Scientific name	Authority	First published in
Boberella halimifolia	(Mill.) E.H.L.Krause	Deutschl. Fl. (Sturm), ed. 2, 10: 55. 1903
Jasminoides flaccidum	Moench	Methodus (Moench) 470. 1794 [4 May 1794]
Lycium barbarum	Mill.	Gard. Dict., ed. 8. n. 4. 1768 [16 Apr 1768]
Lycium barbarum var. auranticarpum	K.F.Ching	Fl. Reipubl. Popularis Sin. 67(1): 158. 1978
Lycium chinense var. turbinatum	(Loisel.) A.Terracc.	Malpighia 4: 515. 1891.
Lycium dunalianum	Bubani ex Dunal	Prodr. [A. P. de Candolle] 13(1): 509. 1852 [10 May 1852]
Lycium lanceolata	(Loisel.) A.Terracc.	A.Terracc. et al., Malpighia 4: 516. 1891., 1891.
Lycium halimifolium	Mill.	Gard. Dict., ed. 8. n. 6. 1768 [16 Apr 1768]
Lycium lanceolatum	Loisel.	Traité Arbr. Arbust. (Duhamel), nouv. éd. 1: 123. 1812?
Lycium turbinatum	Loisel.	Traité Arbr. Arbust. (Duhamel), nouv. éd. 1: 119. 1812?
Lycium turcomanicum	Miers	Ann. Mag. Nat. Hist. ser. 2, 14: 183. 1854 [Aug 1854]
Lycium vulgare	Dunal	Prodr. [A. P. de Candolle] 13(1): 509. 1852 [10 May 1852]
Lycium vulgare subsp. barbarum	(L.) A.Terracc.	Malpighia 4: 512. 1891.
Lycium turcomanica	(Miers) A.Terracc.	(S. ) A.Terracc., (M. ) A.Terracc., (D. ) A.Terracc., (M. ) A.Terracc., and (M. ) A.Terracc., Malpighia 4: 513. 1891., 1891.
Lycium europaeum f. lanceolata	(Loisel.) A.Terracc.
Lycium vulgare subf. turcomanica	(Miers) A.Terracc.

Common names Top

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Filter by language:

Language	Common/alternative name
English	matrimony vine
English	murali
English	barbary matrimony vine
English	chinese boxthorn
English	chinese wolfberry
English	duke of argyll's tea plant
English	duke of argyll's tea tree
English	himalayan goji
English	mede berry
English	red medlar
English	tibetan goji
English	goji berries
Spanish	goji
Spanish	teremis elliptica
Spanish	baya de goji
Spanish	baya del goji
Spanish	bayas de goji
Spanish	cambronera de berberia
Spanish	cambronera de berbería
Arabic	العوسج
Arabic	عوسج
Arabic	غرقد بربري
Azerbaijani	adi itiüzümü
Belarusian	козірог
Belarusian	ліцый звычайны
Tibetan	འཕང་འབྲས།
Catalan	arç negre
cdo	gēu-kī
Czech	kustovnice cizí
Welsh	ysbeinwydden hardd
Danish	goji
Danish	goji-bær
Danish	almindelig bukketorn
German	gewöhnlicher bocksdorn
German	bocksdorn
German	goji
German	gojibeere
German	gemeiner bocksdorn
Estonian	goji
Estonian	goji marjad
Estonian	teremis elliptica
Estonian	harilik taralõng
Persian	دیوخار
Finnish	aitapukinpensas
Finnish	pukinkoiso
Finnish	pukinpensas
French	lyciet
French	goji
French	baies de goji
French	gou qi zi
French	baie de goji
Galician	cambroeira chinesa
Galician	goxis
Hebrew	ברי, (ג'וז'י ברי או וולפברי)
Hebrew	גוג'י
Croatian	kustovnica
Hungarian	semfa
Hungarian	semfű
Hungarian	közönséges ördögcérna
Armenian	հազազ բերբերի
Japanese	寧波クコ
Japanese	寧波枸杞
Japanese	長葉クコ
Japanese	長葉枸杞
Japanese	ナガバクコ
jv	goji beri
Georgian	khvicha
Kabyle	awǧez
Korean	영하구기자
Lithuanian	dygliuotasis ožerškis
Macedonian	плетиплотка
Norwegian Bokmål	bukketorn
Dutch	boksdoorn
Dutch	bokdoorn
Dutch	goji bes
Dutch	goji-bes
Polish	goji
Polish	kolcowój pospolity
Portuguese	gǒuqǐ níngxià
Portuguese	goji
Romanian	goji
Romanian	cătina de garduri
Romanian	cătină de garduri
Russian	Волчья ягода
Russian	Дереза берберов
Russian	Дереза варварская
Russian	Дереза обыкновенная
Russian	ягода годжи
Russian	Лиций обыкновенный
Slovak	kustovnica cudzia
Slovenian	goji
Slovenian	navadna kustovnica
Serbian	Гоџи
Swedish	goji
Swedish	gojibär
Swedish	bocktörne
Thai	เก๋ากี้
Thai	เก๋ากี๋
Thai	โกจิเบอรี่
Thai	เก๋ากี่
ug	ئالقات
Ukrainian	дереза звичайна
Ukrainian	повій звичайний
Vietnamese	kỷ tử
za	gaeujgij
Chinese	枸杞
Chinese	地骨皮
Chinese	枸杞子
Chinese	宁夏枸杞
Chinese	中宁枸杞
Chinese	山枸杞
Chinese	津枸杞
Chinese	杞子
Chinese	津杞
Chinese	甘杞
Chinese	寧夏枸杞

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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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!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Mauritius

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Qinghai
  - Xinjiang
- Eastern Asia
  - Korea
- Middle Asia
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Nepal
- Indo-China
  - Vietnam

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - South Australia
  - Tasmania
  - Victoria

Europe click to expand
- Eastern Europe
  - Central European Russia
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Spain

Northern America click to expand
- Eastern Canada
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - 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.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
  - Nevada
  - Utah
- Western Canada
  - Alberta
  - British Columbia
  - Saskatchewan

Southern America click to expand
- Southern South America
  - Argentina South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001022663
UNII	81Z5L86W8G
Canadensys	9354
USDA Plants	LYBA4
Tropicos	29600019
INPN	106965
Flora of Italy	4694
KEW	urn:lsid:ipni.org:names:816356-1
The Plant List	kew-2499019
Open Tree Of Life	40038
Observations.org	7019
NCBI Taxonomy	112863
NBN Atlas	NBNSYS0000004032
Nature Serve	2.133162
IPNI	816356-1
iNaturalist	77902
GBIF	2928835
WisFlora	9037
EPPO	LYUHA
EOL	487010
Elurikkus	5594
Calflora (Californian flora)	5231
USDA GRIN	22939
Wikipedia	Lycium_barbarum
CMAUP	NPO23429
Plantarium	23448
Missouri Botanical Garden	369042

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
GCF_019175385.1	ASM1917538v2	Chromosome	Fujian Agriculture and Forestry University	2021-07-08	114.5x	1.55 Gb

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

Analysis and validation of biomarkers of immune cell-related genes in postmenopausal osteoporosis: An observational study

Chen L, Zhao Y, Qiu J, Lin X

Medicine (Baltimore)

10-May-2024

PMCID:	PMC11081595
doi:	10.1097/MD.0000000000038042
PMID:	38728482

Retraction: Lycium barbarum polysaccharide induced apoptosis and inhibited proliferation in infantile hemangioma endothelial cells via down-regulation of PI3K/AKT signaling pathway

N/A

Biosci Rep

08-May-2024

PMCID:	PMC11081942
doi:	10.1042/BSR-2019-1182_RET
PMID:	38716539

Acetylation proteomics and metabolomics analyses reveal the involvement of starch synthase undergoing acetylation modification during UV-B stress resistance in Rhododendron Chrysanthum Pall

Liu M, Sun L, Cao Y, Xu H, Zhou X

Hereditas

03-May-2024

PMCID:	PMC11067277
doi:	10.1186/s41065-024-00320-4
PMID:	38702800

Anti-Metastatic Effects of Standardized Polysaccharide Fraction from Diospyros kaki Leaves via GSK3β/β-Catenin and JNK Inactivation in Human Colon Cancer Cells

Lee WS, Shin JS, Jang SY, Chung KS, Kim SD, Cho CW, Hong HD, Rhee YK, Lee KT

Polymers (Basel)

03-May-2024

PMCID:	PMC11085380
doi:	10.3390/polym16091275
PMID:	38732748

Huaier Polysaccharide Alleviates Dextran Sulphate Sodium Salt-Induced Colitis by Inhibiting Inflammation and Oxidative Stress, Maintaining the Intestinal Barrier, and Modulating Gut Microbiota

Tang YF, Xie WY, Wu HY, Guo HX, Wei FH, Ren WZ, Gao W, Yuan B

Nutrients

30-Apr-2024

PMCID:	PMC11085394
doi:	10.3390/nu16091368
PMID:	38732614

Arbuscular Mycorrhizal Fungi Improve Lycium barbarum Potassium Uptake by Activating the Expression of LbHAK

Zhang Y, Han X, Ren W, Zhang H, Tang M

Plants (Basel)

30-Apr-2024

PMCID:	PMC11085931
doi:	10.3390/plants13091244
PMID:	38732459

Lung function benefits of traditional Chinese medicine Qiju granules against fine particulate air pollution exposure: a randomized controlled trial

Chen R, Zhang L, Gu W, Li R, Hong H, Zhou L, Zhang J, Wang Y, Ni P, Xu S, Wang Z, Sun Q, Liu C, Yang J

Front Med (Lausanne)

29-Apr-2024

PMCID:	PMC11089203
doi:	10.3389/fmed.2024.1370657
PMID:	38741765

Altitudinal variation of dragon fruit metabolite profiles as revealed by UPLC-MS/MS-based widely targeted metabolomics analysis

Zhao Z, Wang L, Chen J, Zhang N, Zhou W, Song Y

BMC Plant Biol

29-Apr-2024

PMCID:	PMC11057076
doi:	10.1186/s12870-024-05011-w
PMID:	38684949

Comparative metabolomics combined with genome sequencing provides insights into novel wolfberry-specific metabolites and their formation mechanisms

Long Q, Zhang C, Zhu H, Zhou Y, Liu S, Liu Y, Ma X, An W, Zhou J, Zhao J, Zhang Y, Jin C

Front Plant Sci

26-Apr-2024

PMCID:	PMC11082402
doi:	10.3389/fpls.2024.1392175
PMID:	38736439

Commodity risk assessment of Petunia spp. and Calibrachoa spp. unrooted cuttings from Kenya

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Lacomme C, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R

EFSA J

25-Apr-2024

PMCID:	PMC11044013
doi:	10.2903/j.efsa.2024.8742
PMID:	38665158

Effects of different nitrogen application rates and picking batches on the nutritional components of Lycium barbarum L. fruits

Liang X, An W, Li Y, Qin X, Zhao J, Su S

Front Plant Sci

24-Apr-2024

PMCID:	PMC11076786
doi:	10.3389/fpls.2024.1355832
PMID:	38721340

Editorial: Potential of the plant rhizomicrobiome for bioremediation of contaminants in agroecosystems

Bhandari G, Gangola S, Bhatt P, Rafatullah M

Front Plant Sci

22-Apr-2024

PMCID:	PMC11070560
doi:	10.3389/fpls.2024.1397360
PMID:	38711602

Unlocking the Power of Light on the Skin: A Comprehensive Review on Photobiomodulation

Hernández-Bule ML, Naharro-Rodríguez J, Bacci S, Fernández-Guarino M

Int J Mol Sci

19-Apr-2024

PMCID:	PMC11049838
doi:	10.3390/ijms25084483
PMID:	38674067

Active metabolites combination therapies: towards the next paradigm for more efficient and more scientific Chinese medicine

Gao Q, Wu H, Chen M, Gu X, Wu Q, Xie T, Sui X

Front Pharmacol

18-Apr-2024

PMCID:	PMC11063311
doi:	10.3389/fphar.2024.1392196
PMID:	38698817

Natural products in atherosclerosis therapy by targeting PPARs: a review focusing on lipid metabolism and inflammation

Zhang Y, Zhang XY, Shi SR, Ma CN, Lin YP, Song WG, Guo SD

Front Cardiovasc Med

18-Apr-2024

PMCID:	PMC11064802
doi:	10.3389/fcvm.2024.1372055
PMID:	38699583

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 / Tropane alkaloids
(+)-Hyoscyamine	637577	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) (2R)-3-hydroxy-2-phenylpropanoate	25817	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
Atropine	174174	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1055/S-0029-1186218
Hyoscyamine	154417	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
L-Hyoscyamine	64692	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
L-Hyoscyamine	3661	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-hydroxy-3-methoxy-6-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione	5320543	Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(=O)C5=C(C2=O)C=C(C=C5O)OC	608.50	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives
1,2,3,5-Tetramethylbenzene	10695	Click to see CC1=CC(=C(C(=C1)C)C)C	134.22	unknown	via CMAUP database
Benzaldehyde, oxime, (Z)-	5324470	Click to see C1=CC=C(C=C1)C=NO	121.14	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[5,9-Dihydroxy-6,20,22-trimethoxy-17-(methoxymethyl)-10,14-dimethyl-14-azahexacyclo[9.9.2.12,5.01,12.03,10.017,21]tricosan-4-yl] benzoate	53399238	Click to see CC12C(CCC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CCC7(C5C(C2C6CN(CC7)C)OC)COC)OC)O)OC)O	627.80	unknown	via CMAUP database
> 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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxysalicylic acid	75231	Click to see COC1=CC(=C(C=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	via CMAUP database
> Benzenoids / Naphthalenes
1-Methylnaphthalene	7002	Click to see CC1=CC=CC2=CC=CC=C12	142.20	unknown	via CMAUP database
2-Methylnaphthalene	7055	Click to see CC1=CC2=CC=CC=C2C=C1	142.20	unknown	via CMAUP database
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Dihydro-N-Caffeoyltyramine	16119668	Click to see C1=CC(=CC=C1CCNC(=O)CCC2=CC(=C(C=C2)O)O)O	301.34	unknown	via CMAUP database
Kukoamine B	10346914	Click to see C1=CC(=C(C=C1CCC(=O)NCCCNCCCCN(CCCN)C(=O)CCC2=CC(=C(C=C2)O)O)O)O	530.70	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane	15600	Click to see CCCCCCCCCC	142.28	unknown	via CMAUP database
Dodecane	8182	Click to see CCCCCCCCCCCC	170.33	unknown	via CMAUP database
Tetradecane	12389	Click to see CCCCCCCCCCCCCC	198.39	unknown	via CMAUP database
Tridecane	12388	Click to see CCCCCCCCCCCCC	184.36	unknown	via CMAUP database
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2,2,4,6,6-Pentamethylheptane	26058	Click to see CC(CC(C)(C)C)CC(C)(C)C	170.33	unknown	via CMAUP database
2,3,5,8-Tetramethyldecane	545611	Click to see CCC(C)CCC(C)CC(C)C(C)C	198.39	unknown	via CMAUP database
3-Methylnonane	22202	Click to see CCCCCCC(C)CC	142.28	unknown	via CMAUP database
3-Methyltridecane	110848	Click to see CCCCCCCCCCC(C)CC	198.39	unknown	via CMAUP database
3-Methylundecane	13845	Click to see CCCCCCCCC(C)CC	170.33	unknown	via CMAUP database
4-Methylundecane	520454	Click to see CCCCCCCC(C)CCC	170.33	unknown	via CMAUP database
5-Ethyldecane	529848	Click to see CCCCCC(CC)CCCC	170.33	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2-Ethyl-1-decene	550798	Click to see CCCCCCCCC(=C)CC	168.32	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Dodecene	8183	Click to see CCCCCCCCCCC=C	168.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2,3-Dimethylacrylic acid, (E)-	125468	Click to see CC=C(C)C(=O)O	100.12	unknown	via CMAUP database
2,3-Dimethylacrylic acid, (Z)-	643915	Click to see CC=C(C)C(=O)O	100.12	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
12-Octadecenoic acid	5282762	Click to see CCCCCC=CCCCCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
cis-12-Octadecenoic acid	446285	Click to see CCCCCC=CCCCCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
Octadec-12-enoic acid	151512	Click to see CCCCCC=CCCCCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[4-(2,4-Dihydroxy-2,6,6-trimethylcyclohexylidene)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	14846177	Click to see CC(C=C=C1C(CC(CC1(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	https://doi.org/10.1016/S0040-4039(00)97106-5
2-o-beta-d-Glucopyranosyl-l-ascorbic acid	54706833	Click to see C(C1C(C(C(C(O1)OC2=C(C(OC2=O)C(CO)O)O)O)O)O)O	338.26	unknown	https://doi.org/10.1021/JF035445W
AA-2betaG	54725703	Click to see C(C1C(C(C(C(O1)OC2=C(C(OC2=O)C(CO)O)O)O)O)O)O	338.26	unknown	https://doi.org/10.1021/JF035445W
CID 101017493	101017493	Click to see CC(C=C=C1C(CC(CC1(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O	388.50	unknown	https://doi.org/10.1016/S0040-4039(00)97106-5
> 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	via CMAUP database
(3R)-octan-3-ol	445789	Click to see CCCCCC(CC)O	130.23	unknown	via CMAUP database
(S)-(+)-3-Octanol	6999002	Click to see CCCCCC(CC)O	130.23	unknown	via CMAUP database
(S)-1-Octen-3-ol	2724898	Click to see CCCCCC(C=C)O	128.21	unknown	via CMAUP database
1-Heptanol	8129	Click to see CCCCCCCO	116.20	unknown	via CMAUP database
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	via CMAUP database
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	via CMAUP database
1-Octen-3-Ol	18827	Click to see CCCCCC(C=C)O	128.21	unknown	via CMAUP database
3-Octanol	11527	Click to see CCCCCC(CC)O	130.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid	3931	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
9,12-Octadecadienoic acid, (E,Z)-	5282798	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
9,12,15-Octadecatrienoic acid	860	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
9Z,12E-octadecadienoic acid	5282797	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Elaidolinolenic acid	5282822	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
Linoelaidic acid	5282457	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / 3-O-beta-D-digalactosyl-sn-glycerols
[(2S,3R,4S,5S,6R)-2-[[(2R,3R,4S,5R,6R)-6-[(2S)-3-hexadecanoyloxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]oxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate	102031334	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCC=CCC=CCC=CCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1175.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S,3R,4S,5S,6R)-2-[[(2R,3R,4S,5R,6R)-6-[(2S)-3-hexadecanoyloxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]oxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (9Z,12Z)-octadeca-9,12-dienoate	102031332	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1177.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] (Z)-nonadec-9-enoate	162934539	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCCC	933.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-6-[[(2S,3R,4S,5S,6R)-4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropan-2-yl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate	102031331	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1153.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-6-[[(2S,3R,4S,5S,6R)-4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropan-2-yl] (9Z,12Z)-octadeca-9,12-dienoate	102031333	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	1155.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-2-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-6-[[(2S,3R,4S,5S,6R)-4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropyl] hexadecanoate	102092528	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC	1131.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
Dgdg	57400365	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	937.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
Digalactosyldiacylglycerol	10724471	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	917.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2S)-1-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] (9Z,12Z)-octadeca-9,12-dienoate	132506182	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)COC(=O)CCCCCCCC=CCC=CCC=CCC	939.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate	101684924	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	753.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (9Z,12Z)-octadeca-9,12-dienoate	101986482	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	755.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate	10843454	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	915.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadecanoate	10701056	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	945.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[(2S)-2-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] hexadecanoate	51035390	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC	893.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] nonadec-9-enoate	163038432	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCCC	771.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] octadeca-9,12-dienoate	74381412	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	755.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] octadeca-9,12,15-trienoate	74382274	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	753.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] nonadec-9-enoate	162934538	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCCC	933.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[6-[[4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropan-2-yl] octadeca-9,12-dienoate	162849514	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	1155.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Hexadecanoyloxy-3-[6-[[4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropan-2-yl] octadeca-9,12,15-trienoate	163080050	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1153.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[1-Octadeca-9,12,15-trienoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] octadeca-9,12-dienoate	25203629	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)COC(=O)CCCCCCCC=CCC=CCC=CCC	939.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[2-[[6-(3-Hexadecanoyloxy-2-octadeca-9,12,15-trienoyloxypropoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] octadeca-9,12-dienoate	162906078	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1177.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[2-[[6-(3-Hexadecanoyloxy-2-octadeca-9,12,15-trienoyloxypropoxy)-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] octadeca-9,12,15-trienoate	162846464	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCC=CCC=CCC=CCC)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	1175.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[2-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] hexadecanoate	15608207	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC	893.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[2-Octadeca-9,12-dienoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadecanoate	25202928	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	945.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
[2-Octadeca-9,12,15-trienoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadeca-9,12,15-trienoate	25200977	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	937.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
CID 85229953	85229953	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)OC(=O)CCCCCCCCCCCCCCC)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC	1131.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (Z)-nonadec-9-enoate	163038433	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCCC	771.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
6,10-Dimethylundeca-5,9-dien-2-one	19633	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	via CMAUP database
Geranylacetone	1549778	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	via CMAUP database
Nerylacetone	1713001	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-{[5-Methyl-2-(propan-2-yl)cyclohexyl]oxy}-4-oxobutanoate	18676664	Click to see CC1CCC(C(C1)OC(=O)CCC(=O)[O-])C(C)C	255.33	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Monomenthyl succinate	10199004	Click to see CC1CCC(C(C1)OC(=O)CCC(=O)O)C(C)C	256.34	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5-Methoxy-3,3,7b-trimethyl-1,1a,2,4,4a,6,7,7a-octahydrocyclopropa[e]azulen-5-yl)methanol	73819953	Click to see CC1(CC2CC2(C3CCC(C3C1)(CO)OC)C)C	252.39	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
CID 46173863	46173863	Click to see CC1=CCCC2(C(O2)C(=O)C3=C(C1)OC=C3C)C	246.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	6433159	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	25245095	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
(1S)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	448437	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
1,5,5-trimethyl-6-[(1E,3Z,5Z,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-7-oxabicyclo[4.1.0]heptan-3-ol	5316151	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C	568.90	unknown	via CMAUP database
4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-2-en-1-ol	5368396	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
4-[18-(4-Hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	181579	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
all-trans-Neoxanthin	5281247	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=C=C1C(CC(CC1(C)O)O)(C)C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C	600.90	unknown	via CMAUP database
Beta, e-carotene-3, 3'-diol	102514741	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
Cryptoxanthin	5281235	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	552.90	unknown	via CMAUP database
Lutein	5281243	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
Physalien	5281250	Click to see CCCCCCCCCCCCCCCC(=O)OC1CC(=C(C(C1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)OC(=O)CCCCCCCCCCCCCCC)C)C)C)C	1045.70	unknown	via CMAUP database
Zeaxanthin	5280899	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	568.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Acetic acid, (Z)-	9904352	Click to see CCN1C(=CC(=O)OCC)SC(C1=O)N2CCCCC2	298.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
D-ornithine	71082	Click to see C(CC(C(=O)O)N)CN	132.16	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-2,5-diaminopentanoate;hydron	88747248	Click to see [H+].C(CC(C(=O)[O-])N)CN	132.16	unknown	via CMAUP database
(E,2S)-2-amino-4-[(R)-methylsulfinyl]but-3-enoic acid	56932118	Click to see CS(=O)C=CC(C(=O)O)N	163.20	unknown	via CMAUP database
L-ornithinium(1+)	59565831	Click to see C(CC(C(=O)O)N)C[NH3+]	133.17	unknown	via CMAUP database
L-ornithinium(2+)	449468	Click to see C(CC(C(=O)O)[NH3+])C[NH3+]	134.18	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(2S)-2-ammonio-4-(methylsulfanyl)butanoate	6992087	Click to see CSCCC(C(=O)[O-])[NH3+]	149.21	unknown	via CMAUP database
2-Azaniumyl-4-methylsulfanylbutanoate	5255805	Click to see CSCCC(C(=O)[O-])[NH3+]	149.21	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
L-Phenylalanine, 23	57397115	Click to see C1=CC=C(C=C1)CC(C(=O)[O-])[NH3+]	165.19	unknown	via CMAUP database
Phenylalanine	6140	Click to see C1=CC=C(C=C1)CC(C(=O)O)N	165.19	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Aminobutanoate	6992099	Click to see C(CC(=O)[O-])C[NH3+]	103.12	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Lyciumin C	44584331	Click to see CC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CC2=CN(C(C(=O)N1)NC(=O)C(CC3=CC=C(C=C3)O)NC(=O)C4CCCN4C(=O)C5CCC(=O)N5)C6=CC=CC=C26)C(=O)OC)CO)CC7=CC=CC=C7	978.10	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(R)-Ethyl 2-hydroxypropanoate	637513	Click to see CCOC(=O)C(C)O	118.13	unknown	via CMAUP database
ethyl (2S)-2-hydroxypropanoate	92831	Click to see CCOC(=O)C(C)O	118.13	unknown	via CMAUP database
Ethyl Lactate	7344	Click to see CCOC(=O)C(C)O	118.13	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Hydron;acetate	21980959	Click to see [H+].CC(=O)[O-]	60.05	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[3,4,5-Triacetyloxy-6-[4-(4-acetyloxy-2-hydroxy-2,6,6-trimethylcyclohexylidene)but-3-en-2-yloxy]oxan-2-yl]methyl acetate	14846179	Click to see CC(C=C=C1C(CC(CC1(C)O)OC(=O)C)(C)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	598.60	unknown	https://doi.org/10.1016/S0040-4039(00)97106-5
CID 162945599	162945599	Click to see CC(C=C=C1C(CC(CC1(C)O)OC(=O)C)(C)C)OC2C(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	598.60	unknown	https://doi.org/10.1016/S0040-4039(00)97106-5
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid	1060	Click to see CC(=O)C(=O)O	88.06	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see C(CS(=O)(=O)O)N	125.15	unknown	via CMAUP database
> Organic oxygen compounds / Organic oxides
beta-Cyclocitral	9895	Click to see CC1=C(C(CCC1)(C)C)C=O	152.23	unknown	via CMAUP database
Safranal	61041	Click to see CC1=C(C(CC=C1)(C)C)C=O	150.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,4-Dicaffeoylquinic acid	12358846	Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	via CMAUP database
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	via CMAUP database
cis-Chlorogenic acid	1794425	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	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2S,3S)-butane-2,3-diol	439888	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
(R,R)-2,3-butanediol	225936	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
2,3-Butanediol	262	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol	6276	Click to see CCCCCO	88.15	unknown	via CMAUP database
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]hexadeca-1,3,5,7,9,11,13,15-octaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	29921731	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC=CC=CC=CC=CC=CC=CC=CC2=C(CC(CC2(C)C)O)C	486.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin	440936	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Amylose	871	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O	504.40	unknown	https://doi.org/10.1016/J.EXGER.2005.06.010
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin	753	Click to see C(C(CO)O)O	92.09	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(R)-acetoin	439314	Click to see CC(C(=O)C)O	88.11	unknown	via CMAUP database
Acetoin	179	Click to see CC(C(=O)C)O	88.11	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde	11552	Click to see CC(C)CC=O	86.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hepten-1-al	17167	Click to see CCCCC=CC=O	112.17	unknown	via CMAUP database
2-Heptenal	5283316	Click to see CCCCC=CC=O	112.17	unknown	via CMAUP database
2-Heptenal, (Z)-	5362616	Click to see CCCCC=CC=O	112.17	unknown	via CMAUP database
Heptanal	8130	Click to see CCCCCCC=O	114.19	unknown	via CMAUP database
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	via CMAUP database
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
Octanal	454	Click to see CCCCCCCC=O	128.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylfuran	14505	Click to see CC(=O)C1=CC=CO1	110.11	unknown	via CMAUP database
2-Acetylpyrrole	14079	Click to see CC(=O)C1=CC=CN1	109.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(4aS,7R)-4a-methyl-7-prop-1-en-2-yl-5,6,7,8-tetrahydronaphthalen-2-one	15726782	Click to see CC(=C)C1CCC2(C=CC(=O)C=C2C1)C	202.29	unknown	via CMAUP database
(R)-2,2,6-Trimethylcyclohexanone	6999893	Click to see CC1CCCC(C1=O)(C)C	140.22	unknown	via CMAUP database
(S)-2,2,6-Trimethylcyclohexanone	6992946	Click to see CC1CCCC(C1=O)(C)C	140.22	unknown	via CMAUP database
2,2,6-Trimethylcyclohexane-1,4-dione	30181	Click to see CC1CC(=O)CC(C1=O)(C)C	154.21	unknown	via CMAUP database
2,2,6-Trimethylcyclohexanone	17000	Click to see CC1CCCC(C1=O)(C)C	140.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	via CMAUP database
Methoxyacetone	22172	Click to see CC(=O)COC	88.11	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2-Isobutyl-3,5,6-trimethylpyrazine	521191	Click to see CC1=C(N=C(C(=N1)C)CC(C)C)C	178.27	unknown	via CMAUP database
2,3,5-Trimethylpyrazine	26808	Click to see CC1=CN=C(C(=N1)C)C	122.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones
2-Methyltetrahydrofuran-3-one	18522	Click to see CC1C(=O)CCO1	100.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran	19602	Click to see CCCCCC1=CC=CO1	138.21	unknown	via CMAUP database
5-Methylfurfuryl alcohol	520911	Click to see CC1=CC=C(O1)CO	112.13	unknown	via CMAUP database
Furfuryl alcohol	7361	Click to see C1=COC(=C1)CO	98.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
(-)-beta-Butyrolactone	6998969	Click to see CC1CC(=O)O1	86.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
gamma-Butyrolactone	7302	Click to see C1CC(=O)OC1	86.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide	936	Click to see C1=CC(=CN=C1)C(=O)N	122.12	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(e)-N-(2-hydroxy-2-(4-hydroxyphenyl) ethyl)-3-(3-hydroxy-4-methoxyphenyl)acrylamide	70681748	Click to see COC1=C(C=C(C=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	via CMAUP database
(E)-N-[(2S)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide	10042201	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	via CMAUP database
Cis-N-Feruloyloctopamine	68976271	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	via CMAUP database
N-Caffeoyltyramine	9994897	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O	299.32	unknown	via CMAUP database
Tamgermanetin	11289949	Click to see COC1=C(C=C(C=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
> 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	via CMAUP database
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
cis-p-Coumaric acid	1549106	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrochromen-2-one	11953803	Click to see COC1=C(C=C2C(=C1)CCC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	356.32	unknown	via CMAUP database
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin	3083616	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC	222.19	unknown	via CMAUP database
Isoscopoletin	69894	Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
> 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	via CMAUP database
Quercetin-7-olate	46906036	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O	301.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550363/
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550363/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	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://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550363/
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	45933931	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)OC)O)O)O)O)O)O	624.50	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-glucopyranoside	17751019	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)OC)O)O)O)O)O)O	624.50	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	20055286	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	594.50	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	24211973	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	594.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	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	594.50	unknown	via CMAUP database
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550363/
Narcissin	5481663	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)OC)O)O)O)O)O)O	624.50	unknown	via CMAUP database
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550363/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	163188021	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)OC6C(C(C(C(O6)CO)OC(=O)C=CC7=CC=C(C=C7)O)O)O)O)CO)O	772.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.09.002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dihydroxyphenyl)propionic acid	348154	Click to see C1=CC(=C(C=C1CCC(=O)O)O)O	182.17	unknown	via CMAUP database

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Lycium barbarum

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