Musanga cecropioides - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

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

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

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

Common names Top

Add a new one! Suggest a correction!

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

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
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
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
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
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Spatial patterns of light‐demanding tree species in the Yangambi rainforest (Democratic Republic of Congo) Luambua NK, Hubau W, Salako KV, Amani C, Bonyoma B, Musepena D, Rousseau M, Bourland N, Nshimba HS, Ewango C, Beeckman H, Hardy OJ Ecol Evol 20-Dec-2021
PMCID:PMC8717288
doi:10.1002/ece3.8443
PMID:35003702

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Oct-2-enyl acetate 102248 Click to see CCCCCC=CCOC(=O)C 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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 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
(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
(1S,2R,4aS,6aR,6aS,6bR,10R,11R,12aR,14bR)-11-acetyloxy-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-carboxylic acid 192258 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC(=O)C)C)C)C2C1C)C)C(=O)O 514.70 unknown https://doi.org/10.1055/S-2006-960959
2-Acetyltormentic acid 178932 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)O 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
CID 3838010 3838010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP50061A005
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP50061A005
Euscaphic acid 471426 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/10.1016/S0031-9422(97)00789-9
https://doi.org/10.1021/NP50038A034
https://doi.org/10.1016/0031-9422(92)80459-R
https://doi.org/10.1055/S-2006-960959
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0040-4039(00)96945-4
https://doi.org/10.1021/NP50061A005
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 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 (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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)OC 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 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 (4aS,6aR,6aS,6bR,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 3082208 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 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 acuminate 14314584 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
Methyl maslinate 13653327 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1055/S-2006-957404
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1055/S-2006-957404
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP50061A005
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 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/10.1016/S0031-9422(97)00789-9
https://doi.org/10.1055/S-2006-960959
https://doi.org/10.1016/S0040-4039(00)96945-4
https://doi.org/10.1021/NP50061A005
https://doi.org/10.1021/NP50038A034
https://doi.org/10.1016/0031-9422(92)80459-R
Tormentic acid methyl ester 14314585 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/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/S0031-9422(97)00789-9
https://doi.org/10.1016/0031-9422(92)80459-R
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP50061A005
https://doi.org/10.1016/S0040-4039(00)96945-4
Ursolic acid methyl ester 89432794 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1055/S-2006-957404
> 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 CC1CCC2(CC(C3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)OC)O)C)C)C2C1(C)O)C)O)C(=O)OC 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 CC1CCC2(CC(C3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)OC)O)C)C)C2C1(C)O)C)O)C(=O)OC 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 CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)OC)O)C)C)C2C1(C)O)C)C(=O)OC)O 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 CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)OC)O)C)C)C2C1(C)O)C)C(=O)OC)O 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 CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)O)C)C2C1(C)O)C)C(=O)O 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 CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)O)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0040-4039(00)96945-4
19alpha-Hydroxy-2,3-secours-12-ene-2,3,28-trioic acid trimethyl ester 14312911 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)C(=O)OC 560.80 unknown https://doi.org/10.1016/0031-9422(91)84220-M
CID 101603364 101603364 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)C(=O)OC 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 (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 CC1CC(C2(CCC3(C(C2C1(C)O)CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C)C(=O)OC)O 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 CC1CCC2(CC(C3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)O)C(=O)OC 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 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
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 CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)C(=O)OC 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 CC1CCC2(CC(C3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)O)C(=O)OC 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 CC1CCC2(CC(C3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)O)O)C)C)C2C1(C)O)C)O)C(=O)O 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 CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CC(C5(C)C)(C(=O)O)O)C)C)C2C1(C)O)C)C(=O)O)O 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-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-2006-960959
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-2006-960959
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1078/0944-7113-00003
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1078/0944-7113-00003
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1078/0944-7113-00003
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 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 C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1078/0944-7113-00003

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.