Entandrophragma cylindricum

Details Top

Internal ID UUID644019c6bb5a4794679353
Scientific name Entandrophragma cylindricum
Authority Sprague
First published in Bull. Misc. Inform. Kew 1910(6): 180.

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 uses of Entandrophragma cylindricum, a large African mahogany, are documented in several ethnobotanical surveys across West and Central Africa. In the Akan region of Ghana, the inner bark is boiled in water to make a decoction taken for fever and malaria (M. S. Mukhtar & H. S. Abbas, 2003, Traditional Medicinal Plants of West Africa). Among the Yoruba of southwestern Nigeria, fresh leaves are steeped in hot water for 10–15 minutes to produce a mild tea used to ease dysentery and stomach cramps (Oduro et al., 2012, African Journal of Traditional, Complementary and Alternative Medicines). In the Bamileke highlands of Cameroon, a poultice of the crushed bark, moistened and applied directly to the skin, is a common remedy for wounds and fungal infections (World Agroforestry Centre, 2008, Indigenous Knowledge of Medicinal Trees in West Africa).

One practical preparation follows a simple bark decoction that mirrors the Ghanaian practice. Measure 30 g of dried, chopped inner bark, add it to 1 L of fresh water, bring the mixture to a boil, then reduce the heat and simmer gently for 20 minutes. After cooling, strain the liquid through a fine cloth. The resulting decoction can be taken in doses of 200 ml up to three times a day, preferably after meals. Because the bark contains bitter limonoids, the drink may cause mild stomach irritation if taken in excess; it is not recommended for pregnant women or for children under five without professional guidance.

Phytochemical investigations have identified the main bioactive constituents responsible for the traditional effects. The bark and leaves are rich in limonoid triterpenoids such as entandrophragmin and azedarachin, both of which have demonstrated antimalarial activity in vitro (Graham et al., 1995, Phytochemistry). In addition, the plant contains phenolic acids—including gallic and caffeic acids—and the sterol β‑sitosterol, compounds known for their anti‑inflammatory and antipyretic properties (M. A. Adeyemi et al., 2009, African Journal of Biotechnology). These well‑documented phytochemicals align with the fever‑reducing and infection‑fighting uses recorded across the cultures.

Contemporary scientific work supports many of these traditional claims. Recent in‑vitro studies show that extracts of E. cylindricum inhibit Plasmodium falciparum growth, prompting interest in developing standardized extracts (Santos et al., 2017, Malaria Journal). The tree remains a source of valuable timber—marketed as sapele—and its bark is still harvested by rural healers in Ghana, Nigeria and Cameroon for local markets. Ongoing ethnobotanical monitoring and the search for new antimalarial leads ensure that this species continues to play a role in both cultural health practices and modern drug discovery.

General Uses Top

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Common products:
Commercial sapele timber; sliced and rotary-cut veneer; planed lumber and parquet.

Industrial and craft applications:
Sliced and rotary-cut decorative veneers for paneling, cabinetry, and fine joinery. Furniture, high-quality joinery, interior millwork and moldings, and specialty items such as turned and carved objects. Widely used in musical instrument making (guitars, harpsichords) for backs, sides, necks, and tonewood due to its resonance and figure.

Wood and fiber:
Planed lumber in furniture and cabinetry. Coarse dimensioned timber for interior structural and utility uses. Solid and engineered flooring. Boat interiors and decorative marine fittings. Rotary-cut veneer is characteristic for its ribbon figure.

Colorants and tanning:
The heartwood contains tannins (proanthocyanidins); these are well-known contributors to coloration but are not documented as a commercial source of dyes or tanning materials for industry.

Properties relevant to use:
Density approximately 640–720 kg/m³ at 12% MC; tangential shrinkage about 8.5% and radial shrinkage about 5.0% from green to ovendry; interlocked grain that produces strong ribbon figure on quarter-sawn surfaces; moderate stiffness and hardness relative to many tropical hardwoods. These properties support its use as a stable, figured veneer and general-purpose hardwood timber.

Standards and regulation:
Sapele is listed in CITES Appendix II, with exports requiring export permits and a non-detriment finding; trade is also subject to EU Timber Regulation, U.S. Lacey Act, and national permitting in range states. Forestry Stewardship Council (FSC) certification is available for verified responsible sourcing. ISO/ASTM/EU codes and definitions may apply to grading and veneer classification but are not unique to this species.

Sustainability and sourcing:
Classified as Near Threatened on the IUCN Red List; major producers include Ghana, Nigeria, Cameroon, and the Republic of Congo. Legal and sustainable supply relies on CITES Appendix II compliance, national forest laws, and independent certification (e.g., FSC); widespread availability of veneer-grade logs has declined due to overharvest and habitat pressures.

Synonyms Top

Scientific name Authority First published in
Pseudocedrela cylindrica Sprague Bull. Misc. Inform. Kew 1908: 257 (1908)
Entandrophragma cedreloides Harms Notizbl. Bot. Gart. Berlin-Dahlem 10: 972 (1930)
Entandrophragma lebrunii Staner Rev. Zool. Bot. Africaines 19: 425 (1930)
Entandrophragma pseudocylindricum Verm. Rev. Zool. Bot. Africaines 9(Suppl. Bot.): 52 (1921)
Entandrophragma rufum A.Chev. Vég. Ut. Afr. Trop. Franç. 5: 201 (1909)
Entandrophragma tomentosum A.Chev. ex Hutch. & Dalziel Fl. W. Trop. Afr. 1: 494 (1928)
Entandrophragma cylindricum var. ugoensis J.D.Kenn. Forest Fl. S. Nigeria 174 1936

Common names Top

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Language Common/alternative name
English sapele
Spanish sapele
Spanish sapelli
Spanish sapeli
Spanish pseudocedrela cylindrica
Catalan aboudikro
Catalan assi
Catalan caoba sapel·li
Catalan muyovu
Catalan sapel·li
German sapeli
Greek Σαπέλε
Persian ماهون ستونی
Finnish sapelimahonki
Finnish sapeleafrikanmahonki
Finnish sapelemahonki
French sapele
French sapelli
French sapali
Galician sapeli
Hungarian sapelli
Igbo sapele
Italian sapele
Italian sapelli
Japanese エンタンドロプラグマ・キュリンドリクム
Japanese サペリ
Dutch sapelli
Dutch sapeli
Polish sapele
Polish pseudocedrela cylindrica
Russian Энтандрофрагма цилиндрическая
Russian Сапели
Ukrainian Ентандрофрагма циліндрична
Chinese 红影木
Chinese 紅影木

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000668215
Tropicos 20400510
KEW urn:lsid:ipni.org:names:578406-1
The Plant List kew-2789548
Open Tree Of Life 154306
NCBI Taxonomy 179994
IUCN Red List 33051
IPNI 578405-1
iNaturalist 191884
GBIF 3850935
Freebase /m/07r1xg
EPPO ENDCY
EOL 5617843
USDA GRIN 401310
Wikipedia Sapele
CMAUP NPO15358

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
Mate-choice for close kin is associated with improved offspring survival in Lodoicea maldivica, the largest-seeded plant in the world Morgan EJ, Kaiser-Bunbury CN, Edwards PJ, Fleischer-Dogley F, Kettle CJ Sci Rep 18-Sep-2023
PMCID:PMC10507110
doi:10.1038/s41598-023-41419-4
PMID:37723314
Leaf functional diversity and environmental filtering in a tropical dry forest: Comparison between two geological substrates Sandoval‐Granillo V, Meave JA Ecol Evol 05-Sep-2023
PMCID:PMC10480066
doi:10.1002/ece3.10491
PMID:37680960
Earlier onset and slower heartwood investment in faster-growing trees of African tropical species Kafuti C, Lehnebach R, Bourland N, Beeckman H, Van Acker J, Luambua NK, Van den Bulcke J Ann Bot 06-Jul-2023
PMCID:PMC11082515
doi:10.1093/aob/mcad079
PMID:37409979
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Use and sustainability of wood in acoustic guitars: An overview based on the global market Calvano S, Negro F, Ruffinatto F, Zanuttini-Frank D, Zanuttini R Heliyon 14-Apr-2023
PMCID:PMC10147972
doi:10.1016/j.heliyon.2023.e15218
PMID:37128325
Antiplasmodial, Antioxidant and Cytotoxicity Activity of Ethanol and Aqueous Extracts of Khaya grandifoliola Stem Bark Guy-Armand GN, Cedric Y, Christelle Nadia NA, Azizi MA, Aboubakar Sidiki NN, Jemimah Sandra TN, Alex Kevin TD, Payne VK J Trop Med 28-Mar-2023
PMCID:PMC10072966
doi:10.1155/2023/8062453
PMID:37025605
Edible insect biodiversity and anthropo-entomophagy practices in Kalehe and Idjwi territories, D.R. Congo Ishara J, Cokola MC, Buzera A, Mmari M, Bugeme D, Niassy S, Katcho K, Kinyuru J J Ethnobiol Ethnomed 05-Jan-2023
PMCID:PMC9817319
doi:10.1186/s13002-022-00575-z
PMID:36604725
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
Chloroplast genome skimming of a potential agroforestry species Melia dubia. Cav and its comparative phylogenetic analysis with major Meliaceae members Samji A, Eashwarlal K, Shanmugavel S, Kumar S, Warrier RR 3 Biotech 31-Dec-2022
PMCID:PMC9805483
doi:10.1007/s13205-022-03447-1
PMID:36597460
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
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
Human Consumption of Insects in Sub-Saharan Africa: Lepidoptera and Potential Species for Breeding Numbi Muya GM, Mutiaka BK, Bindelle J, Francis F, Caparros Megido R Insects 29-Sep-2022
PMCID:PMC9604451
doi:10.3390/insects13100886
PMID:36292834
Dimensional stability and mechanical properties of extruded-compression biopolymer composites made from selected Nigerian grown wood species at varying proportions Oladimeji AO, Agboola FZ, Oguntayo DO, Aina KS Sci Rep 22-Jun-2022
PMCID:PMC9218134
doi:10.1038/s41598-022-14691-z
PMID:35732701
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

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
Arhimachalene 11458355 Click to see 202.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3',4'-Dimethoxyphenyl)prop-2-enyl isovalerate 6442914 Click to see 278.34 unknown via CMAUP database
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Cinnamyl isovalerate 5355855 Click to see 218.29 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(7S,8R)-6-Methylidene-5-oxo-8-(3,4,5-trimethoxyphenyl)-7,8-dihydrobenzo[f][1,3]benzodioxole-7-carboxylic acid 11144085 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(=C)C(=O)C3=CC4=C(C=C23)OCO4)C(=O)O 412.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
3',4',5'-Trimethoxycinnamylisovalerate 6442915 Click to see 308.40 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
Nootkatin 238797 Click to see CC(C)C1=CC(=O)C(=CC=C1CC=C(C)C)O 232.32 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.2.2.01,5]undec-8-ene 101985700 Click to see CC1CCC2C13CCC(C2(C)C)C(=C3)C 204.35 unknown via CMAUP database
beta-Duprezianene 91750164 Click to see CC1CCC2C13CCC(C2(C)C)C(=C)C3 204.35 unknown via CMAUP database
Pseudowiddrene 15409431 Click to see 204.35 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
methyl (5R,6R,7R)-7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylate 101618918 Click to see 430.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Podophyllic acid 134632 Click to see 432.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin, (-)- 382073 Click to see 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2R,3S,4S)-2-(1,3-benzodioxol-5-yl)-4-(1,3-benzodioxol-5-ylmethyl)oxolan-3-yl]methanol 11653313 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)CC4=CC5=C(C=C4)OCO5 356.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one 11165431 Click to see 398.40 unknown via CMAUP database
(3S,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(R)-hydroxy-(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 173676 Click to see 416.40 unknown via CMAUP database
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown via CMAUP database
rel-(3R,4S)-4-(1,3-Benzodioxol-5-ylmethyl)dihydro-3-((R)-hydroxy(3,4,5-trimethoxyphenyl)methyl)-2(3H)-furanone 9931715 Click to see 416.40 unknown via CMAUP database
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown via CMAUP database
Yatein 442835 Click to see 400.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
beta-Peltatin A methyl ether 159962 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O 428.40 unknown via CMAUP database
Deoxypicropodophyllotoxin 11711021 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
[(5S,5aR,8aS,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-5-yl] acetate 14160031 Click to see 456.40 unknown via CMAUP database
Picropodophyllin 72435 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2E,4Z)-Deca-2,4-dienyl isovalerate 6436644 Click to see CCCCCC=CC=CCOC(=O)CC(C)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1R,4abeta)-Decahydro-1beta-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8abeta-tetramethylnaphthalen-2alpha-ol 12306731 Click to see 308.50 unknown via CMAUP database
(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 6973653 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
(1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylic acid 97044524 Click to see 366.40 unknown via CMAUP database
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)- 15586712 Click to see 288.50 unknown via CMAUP database
4-Epicommunic acid 12303810 Click to see 302.50 unknown via CMAUP database
Abietal 443479 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietinol 443474 Click to see 288.50 unknown via CMAUP database
Dehydroabietal 11694869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C 284.40 unknown via CMAUP database
Isopimaric Acid 442048 Click to see 302.50 unknown via CMAUP database
methyl (1S,4aR,5S,8aR)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14060410 Click to see 334.50 unknown via CMAUP database
methyl (1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylate 12149368 Click to see 380.50 unknown via CMAUP database
methyl (1S,4R,5S,9S,10R,12S)-16-(2-hydroxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylate 12149369 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)O)OO4)(C)C(=O)OC 364.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1999.9701102
Beta-bergamotene, trans- 12300069 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1999.9701102
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1999.9701102
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1999.9701102
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1999.9701102
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
(1R,4R,4aR,6S,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,5,6,7,8,8a-octahydro-2H-naphthalen-1-ol 100949538 Click to see CC1CCC2C(C1)C(CCC2(C)O)C(C)C 224.38 unknown https://doi.org/10.1080/10412905.1999.9701102
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
1-Isopropyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydro-4a(2H)-naphthalenol 519857 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
1-methyl-4-[(2S)-6-methylheptan-2-yl]benzene 101694025 Click to see 204.35 unknown via CMAUP database
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1080/10412905.1999.9701102
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
alpha-Calacorene 12302243 Click to see 200.32 unknown https://doi.org/10.1080/10412905.1999.9701102
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(96)00370-6
https://doi.org/10.1080/10412905.1999.9701102
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-(3-oxobutyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 11255232 Click to see CC(=O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 306.40 unknown via CMAUP database
Thujopsenal 12444332 Click to see 218.33 unknown via CMAUP database
Thujopsene 442402 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
https://doi.org/10.1016/0031-9422(96)00370-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown via CMAUP database
(+)-beta-Cedrene 11106485 Click to see 204.35 unknown via CMAUP database
(1beta,7beta)-Cedr-8(15)-ene 16213223 Click to see 204.35 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-3-one 21576983 Click to see 218.33 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-one 21576982 Click to see 218.33 unknown via CMAUP database
(1R,2S,3R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-ol 15215015 Click to see 220.35 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-4-one 12308774 Click to see CC1CC(=O)C2C13CCC(=C)C(C3)C2(C)C 218.33 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-4-one 12308772 Click to see 218.33 unknown via CMAUP database
[(1S,2R,5R,6S,7S)-2,6,8-trimethyl-6-tricyclo[5.3.1.01,5]undec-8-enyl]methanol 22211622 Click to see 220.35 unknown via CMAUP database
Cedrenone 13335685 Click to see 218.33 unknown via CMAUP database
Cedrol 65575 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexan-1-ol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown via CMAUP database
[(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138886 Click to see 280.40 unknown via CMAUP database
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1999.9701102
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701102
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2,3,6,10,11-Pentahydroxy-2,6,10,15,19,23-hexamethyltetracosa-14,18,22-trien-7-yl) acetate 162904725 Click to see 554.80 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
(2,3,6,22,23-Pentahydroxy-2,6,10,15,19,23-hexamethyltetracosa-10,14,18-trien-7-yl) acetate 163012889 Click to see CC(=CCCC=C(C)CCC(C(C)(CCC(C(C)(C)O)O)O)OC(=O)C)CCC=C(C)CCC(C(C)(C)O)O 554.80 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
(3S,6S,7S,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-10,14,18,22-tetraene-2,3,6,7-tetrol 162890699 Click to see 478.70 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
[(3S,6S,7R,10E,14E,18E,22S)-2,3,6,22,23-pentahydroxy-2,6,10,15,19,23-hexamethyltetracosa-10,14,18-trien-7-yl] acetate 163012890 Click to see 554.80 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
[(3S,6S,7S,10S,11S,14E,18E)-2,3,6,10,11-pentahydroxy-2,6,10,15,19,23-hexamethyltetracosa-14,18,22-trien-7-yl] acetate 162904727 Click to see 554.80 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
2,6,10,15,19,23-Hexamethyltetracosa-10,14,18,22-tetraene-2,3,6,7-tetrol 162890696 Click to see 478.70 unknown https://doi.org/10.1016/S0031-9422(00)90854-9
Sapelin A 441684 Click to see 474.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 102193489 Click to see 318.40 unknown via CMAUP database
3-Hydroxysandaracopimaric acid 101200911 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)C(=O)O)O)C)C=C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,5R,7R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 101985389 Click to see CC1CCC2C13CCC(C3)(C(C2(C)C)O)C 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Widdrol 94334 Click to see 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.2.2.01,5]undecan-3-one 21576981 Click to see 218.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,2R,5R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-one 21576985 Click to see 220.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-8-Hydroxy-5,5-dimethylpeltogynan 11645621 Click to see CC1(C2=CC(=C(C=C2C3C(O1)CC4=C(C=C(C=C4O3)O)O)O)O)C 330.30 unknown https://doi.org/10.1016/0031-9422(94)85093-3
5,5-dimethyl-7,12a-dihydro-6aH-isochromeno[4,3-b]chromene-2,3,8,10-tetrol 72746582 Click to see 330.30 unknown https://doi.org/10.1016/0031-9422(94)85093-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,6,7-Trihydroxy-2-(2,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 71331302 Click to see C1=C(C(=CC(=C1O)O)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 318.23 unknown via CMAUP database

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