Eugenia uniflora, also known as pitanga, Suriname cherry, or Brazilian cherry, is a flowering plant native to tropical South America. It is often used as a hedge or screen in gardens and has been introduced to other regions, such as Bermuda and Florida. The plant produces small, edible fruits that are high in vitamin C and can be used in jams and jellies. Its leaves are also used for tea and as an insect repellent. Additionally, Eugenia uniflora has medicinal properties, including anti-inflammatory and antiviral effects, and is used in traditional medicine to treat stomach ailments.

Synonyms Top

Scientific name	Authority	First published in
Luma arechavaletae	(Herter) Herter	Revista Sudamer. Bot. 7: 218 (1943)
Luma costata	(Cambess.) Herter	Revista Sudamer. Bot. 7: 219 (1943)
Luma dasyblasta	(O.Berg) Herter	Revista Sudamer. Bot. 7: 219 (1943)
Luma strigosa	(O.Berg) Herter	Revista Sudamer. Bot. 7: 220 (1943)
Myrtus brasiliana	L.	Sp. Pl. : 701 (1753)
Myrtus willdenowii	Spreng.	Syst. Veg. 2: 480 (1825)
Plinia pedunculata	L.f.	Suppl. Pl. : 253 (1782)
Plinia petiolata	L.	Pl. Surin. : 10 (1775)
Plinia rubra	L.	Mant. Pl. 2: 243 (1771)
Plinia tetrapetala	L.	Mant. Pl. 2: 402 (1771)
Stenocalyx affinis	O.Berg	Fl. Bras. 14(1): 336 (1857)
Stenocalyx brunneus	O.Berg	Fl. Bras. 14(1): 335 (1857)
Stenocalyx costatus	O.Berg	Linnaea 27: 311 (1856)
Stenocalyx dasyblastus	O.Berg	Fl. Bras. (Martius) 14(1): 337. 1857 [15 May 1857]
Stenocalyx glaber	O.Berg	Fl. Bras. 14(1): 337 (1857)
Stenocalyx impunctatus	O.Berg	Fl. Bras. 14(1): 336 (1857)
Stenocalyx lucidus	O.Berg	Fl. Bras. 14(1): 337 (1857)
Stenocalyx michelii	O.Berg	Linnaea 27: 310 (1856)
Stenocalyx oblongifolius	O.Berg	Fl. Bras. 14(1): 339 (1857)
Stenocalyx rhampiri	Barb.Rodr.	Myrt. Paraguay : 8 (1903)
Stenocalyx ruber	(L.) Kausel	Ark. Bot. , a.s., 3: 495 (1956)
Stenocalyx strigosus	O.Berg	Fl. Bras. 14(1): 335 (1857)
Stenocalyx uniflorus	(L.) Kausel	Lilloa 32: 331 (1967)
Syzygium michelii	Duthie	Fl. Brit. India 2: 505 (1879)
Myrtus brasiliana var. diversifolia	Kuntze	Revis. Gen. Pl. 3(2): 90 (1898)
Myrtus brasiliana var. lanceolata	Kuntze	Revis. Gen. Pl. 3(2): 90 (1898)
Myrtus brasiliana var. lucida	(O.Berg ex Mart.) Kuntze	Revis. Gen. Pl. 3(2): 90 (1898)
Stenocalyx michelii var. membranacea	O.Berg	Fl. Bras. 14(1): 338 (1857)
Stenocalyx michelii var. rigida	O.Berg	Fl. Bras. 14(1): 338 (1857)
Myrtus willdenowii var. portoriccensis	Spreng. ex DC.	Prodr. [A. P. de Candolle] 3: 266. 1828
Eugenia arechavaletae	Herter	Estud. Bot. Reg. Uruguay 4: 93 (1931)
Eugenia costata	Cambess.	Fl. Bras. Merid. 2: 359 (1833)
Eugenia dasyblasta	Nied.	Nat. Pflanzenfam. 3(7): 82 (1893)
Eugenia decidua	Merr.	Philipp. J. Sci., C 9: 121 (1914)
Eugenia michelii	Lam.	Encycl. 3: 203 (1789)
Eugenia myrtifolia	Salisb.	Prodr. Stirp. Chap. Allerton : 353 (1796)
Eugenia oblongifolia	Arechav.	Anales Mus. Nac. Montevideo 5: 62 (1905)
Eugenia strigosa	Arechav.	Anales Mus. Nac. Montevideo 5: 60 (1905)
Eugenia uniflora var. atropurpurea	Mattos	Loefgrenia 85: 2 (1984)
Eugenia willdenowii	DC.	Prodr. 3: 265 (1828)
Eugenia zeylanica	Willd.	Sp. Pl., ed. 4 , 2: 963 (1799)
Eugenia lacustris	Barb.Rodr.	Bull. Herb. Boissier ser. 2, 7: 806. 1907
Eugenia microphylla	Barb.Rodr.	Bull. Herb. Boissier ser. 2, 7: 807. 1907
Stenocalyx nhamperi	Barb.Rodr.	Myrt. Paraguay 8, pl. 10. 1903
Myrtus brasiliana var. normalis	Kuntze	Revis. Gen. Pl. 3(2): 90 (1898)

Common names Top

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Filter by language:

Language	Common/alternative name
English	brazilian cherry
English	cayenne cherry
English	cerisier carre
English	cerisier carré
English	pitanga
English	suriname cherry
English	surinam cherry
Arabic	يوجينة أحادية الزهرة
Bulgarian	суринамска череша
Czech	eugenie jednokvětá
German	kirschmyrte
German	surinamkirsche
Esperanto	pitango
French	cerisier de cayenne
frr	pitanga
gn	Ñangapiry
Hebrew	פיטנגו
Indonesian	ceremai belanda
Japanese	ピタンガ
jv	dewandaru
Korean	수리남체리
Lithuanian	vienažiedė eugenija
Malayalam	സൂരിനാം ചെറി
Malay	cermai belanda
Dutch	surinaamse kers
Polish	goździkowiec jednokwiatowy
Polish	pitanga
Polish	piernia jednokwiatowa
Portuguese	pitanga
Russian	Суринамская вишня
Thai	มะยมฝรั่ง
Tonga	polokanite
Tonga	phyllanthus acidus
Tonga	grossularia redinata
Turkish	surinam kirazı
Chinese	苏里南苦樱桃
Chinese	巴西红果
Chinese	红果仔
Chinese	稜果蒲桃
Chinese	扁樱桃
Chinese	一种维管植物

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

Africa click to expand
- West Tropical Africa
  - Benin
  - Guinea
  - Guinea-Bissau
  - Senegal
- West-central Tropical Africa
  - Central African Republic
  - Gabon
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Sri Lanka
- Malesia
  - Philippines

Australasia click to expand
- Australia
  - Norfolk Island

Northern America click to expand
- Mexico
  - Mexico Southeast
- Southeastern U.S.A.
  - Florida

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Marianas
- South-central Pacific
  - Cook Islands
  - Marquesas
  - Pitcairn Islands
  - Society Islands
  - Tuamotu
- Southwestern Pacific
  - Niue

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
- Caribbean
  - Bahamas
  - Bermuda
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Panamá
- Northern South America
  - Suriname
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000959411
UNII	Q25FZX4MB9
Florida Plant Atlas	1388
USDA Plants	EUUN2
Tropicos	22101634
INPN	447398
KEW	urn:lsid:ipni.org:names:596263-1
The Plant List	kew-77153
Open Tree Of Life	1001992
Observations.org	199459
NCBI Taxonomy	119951
Nature Serve	2.159032
IUCN Red List	60330325
IPNI	596263-1
iNaturalist	83642
GBIF	5416458
Freebase	/m/06dwlp
EPPO	EUEUN
EOL	2508562
Elurikkus	4685
USDA GRIN	16210
Wikipedia	Eugenia_uniflora

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_004012085.1	ASM401208v1	Contig	Universidade Federal do Pampa	2019-01-11	0.0x	3.01 Mb

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

Gas Chromatography–Mass Spectrometry Chemical Profiling of Commiphora myrrha Resin Extracts and Evaluation of Larvicidal, Antioxidant, and Cytotoxic Activities

Alanazi NA, Alamri AA, Mashlawi AM, Almuzaini N, Mohamed G, Salama SA

Molecules

13-Apr-2024

PMCID:	PMC11051918
doi:	10.3390/molecules29081778
PMID:	38675598

Antidiabetic Property Optimization from Green Leafy Vegetables Using Ultrasound-Assisted Extraction to Improve Cracker Production

Maser WH, Maiyah N, Karnjanapratum S, Nukthamna P, Thompson AK, Huda N, Moula Ali AM, Bavisetty SC

Prev Nutr Food Sci

31-Mar-2024

PMCID:	PMC10987381
doi:	10.3746/pnf.2024.29.1.47
PMID:	38576886

Mechanism of action of microRNA166 on nitric oxide in alfalfa (Medicago sativa L.) under drought stress

Wei B, Wang Y, Ruan Q, Zhu X, Wang X, Wang T, Zhao Y, Wei X

BMC Genomics

28-Mar-2024

PMCID:	PMC10976769
doi:	10.1186/s12864-024-10095-7
PMID:	38549050

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

07-Mar-2024

PMCID:	PMC10918603
doi:	10.2903/j.efsa.2024.8648
PMID:	38455154

Citizen science data on urban forageable plants: a case study in Brazil

Soares FM, Ferreira Pires L, Garcia MC, Coradin L, Ghilardi-Lopes NP, Silva RR, de Carvalho AM, Gavai A, Bouzembrak Y, Maculan BC, Koffler S, Montedo UB, Drucker DP, Santiago R, de Carvalho MC, Lima AC, Gabriel HD, de França SG, de Almeida KR, dos Santos BJ, Saraiva AM

GigaByte

21-Feb-2024

PMCID:	PMC10905257
doi:	10.46471/gigabyte.107
PMID:	38434929

DOF gene family expansion and diversification

Waschburger EL, Filgueiras JP, Turchetto-Zolet AC

Genet Mol Biol

05-Feb-2024

PMCID:	PMC10842470
doi:	10.1590/1678-4685-GMB-2023-0109
PMID:	38315880

Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data

Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L

Biomedicines

04-Feb-2024

PMCID:	PMC10886757
doi:	10.3390/biomedicines12020365
PMID:	38397967

Potential Effects of Essential Oil from Plinia cauliflora (Mart.) Kausel on Leishmania: In Vivo, In Vitro, and In Silico Approaches

Holanda VN, Brito TG, de Oliveira JR, da Cunha RX, da Silva AP, da Silva WV, Araújo TF, Tavares JF, dos Santos SG, Figueiredo RC, Lima VL

Microorganisms

19-Jan-2024

PMCID:	PMC10819817
doi:	10.3390/microorganisms12010207
PMID:	38276192

Antimicrobial, antioxidant and antiproliferative activities of a galactose-binding seed lectin from Manilkara zapota

Podder MK, Hossain MM, Kabir SR, Asaduzzaman AK, Hasan I

Heliyon

17-Jan-2024

PMCID:	PMC10835259
doi:	10.1016/j.heliyon.2024.e24592
PMID:	38312555

Update of Natural Products and Their Derivatives Targeting Epstein–Barr Infection

Pennisi R, Trischitta P, Costa M, Venuti A, Tamburello MP, Sciortino MT

Viruses

15-Jan-2024

PMCID:	PMC10818872
doi:	10.3390/v16010124
PMID:	38257824

Native Fauna of Tardigrades from Two Natural Areas of the Argentina Republic

Ostertag BR, González-Reyes AX, Grabosky A, Meier F, Doma IL, Corronca J, Rocha AM

Zool Stud

29-Dec-2023

PMCID:	PMC11019430
doi:	10.6620/ZS.2023.62-57
PMID:	38628161

Applications of Plant Bioactive Compounds as Replacers of Synthetic Additives in the Food Industry

Nieto G, Martínez-Zamora L, Peñalver R, Marín-Iniesta F, Taboada-Rodríguez A, López-Gómez A, Martínez-Hernández GB

Foods

21-Dec-2023

PMCID:	PMC10778451
doi:	10.3390/foods13010047
PMID:	38201075

Hormetic Effect Caused by Sublethal Doses of Glyphosate on Toona ciliata M. Roem

de Faria GS, Carlos L, Jakelaitis A, de Freitas ST, Vicentini TA, Silva IO, Vasconcelos Filho SC, Lourenço LL, Farnese FS, Batista MA, Vitorino LC

Plants (Basel)

15-Dec-2023

PMCID:	PMC10747235
doi:	10.3390/plants12244163
PMID:	38140490

NADES-Assisted Extraction of Polyphenols from Coriander Seeds: A Systematic Optimization Study

Ianni F, Scandar S, Mangiapelo L, Blasi F, Marcotullio MC, Cossignani L

Antioxidants (Basel)

27-Nov-2023

PMCID:	PMC10741060
doi:	10.3390/antiox12122048
PMID:	38136168

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(3Z)-3,8-dimethylnona-1,3,7-triene	10931614	Click to see CC(=CCCC=C(C)C=C)C	150.26	unknown	https://doi.org/10.1590/S0103-50532010000500012
3,8-Dimethylnona-1,3,7-triene	85320695	Click to see CC(=CCCC=C(C)C=C)C	150.26	unknown	https://doi.org/10.1590/S0103-50532010000500012
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol	68171	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO	382.70	unknown	https://doi.org/10.1055/S-0028-1097540
1-Octacosanol	68406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO	410.80	unknown	https://doi.org/10.1055/S-0028-1097540
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1590/S0103-50532010000500012
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1590/S0103-50532010000500012
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1590/S0103-50532010000500012
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1590/S0103-50532010000500012
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)-	26318	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
gamma-Selinene	521334	Click to see CC(=C1CCC2(CCCC(=C)C2C1)C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1055/S-0028-1097540
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Isocaryophyllene oxide	1742211	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Selina-4(15),7(11)-diene	10655819	Click to see CC(=C1CCC2(CCCC(=C)C2C1)C)C	204.35	unknown	https://doi.org/10.1055/S-0028-1097540 https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7R,7aR,7bS)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	94249463	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1002/CBDV.201600089
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
beta-Spathulenol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1002/CBDV.201600089
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-	9859094	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel-	10583	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2,3,4,4a,5,6,7,8-Octahydro-4,4a-dimethyl-6-(1-methylvinyl)-2-naphthol	103814	Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Atractylol	5321065	Click to see CC1=COC2=C1CC3C(=C)CCCC3(C2)C	216.32	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1016/J.PHYMED.2009.03.009
Atractylon	3080635	Click to see CC1=COC2=C1CC3C(=C)CCCC3(C2)C	216.32	unknown	https://doi.org/10.1016/J.PHYMED.2009.03.009 https://doi.org/10.1590/S0103-50532010000500012
Nootkatol	182645	Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O	220.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene	519361	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
1,5-Dimethyl-8-(propan-2-ylidene)cyclodeca-1,5-diene	177602	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1055/S-0028-1097540
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-	91104	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012 https://doi.org/10.1055/S-0028-1097540
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1590/S0103-50532010000500012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Epifriedelanol	119242	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1055/S-0028-1097540
Friedelan-3-one	244297	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097540
Friedelanol	348029	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1055/S-0028-1097540
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097540
> Organoheterocyclic compounds / Indolizidines
(-)-uniflorine A	9794258	Click to see C1C(C(C2N1CC(C(C2O)O)O)O)O	205.21	unknown	https://doi.org/10.1076/1388-0209(200009)3841-AFT302
uniflorine B	46879415	Click to see C1C(C(C2C(C(CN2C1O)O)O)O)O	205.21	unknown	https://doi.org/10.1076/1388-0209(200009)3841-AFT302
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Procyanidin	107876	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C=C6)O)O	594.50	unknown	https://doi.org/10.1016/0305-1978(92)90062-I
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Flavan-3,3',4',5,5',7-hexol	1249	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/S0304-3835(00)00353-0 https://doi.org/10.1016/S0031-9422(96)00702-9
Prodelphiniline	285704	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C(=C6)O)O)O	610.50	unknown	https://doi.org/10.1016/0305-1978(92)90062-I
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1016/0378-8741(87)90128-0
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/10.1016/0305-1978(92)90062-I https://doi.org/10.1016/0378-8741(87)90128-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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(96)00702-9
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(96)00702-9 https://doi.org/10.1016/0378-8741(87)90128-0
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://doi.org/10.1016/0378-8741(87)90128-0
> Phenylpropanoids and polyketides / Tannins
1,2,4,6-Tetragalloyl-beta-D-glucopyranose	14464350	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)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
1,2,4,6-Tetragalloylglucose	11297287	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)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(11R,12R,14R,15R,29R,30R,37R,38R,40R,57R,58S,65S)-4,5,6,12,20,21,22,25,30,31,31,38,46,47,48,51,52-heptadecahydroxy-9,17,32,35,43,55,62-heptaoxo-65-(3,4,5-trihydroxybenzoyl)oxy-2,10,13,16,28,36,39,42,56,59,63-undecaoxadodecacyclo[35.15.6.514,27.111,15.126,30.03,8.018,23.029,34.040,57.044,49.050,54.024,61]pentahexaconta-1(52),3,5,7,18,20,22,24,26,33,44,46,48,50,53,60-hexadecaen-58-yl] 3,4,5-trihydroxybenzoate	163028110	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=O)C(C5(C4OC6=C(O5)C(=C7C(=C6)C(=O)OCC8C(C(C(C(O8)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C17)O)O)O)O)O)(O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1585.10	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
[(11R,12R,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyl)oxy-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	163017507	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC8C(C(C(C(O8)CO)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1731.20	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
[(11R,12S,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,12,20,21,22,25,26,30,31,32,38,46,47,48,51,52-octadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyl)oxy-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16135666	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1569.10	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(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-12-yl] 2-[[3,4,5,12,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(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-21-yl]oxy]-3,4,5-trihydroxybenzoate	16174339	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C95)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1571.10	unknown	https://doi.org/10.1016/S0304-3835(00)00353-0
[4,5,6,12,20,21,22,25,30,31,31,38,46,47,48,51,52-Heptadecahydroxy-9,17,32,35,43,55,62-heptaoxo-65-(3,4,5-trihydroxybenzoyl)oxy-2,10,13,16,28,36,39,42,56,59,63-undecaoxadodecacyclo[35.15.6.514,27.111,15.126,30.03,8.018,23.029,34.040,57.044,49.050,54.024,61]pentahexaconta-1(52),3,5,7,18,20,22,24,26,33,44,46,48,50,53,60-hexadecaen-58-yl] 3,4,5-trihydroxybenzoate	163028109	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=O)C(C5(C4OC6=C(O5)C(=C7C(=C6)C(=O)OCC8C(C(C(C(O8)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C17)O)O)O)O)O)(O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1585.10	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
[4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-Heptadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyl)oxy-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	163017506	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC8C(C(C(C(O8)CO)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1731.20	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9
Oenothein B	16129800	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1569.10	unknown	https://doi.org/10.1016/S0031-9422(96)00702-9

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Eugenia uniflora

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