Musanga cecropioides

Details Top

Internal ID UUID643ff5b9c3bfb064645431
Scientific name Musanga cecropioides
Authority R.Br. ex Tedlie
First published in Miss. Ashantee : 372 (1819)

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.

Across West and Central Africa, Musanga cecropioides is best known as a fever plant, but the parts used and how they are prepared differ by locale. In southern Nigeria, healers collect mature leaves and steep them in near-boiling water to make an antimalarial tea (Watson et al., 1989). In the southern parts of the Republic of Congo, a light leaf infusion is taken for fevers and general malaise (Bouquet, 1971), while in southern Cameroon villagers use a bark decoction as a febrifuge and for “bile” complaints (Betti, 2004). A different sort of drink—bark macerated in warm water—is taken in some Central African communities for treating diarrhea and stomach pains (Betti, 2004). The same general pattern of using the leaf for fevers and the bark for digestive problems also appears in the western Congo basin, where infusions and decoctions are both recorded (Boulvert, 1982). Taken together, these records show that water extracts—teas, infusions, decoctions, and short macerations—are the preferred traditional forms.

For those who wish to try a mild leaf tea, the following method is typical of what healers describe. Simmer 5 g of freshly chopped leaves in 250 ml of water for 5 minutes, then remove from heat and steep covered for 10 minutes. Cool to comfortable drinking temperature. This is a mild, general-purpose febrifuge tea as practiced in Nigeria and Congo. Use cautiously: it is not for heavy daily use, should not be taken by children, and avoid in pregnancy and if you are using anticoagulants, since alkaloids in the plant can interfere with clotting medicines (African Herbal Pharmacopoeia, 2010).

Pharmacologically, the leaf and bark of Musanga cecropioides are rich in saponins, tannins, alkaloids, and flavonoids such as quercetin and kaempferol (Tchinda et al., 2000). These classes of compounds are well known to provide antipyretic, antimicrobial, and astringent effects in other species and give a credible chemical basis for the fever‑relieving and antidiarrheal uses described above.

Today the umbrella tree is still collected and prepared as tea or decoction in rural clinics and by healers in Cameroon, the Republic of Congo, and the Democratic Republic of the Congo, and the species appears in community pharmacopeias of the Congo basin (Betti, 2004). Small quantities of powdered bark and leaf are sold in local markets, and modern studies continue to evaluate the plant’s antimicrobial and antiparasitic properties, keeping a long‑standing fever remedy relevant to current practice.

General Uses Top

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Wood and fiber:
The timber is a lightweight, soft hardwood with a specific gravity approximately 0.38–0.44, yielding large logs with a high proportion of sapwood and a relatively low resistance to fungi and insects. The wood is employed in interior carpentry, light construction, paneling, crates, match blocks and splints, and fiberboard or particleboard. Bast fibers from the bark have been used for rope and cordage, while the pith is suited for match production.

Industrial and craft applications:
A principal industrial use is in match manufacture, where the species supplies both splints and friction strips. The wood’s low density, ease of processing, and workability make it suitable for mass-produced items such as boxes and light joinery. It is also used as a fuelwood and for charcoal production.

Properties relevant to use:
The material’s low specific gravity and consistent texture permit efficient cutting, planing, and machining. The match-grade performance is related to the uniformity of short fibers and relatively low resin content. Its susceptibility to decay is mitigated by the wood’s use in short-term, low-stress applications or treated components.

Sustainability and sourcing:
Musanga cecropioides occurs commonly in secondary forests across West and Central Africa. Its rapid growth and pioneer status support sustainable harvesting and plantation establishment; however, durability limitations restrict external or load-bearing applications without protective treatment.

Synonyms Top

Scientific name Authority First published in
Musanga smithii R.Br. Pl. Jav. Rar. : 49 (1838)

Common names Top

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Language Common/alternative name
Persian درخت چوبپنبهای آفریقا
French parasolier
Chinese 伞树

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • 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-0000374733
Tropicos 21300990
KEW urn:lsid:ipni.org:names:584392-1
The Plant List kew-2369493
Open Tree Of Life 4729816
NCBI Taxonomy 1317686
IUCN Red List 61967837
IPNI 584392-1
iNaturalist 341036
GBIF 5643189
Freebase /m/056n4j
EPPO MUGCE
EOL 5719746
USDA GRIN 405240
Wikipedia Musanga_cecropioides

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
Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M Heliyon 21-Mar-2024
PMCID:PMC10999872
doi:10.1016/j.heliyon.2024.e28247
PMID:38590891
Antiproliferative activities of some selected Nigerian medicinal plants against breast, liver, and cervical cancer cells Olaleye OO, Kim DH, Spriggs KA BMC Complement Med Ther 06-Mar-2024
PMCID:PMC10916328
doi:10.1186/s12906-024-04365-w
PMID:38448883
Immunomodulatory effects of epiphytic Loranthus micranthus leaf extracts collected from two host plants: Psidium guajava and Parkia biglobosa Idoko ND, Chukwuma IF, Nworah FN, Mba SE, Joshua PE, Nwodo OF, Abusudah WF, Almohmadi NH, de Waard M BMC Complement Med Ther 02-Jan-2024
PMCID:PMC10759741
doi:10.1186/s12906-023-04282-4
PMID:38166988
Finding umbrella trees: cultivating inclusion and more than survival in a post-affirmative action academy Montgomery BL Plant Cell 11-Oct-2023
PMCID:PMC10734612
doi:10.1093/plcell/koad261
PMID:37820739
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Foraging and mating behaviors of Hypsignathus monstrosus at the bat‐human interface in a central African rainforest Schloesing E, Caron A, Chambon R, Courbin N, Labadie M, Nina R, Mouiti Mbadinga F, Ngoubili W, Sandiala D, N’Kaya Tobi, Bourgarel M, De Nys HM, Cappelle J Ecol Evol 08-Jul-2023
PMCID:PMC10329260
doi:10.1002/ece3.10240
PMID:37424939
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
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
First evidence of a monodominant (Englerodendron, Amherstieae, Detarioideae, Leguminosae) tropical moist forest from the early Miocene (21.73 Ma) of Ethiopia Pan AD, Jacobs BF, Bush RT, de la Estrella M, Grímsson F, Herendeen PS, van der Burgt XM, Currano ED PLoS One 11-Jan-2023
PMCID:PMC9833558
doi:10.1371/journal.pone.0279491
PMID:36630378
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Acute and Subchronic Toxicity Studies on the Aqueous Extract of the Plant Mixture (Bidens pilosa and Cymbopogon citratus Aerial Parts) in Rat Model Tcheutchoua YC, Bilanda DC, Mengue Ngadena YS, Djomeni Dzeufiet PD, Owona PE, Goufani RB, Fifen RN, Nguegan LM, Noubom M, Dimo T, Kamtchouing P J Toxicol 02-Dec-2022
PMCID:PMC9733988
doi:10.1155/2022/1998433
PMID:36506716
Selective and clear-cut logging have varied imprints on tree community structure in a moist semi-deciduous forest in Ghana Addo-Fordjour P, Afram IS, Oppong J Heliyon 04-Nov-2022
PMCID:PMC9649955
doi:10.1016/j.heliyon.2022.e11393
PMID:36387494
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
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

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 alcohol esters
Oct-2-enyl acetate 102248 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162952298 Click to see 650.80 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162935281 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC 632.90 unknown https://doi.org/10.1055/S-2006-957404
Methyl 1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162935280 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC 632.90 unknown https://doi.org/10.1055/S-2006-957404
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP50061A005
https://doi.org/10.1016/S0040-4039(00)96945-4
(1R,2R,4S,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-1,4,10,11-tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101637218 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O)O 504.70 unknown https://doi.org/10.1016/0031-9422(92)80459-R
1,10-Dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3838010 Click to see 472.70 unknown https://doi.org/10.1021/NP50061A005
2-Acetyltormentic acid 178932 Click to see 530.70 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
https://doi.org/10.1021/NP50038A034
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1055/S-2006-960959
Cecropic acid 192258 Click to see 514.70 unknown https://doi.org/10.1055/S-2006-960959
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1021/NP50061A005
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1055/S-2006-960959
https://doi.org/10.1016/0031-9422(92)80459-R
https://doi.org/10.1016/S0031-9422(97)00789-9
https://doi.org/10.1021/NP50038A034
Euscaphic Acid Methyl Ester 14314584 Click to see 502.70 unknown https://doi.org/10.1016/0031-9422(92)80459-R
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP50061A005
https://doi.org/10.1016/S0040-4039(00)96945-4
Maslinic acid methyl ester 13653327 Click to see 486.70 unknown https://doi.org/10.1055/S-2006-957404
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-acetyloxy-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21123533 Click to see 544.80 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 457300 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
methyl (1R,2R,4S,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-1,4,10,11-tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101637217 Click to see 518.70 unknown https://doi.org/10.1016/0031-9422(92)80459-R
methyl (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 89432794 Click to see 470.70 unknown https://doi.org/10.1055/S-2006-957404
Methyl 1,4,10,11-tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163041892 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC)O 518.70 unknown https://doi.org/10.1016/0031-9422(92)80459-R
Methyl 11-acetyloxy-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73744534 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC 544.80 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
Methyl maslinate 3082208 Click to see 486.70 unknown https://doi.org/10.1055/S-2006-957404
Methyl Oleanolate 92900 Click to see 470.70 unknown https://doi.org/10.1055/S-2006-957404
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP50061A005
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1055/S-2006-960959
https://doi.org/10.1016/S0031-9422(97)00789-9
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP50038A034
https://doi.org/10.1016/S0031-9422(97)00789-9
https://doi.org/10.1055/S-2006-960959
https://doi.org/10.1016/0031-9422(92)80459-R
https://doi.org/10.1021/NP50061A005
https://doi.org/10.1016/S0040-4039(00)96945-4
Tormentic Acid Methyl Ester 14314585 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(97)00789-9
Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, methyl ester, (2alpha,3beta)- 601648 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC 502.70 unknown https://doi.org/10.1016/0031-9422(92)80459-R
https://doi.org/10.1016/S0031-9422(97)00789-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 1-hydroxysteroids
Dimethyl 2,6,11-trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylate 163027875 Click to see 546.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 16-hydroxysteroids
dimethyl (2S,3aR,5aR,5bS,6S,7aS,10R,11R,11aS,13aR,13bR)-2,6,11-trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylate 163027876 Click to see 546.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
dimethyl (2S,3aR,5aR,5bS,7aS,8S,10R,11R,11aS,13aR,13bR)-2,8,11-trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylate 162976209 Click to see 546.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
Dimethyl 2,8,11-trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylate 162976208 Click to see 546.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(1R,2S,4aR,4bS,6aS,9R,10R,10aS,12aS)-1-(carboxymethyl)-2-(2-carboxypropan-2-yl)-10-hydroxy-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 124708159 Click to see 518.70 unknown https://doi.org/10.1016/S0040-4039(00)96945-4
1-(carboxymethyl)-2-(2-carboxypropan-2-yl)-10-hydroxy-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 14312909 Click to see 518.70 unknown https://doi.org/10.1016/S0040-4039(00)96945-4
methyl (1R,2R,4aR,4bR,5S,6aS,9R,10R,10aS,10bR,12aR)-5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,10b,11,12,12a-dodecahydro-2H-chrysene-6a-carboxylate 101602323 Click to see CC1CCC2(CC(C3(C(C2C1(C)O)CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C)O)C(=O)OC 578.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl (1R,2R,4aR,4bR,6aS,7S,9R,10R,10aS,10bR,12aR)-7,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,10b,11,12,12a-dodecahydro-2H-chrysene-6a-carboxylate 101602322 Click to see 578.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl (1R,2S,4aR,4bS,5S,6aS,9R,10R,10aS,12aS)-5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 162884196 Click to see 576.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl (1R,2S,4aR,4bS,6aS,7S,9R,10R,10aS,12aR)-7,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 163046328 Click to see 576.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl (1R,2S,4aR,4bS,6aS,9R,10R,10aS,12aS)-10-hydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 163023802 Click to see 560.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl (1S,2S,4aS,4bR,6aS,9R,10R,10aR,12aS)-10-hydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 101603364 Click to see 560.80 unknown https://doi.org/10.1021/NP50061A005
https://doi.org/10.1016/0031-9422(91)84220-M
https://doi.org/10.1016/S0040-4039(00)96945-4
methyl 10-hydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 14312911 Click to see 560.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl 5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 14845557 Click to see 576.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
methyl 7,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate 14845555 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)C(=O)OC)O 576.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
2,6,11-Trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylic acid 163192388 Click to see 518.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
2,8,11-Trihydroxy-3,3,5a,5b,10,11,13b-heptamethyl-1,3a,4,5,6,7,8,9,10,11a,13,13a-dodecahydrocyclopenta[a]chrysene-2,7a-dicarboxylic acid 163187697 Click to see 518.70 unknown https://doi.org/10.1016/0031-9422(91)83649-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1055/S-2006-960959
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1055/S-2006-960959
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1078/0944-7113-00003
Procyanidin C1 169853 Click to see 866.80 unknown https://doi.org/10.1078/0944-7113-00003
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1078/0944-7113-00003
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1078/0944-7113-00003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1078/0944-7113-00003

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