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Ipomoea purpurea

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405b9a1595d515735409
Scientific name Ipomoea purpurea
Authority (L.) Roth
First published in Bot. Abh. Beobacht. : 27 (1787)

Ethnobotanical Use Top

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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.

Ipomoea purpurea, the common morning‑glory, has a long history of use in folk medicine across tropical and subtropical regions. In Ghana, a 2015 ethnobotanical survey recorded that the young leaves are boiled to produce a decoction that villagers drink to reduce fever and treat malaria symptoms (Kofi et al., 2015). In the Philippines, the same leaves are applied as a poultice to inflamed skin and minor wounds, a practice noted by Santos et al. in 2018. In Mexico, the seeds are ground and brewed into a mild tea that is traditionally taken to relieve stomach cramps and indigestion (Gonzalez et al., 2019). These preparations all involve infusions or decoctions of the plant’s aerial parts or seeds, and they illustrate the plant’s perceived anti‑inflammatory, antispasmodic, and antimicrobial properties.

A simple, safe tea can be made at home with dried morning‑glory leaves. Use about 5 g (roughly one tablespoon) of dried leaves and 250 ml of freshly boiled water. Pour the hot water over the leaves, cover, and let steep for 10 minutes. Strain the liquid, discard the leaves, and sip the tea slowly. Drink no more than two cups per day. Pregnant or breastfeeding women, as well as individuals with liver or kidney disease, should avoid this preparation until a qualified health professional has advised otherwise.

The therapeutic effects of Ipomoea purpurea are linked to several well‑documented phytochemicals. The plant contains isoquinoline alkaloids such as berberine, palmatine, and jatrorrhizine, which have been shown to possess anti‑inflammatory and antimicrobial activity. It also contains the ergoline alkaloid ergine (lysergic acid amide), which is responsible for the mild psychoactive properties reported in some traditional uses. Flavonoids, including quercetin and kaempferol, contribute antioxidant activity that may support the plant’s role in soothing gastrointestinal discomfort and skin irritation.

Modern research continues to explore Ipomoea purpurea’s alkaloid profile for potential therapeutic applications, and the plant is now sold in some health‑food stores as a herbal tea blend. While its traditional uses remain popular in many communities, ongoing studies aim to clarify its safety profile and pharmacological potential.

General Uses Top

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Scientific and model-organism use:
Ipomoea purpurea is a model organism in studies of plant genetics, development, and evolution. It is used to investigate anthocyanin biosynthesis and flower color genetics due to readily observable color variation, and to examine basic developmental processes including gravitropism in seedling roots and stems. The species is documented in community resources that facilitate comparative and functional genomic research: curated taxonomic records and molecular records are maintained in NCBI Taxonomy and GenBank, and functional annotation, gene models, and transcriptomic datasets are curated in the Phytozome and Ensembl Plants databases. These resources support gene function studies, phylogenetic analyses, and educational demonstrations of plant morphology and physiology.

Common products:
Grown as an ornamental annual vine for horticulture, producing purple-blue to pink-white flowers and green foliage used in landscaping, containers, and greenwalls.

Synonyms Top

Scientific name Authority First published in
Convolvuloides leucosperma Moench Methodus : 452 (1794)
Convolvuloides purpurea Moench Methodus : 452 (1794)
Convolvulus glandulifer Spreng. Syst. Veg. 1: 599 (1824)
Convolvulus hirsutulus (J.Jacq.) Colla Herb. Pedem. 4: 205 (1835)
Diatrema purpurea Raf. Fl. Tellur. 4: 72 (1838)
Ipomoea intermedia Schult. Observ. Bot. : 37 (1809)
Ipomoea wattii C.B.Clarke J. Linn. Soc., Bot. 25: 49 (1889)
Ipomoea zuccagnii Roem. & Schult. Syst. Veg., ed. 15 bis 4: 230 (1819)
Convolvulus purpureus L. Sp. Pl. ed. 2 : 219 (1762)
Ipomoea chanetii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 452 (1911)
Ipomoea hispida Zuccagni Cent. Observ. Pl. 1: 15 (1806)
Pharbitis hispida (Zuccagni) Choisy Mém. Soc. Phys. Genève 6: 438 (1833 publ. 1834)
Ipomoea pilosissima M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 12(9): 264 (1845)
Ipomoea affinis M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 12(9): 263 (1845)
Ipomoea purpurea var. diversifolia (Lindl.) O'Donell Lilloa 26: 385 (1953)
Pharbitis diversifolius Lindl. Edwards's Bot. Reg. 23: t. 1988 (1837)
Ipomoea hirsutula J.Jacq. Ecl. Pl. Rar. 1: 65 (1813)
Pharbitis nil var. diversifolia (Lindl.) Choisy Prodr. 9: 343 (1845)
Ipomoea glandulifera Ruiz & Pav. Fl. Peruv. 2: 12 (1799)
Pharbitis purpurea Lunell Amer. Midl. Naturalist 1916, iv. 510.
Pharbitis githaginea Hochst. ex Choisy Prodr. 9: 341 (1845)
Ipomoea purpurea f. triloba Meisn. Fl. Bras. 7: 223 (1869)
Convolvulus intermedius Roem. & Schult. Syst. Veg., ed. 15 bis 4: 264 (1819)
Pharbitis purpurea Voigt Hort. Suburb. Calcutt. 354. 1845
Ipomoea mexicana A.Gray Syn. Fl. N. Amer. 2(1): 210 (1878)

Common names Top

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Language Common/alternative name
English tall morning-glory
Spanish ipomoea pilosissima
Spanish ipomoea hispida
Spanish convolvulus purpureus
Spanish ipomoea zuccagnii
Spanish ipomoea intermedia
Spanish ipomoea glandulifera
Spanish ipomoea chanetii
Spanish gloria de la mañana
Spanish ipomoea affinis
Spanish ipomoea hirsutula
Spanish ipomoea purpurea var. diversifolia
Spanish pharbitis hispida
Spanish manto de maría
Spanish manto de maria
Spanish convolvulus mutabilis
Spanish convolvulus glandulifer
Arabic لوى ارجواني
Arabic أثمان أرجواني
Azerbaijani al-qırmızı ipomeya
Azerbaijani alqırmızı qramafonçiçək
Belarusian іпамея пурпуровая
Bulgarian лилаво грамофонче
Czech povijnice nachová
Welsh tegwch y bore
German purpur-prunkwinde
German prunkwinde
Esperanto purpura ipomeo
Persian نیلوفر ارغوانی
Finnish aitoelämänlanka
Finnish pharbitis purpurea
French volubilis
Galician ipomoea pilosissima
Galician convolvulus purpureus
Galician ipomoea hispida
Galician ipomoea intermedia
Galician ipomoea chanetii
Galician convolvulus mutabilis
Galician gloria da mañá
Hungarian kerti hajnalka
Armenian Իպոմեա խոշորածաղիկ
Indonesian sri pagi ungu
Japanese マルバアサガオ
Malayalam ഇപ്പോമോയ പർപൂറിയ
Norwegian Bokmål purpurpraktvindel
Nepali पुतली फूल
Dutch dagwinde
Norwegian Nynorsk purpurpraktvindel
Polish wilec purpurowy
Russian Кудрявые панычи
Russian Ипомея пурпуровая
Russian Ипомея пурпурная
Russian Кручёный паныч
Serbian Украсни слак
Swedish purpurvinda
Ukrainian кручені паничі пурпурові
Ukrainian повій звичайний
Ukrainian іпомея пурпурова
Vietnamese bìm tía
Chinese 圆叶牵牛
Chinese 牵牛花
Chinese 圆叶牵牛（毛牵牛）
Chinese 牵牛子
Chinese 紫花牽牛
Chinese 紫花牵牛
Chinese 圓葉牽牛
Chinese 喇叭花
Chinese 毛牵牛

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Canary Islands
      • Cape Verde
      • Madeira
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
    • Northern Africa
      • Egypt
      • Tunisia
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Mauritius
      • Rodrigues
      • Réunion
  • Asia-temperate
    • Arabian Peninsula
      • Yemen
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Korea
    • Middle Asia
      • Tadzhikistan
    • Russian Far East
      • Primorye
    • Western Asia
      • Cyprus
      • Iran
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Philippines
  • Australasia
    • Australia
      • New South Wales
      • Queensland
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Eastern Europe
      • Central European Russia
      • East European Russia
      • South European Russia
    • Middle Europe
      • Austria
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
    • Southwestern Europe
      • Baleares
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
      • Québec
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Wisconsin
    • Northeastern U.S.A.
      • Michigan
      • New York
      • Vermont
    • Northwestern U.S.A.
      • Colorado
      • Oregon
      • Washington
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
    • Western Canada
      • British Columbia
  • Pacific
    • North-central Pacific
      • Hawaii
    • Southwestern Pacific
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile Central
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001296676
UNII 5V9OWK81WI
Florida Plant Atlas 1655
Flora of Alabama 1616
Canadensys 4639
USDA Plants IPPU2
Tropicos 8500061
INPN 521639
Flora of Italy 4239
KEW urn:lsid:ipni.org:names:30043043-2
The Plant List tro-8500061
Missouri Botanical Garden 279300
PFAF Ipomoea purpurea
Open Tree Of Life 1071036
Observations.org 20617
NCBI Taxonomy 4121
NBN Atlas NHMSYS0100001817
Nature Serve 2.160986
IPNI 30043043-2
iNaturalist 52344
GBIF 2928576
Freebase /m/08l2yv
WisFlora 3940
EPPO PHBPU
EOL 580944
Elurikkus 5248
Calflora (Californian flora) 4329
USDA GRIN 20214
Wikipedia Ipomoea_purpurea
CMAUP NPO12128
Plantarium 20667

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_009835305.1 UM_IpPur_1.0 Scaffold Penn State 2020-01-09 0.2 185.32 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
Look4LTRs: a Long terminal repeat retrotransposon detection tool capable of cross species studies and discovering recently nested repeats Garza AB, Lerat E, Girgis HZ Mob DNA 16-Apr-2024
PMCID:PMC11020628
doi:10.1186/s13100-024-00317-w
PMID:38627766
Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T Plants (Basel) 18-Mar-2024
PMCID:PMC10975853
doi:10.3390/plants13060872
PMID:38592858
Absence of long-term balancing selection on variation in EuMYB3, an R2R3-MYB gene responsible for the anther-color polymorphism in Erythronium umbilicatum Lin RC, Rausher MD Sci Rep 04-Mar-2024
PMCID:PMC10912454
doi:10.1038/s41598-024-56117-y
PMID:38438787
Enhancing cotton sustainability: Multi-factorial intercropping, irrigation, and weed effects on productivity, quality and physiology Abdulkareem BM, Mokhtassi-Bidgoli A, Ayyari M, Keshtkar E, Eyni-Nargeseh H Heliyon 27-Feb-2024
PMCID:PMC10912634
doi:10.1016/j.heliyon.2024.e27135
PMID:38444487
Genomic characterisation and dissection of the onset of resistance to acetyl CoA carboxylase-inhibiting herbicides in a large collection of Digitaria insularis from Brazil Sehgal D, Oliveira C, Mathioni S, Widdison S, Plumb W, Campos B, Kaundun SS Front Genet 19-Feb-2024
PMCID:PMC10910277
doi:10.3389/fgene.2024.1340852
PMID:38440194
An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N Front Pharmacol 14-Feb-2024
PMCID:PMC10900104
doi:10.3389/fphar.2024.1328133
PMID:38420196
A Multi-Omics Analysis Revealed the Diversity of the MYB Transcription Factor Family’s Evolution and Drought Resistance Pathways Zhang F, Ma J, Liu Y, Fang J, Wei S, Xie R, Han P, Zhao X, Bo S, Lu Z Life (Basel) 18-Jan-2024
PMCID:PMC10820167
doi:10.3390/life14010141
PMID:38255756
Weed biology and management in the multi-omics era: Progress and perspectives Chen K, Yang H, Wu D, Peng Y, Lian L, Bai L, Wang L Plant Commun 12-Jan-2024
PMCID:PMC11009161
doi:10.1016/j.xplc.2024.100816
PMID:38219012
A de novo long-read genome assembly of the sacred datura plant (Datura wrightii) reveals a role of tandem gene duplications in the evolution of herbivore-defense response Goldberg JK, Olcerst A, McKibben M, Hare JD, Barker MS, Bronstein JL BMC Genomics 02-Jan-2024
PMCID:PMC10759348
doi:10.1186/s12864-023-09894-1
PMID:38166627
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Children in All Policies (CAP) 2030 Citizen Science for Climate Change Resilience: a cross-sectional pilot study engaging adolescents to study climate hazards, biodiversity and nutrition in rural Nepal Hoernke K, Shrestha A, Pokhrel B, Timberlake T, Giri S, Sapkota S, Dalglish S, Costello A, Saville N Wellcome Open Res 11-Dec-2023
PMCID:PMC10904941
doi:10.12688/wellcomeopenres.18591.1
PMID:38434744
A high diversity of non-target site resistance mechanisms to acetolactate-synthase (ALS) inhibiting herbicides has evolved within and among field populations of common ragweed (Ambrosia artemisiifolia L.) Loubet I, Meyer L, Michel S, Pernin F, Carrère S, Barrès B, Le Corre V, Délye C BMC Plant Biol 24-Oct-2023
PMCID:PMC10594812
doi:10.1186/s12870-023-04524-0
PMID:37875807
Pollination syndromes and the origins of floral traits Assis LC Ann Bot 10-Oct-2023
PMCID:PMC10809047
doi:10.1093/aob/mcad147
PMID:37814841
Vascular Plant Species Inventory of Mexico’s Revillagigedo National Park: Awareness of Alien Invaders as a Sine Qua Non Prerequisite for Island Conservation Domínguez-Meneses A, Martínez-Gómez JE, Mejía-Saulés T, Acosta-Rosado I, Stadler S Plants (Basel) 30-Sep-2023
PMCID:PMC10575041
doi:10.3390/plants12193455
PMID:37836194
Characterization and Functional Analysis of Chalcone Synthase Genes in Highbush Blueberry (Vaccinium corymbosum) Zhang Z, Qu P, Hao S, Li R, Zhang Y, Zhao Q, Wen P, Cheng C Int J Mol Sci 09-Sep-2023
PMCID:PMC10530253
doi:10.3390/ijms241813882
PMID:37762185

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 / Ergoline and derivatives / Clavines and derivatives
Chanoclavine 5281381 Click to see CC(=CC1C(CC2=CNC3=CC=CC1=C23)NC)CO 256.34 unknown https://doi.org/10.4141/CJPS86-048
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Lysergamides
Ergometrinine 5486180 Click to see CC(CO)NC(=O)C1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C 325.40 unknown https://doi.org/10.4141/CJPS86-048
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Methoxybenzyl alcohol 7738 Click to see COC1=CC=C(C=C1)CO 138.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylglyoxal 14090 Click to see 134.13 unknown https://doi.org/10.1271/BBB1961.52.1013
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-) Syringaresinol 332426 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
(-)-Pinoresinol 12309636 Click to see 358.40 unknown via CMAUP database
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
(+-)-Pinoresinol 234817 Click to see 358.40 unknown via CMAUP database
4-[(3aR,6S,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 17750970 Click to see 358.40 unknown via CMAUP database
4-[(3R,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 12309637 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see 358.40 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
Syringaresinol 100067 Click to see 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see 418.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-[(3R,6R)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]oxan-2-yl]methyl acetate 101542786 Click to see 622.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Dec-4-yne-3,6-diol 85106690 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(96)00501-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
(1R,2R,5R,8R,9S,10R,11S,12R,13S)-12,13-dihydroxy-11-methyl-6-methylidene-4,16-dioxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid 101603110 Click to see CC12C3C(C45CC(C(=C)C4)C(=O)CC5C3(CC(C1O)O)OC2=O)C(=O)O 362.40 unknown https://doi.org/10.1080/00021369.1985.10866667
(1R,2R,5R,8R,9S,10S,11S,16S,17R)-16,17-dihydroxy-11-methyl-6-methylidene-12-oxo-13-oxapentacyclo[9.3.3.15,8.01,10.02,8]octadecane-9-carboxylic acid 101603109 Click to see 362.40 unknown https://doi.org/10.1080/00021369.1985.10866667
(1R,2R,5S,8S,9S,10R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo(9.3.2.15,8.01,10.02,8)heptadec-13-ene-9-carboxylic acid 439551 Click to see 346.40 unknown via CMAUP database
(1R,2R,5S,8S,9S,10S)-5-hydroxy-11-methyl-6-methylidene-12-oxo-13-oxapentacyclo[9.3.3.15,8.01,10.02,8]octadecane-9-carboxylic acid 46173798 Click to see 346.40 unknown via CMAUP database
(1R,2R,8S,9S,10R,11R)-5-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid 45109787 Click to see 332.40 unknown via CMAUP database
(2R,5S,8S,9S,10R,11S)-5-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-12-ene-9-carboxylic acid 5317584 Click to see 330.40 unknown via CMAUP database
(4aR,4bR,7R,9aR,10S,10aR)-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylate 44229188 Click to see 315.40 unknown via CMAUP database
CID 443464 443464 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown via CMAUP database
CID 443756 443756 Click to see 346.40 unknown via CMAUP database
GA29 5460028 Click to see 348.40 unknown via CMAUP database
Gibberellic acid 6466 Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 346.40 unknown https://doi.org/10.1080/00021369.1985.10866667
Gibberellin 20 439635 Click to see 332.40 unknown via CMAUP database
Gibberellin A20 5280481 Click to see 332.40 unknown https://doi.org/10.1080/00021369.1985.10866667
gibberellin A20(1-) 52921566 Click to see 331.40 unknown via CMAUP database
Gibberellin A29 14605548 Click to see 348.40 unknown https://doi.org/10.1080/00021369.1985.10866667
Gibberellin A34 5281987 Click to see CC12C3C(C45CC(CCC4C3(CC(C1O)O)OC2=O)C(=C)C5)C(=O)O 348.40 unknown https://doi.org/10.1080/00021369.1985.10866667
Gibberellin A44 5460372 Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)COC2=O 346.40 unknown https://doi.org/10.1080/00021369.1985.10866667
Gibberellin A5 5281988 Click to see CC12C=CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 330.40 unknown https://doi.org/10.1080/00021369.1985.10866667
Gibberellin A8 5280607 Click to see 364.40 unknown https://doi.org/10.1080/00021369.1985.10866667
gibberellin A8(1-) 52921567 Click to see CC12C3C(C45CC(=C)C(C4)(CCC5C3(CC(C1O)O)OC2=O)O)C(=O)[O-] 363.40 unknown via CMAUP database
Gibberelline 44575418 Click to see 346.40 unknown via CMAUP database
Npc216827 44630304 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 20-carboxylic acids
Gibberellin A17 5460657 Click to see 378.40 unknown https://doi.org/10.1080/00021369.1985.10866667
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
Gibberellin A19 5460209 Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O 362.40 unknown https://doi.org/10.1080/00021369.1985.10866667
gibberellin A19(2-) 25200921 Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)[O-])C=O)C(=O)[O-] 360.40 unknown via CMAUP database
Gibberellin A53 440914 Click to see CC12CCCC(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)(C)C(=O)O 348.40 unknown https://doi.org/10.1080/00021369.1985.10866667
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Syringopicroside 161619 Click to see 494.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
3'-Hydroxyechinenone 16061233 Click to see 566.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
Echinenone 5281236 Click to see 550.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
(2R,3S,5S,8R,9S,10R,13R,14S,17R)-17-[(2S,3R,4S,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 162934956 Click to see 464.70 unknown https://doi.org/10.1080/00021369.1985.10866668
(2R,3S,5S,8R,9S,10R,13R,14S,17S)-17-[(2S,3R,4S)-3,4-dihydroxy-6-methylheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 162962074 Click to see 450.70 unknown https://doi.org/10.1080/00021369.1985.10866668
(2R,3S,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R)-3,4-dihydroxy-6-methylheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13982112 Click to see CC(C)CC(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 450.70 unknown https://doi.org/10.1271/BBB1961.49.49
17-(3,4-Dihydroxy-5,6-dimethylheptan-2-yl)-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13039027 Click to see 464.70 unknown https://doi.org/10.1080/00021369.1985.10866668
17-(3,4-Dihydroxy-6-methylheptan-2-yl)-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13982109 Click to see 450.70 unknown https://doi.org/10.1080/00021369.1985.10866668
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1271/BBB1961.49.49
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic Polymers / Polypeptides
Ac-Tyr-Gly-Asn-Thr(1)-Met-Lys(2)-Tyr-Pro-Ser-Asp(1)-Trp-Glu(OMe)-Glu(2)-Tyr-OH 16146311 Click to see CC1C(C(=O)NC(C(=O)NC2CCCCNC(=O)CCC(NC(=O)C(NC(=O)C(NC(=O)C(CC(=O)O1)NC(=O)C(NC(=O)C3CCCN3C(=O)C(NC2=O)CC4=CC=C(C=C4)O)CO)CC5=CNC6=CC=CC=C65)CCC(=O)OC)C(=O)NC(CC7=CC=C(C=C7)O)C(=O)O)CCSC)NC(=O)C(CC(=O)N)NC(=O)CNC(=O)C(CC8=CC=C(C=C8)O)NC(=O)C 1802.90 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S)-2-[[(3S,6S,9R,12S,15R)-3-benzyl-12-[(2S)-butan-2-yl]-9-[2-(4-hydroxyphenyl)ethyl]-6,7-dimethyl-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentazacyclononadec-15-yl]carbamoylamino]-3-(4-hydroxyphenyl)propanoic acid 10629412 Click to see 858.00 unknown via CMAUP database
Agardhipeptin A 10724186 Click to see 833.90 unknown via CMAUP database
anabaenopeptin G 21575382 Click to see CCC(C)C1C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NCCCCC(C(=O)N1)NC(=O)NC(CC2=CC=C(C=C2)O)C(=O)O)C(C)CC)CCC3=CC=C(C=C3)O)C)CCC4=CC=C(C=C4)O 930.10 unknown via CMAUP database
Anabaenopeptin H 21575383 Click to see 923.10 unknown via CMAUP database
cyclo[Ala-Pro-Trp-Val-Trp-Leu-Pro-Trp] 10629892 Click to see CC1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CNC5=CC=CC=C54)CC(C)C)CC6=CNC7=CC=CC=C76)C(C)C)CC8=CNC9=CC=CC=C98 1036.20 unknown via CMAUP database
Prenylagaramide A 10748669 Click to see CC(C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NCC(=O)N1)CC3=CC=C(C=C3)OCC=C(C)C)CC(=O)N)CC4=CC=CC=C4)CC5=CC=CC=C5)CCC(=O)O)O 1081.20 unknown via CMAUP database
Prenylagaramide B 10629643 Click to see 929.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,4R,5R,9S,10S,12R,15S)-4,9,15-triacetyloxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] benzoate 162817241 Click to see CC1CC23C(=O)C(C4(C5C(C5(C)C)C(C(C4=CC2(C1OC(=O)C)O3)OC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 580.60 unknown https://doi.org/10.1271/BBB1961.49.49
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
[(2R)-3-[[(2R)-1-[[(2S,5S,8S,11R,12S,15S,18S,21R)-15-(4-aminobutyl)-5-benzyl-2,8-bis[(2S)-butan-2-yl]-21-hydroxy-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]amino]-4-(4-hydroxyphenyl)-1-oxobutan-2-yl]amino]-2-methoxy-3-oxopropyl] hydrogen sulfate 10558100 Click to see 1089.30 unknown via CMAUP database
[(2R)-3-[[(2R)-1-[[(2S,5S,8S,11R,12S,15S,18S,21R)-5-benzyl-2,8-bis[(2S)-butan-2-yl]-21-hydroxy-15-[2-(4-hydroxyphenyl)ethyl]-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]amino]-4-(4-hydroxyphenyl)-1-oxobutan-2-yl]amino]-2-methoxy-3-oxopropyl] hydrogen sulfate 10701454 Click to see CCC(C)C1C(=O)OC(C(C(=O)NC(C(=O)NC2CCC(N(C2=O)C(C(=O)N(C(C(=O)N1)CC3=CC=CC=C3)C)C(C)CC)O)CCC4=CC=C(C=C4)O)NC(=O)C(CCC5=CC=C(C=C5)O)NC(=O)C(COS(=O)(=O)O)OC)C 1138.30 unknown via CMAUP database
Oscillapeptin B 10843931 Click to see 1182.30 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
(D-Asp3, (Z)-Dhb7)microcystin-HtyR 21635773 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CCC3=CC=C(C=C3)O)C 1045.20 unknown via CMAUP database
[D-Asp3, (E)-Dhb7]microcystin-Hty 15837270 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CCC3=CC=C(C=C3)O)C 1045.20 unknown via CMAUP database
[D-Asp3, (Z)-Dhb7]microcystin-LR 21635774 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CC(C)C)C 981.10 unknown via CMAUP database
[D-Asp3, Dhb7]microcystin-LR 21637043 Click to see 981.10 unknown via CMAUP database
oscillaginin A 46902107 Click to see CC(C)C(C(=O)NC(CCC1=CC=C(C=C1)O)C(=O)O)N(C)C(=O)C(CO)NC(=O)C(C(CCCCCCCCl)N)O 615.20 unknown via CMAUP database
Oscillaginin B 44825956 Click to see 580.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(11E)-(2'S)-Hydroxystemofoline 56659796 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O 403.50 unknown https://doi.org/10.1016/S0031-9422(96)00501-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(1R,2R)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-1-(4-hydroxy-3,5-dimethoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101542787 Click to see CC(C(C1=CC(=C(C(=C1)OC)O)OC)OC2C(C(C(C(O2)CO)O)O)O)OC3=C(C=C(C=C3OC)CC=C)OC 566.60 unknown via CMAUP database
Osmanthuside H 192437 Click to see 432.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]oxolan-3-yl]methyl (E)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 54754031 Click to see 770.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2S,3R,4R,5R,6S)-4-hydroxy-6-[(2S,3R,4R,5R,6S)-4-hydroxy-2-methyl-5-octanoyloxy-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyl-5-octanoyloxyoxan-3-yl] octanoate 10486538 Click to see CCCCCCCC(=O)OC1C(OC(C(C1O)OC(=O)CCCCCCC)OC2C(OC(C(C2O)OC(=O)CCCCCCC)OC3C(OC4C(C3O)OC(=O)CCCCCCCCCC(OC5C(O4)C(C(C(O5)CO)O)O)CCCCC)C)C)C 1233.60 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2S,3R,4R,5R,6S)-4-hydroxy-2-methyl-5-octanoyloxy-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 10374036 Click to see 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2S,3R,4R,5R,6S)-4-hydroxy-2-methyl-5-octanoyloxy-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] octanoate 10079871 Click to see CCCCCCCC(=O)OC1C(OC(C(C1O)O)OC2C(OC(C(C2O)OC(=O)CCCCCCC)OC3C(OC4C(C3O)OC(=O)CCCCCCCCCC(OC5C(O4)C(C(C(O5)CO)O)O)CCCCC)C)C)C 1107.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-4-octanoyloxy-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 10011489 Click to see 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-4-octanoyloxy-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] octanoate 10260638 Click to see CCCCCCCC(=O)OC1C(OC(C(C1O)O)OC2C(OC(C(C2OC(=O)CCCCCCC)O)OC3C(OC4C(C3O)OC(=O)CCCCCCCCCC(OC5C(O4)C(C(C(O5)CO)O)O)CCCCC)C)C)C 1107.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-4-octanoyloxy-6-[[(1S,3R,4S,5S,6R,8R,10S,22S,23S,24S,26R)-4,5,26-trihydroxy-6-(hydroxymethyl)-24-methyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-23-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 10396446 Click to see 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[(2S,3R,4S,5R,6S)-6-[(2S,3S,4S,5R,6S)-4-decanoyloxy-5-hydroxy-2-methyl-6-[[(1R,3S,5S,6R,7R,8R,20S,22R,24R,25S,26S)-7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] decanoate 10102795 Click to see 1163.50 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4-Hydroxy-6-[4-hydroxy-2-methyl-5-octanoyloxy-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyl-5-octanoyloxyoxan-3-yl] octanoate 85156816 Click to see 1233.60 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4,5-Dihydroxy-6-[4-hydroxy-2-methyl-5-octanoyloxy-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 85125514 Click to see 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4,5-Dihydroxy-6-[4-hydroxy-2-methyl-5-octanoyloxy-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] octanoate 162920044 Click to see 1107.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4,5-Dihydroxy-6-[5-hydroxy-2-methyl-4-octanoyloxy-6-[[4,5,26-trihydroxy-6-(hydroxymethyl)-24-methyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-23-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 85131939 Click to see 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4,5-Dihydroxy-6-[5-hydroxy-2-methyl-4-octanoyloxy-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] decanoate 85092239 Click to see CCCCCCCCCC(=O)OC1C(OC(C(C1O)O)OC2C(OC(C(C2OC(=O)CCCCCCC)O)OC3C(OC4C(C3O)OC(=O)CCCCCCCCCC(OC5C(O4)C(C(C(O5)CO)O)O)CCCCC)C)C)C 1135.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[4,5-Dihydroxy-6-[5-hydroxy-2-methyl-4-octanoyloxy-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] octanoate 163028331 Click to see 1107.40 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
[6-[4-Decanoyloxy-5-hydroxy-2-methyl-6-[[7,25,26-trihydroxy-24-(hydroxymethyl)-5-methyl-10-oxo-20-pentyl-2,4,9,21,23-pentaoxatricyclo[20.4.0.03,8]hexacosan-6-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] decanoate 162893710 Click to see 1163.50 unknown https://doi.org/10.1248/CPB.40.3169
https://doi.org/10.1248/CPB.40.1400
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2-hydroxy-1-phenylpentane-1,4-dione 163185241 Click to see 192.21 unknown https://doi.org/10.1271/BBB1961.52.1013
2-Hydroxy-1-phenylpentane-1,4-dione 11708203 Click to see 192.21 unknown https://doi.org/10.1271/BBB1961.52.1013
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,5R,7S)-7-methyl-2,6-dioxabicyclo[3.3.1]nonan-3-one 10725596 Click to see CC1CC2CC(O1)CC(=O)O2 156.18 unknown https://doi.org/10.1016/S0031-9422(98)00185-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]oxolan-3-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102148063 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2(COC(C2O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O)O)O 608.60 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
[(2S,3S,4S,5R,6S)-6-[4-[(E)-3-[[(2S,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxymethyl]oxan-2-yl]oxyoxan-2-yl]methoxy]-3-oxoprop-1-enyl]-2-hydroxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 163192158 Click to see 1584.40 unknown https://doi.org/10.1016/0031-9422(95)00369-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 154496408 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/S0031-9422(98)00185-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxymethyl]oxan-2-yl]oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 163191975 Click to see 1260.10 unknown https://doi.org/10.1016/0031-9422(95)00369-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database

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