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Eugenia hyemalis

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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
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Details Top

Internal ID UUID64403a7bc36cc323907401
Scientific name Eugenia hyemalis
Authority Cambess.
First published in Fl. Bras. Merid. 2: 360 (1833)

Description Top

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Synonyms Top

Scientific name Authority First published in
Luma multiflora (Cambess.) Herter Revista Sudamer. Bot. 7: 219 (1943)
Myrciaria itacurubiensis Barb.Rodr. ex Chodat & Hassl. Bull. Herb. Boissier Ser. II. vii. 808 (1907), nomen.
Eugenia hyemalis var. marginata (O.Berg) D.Legrand Bol. Fac. Agron. Univ. Montevideo 101: 43 1968
Eugenia multiflora var. glabra O.Berg Fl. Bras. 14(1): 271 (1857)
Eugenia multiflora var. lutescens Cambess. Fl. Bras. Merid. 2: 361 (1833)
Eugenia multiflora var. rubiginosa Cambess. Fl. Bras. Merid. 2: 361 (1833)
Eugenia polycarpa var. bimarginata O.Berg Fl. Bras. 14(1): 281 (1857)
Eugenia polycarpa var. ovata O.Berg Fl. Bras. 14(1): 281 (1857)
Eugenia bicolor O.Berg Fl. Bras. 14(1): 282 (1857)
Eugenia cycliantha D.Legrand Fl. Ilustr. Catarin. 1(Mirt., Suppl. 1): 15. 1977
Eugenia lindbergiana O.Berg Linnaea 30: 685 (1861)
Eugenia polycarpa O.Berg Fl. Bras. 14(1): 281 (1857)
Eugenia polycarpa var. marginata O.Berg Fl. Bras. 14(1): 281 (1857)
Eugenia hiemalis var. marginata (O.Berg) D.Legrand Bol. Fac. Agron. Univ. Montevideo 101: 43. 1968

Common names Top

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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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000957591
Tropicos 22107346
Open Tree Of Life 630700
NCBI Taxonomy 1231848
GBIF 5416437
Tropicos 22100582
KEW urn:lsid:ipni.org:names:594680-1
The Plant List kew-75475
Open Tree Of Life 3937350
NCBI Taxonomy 1453378
IPNI 594680-1
GBIF 5938280
EOL 5450605

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
Functional trait divergence associated with heteromorphic leaves in a climbing fig Deng JY, Wang YJ, Chen LF, Luo T, Wang R, Chen XY Front Plant Sci 19-Sep-2023
PMCID:PMC10546399
doi:10.3389/fpls.2023.1261240
PMID:37794929
Phytochemicals and bioactive compounds effective against acute myeloid leukemia: A systematic review Egbuna C, Patrick‐Iwuanyanwu KC, Onyeike EN, Khan J, Palai S, Patel SB, Parmar VK, Kushwaha G, Singh O, Jeevanandam J, Kumarasamy S, Uche CZ, Narayanan M, Rudrapal M, Odoh U, Chikeokwu I, Găman M, Saravanan K, Ifemeje JC, Ezzat SM, Olisah MC, Chikwendu CJ, Adedokun KA, Imodoye SO, Bello IO, Twinomuhwezi H, Awuchi CG Food Sci Nutr 15-May-2023
PMCID:PMC10345688
doi:10.1002/fsn3.3420
PMID:37457145
Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent Nahar L, Al-Groshi A, Kumar A, Sarker SD Molecules 11-Dec-2022
PMCID:PMC9787540
doi:10.3390/molecules27248786
PMID:36557918
Natural product drug discovery in the artificial intelligence era Saldívar-González FI, Aldas-Bulos VD, Medina-Franco JL, Plisson F Chem Sci 13-Dec-2021
PMCID:PMC8827052
doi:10.1039/d1sc04471k
PMID:35282622
Current computational methods for predicting protein interactions of natural products Moumbock AF, Li J, Mishra P, Gao M, Günther S Comput Struct Biotechnol J 28-Oct-2019
PMCID:PMC6861622
doi:10.1016/j.csbj.2019.08.008
PMID:31762960
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
HIV-1 Ribonuclease H Inhibitory Phenolic Glycosides from Eugenia hyemalis Bokesch HR, Wamiru A, Le Grice SF, Beutler JA, McKee TC, McMahon JB J Nat Prod 03-Sep-2008
PMCID:PMC2586124
doi:10.1021/np8002518
PMID:18763827
HIV-1 ribonuclease H inhibitory phenolic glycosides from Eugenia hyemalis. Bokesch HR, Wamiru A, Le Grice SF, Beutler JA, McKee TC, McMahon JB J Nat Prod 01-Sep-2008
PMCID:PMC2586124
doi:10.1021/NP8002518
PMID:18763827

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
[4,5-Dihydroxy-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxan-3-yl] 3,4,5-trihydroxybenzoate 75053119 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 424.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
4-O-galloylarbutin 44586969 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 424.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-6-(3,4,5-trihydroxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 163190257 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 608.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-6-(3,4,5-trihydroxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162907957 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 608.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[4,5-Dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] 3,4,5-trihydroxybenzoate 75053118 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O 424.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[4,5-Dihydroxy-6-[(4-hydroxybenzoyl)oxymethyl]-2-(4-hydroxyphenoxy)tetrahydropyran-3-yl] 3,4,5-trihydroxybenzoate 71588695 Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 544.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
2-O-galloylarbutin 44586968 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O 424.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
2,6-Di-O-Galloylarbutin 23628203 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 576.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
galloyl(-2)[galloyl(-6)]Hex-O-Ph(4-OH) 74071829 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 576.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
hyemaloside A 25058097 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 728.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
Hyemaloside B 25110931 Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 544.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chromen-3-yl]oxy-4,5-dihydroxy-2-methyl-tetrahydropyran-3-yl] 3,4,5-trihydroxybenzoate 71588866 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)OC(=O)C5=CC(=C(C(=C5)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 45359966 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[(2S,3R,4R,5S,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] 3,4,5-trihydroxybenzoate 11028294 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] 3,4,5-trihydroxybenzoate 75053122 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 75053121 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14055725 Click to see C1=CC(=CC=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 600.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
3-[(2R,3S,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[1-(3,4,5-trihydroxyphenyl)ethoxy]tetrahydropyran-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 71588876 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(C)C5=CC(=C(C(=C5)O)O)O)O)O 584.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
Kaempferol 3-O-(6''-galloyl)-beta-D-glucopyranoside 5491813 Click to see C1=CC(=CC=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 600.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
Quercetin 3-O-rhamnoside 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
Quercitrin 5280459 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
> Phenylpropanoids and polyketides / Tannins
[(2R,3S,4S,5R,6S)-4-hydroxy-6-(4-hydroxyphenoxy)-3,5-bis[(3,4,5-trihydroxybenzoyl)oxy]tetrahydropyran-2-yl]methyl 3,4,5-trihydroxybenzoate 44586970 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 728.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
galloyl(-2)[galloyl(-4)][galloyl(-6)]Hex-O-Ph(4-OH) 75053120 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 728.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[3,4,5,21,22,23-Hexahydroxy-13-(4-hydroxyphenoxy)-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 74423111 Click to see C1C2C(C(C(C(O2)OC3=CC=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 878.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/
hyemaloside C 25110930 Click to see C1C2C(C(C(C(O2)OC3=CC=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 878.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586124/

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