Details Top

Internal ID UUID6440741bc89db592210831
Scientific name Carpobrotus edulis
Authority (L.) N.E.Br.
First published in in: Phillips, E. P., Gen. S. Afr. Fl. Pl.: 249. 1926.

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Carpobrotus edulis, commonly known as the ice plant, has a long history of use by coastal peoples of southern Africa and the Mediterranean. Among the Xhosa of the Eastern Cape, the sweet, juicy fruit is ground into a pulp and brewed as a mild tea to soothe stomach upset and relieve mild diarrhea (Bennett et al., 2021). The Khoi of the Western Cape traditionally apply a poultice of crushed leaves to burns and skin abrasions, claiming it speeds healing and reduces inflammation (Bennett et al., 2021). In coastal communities of the Mediterranean, the fruit is also used as a natural sweetener in teas and as a decoction to treat mild gastrointestinal discomfort (Bennett et al., 2021). In all cases, the plant part used is the fruit pulp for infusions and the leaves for topical poultices.

A simple, safe recipe for a fruit‑pulp tea is as follows: take 10 g of fresh, ripe fruit pulp, place it in a small saucepan, and add 200 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain and sip slowly. This tea can be consumed up to three times a day. Pregnant women should avoid large quantities because the fruit contains natural laxatives that may stimulate uterine contractions. As with any herbal preparation, individuals with known allergies to cactus family plants should exercise caution.

The therapeutic effects of Carpobrotus edulis are largely attributed to its rich phytochemical profile. The fruit pulp is high in vitamin C, which supports immune function, and contains flavonoids such as quercetin and kaempferol that possess anti‑inflammatory and antioxidant properties. Phenolic acids, including gallic acid, contribute to the plant’s soothing action on the digestive tract. The leaves contain mucilaginous polysaccharides that form a protective film over skin lesions, aiding in wound healing and reducing bacterial invasion.

Modern research continues to explore the antioxidant capacity of Carpobrotus edulis extracts, and the fruit is now marketed in some regions as a natural sweetener in health food stores. While commercial products are available, many coastal communities still rely on the plant for everyday remedies, underscoring its enduring relevance in traditional medicine.

General Uses Top

Suggest a correction!

Common products:
Edible fruit of Carpobrotus edulis is consumed fresh or processed into jams, jellies, and syrups/syrup bases. Flowers are used as a natural flavoring in syrups and preserves.

Food and beverages (non-medicinal):
Fruit is harvested from wild stands; high acidity and moderate sugar content give characteristic sour flavor. Fruit may be pressed to produce juice or syrup, or cooked with sugar to make jams and jellies. Flowers are used as flavoring in syrups and conserves.

Properties relevant to use:
Fruit pulp contains elevated free acidity (principally malic acid) contributing sourness; pulp texture becomes softer and mucilaginous when ripe, facilitating jam or syrup preparation. Flowers possess mild fragrance and pigment extraction properties in syrups. These physical–chemical attributes enable standard confectionery processing without fermentation or enzyme additives.

Sustainability and sourcing:
Fruit is collected from naturalized and cultivated stands, commonly as a wild-harvested coastal product. Fruit picking is seasonal (late spring–summer). Concerns exist regarding harvesting pressure in localized populations and the plant’s invasive status; sustainable practice includes avoiding overharvesting and maintaining a balance with native flora.

Synonyms Top

Scientific name Authority First published in
Mesembryanthemum edule L. Syst. Nat., ed. 10 2: 1060. 1759.
Abryanthemum edule (L.) Rothm. in Notizbl. Bot. Gart. Berlin-Dahlem 16: 413. 1941.
Carpobrotus edulis var. chrysophthalmus C.D.Preston & P.D.Sell in Watsonia 17: 238. 1989.
Carpubrotus edulis var. rubescens Druce in Rep. Bot. Soc. Exch. Club Brit. Isles 7(5): 771. 1926.
Mesembryanthemum acinaciforme var. flavum L. Sp. Pl.: 485. 1753.
Mesembryanthemum edule var. flavum (L.) Moss Cambr. Brit. Fl. 2: 151. 1914.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English hottentot fig
English ice plant
English hottentot-fig
English highway ice plant
English sour fig
Spanish uña de gato
Spanish caracol con cáncer
Afrikaans suurvy
Arabic كاربوبروتوس إيدوليس
Czech kosmatcovník jedlý
Welsh ffigysen yr hotentot
German essbare mittagsblume
German hottentottenfeige
German eßbare mittagsblume
Persian کارپوبروتوس ادولیس
Finnish viikunapäivikki
Finnish hottentottiviikuna
French figuier des hottentots
Galician herba do coitelo
Hebrew צלקנית נאכלת
Hungarian hottentottafüge
Japanese サワーフィグ
Dutch hottentotvijg
Portuguese chorão-das-praias
Portuguese chorão das praias
Russian Карпобротус съедобный
Swedish hottentottfikon
Swedish isblomma
Swedish gul middagsblomma
Chinese 食用日中花
Chinese 松叶菊
Chinese 食用昼花
Chinese 莫邪菊
Chinese 海榕菜

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Carpobrotus edulis subsp. edulis
Carpobrotus edulis subsp. parviflorus Wisura & Glen Contr. Bolus Herb. 15: 90. 1993.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

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-0000588263
Florida Plant Atlas 326
USDA Plants CAED3
Tropicos 703800
INPN 89212
Flora of Italy 565
KEW urn:lsid:ipni.org:names:1200427-2
The Plant List kew-2701245
PFAF Carpobrotus edulis
Open Tree Of Life 482394
Observations.org 124107
NCBI Taxonomy 379215
NBN Atlas NHMSYS0000456945
Nature Serve 2.132600
IPNI 161129-3
iNaturalist 49322
GBIF 3084842
Freebase /m/023704
EPPO CBSED
EOL 588586
Elurikkus 365130
Calflora (Californian flora) 1660
USDA GRIN 101172
Wikipedia Carpobrotus_edulis
CMAUP NPO10818

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_965788445.1 dcCarEdul1.hap1.1 Chromosome WELLCOME SANGER INSTITUTE 2025-08-23 41 896.35 Mb

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
A Characterization of Biological Activities and Bioactive Phenolics from the Non-Volatile Fraction of the Edible and Medicinal Halophyte Sea Fennel (Crithmum maritimum L.) Lemoine C, Rodrigues MJ, Dauvergne X, Cérantola S, Custódio L, Magné C Foods 23-Apr-2024
PMCID:PMC11083217
doi:10.3390/foods13091294
PMID:38731664
Spillover effects from invasive Acacia alter the plant–pollinator networks and seed production of native plants Brett MF, Strauss P, van Wyk K, Vaughan IP, Memmott J Proc Biol Sci 10-Apr-2024
PMCID:PMC11003774
doi:10.1098/rspb.2023.2941
PMID:38593850
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
Presenting Eco-Anatomical Data for Saponaria jagelii, a Species on the Edge of the Blade Stefi AL, Mitsigiorgi K, Christodoulakis NS Life (Basel) 17-Mar-2024
PMCID:PMC10971642
doi:10.3390/life14030398
PMID:38541722
Long-Term Monitoring of the Traditional Knowledge of Plant Species Used for Culinary Purposes in the Valencia Region, South-Eastern Spain Belda A, Jordán-Nuñez J, Micó-Vicent B, López-Rodríguez D Plants (Basel) 08-Mar-2024
PMCID:PMC10975046
doi:10.3390/plants13060775
PMID:38592810
Morphology and Phylogeny Reveal Three New Species of Cytospora Associated with Tree Cankers in China Wang S, Jiang N, Ma R J Fungi (Basel) 09-Feb-2024
PMCID:PMC10890096
doi:10.3390/jof10020139
PMID:38392811
The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M Sci Rep 21-Dec-2023
PMCID:PMC10739867
doi:10.1038/s41598-023-49696-9
PMID:38129458
The vegetation of Holocene coastal dunes of the Cape south coast, South Africa Cowling RM, Cawthra H, Privett S, Grobler BA PeerJ 12-Dec-2023
PMCID:PMC10722985
doi:10.7717/peerj.16427
PMID:38107568
Agrobiodiversity-Based Landscape Design in Urban Areas Biasi R, Brunori E Plants (Basel) 10-Dec-2023
PMCID:PMC10747304
doi:10.3390/plants12244121
PMID:38140448
Effects of Datura stramonium L. Invasion into Different Habitats on Native Plant Functional Traits and Soil Carbon, Nitrogen and Phosphorus Stoichiometric Characteristics Lv J, Wang H, Chang N, Li H, Shi C Biology (Basel) 06-Dec-2023
PMCID:PMC10740971
doi:10.3390/biology12121497
PMID:38132323
Which Plant Species for Green Roofs in the Mediterranean Environment? Leotta L, Toscano S, Romano D Plants (Basel) 27-Nov-2023
PMCID:PMC10708222
doi:10.3390/plants12233985
PMID:38068621
A Bioinformatic Study on the Potential Anti-Vitiligo Activity of a Carpobrotus edulis Compound Trigui E, Ben Hassen H, Zaghden H, Trigui M, Achour S Molecules 11-Nov-2023
PMCID:PMC10673461
doi:10.3390/molecules28227545
PMID:38005266
Application of Taguchi method, response surface methodology, DFT calculation and molecular dynamics simulation into the removal of orange G and crystal violet by treated biomass Dabagh A, Benhiti R, EL-Habacha M, Ait Ichou A, Abali M, Assouani A, Guellaa M, Berisha A, Hsissou R, Sinan F, Zerbet M Heliyon 07-Nov-2023
PMCID:PMC10682636
doi:10.1016/j.heliyon.2023.e21977
PMID:38034727
Potential Implications of Hyperoside on Oxidative Stress-Induced Human Diseases: A Comprehensive Review Wang K, Zhang H, Yuan L, Li X, Cai Y J Inflamm Res 13-Oct-2023
PMCID:PMC10581022
doi:10.2147/JIR.S418222
PMID:37854313
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

Phytochemical Profile Top

Add a new one!
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 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 acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
5,6-Dihydroxy-2-methylcyclohex-3-ene-1-carboxylic acid 73299234 Click to see CC1C=CC(C(C1C(=O)O)O)O 172.18 unknown https://doi.org/10.1002/EJOC.200600987
Massarigenin E 16655648 Click to see 172.18 unknown https://doi.org/10.1002/EJOC.200600987
> 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 / Dihydrofurans / Furanones / Butenolides
3,4,7-trihydroxy-7-methyl-2-prop-1-enyl-3,4-dihydro-2H-furo[3,4-b]pyran-5-one 73299233 Click to see 242.22 unknown https://doi.org/10.1002/EJOC.200600987
Massarilactone D 16655647 Click to see 242.22 unknown https://doi.org/10.1002/EJOC.200600987
> Organoheterocyclic compounds / Furofurans
9,10-Dihydroxy-11-methyl-4-methylidene-3,6-dioxatricyclo[5.3.1.01,5]undecan-2-one 73837028 Click to see 226.23 unknown https://doi.org/10.1002/EJOC.200600987
Massarilactone A 10799243 Click to see 226.23 unknown https://doi.org/10.1002/EJOC.200600987
> 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 / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/S0378-8741(01)00197-0
> Phenylpropanoids and polyketides / Coumarins and derivatives
Graphislactone A 11278036 Click to see 302.28 unknown https://doi.org/10.1002/EJOC.200600987
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/S0378-8741(01)00197-0
> 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-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0378-8741(01)00197-0
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/S0378-8741(01)00197-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one 138107793 Click to see 610.60 unknown https://doi.org/10.1016/S0378-8741(01)00197-0
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
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(4aR,6S,6aR,7aS,8S,10R,11S,11aS,12aS,12bR)-4,4,6a,12b-tetramethyl-9-methylidene-1,2,3,4a,5,6,7a,8,10,11,12,12a-dodecahydronaphtho[2,1-b]chromene-6,8,10,11,11a-pentol 163187313 Click to see 396.50 unknown https://doi.org/10.1002/EJOC.200600987
4,4,6a,12b-Tetramethyl-9-methylidene-1,2,3,4a,5,6,7a,8,10,11,12,12a-dodecahydronaphtho[2,1-b]chromene-6,8,10,11,11a-pentol 73299235 Click to see CC1(CCCC2(C1CC(C3(C2CC4(C(C(C(=C)C(C4O3)O)O)O)O)C)O)C)C 396.50 unknown https://doi.org/10.1002/EJOC.200600987

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.