Details Top

Internal ID UUID64402ccb0c7fd622497285
Scientific name Ceratophyllum submersum
Authority L.
First published in Sp. Pl. ed. 2 : 1409 (1763)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Ceratophyllum submersum is cultivated and marketed as an ornamental aquarium and pond plant. Commercial growers supply it as live potted plants, loose bunches, or as a component of aquascaping starter kits, often under trade names such as “Soft Hornwort” (Tropica product catalogue; The Encyclopedia of Aquarium Plants, 2nd ed.). The species appears on the International Aquatic Plant Society’s list of recommended aquarium plants and is a standard background or mid‑ground plant in community tanks, garden ponds, and indoor aquascapes. In addition to the hobby trade, live material is sold to research institutions as a model submerged aquatic plant for laboratory studies of photosynthesis, nutrient uptake, and phytoremediation (peer‑reviewed studies on nutrient removal with C. submersum).

Properties relevant to use:
The plant’s morphology—highly dissected, whorled leaves that form dense, intertwining mats—provides a large surface‑area‑to‑volume ratio, facilitating efficient gas exchange and nutrient capture in water. It tolerates low‑light conditions (photosynthetically active radiation down to ~20 µmol m⁻² s⁻¹) and grows within a temperature range of 15 °C to 28 °C and a pH of 6.5–8.0. Vegetative propagation by simple fragmentation enables rapid, clonal production without reliance on seed. Chemical analyses report high polysaccharide content in the leaves, which contributes to a gelatinous biofilm that adsorbs dissolved nutrients and suspended particles. Laboratory incubations have documented oxygen evolution rates comparable to other submerged macrophytes, and the dense mats reduce light penetration, suppressing algal growth in controlled systems.

Sustainability and sourcing:
Commercial supply is generated primarily from horticultural nurseries that propagate the species vegetatively under controlled greenhouse conditions, limiting wild‑collection pressure. Where wild material is collected, it is generally limited to regulated populations and must comply with national plant‑health regulations (e.g., the European Union Plant Health Regulation). Life‑cycle assessments of nursery production indicate relatively low inputs of fertilizers and water compared with terrestrial crops, and the plant’s capacity for nutrient sequestration can offset part of the transport carbon footprint. Certification schemes for aquarium plants, such as the Aquatic Plant Association’s “Certified Sustainable” label, increasingly include C. submersum, encouraging traceability and responsible sourcing. The species is not listed in CITES Appendices and is assessed as low‑risk in trade databases.

Synonyms Top

Scientific name Authority First published in
Ceratophyllum submersum var. granulosum (Schur) Nyman Consp. Fl. Eur. 251. 1879
Ceratophyllum demersum var. laeve Crép. Man. Fl. Belgique ed. 5: 325. 1884
Ceratophyllum submersum var. inerme Van Haes. Ann. Soc. Méd. Anvers 1841: 394.

Common names Top

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Language Common/alternative name
English soft hornwort
Spanish hierba laguna
Arabic بشت القرد
Arabic حامول المياه
Arabic حامول الماء
Arabic حامول
Arabic حامُول الماء
Arabic بَشْت القِرد
Arabic شمبلان غارق
Belarusian Рагаліснік напаўапушчаны
Bulgarian потопен роголистник
Catalan cératophylle submergé
Czech růžkatec potopený
Czech růžkatec bradavčitý
Welsh cyrnddail meddal
Danish tornløs hornblad
German zartes hornblatt
German cératophylle submergé
Estonian sile kardhein
Finnish hentokarvalehti
French cératophylle submergé
Hebrew קרנן טבול
Croatian mekana voščika
Upper Sorbian hładki rohačk
Japanese セイロンマツモ
Lithuanian gležnalapė nertis
Lithuanian cératophylle submergé
Dutch fijn hoornblad
Polish rogatek krótkoszyjkowy
Romanian cosor
Russian роголистник полупогружённый
Swedish vårtsärv
Swedish cératophylle submergé
Chinese 细金鱼藻

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Ceratophyllum submersum var. haynaldianum (Borbás) Wilmot-Dear Kew Bull. 40: 266 (1985)
Ceratophyllum submersum var. submersum Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Chad
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Zaïre
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • Caucasus
      • North Caucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Uzbekistan
    • Siberia
      • Altay
      • West Siberia
    • Western Asia
      • Palestine
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000832288
USDA Plants CESU6
Tropicos 7000007
INPN 90222
KEW urn:lsid:ipni.org:names:163088-1
The Plant List kew-36951
PaleoBotany 23523
Open Tree Of Life 531469
Observations.org 6584
NCBI Taxonomy 108412
NBN Atlas NBNSYS0000002762
IUCN Red List 167833
IPNI 163088-1
iNaturalist 273940
IFPNI 514E13A9-920D-4663-BDCD-C61726923009
GBIF 2882404
Freebase /m/0k3mfw6
EPPO CEYSU
EOL 596308
Elurikkus 3595
USDA GRIN 450287
Wikipedia Ceratophyllum_submersum
CMAUP NPO14845

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
Characteristics of turion development in two aquatic carnivorous plants: Hormonal profiles, gas exchange and mineral nutrient content Adamec L, Plačková L, Doležal K Plant Direct 11-Jan-2024
PMCID:PMC10784648
doi:10.1002/pld3.558
PMID:38222932
Beyond taxonomic diversity patterns – investigating how α and β components of macrophyte functional diversity respond to environmental gradients in lotic ecosystems of Greece Stefanidis K, Oikonomou A, Dimitrellos G, Tsoukalas D, Papastergiadou E Front Plant Sci 08-Sep-2023
PMCID:PMC10514920
doi:10.3389/fpls.2023.1204383
PMID:37746009
Phylogenetic placement of Ceratophyllum submersum based on a complete plastome sequence derived from nanopore long read sequencing data Meckoni SN, Nass B, Pucker B BMC Res Notes 25-Aug-2023
PMCID:PMC10464454
doi:10.1186/s13104-023-06459-z
PMID:37626355
Polysaccharides from marine biological resources and their anticancer activity on breast cancer Yang S, Li D, Liu W, Chen X RSC Med Chem 13-Apr-2023
PMCID:PMC10285744
doi:10.1039/d3md00035d
PMID:37360387
Resource availability modulates the effect of body size on reproductive development Gergely R, Tökölyi J Ecol Evol 06-Jan-2023
PMCID:PMC9817193
doi:10.1002/ece3.9722
PMID:36620418
Nonlinear effects of environmental drivers shape macroinvertebrate biodiversity in an agricultural pondscape Musseau CL, Onandia G, Petermann JS, Sagouis A, Lischeid G, Jeschke JM Ecol Evol 08-Nov-2022
PMCID:PMC9643126
doi:10.1002/ece3.9458
PMID:36381394
Seasonal variation of genotypes and reproductive plasticity in a facultative clonal freshwater invertebrate animal (Hydra oligactis) living in a temperate lake Miklós M, Laczkó L, Sramkó G, Barta Z, Tökölyi J Ecol Evol 14-Jul-2022
PMCID:PMC9280439
doi:10.1002/ece3.9096
PMID:35845371
Refined Interpretation of the Pistillate Flower in Ceratophyllum Sheds Fresh Light on Gynoecium Evolution in Angiosperms Sokoloff DD, El ES, Pechenyuk EV, Carrive L, Nadot S, Rudall PJ, Remizowa MV Front Cell Dev Biol 28-Apr-2022
PMCID:PMC9098228
doi:10.3389/fcell.2022.868352
PMID:35573671
Anthropogenic Stressors in Upland Rivers: Aquatic Macrophyte Responses. A Case Study from Bulgaria Gecheva G, Pall K, Todorov M, Traykov I, Gribacheva N, Stankova S, Birk S Plants (Basel) 09-Dec-2021
PMCID:PMC8703415
doi:10.3390/plants10122708
PMID:34961179
Known but not called by name: recreational fishers’ ecological knowledge of freshwater plants in Hungary Löki V, Nagy J, Nagy A, Babai D, Molnár Z, Lukács BA J Ethnobiol Ethnomed 04-Nov-2021
PMCID:PMC8567722
doi:10.1186/s13002-021-00489-2
PMID:34736491
Wetland Restoration with Hydrophytes: A Review Rodrigo MA Plants (Basel) 21-May-2021
PMCID:PMC8223994
doi:10.3390/plants10061035
PMID:34063930
Subcellular Alterations Induced by Cyanotoxins in Vascular Plants—A Review Máthé C, M-Hamvas M, Vasas G, Garda T, Freytag C Plants (Basel) 14-May-2021
PMCID:PMC8157112
doi:10.3390/plants10050984
PMID:34069255
Key drivers structuring rotifer communities in ponds: insights into an agricultural landscape Onandia G, Maassen S, Musseau CL, Berger SA, Olmo C, Jeschke JM, Lischeid G J Plankton Res 06-May-2021
PMCID:PMC8163045
doi:10.1093/plankt/fbab033
PMID:34084088
Assessment of the impact of land use in an agricultural catchment area on water quality of lowland rivers Kupiec JM, Staniszewski R, Jusik S PeerJ 17-Feb-2021
PMCID:PMC7896503
doi:10.7717/peerj.10564
PMID:33643698
The Future of Freshwater Macrophytes in a Changing World: Dissolved Organic Carbon Quantity and Quality and Its Interactions With Macrophytes Reitsema RE, Meire P, Schoelynck J Front Plant Sci 14-May-2018
PMCID:PMC5960680
doi:10.3389/fpls.2018.00629
PMID:29868084

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
> Alkaloids and derivatives / Harmala alkaloids
Flazin 5377686 Click to see 308.29 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
Amaroridine 14463028 Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown via CMAUP database
Bruceolline B 190940 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O 560.50 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 24970879 Click to see 416.40 unknown via CMAUP database
9H-Pyrano(2,3-f)-1,4-benzodioxin-9-one, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-, trans-(+-)- 11982428 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown via CMAUP database
Cleomiscosin A 442510 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(-)-Hydnocarpin 44582381 Click to see 464.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Medioresinol, (+)- 181681 Click to see 388.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadecanoic acid, 8-hydroxy-, (S)- 5312819 Click to see 272.42 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Diolein 5497165 Click to see 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cucumegastigmane I 16105430 Click to see 240.29 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(11beta,12alpha,15beta)-13,20-Epoxy-3,11,12-trihydroxy-15-[[(2E)-4-hydroxy-3,4-dimethyl-1-oxo-2-penten-1-yl]oxy]-2,16-dioxopicras-3-en-21-oic acid 5315509 Click to see 564.60 unknown via CMAUP database
(1beta,2alpha,11beta,12alpha,15beta)-13,20-Epoxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one 5315510 Click to see 412.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,11,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 5315511 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O)O 428.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-9,13,17-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 101273517 Click to see 574.60 unknown via CMAUP database
(1R,2R,3R,6R,8S,12R,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-13,17-dimethyl-9-methylidene-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-en-4-one 101600137 Click to see CC12C(CC3C45C1C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C(=C)C=CC2O 394.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R,19S)-2,3,12,15,16,19-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 11304852 Click to see 426.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,9R,10R,11S,12R)-2,3,10,11-tetrahydroxy-8,12-dimethyl-8-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-5,13-dioxatetracyclo[7.5.0.01,6.02,12]tetradecan-4-one 21769824 Click to see 396.40 unknown via CMAUP database
(1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylic acid 10391474 Click to see 506.50 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 10556620 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-Dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 3000803 Click to see 670.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 21606955 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6S,7R,8S,13S,14R,15R,16S,17S)-3,7,15,16-tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102059835 Click to see 394.40 unknown via CMAUP database
Bruceantin 5281304 Click to see 548.60 unknown via CMAUP database
Bruceantinol A 23656477 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)O)O)O)C)O 592.60 unknown via CMAUP database
Brucein D 441788 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown via CMAUP database
Bruceine A 160006 Click to see 522.50 unknown via CMAUP database
Bruceine H 10320238 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O 426.40 unknown via CMAUP database
Bruceine J 23656476 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)O)O)O)C)O 508.50 unknown via CMAUP database
Bruceolide 99531 Click to see 438.40 unknown via CMAUP database
bruceosideB 3000796 Click to see 682.70 unknown via CMAUP database
Brusatol 73432 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O 520.50 unknown via CMAUP database
butyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10556847 Click to see 724.70 unknown via CMAUP database
CID 11765370 11765370 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown via CMAUP database
CID 21606956 21606956 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown via CMAUP database
CID 21636148 21636148 Click to see 642.60 unknown via CMAUP database
Dehydrobruceantinol 54604632 Click to see 604.60 unknown via CMAUP database
Dehydrobruceine B 101967133 Click to see 478.40 unknown via CMAUP database
Dehydrobrusatol 59087297 Click to see 518.50 unknown via CMAUP database
Javanicolide C 11214625 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)O)C)O)O)C(=O)OC 524.60 unknown via CMAUP database
Javanicolide D 11455840 Click to see 566.60 unknown via CMAUP database
Javanicolide E 70686049 Click to see 522.50 unknown via CMAUP database
Javanicoside B 11169907 Click to see 684.70 unknown via CMAUP database
Javanicoside C 11169890 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 680.60 unknown via CMAUP database
Javanicoside D 11227971 Click to see 740.70 unknown via CMAUP database
Javanicoside F 11445415 Click to see 696.70 unknown via CMAUP database
Javanicoside H 12086836 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC 738.70 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(((2E)-4-(acetyloxy)-3,4-dimethyl-1-oxo-2-penten-1-yl)oxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 5281305 Click to see 606.60 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(acetyloxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 161496 Click to see 480.50 unknown via CMAUP database
Methyl (1R,2R,6S,7R,8R,13R,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-7-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21115217 Click to see 682.70 unknown via CMAUP database
Methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-11,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 21125878 Click to see 520.50 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636149 Click to see 726.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636147 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-(3,4-dimethylpent-2-enoyloxy)-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 441786 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11411443 Click to see 704.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11479645 Click to see 728.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659160 Click to see 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659162 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-3-acetyloxy-12,15,16-trihydroxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659159 Click to see 644.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11490891 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 101499202 Click to see 608.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10S,11R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 11250992 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-(3-hydroxy-3-methylbutanoyl)oxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659163 Click to see 700.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 12086835 Click to see 652.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3-ethyl-4-methylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10417797 Click to see 782.80 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659161 Click to see 768.80 unknown via CMAUP database
Methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-acetyloxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 3000798 Click to see 642.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 11445340 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 101659164 Click to see 710.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-((3-methyl-1-oxo-2-buten-1-yl)oxy)-3,16-dioxo-, methyl ester, (11beta,12alpha,15beta)- 441789 Click to see 682.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-[(4-hydroxy-3,4-dimethyl-1-oxo-2-pentenyl)oxy]-3,16-dioxo-, methyl ester, [11beta,12alpha,15beta(E)]- 101659158 Click to see 726.70 unknown via CMAUP database
Yadanziolide B 11744055 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)O)C)O 442.40 unknown via CMAUP database
Yadanziolide C 10409280 Click to see 410.40 unknown via CMAUP database
Yadanzioside K 14060346 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 768.80 unknown via CMAUP database
Yadanzioside M 21115200 Click to see 704.70 unknown via CMAUP database
YadanziosideA 101659157 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 684.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10E,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 49799780 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Macedonic acid 193076 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8R,9R,10R,13S,17S)-17-[(2S,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-methoxyoxolan-3-yl]-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 10414931 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC)C6C(O6)(C)C)C)C)(C)C 540.70 unknown via CMAUP database
[(5R,7R,8R,9R,10S,11R,13S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-11-hydroxy-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 71544782 Click to see 574.70 unknown via CMAUP database
1,2-Dihydrobruceajavanin A 10076750 Click to see CC(=O)OC1CC2C(C(=O)CCC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C 570.80 unknown via CMAUP database
Bruceajavanin A 10030889 Click to see 568.70 unknown via CMAUP database
Bruceajavanone A 44582338 Click to see 640.80 unknown via CMAUP database
Bruceajavanone A 7-Acetate 44582339 Click to see 682.90 unknown via CMAUP database
Bruceajavanone B 44582340 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 101916318 Click to see 450.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
2-[(1R,2S,3R,6R,8S,9S,10R,11R,12S,13S)-11,12-dihydroxy-13-methoxycarbonyl-8-[(2S)-1-methoxy-1-oxopropan-2-yl]-9-methyl-3-(3-methylbut-2-enoyloxy)-4-oxo-5,14-dioxatetracyclo[8.5.0.01,6.02,13]pentadecan-9-yl]acetic acid 70692363 Click to see 568.60 unknown via CMAUP database
Javanic Acid A 70694422 Click to see 554.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Bruceanic Acid E 70681802 Click to see 524.50 unknown via CMAUP database
Bruceanic Acid E Methyl Ester 70688171 Click to see 538.50 unknown via CMAUP database
Bruceanic Acid F 70681803 Click to see 510.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1S,2R,3R,4S,6R,7R,10R,11R,12R)-2,6,11,12-tetrahydroxy-4,10-dimethyl-4-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-9,14-dioxatetracyclo[8.4.0.03,7.07,11]tetradecan-13-one 10453339 Click to see 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Ethoxycarbonyl-2-quinolone 160782 Click to see 217.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Luteolin-7-O-galactoside 5488493 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Thevetiaflavone 5315202 Click to see 284.26 unknown via CMAUP database

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