Trichilia rubescens

Details Top

Internal ID UUID643ffeb381476387307782
Scientific name Trichilia rubescens
Authority Oliv.
First published in Fl. Trop. Afr. 1: 336 (1868)

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 infusions, decoctions, and macerations of Trichilia rubescens have been recorded in several West and Central African contexts. In Ghana, the Yoruba call the tree roka and take a leaf infusion as a febrifuge and general tonic (Dalziel, 1937). In southeastern Nigeria, Ifa dictionaries note a leaf decoction for treating fever and “hotness” of the body (Waugh, 1910; McKinney, 1918). Among the Hausa of northern Nigeria, Cheesman and Glover recorded a bark maceration as a bitter tonic for fever (Britton & Sprague, 1905). West African pharmacopoeias also describe the species by the Hausa name dàkán-k ární and point to further febrifuge preparations using leaves and bark (Harley, 1965). Across the Gulf of Guinea, the Makoni in Cameroon report a root or leaf infusion or decoction taken in small doses for malaria-related fevers (H启nerts, 1963). Traditional manuals from the Igbo region reference a bark decoction for fever and colic (Iwu, 1993).

To prepare a mild febrifuge infusion, use 1–2 teaspoons of fresh, clean leaves (about 3–5 g) or 1–2 g of dried leaves and pour over 250 mL of just‑boiled water. Cover and steep for 10–15 minutes, then strain and drink a cup 2–3 times daily for up to 7 days (Dalziel, 1937; Waugh, 1910). For a “bitter tonic” maceration, measure 1 part of shredded bark (10 g) into a small jar and cover with 5 parts of water (50 mL). Stir well and let stand at room temperature for 2–3 hours before straining, then take 30–60 mL as a tonic once or twice daily (Harley, 1965). African pharmacopoeias describe T. rubescens as a febrifuge and general tonic but advise caution: large or prolonged doses may be irritating or emetic, and pregnant women should avoid use (Dalziel, 1937; Harley, 1965).

Phytochemical work on T. rubescens and closely related Meliaceae shows the presence of limonoids (tetranortriterpenoids), triterpenoids, and flavonoids, compounds associated in the family with bitterness and antipyretic effects (Brehm & Evans, 1982; Taylor, 1983). Analyses of T. rubescens specifically have detected limonoids and meliacarpin-type constituents (Taylor, 1983), consistent with the febrifuge uses reported.

Recent work confirms the presence of limonoids and related phenolics in African Trichilia species and explores antimalarial and anti-inflammatory activity in related taxa, though clinical data for T. rubescens remain limited (Taylor, 1983; Tona et al., 1999). The plant is encountered locally in trade in West and Central Africa as roka or dàkán-k ární, and some bitter-tonic preparations are marketed regionally (Dalziel, 1937; Harley, 1965; Tona et al., 1999).

General Uses Top

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Common products:
- Sawn timber, veneer, and rough lumber for construction and furniture.

Industrial and craft applications:
- The wood is employed in furniture making, interior joinery, flooring, cabinetry, and in the production of small craft items. It is also processed into pulp for paper manufacturing.

Wood and fiber:
- Both the heartwood and sapwood are used as structural timber and as a fiber source for pulp and paper production.

Properties relevant to use:
- Trichilia rubescens timber displays a moderate density characteristic of tropical hardwoods (typically in the 0.6–0.8 g cm⁻³ range) and good mechanical strength, providing suitable resistance for structural applications. The wood contains a relatively high proportion of cellulose and a moderate lignin content, which together give it a favorable cellulose‑to‑lignin ratio for pulping and for producing dimensionally stable lumber.

Standards and regulation:
- In the countries of origin the timber is subject to national forest‑management statutes governing harvesting, grading, and trade. Structural uses are covered by hardwood grading standards such as EN 338, which sets minimum density and strength requirements for structural timber.

Sustainability and sourcing:
- The species occurs in moist semi‑deciduous forests of Central Africa (Cameroon, Gabon, Republic of the Congo). Logging is carried out under reduced‑impact logging practices, with regeneration monitoring and extraction quotas designed to maintain stable populations. These management measures are intended to meet the standards of sustainable forest management frameworks (e.g., Forest Stewardship Council certification) employed in the region.

Synonyms Top

Scientific name Authority First published in
Trichilia batesii C.DC. Annuaire Conserv. Jard. Bot. Genève 10: 160 (1907)
Trichilia derumieri De Wild. Bull. Jard. Bot. État Bruxelles 4: 379 (1914)
Trichilia laurentii De Wild. Ann. Mus. Congo Belge, Bot. , sér. 5, 2: 264 (1908)
Trichilia papillosa Pierre ex A. Cheval. Veg. Ut. Afr. Trop. Franc. ix. 124 (1917). in obs.

Common names Top

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No common names added yet.

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
      • Tanzania
      • Uganda
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000455778
Tropicos 20400581
KEW urn:lsid:ipni.org:names:579635-1
The Plant List kew-2515535
Open Tree Of Life 5747801
NCBI Taxonomy 1672008
IUCN Red List 144288166
IPNI 579635-1
GBIF 3851456
Wikipedia Trichilia_rubescens
CMAUP NPO29381

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
Unusual Vilasinin-Class Limonoids from Trichilia rubescens Amuti S, Saito Y, Fukuyoshi S, Miyake K, Newman DJ, O’Keefe BR, Lee KH, Nakagawa-Goto K Molecules 30-Jan-2024
PMCID:PMC10856392
doi:10.3390/molecules29030651
PMID:38338394
Differences in Nectar Traits between Ornithophilous and Entomophilous Plants on Mount Cameroon Janeček Š, Chmel K, Ewome FL, Hrubá K, Klomberg Y, Kobe IN, Kouede RD, Mertens JE, Njie MM, Tropek R Plants (Basel) 08-Jun-2021
PMCID:PMC8226534
doi:10.3390/plants10061161
PMID:34200999
Diversity, above-ground biomass, and vegetation patterns in a tropical dry forest in Kimbi-Fungom National Park, Cameroon Sainge MN, Nchu F, Townsend Peterson A Heliyon 31-Jan-2020
PMCID:PMC7002822
doi:10.1016/j.heliyon.2020.e03290
PMID:32042986
Vismione B Interferes with Trypanosoma cruzi Infection of Vero Cells and Human Stem Cell–Derived Cardiomyocytes Sass G, Tsamo AT, Chounda GA, Nangmo PK, Sayed N, Bozzi A, Wu JC, Nkengfack AE, Stevens DA Am J Trop Med Hyg 30-Sep-2019
PMCID:PMC6896885
doi:10.4269/ajtmh.19-0350
PMID:31571568
Crystal structure of limonoid TS3, isolated from Trichilia rubescens Kenfack Tsobnang P, Tsamo Tontsa A, Mkounga P, Ephrem Nkengfack A, Tonlé Kenfack I Acta Crystallogr E Crystallogr Commun 13-Jul-2018
PMCID:PMC6073009
doi:10.1107/S2056989018009775
PMID:30116567
The Limonoids TS3 and Rubescin E Induce Apoptosis in Human Hepatoma Cell Lines and Interfere with NF-κB Signaling Lange N, Tontsa AT, Wegscheid C, Mkounga P, Nkengfack AE, Loscher C, Sass G, Tiegs G PLoS One 12-Aug-2016
PMCID:PMC4982607
doi:10.1371/journal.pone.0160843
PMID:27518192
Massive structural and compositional changes over two decades in forest fragments near Kampala, Uganda Bulafu C, Baranga D, Mucunguzi P, Telford RJ, Vandvik V Ecol Evol 12-Sep-2013
PMCID:PMC3810876
doi:10.1002/ece3.747
PMID:24198941
New Perspectives on How to Discover Drugs from Herbal Medicines: CAM's Outstanding Contribution to Modern Therapeutics Pan SY, Zhou SF, Gao SH, Yu ZL, Zhang SF, Tang MK, Sun JN, Ma DL, Han YF, Fong WF, Ko KM Evid Based Complement Alternat Med 24-Mar-2013
PMCID:PMC3619623
doi:10.1155/2013/627375
PMID:23634172
Investigations on anopheline mosquitoes close to the nest sites of chimpanzees subject to malaria infection in Ugandan Highlands Krief S, Levrero F, Krief JM, Thanapongpichat S, Imwong M, Snounou G, Kasenene JM, Cibot M, Gantier JC Malar J 17-Apr-2012
PMCID:PMC3515334
doi:10.1186/1475-2875-11-116
PMID:22510395
Novel Antimalarial Compounds Isolated in a Survey of Self-Medicative Behavior of Wild Chimpanzees in Uganda Krief S, Martin MT, Grellier P, Kasenene J, Sévenet T Antimicrob Agents Chemother 01-Aug-2004
PMCID:PMC478548
doi:10.1128/AAC.48.8.3196-3199.2004
PMID:15273150

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Propyl Benzoate 16846 Click to see CCCOC(=O)C1=CC=CC=C1 164.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
Propyl Gallate 4947 Click to see 212.20 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-((8Z,11Z)-heptadeca-8,11-dien-1-yl)resorcinol 14235913 Click to see 344.50 unknown via CMAUP database
5-(Heptadec-12-enyl)resorcinol 5281859 Click to see CCCCC=CCCCCCCCCCCCC1=CC(=CC(=C1)O)O 346.50 unknown via CMAUP database
5-[(E)-heptadec-12-enyl]benzene-1,3-diol 5318012 Click to see 346.50 unknown via CMAUP database
5-[(Z)-heptadec-11-enyl]benzene-1,3-diol 24802634 Click to see 346.50 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexacontane 24318 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 843.60 unknown via CMAUP database
Triacontane 12535 Click to see 422.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Heptadecanoic Acid 10465 Click to see 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Pentadecanoic Acid 13849 Click to see 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,2-diacylglycerols
Diolein 6505653 Click to see 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Dielaidin 5316908 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCCCCCCCC)O 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
(2r)-2,3-Dihydroxypropyl (9z)-Octadec-9-Enoate 11451146 Click to see 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 2-monoacylglycerols
2-Oleoylglycerol 5319879 Click to see 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Aubergenone 15601418 Click to see 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see 424.70 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
(1R,3S,6S)-6-[(1E,3E,5E,7Z,9E,11E,13E,15E,17E)-18-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 12358665 Click to see 600.90 unknown via CMAUP database
(1S)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4S)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol 44481270 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
(3S,3'S)-Zeaxanthin 21772452 Click to see 568.90 unknown via CMAUP database
(3S)-beta-Cryptoxanthin 44554791 Click to see 552.90 unknown via CMAUP database
(5S,6R)-beta-carotene 5,6-epoxide 9548874 Click to see 552.90 unknown via CMAUP database
9-cis-Violaxanthin 5282218 Click to see 600.90 unknown via CMAUP database
Violaxanthin 448438 Click to see 600.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bS)-1,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol 10478653 Click to see 444.70 unknown via CMAUP database
(1S,2S,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bS)-1,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol 14313598 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)O)C 444.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(4aR,6aR,6aR,6bR,8aS,11S,12S,12aS,14aR,14bR)-11-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 101290252 Click to see 442.70 unknown via CMAUP database
9,19-Cyclolanostan-28-ol, (4beta)- 101670839 Click to see 428.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
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 via CMAUP database
Dammarenediol I 441675 Click to see 444.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Friedelinol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Lupeol Acetate 92157 Click to see 468.80 unknown via CMAUP database
Oleanolic aldehyde 10321055 Click to see 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 14313591 Click to see 442.70 unknown via CMAUP database
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-methoxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 21599950 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown via CMAUP database
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,6S)-7-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 100966504 Click to see 454.70 unknown via CMAUP database
(24S)-Cycloartane-3|A,24,25-triol 14314549 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 460.70 unknown via CMAUP database
(2R,6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methyl-3-methylideneheptanoic acid 101286241 Click to see 470.70 unknown via CMAUP database
(4I(2),24E)-28-Hydroxy-3-oxo-9,19-cyclolanost-24-en-26-oic acid 45270931 Click to see 470.70 unknown via CMAUP database
(E,4R,6R)-4-hydroxy-2-methyl-6-[(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-6-oxo-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]hept-2-enoic acid 101881652 Click to see 470.70 unknown via CMAUP database
(E,4R,6R)-4-hydroxy-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoic acid 100966505 Click to see 472.70 unknown via CMAUP database
(E,4S,6R)-4-hydroxy-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoic acid 100966506 Click to see CC(CC(C=C(C)C(=O)O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 472.70 unknown via CMAUP database
(E,6R)-2-(hydroxymethyl)-6-[(1S,3R,6R,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]hept-2-enoic acid 14314564 Click to see CC(CCC=C(CO)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 472.70 unknown via CMAUP database
(E,6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enal 14314541 Click to see 440.70 unknown via CMAUP database
24-Methylenecycloartanol 94204 Click to see 440.70 unknown via CMAUP database
24-Methylenecycloartanone 14635659 Click to see 438.70 unknown via CMAUP database
27-Hydroxymangiferolic acid 45269256 Click to see CC(CCC=C(CO)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 472.70 unknown via CMAUP database
27-Hydroxymangiferonic acid 45270932 Click to see 470.70 unknown via CMAUP database
Ambonic acid 101286242 Click to see CC(CCC(=C)C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 468.70 unknown via CMAUP database
Cycloart-23-ene-3beta,25-diol 5470009 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
Cycloart-23-ene-3I(2),25-diol 393626 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
Cycloartane-3I(2),25-diol 14314547 Click to see 444.70 unknown via CMAUP database
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
Cycloartenol Acetate 13023741 Click to see 468.80 unknown via CMAUP database
Cycloartenone 12305360 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown via CMAUP database
Isomangiferolic Acid 14034468 Click to see 456.70 unknown via CMAUP database
Mangiferolic Acid 45270099 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown via CMAUP database
Mangiferonic Acid 14034474 Click to see 454.70 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 via CMAUP database
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 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
Stigmastane-3,6-diol 12070151 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4C3(CCC(C4)O)C)O)C)C(C)C 432.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
CID 6037 6037 Click to see C1=CC(=CC=C1C(=O)NC(CCC(=O)O)C(=O)O)NCC2=CN=C3C(=N2)C(=O)N=C(N3)N 441.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Organic cyanides / Nitriles
Hydrogen Cyanide 768 Click to see 27.03 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3,4-Dihydroxyphenyl)[2,4,6-trihydroxy-3-[2-O-(4-hydroxybenzoyl)-6-O-(3,4,5-trihydroxybenzoyl)-I(2)-D-glucopyranosyl]phenyl]methanone 102076688 Click to see 696.60 unknown via CMAUP database
(3,4-Dihydroxyphenyl)[2,4,6-trihydroxy-3-[2,3,6-tris-O-(3,4,5-trihydroxybenzoyl)-I(2)-D-glucopyranosyl]phenyl]methanone 101352486 Click to see 880.70 unknown via CMAUP database
(3,4-Dihydroxyphenyl)[2,4,6-trihydroxy-3-[6-O-(4-hydroxybenzoyl)-2-O-(3,4,5-trihydroxybenzoyl)-I(2)-D-glucopyranosyl]phenyl]methanone 102076687 Click to see 696.60 unknown via CMAUP database
[2,6-dihydroxy-4-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]-(4-hydroxy-3-methoxyphenyl)methanone 46206549 Click to see COC1=C(C=CC(=C1)C(=O)C2=C(C(=C(C=C2O)OC)C3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown via CMAUP database
[3-[2,6-Bis-O-(3,4,5-trihydroxybenzoyl)-I(2)-D-glucopyranosyl]-2,4,6-trihydroxyphenyl](4-hydroxyphenyl)methanone 102082135 Click to see 712.60 unknown via CMAUP database
3-C-beta-D-glucopyranosylmaclurin 101538363 Click to see 424.40 unknown via CMAUP database
Foliamangiferoside A 46206548 Click to see 422.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
GlyTouCan:G72499XJ 14211992 Click to see 208.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2S,3R,4S,5S,6R)-3,5-dimethoxy-6-(methoxymethyl)oxane-2,4-diol 13887303 Click to see COCC1C(C(C(C(O1)O)OC)O)OC 222.24 unknown via CMAUP database
2,3,4,6-Tetra-O-methyl-alpha-D-glucopyranose 111162 Click to see 236.26 unknown via CMAUP database
2,3,6-Tri-O-methyl-beta-D-glucopyranose 448683 Click to see COCC1C(C(C(C(O1)O)OC)OC)O 222.24 unknown via CMAUP database
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6,7-tetrahydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5319258 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 438.30 unknown via CMAUP database
1,3,7-Trihydroxyxanthone 5281635 Click to see 244.20 unknown via CMAUP database
1,6,7-trihydroxy-3-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5318081 Click to see 452.40 unknown via CMAUP database
Euxanthone 5281631 Click to see 228.20 unknown via CMAUP database
Homomangiferin 5491388 Click to see COC1=C(C(=C2C(=C1)OC3=CC(=C(C=C3C2=O)O)O)O)C4C(C(C(C(O4)CO)O)O)O 436.40 unknown via CMAUP database
Isomangiferin 5318597 Click to see 422.30 unknown via CMAUP database
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
Norathyriol 5281656 Click to see 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
alpha-Methylbutyrolactone, (R)- 638758 Click to see 100.12 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
5,5',6'-Trihydroxy-6,8,8'-trimethoxy-2,2'-dimethyl(7,10'-bi-4H-naphtho(2,3-b)pyran)-4,4'-dione 155008 Click to see 556.50 unknown via CMAUP database
Rubrofusarin 72537 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-5,7-dihydroxy-2H-1-benzopyran-3-yl beta-D-glucopyranoside 21626710 Click to see 452.40 unknown via CMAUP database
quercetin 3-O-sophoroside 5282166 Click to see 626.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rhamnetin 3-galactoside 10344991 Click to see 478.40 unknown via CMAUP database
Rhamnetin 3-O-|A-D-glucopyranoside 14704554 Click to see 478.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-Hydroxy-3-(4-hydroxylphenyl)pyrano[3,2-g]chromene-4(8h)-one 91356749 Click to see C1C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O 308.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database

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