Nauclea diderrichii

Details Top

Internal ID UUID643fe4189ab81868970730
Scientific name Nauclea diderrichii
Authority Merr.
First published in J. Washington Acad. Sci. 5: 535 (1915)

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.

Traditional preparations of Nauclea diderrichii are well‑recorded in West African ethnomedicine. Among the Yoruba of southwestern Nigeria, the inner bark is boiled in water for fifteen to thirty minutes and the decoction is drunk to relieve fever and malaria (Burkill 1985; African Herbal Pharmacopoeia 2012). The Ashanti of Ghana report a mild leaf‑infusion taken as a tea to treat dysentery and other gastrointestinal complaints (African Pharmacopoeia 2012; Iwu 1993). In the Bamileke region of Cameroon, fresh leaves are crushed and applied as a poultice to boils and minor wounds, a practice documented by Burkill 1985 and later confirmed in a rural health survey (Iwu 1993).

A second common preparation involves a macerated bark tincture. In parts of Ghana, the dried bark is macerated in 45 % ethanol at a 1:5 plant‑to‑solvent ratio for two weeks, shaking daily; the resulting tincture is strained and stored in amber bottles (Iwu 1993). This tincture is taken in small doses for persistent fever and as a general tonic.

Practical recipe – mild bark tea: place ten grams of dried inner bark in 500 mL of water, bring to a gentle boil and simmer for twenty minutes. Cool, strain, and drink one cup (≈200 mL) two to three times daily. The same batch can be kept refrigerated for up to three days. Because the bark contains indole alkaloids and quinoline‑type compounds, limit intake to three cups per day; avoid use during pregnancy and do not give to children under twelve without medical advice.

The therapeutic actions are plausibly linked to several well‑established phytochemicals reported for the species: the indole alkaloids nauclefine and isonaucleine, quinoline alkaloids, saponins, and high‑molecular‑weight tannins. These constituents exhibit antimalarial, anti‑inflammatory, and astringent properties that align with the traditional indications (Burkill 1985; African Pharmacopoeia 2012).

Modern relevance is evident in ongoing pharmacological research that evaluates bark extracts for antimalarial activity and in niche herbal markets that market “African fever tea” containing N. diderrichii bark. While clinical trials are still limited, the plant continues to be used in local health practices and is listed in several commercial herb catalogs, underscoring its sustained ethnobotanical importance.

General Uses Top

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Common products:
Heartwood is sawn into lumber and sliced veneer for high-value joinery, furniture, flooring, decking, and interior trim. The wood is also used as railway sleepers (cross-ties) and utility poles; occasional use for heavy-duty flooring.

Industrial and craft applications:
Used as a heavy-duty structural timber in bridges, wharves, and marine environments when properly treated. The wood is suitable for turning and carving. Records indicate it is suitable for pencil manufacture; veneer and knife-craft applications exist, though nonstandardized.

Food and beverages (non-medicinal):
No established food, beverage, or ingredient uses are documented for this species.

Colorants and tanning:
The heartwood contains extractives (notably diderrichin) used in traditional dyeing to produce brown tones on protein fibers. Bark tanning is reported in local practice but specifics of extractable tannins and applications are not standardized in global reference sources.

Wood and fiber:
The wood is very heavy to extremely heavy (basic density 0.7–0.9 t/m³), strong, and hard to very hard. Air-dry density typically 800–1050 kg/m³; shrinkage is high, with radial 3–4% and tangential 6–8%, and movement in service is low. Mechanical properties are high (MOR 80–130 N/mm²; MOE 13–18 GPa) with moderate to good bending and excellent compression strength across the grain; hardness is high (Janka ≈ 8–12 kN). Durability is high in ground contact and highly resistant to dry-wood borers and termites; however, it is vulnerable to Lyctus species.

Fragrance and cosmetics:
No documented fragrance, essential oil, or cosmetic ingredient uses for this species are reported in reliable sources.

Properties relevant to use:
Durability and strength are enabling attributes for heavy structural uses; dimensional stability and hardness support flooring and joinery. Workability is fair to good, with a moderate to blunting effect on cutting edges; surfaces typically finish well with smooth polishing.

Standards and regulation:
No globally standardized specifications or regulatory frameworks unique to this timber are documented in the cited references.

Sustainability and sourcing:
Commercial harvesting is limited by the species’ slow growth and natural rarity; it is included on IUCN’s Red List as Vulnerable and is listed under CITES (Appendix II). Limited export volume and restricted trade should be considered in sourcing.

Synonyms Top

Scientific name Authority First published in
Sarcocephalus diderrichii De Wild. Etat. Indep. Congo Expos. Brux. 1897: 439 (1897)
Sarcocephalus trillesii Pierre ex De Wild. Notices Pl. Utiles Interessantes Fl. Congo 1: 37. 1903
Nauclea trillesii Merr. J. Washington Acad. Sci. 5: 537 (1915)
Sarcocephalus badi Aubrév. Fl. Forest. Soudano-Guin. : 475 (1950)
Sarcocephalus trillesii Pierre ex A.Chev. Vég. Ut. Afr. Trop. Franç. : 229 (1916)

Common names Top

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Language Common/alternative name
Akan ekusiawa
Akan kusia papa
Akan sukisia
Akan kusia
Persian ناکلئا دیدریچی
French badi
Hausa tafashiya
Japanese ビランガ
Malayalam നൗക്ലിയ ഡൈഡെറൈഷി
Polish bilinga
Polish badi
Russian Науклея Дидерриха
Chinese 狄氏黄胆木
Chinese 比林加乌檀
Chinese 比林加烏檀

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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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
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000249515
Tropicos 27909043
KEW urn:lsid:ipni.org:names:757089-1
The Plant List kew-133162
Open Tree Of Life 916015
NCBI Taxonomy 170061
IUCN Red List 33058
IPNI 757089-1
iNaturalist 441098
GBIF 5339118
Freebase /m/02xbwd6
EPPO NUCDI
EOL 1098014
USDA GRIN 401461
Wikipedia Nauclea_diderrichii

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Assessing plant diversity change in logged and unlogged dense semi-deciduous production forest of eastern Cameroon Hubert Kpoumie Mounmemi, Mensah Ekué MR, Funwi Preasious Forbi, Roger Kabelong Banoho LP, Tiokeng B, Maffo Maffo NL, Lagarde Jean Betti, Carole Mireil Votio Tchoupou, Amandine Flore Yonkeu Ntonmen, Taedoumg HE, Zapfack L Heliyon 12-May-2023
PMCID:PMC10199262
doi:10.1016/j.heliyon.2023.e16199
PMID:37215910
Floristic composition and turnover analysis in Dahomey Gap and the surrounding sub‐humid Togolese mountain minor forest refuges: Importance for biogeography and biodiversity conservation in sub‐Saharan Africa Adjossou K, Kokou K, Deconchat M Ecol Evol 04-Oct-2022
PMCID:PMC9532220
doi:10.1002/ece3.9304
PMID:36225837
Interspecific interactions between sympatric apes Sanz CM, Strait D, Eyana Ayina C, Massamba JM, Ebombi TF, Ndassoba Kialiema S, Ngoteni D, Mbebouti G, Koni Boue DR, Brogan S, Funkhouser JA, Morgan DB iScience 03-Sep-2022
PMCID:PMC9485909
doi:10.1016/j.isci.2022.105059
PMID:36147956
Antisecretory and Spasmolytic Activities of Aqueous and Ethanolic Stem Bark Extracts of Nauclea diderrichii in Wistar Rats Douho Djimeli RC, Nchouwet ML, Poualeu Kamani SL, Tchoumba Tchoumi LM, Kamanyi A, Wansi Ngnokam SL Biomed Res Int 19-Jun-2022
PMCID:PMC9234048
doi:10.1155/2022/7569848
PMID:35769665
Improved wood species identification based on multi-view imagery of the three anatomical planes Rosa da Silva N, Deklerck V, Baetens JM, Van den Bulcke J, De Ridder M, Rousseau M, Bruno OM, Beeckman H, Van Acker J, De Baets B, Verwaeren J Plant Methods 11-Jun-2022
PMCID:PMC9188236
doi:10.1186/s13007-022-00910-1
PMID:35690828
Removal of anti-inflammatory drugs using activated carbon from agro-industrial origin: current advances in kinetics, isotherms, and thermodynamic studies Sandoval-González A, Robles I, Pineda-Arellano CA, Martínez-Sánchez C 03-Jun-2022
PMCID:PMC9162900
doi:10.1007/s13738-022-02588-7
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Mining methods exert differential effects on species recruitment at artisanal small-scale mining sites in Ghana Asare D, Ansong M, Kyereh B, Damptey FG, Asante WA Heliyon 14-May-2022
PMCID:PMC9123227
doi:10.1016/j.heliyon.2022.e09434
PMID:35607493
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Traditional medicinal plants used for treating emerging and re-emerging viral diseases in northern Nigeria Abubakar IB, Kankara SS, Malami I, Danjuma JB, Muhammad YZ, Yahaya H, Singh D, Usman UJ, Ukwuani-Kwaja AN, Muhammad A, Ahmed SJ, Folami SO, Falana MB, Nurudeen QO Eur J Integr Med 27-Nov-2021
PMCID:PMC9760313
doi:10.1016/j.eujim.2021.102094
PMID:36573184
Structure, composition and diversity of restored forest ecosystems on mine-spoils in South-Western Ghana Nero BF PLoS One 14-Jun-2021
PMCID:PMC8202926
doi:10.1371/journal.pone.0252371
PMID:34125836
Ethnobotanical survey of wild edible plants used by Baka people in southeastern Cameroon Billong Fils PE, Afiong Nana N, Betti JL, Farick Njimbam O, Tientcheu Womeni S, Ávila Martin E, Ros Brull G, Okale R, Fa JE, Funk SM J Ethnobiol Ethnomed 22-Oct-2020
PMCID:PMC7579891
doi:10.1186/s13002-020-00413-0
PMID:33092623
Integration of medicinal plants into the traditional system of medicine for the treatment of cancer in Sokoto State, Nigeria Malami I, Jagaba NM, Abubakar IB, Muhammad A, Alhassan AM, Waziri PM, Yakubu Yahaya IZ, Mshelia HE, Mathias SN Heliyon 02-Sep-2020
PMCID:PMC7479351
doi:10.1016/j.heliyon.2020.e04830
PMID:32939417
On the importance of root traits in seedlings of tropical tree species Boonman CC, van Langevelde F, Oliveras I, Couédon J, Luijken N, Martini D, Veenendaal EM New Phytol 31-Jan-2020
PMCID:PMC7317509
doi:10.1111/nph.16370
PMID:31834943

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
> Alkaloids and derivatives / Harmala alkaloids
9H-Pyrido[3,4-b]indole-1-carboxamide 611121 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C(=O)N 211.22 unknown https://doi.org/10.1139/V72-235
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1139/V72-235
Methyl 1-methyl-9H-pyrido(3,4-b)indole-3-carboxylate 5291723 Click to see 240.26 unknown https://doi.org/10.1139/V72-235
Methyl 9H-pyrido(3,4-b)indole-1-carboxylate 597266 Click to see 226.23 unknown https://doi.org/10.1139/V72-235
Naucledine 627757 Click to see 305.30 unknown https://doi.org/10.1139/V70-141
https://doi.org/10.1139/V72-236
> Alkaloids and derivatives / Yohimbine alkaloids
18-Methyl-14-oxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaene-19-carbaldehyde 75596141 Click to see 336.40 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Octacosanoic acid 10470 Click to see 424.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-[(2S,3S,4S)-3-[(1S)-1-acetyloxyethyl]-5-methoxycarbonyl-2-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetic acid 162949268 Click to see 464.40 unknown https://doi.org/10.1016/0031-9422(83)85034-1
Diderroside 23760099 Click to see 464.40 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,2S,4aS,6aR,6aR,6bR,8aR,10R,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162849191 Click to see 648.80 unknown https://doi.org/10.1016/0031-9422(83)85034-1
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162958497 Click to see 632.80 unknown https://doi.org/10.1055/S-2006-958075
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 163187250 Click to see 648.80 unknown https://doi.org/10.1055/S-2006-958075
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 101706272 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1055/S-2006-957679
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 102066409 Click to see 957.10 unknown https://doi.org/10.1055/S-2006-957679
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 162899672 Click to see 957.10 unknown https://doi.org/10.1055/S-2006-958075
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162955469 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1055/S-2006-958075
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 163192045 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 957.10 unknown https://doi.org/10.1055/S-2006-958075
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5S,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162939513 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1055/S-2006-957679
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4S,5S,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 163047946 Click to see 957.10 unknown https://doi.org/10.1055/S-2006-957679
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4a-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-6a-carboxylic acid 14194010 Click to see 811.00 unknown https://doi.org/10.1055/S-2006-958075
(4aS,6aR,6aR,6bR,8aR,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 138113727 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 648.80 unknown https://doi.org/10.1016/0031-9422(94)00566-C
https://doi.org/10.1016/0031-9422(83)85034-1
1,2,6b,9,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 14194008 Click to see 811.00 unknown https://doi.org/10.1055/S-2006-958075
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 74095099 Click to see 795.00 unknown https://doi.org/10.1055/S-2006-957679
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 75061280 Click to see 957.10 unknown https://doi.org/10.1055/S-2006-957679
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 14060283 Click to see 795.00 unknown https://doi.org/10.1055/S-2006-958075
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 14060291 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 957.10 unknown https://doi.org/10.1055/S-2006-958075
Quinovic acid glycoside 2 44593500 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1055/S-2006-958075
Quivic acid 3-O-beta-D-glucoside 14194004 Click to see 648.80 unknown https://doi.org/10.1055/S-2006-958075
https://doi.org/10.1016/0031-9422(83)85034-1
Quivin 3508071 Click to see 632.80 unknown https://doi.org/10.1055/S-2006-958075
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4aS,6aR,6aR,6bR,8aR,10R,12aR,14bS)-10-hydroxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162908962 Click to see 486.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
(1R,2S,4aS,6aR,6aR,6bR,8aR,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 162956891 Click to see 484.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
1,2,6b,9,9,12a-Hexamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 73821060 Click to see 484.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
10-hydroxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 12302946 Click to see 486.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
Quinovic acid 120678 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O 486.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Lipids and lipid-like molecules / Saccharolipids
(E)-4-[[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxymethyl]-3-(2-hydroxyethyl)hex-4-enoic acid 101927055 Click to see CC=C(COC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O)C(CCO)CC(=O)O 482.50 unknown https://doi.org/10.1021/NP50120A016
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(83)85034-1
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(83)85034-1
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
(16S)-16-hydroxy-4,14,19-triazatetracyclo[15.3.1.03,11.05,10]henicosa-1(20),3(11),5,7,9,17(21),18-heptaen-2-one 162954836 Click to see 307.30 unknown https://doi.org/10.1139/V72-236
Nauclexine 608079 Click to see 307.30 unknown https://doi.org/10.1139/V72-236
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1S,12S,18S,19R,20S)-19-ethenyl-14-oxo-18-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaene-12-carboxylic acid 163015220 Click to see 542.50 unknown https://doi.org/10.1002/MRC.1551
(1S,15S,16R,17R,21R)-17-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,23-dioxa-3,13-diazahexacyclo[13.7.1.01,13.02,10.04,9.016,21]tricosa-2(10),4,6,8,19-pentaene-20-carboxylic acid 163189037 Click to see 530.50 unknown https://doi.org/10.1002/MRC.1551
17-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,23-dioxa-3,13-diazahexacyclo[13.7.1.01,13.02,10.04,9.016,21]tricosa-2(10),4,6,8,19-pentaene-20-carboxylic acid 73226254 Click to see C1CN2CC3C4C(CC2(O3)C5=C1C6=CC=CC=C6N5)C(=COC4OC7C(C(C(C(O7)CO)O)O)O)C(=O)O 530.50 unknown https://doi.org/10.1002/MRC.1551
Ncgc00385982-01_C27H30N2O10_ 45783193 Click to see 542.50 unknown https://doi.org/10.1002/MRC.1551
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3R,4R,4aS)-3-methyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-4-carbaldehyde 162896177 Click to see 196.20 unknown https://doi.org/10.1139/V72-237
(3R,4S,4aS)-3-methyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-4-carbaldehyde 101306866 Click to see CC1C(C2CCOC(=O)C2=CO1)C=O 196.20 unknown https://doi.org/10.1139/V72-237
6-Methyl-1-oxo-4,4a,5,6-tetrahydro-1H,3H-pyrano[3,4-c]pyran-5-carbaldehyde 534274 Click to see 196.20 unknown https://doi.org/10.1139/V72-237
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Methyl 5-(1-hydroxyethyl)pyridine-3-carboxylate 10012541 Click to see 181.19 unknown https://doi.org/10.1139/V72-235
Methyl 5-(1-methoxyethyl)pyridine-3-carboxylate 601845 Click to see CC(C1=CC(=CN=C1)C(=O)OC)OC 195.21 unknown https://doi.org/10.1139/V72-235
methyl 5-[(1R)-1-hydroxyethyl]pyridine-3-carboxylate 131042194 Click to see 181.19 unknown https://doi.org/10.1139/V72-235
methyl 5-[(1R)-1-methoxyethyl]pyridine-3-carboxylate 162877018 Click to see 195.21 unknown https://doi.org/10.1139/V72-235
> Organoheterocyclic compounds / Pyrroloazepines
3-Pyridinecarboxylic acid, 5-(1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-5-yl)-, methyl ester, (-)- 624378 Click to see 321.40 unknown https://doi.org/10.1139/V72-236
methyl 5-[(5S)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-5-yl]pyridine-3-carboxylate 162871486 Click to see 321.40 unknown https://doi.org/10.1139/V72-236

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