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Leopoldia comosa

Leopoldia comosa - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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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

Common names Top

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Language Common/alternative name
Czech modřenec chocholatý
Greek mούσκαρι το εύκομον
Croatian kitnjasta presličica
Hungarian muscari comosum
Hungarian Üstökös gyöngyike
Chinese 丛毛蓝壶花
Chinese 丛生蓝壶花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

Suggest others/fix!
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
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
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
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
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
Ethnopharmacological Survey, Mineral and Chemical Content, In Vitro Antioxidant, and Antibacterial Activities of Aqueous and Organic Extracts of Chamaerops humilis L. var. argentea Andre Leaves Lachkar N, Lamchouri F, Toufik H Biomed Res Int 05-Aug-2022
PMCID:PMC9410792
doi:10.1155/2022/1091247
PMID:36033551
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Vegetation Dynamics in a Loess Grassland: Plant Traits Indicate Stability Based on Species Presence, but Directional Change When Cover Is Considered Csontos P, Tamás J, Kovács Z, Schellenberger J, Penksza K, Szili-Kovács T, Kalapos T Plants (Basel) 13-Mar-2022
PMCID:PMC8950867
doi:10.3390/plants11060763
PMID:35336646
Diet Selection by the Italian Hare (Lepus corsicanus de Winton, 1898) in Two Protected Coastal Areas of Latium Freschi P, Fascetti S, Riga F, Rizzardini G, Fortebraccio M, Ragni M, Paolino R, Cosentino C Animals (Basel) 09-Mar-2022
PMCID:PMC8944817
doi:10.3390/ani12060687
PMID:35327084
Pangenomes as a Resource to Accelerate Breeding of Under-Utilised Crop Species Tay Fernandez CG, Nestor BJ, Danilevicz MF, Gill M, Petereit J, Bayer PE, Finnegan PM, Batley J, Edwards D Int J Mol Sci 28-Feb-2022
PMCID:PMC8910360
doi:10.3390/ijms23052671
PMID:35269811

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 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
(23S)-17,23-Epoxy-29-hydroxy-3beta-[6-O-[2-O-(2-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl)-alpha-L-arabinopyranosyl]-beta-D-glucopyranosyloxy]-27-norlanosta-8-ene-15,24-dione 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
(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 CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)O)C)C)C)C 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/V84-485
https://doi.org/10.1139/V84-199
(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 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,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 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
(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-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 CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)O)C)C)C)C 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 CCC(=O)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)O)OC9C(C(CO9)(CO)O)O)O)O)O)C)C)C)C 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 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
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 CCC(=O)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)O)OC9C(C(CO9)(CO)O)O)O)O)O)C)C)C)C 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 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
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/V87-387
https://doi.org/10.1139/V84-199
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 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
> 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
(-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone 9971218 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
(3R)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-methoxy-2,3-dihydrochromen-4-one 132555989 Click to see COC1=C(C=C(C2=C1OCC(C2=O)CC3=CC=C(C=C3)O)O)O 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 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
(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 COC1=C(C2=C(C(=C1)O)C(=O)C(CO2)CC3=CC=C(C=C3)O)O 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
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 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
5-Hydroxy-3-(4-hydroxybenzyl)-7,8-dimethoxy-4-chromanone 21627906 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
5,7-Dihydroxy-3-[(4-hydroxyphenyl)methyl]-8-methoxy-2,3-dihydrochromen-4-one 21627905 Click to see COC1=C(C=C(C2=C1OCC(C2=O)CC3=CC=C(C=C3)O)O)O 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 COC1=C(C2=C(C(=C1)O)C(=O)C(CO2)CC3=CC=C(C=C3)O)O 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 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
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 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
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 CC(=O)OCC1(COC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)OC)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1
Comosin 21676269 Click to see CC(=O)OCC1(COC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)OC)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)83055-1

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