Alibertia edulis - Unknown
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Internal ID UUID6440384b7efba719087731
Scientific name Alibertia edulis
Authority (Rich.) A.Rich. ex DC.
First published in Prodr. 4: 443 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sabicea edulis Seem. ex B.D.Jacks. Index Kew. 2(4): 772. 1895 , a sphalm.
Cordiera edulis (Rich.) Kuntze Revis. Gen. Pl. 1: 279 (1891)
Amaioua edulis Baill. Hist. Pl. 7: 387 (1880)
Gardenia edulis (Rich.) Poir. Encycl. , Suppl. 2: 708 (1812)
Genipa edulis Rich. Actes Soc. Hist. Nat. Paris 1: 107. 1792 [Oct 1792]

Common names Top

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Language Common/alternative name
German wilde guave
Persian امرود وحشی
Chinese 普瑞果
Chinese 普鲁伊
Chinese 普魯伊(水果)

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Alibertia edulis var. edulis Unknown
Alibertia edulis var. manuana Delprete & C.H.Perss.
Alibertia edulis var. obtusiuscula (Steyerm.) Delprete & C.H.Perss. Fl. Venez. Guayana 8: 514 (2004)
Alibertia edulis var. premontana (C.M.Taylor) Delprete & C.H.Perss. Novon 21: 137 (2011)

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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Southwest Caribbean
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000941730
Tropicos 27900261
INPN 629048
KEW urn:lsid:ipni.org:names:743001-1
The Plant List kew-6016
Open Tree Of Life 952905
NCBI Taxonomy 58508
IUCN Red List 150111913
IPNI 743001-1
iNaturalist 316789
GBIF 5335670
Freebase /m/012hmr0c
EPPO AJBED
EOL 1109790
USDA GRIN 2200
Wikipedia Alibertia_edulis

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
Carbon Storage in Different Compartments in Eucalyptus Stands and Native Cerrado Vegetation Ribeiro FP, Gatto A, de Oliveira AD, Pulrolnik K, Valadão MB, Araújo JB, de Carvalho AM, Ferreira EA Plants (Basel) 24-Jul-2023
PMCID:PMC10386474
doi:10.3390/plants12142751
PMID:37514365
Comparative genomics uncovers the evolutionary history, demography, and molecular adaptations of South American canids Chavez DE, Gronau I, Hains T, Dikow RB, Frandsen PB, Figueiró HV, Garcez FS, Tchaicka L, de Paula RC, Rodrigues FH, Jorge RS, Lima ES, Songsasen N, Johnson WE, Eizirik E, Koepfli KP, Wayne RK Proc Natl Acad Sci U S A 15-Aug-2022
PMCID:PMC9407222
doi:10.1073/pnas.2205986119
PMID:35969758
Phylogenomic and comparative analyses of Coffeeae alliance (Rubiaceae): deep insights into phylogenetic relationships and plastome evolution Amenu SG, Wei N, Wu L, Oyebanji O, Hu G, Zhou Y, Wang Q BMC Plant Biol 26-Feb-2022
PMCID:PMC8881883
doi:10.1186/s12870-022-03480-5
PMID:35219317
An approach for evaluating the bioavailability and risk assessment of potentially toxic elements using edible and inedible plants—the Remance (Panama) mining area as a model González-Valoys AC, Jiménez Salgado JU, Rodríguez R, Monteza-Destro T, Vargas-Lombardo M, García-Noguero EM, Esbrí JM, Jiménez-Ballesta R, García-Navarro FJ, Higueras P Environ Geochem Health 22-Oct-2021
PMCID:PMC9867682
doi:10.1007/s10653-021-01086-8
PMID:34677729
Cabbage Production in West Africa and IPM with a Focus on Plant-Based Extracts and a Complementary Worldwide Vision Mondédji AD, Silvie P, Nyamador WS, Martin P, Agboyi LK, Amévoin K, Ketoh GK, Glitho IA Plants (Basel) 11-Mar-2021
PMCID:PMC7998567
doi:10.3390/plants10030529
PMID:33799877
Edible Fruit Plant Species in the Amazon Forest Rely Mostly on Bees and Beetles as Pollinators Paz FS, Pinto CE, de Brito RM, Imperatriz-Fonseca VL, Giannini TC J Econ Entomol 13-Jan-2021
PMCID:PMC8042744
doi:10.1093/jee/toaa284
PMID:33440000
Effects of subacute oral administration of aqueous extract of Macaranga barteri Müll.Arg (Euphorbiaceae) leaf on anthropometric and haematological parameters in rats Ehilé EH, Goze NB, Kouakou KL, Yapo AP, Ehilé EE Toxicol Res 03-Jun-2020
PMCID:PMC7806691
doi:10.1007/s43188-020-00048-z
PMID:33489864
Chloroplast genomes of Rubiaceae: Comparative genomics and molecular phylogeny in subfamily Ixoroideae Ly SN, Garavito A, De Block P, Asselman P, Guyeux C, Charr JC, Janssens S, Mouly A, Hamon P, Guyot R PLoS One 30-Apr-2020
PMCID:PMC7192488
doi:10.1371/journal.pone.0232295
PMID:32353023
A Structure Shaped by Fire, but Also Water: Ecological Consequences of the Variability in Bark Properties Across 31 Species From the Brazilian Cerrado Loram-Lourenço L, Farnese FD, de Sousa LF, Alves RD, de Andrade MC, Almeida SE, Moura LM, Costa AC, Silva FG, Galmés J, Cochard H, Franco AC, Menezes-Silva PE Front Plant Sci 22-Jan-2020
PMCID:PMC6987451
doi:10.3389/fpls.2019.01718
PMID:32038687
Inventory data on Brazilian Amazon׳s non-wood native biomass sources for bioenergy production Flores JA, Konrad O, Flores CR, Schroder NT Data Brief 22-Sep-2018
PMCID:PMC6171085
doi:10.1016/j.dib.2018.09.050
PMID:30294647
Chemical Compounds and Bioactivity of Aqueous Extracts of Alibertia spp. in the Control of Plutella xylostella L. (Lepidoptera: Plutellidae) Peres LL, Sobreiro AI, Couto IF, Silva RM, Pereira FF, Heredia-Vieira SC, Cardoso CA, Mauad M, Scalon SP, Verza SS, Mussury RM Insects 22-Nov-2017
PMCID:PMC5746808
doi:10.3390/insects8040125
PMID:29165339
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
Nature and Age of Neighbours Matter: Interspecific Associations among Tree Species Exist and Vary across Life Stages in Tropical Forests Ledo A PLoS One 18-Nov-2015
PMCID:PMC4651535
doi:10.1371/journal.pone.0141387
PMID:26581110
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Knowledge and use of wild edible plants in rural communities along Paraguay River, Pantanal, Brazil Bortolotto IM, Amorozo MC, Neto GG, Oldeland J, Damasceno-Junior GA J Ethnobiol Ethnomed 30-May-2015
PMCID:PMC4469002
doi:10.1186/s13002-015-0026-2
PMID:26025294

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Tropanserin 68600 Click to see CC1=CC(=CC(=C1)C(=O)OC2CC3CCC(C2)N3C)C 273.37 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
cis-Phytol 6430833 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
1-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4,7-dicarboxylic acid 75051789 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 388.32 unknown https://doi.org/10.1002/HLCA.200890147
Ixoside 44583801 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 388.32 unknown https://doi.org/10.1002/HLCA.200890147
methyl 5,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 13892721 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1002/HLCA.200890147
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aS,6bR,10S,12aR)-10-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-hydroxy-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 163049343 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O 1105.30 unknown https://doi.org/10.1002/HLCA.200890147
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-hydroxy-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 85106379 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O 1105.30 unknown https://doi.org/10.1002/HLCA.200890147
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
https://doi.org/10.1590/S0100-40422003000500003
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Clethric acid 20055826 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1590/S0100-40422003000500003
https://doi.org/10.1016/S0031-9422(00)89654-5
Hederagenin methyl ester 11752118 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-acetyloxy-9,9-bis(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162931969 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(COC(=O)C)COC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC 644.80 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1R,2R,4aS,6aS,6bR,10S,12aR)-1,10-dihydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162820471 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1(C)O)C)C(=O)OC 518.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1R,2R,4aS,6aS,6bR,10S,12aR)-10-acetyloxy-9,9-bis(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162931971 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(COC(=O)C)COC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC 644.80 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1S,2R,4aS,6aR,6aS,6bR,9R,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 163030380 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-acetyloxy-9,9-bis(acetyloxymethyl)-1-hydroxy-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162842426 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1OC(=O)C)C)CC=C4C3(CCC5(C4C(C(CC5)(C)C)O)C(=O)OC)C)C)COC(=O)C 644.80 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl (1S,4aR,6aS,6bR,10S,12aR)-1,10-dihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162924497 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1O)C)C(=O)OC)C 518.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Methyl 1,10-dihydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73821063 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1(C)O)C)C(=O)OC 518.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Methyl 1,10-dihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162924494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)O)C)C)C2C1O)C)C(=O)OC)C 518.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Methyl 10-acetyloxy-9,9-bis(acetyloxymethyl)-1-hydroxy-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162931968 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(COC(=O)C)COC(=O)C)OC(=O)C)C)C)C2C1(C)O)C)C(=O)OC 644.80 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Methyl 10-acetyloxy-9,9-bis(acetyloxymethyl)-1-hydroxy-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162842425 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1OC(=O)C)C)CC=C4C3(CCC5(C4C(C(CC5)(C)C)O)C(=O)OC)C)C)COC(=O)C 644.80 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
methyl 10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 13890854 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Methyl 10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 12526650 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
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/10.1016/S0031-9422(00)89654-5
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
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/10.1016/S0031-9422(00)89654-5
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89654-5
https://doi.org/10.1590/S0100-40422003000500003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
methyl (1S,4aS,5S,6S,7aS)-5,6-dihydroxy-7-methylidene-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 24938675 Click to see COC(=O)C1=COC(C2C1C(C(C2=C)O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1002/HLCA.200890147
methyl 5,6-dihydroxy-7-methylidene-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 74368795 Click to see COC(=O)C1=COC(C2C1C(C(C2=C)O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1002/HLCA.200890147
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922633 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1002/HLCA.200890147
Kelampayoside A 10552637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1002/HLCA.200890147

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