Zantedeschia aethiopica - Unknown
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Details Top

Internal ID UUID643ff0ef57ace504555801
Scientific name Zantedeschia aethiopica
Authority (L.) Spreng.
First published in Syst. Veg. 3: 765 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Otosma ethiopica Raf. New Fl. [Rafinesque] ii. 90 (1836); et Fl. Tellur. iv. 8 (1836).
Arodes aethiopica Kuntze Revis. Gen. Pl. 2: 740 (1891)
Pseudohomalomena pastoensis A.D.Hawkes Madroño 11: 147 (1951)
Richardia aethiopica (L.) Spreng. Syst. Veg., ed. 16 [Sprengel] 3: 765. 1826 [Jan-Mar 1826] ; 5: 594, sphalm
Richardia africana Kunth Mém. Mus. Hist. Nat. 4: 433. 1818
Calla aethiopica L. Sp. Pl. : 968 (1753)
Calla ambigua Salisb. Prodr. Stirp. Chap. Allerton : 262 (1796)
Colocasia aethiopica Link Diss. Bot. : 77 (1795)

Common names Top

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Language Common/alternative name
English calla lily
English arum lily
Spanish lirio de etiopía
Spanish lirio de etiopia
Spanish cala de etiopía
Spanish cala de etiopia
Spanish aro de etiopía
Spanish aro de etiopia
Spanish cartucho
Afrikaans varkblom
Czech kornoutice africká
Czech kornoutovka africká
Welsh lili‘r pasg
Welsh lili`r pasg
Estonian harilik kalla
Basque kala
Persian گل شیپوری اتیوپیایی
Finnish valkokalla
Finnish valkohuonevehka
French calla
Croatian sobna kala
Upper Sorbian aronowa lilija
Hungarian fehér kála
Hungarian fehér tölcsérvirág
Indonesian kala lili
Italian calla aethiopica
Italian richardia africana
Italian colocasia aethiopica
Lithuanian abisininė kalija
Malayalam സാന്തെഡെഷിയ എത്യോപിക്ക
nah canāuhxōchitl
nah canauhxochitl
Dutch witte aronskelk
Polish cantedeskia etiopska
Polish zantedeschia etiopska
Polish kallijka etiopska
Polish cantodeskia etiopska
Polish bielikrasa etiopska
Portuguese boca de jarro
Portuguese jarro
Slovak kornútovka africká
Uzbek kalla
Vietnamese loa kèn sông nin
Chinese 馬蹄蓮
Chinese 慈姑花
Chinese 馬蹄蘭
Chinese 马蹄莲
Chinese 海芋

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 at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
remove green photosynthesizing capsule which inhibits germination

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland
    • Western Indian Ocean
      • Réunion
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
    • Malesia
      • Philippines
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
    • New Zealand
      • New Zealand North
  • Europe
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Southwest
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California
  • Pacific
    • North-central Pacific
      • Hawaii
    • South-central Pacific
      • Society Islands
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Bermuda
      • Dominican Republic
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • Costa Rica
      • Nicaragua
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000335148
UNII 0W4EP139UA
USDA Plants ZAAE
Tropicos 2104736
INPN 130605
Flora of Italy 7849
KEW urn:lsid:ipni.org:names:89403-1
The Plant List kew-215527
Missouri Botanical Garden 276469
PFAF Zantedeschia aethiopica
Open Tree Of Life 549269
Observations.org 123600
NCBI Taxonomy 69721
NBN Atlas NHMSYS0000465223
Nature Serve 2.131475
IUCN Red List 164507
IPNI 89403-1
iNaturalist 56006
iNaturalist 414930
GBIF 2868827
Freebase /m/025s2mp
EPPO ZNTAE
EOL 1127679
Elurikkus 210954
Calflora (Californian flora) 8380
USDA GRIN 42173
Wikipedia Zantedeschia_aethiopica

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
Phytoremediation potential of Pistia stratiotes, Eichhornia crassipes, and Typha latifolia for chromium with stimulation of secondary metabolites Rizvi ZF, Jamal M, Parveen H, Sarfraz W, Nasreen S, Khalid N, Muzammil K Heliyon 03-Apr-2024
PMCID:PMC11004193
doi:10.1016/j.heliyon.2024.e29078
PMID:38601583
A survey to document toxic hazards in the zone surrounding volcanoes national park, a habitat for mountain gorillas, an endangered wildlife species in Rwanda Kwizera E, Rumbeiha WK, Nishimwe K, Nziza J Front Vet Sci 03-Jan-2024
PMCID:PMC10791935
doi:10.3389/fvets.2023.1320162
PMID:38234986
Endomicrobiome of in vitro and natural plants deciphering the endophytes-associated secondary metabolite biosynthesis in Picrorhiza kurrooa, a Himalayan medicinal herb Tamang A, Swarnkar M, Kumar P, Kumar D, Pandey SS, Hallan V Microbiol Spectr 09-Oct-2023
PMCID:PMC10715050
doi:10.1128/spectrum.02279-23
PMID:37811959
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
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
Research Progress on Anthocyanin-Mediated Regulation of ‘Black’ Phenotypes of Plant Organs Wang F, Chen J, Tang R, Wang R, Ahmad S, Liu Z, Peng D Curr Issues Mol Biol 01-Sep-2023
PMCID:PMC10527681
doi:10.3390/cimb45090458
PMID:37754242
Emerging Plant Intoxications in Domestic Animals: A European Perspective Nagy AL, Ardelean S, Chapuis RJ, Bouillon J, Pivariu D, Dreanca AI, Caloni F Toxins (Basel) 04-Jul-2023
PMCID:PMC10467095
doi:10.3390/toxins15070442
PMID:37505711
Insight into biodiversity of the recently rearranged genus Dickeya Hugouvieux-Cotte-Pattat N, Pédron J, Van Gijsegem F Front Plant Sci 20-Jun-2023
PMCID:PMC10319131
doi:10.3389/fpls.2023.1168480
PMID:37409305
Assembly and Comparative Analysis of the Complete Mitochondrial Genome of Two Species of Calla Lilies (Zantedeschia, Araceae) Guo Y, Li Z, Jin S, Chen S, Li F, Wu H Int J Mol Sci 31-May-2023
PMCID:PMC10254018
doi:10.3390/ijms24119566
PMID:37298515
Toxicity of House Plants to Pet Animals Siroka Z Toxins (Basel) 19-May-2023
PMCID:PMC10220692
doi:10.3390/toxins15050346
PMID:37235380
Exogenous applications of gibberellic acid modulate the growth, flowering and longevity of calla lily Chandel A, Thakur M, Rakwal A, Chauhan S, Bhargava B Heliyon 15-May-2023
PMCID:PMC10208936
doi:10.1016/j.heliyon.2023.e16319
PMID:37251873
Melissopalynological analysis and floral spectra of Apis mellifera scutellata Lepeletier bees in different agroecologies of southwest Ethiopia Tulu D, Aleme M, Mengistu G, Bogale A, Bezabeh A, Mendesil E Heliyon 11-May-2023
PMCID:PMC10199175
doi:10.1016/j.heliyon.2023.e16047
PMID:37215831
Inhibition of AcrAB-TolC enhances antimicrobial activity of phytochemicals in Pectobacterium brasiliense Pun M, Khazanov N, Galsurker O, Kerem Z, Senderowitz H, Yedidia I Front Plant Sci 09-May-2023
PMCID:PMC10203483
doi:10.3389/fpls.2023.1161702
PMID:37229130
Combined analyses of transcriptome and metabolome reveal the mechanism of exogenous strigolactone regulating the response of elephant grass to drought stress Zhou J, Liu Y, Li Y, Ling W, Fan X, Feng Q, Ming R, Yang F Front Plant Sci 08-May-2023
PMCID:PMC10200884
doi:10.3389/fpls.2023.1186718
PMID:37223793
Valorization of Wild Edible Plants as Food Ingredients and Their Economic Value Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 27-Feb-2023
PMCID:PMC10001278
doi:10.3390/foods12051012
PMID:36900530

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
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1016/0031-9422(80)85057-6
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine 681 Click to see C1=CC(=C(C=C1CCN)O)O 153.18 unknown https://doi.org/10.1016/0031-9422(80)85057-6
> Benzenoids / Phenols / Methoxyphenols
1,2-Propanediol, 3-(4-hydroxy-3-methoxyphenyl)-, (2S)- 10750461 Click to see COC1=C(C=CC(=C1)CC(CO)O)O 198.22 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
3-(4-Hydroxy-3-methoxyphenyl)propane-1,2-diol 161566 Click to see COC1=C(C=CC(=C1)CC(CO)O)O 198.22 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Guaiacylglycerol 14579 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
threo-Guaiacylglycerol 11063784 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lignans, neolignans and related compounds
(1R,2R)-1-(4-Hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-[(1S,2S)-1,2,3-trihydroxypropyl]phenoxy]-1,3-propanediol 101416577 Click to see COC1=C(C=CC(=C1)C(C(CO)OC2=C(C=C(C=C2)C(C(CO)O)O)OC)O)O 410.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
(1R,2R)-2-[4-[(2R)-2,3-dihydroxypropyl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 162861017 Click to see COC1=C(C=CC(=C1)CC(CO)O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
(1S,2S)-2-[4-[(2S)-2,3-dihydroxypropyl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 10572687 Click to see COC1=C(C=CC(=C1)CC(CO)O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
2-[4-(2,3-Dihydroxypropyl)-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 85190107 Click to see COC1=C(C=CC(=C1)CC(CO)O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Threo,threo-1-[4-(2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-(hydroxymethyl)ethoxy)-3-methoxyphenyl]-1,2,3-propanetriol 76417856 Click to see COC1=C(C=CC(=C1)C(C(CO)OC2=C(C=C(C=C2)C(C(CO)O)O)OC)O)O 410.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(E)-Isoconiferin 10914828 Click to see COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)O 342.34 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
(E)-Isosyringin 14861368 Click to see COC1=CC(=CC(=C1O)OC)C=CCOC2C(C(C(C(O2)CO)O)O)O 372.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
2-[3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85313722 Click to see COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)O 342.34 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
2-[3-(4-Hydroxy-3,5-dimethoxyphenyl)prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72740199 Click to see COC1=CC(=CC(=C1O)OC)C=CCOC2C(C(C(C(O2)CO)O)O)O 372.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
24-Methylenecycloartanol 94204 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
3beta-24-Methylenecycloartan-3-ol 544165 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-en-6-ol 162820419 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)O)C)C 438.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
9,19-Cyclo-9beta-lanost-24-en-3beta-ol 500213 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 633877 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Ergosterol peroxide 5351516 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,4S,5R,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162910425 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
(3S,5R,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 139585457 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
10,13-dimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12309689 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
4,10,13-trimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 625278 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
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/10.1016/S0031-9422(98)00092-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol 5318414 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
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/10.1016/S0031-9422(98)00092-2
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
3beta-Hydroxyporiferast-5-en-7-one 14779505 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
7beta-Hydroxysitosterol 12309569 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Ikshusterol 161816 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3,4-dihydroxyphenyl)-ethyl-O-beta-D-glucopyranoside 5316821 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one 73829966 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 14583621 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 14583620 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Isoswertiajaponin 21721993 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2
Isoswertisin 44258317 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(98)00092-2

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