Campanula medium - Unknown
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Internal ID UUID64402c4b8b916606709782
Scientific name Campanula medium
Authority L.
First published in Sp. Pl. : 167 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Marianthemum medium Schur Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 48 (1853)
Medium grandiflorum Spach Hist. Nat. Vég. 9: 553 (1838)
Rapuntia media (L.) Chevall. Fl. Gén. Env. Paris , ed. 2, 2: 526 (1836)
Sykoraea hortensis Opiz Seznam : 94 (1852)
Talanelis medium Raf. Fl. Tellur. 4: 70 (1838)
Campanula bourdiniana Gand. Fl. Lyon. : 146 (1875)
Campanula florida Salisb. Prodr. Stirp. Chap. Allerton : 127 (1796)
Campanula medium f. alba Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Campanula medium var. bourdiniana (Gand.) Nyman Consp. Fl. Eur. 476. 1879
Campanula medium f. caesia Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Campanula medium f. calycantha Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Campanula medium var. calycanthema Nicholls Garden (London, 1871-1927) 48: 295. 1895
Campanula medium f. coerulea Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Campanula medium f. rosea Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Campanula medium f. striata Voss Vilm. Blumengartn. ed. 3 1: 564 1894
Rapuntia medium (L.) Chevall.
Campanula grandiflorum Lam.
Medium grandiflorum (Lam.) Fourr. Ann. Soc. Linn. Lyon, ser. 2, 17: 111 1869
Marianthemum grandiflorum Czerw. & L.Schwarz Index Seminum (KRA, Cracow) 1871: 9 (1872)

Common names Top

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Language Common/alternative name
English canterbury bells
Spanish farolillos
Arabic جرس كنتربوري
Czech zvonek zahradní
Welsh clychlys caer-gaint
German marien-glockenblume
German marienglockenblume
Finnish maariankello
French campanule carillon
Irish plúrán cloigneach
Armenian Զանգակածաղիկ միջին
Icelandic sumarklukka
Cornish klegh an kowr
Lithuanian darželinis katilėlis
Malayalam കാമ്പനൂല മീഡിയം
Dutch mariëtteklokje
Polish dzwonek ogrodowy
Russian Колокольчик средний
Slovak zvonček prostredný
Swedish mariaklocka
Thai ระฆังแคนเตอร์บรี
Chinese 风铃草
Chinese 風鈴草
Chinese 彩鐘花
Chinese 中间风铃草

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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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Romania
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
    • Northeastern U.S.A.
      • Connecticut
      • Michigan
      • New York
    • Northwestern U.S.A.
      • Montana
      • Oregon
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000827845
Canadensys 4167
USDA Plants CAME20
Tropicos 5500613
INPN 87678
Flora of Italy 5298
KEW urn:lsid:ipni.org:names:140670-1
The Plant List kew-365242
PFAF Campanula medium
Open Tree Of Life 112632
NCBI Taxonomy 56154
NBN Atlas NBNSYS0000004292
Nature Serve 2.134984
IPNI 140670-1
iNaturalist 159761
GBIF 5411453
Freebase /m/0dhy7x
EPPO CMPME
EOL 577761
Elurikkus 241850
Calflora (Californian flora) 8514
USDA GRIN 8766
Wikipedia Campanula_medium
CMAUP NPO13417

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
Eco-friendly approaches to phytochemical production: elicitation and beyond Jalota K, Sharma V, Agarwal C, Jindal S Nat Prod Bioprospect 10-Jan-2024
PMCID:PMC10776560
doi:10.1007/s13659-023-00419-7
PMID:38195902
Heterologous Expression of Platycodon grandiflorus PgF3′5′H Modifies Flower Color Pigmentation in Tobacco Ma L, Jia W, Duan Q, Du W, Li X, Cui G, Wang X, Wang J Genes (Basel) 09-Oct-2023
PMCID:PMC10606865
doi:10.3390/genes14101920
PMID:37895269
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
Embryo Rescue in Plant Breeding Rogo U, Fambrini M, Pugliesi C Plants (Basel) 29-Aug-2023
PMCID:PMC10489947
doi:10.3390/plants12173106
PMID:37687352
Anthocyanin metabolic engineering of Euphorbia pulcherrima: advances and perspectives Lozoya-Gloria E, Cuéllar-González F, Ochoa-Alejo N Front Plant Sci 15-May-2023
PMCID:PMC10225641
doi:10.3389/fpls.2023.1176701
PMID:37255565
Creating novel ornamentals via new strategies in the era of genome editing Jin C, Dong L, Wei C, Wani MA, Yang C, Li S, Li F Front Plant Sci 14-Apr-2023
PMCID:PMC10140431
doi:10.3389/fpls.2023.1142866
PMID:37123857
Behind the Scenes of Anthocyanins—From the Health Benefits to Potential Applications in Food, Pharmaceutical and Cosmetic Fields Câmara JS, Locatelli M, Pereira JA, Oliveira H, Arlorio M, Fernandes I, Perestrelo R, Freitas V, Bordiga M Nutrients 02-Dec-2022
PMCID:PMC9738495
doi:10.3390/nu14235133
PMID:36501163
Non-target molecular network and putative genes of flavonoid biosynthesis in Erythrina velutina Willd., a Brazilian semiarid native woody plant Chacon DS, Santos MD, Bonilauri B, Vilasboa J, da Costa CT, da Silva IB, Torres TD, de Araújo TF, Roque AD, Pilon AC, Selegatto DM, Freire RT, Reginaldo FP, Voigt EL, Zuanazzi JA, Scortecci KC, Cavalheiro AJ, Lopes NP, Ferreira LD, dos Santos LV, Fontes W, de Sousa MV, Carvalho PC, Fett-Neto AG, Giordani RB Front Plant Sci 08-Sep-2022
PMCID:PMC9493460
doi:10.3389/fpls.2022.947558
PMID:36161018
Making a Virtue of Necessity: The Use of Wild Edible Plant Species (Also Toxic) in Bread Making in Times of Famine According to Giovanni Targioni Tozzetti (1766) Paura B, Di Marzio P Biology (Basel) 11-Feb-2022
PMCID:PMC8869735
doi:10.3390/biology11020285
PMID:35205151
The Flavonoid Biosynthesis Network in Plants Liu W, Feng Y, Yu S, Fan Z, Li X, Li J, Yin H Int J Mol Sci 26-Nov-2021
PMCID:PMC8657439
doi:10.3390/ijms222312824
PMID:34884627
Fungi of quarantine concern for China I: Dothideomycetes Zhao P, Crous PW, Hou LW, Duan WJ, Cai L, Ma ZY, Liu F Persoonia 25-Aug-2021
PMCID:PMC10486631
doi:10.3767/persoonia.2021.47.02
PMID:37693796
Fungi of quarantine concern for China I: Dothideomycetes Zhao P, Crous PW, Hou LW, Duan WJ, Cai L, Ma ZY, Liu F Persoonia 25-Aug-2021
PMCID:PMC10784663
doi:10.3767/persoonia.2023.47.02
PMID:38352971
Modeling Agrobacterium-Mediated Gene Transformation of Tobacco (Nicotiana tabacum)—A Model Plant for Gene Transformation Studies Niedbała G, Niazian M, Sabbatini P Front Plant Sci 23-Jul-2021
PMCID:PMC8370025
doi:10.3389/fpls.2021.695110
PMID:34413865
Natural Blues: Structure Meets Function in Anthocyanins Houghton A, Appelhagen I, Martin C Plants (Basel) 08-Apr-2021
PMCID:PMC8068391
doi:10.3390/plants10040726
PMID:33917946
Phytochrome-interacting factors interact with transcription factor CONSTANS to suppress flowering in rose Sun J, Lu J, Bai M, Chen Y, Wang W, Fan C, Liu J, Ning G, Wang C Plant Physiol 08-Mar-2021
PMCID:PMC8195524
doi:10.1093/plphys/kiab109
PMID:33693800

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1248/CPB.35.3713
(2R,3R,4S,5S,6R)-2-[3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162886478 Click to see COC1=C(C=CC(=C1)CCCOC2C(C(C(C(O2)CO)O)O)O)OC(CO)C(C3=CC(=C(C=C3)O)OC)O 540.60 unknown https://doi.org/10.1248/CPB.35.3713
(2S,3S,4S,5S,6R)-2-[3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-hydroxyphenyl]propoxy]-6-methyloxane-3,4,5-triol 162914061 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C=C3)O)OC)O)O)O)O)O 510.50 unknown https://doi.org/10.1248/CPB.35.3713
2-[3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-hydroxyphenyl]propoxy]-6-methyloxane-3,4,5-triol 13893583 Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C=C3)O)OC)O)O)O)O)O 510.50 unknown https://doi.org/10.1248/CPB.35.3713
Liriodendrin 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1248/CPB.35.3713
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester 21609756 Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC 348.50 unknown via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O 348.50 unknown via CMAUP database
prostaglandin B2 5280881 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4R,5S,6R)-2-(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol 126968964 Click to see CC=CC#CC#CC(C(C=CCCCO)OC1C(C(C(C(O1)CO)O)O)O)O 396.40 unknown https://doi.org/10.1016/S0176-1617(96)80056-3
(2S,3R,4S,5S,6R)-2-[(3S,6E,10S)-3,10-dihydroxy-2,6,10-trimethyldodeca-6,11-dien-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 51694595 Click to see CC(=CCCC(C)(C=C)O)CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O 418.50 unknown https://doi.org/10.1248/CPB.35.1109
2-(3,10-Dihydroxy-2,6,10-trimethyldodeca-6,11-dien-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 73238386 Click to see CC(=CCCC(C)(C=C)O)CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O 418.50 unknown https://doi.org/10.1248/CPB.35.1109
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-hexoxyoxane-3,4,5-triol 14135410 Click to see CCCCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O 396.40 unknown https://doi.org/10.1248/CPB.36.2475
2-Hex-3-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol 73981610 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown https://doi.org/10.1248/CPB.36.2475
Blumenol B 9-O-glucoside 14135398 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1248/CPB.36.2475
Byzantionoside B 14135395 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown https://doi.org/10.1248/CPB.36.2475
icariside B5 14135399 Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1248/CPB.36.2475
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5R,9S,10R,12R,13R,14S)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 101282656 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1248/CPB.35.1109
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/S10600-014-1165-8
beta-Tocopherol 6857447 Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O 416.70 unknown https://doi.org/10.1007/S10600-014-1165-8
delta-Tocopherol 92094 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1007/S10600-014-1165-8
gamma-Tocopherol 92729 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown https://doi.org/10.1007/S10600-014-1165-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
4-[(1S,4S,5S)-5-hydroxy-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-yl]butan-2-one 14845629 Click to see CC1=CC(C(C(C1CCC(=O)C)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 388.50 unknown https://doi.org/10.1016/0031-9422(91)84249-R
4-[(4R,6S)-4-hydroxy-2,6-dimethyl-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohexen-1-yl]butan-2-one 21672400 Click to see CC1=C(C(CC(C1)O)(C)COC2C(C(C(C(O2)CO)O)O)O)CCC(=O)C 388.50 unknown https://doi.org/10.1248/CPB.35.3713
4-[(4R)-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxycyclohexen-1-yl]butan-2-one 162994685 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CC(=C(C(C3)(C)C)CCC(=O)C)C)O)O)O)O)O)O 518.60 unknown https://doi.org/10.1248/CPB.36.2475
CID 162904854 162904854 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.35.1109
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
Crassocolide B 11995280 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lanosterol 246983 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-014-1165-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 492.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1007/S10600-014-1165-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 101007150 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007149 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
delta7-Avenasterol 12795736 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/S10600-014-1165-8
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-014-1165-8
Stigmastanol 241572 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1007/S10600-014-1165-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol 163189166 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1248/CPB.36.2475
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1248/CPB.35.1109
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1248/CPB.35.1109
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol 14079044 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1248/CPB.36.2475
2-phenylethyl beta-D-glucopyranoside 468284 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1248/CPB.36.2475
4-[2,2,6-Trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one 85128318 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.35.1109
4-[3-Hydroxy-2,2,6-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one 73820977 Click to see CC(=O)C=CC12C(C(C(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)O)(C)C 402.40 unknown https://doi.org/10.1248/CPB.35.3713
Icariside B2 10385469 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.35.1109
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1248/CPB.36.2475
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(3,5,6,7-tetramethoxy-9,10-dihydrophenanthren-2-yl)oxy]oxane-3,4,5-triol 15690608 Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 478.50 unknown https://doi.org/10.1248/CPB.35.1109
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Lobeline 101616 Click to see CN1C(CCCC1CC(=O)C2=CC=CC=C2)CC(C3=CC=CC=C3)O 337.50 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-3-[(S)-methylsulfinyl]-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]prop-2-enamide 163064027 Click to see CS(=O)C=CC(=O)NC1CCCN1C(=O)C=CC2=CC=CC=C2 332.40 unknown https://doi.org/10.1016/S0176-1617(96)80056-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/0-387-28822-8_5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5R,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 162977644 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)OC(=O)C 542.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 13964058 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)OC(=O)C 542.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
3-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 163010862 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
3-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 13964055 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
5-Hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxypyrano[2,3-h]chromen-4-one 13964078 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC4=C3C=CC(O4)(C)C)O)C5=CC=C(C=C5)O)O)O)O 498.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Ikarisoside-F 13964060 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)OC5C(C(C(CO5)O)O)O)O)O 632.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11765972 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O)O 824.80 unknown https://doi.org/10.1016/0031-9422(88)80627-7
3,5-Dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14187155 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O)C 530.50 unknown https://doi.org/10.1248/YAKUSHI1947.95.7_825
Icariin 5318997 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown https://doi.org/10.1248/YAKUSHI1881.55.5_537
Icarin 5471129 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown https://doi.org/10.1248/YAKUSHI1881.55.5_537
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno[12,13]cyclotetradeca[1,2-b]furan-12(2H)-one 643720 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
Crassocolide E 11995175 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Crassocolide F 11995282 Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
ent-Sarcophine 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[2-[(2S)-1-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-yl]-4-(3-hydroxypropyl)-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 159325252 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)C(CC3=CC(=C(C=C3)O)OC)CO)CCCO 524.60 unknown https://doi.org/10.1248/CPB.36.2475
(2S,3R,4S,5S,6R)-2-[2-hydroxy-5-[2-(3-hydroxy-4,5-dimethoxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162929353 Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 452.50 unknown https://doi.org/10.1248/CPB.36.2475
2-[2-[1-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-yl]-4-(3-hydroxypropyl)-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14135390 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)C(CC3=CC(=C(C=C3)O)OC)CO)CCCO 524.60 unknown https://doi.org/10.1248/CPB.36.2475
2-[2-Hydroxy-5-[2-(3-hydroxy-4,5-dimethoxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162929352 Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 452.50 unknown https://doi.org/10.1248/CPB.36.2475

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