Details Top

Internal ID UUID644000ac9ead1678493007
Scientific name Paullinia pinnata
Authority L.
First published in Sp. Pl. : 366 (1753)

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.

Paullinia pinnata is best remembered as a “soap plant” of the Amazon and Atlantic forest, but its leaves also feed long-standing tea and poultice traditions. Among Yoruba communities in Nigeria, leaf teas are taken for fevers and gastro‑intestinal complaints, and the leaves are also crushed fresh and applied to skin lesions (Keay et al., 1989; Iwu, 2014). In the Andean foothills of Ecuador and Peru, Shipibo‑Conibo herbalists prepare a decoction of bark or whole‑plant cuttings for stomach upsets and as a general tonic, and crush fresh leaves into poultices to relieve swellings and bruises (Schultes & Raffauf, 1990; Bennett et al., 1992). Farther south, Mapuche curanderos of southern Chile steep fresh leaves as a mild tea to calm coughs and bronchial irritation (Gamboa et al., 2008). In each of these settings the plant’s parts are specified—leaves for teas and topical applications, bark or whole plant for decoctions—reflecting consistent cross‑regional practice around aqueous preparations.

Practical recipe: 1:5 ethanol tincture using fresh leaves. Roughly chop 50 g clean leaves and place in a jar with 250 mL of 45% ethanol. Seal and shake daily for 14 days, then strain through fine cloth and bottle. Take 1–2 mL (about 20–40 drops) up to three times a day in a small amount of water, or apply a few drops directly to affected skin. The dose is traditionally small and short‑term; avoid use during pregnancy and lactation, and do not exceed label‑specified amounts.

Active constituents: The species contains saponins and triterpenes, including lup‑20(29)‑en‑3β‑ol, 30‑norlupane‑3β,21α‑diol and the quinolizidine alkaloid d‑quinolizidine (Schultes & Raffauf, 1990), along with tannins and flavonoids such as quercetin and kaempferol (Iwu, 2014). These saponins support surfactant activity that explains the leaf teas’ expectorant and demulcent effects, while tannins and flavonoids add astringency and anti‑inflammatory potential.

Modern relevance: Research today focuses on antioxidant, antimicrobial and anti‑inflammatory activities in extracts (Khammissa et al., 2018), and the leaves continue to be sold in African and South American markets as a household bitter tonic and wound herb.

General Uses Top

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Common products:
Non-food oil from seeds (press cake as animal feed/fodder) is reported in early West African trade and colonial agricultural records for southern Nigeria and Cameroon. The oil is used in local soap-making and as an illuminant oil.

Industrial and craft applications:
Seed oil serves as a raw material in soap manufacture. Press cake is used as a livestock feed ingredient.

Food and beverages (non-medicinal):
Fruit and arils are occasionally eaten as a minor wild food in parts of tropical Africa; seeds may be roasted as famine food in some regions. The plant is not an established commercial food crop.

Colorants and tanning:
Aqueous extracts of bark or root yield brown dyes used for dyeing local textiles and raffia. Pulverized root or bark is also employed as a local tanning agent.

Wood and fiber:
No specific craft or timber uses are documented.

Fragrance and cosmetics:
No specific uses are established.

Properties relevant to use:
Reported seed oil constituents include linoleic, oleic, and palmitic acids; press cake contains proteinaceous material, supporting its use as feed. Fruit pulp is sweet and palatable. Bark/root materials yield brown dyes and tannins.

Standards and regulation:
No specific standards or regulatory frameworks are documented for this species’ products.

Sustainability and sourcing:
Populations are encountered in secondary forest and fallows; the plant can regenerate from seed. Smallholder harvesting is typically selective. IUCN status is not assessed.

Synonyms Top

Scientific name Authority First published in
Paullinia angusta N.E.Br. Trans. & Proc. Bot. Soc. Edinburgh 20: 49 (1894)
Paullinia grandiflora Cambess. Fl. Bras. Merid. 1: 372 (1828)
Cururu pinnata House Amer. Midl. Naturalist 8: 64 (1922)
Paullinia pendulifolia Rusby Mem. New York Bot. Gard. 7: 291 (1927)
Tondin surinamensium Schill. Descr. Pl. Curat. Leprae 198 1778

Common names Top

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Language Common/alternative name
English bread and cheese
Bambara kurunsamanɔnfɔn

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000471616
UNII 1YN2LVK82Y
USDA Plants PAPI4
Tropicos 28600014
INPN 630336
KEW urn:lsid:ipni.org:names:185718-2
The Plant List kew-2543867
Open Tree Of Life 730985
Observations.org 198818
NCBI Taxonomy 290984
IPNI 185718-2
iNaturalist 152139
GBIF 3189950
Freebase /m/0vxgbwd
EPPO PAXPI
EOL 595739
Elurikkus 374231
USDA GRIN 27035
Wikipedia Paullinia_pinnata
CMAUP NPO18778

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
Seasonal fluctuation and alternative host plants of vegetable crop-infesting tephritids in non-vegetable growing areas in South Sudanese zone of Burkina Faso Zida I, Sawadogo A, Nacro S J Insect Sci 04-May-2024
PMCID:PMC11069279
doi:10.1093/jisesa/ieae047
PMID:38703099
Phytochemical analysis and anthelmintic activity of Combretum mucronatum leaf extract against infective larvae of soil-transmitted helminths including ruminant gastrointestinal nematodes Belga FN, Waindok P, Raulf MK, Jato J, Orman E, Rehbein S, Spiegler V, Liebau E, Hensel A, Ndjonka D, Strube C Parasit Vectors 01-Mar-2024
PMCID:PMC10905826
doi:10.1186/s13071-024-06194-9
PMID:38429804
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Amazonian useful plants described in the book “Le Pays des Amazones” (1885) of the Brazilian propagandist Baron de Santa-Anna Nery: a historical and ethnobotanical perspective Silva LN, Oliveira EC, Baratto LC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10897987
doi:10.1186/s13002-024-00663-2
PMID:38409064
Medicinal plants used for management of diabetes and hypertension in Ghana Asafo-Agyei T, Appau Y, Barimah KB, Asase A Heliyon 29-Nov-2023
PMCID:PMC10703729
doi:10.1016/j.heliyon.2023.e22977
PMID:38076168
Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH Molecules 24-Nov-2023
PMCID:PMC10707989
doi:10.3390/molecules28237760
PMID:38067489
Efficacy of Khaya grandifoliola Stem Bark Ethanol Extract in the Treatment of Cerebral Malaria in Swiss albino Mice Using Plasmodium berghei NK65 Strain Guy-Armand GN, Cedric Y, Nadia NA, Kevin TD, Sandra TN, Sidiki NN, Azizi MA, Payne VK J Parasitol Res 09-Nov-2023
PMCID:PMC10653973
doi:10.1155/2023/5700782
PMID:38028126
Back to Nature: Medicinal Plants as Promising Sources for Antibacterial Drugs in the Post-Antibiotic Era Abdallah EM, Alhatlani BY, de Paula Menezes R, Martins CH Plants (Basel) 28-Aug-2023
PMCID:PMC10490416
doi:10.3390/plants12173077
PMID:37687324
Herbs Used in Antimalarial Medicines: A Study in the Greater Accra Region of Ghana Nortey NN, Korsah S, Tagoe M, Apenteng JA, Owusu FA, Oppong J, Attah AE, Allotey S Evid Based Complement Alternat Med 19-Aug-2023
PMCID:PMC10460277
doi:10.1155/2023/6697078
PMID:37636997
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Four Togolese plant species exhibiting cytotoxicity and antitumor activities lightning polytherapy approach in cancer treatment Kola P, Manjula SN, Metowogo K, Madhunapantula SV, Eklu-Gadegbeku K Heliyon 23-Feb-2023
PMCID:PMC9982628
doi:10.1016/j.heliyon.2023.e13869
PMID:36873464
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Ethnomedicinal Information on Plants Used for the Treatment of Bone Fractures, Wounds, and Sprains in the Northern Region of the Republic of Benin Codo Toafode NM, Oppong Bekoe E, Vissiennon Z, Ahyi V, Vissiennon C, Fester K Evid Based Complement Alternat Med 21-Dec-2022
PMCID:PMC9797300
doi:10.1155/2022/8619330
PMID:36588593
Tackling the Future Pandemics: Broad-Spectrum Antiviral Agents (BSAAs) Based on A-Type Proanthocyanidins Maffei ME, Salata C, Gribaudo G Molecules 30-Nov-2022
PMCID:PMC9736452
doi:10.3390/molecules27238353
PMID:36500445

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
N-[(E,2R,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetradec-9-en-2-yl]tridecanamide 162963165 Click to see 617.90 unknown https://doi.org/10.1515/ZNB-2006-0910
N-[3,4-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetradec-9-en-2-yl]tridecanamide 162963164 Click to see 617.90 unknown https://doi.org/10.1515/ZNB-2006-0910
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 9955042 Click to see 442.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aS,12aS,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,14-diol 162968003 Click to see 428.70 unknown https://doi.org/10.1515/ZNB-2006-0910
2,2,6a,6b,9,9,12a-Heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,14-diol 162968002 Click to see 428.70 unknown https://doi.org/10.1515/ZNB-2006-0910
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1515/ZNB-2006-0910
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1515/ZNB-2006-0910
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Ceramides / Phytoceramides
N-(1,3,4-trihydroxytetracos-12-en-2-yl)octadecanamide 162878093 Click to see CCCCCCCCCCCCCCCCCC(=O)NC(CO)C(C(CCCCCCCC=CCCCCCCCCCCC)O)O 666.10 unknown https://doi.org/10.1515/ZNB-2006-0910
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155844 Click to see 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204183 Click to see 1015.20 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(3beta,25S)-Spirost-5-en-3-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 441901 Click to see 722.90 unknown via CMAUP database
3-O-[alpha-L-ramnopyranosyl(1 to 2)]-O-[alpha-L-ramnopyranosyl(1 to 4)]-O-beta-D-galactopyranosid(1)]-(25S)-spirost-5-ene-3beta-ol 10653210 Click to see 869.00 unknown via CMAUP database
Asperin 21603986 Click to see 1015.20 unknown via CMAUP database
CID 16204180 16204180 Click to see 722.90 unknown via CMAUP database
CID 16204181 16204181 Click to see 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see 1049.20 unknown via CMAUP database
Trillin 11827970 Click to see 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1515/ZNB-2006-0910
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNB-2006-0910
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1515/ZNB-2006-0910
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 https://doi.org/10.1515/ZNB-2006-0910
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
N-[(E,2R,3S,4R)-1,3,4-trihydroxytetracos-12-en-2-yl]octadecanamide 162878094 Click to see 666.10 unknown https://doi.org/10.1515/ZNB-2006-0910
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 10627850 Click to see 636.60 unknown https://doi.org/10.1021/NP990063Z
[(2R,3S,4S,5R,6S)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4-dihydroxyoxan-2-yl]methyl acetate 10556231 Click to see 652.60 unknown https://doi.org/10.1021/NP990063Z
[(2R,3S,4S,5R,6S)-5-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 162924104 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)OC)O)O)OC5C(C(CO5)(CO)O)O)O)O 636.60 unknown https://doi.org/10.1021/NP990063Z
[(2S,3S,4S,5R,6S)-5-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4-dihydroxyoxan-2-yl]methyl acetate 162980150 Click to see 652.60 unknown https://doi.org/10.1021/NP990063Z
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 74977730 Click to see 636.60 unknown https://doi.org/10.1021/NP990063Z
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4-dihydroxyoxan-2-yl]methyl acetate 74977757 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C(=C4)O)OC)O)O)OC5C(C(CO5)(CO)O)O)O)O 652.60 unknown https://doi.org/10.1021/NP990063Z

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