Allspice, also known as Jamaica pepper, is a dried unripe berry from the Pimenta dioica tree, native to the Greater Antilles, southern Mexico, and Central America. It is now cultivated in many warm parts of the world. The name allspice was given by the English in the 17th century, who valued it for its combination of cinnamon, nutmeg, and clove flavors. Allspice is used in a variety of cuisines, including Caribbean, Mexican, Middle Eastern, and European. It is also an important part of traditional stews and meat dishes in Arab cuisine. The allspice tree can grow up to 18 meters tall and can be grown outdoors in the tropics and subtropics. Christopher Columbus first discovered allspice on his second voyage to the New World, and it soon became a popular spice in Europe. Today, Jamaica remains the leading producer of allspice, but it is also grown in other countries in the same region.

Synonyms Top

Scientific name	Authority	First published in
Myrtus aromatica	Salisb.	Prodr. Stirp. Chap. Allerton : 354 (1796)
Myrtus dioica	L.	Syst. Nat. ed. 10 , 2: 1056 (1759)
Myrtus pimenta	L.	Sp. Pl. : 472 (1753)
Myrtus piperita	Sessé & Moc.	Fl. Mexic. , ed. 2: 124 (1894)
Pimenta aromatica	Kostel.	Allg. Med.-Pharm. Fl. 4: 1525 (1835)
Pimenta communis	Benth. & Hook.f.	Gen. Pl. 1: 717 (1865)
Pimenta officinalis	Lindl.	Coll. Bot. : t. 19 (1821)
Pimenta officinalis var. cumanensis	Schiede & Deppe	Linnaea 27: 424 1856
Pimenta pimenta	H.Karst.	Deut. Fl. : 790 (1882)
Pimenta vulgaris	Bello	Anales Soc. Esp. Hist. Nat. 10: 270 (1881)
Pimenta vulgaris	Lindl.	Encycl. Pl. : 418 (1829)
Pimentus aromatica	Raf.	Sylva Tellur. : 158 (1838)
Pimentus geminata	Raf.	Sylva Tellur. : 105 (1838)
Pimentus vera	Raf.	Sylva Tellur. : 105 (1838)
Eugenia pimenta var. longifolia	DC.	Prodr. 3: 285 (1828)
Eugenia pimenta var. ovalifolia	DC.	Prodr. 3: 285 (1828)
Myrtus pimenta var. brevifolia	Hayne	Getreue Darstell. Gew. 9: t. 37 1825
Myrtus pimenta var. longifolia	Sims	Bot. Mag. 30: t. 1236 (1809)
Pimenta officinalis var. longifolia	(Sims) O.Berg	Linnaea 27: 423 (1856)
Pimenta officinalis var. ovalifolia	(DC.) O.Berg	Linnaea 27: 424 (1856)
Caryophyllus pimenta	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Eugenia micrantha	Bertol.	Fl. Guatimal. : 22 (1840)
Eugenia pimenta	DC.	Prodr. 3: 285 (1828)
Pimenta communis	Lindl.	Coll. Bot. 19
Evanesca micrantha	Bertol.	Novi Comment. Acad. Sci. Inst. Bononiensis 4: 442 1840
Pimenta officinalis var. tenuifolia	O.Berg	Handb. Pharmaceut. Bot. 339 1855

Common names Top

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Filter by language:

Language	Common/alternative name
English	jamaican pepper
English	allspice
Spanish	malagueta
Spanish	pimienta de jamaica
Spanish	pimienta de tabasco
Spanish	myrtus tabasco
Afrikaans	wonderpeper
Arabic	فلفل حلو
Arabic	فلفل إفرنجي
Azerbaijani	İkievli pimenta
bar	neugewürz
bar	piment
bar	naigwirz
Belarusian	Пімента двудомная
Belarusian	Пімента лекавая
Bulgarian	бахар
Catalan	pebre de jamaica
Catalan	totesespícies
Catalan	totespècia
Catalan	pebrer de jamaica
Czech	pimentovník pravý
Czech	nové koření
Danish	allehånde
German	pimentpflanze
German	wunderpfeffer
German	viergewürz
German	neugewürz
German	jamaikapfeffer
German	gewürzkörner
German	allgewürz
German	piment
German	nelkenpfeffer
Greek	Μπαχάρι
Esperanto	dioika pimento
Estonian	harilik pimendipuu
Persian	فلفل فرنگی
Finnish	maustepippuri
French	myrte-piment
French	grand piment
French	malaguette
French	tout-épice
French	quatre-épices
French	piment de la jamaique
French	yeni bahar
French	piment de la jamaïque
French	yenibahar
Irish	ilspíosra
Hebrew	פלפל ג'מייקה
Hebrew	פלפל אנגלי
Upper Sorbian	wšědny korjenjownik
Upper Sorbian	wšědny piment
ht	malagèt
Hungarian	szegfűbors
Indonesian	merica jamaika
Icelandic	allrahanda
Italian	pepe della giamaica
Italian	pimento
Japanese	オールスパイス
Korean	올스파이스나무
Korean	올스파이스
Lithuanian	kvapusis pimentas
Lithuanian	kvapusis pipiras
Lithuanian	kvapnieji pipirai
Lithuanian	kvapieji pipirai
Malayalam	സർവ സുഗന്ധി
Norwegian Bokmål	allehånde
nds	piment
Dutch	pimentbes
Dutch	jamaicapeper
Dutch	nagelpeper
Dutch	piment
Norwegian Nynorsk	allehande
Polish	korzennik lekarski
Polish	ziele angielskie
Romanian	ienibahar
Russian	Пимента лекарственная
Russian	Пимента двудомная
Slovenian	pimentovec
Slovenian	piment
Serbian	Најгвирц
Swedish	kryddpeppar
Tamil	ஆல்ஸ்பைஸ்
Thai	ออลสไปซ์
Tonga	sipaisi
Turkish	yeni bahar
Turkish	yenibahar
Ukrainian	Духмяний перець
Ukrainian	Англійський перець
Ukrainian	Перець духмяний
Ukrainian	Ямайський перець
Chinese	多香果
Chinese	众香树
Chinese	眾香子
Chinese	牙買加胡椒

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

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

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
- South-central Pacific
  - Society Islands

Southern America click to expand
- Caribbean
  - Bahamas
  - Bermuda
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Jamaica
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
- Northern South America
  - Venezuela
- Western South America
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000273391
UNII	25VLG4CLNR
Florida Plant Atlas	4321
USDA Plants	PIDI2
Tropicos	22101787
INPN	706657
KEW	urn:lsid:ipni.org:names:196799-2
The Plant List	kew-156136
Missouri Botanical Garden	282860
Open Tree Of Life	1011084
Observations.org	346312
NCBI Taxonomy	375272
Nature Serve	2.139940
IUCN Red List	103121329
IPNI	196799-2
iNaturalist	122811
GBIF	3186061
Freebase	/m/01bp2v
EPPO	PMTDI
EOL	2508608
Elurikkus	373457
USDA GRIN	28390
Wikipedia	Allspice

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

Discovery of bitter masking compounds from Allspice (Pimenta dioica) using sensory guided isolation

An JP, Liu X, Wang Y

Food Chem X

28-Apr-2024

PMCID:	PMC11087956
doi:	10.1016/j.fochx.2024.101426
PMID:	38736983

Unveiling the aesthetic secrets: exploring connections between genetic makeup, chemical, and environmental factors for enhancing/improving the color and fragrance/aroma of Chimonanthus praecox

Zhao H, Masood HA, Muhammad S

PeerJ

19-Apr-2024

PMCID:	PMC11034496
doi:	10.7717/peerj.17238
PMID:	38650650

Natural Polymers as Carriers for Encapsulation of Volatile Oils: Applications and Perspectives in Food Products

Tița O, Constantinescu MA, Rusu L, Tița MA

Polymers (Basel)

09-Apr-2024

PMCID:	PMC11054478
doi:	10.3390/polym16081026
PMID:	38674945

SAR, Molecular Docking and Molecular Dynamic Simulation of Natural Inhibitors against SARS-CoV-2 Mpro Spike Protein

Salamat A, Kosar N, Mohyuddin A, Imran M, Zahid MN, Mahmood T

Molecules

04-Mar-2024

PMCID:	PMC10934104
doi:	10.3390/molecules29051144
PMID:	38474656

Quantitative NMR Spectrometry of Phenylpropanoids, including Isoeugenol in Herbs, Spices, and Essential Oils

Fabry P, Weber S, Teipel J, Richling E, Walch SG, Lachenmeier DW

Foods

27-Feb-2024

PMCID:	PMC10930604
doi:	10.3390/foods13050720
PMID:	38472833

In Vitro Evaluation of Essential Oils and Saturated Fatty Acids for Repellency against the Old-World Sand Fly, Phlebotomus papatasi (Scopoli) (Diptera: Psychodidae)

Temeyer KB, Schlechte KG, Coats JR, Cantrell CL, Rosario-Cruz R, Lohmeyer KH, Pérez de León AA, Li AY

Insects

24-Feb-2024

PMCID:	PMC10970923
doi:	10.3390/insects15030155
PMID:	38535351

Plant-Based Films and Hydrogels for Wound Healing

Lopes AI, Pintado MM, Tavaria FK

Microorganisms

21-Feb-2024

PMCID:	PMC10972459
doi:	10.3390/microorganisms12030438
PMID:	38543489

Magnetic iron oxide-based nanozymes: from synthesis to application

Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A

Nanoscale Adv

19-Feb-2024

PMCID:	PMC10929596
doi:	10.1039/d3na00903c
PMID:	38482039

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Special Issue “Drug Discovery of Antiprotozoal Agents”

Mendonça-Junior FJ

Pharmaceuticals (Basel)

30-Jan-2024

PMCID:	PMC10891929
doi:	10.3390/ph17020176
PMID:	38399391

Geometric entropy of plant leaves: A measure of morphological complexity

Muraleedharan V, Rajan SC, R J

PLoS One

02-Jan-2024

PMCID:	PMC10760904
doi:	10.1371/journal.pone.0293596
PMID:	38166118

Eugenol-Rich Essential Oil from Pimenta dioica: In Vitro and In Vivo Potentialities against Leishmania amazonensis

Monzote L, Machín L, González A, Scull R, Gutiérrez YI, Satyal P, Gille L, Setzer WN

Pharmaceuticals (Basel)

29-Dec-2023

PMCID:	PMC10819736
doi:	10.3390/ph17010064
PMID:	38256897

Latin American Plants against Microorganisms

Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR

Plants (Basel)

28-Nov-2023

PMCID:	PMC10708099
doi:	10.3390/plants12233997
PMID:	38068631

Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida

Pemberton RW

Insects

27-Nov-2023

PMCID:	PMC10743517
doi:	10.3390/insects14120909
PMID:	38132583

Phenolic content, antioxidant and antimicrobial activities evaluation and relationship of commercial spices in the lebanese market

Rayess YE, Nehme L, Ghanem C, Beyrouthy ME, Sadaka C, Azzi-Achkouty S, Nehme N, Gürer ES, Sharifi-Rad J

BMC Chem

20-Nov-2023

PMCID:	PMC10662694
doi:	10.1186/s13065-023-01074-2
PMID:	37986193

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 / 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/10.1021/NP9906121
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4S,5S)-4-hydroxy-5-(hydroxymethyl)-2-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(1R)-4-methylcyclohex-3-en-1-yl]propan-2-yloxy]oxan-2-yl]methoxy]oxolan-3-yl] 3,4,5-trihydroxybenzoate	24879406	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	600.60	unknown	https://doi.org/10.1021/NP0705615
[(2R,3R,4S,5S)-4-hydroxy-5-(hydroxymethyl)-2-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yloxy]oxan-2-yl]methoxy]oxolan-3-yl] 3,4,5-trihydroxybenzoate	24879475	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	600.60	unknown	https://doi.org/10.1021/NP0705615
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(2R)-1-hydroxy-3-(3-methoxy-4-methylphenyl)propan-2-yl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162984324	Click to see CC1=C(C=C(C=C1)CC(CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC	510.50	unknown	https://doi.org/10.1021/NP9906121
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(1R)-4-methylcyclohex-3-en-1-yl]propan-2-yloxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	10695593	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	468.50	unknown	https://doi.org/10.1021/NP9906121
[3,4,5-Trihydroxy-6-[1-hydroxy-3-(3-methoxy-4-methylphenyl)propan-2-yl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162984323	Click to see CC1=C(C=C(C=C1)CC(CO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC	510.50	unknown	https://doi.org/10.1021/NP9906121
[3,4,5-Trihydroxy-6-[2-(4-methylcyclohex-3-en-1-yl)propan-2-yloxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	74105555	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	468.50	unknown	https://doi.org/10.1021/NP9906121
[4-Hydroxy-5-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-[2-(4-methylcyclohex-3-en-1-yl)propan-2-yloxy]oxan-2-yl]methoxy]oxolan-3-yl] 3,4,5-trihydroxybenzoate	74342788	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	600.60	unknown	https://doi.org/10.1021/NP0705615
1-[(1S)-4-Methyl-3-cyclohexenyl]-1-methylethyl 6-O-galloyl-beta-D-glucopyranoside	10552230	Click to see CC1=CCC(CC1)C(C)(C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	468.50	unknown	https://doi.org/10.1021/NP9906121
> Benzenoids / Phenol ethers / Anisoles
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	148.20	unknown	https://doi.org/10.1080/10412905.1997.9700812
> Benzenoids / Phenols / Methoxyphenols
(1R,2S)-3-chloro-1-(4-hydroxy-3-methoxyphenyl)propane-1,2-diol	71415915	Click to see COC1=C(C=CC(=C1)C(C(CCl)O)O)O	232.66	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
(1S,2R)-3-chloro-1-(4-hydroxy-3-methoxyphenyl)propane-1,2-diol	10847213	Click to see COC1=C(C=CC(=C1)C(C(CCl)O)O)O	232.66	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
(2r)-3-(4-Hydroxy-3-methoxyphenyl)-1,2-propanediol	101154580	Click to see COC1=C(C=CC(=C1)CC(CO)O)O	198.22	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
1,2-Propanediol, 3-(4-hydroxy-3-methoxyphenyl)-, (2S)-	10750461	Click to see COC1=C(C=CC(=C1)CC(CO)O)O	198.22	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)-	9984	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
3-(4-Hydroxy-3-methoxyphenyl)propane-1,2-diol	161566	Click to see COC1=C(C=CC(=C1)CC(CO)O)O	198.22	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
3-Chloro-1-(4-hydroxy-3-methoxyphenyl)-1,2-propanediol	78067769	Click to see COC1=C(C=CC(=C1)C(C(CCl)O)O)O	232.66	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1080/10412905.1997.9700812 https://doi.org/10.1016/S0031-9422(99)00406-9 https://doi.org/10.1080/10412905.1991.9700504
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[(1R,2R)-3-oxo-2-[(Z)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]oxypent-2-enyl]cyclopentyl]acetic acid	24879474	Click to see C1CC(=O)C(C1CC(=O)O)CC=CCCOC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	540.50	unknown	https://doi.org/10.1021/NP0705615
2-[3-Oxo-2-[5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]oxypent-2-enyl]cyclopentyl]acetic acid	74342823	Click to see C1CC(=O)C(C1CC(=O)O)CC=CCCOC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	540.50	unknown	https://doi.org/10.1021/NP0705615
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700812
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1997.9700812
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700812
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700812
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700812
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700812
Menthol	1254	Click to see CC1CCC(C(C1)O)C(C)C	156.26	unknown	https://doi.org/10.1080/10412905.1997.9700812
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700812
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700812
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1080/10412905.1997.9700812
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1080/10412905.1997.9700812
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700812
alpha-Calacorene	12302243	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1080/10412905.1997.9700812
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1080/10412905.1997.9700812
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700812
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700812
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-hydroxy-3-methoxy-5-prop-2-enylphenoxy)oxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	24879405	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3O)OC)CC=C)O)O)O	548.50	unknown	https://doi.org/10.1021/NP0705615
[3,4,5-Trihydroxy-6-(2-hydroxy-3-methoxy-5-prop-2-enylphenoxy)oxan-2-yl]methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	74342787	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3O)OC)CC=C)O)O)O	548.50	unknown	https://doi.org/10.1021/NP0705615
2-Methoxy-4-(2-propen-1-yl)phenyl I(2)-D-glucopyranoside 6-(3,4,5-trihydroxybenzoate)	44583693	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP9906121
Eugenol O-[3,4,5-Trihydroxybenzoyl-(->6)-b-D-glucopyranoside]	75051748	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP9906121
Pimentol	9917512	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1021/NP9906121 https://doi.org/10.1271/BBB.61.263
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(3,4-Dimethoxyphenyl)-2-propenal	107557	Click to see COC1=C(C=C(C=C1)C=CC=O)OC	192.21	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
3,4-Dimethoxy cinnamaldehyde	5375268	Click to see COC1=C(C=C(C=C1)C=CC=O)OC	192.21	unknown	https://doi.org/10.1016/S0031-9422(99)00406-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one	5153580	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1021/NP0705615
Dihydromyricetin	161557	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1021/NP0705615
> 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/10.1021/NP0705615
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/10.1021/NP0705615
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Methyl 6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	73829983	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	492.40	unknown	https://doi.org/10.1021/NP0705615
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER	21722016	Click to see COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	492.40	unknown	https://doi.org/10.1021/NP0705615
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1021/NP0705615
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51521831	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/10.1021/NP0705615
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/10.1021/NP0705615
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/10.1021/NP0705615
3-[(2S,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308708	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/10.1021/NP0705615
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	5320668	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/10.1021/NP0705615
Avicularin	5490064	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/10.1021/NP0705615
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/10.1021/NP0705615
Myricetin 3-beta-D-glucopyranoside	12311099	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1021/NP0705615
Myricetin 3-galactoside	5491408	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1021/NP0705615
myricetin 3-O-beta-L-galactopyranoside	72551438	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1021/NP0705615
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://doi.org/10.1021/NP0705615

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Pimenta dioica

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