Attalea phalerata, also known as urucuri palm, is a species of palm tree native to Brazil, Bolivia, Paraguay, and Peru. It is the most common palm tree in the Pantanal region and can grow up to 18 meters tall with feather-like leaves and bright orange fruits. This palm is ecologically important and is dispersed by various animals such as tapirs, rheas, and macaws. It is also commonly pollinated by sap beetles and weevils. The tree has various human uses, including thatching rooftops, feeding livestock, and producing vegetable oil. In Bolivia, it is known as motacú and is considered one of the most economically important palm species.

Synonyms Top

Scientific name	Authority	First published in
Attalea excelsa	Mart.	Hist. Nat. Palm. 2: 138 (1826)
Scheelea corumbaensis	Barb.Rodr.	Sert. Palm. Brasil. 1: 54 (1903)
Scheelea martiana	Burret	Notizbl. Bot. Gart. Berlin-Dahlem 10: 541 (1929)
Scheelea microspadix	Burret	Notizbl. Bot. Gart. Berlin-Dahlem 15: 104 (1940)
Scheelea phalerata	(Mart. ex Spreng.) Burret	Notizbl. Bot. Gart. Berlin-Dahlem 10: 541 (1929)
Scheelea princeps var. corumbaensis	Barb.Rodr.	Palm. Mattogross. Nov. : 66 (1898)
Attalea phalerata var. concinna	L.R.Moreno & O.I.Moreno	Revista Soc. Boliv. Bot. 4: 68 (2003)
Attalea excelsa	Mart. ex Spreng.	Syst. Veg., ed. 16 [Sprengel] 2: 624. 1825 [Jan-May 1825]

Common names Top

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Filter by language:

Language	Common/alternative name
English	urucuri palm
gn	mbakuri
Chinese	直叶椰子
Chinese	尤鲁库里棕榈
Chinese	尤鲁庫里棕櫚
Chinese	皮沙巴直葉椰子

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central
- Southern South America
  - Paraguay
- Western South America
  - Bolivia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000296432
Tropicos	50065600
KEW	urn:lsid:ipni.org:names:26580-2
The Plant List	kew-17822
Open Tree Of Life	293018
NCBI Taxonomy	290273
IUCN Red List	67532499
IPNI	26580-2
iNaturalist	67511
GBIF	2732758
Freebase	/m/0kv1gnx
EPPO	ATTPH
EOL	1131719
USDA GRIN	411794
Wikipedia	Attalea_phalerata
CMAUP	NPO1776

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

Resveratrol-Loaded Attalea funifera Oil Organogel Nanoparticles: A Potential Nanocarrier against A375 Human Melanoma Cells

Dourado D, Batista FP, Philadelpho BO, de Souza ML, de Cerqueira e Silva MB, de Grandis RA, Miranda PA, Colauto NB, Pereira DT, Formiga FR, Cilli EM, Pavan FR, Oliveira de Souza C, Ferreira ED

Int J Mol Sci

28-Jul-2023

PMCID:	PMC10419039
doi:	10.3390/ijms241512112
PMID:	37569487

Palm Sunday in central Mexico: among sellers, palms and syncretism

Briseño-Tellez JM, Pulido Silva MT, Bautista K, García Mera A, Larios-Lozano O, López Gutiérrez BN, López López YA, Mendoza Cruz Y, Monzalvo R, Ortega-Meza D, Sánchez Trejo EC, Zepeda-Hernández ZK

J Ethnobiol Ethnomed

03-Jun-2023

PMCID:	PMC10239146
doi:	10.1186/s13002-023-00587-3
PMID:	37268987

“Mi Casa, Tu Casa”: the coati nest as a hub of Trypanosoma cruzi transmission in the southern Pantanal biome revealed by molecular blood meal source identification in triatomines

Pessanha TS, Herrera HM, Jansen AM, Iñiguez AM

Parasit Vectors

23-Jan-2023

PMCID:	PMC9872340
doi:	10.1186/s13071-022-05616-w
PMID:	36691054

Unveiling demographic and mating strategies of Panthera onca in the Pantanal, Brazil

Fragoso CE, Rampim LE, Quigley H, Buhrke Haberfeld M, Ayala Espíndola W, Cabral Araújo V, Rodrigues Sartorello L, May Júnior JA

J Mammal

12-Jan-2023

PMCID:	PMC10075339
doi:	10.1093/jmammal/gyac123
PMID:	37032705

Rhodnius (Stål, 1859) (Hemiptera, Triatominae) genus in Bolivian Amazonia: a risk for human populations?

Depickère S, Villacís AG, Santillán-Guayasamín S, Callapa Rafael JE, Brenière SF, Revollo Zepita S

Parasit Vectors

29-Aug-2022

PMCID:	PMC9426019
doi:	10.1186/s13071-022-05423-3
PMID:	36038947

Toxic Potential of Cerrado Plants on Different Organisms

Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF

Int J Mol Sci

22-Mar-2022

PMCID:	PMC8998518
doi:	10.3390/ijms23073413
PMID:	35408775

Intra- and interspecific variation in self-control capacities of parrots in a delay of gratification task

Brucks D, Petelle M, Baldoni C, Krasheninnikova A, Rovegno E, von Bayern AM

Anim Cogn

21-Oct-2021

PMCID:	PMC8940755
doi:	10.1007/s10071-021-01565-6
PMID:	34671864

Do the new triatomine species pose new challenges or strategies for monitoring Chagas disease? An overview from 1979-2021

Costa J, Dale C, Galvão C, Almeida CE, Dujardin JP

Mem Inst Oswaldo Cruz

31-May-2021

PMCID:	PMC8186471
doi:	10.1590/0074-02760210015
PMID:	34076075

Co-occurrence or dependence? Using spatial analyses to explore the interaction between palms and Rhodnius triatomines

Calderón JM, González C

Parasit Vectors

22-Apr-2020

PMCID:	PMC7178562
doi:	10.1186/s13071-020-04088-0
PMID:	32321545

Persistent Early to Middle Holocene tropical foraging in southwestern Amazonia

Capriles JM, Lombardo U, Maley B, Zuna C, Veit H, Kennett DJ

Sci Adv

24-Apr-2019

PMCID:	PMC6482008
doi:	10.1126/sciadv.aav5449
PMID:	31032413

Plants used by the rural community of Bananal, Mato Grosso, Brazil: Aspects of popular knowledge

Miguéis GD, da Silva RH, Damasceno Júnior GA, Guarim-Neto G

PLoS One

30-Jan-2019

PMCID:	PMC6353550
doi:	10.1371/journal.pone.0210488
PMID:	30699133

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

Beetles, ants, wasps, or flies? An ethnobiological study of edible insects among the Awajún Amerindians in Amazonas, Peru

Casas Reátegui R, Pawera L, Villegas Panduro PP, Polesny Z

J Ethnobiol Ethnomed

09-Aug-2018

PMCID:	PMC6085703
doi:	10.1186/s13002-018-0252-5
PMID:	30092837

The Chemical Composition and Metabolic Effects of Attalea phalerata Nut Oil in Hyperlipidemic Rats Induced by a High-Fructose Diet

Baldivia DD, Sanjinez-Argandonã EJ, Antunes KÁ, Moraes IC, dos Santos EL, de Picoli Souza K

Molecules

20-Apr-2018

PMCID:	PMC6017791
doi:	10.3390/molecules23040960
PMID:	29677105

Anti-inflammatory, antiproliferative and cytoprotective potential of the Attalea phalerata Mart. ex Spreng. pulp oil

Freitas de Lima F, Lescano CH, Arrigo JD, Cardoso CA, Coutinho JP, Moslaves IS, Ximenes TV, Kadri MC, Weber SS, Perdomo RT, Kassuya CA, Vieira MD, Sanjinez-Argandoña EJ

PLoS One

10-Apr-2018

PMCID:	PMC5892912
doi:	10.1371/journal.pone.0195678
PMID:	29634766

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
4-Hydroxy-2-methoxybenzoic acid	12695575	Click to see COC1=C(C=CC(=C1)O)C(=O)O	168.15	unknown	via CMAUP database
> Benzenoids / Indanes / Indanones
(2R-trans)-2,3-Dihydro-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-1H-inden-1-one	169729	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O	234.29	unknown	via CMAUP database
(2R)-2-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-3H-inden-1-one	46849571	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)O	234.29	unknown	via CMAUP database
(2S-trans)-6-(2-Chloroethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-1H-inden-1-one	148419	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCCl)C)O	252.73	unknown	via CMAUP database
(2S,3R)-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one	46850078	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O	234.29	unknown	via CMAUP database
(2S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one	12314748	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C	218.29	unknown	via CMAUP database
(3R)-6-(2-chloroethyl)-3-hydroxy-2,2,5,7-tetramethyl-3H-inden-1-one	23260004	Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2O)(C)C	266.76	unknown	via CMAUP database
(3S)-3-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one	71361396	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C	248.32	unknown	via CMAUP database
(S)-2,3-Dihydro-2-(hydroxymethyl)-6-(2-methoxyethyl)-2,5,7-trimethyl-1H-inden-1-one	134443	Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)CO	262.34	unknown	via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one	169739	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)CO	234.29	unknown	via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-5-(hydroxymethyl)-2,7-dimethyl-1H-inden-1-one	151323	Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCO)CO	234.29	unknown	via CMAUP database
1-Indanone	6735	Click to see C1CC(=O)C2=CC=CC=C21	132.16	unknown	via CMAUP database
2S,3S-acetylpterosin C	21122778	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC(=O)C)C)O	276.33	unknown	via CMAUP database
Epipterosin L	46848746	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO	264.32	unknown	via CMAUP database
Pterosin A	135017	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)CO	248.32	unknown	via CMAUP database
Pterosin B	115049	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C	218.29	unknown	via CMAUP database
Pterosin C	186209	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O	234.29	unknown	via CMAUP database
Pterosin D	147559	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C	248.32	unknown	via CMAUP database
Pterosin E	148588	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CC(=O)O)C	232.27	unknown	via CMAUP database
Pterosin H	135029	Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)C	250.76	unknown	via CMAUP database
Pterosin I	161891	Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)C	246.34	unknown	via CMAUP database
Pterosin K	148420	Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)CO	266.76	unknown	via CMAUP database
Pterosin L	21633068	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO	264.32	unknown	via CMAUP database
Pterosin O	135255	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC)C	232.32	unknown	via CMAUP database
Pterosin Z	134977	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)C	232.32	unknown	via CMAUP database
Pterosinf	46849741	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C	236.73	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Pteridicacid A	11013967	Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C	364.50	unknown	via CMAUP database
Pteridicacid B	10883014	Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C	364.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tripalmitin	11147	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC	807.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Ptaquiloside Z	101242525	Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)(C)C)OC4C(C(C(C(O4)CO)O)O)O	412.50	unknown	via CMAUP database
Pteridanoside	11795946	Click to see CC1(CC2C(C1=O)C3(CCC3=C(C2O)COC4C(C(C(C(O4)CO)O)O)O)C)C	412.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	via CMAUP database
3alpha-Hydroxyecdysone	70686927	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	via CMAUP database
Pterosterone	441836	Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O	480.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3-Epiecdysone	23724769	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O	464.60	unknown	via CMAUP database
Ecdysone	19212	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O	464.60	unknown	via CMAUP database
Ponasterone A	115127	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	464.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Ponasteroside A	12314455	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(C(O5)CO)O)O)O)O)C)C)O)O)O	626.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R)-3-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one	46848577	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O	396.40	unknown	via CMAUP database
(2S,3S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroinden-1-one	23260007	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O	396.40	unknown	via CMAUP database
(2S)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one	46848576	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C	380.40	unknown	via CMAUP database
(3R)-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3H-inden-1-one	46848743	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C	410.50	unknown	via CMAUP database
Ptaquiloside	13962857	Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O	398.40	unknown	via CMAUP database
Pteroside A	169727	Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)CO	410.50	unknown	via CMAUP database
Pteroside B	134279	Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C	380.40	unknown	via CMAUP database
Pteroside C	169728	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O	396.40	unknown	via CMAUP database
Pteroside D	169738	Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2O)(C)C	410.50	unknown	via CMAUP database
Pteroside P	148715	Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)CO	396.40	unknown	via CMAUP database
Pteroside Z	169737	Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)C	394.50	unknown	via CMAUP database
pterosin C 3-O-glucoside	44201982	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O	396.40	unknown	via CMAUP database
Pterosin D 3-O-glucoside	21670079	Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C	410.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Ethenylphenyl beta-D-glucopyranoside	182338	Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O	282.29	unknown	via CMAUP database
beta-D-Glucopyranoside, 4-ethenylphenyl 6-O-beta-D-xylopyranosyl-	185053	Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O	414.40	unknown	via CMAUP database
Ptelatoside b	130179	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C=C)CO)O)O)O)O)O	428.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
(5R)-5-methoxypyrrolidin-2-one	643445	Click to see COC1CCC(=O)N1	115.13	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
5-Caffeoylshikimic acid	5281762	Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	336.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
kaempferol 3-O-(6"-O-feruloyl)-glucoside	23265189	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	624.50	unknown	via CMAUP database
Tiliroside	5320686	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
kaempferol 5-O-beta-L-glucopyranoside	72551435	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one	101714010	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)O)O)O	640.50	unknown	via CMAUP database
3-[(3-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one	101683505	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	640.50	unknown	via CMAUP database
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Isoquercitin	10813969	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside	9911508	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
Quercetin 3-laminaribioside	101683504	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O	626.50	unknown	via CMAUP database
Trifolin	5282149	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 7-O-alpha-L-rhamnopyranoside-4'-O-beta-D-glucopyranoside	101949540	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	594.50	unknown	via CMAUP database

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Attalea phalerata

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