Scientific name	Authority	First published in
Jambosa jambos	Millsp.	Publ. Field Columb. Mus., Bot. Ser. 2: 80 (1900)
Jambosa leptostachya	Blume	Mus. Bot. 1: 99 (1850)
Jambosa malaccensis f. cericarpa	O.Deg.	Fl. Hawaiiensis 273: s.p. 1933
Jambosa palembanica	Blume	Mus. Bot. 1: 93 (1850)
Myrtus jambos	Kunth	Nov. Gen. Sp. 6: 144 (1823)
Plinia jambos	M.Gómez	Fl. Haban. : 292 (1914)
Syzygium jambos var. linearilimbum	H.T.Chang & R.H.Miao	Acta Bot. Yunnan. 4: 17 (1982)
Syzygium leptostachyum	(Blume) Merr. & L.M.Perry	Mem. Amer. Acad. Arts , n.s., 18: 175 (1939)
Syzygium merrillii	Masam.	Enum. Phan. Born. : 534 (1942)
Syzygium monanthum	(Merr.) Merr. & L.M.Perry	Mem. Amer. Acad. Arts , n.s., 18: 163 (1939)
Eugenia decora	Salisb.	Prodr. Stirp. Chap. Allerton : 353 (1796)
Eugenia jamboides	Wender.	Schriften Ges. Beförd. Gesammten Naturwiss. Marburg 2: 254 (1831)
Eugenia jambos	L.	Sp. Pl. : 470 (1753)
Eugenia jambosa	Crantz	Inst. Rei Herb. 2: 201 (1766)
Eugenia malaccensis f. cericarpa	(O.Deg.) St.John.	Mem. Pacific Trop. Bot. Gard. 1: 252 (1973)
Eugenia monantha	Merr.	J. Straits Branch Roy. Asiat. Soc. 79: 22 (1918)
Eugenia vulgaris	Baill.	Hist. Pl. 6: 345 (1876)

Common names Top

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Filter by language:

Language	Common/alternative name
English	plum rose
English	malabar plum
English	rose apple
Spanish	manzana malaya
Spanish	marañón japonés
Spanish	ciruela malabar
Spanish	jambolian
Spanish	macupa
Spanish	malarrosa
Spanish	manzana de rosa
Spanish	manzana malasia
Spanish	pomarosa
Spanish	maranon japones
Spanish	maranon japonés
Spanish	maranón japones
Spanish	maranón japonés
Spanish	marañon japones
Spanish	marañon japonés
Spanish	marañón japones
Spanish	pomarrosa
Arabic	جنبوزة
Azerbaijani	Çəhrayı alma
Bengali	গোলাপজাম
Czech	hřebíčkovec jambos
German	rosenapfel
Finnish	rusojambolaani
French	jam-rose
French	jamrose
French	jambosier
French	jambrosade
French	jamrosa
French	pomme rose
French	pommier rose
French	jamrosat
Hebrew	תפוח הוורד
Upper Sorbian	róžowy nalikowc
Indonesian	jambu mawar
Indonesian	jambu kraton
Japanese	フトモモ
Japanese	蒲桃
jv	jambu mawar
Kannada	ಪನ್ನೇರಳೆ
Korean	로즈애플
Lithuanian	rausvasis gvazdikmedis
Malayalam	ജാംബ
Malayalam	പനിനീർച്ചാമ്പ
Malayalam	പനിനീർ ചാമ്പ
Malay	pokok jambu mawar
Burmese	ဇမ္ဗူ့သပြေပင်
Norwegian Bokmål	roseneple
Nepali	गुलाब जामुन
Dutch	djamboe air mawar
Dutch	djamboe mawar
Dutch	rozenappel
Dutch	djamboe aer mawar
Polish	czapetka jambos
Portuguese	jambos
Portuguese	jambo
Russian	Розовое яблоко
sa	जम्बूवृक्षः
su	jambu mawar
Swedish	rosenäpple
Telugu	రోజ్ యాపిల్
Thai	ชมพู่น้ำดอกไม้
Tonga	fekika papālangi
Tonga	caryophyllus jambos
Vietnamese	roi hoa vàng
Chinese	葡桃
Chinese	香果
Chinese	蒲桃
Chinese	水蒲桃
Chinese	水石榴
Chinese	水桃树
Chinese	蒲桃种子
Chinese	蒲桃根皮
Chinese	蒲桃壳
Chinese	蒲桃叶
Chinese	乌墨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Macaronesia
  - Madeira
- Middle Atlantic Ocean
  - Saint Helena
- South Tropical Africa
  - Angola
- West Tropical Africa
  - Guinea
  - Guinea-Bissau
- West-central Tropical Africa
  - Central African Republic
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Ogasawara-Shoto

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sumatera

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

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- South-central Pacific
  - Cook Islands
  - Easter Island
  - Marquesas
  - Pitcairn Islands
  - Society Islands
  - Tuamotu
  - Tubuai Islands
- Southwestern Pacific
  - New Caledonia
  - Tonga
  - Vanuatu
  - Wallis-Futuna Islands

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil Southeast
- Caribbean
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - Venezuela
- Western South America
  - Bolivia
  - Galápagos

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000318809
UNII	Q08F068PCS
Florida Plant Atlas	434
USDA Plants	SYJA
Tropicos	22101929
INPN	447411
KEW	urn:lsid:ipni.org:names:601802-1
The Plant List	kew-199743
Open Tree Of Life	731939
Observations.org	199502
NCBI Taxonomy	334483
Nature Serve	2.142480
IUCN Red List	49487025
IPNI	601802-1
iNaturalist	84838
GBIF	3183534
Freebase	/m/0clq3_
EPPO	SYZJA
EOL	2508661
Elurikkus	7639
USDA GRIN	50070
Wikipedia	Syzygium_jambos
CMAUP	NPO13199

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_031216235.1	ASM3121623v1	Chromosome	Philip Morris International R&D	2023-09-07	150.0x	406.42 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

Potential of Wormwood and Oak Bark-Based Supplement in Health Improvement of Nosema ceranae-Infected Honey Bees

Glavinic U, Jovanovic NM, Dominikovic N, Lakic N, Ćosić M, Stevanovic J, Stanimirovic Z

Animals (Basel)

16-Apr-2024

PMCID:	PMC11047348
doi:	10.3390/ani14081195
PMID:	38672343

Yams (Dioscorea spp.) in shellmounds and swiddens: ancient history in Babitonga Bay, Santa Catarina State, southern Brazil

da Silva Souza DA, da Bandeira DR, Peroni N

J Ethnobiol Ethnomed

02-Feb-2024

PMCID:	PMC10836009
doi:	10.1186/s13002-024-00653-4
PMID:	38308263

Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review

Islam Shawon S, Nargis Reyda R, Qais N

Heliyon

01-Feb-2024

PMCID:	PMC10864916
doi:	10.1016/j.heliyon.2024.e25340
PMID:	38356556

Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196

He Y, Xu Y, Chen X

Insects

31-Jan-2024

PMCID:	PMC10889426
doi:	10.3390/insects15020093
PMID:	38392559

Malinzi, a traditional medicinal plants: Comprehensive review of botany, medical application, chemical composition, and pharmacology

Zhai RX, Fu XJ, Ren X

Heliyon

30-Jan-2024

PMCID:	PMC10850416
doi:	10.1016/j.heliyon.2024.e24986
PMID:	38333853

Chemical profiling and dermatological and anti-aging properties of Syzygium jambos L. (Alston): evidence from molecular docking, molecular dynamics, and in vitro experiments

Mahdi I, Imbimbo P, Ortaakarsu AB, Adhiambo Ochieng M, Ben Bakrim W, Drissi BE, Ibrahim MA, Abdelfattah MA, Mahmoud MF, Monti DM, Sobeh M

Front Mol Biosci

05-Jan-2024

PMCID:	PMC10797028
doi:	10.3389/fmolb.2023.1331059
PMID:	38250734

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

Assessing deep convolutional neural network models and their comparative performance for automated medicinal plant identification from leaf images

Dey B, Ferdous J, Ahmed R, Hossain J

Heliyon

13-Dec-2023

PMCID:	PMC10767391
doi:	10.1016/j.heliyon.2023.e23655
PMID:	38187334

Evaluation of Bioactive Compounds and Antioxidant Activity in 51 Minor Tropical Fruits of Ecuador

Coyago-Cruz E, Guachamin A, Villacís M, Rivera J, Neto M, Méndez G, Heredia-Moya J, Vera E

Foods

11-Dec-2023

PMCID:	PMC10742603
doi:	10.3390/foods12244439
PMID:	38137243

Double-stranded RNA prevents and cures infection by rust fungi

Degnan RM, Shuey LS, Radford-Smith J, Gardiner DM, Carroll BJ, Mitter N, McTaggart AR, Sawyer A

Commun Biol

06-Dec-2023

PMCID:	PMC10700371
doi:	10.1038/s42003-023-05618-z
PMID:	38057635

Nutritional and Technological Properties of Albino Peach Palm (Bactris gasipaes) from the Amazon: Influence of Cooking and Drying

Soares SD, dos Santos OV, da Conceição LR, Costi HT, Silva Júnior JO, do Nascimento FD, Pena RD

Foods

01-Dec-2023

PMCID:	PMC10706845
doi:	10.3390/foods12234344
PMID:	38231871

Do Native and Alien Species Differ in Their Ecological Strategies? A Test with Woody Plants in Tropical Rainforests on Réunion Island (Mascarene Archipelago, Indian Ocean)

Heymans L, Meyer JY, Ah-Peng C, Ethève Q, Flores O, Lavergne C, Mallet B, Parlevliet H, Strasberg D, Pouteau R

Plants (Basel)

27-Nov-2023

PMCID:	PMC10708162
doi:	10.3390/plants12233990
PMID:	38068626

Antibacterial potential of silver nanoparticles (SP-AgNPs) synthesized from Syzygium polyanthum (Wight) Walp. against selected foodborne pathogens

Khan S, Rukayadi Y, Jaafar AH, Ahmad NH

Heliyon

22-Nov-2023

PMCID:	PMC10730589
doi:	10.1016/j.heliyon.2023.e22771
PMID:	38125456

Pest categorisation of Diaprepes abbreviatus

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

EFSA J

15-Nov-2023

PMCID:	PMC10648563
doi:	10.2903/j.efsa.2023.8318
PMID:	38027434

Intra- and interspecific ecophysiological responses to waterlogging stress in two contrasting waterlogging-tolerant arbor species

Tian M, Li D, Cisse EH, Miao L, Zhou J, Yang W, Chen B, Li L, Tian H, Ye B, Yang F

Front Plant Sci

13-Nov-2023

PMCID:	PMC10679334
doi:	10.3389/fpls.2023.1257730
PMID:	38023841

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione	54752972	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=CC(=C(C(=C3C2=O)O)C4=C(C=C5C(=C4O)C(=O)C6=C(C5=O)C(=CC(=C6)C)O)O)O	538.50	unknown	via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione	54752971	Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O	300.26	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives
3-Phenyl-1-propanol	31234	Click to see C1=CC=C(C=C1)CCCO	136.19	unknown	https://doi.org/10.1080/10412905.1991.9697916
3-Phenylpropanal	7707	Click to see C1=CC=C(C=C1)CCC=O	134.17	unknown	https://doi.org/10.1080/10412905.1991.9697916
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
(5aR,10bR)-8,10-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-5a-propan-2-yl-10bH-[1]benzofuro[2,3-b][1]benzofuran-1,3-dione	102521923	Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC3(C2C4=C(O3)C(C(=O)C(C4=O)(C)C)(C)C)C(C)C)O)O	456.50	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
(Z)-Cinnamyl acetate	5315912	Click to see CC(=O)OCC=CC1=CC=CC=C1	176.21	unknown	https://doi.org/10.1080/10412905.1991.9697916
Cinnamyl acetate	5282110	Click to see CC(=O)OCC=CC1=CC=CC=C1	176.21	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol	10439806	Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O	714.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (E)-3-methyl-5-[(1S,6R)-1,2,6-trimethylcyclohex-2-en-1-yl]pent-2-enoate	11043181	Click to see CC1CCC=C(C1(C)CCC(=CC(=O)OC)C)C	250.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linolenate	5319706	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC	292.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(21R)-Hopa-22(29)-ene-3beta,30-diol	102032092	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5C4(CCC5C(=C)CO)C)C)C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	https://doi.org/10.1080/10412905.1991.9697916
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1991.9697916
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1991.9697916
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol	14985	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	11876093	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	10836206	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	7061300	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate	479957	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO	484.80	unknown	via CMAUP database
11-Oxo-beta-amyrin	20055661	Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	440.70	unknown	via CMAUP database
3-O-p-Coumaroyloleanolic acid	10579517	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1)C)C(=O)O)C	602.80	unknown	via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide	21626351	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C	512.70	unknown	via CMAUP database
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Betulonic acid	122844	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	40884490	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC	470.70	unknown	via CMAUP database
Methyl Betulonate	10766700	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC	468.70	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 / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
Sollasin B	44575909	Click to see CC1CCC=C(C1(C)CCC(=CC(=O)NC2CCCNC2=O)C)C	332.50	unknown	via CMAUP database
Sollasin C	44575910	Click to see CC1CCC=C(C1(C)CCC(=CC(=O)NC2CCCCNC2=O)C)C	346.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione	44281346	Click to see CC1(C=C2C(=O)C(C(=O)C(C2(OO1)O)(C)C)(C)C)C	268.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Hotrienol	5366264	Click to see CC(=C)C=CCC(C)(C=C)O	152.23	unknown	https://doi.org/10.1080/10412905.1991.9697916
Linalool, oxide	102611	Click to see CC(=CCCC(C)(C1CO1)O)C	170.25	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone	56929125	Click to see CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O	688.80	unknown	via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione	102521922	Click to see CC(C)CC1C2=C(C(=C(C=C2O)O)C(=O)CC(C)C)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C	442.50	unknown	via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione	26202536	Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C	442.50	unknown	via CMAUP database
Rhodomyrtone	12050020	Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C	442.50	unknown	via CMAUP database
Tomentosone A	56929124	Click to see CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O	688.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Sollasin D	10335934	Click to see CC1CCC=C(C1(C)CCC(=CC2=CC(=CC(=O)O2)OC)C)C	316.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde	637511	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	https://doi.org/10.1080/10412905.1991.9697916
cis-Cinnamaldehyde	6428995	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate	14213589	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	585.00	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(Z)-3-Phenyl-2-propen-1-ol	5280511	Click to see C1=CC=C(C=C1)C=CCO	134.17	unknown	https://doi.org/10.1080/10412905.1991.9697916
Cinnamyl alcohol	5315892	Click to see C1=CC=C(C=C1)C=CCO	134.17	unknown	https://doi.org/10.1080/10412905.1991.9697916
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> 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	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> 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/10.1016/0305-1978(92)90062-I
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/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	101674015	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(CO5)O)O)O)O)O	580.50	unknown	https://doi.org/10.1016/0031-9422(94)85036-4
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	101674016	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)OC5C(C(C(CO5)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/0031-9422(94)85036-4
3-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	74978299	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)OC5C(C(C(CO5)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/0031-9422(94)85036-4
quercetin-3-O-deoxyhexosyl(1-2)pentoside	13784485	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(CO5)O)O)O)O)O	580.50	unknown	https://doi.org/10.1016/0031-9422(94)85036-4
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	129010093	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O	580.50	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
Naringin	442428	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O	580.50	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 5-hydroxyflavonoids
Delfinidin	25203213	Click to see C1=C(C=C(C(=C1O)[O-])O)C2=C(C=C3C(=CC(=O)C=C3O2)O)O	301.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Malvidin	159287	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	331.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin	72281	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O	302.28	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol	12303802	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)OC)O	388.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Tangeretin	68077	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	372.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein	5281708	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O	254.24	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O	284.26	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	https://doi.org/10.1002/(SICI)1099-1565(199707)8:4<176::AID-PCA351>3.0.CO;2-K
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,46-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-37-yl] 3,4,5-trihydroxybenzoate	102231177	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1086.70	unknown	https://doi.org/10.1016/S0304-3835(00)00477-8
2,3,8-Tri-O-methylellagic acid	5281860	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC	344.30	unknown	via CMAUP database
beta-Pedunculagin	5320441	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	via CMAUP database
Casuariin	14035442	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1016/S0304-3835(00)00477-8
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1016/S0031-9422(00)86652-2
S45A8T6Q4C	13834145	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	via CMAUP database

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Syzygium jambos

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