PlantaeDB Logo
Login Sign-up

Eugenia selloi

We don't have an image yet. Upload an image!

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64403aabcab77420944447
Scientific name Eugenia selloi
Authority B.D.Jacks.
First published in Index Kew. 1: 911 (1893)

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
Phyllocalyx edulis O.Berg Fl. Bras. 14(1): 327 (1857)
Phyllocalyx edulis var. depauperata O.Berg Fl. Bras. 14(1): 327 (1857)
Phyllocalyx edulis var. dives O.Berg Fl. Bras. 14(1): 327 (1857)
Eugenia neonitida Sobral Napaea 11: 36 (1995)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000959028
Tropicos 100189984
KEW urn:lsid:ipni.org:names:60464874-2
The Plant List kew-76800
Open Tree Of Life 3936437
NCBI Taxonomy 2014562
IUCN Red List 149206108
IPNI 60464874-2
iNaturalist 430997
GBIF 5418007
USDA GRIN 438370

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
The phytoactive constituents of Eugenia selloi B.D. Jacks (pitangatuba): Toxicity and elucidation of their anti-inflammatory mechanism(s) of action Lazarini JG, Massarioli AP, Soares JC, Nani BD, Charo N, Oliveira DS, Camargo L, Alvarez-Flores MP, Batista ID, Chudzinski-Tavassi AM, Alencar SM, Franchin M, Rosalen PL Food Chem (Oxf) 07-Mar-2022
PMCID:PMC8991978
doi:10.1016/j.fochms.2022.100093
PMID:35415693
The role of schools as an opportunity for transmission of local knowledge about useful Restinga plants: experiences in southeastern Brazil van Luijk N, Soldati GT, da Fonseca-Kruel VS J Ethnobiol Ethnomed 17-May-2021
PMCID:PMC8130333
doi:10.1186/s13002-021-00461-0
PMID:34001189
The resilient frugivorous fauna of an urban forest fragment and its potential role in vegetation enrichment Rigacci ED, Paes ND, Félix GM, Silva WR Urban Ecosyst 06-Jan-2021
PMCID:PMC7787706
doi:10.1007/s11252-020-01080-5
PMID:33432262
Complete chloroplast genome sequence and phylogenetic analysis of Syzygium malaccense Tao L, Shi ZG, Long QY Mitochondrial DNA B Resour 09-Oct-2020
PMCID:PMC7782888
doi:10.1080/23802359.2020.1829132
PMID:33458237
Anti-inflammatory and antioxidant potential, in vivo toxicity, and polyphenolic composition of Eugenia selloi B.D.Jacks. (pitangatuba), a Brazilian native fruit Lazarini JG, Franchin M, Soares JC, Nani BD, Massarioli AP, de Alencar SM, Rosalen PL PLoS One 09-Jun-2020
PMCID:PMC7282636
doi:10.1371/journal.pone.0234157
PMID:32516332
The evolutionary history of Eugenia sect. Phyllocalyx (Myrtaceae) corroborates historically stable areas in the southern Atlantic forests de Oliveira Bünger M, Fernanda Mazine F, Forest F, Leandro Bueno M, Renato Stehmann J, Lucas EJ Ann Bot 09-Dec-2016
PMCID:PMC5155605
doi:10.1093/aob/mcw209
PMID:27974324
Polyoxygenated flavonoids from Eugenia edulis. Hussein SA, Hashem AN, Seliem MA, Lindequist U, Nawwar MA Phytochemistry 01-Oct-2003
doi:10.1016/S0031-9422(03)00437-0
PMID:14559286

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 / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
> 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 https://doi.org/10.1016/S0031-9422(03)00437-0
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 https://doi.org/10.1016/S0031-9422(03)00437-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-dihydroxyphenyl)-7-hydroxy-3,8-dimethoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101762773 Click to see COC1=C2C(=C(C=C1O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C(=C(O2)C4=CC(=C(C=C4)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
2-(3,4-Dihydroxyphenyl)-7-hydroxy-3,8-dimethoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978557 Click to see COC1=C2C(=C(C=C1O)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C(=C(O2)C4=CC(=C(C=C4)O)O)OC 508.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14055723 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1016/S0031-9422(03)00437-0
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
3-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 86328068 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13245583 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 12308704 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 129010103 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
Hyperoside 5281643 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 https://doi.org/10.1016/S0031-9422(03)00437-0
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
Quercetin 3-O-(6''-galloyl)-beta-D-glucopyranoside 9830456 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
Quercetin-3-o-alpha-d-arabinofuranoside 11968848 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7,4',5'-Trihydroxy-3,5,3'-trimethoxyflavone 44259711 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)O)OC 360.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0
7,8,3',4'-Trihydroxy-3,5-dimethoxyflavone 5323591 Click to see COC1=C2C(=C(C(=C1)O)O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(03)00437-0

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.