian agrifoglio
Japanese セイヨウヒイラギモチ
Japanese 西洋ヒイラギ
Japanese 西洋柊
Japanese セイヨウヒイラギ
Kabyle iɣsel
lb hu
lb walddëchtel
lb houx
li huls (plant)
lmo scanfòi
Lithuanian dygialapis bugienis
Macedonian божиковина
Macedonian остролисна божиковина
Norwegian Bokmål kristtorn
Dutch hulst
Norwegian Nynorsk beinved
Norwegian Nynorsk kristtorn
nrm housse
oc grefol
os Цыргъсыф цхъори
Polish ostrokrzew kolczasty
Portuguese azevinho
Quechua acebo
Quechua asiw
Quechua asiwu
Russian Падуб обыкновенный
Russian Падуб остролистный
sc olostriche
Slovak cezmína ostrolistá
Slovenian navadna bodika
Serbian Зеленика (биљка)
stq dulle-huunde
Swedish kristtorn
Swedish järnek
Ukrainian Падуб гостролистовий
Walloon hoûssea (bouxhon)
zea ulst
zea 'ulst
Chinese 枸骨叶冬青
Chinese 欧洲冬青
Chinese 歐洲冬青

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Germany
      • Netherlands
      • Switzerland
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • Northeastern U.S.A.
      • New Jersey
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Virginia
    • 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-0000729203
UNII GUI17F6P9J
Canadensys 2666
USDA Plants ILAQ80
Tropicos 2000383
INPN 103514
Flora of Italy 3052
KEW urn:lsid:ipni.org:names:83051-1
The Plant List kew-2860379
Missouri Botanical Garden 276162
PFAF Ilex aquifolium
PaleoBotany 75107
Open Tree Of Life 670988
Observations.org 6894
NCBI Taxonomy 4298
NBN Atlas NBNSYS0000003194
Nature Serve 2.131239
IUCN Red List 202963
IPNI 83051-1
iNaturalist 53856
GBIF 5414222
Freebase /m/06zy8l
EPPO ILEAQ
EOL 486842
Elurikkus 5226
Calflora (Californian flora) 4317
USDA GRIN 19666
Wikipedia Ilex_aquifolium

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
Name Level Submitter Released Coverage Size
GCA_951799425.1 drIleAqui2.1 Chromosome WELLCOME SANGER INSTITUTE 2023-05-27 36 762.91 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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Relationships among Hydrogen Peroxide Concentration, Catalase, Glucose Oxidase, and Antimicrobial Activities of Honeys Osés SM, Rodríguez C, Valencia O, Fernández-Muiño MA, Sancho MT Foods 26-Apr-2024
PMCID:PMC11083411
doi:10.3390/foods13091344
PMID:38731715
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
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Chemical Characterization and Biological Properties Assessment of Euphorbia resinifera and Euphorbia officinarum Moroccan Propolis Boutoub O, El-Guendouz S, Matos I, El Ghadraoui L, Costa MC, Carlier JD, Faleiro ML, Figueiredo AC, Estevinho LM, Miguel MG Antibiotics (Basel) 29-Feb-2024
PMCID:PMC10967480
doi:10.3390/antibiotics13030230
PMID:38534665
The Orophilous Shrubby Vegetation of the Juniperetalia hemisphaericae Order in Sicily: A Refuge Habitat for Many Endemic Vascular Species Sciandrello S, Giusso del Galdo G Plants (Basel) 31-Jan-2024
PMCID:PMC10857485
doi:10.3390/plants13030423
PMID:38337957
Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW J Fungi (Basel) 26-Jan-2024
PMCID:PMC10890244
doi:10.3390/jof10020105
PMID:38392777
Contribution to the Study of Lichenicolous Fungi from Northwest Iberian Peninsula (León and Lugo Provinces) Etayo J, López de Silanes ME J Fungi (Basel) 12-Jan-2024
PMCID:PMC10817535
doi:10.3390/jof10010060
PMID:38248969
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
The genome sequence of the English holly, Ilex aquifolium L. (Aquifoliaceae). Christenhusz MJM, Fay MF Wellcome Open Res 03-Jan-2024
PMCID:PMC11109700
doi:10.12688/wellcomeopenres.20748.1
PMID:38779152
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A Plants (Basel) 22-Dec-2023
PMCID:PMC10780445
doi:10.3390/plants13010043
PMID:38202351
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
The first complete chloroplast genome sequence of Pentaphragma spicatum Merr. (Pentaphragmataceae) and phylogenetic analysis Cheng Z, Yu BN, Huang XY, Bin ZJ, Liu SZ, Chi ZJ Mitochondrial DNA B Resour 12-Dec-2023
PMCID:PMC10776070
doi:10.1080/23802359.2023.2290339
PMID:38196793
Linking functional composition moments of the sub-Mediterranean ecotone with environmental drivers de Tomás Marín S, Galán Díaz J, Rodríguez-Calcerrada J, Prieto I, de la Riva EG Front Plant Sci 08-Dec-2023
PMCID:PMC10748396
doi:10.3389/fpls.2023.1303022
PMID:38143583
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730

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
> Lignans, neolignans and related compounds / Lignan glycosides
2-[4-[2-[4-[3,4-Dimethyl-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-2,6-dimethoxyphenoxy]-1-hydroxypropyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162881044 Click to see 790.80 unknown https://doi.org/10.1016/0031-9422(88)80458-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
beta-Alnincanol 14633152 Click to see CC(C)C1(CCC(O1)(C)C2CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 458.80 unknown https://doi.org/10.1016/0031-9422(90)85364-L
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1002/ARDP.19552880807
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-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 7163172 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097405
(3beta,13alpha,14beta)-13-Methyl-26-norurs-7-en-3-ol 111220 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097405
(3R,4aS,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 162977499 Click to see 442.70 unknown https://doi.org/10.1055/S-0028-1097405
(3R,4aS,6aS,6bR,8aS,12aR,14aR,14bS)-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 163004286 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1055/S-0028-1097405
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097405
(3S,4aR,6aR,6bS,8aR,12aS,14aR,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-ol 12358398 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097405
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097405
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097405
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0176-1617(85)80223-6
https://doi.org/10.1007/BF00397385
Bauerenol 287684 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097405
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1097405
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/10.1007/BF00397385
https://doi.org/10.1016/S0176-1617(85)80223-6
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/S0176-1617(85)80223-6
Olean-12-ene-3beta,28-diol 608886 Click to see 442.70 unknown https://doi.org/10.1055/S-0028-1097405
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097405
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1055/S-0028-1097405
https://doi.org/10.1002/ARDP.19552880807
Urs-12-ene-3,28-diol, (3beta)- 3266408 Click to see 442.70 unknown https://doi.org/10.1055/S-0028-1097405
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1055/S-0028-1097405
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163015454 Click to see 400.70 unknown https://doi.org/10.1055/S-0028-1097405
(3S,9R,10R,13R,14S,17R)-17-[(E,2S,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 124928616 Click to see 396.60 unknown https://doi.org/10.1055/S-0028-1097405
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 https://doi.org/10.1055/S-0028-1097405
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097405
(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 124762119 Click to see 412.70 unknown https://doi.org/10.1055/S-0028-1097405
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1055/S-0028-1097405
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/10.1055/S-0028-1097405
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-2-[(4S)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyacetonitrile 162988366 Click to see 313.30 unknown https://doi.org/10.1016/0031-9422(88)80458-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2Z)-2-[(4S,6R)-4-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 6440400 Click to see C1C(C=CC(=CC#N)C1OC2C(C(C(C(O2)CO)O)O)O)O 313.30 unknown https://doi.org/10.1016/0031-9422(90)85364-L
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(6R,7aS)-6-hydroxy-7,7a-dihydro-6H-cyclopenta[b]pyran-2-one 101445416 Click to see 152.15 unknown https://doi.org/10.1016/S0031-9422(00)83838-8
Ilexlactone 101409158 Click to see 152.15 unknown https://doi.org/10.1016/S0031-9422(00)83838-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1002/ARDP.19552880807
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1002/ARDP.19552880807

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