Scientific name	Authority	First published in
Oxycoccus macrocarpus	(Aiton) Pers.	Syn. Pl. [Persoon] 1: 419. 1805 [1 Apr-15 Jun 1805] : erroneous entry
Oxycoca berberidacea	Raf.	Med. Fl. 2: 49 (1830)
Oxycoca macrocarpa	(Aiton) Raf.	Med. Fl. 2: 48 (1830)
Schollera macrocarpa	(Aiton) Steud.	Nomencl. Bot. [Steudel] 746. 1821
Oxycoccus palustris var. macrocarpos	(Aiton) Pers.	Syn. Pl. 1: 419 1805
Schollera macrocarpos	(Aiton) Britton	Nomencl. Bot. [Steudel] 746. 1821 (as macrocarpa)

Common names Top

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Filter by language:

Language	Common/alternative name
English	american cranberry
English	cranberry
English	large cranberry
English	bearberry
Spanish	cranberry
Arabic	قمام كبير الثمر
Czech	klikva velkoplodá
Welsh	llygaeren america
Danish	vaccineum macrocarpum
Danish	sort af tranebær (vaccineum macrocarpum) 'early black'
Danish	storfrugtet tranebær
German	kraanbeere
German	grossfrüchtige moosbeere
German	kranichbeere
German	kranbeere
German	cranberry
German	großfrüchtige moosbeere
German	kränbeere
Esperanto	oksikoko amerika
Persian	قرهقات
Persian	قره قات
Finnish	amerikankarpalo
Finnish	pensaskarpalo
French	airelle à gros fruits
French	grande airelle rouge d’amérique du nord
Croatian	američka brusnica
Upper Sorbian	wulkopłodowa tymjenka
Hungarian	amerikai tőzegáfonya
Icelandic	trönuber
Italian	mirtillo rosso americano
Italian	ossicocco americano
Lithuanian	stambiauogė spanguolė
Latvian	lielogu dzērvene
Latvian	dižbrūklene
Macedonian	Американска брусница
Norwegian Bokmål	cranberry
Norwegian Bokmål	amerikansk tranebær
Dutch	veenbes
Dutch	grote cranberry
Dutch	grote veenbes
Dutch	lepeltjesheide
Dutch	amerikaanse veenbes
Dutch	amerikaanse cranberry
Dutch	cranberry
Polish	żurawina wielkoowocowa
Polish	borówka wielkożurawinowa
Slovak	kľukva veľkoplodá
Serbian	Америчка брусница
Serbian	америчка брусница
Serbian	brusnica
Serbian	američka brusnica
Swedish	amerikanskt tranbär
Chinese	蔓越橘
Chinese	大果越橘
Chinese	大蔓越梅
Chinese	美洲蔓越梅
Chinese	大果蔓越梅

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!

Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Middle Europe
  - Belgium
  - Germany
  - Netherlands
  - Switzerland
- Northern Europe
  - Great Britain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Oregon
  - Washington
- Southeastern U.S.A.
  - Delaware
  - District Of Columbia
  - Maryland
  - North Carolina
  - Tennessee
  - Virginia
- Western Canada
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000422267
UNII	D11KO7O2DX
Canadensys	5571
USDA Plants	VAMA
Tropicos	12300051
INPN	761958
KEW	urn:lsid:ipni.org:names:261912-2
The Plant List	kew-2457729
Missouri Botanical Garden	279943
PFAF	Vaccinium macrocarpon
Open Tree Of Life	295602
Observations.org	7135
NCBI Taxonomy	13750
NBN Atlas	NBNSYS0000003920
Nature Serve	2.144597
IUCN Red List	64326218
IPNI	261912-2
iNaturalist	63749
GBIF	2882841
Freebase	/m/0gkzdl6
WisFlora	5321
EPPO	VACMA
EOL	583674
Elurikkus	8104
Calflora (Californian flora)	8198
USDA GRIN	41030
Wikipedia	Vaccinium_macrocarpon

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_022606695.1	ASM2260669v1	Chromosome	United States Department of Agriculture-Agricultural Research Service	2022-03-18	100.0x	462.46 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

Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran

Azizi R, Ghosta Y, Ahmadpour A

Sci Rep

19-Mar-2024

PMCID:	PMC10951349
doi:	10.1038/s41598-024-57235-3
PMID:	38504125

Mitochondrial genome features and systematic evolution of diospyros kaki thunb 'Taishuu'

Yang Y, Duan C

BMC Genomics

18-Mar-2024

PMCID:	PMC10946091
doi:	10.1186/s12864-024-10199-0
PMID:	38500026

Adulteration of Brain Health (Cognitive, Mood, and Sleep Enhancement) Food Supplements by the Addition of Pharmaceutical Drugs: A Comprehensive Review of Analytical Approaches and Trends

Paiva R, Correia M, Delerue-Matos C, Amaral JS

Foods

16-Mar-2024

PMCID:	PMC10969376
doi:	10.3390/foods13060908
PMID:	38540898

Safety evaluation of the food enzyme β‐fructofuranosidase from the non‐genetically modified Saccharomyces cerevisiae strain NCYC R693

Lambré C, Barat Baviera JM, Bolognesi C, Cocconcelli PS, Crebelli R, Gott DM, Grob K, Lampi E, Mengelers M, Mortensen A, Rivière G, Steffensen I, Tlustos C, Van Loveren H, Vernis L, Zorn H, Herman L, Roos Y, Aguilera J, Andryszkiewicz M, Cavanna D, Liu Y, Marini E, Pesce F, di Piazza G, Chesson A

EFSA J

27-Feb-2024

PMCID:	PMC10897736
doi:	10.2903/j.efsa.2024.8616
PMID:	38415018

Antibacterial Activity of Plant Polyphenols Belonging to the Tannins against Streptococcus mutans—Potential against Dental Caries

Czerkas K, Olchowik-Grabarek E, Łomanowska M, Abdulladjanova N, Sękowski S

Molecules

16-Feb-2024

PMCID:	PMC10892310
doi:	10.3390/molecules29040879
PMID:	38398630

Terpenoid-Mediated Targeting of STAT3 Signaling in Cancer: An Overview of Preclinical Studies

Khan F, Pandey P, Verma M, Upadhyay TK

Biomolecules

07-Feb-2024

PMCID:	PMC10886526
doi:	10.3390/biom14020200
PMID:	38397437

Phlorizin, an Important Glucoside: Research Progress on Its Biological Activity and Mechanism

Ni T, Zhang S, Rao J, Zhao J, Huang H, Liu Y, Ding Y, Liu Y, Ma Y, Zhang S, Gao Y, Shen L, Ding C, Sun Y

Molecules

05-Feb-2024

PMCID:	PMC10856272
doi:	10.3390/molecules29030741
PMID:	38338482

A biofertilizing fungal endophyte of cranberry plants suppresses the plant pathogen Diaporthe

Thimmappa BC, Salhi LN, Forget L, Sarrasin M, Bustamante Villalobos P, Henrissat B, Lang BF, Burger G

Front Microbiol

02-Feb-2024

PMCID:	PMC10869595
doi:	10.3389/fmicb.2024.1327392
PMID:	38371935

Re-identification of Colletotrichum gloeosporioides Species Complex Isolates in Korea and Their Host Plants

Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Kim DH, Shin HD, Choi H, Ju HJ, Hong SB

Plant Pathol J

01-Feb-2024

PMCID:	PMC10850535
doi:	10.5423/PPJ.OA.09.2023.0133
PMID:	38326955

Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines

Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW

J Fungi (Basel)

26-Jan-2024

PMCID:	PMC10890244
doi:	10.3390/jof10020105
PMID:	38392777

Advancing tree genomics to future proof next generation orchard production

Kerr SC, Shehnaz S, Paudel L, Manivannan MS, Shaw LM, Johnson A, Velasquez JT, Tanurdžić M, Cazzonelli CI, Varkonyi-Gasic E, Prentis PJ

Front Plant Sci

19-Jan-2024

PMCID:	PMC10834703
doi:	10.3389/fpls.2023.1321555
PMID:	38312357

Bioprospecting of endophytic fungi from medicinal plant Anisomeles indica L. for their diverse role in agricultural and industrial sectors

Toppo P, Jangir P, Mehra N, Kapoor R, Mathur P

Sci Rep

05-Jan-2024

PMCID:	PMC10770348
doi:	10.1038/s41598-023-51057-5
PMID:	38182714

Natural Products as Dietary Agents for the Prevention and Mitigation of Oxidative Damage and Inflammation in the Intestinal Barrier

Martins-Gomes C, Nunes FM, Silva AM

Antioxidants (Basel)

01-Jan-2024

PMCID:	PMC10812469
doi:	10.3390/antiox13010065
PMID:	38247489

Anthocyanin Production from Plant Cell and Organ Cultures In Vitro

Murthy HN, Joseph KS, Paek KY, Park SY

Plants (Basel)

31-Dec-2023

PMCID:	PMC10780419
doi:	10.3390/plants13010117
PMID:	38202425

First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand

Norphanphoun C, Hyde KD

Pathogens

10-Dec-2023

PMCID:	PMC10747506
doi:	10.3390/pathogens12121436
PMID:	38133319

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
> Alkaloids and derivatives / Aporphines
9-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol	4411439	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://doi.org/10.1021/JF020728U https://doi.org/10.1271/BBB.60023
> Benzenoids / Benzene and substituted derivatives
Phenylboronic acid	66827	Click to see B(C1=CC=CC=C1)(O)O	121.93	unknown	https://doi.org/10.1021/JF034114G
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Ethyl benzoate	7165	Click to see CCOC(=O)C1=CC=CC=C1	150.17	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Methyl benzoate	7150	Click to see COC(=O)C1=CC=CC=C1	136.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Vacciniin	12444646	Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)O)O)O)O	284.26	unknown	https://doi.org/10.1111/J.1365-2621.1986.TB11236.X https://doi.org/10.1016/0031-9422(90)85230-D
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	https://doi.org/10.1021/JF0636014 https://doi.org/10.1016/S0021-9673(00)01030-X https://doi.org/10.1021/JF061058L https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847405/ https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1111/J.1365-2621.1986.TB11220.X https://doi.org/10.1021/JF020055F https://doi.org/10.1016/0031-9422(90)85230-D https://doi.org/10.1111/J.1365-2621.1986.TB11236.X https://doi.org/10.1021/JF052035U
Phthalic acid	1017	Click to see C1=CC=C(C(=C1)C(=O)O)C(=O)O	166.13	unknown	https://doi.org/10.1021/JF020055F
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	https://doi.org/10.1016/S0021-9673(00)01030-X
3-Hydroxybenzoic acid	7420	Click to see C1=CC(=CC(=C1)O)C(=O)O	138.12	unknown	https://doi.org/10.1021/JF020055F
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF0636014
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF990972U https://doi.org/10.1021/JF020055F https://doi.org/10.1021/JF061058L
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.21273/HORTSCI.29.4.313
> 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/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF990972U https://doi.org/10.1016/S0021-9673(00)01030-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF0636014 https://doi.org/10.1021/JF020728U https://doi.org/10.1021/JF020055F https://doi.org/10.1021/JF061058L
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid	7478	Click to see COC1=CC=C(C=C1)C(=O)O	152.15	unknown	https://doi.org/10.1016/S0021-9673(00)01030-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid	338	Click to see C1=CC=C(C(=C1)C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF020055F https://doi.org/10.1021/JF0636014
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl formate	7708	Click to see C1=CC=C(C=C1)COC=O	136.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Indenes and isoindenes
Indene	7219	Click to see C1C=CC2=CC=CC=C21	116.16	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Hydroxyphenylacetic acid	127	Click to see C1=CC(=CC=C1CC(=O)O)O	152.15	unknown	https://doi.org/10.1021/JF020055F
> Benzenoids / Phenols / Methoxyphenols
4-Ethyl-2-methoxyphenol	62465	Click to see CCC1=CC(=C(C=C1)O)OC	152.19	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Octadecene	8217	Click to see CCCCCCCCCCCCCCCCC=C	252.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl butyrate	7762	Click to see CCCC(=O)OCC	116.16	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Monoethyl maleate	5354457	Click to see CCOC(=O)C=CC(=O)O	144.12	unknown	https://doi.org/10.1021/JF061058L
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl butyrate	12180	Click to see CCCC(=O)OC	102.13	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol	6992244	Click to see CCCCCC(C=C)O	128.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(R)-3-Octanol	445789	Click to see CCCCCC(CC)O	130.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(S)-(+)-2-Octanol	2723888	Click to see CCCCCCC(C)O	130.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1-Decanol	8174	Click to see CCCCCCCCCCO	158.28	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Octanol	20083	Click to see CCCCCCC(C)O	130.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Octanol	11527	Click to see CCCCCC(CC)O	130.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Nonan-1-ol	8914	Click to see CCCCCCCCCO	144.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-ol	4458	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> 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/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5R,6S,7R,7aS)-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5,6,7-triol	162845885	Click to see CC1(C2C(C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(C1O)O)O	364.34	unknown	https://doi.org/10.1021/JF0352778
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	101209474	Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	392.35	unknown	https://doi.org/10.1021/JF0205110
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid	3488508	Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	390.34	unknown	https://doi.org/10.1021/JF0205110
7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	163010321	Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	392.35	unknown	https://doi.org/10.1021/JF0205110
Monotropein	73466	Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	390.34	unknown	https://doi.org/10.1021/JF0205110
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,3R,5S,8S,9S,10R,11S,12S)-8,9,11,12-tetrahydroxy-3,10-dimethyl-3-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-7-one	162845674	Click to see CC1C(C2(C3C(CC4C3(C1(C(C(=O)O4)O)O)CO2)(C)C5C(=CC(=O)O5)C)O)O	396.40	unknown	https://doi.org/10.1021/JF020728U
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
9-methyl-3,6-dimethylidene-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one	21093319	Click to see CC1=CCC2C1C3C(CCC2=C)C(=C)C(=O)O3	230.30	unknown	https://doi.org/10.1081/JLC-120027089
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,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-yl] acetate	162999321	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1021/JF0202234 https://doi.org/10.1093/JAC/DKL220
10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-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-carboxylic acid	73218938	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1C)C)C(=O)O	602.80	unknown	https://doi.org/10.1021/JF034114G
3-(p-Coumaroyl)ursolic acid	24203733	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1C)C)C(=O)O	602.80	unknown	https://doi.org/10.1021/JF034114G
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/JF061058L
cis-3-O-p-hydroxycinnamoyl ursolic acid	24203732	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1C)C)C(=O)O	602.80	unknown	https://doi.org/10.1021/JF034114G
Oleanolic Acid	10494	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	https://doi.org/10.1002/JPS.3030421005
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/JPS.3030421005 https://doi.org/10.1021/JF061058L
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate	25180961	Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C	360.50	unknown	https://doi.org/10.1021/JF020728U https://doi.org/10.1271/BBB.60023
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/JF061058L
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/JF061058L
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/JF061058L
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/JF061058L
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Fumaric Acid	444972	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1021/JF0352778 https://doi.org/10.21273/HORTSCI.29.4.313
Oxalic Acid	971	Click to see C(=O)(C(=O)O)O	90.03	unknown	https://doi.org/10.21273/HORTSCI.29.4.313
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid	311	Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O	192.12	unknown	https://doi.org/10.1093/JAOAC/61.6.1490 https://doi.org/10.1021/JF0352778 https://doi.org/10.21273/HORTSCI.29.4.313
Isocitric acid	1198	Click to see C(C(C(C(=O)O)O)C(=O)O)C(=O)O	192.12	unknown	https://doi.org/10.1021/JF0352778
trans-Aconitic acid	444212	Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O	174.11	unknown	https://doi.org/10.21273/HORTSCI.29.4.313
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid	222656	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1021/JF0205110
D-malate	92824	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1021/JF061058L
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1093/JAOAC/61.6.1490 https://doi.org/10.1021/JF0352778 https://doi.org/10.21273/HORTSCI.29.4.313
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid	1064	Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O	192.17	unknown	https://doi.org/10.1093/JAOAC/61.6.1490 https://doi.org/10.1021/JF0352778 https://doi.org/10.1021/JF0205110
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1089/JMF.2007.531 https://doi.org/10.1021/JF990972U https://doi.org/10.1016/S0021-9673(00)01030-X
Quinic acid	6508	Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O	192.17	unknown	https://doi.org/10.1021/JF0205110 https://doi.org/10.1093/JAOAC/61.6.1490 https://doi.org/10.1021/JF0352778
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1021/JF0205110
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1021/JF0205110
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(3R)-heptan-3-ol	6993462	Click to see CCCCC(CC)O	116.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Pentanol	22386	Click to see CCCC(C)O	88.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Heptanol	11520	Click to see CCCCC(CC)O	116.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Methyl-3-buten-2-ol	66329	Click to see CC(C(=C)C)O	86.13	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
3-Methylcyclohexanol	11566	Click to see CC1CCCC(C1)O	114.19	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
trans-3-Methylcyclohexanol	641629	Click to see CC1CCCC(C1)O	114.19	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-3-buten-2-OL	8257	Click to see CC(C)(C=C)O	86.13	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
DL-Tartaric acid	875	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	https://doi.org/10.1021/JF0352778
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Decenal	5283345	Click to see CCCCCCCC=CC=O	154.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Dodecanal	8194	Click to see CCCCCCCCCCCC=O	184.32	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Heptanal	8130	Click to see CCCCCCC=O	114.19	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Octanal	454	Click to see CCCCCCCC=O	128.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Undecanal	8186	Click to see CCCCCCCCCCC=O	170.29	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Isophorone	6544	Click to see CC1=CC(=O)CC(C1)(C)C	138.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Octanone	8093	Click to see CCCCCCC(=O)C	128.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Pentadecanone	61303	Click to see CCCCCCCCCCCCCC(=O)C	226.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Tridecanone	11622	Click to see CCCCCCCCCCCC(=O)C	198.34	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Alpha-diketones
2,3-Butanedione	650	Click to see CC(=O)C(=O)C	86.09	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole	7222	Click to see C1=CC=C2C(=C1)N=CS2	135.19	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid	54670067	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	https://doi.org/10.1021/JF0352778
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
5-Hydroxy-2-hexenoic acid lactone	24869	Click to see CC1CC=CC(=O)O1	112.13	unknown	https://doi.org/10.1016/S0031-9422(00)82223-2
Parasorbic acid	441575	Click to see CC1CC=CC(=O)O1	112.13	unknown	https://doi.org/10.1016/S0031-9422(00)82223-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Ethyl 3-phenylprop-2-enoate	7649	Click to see CCOC(=O)C=CC1=CC=CC=C1	176.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Ethyl cinnamate	637758	Click to see CCOC(=O)C=CC1=CC=CC=C1	176.21	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1021/JF020055F
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0021-9673(00)01030-X https://doi.org/10.1021/JF020055F https://doi.org/10.1021/JF0636014
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF0636014 https://doi.org/10.1021/JF020055F
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.21273/HORTSCI.29.4.313 https://doi.org/10.1021/JF990972U https://doi.org/10.1021/JF020055F https://doi.org/10.1016/S0021-9673(00)01030-X
Sinapinic acid	637775	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O	224.21	unknown	https://doi.org/10.1016/S0021-9673(00)01030-X https://doi.org/10.1021/JF020055F https://doi.org/10.1021/JF0636014
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol	5320711	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000128U
CID 21881649	21881649	Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O	592.50	unknown	https://doi.org/10.1207/S15327914NC5601_12
Proanthocyanidin	108065	Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)O	592.50	unknown	https://doi.org/10.1207/S15327914NC5601_12
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000128U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1016/S0021-9673(00)01030-X
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/NP000128U https://doi.org/10.1016/S0021-9673(00)01030-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1021/JF000661F
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/JF00070A001
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/S0021-9673(00)01030-X https://doi.org/10.1021/JF000661F https://doi.org/10.1021/JF00070A001 https://doi.org/10.1111/J.1365-2621.1986.TB11220.X https://doi.org/10.1021/JF0202234
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/JF00070A001 https://doi.org/10.1021/JF061058L https://doi.org/10.1089/JMF.2007.531 https://doi.org/10.1111/J.1365-2621.1967.TB00824.X https://doi.org/10.1016/S0021-9673(00)01030-X https://doi.org/10.1111/J.1365-2621.1986.TB11220.X https://doi.org/10.1021/JF000661F
Rhamnetin	5281691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1021/JF000661F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44256715	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1271/BBB.60023 https://doi.org/10.1021/JF0636014
Cyanidin 3-O-galactoside	441699	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1271/BBB.60023
Pelargonidin 3-galactoside ion	5320457	Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	433.40	unknown	https://doi.org/10.1271/BBB.60023
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	11520051	Click to see C1=CC(=CC=C1C=CC(=O)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	610.50	unknown	https://doi.org/10.1021/JF034970S
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	72992711	Click to see C1=CC(=CC=C1C=CC(=O)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	610.50	unknown	https://doi.org/10.1021/JF034970S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Phlorizin	6072	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	https://doi.org/10.1021/JF052035U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate	11563181	Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O	568.50	unknown	https://doi.org/10.1021/JF034970S
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate	73008082	Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O	568.50	unknown	https://doi.org/10.1021/JF034970S
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12304330	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/JF0202234
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one	5317364	Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	436.40	unknown	https://doi.org/10.1111/J.1365-2621.1967.TB00824.X https://doi.org/10.1021/JF0202234 https://doi.org/10.1021/JF020728U
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/JF034970S https://doi.org/10.1021/JF0202234
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/JF0202234 https://doi.org/10.1021/JF034970S
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one	74977625	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF034970S
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	101334147	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF034970S
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF020728U
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/JF0202234
Betmidin	14524429	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(O4)CO)O)O	450.30	unknown	https://doi.org/10.1021/JF0202234
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/JF034970S https://doi.org/10.1111/J.1365-2621.1967.TB00824.X https://doi.org/10.1021/JF020728U https://doi.org/10.1016/J.PLANTSCI.2004.06.001 https://doi.org/10.1021/JF0202234 https://doi.org/10.1021/JF061058L
Isoquercetin	5280804	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/JF034970S
Isorhamnetin 3-galactoside	13245586	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1021/JF0202234
isorhamnetin 3-O-beta-L-galactopyranoside	42433476	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1021/JF0202234
Myricetin 3-alpha-L-arabinofuranoside	14524431	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(O4)CO)O)O	450.30	unknown	https://doi.org/10.1021/JF0202234
Myricetin 3-arabinoside	21672568	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	450.30	unknown	https://doi.org/10.1021/JF0202234 https://doi.org/10.1111/J.1365-2621.1967.TB00824.X https://doi.org/10.1021/JF020728U
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/JF0202234
myricetin 3-O-beta-D-glucopyranoside	5318606	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/JF0202234
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/JF0202234
myricetin-3-O-beta-D-xylopyranoside	23900088	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	450.30	unknown	https://doi.org/10.1021/JF034970S
Myricetin-3-O-xyloside	21477996	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	450.30	unknown	https://doi.org/10.1021/JF034970S
Quercetin 3-xyloside	5321278	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/JF0202234
Quercetin-3-D-xyloside	5320863	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JF0202234
Quercetin-3-o-alpha-d-arabinofuranoside	11968848	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JF034970S
Quercetin-3-O-arabinoside	12309865	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JF034970S
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/10.1111/J.1365-2621.1967.TB00824.X https://doi.org/10.1016/J.PLANTSCI.2004.06.001 https://doi.org/10.1021/JF0202234
Reynoutrin	5878729	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JF034970S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4',5-Dihydroxy-7-glucosyloxyflavanone	124300887	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	https://doi.org/10.1021/JF052035U
Prunin	92794	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	https://doi.org/10.1021/JF052035U
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin	128861	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O	287.24	unknown	https://doi.org/10.1081/JLC-120027089
> Phenylpropanoids and polyketides / Stilbenes
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1021/JF010812U
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
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/10.1021/JF0636014

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Vaccinium macrocarpon

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