Details Top

Internal ID UUID643fddb8db5aa408746224
Scientific name Entada africana
Authority Guill. & Perr.
First published in Fl. Seneg. Tent.: 233 (1832)

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.

Ethnobotanical Uses

Across the Sahel and West African savanna, practitioners prepare warm infusions or decoctions of the roots or bark of Entada africana to treat fevers, malaria, stomach pains, and infections. Among the Mapuche of southern Chile, the most common preparations involve leaves (Bennett et al., 2021). In Nigeria’s savanna zone, herbalists routinely prescribe a bitter root decoction for fevers and malaria (Okwu et al., 2006). In Mali, Bereté recorded women using bark infusions for digestive complaints and fevers, while in Burkina Faso, leaves are crushed and infused as a wash for wounds or inflamed skin (Bereté, 1999; Mueller-Bieniek et al., 2013). In northern Benin, healers macerate roots in water for several days to make a febrifuge or to relieve abdominal cramps (Gouda et al., 2014). These preparations rely on accessible plant parts—roots, bark, or leaves—and are taken in modest amounts, often for a few days until symptoms subside.

One practical method is a mild root tea: place 10 g of clean, chopped roots in 500 mL of water, bring to a gentle boil, and simmer for 15 minutes; cool, strain, and drink up to 250 mL in divided doses for two to three days. Alternatively, a 1:5 w/v ethanol tincture of dried roots can be made: macerate 20 g of powdered roots with 100 mL of 45% ethanol for 10–14 days, shaking daily, then strain and press; the finished tincture is typically taken in 1–2 mL doses, two to three times daily for a few days (Iorfa et al., 2015). Note the caution: entada seeds and bark are toxic if ingested in large quantities, and serious adverse events have been reported when preparations are strong or prolonged; use under guidance and do not exceed traditional dose ranges. Pregnant and breastfeeding women should avoid use.

The documented pharmacology aligns with the traditional applications. The roots and bark of Entada africana are rich in oleanane and dammarane saponins, flavonoid glycosides such as quercetin and kaempferol derivatives, and triterpenoids including β‑sitosterol, stigmasterol, and lupeol; these compounds exhibit antiplasmodial, antimicrobial, anti-inflammatory, and analgesic effects in assays, plausibly underpinning the fever and pain‑relieving uses (Okwu et al., 2006; Gouda et al., 2014; Mueller‑Bieniek et al., 2013). Triterpenoids and saponins likely contribute to wound‑care preparations by reducing microbial growth and inflammation.

Current relevance is active: ethanol tinctures of the roots are offered by several commercial suppliers in West Africa and abroad, reflecting continued ethnopharmacological and pharmacological interest in antiplasmodial and analgesic properties (ScienceDirect; ResearchGate; MDPI).

General Uses Top

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Common products:
- Wood (timber, poles, structural lumber)
- Bark (tannin‑rich, used for leather tanning)
- Gum exudate (water‑soluble polysaccharide used as a natural binder)

Industrial and craft applications:
- Wood used in construction, furniture, tool handles, turnery, and as fuel/charcoal.
- Wood ash employed historically for potash production in soap and glass making.
- Bark used as a mordant in natural dyeing of cotton and protein fibers.
- Bark tannins employed in chrome‑free leather tanning processes.
- Gum used as binder in paper sizing, printing inks, and textile finishing.
- Gum used as a sizing agent in paper manufacturing to improve water resistance.

Colorants and tanning:
- Bark and heartwood yield brown natural dyes for protein fibers (silk, wool).
- Combined with metal salts, the dyes produce deeper, darker shades for textile coloration.
- High tannin concentration makes the bark suitable for vegetable tanning of leather.

Wood and fiber:
- Wood classified as medium‑density hardwood (density 0.78–0.85 g cm⁻³), suitable for structural and joinery uses.
- Fine grain and moderate hardness make it suitable for carving, turnery, and decorative items.
- Bark fibers, after retting, can be stripped and used for simple cords and small baskets.

Properties relevant to use:
- Wood: density 0.78–0.85 g cm⁻³; lignin content ~28 % of dry weight; moderate compressive strength (≈45–55 MPa); low tangential shrinkage (≈7 %); high durability.
- Bark: hydrolyzable tannins (gallotannins) ≈13–15 % of dry bark; high affinity for collagen; effective for chrome‑free leather tanning.
- Gum: polysaccharide mucilage with high molecular weight; imparts viscosity (≈200–400 cP at 1 % solution) and film‑forming ability; useful as natural binder and sizing agent.

Standards and regulation:
- Listed in the FAO Global Forest Resources Assessment; not listed in CITES Appendix.
- Trade subject to national export permits (e.g., Ghana Forestry Commission, Nigeria’s Department of Forestry).
- In the EU, timber must comply with the EU Timber Regulation (EUTR) and the FLEGT licensing scheme for imported timber.

Sustainability and sourcing:
- Entada africana occurs across West African savanna; population estimates indicate a stable total area of ≈7–10 million ha.
- Classified as a pioneer species with rapid regeneration after disturbance; typical pole production cycles are 5–10 years.
- Sustainable harvest recommendations include a minimum 5‑year cutting interval and replanting of seedlings after harvesting.
- Localized over‑exploitation for charcoal remains a concern; community‑based management and monitoring are encouraged to maintain stand health.

Synonyms Top

Scientific name Authority First published in
Entada sudanica Schweinf. Reliq. Kotschy.: 8 (1868)
Entada ubanguiensis De Wild. Pl. Bequaert.3: 88 (1925)
Pusaetha africana (Guill. & Perr.) Kuntze Revis. Gen. Pl.1: 204 (1891)
Pusaetha sudanica (Schweinf.) Kuntze Revis. Gen. Pl.1: 204 (1891)
Entadopsis sudanica (Schweinf.) G.C.C.Gilbert & Boutique Fl. Congo Belge3: 204 (1952)
Entadopsis sudanica (Schweinf.) G.C.C.Gilbert & Bou

Common names Top

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Language Common/alternative name
Bambara sàmanɛ̀rɛ
dag Ʒugulikɔŋga
Fulah faɗo waanduuhi
Chinese 非洲榼藤

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000207886
Tropicos 13030058
KEW urn:lsid:ipni.org:names:493820-1
The Plant List ild-54
Open Tree Of Life 3918859
NCBI Taxonomy 2005481
IUCN Red List 144292247
IPNI 493820-1
iNaturalist 506865
GBIF 2976222
EOL 703724
USDA GRIN 100211
CMAUP NPO11507
Wikipedia Entada_africana

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
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Ethnobotanical study of medicinal plants used by the people of Mosop, Nandi County in Kenya Maiyo ZC, Njeru SN, Toroitich FJ, Indieka SA, Obonyo MA Front Pharmacol 19-Jan-2024
PMCID:PMC10834697
doi:10.3389/fphar.2023.1328903
PMID:38313073
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
Profiling the Antidiabetic Potential of Compounds Identified from Fractionated Extracts of Entada africana toward Glucokinase Stimulation: Computational Insight Onikanni SA, Lawal B, Munyembaraga V, Bakare OS, Taher M, Khotib J, Susanti D, Oyinloye BE, Noriega L, Famuti A, Fadaka AO, Ajiboye BO Molecules 30-Jul-2023
PMCID:PMC10420681
doi:10.3390/molecules28155752
PMID:37570723
Recent Updates on Viral Oncogenesis: Available Preventive and Therapeutic Entities Chowdhary S, Deka R, Panda K, Kumar R, Solomon AD, Das J, Kanoujiya S, Gupta AK, Sinha S, Ruokolainen J, Kesari KK, Gupta PK Mol Pharm 24-Jul-2023
PMCID:PMC10410670
doi:10.1021/acs.molpharmaceut.2c01080
PMID:37486263
Editorial: Rising stars in ethnopharmacology: 2021 Grienke U, Scotti F, Rollinger JM Front Pharmacol 07-Jun-2023
PMCID:PMC10283002
doi:10.3389/fphar.2023.1224820
PMID:37351515
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
Attenuation of dermal wounds through topical application of ointment containing phenol enriched fraction of Caesalpinia mimosoides Lam. Bhat P, Upadhya V, Hegde GR, Hegde HV, Roy S Front Pharmacol 13-Oct-2022
PMCID:PMC9608657
doi:10.3389/fphar.2022.1025848
PMID:36313327
Anti-Inflammatory Potential of Phenolic Compounds Isolated From Entada africana Guill. & Perr. Used in the Republic of Benin Codo Toafode NM, Marquardt P, Ahyi V, Fester K, Spiegler V, Vissiennon C Front Pharmacol 30-Jun-2022
PMCID:PMC9280145
doi:10.3389/fphar.2022.931240
PMID:35847017
Traditional Medicine Utilisation Among Pregnant Women in Sub-saharan African Countries: A Systematic Review of Literature Mudonhi N, Nunu WN Inquiry 04-May-2022
PMCID:PMC9073130
doi:10.1177/00469580221088618
PMID:35506677
Local perception of ecosystem services and their conservation in Sudanian savannas of Burkina Faso (West Africa) Nabaloum A, Goetze D, Ouédraogo A, Porembski S, Thiombiano A J Ethnobiol Ethnomed 19-Feb-2022
PMCID:PMC8858500
doi:10.1186/s13002-022-00508-w
PMID:35183193
Ethnobotanical and Phytochemical Profiling of Medicinal Plants from Burkina Faso Used to Increase Physical Performance Sama H, Traoré M, Guenné S, Séré I, Hilou A, Dicko MH Medicines (Basel) 28-Jan-2022
PMCID:PMC8878663
doi:10.3390/medicines9020010
PMID:35200754
Sub-Acute Toxicity Effects of Methanolic Stem Bark Extract of Entada abyssinica on Biochemical, Haematological and Histopathological Parameters in Wistar Albino Rats Obakiro SB, Kiprop A, Kigondu E, K’owino I, Kiyimba K, Drago Kato C, Gavamukulya Y Front Pharmacol 07-Sep-2021
PMCID:PMC8452932
doi:10.3389/fphar.2021.740305
PMID:34557104
Antibacterial and Antifungal Activities of Ethiopian Medicinal Plants: A Systematic Review Nigussie D, Davey G, Tufa TB, Brewster M, Legesse BA, Fekadu A, Makonnen E Front Pharmacol 01-Jun-2021
PMCID:PMC8203926
doi:10.3389/fphar.2021.633921
PMID:34140888
Antiviral Activity Exerted by Natural Products against Human Viruses Musarra-Pizzo M, Pennisi R, Ben-Amor I, Mandalari G, Sciortino MT Viruses 04-May-2021
PMCID:PMC8147851
doi:10.3390/v13050828
PMID:34064347

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methylbenzaldehyde 7725 Click to see 120.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
Cleomiscosin C 11464176 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO 416.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aS,6S,6aS)-6-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxy-phenol 12309695 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566574 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O 1660.70 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]oxy-5-hydroxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566572 Click to see 1832.90 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566575 Click to see 1718.80 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566573 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O 1702.80 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566577 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC(=O)C)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O 1702.80 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-5-hydroxy-4-[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxy-3-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]oxyoxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566576 Click to see CC(=CCCC(C)(C=C)O)C(=O)OC1C(COC(C1OC(=O)C=CC2=CC=CC=C2)OC3C(C(OC(C3OC4C(C(C(CO4)O)OC5C(C(CO5)(CO)O)O)O)OC(=O)C67CC(C(CC6C8=CCC9C1(CCC(C(C1CCC9(C8(CC7O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)NC(=O)C)C)(C)C)O)COC(=O)C)O)O 2015.10 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-5-hydroxy-4-[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxy-3-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]oxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566569 Click to see CC(=CCCC(C)(C=C)O)C(=O)OC1C(COC(C1OC(=O)C=CC2=CC=CC=C2)OC3C(C(OC(C3OC4C(C(C(CO4)O)OC5C(C(CO5)(CO)O)O)O)OC(=O)C67CCC(CC6C8=CCC9C1(CCC(C(C1CCC9(C8(CC7O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)NC(=O)C)C)(C)C)COC(=O)C)O)O 1999.10 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-4-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2E,6R)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxyoxan-2-yl]oxy-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxyoxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566571 Click to see 1885.00 unknown https://doi.org/10.1021/NP060257W
[(2S,3R,4S,5R,6R)-6-(acetyloxymethyl)-4-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2E,6R)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxyoxan-2-yl]oxy-3-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 44566570 Click to see 1869.00 unknown https://doi.org/10.1021/NP060257W
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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 oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinethiones
6-Mercaptopurine 667490 Click to see 152.18 unknown https://doi.org/10.1021/NP060257W
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3-Hydroxy-4-methoxy-phenyl)-acrylic acid 92126 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6,7-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 21633144 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)OC 384.30 unknown via CMAUP database
Calycanthoside 5318566 Click to see 384.30 unknown via CMAUP database
Mandshurin 11740722 Click to see 384.30 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Arteminorin B 44178671 Click to see 412.30 unknown via CMAUP database
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Arteminorin C 44178672 Click to see 398.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Arteminorin A 44178670 Click to see 442.40 unknown via CMAUP database
Isofraxidin 5318565 Click to see 222.19 unknown via CMAUP database
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 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 / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-7,4'-dimethoxyflavone 15289454 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Tectorigenin 5281811 Click to see 300.26 unknown via CMAUP database

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