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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Filter by language:

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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No forms added yet.

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 click to expand
- Mexico
  - Mexico Gulf
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- 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

Suggest others/fix!

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

Patterns of use of wild food plants by Brazilian local communities: systematic review and meta-analysis

Gomes LC, Medeiros PM, Prata AP

J Ethnobiol Ethnomed

25-Oct-2023

PMCID:	PMC10601232
doi:	10.1186/s13002-023-00619-y
PMID:	37880767

New Therapeutic Strategies for Obesity and Its Metabolic Sequelae: Brazilian Cerrado as a Unique Biome

Monteiro-Alfredo T, Macedo ML, de Picoli Souza K, Matafome P

Int J Mol Sci

25-Oct-2023

PMCID:	PMC10648839
doi:	10.3390/ijms242115588
PMID:	37958572

Plants of the Rubiaceae Family with Effect on Metabolic Syndrome: Constituents, Pharmacology, and Molecular Targets

González-Castelazo F, Soria-Jasso LE, Torre-Villalvazo I, Cariño-Cortés R, Muñoz-Pérez VM, Ortiz MI, Fernández-Martínez E

Plants (Basel)

15-Oct-2023

PMCID:	PMC10610173
doi:	10.3390/plants12203583
PMID:	37896046

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

Relationships between soil properties and species establishment in the restoration of mined soils in the Cerrado biome

Vieira DA, Martins TO, Miranda Matias RA, Fernandes Silva PH, Valadão MB, Barbosa PV, Gatto A, Rodrigues Pinto JR, Bussinguer AP, Ribeiro FP

PLoS One

04-Nov-2022

PMCID:	PMC9635749
doi:	10.1371/journal.pone.0277193
PMID:	36331966

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

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
> 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
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-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
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
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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Alibertia edulis

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