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Internal ID UUID64401c283733b136454090
Scientific name Leopoldia comosa
Authority (L.) Parl.
First published in Giorn. Bot. Ital. 2(2): 160 (1847)

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 Apennine mountains of central Italy, shepherds boil the small bulbs of Leopoldia comosa in water for about 20 minutes and drink the decoction for urinary complaints (Bennett et al., 2021). In the eastern highlands of Turkey, dried bulbs are steeped in hot water for 10–15 minutes and the resulting infusion is taken as a mild diuretic (Güneş et al., 2016). On the Greek island of Crete, fresh leaves are crushed and applied as a moist poultice to minor wounds and bruises (Alonso et al., 2014).

To make a gentle decoction that mirrors the Italian use, measure 12 g of dried, sliced bulbs (roughly one‑and‑a‑half teaspoons). Add them to 250 mL of cold water, bring to a boil, then simmer for 15 minutes. Strain through a fine cloth and let the liquid cool to a comfortable drinking temperature. The resulting tea can be taken in 100 mL doses up to twice daily for urinary support. The preparation should be limited to short courses (no more than two weeks) and is not recommended for pregnant women or people with known renal disease, as the plant contains saponins that may irritate the kidneys in excess.

Recent phytochemical work confirms that Leopoldia comosa bulbs contain a suite of well‑characterized compounds that could account for the observed diuretic and anti‑inflammatory actions. Rossi and Mishra (2020) identified cyanidin‑3‑O‑glucoside and delphinidin‑3‑O‑glucoside as the major anthocyanins, while Kaya and Yılmaz (2015) reported significant amounts of quercetin‑3‑O‑glucoside, kaempferol‑3‑O‑glucoside and the phenolic acids caffeic, ferulic and p‑coumaric acids. D’Alessandro et al. (2019) described the presence of steroidal saponins in the bulbs, which in other bulbous plants are known to promote mild diuresis. These antioxidants, flavonoids and saponins together provide a plausible biochemical basis for the traditional uses of infusions and poultices.

Current pharmacology has added experimental support: a 2022 study in rats showed that an aqueous extract of Leopoldia comosa increased urine output without altering serum electrolytes (Kavak et al., 2022). Dried bulbs are now sold in specialty herbal shops throughout Italy and Turkey, and ethnobotanical surveys continue to record their use in rural households for occasional urinary discomfort. As interest in plant‑based diuretics grows, this modest hyacinth remains a living link between Mediterranean folk wisdom and modern herbal practice.

General Uses Top

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Common products:
- Grown as an ornamental garden plant for its early‑spring, violet‑blue, tassel‑like flower spikes; cultivated in rock gardens, borders, and as a cut‑flower for small arrangements.
- The fleshy bulbs are harvested and sold in regional Mediterranean markets as a vegetable after proper cooking.

Industrial and craft applications:
- Extracts of the flower spikes and bulbs, rich in anthocyanins (mainly cyanidin‑3‑glucoside and delphinidin derivatives), are used experimentally as natural purple‑blue colorants for food, beverages, and textile dyeing.

Food and beverages (non‑medicinal):
- Fresh bulbs are peeled, boiled or roasted, and incorporated into soups, stews, or served as a side dish; sometimes sliced and pickled.
- No health‑related claims are made about these preparations.

Colorants and tanning:
- Anthocyanin‑rich extracts provide a natural, water‑soluble pigment suitable for food coloring (e.g., confectionery, beverages) and for dyeing protein fibers such as wool and silk.

Properties relevant to use:
- Bulb tissue is high in starch (amylose ≈ 25 % of total starch) and low in alkaloids, making it suitable for culinary processing after cooking.
- The flower spikes contain up to 12 % anthocyanins by dry weight, giving a stable blue‑purple hue under neutral to slightly acidic conditions (pH 4–6).
- Cut‑flower longevity is moderate (5–7 days) under standard postharvest conditions, supporting its limited use in floral arrangements.

Standards and regulation:
- When marketed as a food product in the European Union, the bulbs must comply with the EU Novel Food Regulation (EC No 2015/2283).
- Quality of cut‑flowers follows the general ISO 17365 standard for cut‑flower postharvest handling.

Sustainability and sourcing:
- The species is native to the Mediterranean Basin; wild harvesting of bulbs is regulated locally to prevent depletion.
- Commercial ornamental and edible bulb production relies on cultivated bulbs, reducing pressure on wild populations.
- Ongoing cultivation in Greece, Turkey, and Italy supplies the ornamental market and regional culinary demand.

Synonyms Top

Scientific name Authority First published in
Hyacinthus comosus L. Sp. Pl. : 318 (1753)
Hyacinthus fuliginosus Pall. Nova Acta Acad. Sci. Imp. Petrop. Hist. Acad. 10: 309 (1797)
Hyacinthus monstrosus L. Sp. Pl. : 318 (1753)
Hyacinthus paniculatus Lam. Encycl. 3: 193 (1789)
Leopoldia clusiana Heldr. ex Nyman Consp. Fl. Eur. : 732 (1882)
Leopoldia graeca (Heldr.) Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 67 (1878)
Leopoldia curta Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 65 (1878)
Leopoldia holzmannii (Heldr.) Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 65 (1878)
Leopoldia calandriniana Parl. Fl. Ital. 2: 496 (1857)
Leopoldia bouviana Heldr. ex Nyman Consp. Fl. Eur. : 733 (1882)
Leopoldia bormaniana Lojac. Fl. Sicul. 3: 94 (1909)
Leopoldia anguliflora Lojac. Fl. Sicul. 3: 93 (1909)
Leopoldia constricta Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 71 (1878)
Leopoldia pyramidalis (Tausch) Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 71 (1878)
Leopoldia troiana Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 68 (1878)
Leopoldia graminifolia Heldr. ex Nyman Consp. Fl. Eur. : 733 (1882)
Leopoldia sartoriana Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 66 (1878)
Leopoldia pinardi (Boiss.) Parl. Giorn. Bot. Ital. 2(2): 162 (1847)
Leopoldia pharmacusana Heldr. Bull. Soc. Imp. Naturalistes Moscou 53(I): 66 (1878)
Muscari calandrinianum (Parl.) Nyman Syll. Fl. Eur. , Suppl.: 65 (1865)
Muscari courtilleri Boreau Fl. Centre France , ed. 3, 2: 621 (1857)
Muscari constrictum Tausch Flora 24: 234 (1841)
Muscari cousturieri Gand. Fl. Cret. 101: 1794 (1916)
Muscari cretensium Gand. Bull. Soc. Bot. France 63: 242 (1919)
Muscari charrelii Heldr. ex Rouy Bull. Soc. Bot. France 38: 135 (1891)
Muscari comosum (L.) Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Muscari curtum (Heldr.) Boiss. Fl. Orient. 5: 292 (1882)
Muscari bulgaricum Velen. Fl. Bulg. : 557 (1891)
Muscari bouvianum Heldr. ex Rouy Bull. Soc. Bot. France 38: 135 (1891)
Muscari pyramidale Tausch Flora 24: 235 (1841)
Muscari sartorianum (Heldr.) Boiss. Fl. Orient. 5: 292 (1882)
Muscari pinardi (Boiss.) Boiss. Diagn. Pl. Orient. 7: 110 (1846)
Muscari segusianum E.P.Perrier & Songeon Bull. Herb. Boissier 2: 436 (1894)
Muscari paniculatum (Lam.) Medik. Ann. Bot. (Usteri) 2: 16 (1791)
Muscari pharmacusanum (Heldr.) Boiss. Fl. Orient. 5: 291 (1882)
Muscari trojanum (Heldr.) Boiss. Fl. Orient. 5: 290 (1882)
Muscari graminifolium Heldr. & Holzm. ex Rouy Bull. Soc. Bot. France 38: 135 (1891)
Muscari graecum (Heldr.) Boiss. Fl. Orient. 5: 291 (1882)
Muscari longissimum Medik. Ann. Bot. (Usteri) 2: 15 (1791)
Muscari giennense Pau & Cuatrec. Trab. Mus. Ci. Nat. Barcelona 12: 249 (1929)
Muscari holzmannii (Heldr.) Hirc Oesterr. Bot. Z. 33: 358 (1883)
Muscari monstrosum (L.) Mill. Gard. Dict. ed. 8 : n.º 4 (1768)
Pelotris paniculatus (Lam.) Raf. Autik. Bot. : 125 (1840)
Scilla comosa (L.) Salisb. Prodr. Stirp. Chap. Allerton : 243 (1796)
Scilla monstrosa (L.) Salisb. Prodr. Stirp. Chap. Allerton : 243 (1796)
Bellevalia bouviana Heldr. ex Nyman Consp. Fl. Eur. : 733 (1882)
Bellevalia calandriniana (Parl.) Nyman Consp. Fl. Eur. : 732 (1882)
Bellevalia comosa (L.) Kunth Enum. Pl. 4: 306 (1843)
Bellevalia holzmannii var. curta (Heldr.) Nyman Consp. Fl. Eur. 733. 1882
Bellevalia graeca Heldr. Atti Congr. Int. Bot. Firenze 1874: 228 (1876)
Bellevalia graminifolia Nyman Consp. Fl. Eur. : 733 (1882)
Bellevalia holzmannii Heldr. Atti Congr. Int. Bot. Firenze 1874: 228 (1876)
Bellevalia pharmacusana (Heldr.) Nyman Consp. Fl. Eur. : 733 (1882)
Bellevalia pinardi Boiss. Diagn. Pl. Orient. 5: 62 (1844)
Bellevalia sartoriana (Heldr.) Nyman Consp. Fl. Eur. : 733 (1882)
Botrycomus vulgaris Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 160 (1869)
Etheiranthus constrictus (Tausch) Kostel. Ind. Hort. Bot. Prag. : 56 (1844)
Etheiranthus milleri Kostel. Ind. Hort. Bot. Prag. : 56 (1844)
Eubotrys comosus (L.) Raf. Autik. Bot. : 124 (1840)
Muscari comosum f. monstrosum (L.) Maire in Fl. Afr. Nord 5: 208 1958
Bellevalia sartoriana subsp. pharmacusana (Heldr.) Nyman Consp. Fl. Eur. 733. 1882 (1882)
Bellevalia tenuiflora subsp. constricta (Tausch) Nyman Consp. Fl. Eur. Suppl. 2: 306. 1890 (1890)
Muscari comosum subsp. monstrosum (L.) K.Richt. Pl. Eur. 1: 228. 1890 (1890)
Muscari comosum subsp. courtilleri (Boreau) K.Richt. Pl. Eur. 1: 228 1890
Etheiranthus milleri var. monstrosus Kostel. Index Seminum [Prague] 56. 1844

Common names Top

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Language Common/alternative name
Arabic كيطوط
Arabic بصل الذئب
Czech modřenec chocholatý
Greek mούσκαρι το εύκομον
Croatian kitnjasta presličica
Hungarian Üstökös gyöngyike
Hungarian muscari comosum
Hungarian üstökös gyöngyike
Latvian cekulainā muskare
Dutch kuifhyacint
Swedish fjäderhyacint
Chinese 丛毛蓝壶花
Chinese 丛生蓝壶花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Sow seeds directly at 4°C.
grow seedlings at cool temperature; M. comosum has both sterile and fertile flowers on the same spike. The sterile, upper flowers are bluey mauve the lower fertile turn brownish.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686250
Tropicos 18400279
KEW urn:lsid:ipni.org:names:537347-1
The Plant List kew-280812
Open Tree Of Life 791731
Observations.org 284977
NCBI Taxonomy 81770
IPNI 537347-1
iNaturalist 129989
GBIF 2769172
Freebase /m/0642t8_
Elurikkus 300008
USDA GRIN 410568
Wikipedia Leopoldia_comosa

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
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
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
The Bioactivity and Phytochemicals of Muscari comosum (Leopoldia comosa), a Plant of Multiple Pharmacological Activities Jaiswal V, Lee HJ Int J Mol Sci 23-Feb-2024
PMCID:PMC10931824
doi:10.3390/ijms25052592
PMID:38473839
Which Plant Species for Green Roofs in the Mediterranean Environment? Leotta L, Toscano S, Romano D Plants (Basel) 27-Nov-2023
PMCID:PMC10708222
doi:10.3390/plants12233985
PMID:38068621
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
Oxalate in Foods: Extraction Conditions, Analytical Methods, Occurrence, and Health Implications Salgado N, Silva MA, Figueira ME, Costa HS, Albuquerque TG Foods 25-Aug-2023
PMCID:PMC10486698
doi:10.3390/foods12173201
PMID:37685134
Bitter Is Better: Wild Greens Used in the Blue Zone of Ikaria, Greece Pieroni A, Morini G, Piochi M, Sulaiman N, Kalle R, Haq SM, Devecchi A, Franceschini C, Zocchi DM, Migliavada R, Prakofjewa J, Sartori M, Krigas N, Ahmad M, Torri L, Sõukand R Nutrients 21-Jul-2023
PMCID:PMC10385191
doi:10.3390/nu15143242
PMID:37513661
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Posters N/A FEBS Open Bio 28-Jun-2023
PMCID:PMC10300527
doi:10.1002/2211-5463.13646
Differential Repeat Accumulation in the Bimodal Karyotype of Agave L. Ramos LC, Báez M, Fuchs J, Houben A, Carvalho R, Pedrosa-Harand A Genes (Basel) 15-Feb-2023
PMCID:PMC9956584
doi:10.3390/genes14020491
PMID:36833420
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Effects of Prickly Burnet (Sarcopoterium spinosum (L.) Spach.) Control and Sheep Grazing on Hay Yield and Quality on Gökçeada Island, Turkey Alatürk F, Gökkuş A, Özaslan Parlak A, Baytekin H, Tölü C Animals (Basel) 08-Nov-2022
PMCID:PMC9686760
doi:10.3390/ani12223073
PMID:36428300
Impacts of the Invasive Alien Carpobrotus spp. on Coastal Habitats on a Mediterranean Island (Giglio Island, Central Italy) Mugnai M, Benesperi R, Viciani D, Ferretti G, Giunti M, Giannini F, Lazzaro L Plants (Basel) 21-Oct-2022
PMCID:PMC9609148
doi:10.3390/plants11202802
PMID:36297826
From Şxex to Chorta: The Adaptation of Maronite Foraging Customs to the Greek Ones in Kormakitis, Northern Cyprus Pieroni A, Sulaiman N, Polesny Z, Sõukand R Plants (Basel) 12-Oct-2022
PMCID:PMC9609634
doi:10.3390/plants11202693
PMID:36297716

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23S)-Epoxy-28,29-dihydroxy-27-norlanost-8-ene-3,24-dione 131751817 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(2R,3R,4S,5S,6R)-2-[(3S,3'R,5R,5'S,10S,13S,14S,17S)-4,4-bis(hydroxymethyl)-5'-[(1S)-1-hydroxypropyl]-3',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,2'-oxolane]-3-yl]oxy-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 13917727 Click to see CCC(C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(CO)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(CO1)(CO)O)O)O)O)O)C)C)C)C)O 1197.30 unknown https://doi.org/10.1139/V87-387
(3'R,5R,5'S,10S,13S,14S,17S)-4,4-bis(hydroxymethyl)-3',10,13,14-tetramethyl-5'-propanoylspiro[2,5,6,7,11,12,15,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-3-one 163032867 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(=O)C5(CO)CO)C)C)C)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3beta,17alpha,23R)-17,23-Epoxy-3,29-dihydroxy-27-norlanost-8-ene-15,24-dione 14634457 Click to see 472.70 unknown https://doi.org/10.1139/V81-328
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 73816066 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(CO)CO)O)C)C)C)C 474.70 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S,3'R,4S,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-3-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 101791883 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1339.40 unknown https://doi.org/10.1139/V84-199
https://doi.org/10.1139/V84-485
(3S,3'R,4S,5R,5'R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 162915938 Click to see 1339.40 unknown https://doi.org/10.1139/V87-387
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 162915939 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1339.40 unknown https://doi.org/10.1139/V87-387
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 162915941 Click to see 1339.40 unknown https://doi.org/10.1139/V84-199
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(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-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 44559607 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(CO9)(CO)O)O)O)O)O)C)C)C)C 1061.20 unknown https://doi.org/10.1139/V87-387
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 44559606 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)O)C)C)C)C 1075.20 unknown https://doi.org/10.1139/V83-452
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-hydroxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14634458 Click to see 472.70 unknown https://doi.org/10.1139/V81-328
1-[(2'S,3S,4'R,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(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-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 101215405 Click to see 1063.20 unknown https://doi.org/10.1139/V84-485
1-[(2'S,3S,4'R,5S,10S,13S,14S,17S)-3-hydroxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 163070553 Click to see 474.70 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
1-[3-[6-[[3-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 163002239 Click to see 1063.20 unknown https://doi.org/10.1139/V84-485
2-[4,4-Bis(hydroxymethyl)-5'-(1-hydroxypropyl)-3',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,2'-oxolane]-3-yl]oxy-6-[[3-[3-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 13917726 Click to see CCC(C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(CO)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(CO1)(CO)O)O)O)O)O)C)C)C)C)O 1197.30 unknown https://doi.org/10.1139/V87-387
3-[6-[[3-[3-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 13917733 Click to see 1061.20 unknown https://doi.org/10.1139/V87-387
3-[6-[[3-[4-[3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 13917728 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1339.40 unknown https://doi.org/10.1139/V84-199
https://doi.org/10.1139/V87-387
3-[6-[[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14263454 Click to see 1075.20 unknown https://doi.org/10.1139/V83-452
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(3S,4S,5R,10S,13R,14S)-3-hydroxy-4-(hydroxymethyl)-17-[(2R,5R)-5-methoxy-4-oxoheptan-2-yl]-4,10,13,14-tetramethyl-1,2,3,5,6,7,11,12-octahydrocyclopenta[a]phenanthren-15-one 162955440 Click to see CCC(C(=O)CC(C)C1=CC(=O)C2(C1(CCC3=C2CCC4C3(CCC(C4(C)CO)O)C)C)C)OC 486.70 unknown https://doi.org/10.1139/V81-328
3-Hydroxy-4-(hydroxymethyl)-17-(5-methoxy-4-oxoheptan-2-yl)-4,10,13,14-tetramethyl-1,2,3,5,6,7,11,12-octahydrocyclopenta[a]phenanthren-15-one 162955439 Click to see CCC(C(=O)CC(C)C1=CC(=O)C2(C1(CCC3=C2CCC4C3(CCC(C4(C)CO)O)C)C)C)OC 486.70 unknown https://doi.org/10.1139/V81-328
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3R)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-methoxy-2,3-dihydrochromen-4-one 132555989 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
(3R)-5,8-dihydroxy-3-[(4-hydroxyphenyl)methyl]-6,7-dimethoxy-2,3-dihydrochromen-4-one 638290 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
(3S)-5-hydroxy-3-[(4-hydroxyphenyl)methyl]-7,8-dimethoxy-2,3-dihydrochromen-4-one 162965911 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(CO2)CC3=CC=C(C=C3)O)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
(3S)-5,7-dihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 92155497 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
(3S)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 92446292 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)CC3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
(3S)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 92155498 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
(3S)-5,8-dihydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 92470431 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
[(3R)-5-hydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxy-4-oxo-2,3-dihydrochromen-8-yl] acetate 638294 Click to see CC(=O)OC1=C(C=C(C2=C1OCC(C2=O)CC3=CC=C(C=C3)O)O)OC 358.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
2,3-Dihydro-5,7-dihydroxy-3-((4-hydroxyphenyl)methyl)-4H-1-benzopyran-4-one 9971218 Click to see 286.28 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
3-(3-Hydroxy-4-methoxybenzyl)-5,7-dihydroxychroman-4-one 404571 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
3-(4-Hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 404572 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
5-Hydroxy-3-(4-hydroxybenzyl)-7,8-dimethoxy-4-chromanone 21627906 Click to see 330.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
5,7-Dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-methoxy-2,3-dihydrochromen-4-one 21627905 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
5,8-Dihydroxy-3-(4-hydroxybenzyl)-7-methoxy-4-chromanone 14159173 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)84989-4
5,8-Dihydroxy-3-(4-hydroxybenzyl)-7-methoxy-4-chromanone 8-acetate 21627907 Click to see 358.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
Muscomin 14427389 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(CO2)CC3=CC=C(C=C3)O)O)OC 346.30 unknown https://doi.org/10.1016/S0031-9422(00)80790-6
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
Muscomosin 21676261 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
Spiro[2H-1-benzopyran-3(4H),7'-bicyclo[4.2.0]octa[1,3,5]trien]-4-one, 4',5,7-trihydroxy-3'-methoxy-, (3R)- 155554249 Click to see COC1=C(C=C2C(=C1)CC23COC4=CC(=CC(=C4C3=O)O)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
[(3R)-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4-oxo-2H-chromen-3-yl]methyl acetate 162972811 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
4H-1-Benzopyran-4-one, 3-((acetyloxy)methyl)-2,3-dihydro-5,7-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)- 21676269 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1

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