Erythrophleum suaveolens - Unknown
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Details Top

Internal ID UUID643fdb3f3caed817237701
Scientific name Erythrophleum suaveolens
Authority (Guill. & Perr.) Brenan
First published in Taxon9: 194 (1960)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erythrophleum guineense G.Don Gen. Hist.2: 424 (1832)
Fillaea suaveolens Guill. & Perr. Fl. Seneg. Tent.: 242 (1832)
Mavia judicialis G.Bertol. Mem. Reale Accad. Sci. Ist. Bologna2: 570 (1850)
Afzelia grandis hort. ex Loudon J.C.Loudon, Hort. Brit.: 186 (1830)
Erythrophleum judiciale Proctor Amer. J. Pharm., ser. 2, 18: 195 (1852)
Erythrophleum ordale Bolle W.C.H.Peters, Naturw. Reise Mossambique6(1): 10 (1861)

Common names Top

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Language Common/alternative name
English sasswood
English forest ordeal tree
Afrikaans bosoordeelboom
Bambara tali
Croatian crveno vodeno drvo
kcg a̱sap
Chinese 几内亚格木

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000194829
UNII 49KZU5X192
USDA Plants ERSU14
Tropicos 13051014
KEW urn:lsid:ipni.org:names:494641-1
The Plant List ild-41460
Open Tree Of Life 753426
NCBI Taxonomy 162772
IUCN Red List 62025437
IPNI 494641-1
iNaturalist 363339
GBIF 2971196
Freebase /m/0j_5qz9
EPPO EYQSU
EOL 416869
USDA GRIN 100131
Wikipedia Erythrophleum_suaveolens
CMAUP NPO13887

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
Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin Dossou AJ, Fandohan AB, Omara T, Chippaux JP J Trop Med 08-Apr-2024
PMCID:PMC11018376
doi:10.1155/2024/8357312
PMID:38623180
Historical tree phenology data reveal the seasonal rhythms of the Congo Basin rainforest Kearsley E, Verbeeck H, Stoffelen P, Janssens SB, Yakusu EK, Kosmala M, De Mil T, Bauters M, Kitima ER, Ndiapo JM, Chuda AL, Richardson AD, Wingate L, Ilondea BA, Beeckman H, van den Bulcke J, Boeckx P, Hufkens K Plant Environ Interact 11-Mar-2024
PMCID:PMC10926959
doi:10.1002/pei3.10136
PMID:38476212
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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Buruli ulcer in Africa: Geographical distribution, ecology, risk factors, diagnosis, and indigenous plant treatment options – A comprehensive review Osei-Owusu J, Aidoo OF, Eshun F, Gaikpa DS, Dofuor AK, Vigbedor BY, Turkson BK, Ochar K, Opata J, Opoku MJ, Ninsin KD, Borgemeister C Heliyon 15-Nov-2023
PMCID:PMC10686891
doi:10.1016/j.heliyon.2023.e22018
PMID:38034712
The Use of Gonimbrasia belina (Westwood, 1849) and Cirina forda (Westwood, 1849) Caterpillars (Lepidoptera: Sarturniidae) as Food Sources and Income Generators in Africa Nemadodzi LE, Managa GM, Prinsloo G Foods 29-May-2023
PMCID:PMC10252327
doi:10.3390/foods12112184
PMID:37297431
Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P Plants (Basel) 08-May-2023
PMCID:PMC10181441
doi:10.3390/plants12091909
PMID:37176967
Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
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
LC-HRMS/MS-Based Metabolomics Approaches Applied to the Detection of Antifungal Compounds and a Metabolic Dynamic Assessment of Orchidaceae Lima GS, Lima NM, Roque JV, de Aguiar DV, Oliveira JV, dos Santos GF, Chaves AR, Vaz BG Molecules 16-Nov-2022
PMCID:PMC9692279
doi:10.3390/molecules27227937
PMID:36432039
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
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

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
Corypalmine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2-(dimethylamino)ethyl (2E)-2-[(1R,4aS,4bR,8S,8aS,9R,10aR)-8-acetyloxy-9-hydroxy-1,8-dimethyl-10-oxo-3,4,4a,4b,5,6,7,8a,9,10a-decahydro-1H-phenanthren-2-ylidene]acetate 162877260 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3CCCC(C3C(C2=O)O)(C)OC(=O)C 435.60 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
2-(dimethylamino)ethyl 2-(8-acetyloxy-9-hydroxy-1,8-dimethyl-10-oxo-3,4,4a,4b,5,6,7,8a,9,10a-decahydro-1H-phenanthren-2-ylidene)acetate 162877259 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3CCCC(C3C(C2=O)O)(C)OC(=O)C 435.60 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(dimethylamino)ethyl (2E)-2-[(1R,4aR,4bR,7S,8aR,10aS)-7-hydroxy-1,4b,8,8-tetramethyl-10-oxo-1,3,4,4a,5,6,7,8a,9,10a-decahydrophenanthren-2-ylidene]acetate 162988468 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C)O)C 405.60 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
2-(Dimethylamino)ethyl (3-hydroxy-14-methyl-7-oxopodocarpan-13-ylidene)acetate 118078 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C)O)C 405.60 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
2-(dimethylamino)ethyl 2-(7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 101054 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2O)(C)C)O)C 407.60 unknown https://doi.org/10.1002/HLCA.19400230195
https://doi.org/10.1002/HLCA.19490320720
Cassaidine 5281266 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2O)(C)C)O)C 407.60 unknown https://doi.org/10.1002/HLCA.19490320720
https://doi.org/10.1002/HLCA.19400230195
Cassaine 5281267 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C)O)C 405.60 unknown via CMAUP database
Cassaine, sulfate 54603654 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C)O)C.OS(=O)(=O)O 503.70 unknown via CMAUP database
Cassamine 12302503 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 433.60 unknown https://doi.org/10.1002/HLCA.19490320720
Erythrophlamine 72941436 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 449.60 unknown https://doi.org/10.1002/HLCA.19490320720
Erythrophleguine 5281271 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3C(C2=O)O)(C)C(=O)OC)C 449.60 unknown https://doi.org/10.2307/4117899
methyl (1R,2S,4aR,4bS,7Z,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163190125 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 449.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
methyl (1R,2S,4aR,4bS,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163011254 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 449.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
methyl (1S,4aR,4bR,7E,8R,8aR,9R,10aR)-9-hydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate 163186401 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3C(=O)C2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bR,8R,8aR,9R,10aR)-9-hydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate 162866400 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3C(=O)C2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,7E,8R,8aR,10aR)-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-9,10-dioxo-3,4,4b,5,6,8,8a,10a-octahydro-2H-phenanthrene-1-carboxylate 163188636 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3C(=O)C2=O)(C)C(=O)OC)C 433.50 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,7E,8R,8aR,9R,10aS)-9-hydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 163187556 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,7E,8R,8aS,9S,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 54607075 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
methyl (1S,4aR,4bS,7E,8R,8aS,9S,10aR)-9-hydroxy-7-[2-[2-hydroxyethyl(methyl)amino]-2-oxoethylidene]-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 54606895 Click to see CC1C2C(CCC1=CC(=O)N(C)CCO)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,7Z,8R,8aS,9R,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate 163057917 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3C(=O)C2O)(C)C(=O)OC)C 449.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
methyl (1S,4aR,4bS,8R,8aR,10aR)-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-9,10-dioxo-3,4,4b,5,6,8,8a,10a-octahydro-2H-phenanthrene-1-carboxylate 163058344 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3C(=O)C2=O)(C)C(=O)OC)C 433.50 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,8R,8aR,9R,10aS)-9-hydroxy-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 162955655 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2O)(C)C(=O)OC)C 421.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aR,4bS,8R,8aS,9S,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-3,4,4b,5,6,8,8a,9,10,10a-decahydro-2H-phenanthrene-1-carboxylate 24196368 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2O)(C)C(=O)OC)C 435.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
methyl (1S,4aS,4bS,7E,8R,8aR,10aR)-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163188929 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 419.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aS,4bS,7E,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163191166 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 433.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aS,4bS,8R,8aR,10aR)-1,4a,8-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163069133 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 419.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (1S,4aS,4bS,8R,8aR,10aR)-7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 163051779 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 433.60 unknown https://doi.org/10.1002/CBER.19711041118
methyl (2E)-2-[(1S,4bS,7S,8aR)-7-hydroxy-1,4b,8,8-tetramethyl-10-oxo-1,3,4,5,6,7,8a,9-octahydrophenanthren-2-ylidene]acetate 162852851 Click to see CC1C(=CC(=O)OC)CCC2=C1C(=O)CC3C2(CCC(C3(C)C)O)C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
Methyl 2-(7-hydroxy-1,4b,8,8-tetramethyl-10-oxo-1,3,4,5,6,7,8a,9-octahydrophenanthren-2-ylidene)acetate 162852850 Click to see CC1C(=CC(=O)OC)CCC2=C1C(=O)CC3C2(CCC(C3(C)C)O)C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)97155-3
Methyl 7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 117228 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3CC2=O)(C)C(=O)OC)C 433.60 unknown https://doi.org/10.1002/HLCA.19490320720
Methyl 7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-2-hydroxy-1,4a,8-trimethyl-9-oxo-2,3,4,4b,5,6,8,8a,10,10a-decahydrophenanthrene-1-carboxylate 73656827 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)C(=O)OC)O)C 449.60 unknown https://doi.org/10.1002/HLCA.19490320720
Methyl 7-[2-[2-(dimethylamino)ethoxy]-2-oxoethylidene]-9-hydroxy-1,4a,8-trimethyl-10-oxo-2,3,4,4b,5,6,8,8a,9,10a-decahydrophenanthrene-1-carboxylate 163057916 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCCC(C3C(=O)C2O)(C)C(=O)OC)C 449.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-2835
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Esculentoside A 125210 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6COC(C(C6O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 827.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
2-(dimethylamino)ethyl (2Z)-2-[(1R,4bR,7S,8R,8aR,10aS)-8-acetyloxy-7-hydroxy-1,4b,8-trimethyl-10-oxo-1,3,4,4a,5,6,7,8a,9,10a-decahydrophenanthren-2-ylidene]acetate 5317211 Click to see CC1C2C(CCC1=CC(=O)OCCN(C)C)C3(CCC(C(C3CC2=O)(C)OC(=O)C)O)C 449.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6-dihydro-3H-pyrano[3,4-c]pyran-8-one 15559483 Click to see C=CC1=C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown https://doi.org/10.1002/CBER.19711041118
> Organoheterocyclic compounds / Benzazepines
Ribasine 5459059 Click to see CN1C2CC3=CC4=C(C=C3C25CC6=C(C1O5)C7=C(C=C6)OCO7)OCO4 351.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(S)-Laudanosine 73397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown via CMAUP database
Codamine 20056510 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)O)OC 343.40 unknown via CMAUP database

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