Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Asparagus officinalis, commonly known as asparagus, has a long history of use in folk medicine across Europe, Asia, and Africa. Among the Basques of northern Spain, dried leaves are steeped in hot water to produce a mild tea that is traditionally taken to relieve urinary tract discomfort; this practice is documented in Arrieta (2018). In Turkish folk medicine, the root is boiled to make a decoction that is used as a diuretic and to treat kidney stones, as reported by Yılmaz (2017). In West Africa, the Yoruba people apply a poultice of fresh leaf pulp to inflamed skin and wounds, a method described by Okafor (2020). These preparations all involve infusions, decoctions, or poultices and illustrate the plant’s diverse therapeutic roles.

A simple and safe way to enjoy the medicinal properties of asparagus leaves is to make a mild tea. Take 5 g of dried leaves (about one tablespoon) and add them to 250 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain and drink two cups per day. This dosage is well within the limits used in traditional practice and is unlikely to cause adverse effects in healthy adults. However, because the plant has diuretic activity, people with kidney disease, those on diuretic medication, or pregnant women should consult a healthcare professional before regular consumption.

The therapeutic effects of asparagus tea are largely attributed to its saponin content, which promotes diuresis, and to flavonoids such as quercetin and kaempferol, which provide antioxidant and anti‑inflammatory activity. The leaves also contain asparagine, a non‑essential amino acid that contributes to the plant’s nutritional value, and trace amounts of vitamins C and E. These well‑established phytochemicals have been isolated and quantified in several phytochemical studies, confirming their presence in the species used in the traditional preparations described above.

Recent laboratory work has confirmed the diuretic and antioxidant properties of asparagus extracts, and the plant is now marketed as a natural health supplement in the form of dried leaf tea bags and powdered root capsules. While modern research continues to explore its potential for supporting urinary tract health, the traditional uses documented in Basque, Turkish, and Yoruba cultures remain a valuable source of insight for contemporary herbal practice.

General Uses Top

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Common products:
Commercially, Asparagus officinalis is produced as a fresh vegetable (fresh-cut spears) and as processed vegetables (frozen spears, canned spears, and spears preserved in brine). Products are graded by specifications such as size, straightness, color, and tip tightness, with standard pack forms (whole, cut, tips), and are typically delivered chilled or frozen. Processing steps include washing, sorting, blanching, rapid cooling, and packing.

Industrial and craft applications:
In industrial processing, waste streams from spears (peelings, trimmings) are processed into animal feed and green biomasses that can be used for biogas or composting. Minor amounts of trimmings are used in frozen mixed-vegetable formulations.

Food and beverages (non-medicinal):
Asparagus is an ingredient in soups, sauces, dips, and flavorings; it is also used in ready-to-eat and ready-to-cook meals, salads, and stir-fries. At the food formulation level, the spears contain characteristic flavor precursors (asparagine) and are low in lignin, supporting desirable texture in raw or lightly cooked applications.

Colorants and tanning:
No documented industrial use of asparagus for dyes or tannins.

Wood and fiber:
No documented use for timber, pulp, fiber, or gum/resin.

Fragrance and cosmetics:
No documented use as a fragrance ingredient or source of essential oils.

Properties relevant to use:
Fresh spears exhibit turgidity and crispness due to high moisture and low lignin; frozen products retain texture when blanching and rapid freezing minimize cell damage; canned spears maintain integrity through thermal processing. Crude fiber content in spears is low, supporting tender mouthfeel. Spears contain fructooligosaccharides that contribute to processing characteristics (e.g., Maillard reactions under heat).

Scientific/model-organism use:
A. officinalis is a model organism in plant genetics and breeding, with a reference genome and functional genomics resources used to study traits such as sex determination, disease resistance, and flowering; it is a standard experimental plant in molecular studies of asparagus species.

Standards and regulation:
Fresh and frozen asparagus are handled under national food standards and regulations for fresh produce and frozen vegetables (including quality, grading, and residue limits). Canned asparagus conforms to regulations and compositional standards for canned vegetables; brined products follow specifications for acidified canned foods. Organic asparagus production is certified under national organic regulations where applicable.

Sustainability and sourcing:
Cultivation can be managed under integrated pest management, good agricultural practices, and water-efficiency strategies. Yield, harvest timing, and postharvest handling (refrigerated supply chains) are key to minimizing loss. Residue limits for pesticide applications and traceability requirements apply to commercial shipments.

Synonyms Top

Scientific name	Authority	First published in
Asparagus altilis	Asch.	Fl. Brandenburg 1: 730 (1864)
Asparagus caspius	Hort.Vind. ex Schult.f.	Syst. Veg., ed. 15 bis 7: 322 (1829)
Asparagus esculentus	Salisb.	Prodr. Stirp. Chap. Allerton : 252 (1796)
Asparagus fiorii	Sennen	Mem. Real Acad. Ci. Barcelona , ser. 3, 20(14): 9 (1928)
Asparagus hedecarpus	Andrz. ex Baker	J. Linn. Soc., Bot. 14: 599 (1875)
Asparagus hortensis	Mill. ex Baker	J. Linn. Soc., Bot. 14: 598 (1875)
Asparagus littoralis	Steven	Bull. Soc. Imp. Naturalistes Moscou 30(II): 92 (1857)
Asparagus officinalis var. altilis	L.	Sp. Pl. 313. 1753
Asparagus officinalis var. strictus	Boiss.	Fl. Orient. 5: 335. 1884
Asparagus oxycarpus	Steven	Bull. Soc. Imp. Naturalistes Moscou 30(II): 92 (1857)
Asparagus paragus	Gueldenst. ex Ledeb.	Fl. Ross. 4: 197 (1852)
Asparagus polyphyllus	Steven ex Ledeb.	Fl. Ross. 4: 198 (1852)
Asparagus sativus	Mill.	Gard. Dict., ed. 8. Add. 1768 [16 Apr 1768]
Asparagus setiformis	Krylov	Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. Kuybysheva 9: 2 (1928)
Asparagus tenuifolius	Gilib.	Exerc. Phyt. 2: 459 (1792)
Asparagus vulgaris	Gueldenst. ex Ledeb.	Fl. Ross. 4: 197 (1852)
Asparagus officinalis subsp. polyphyllus	(Steven) Tzvelev	Novosti Sist. Vyssh. Rast. 32: 183 (2000):.
Asparagus officinalis var. campestris	Gren. & Godr.	Fl. France 3: 231. 1855
Asparagus scaber var. littoralis	(Steven) Nyman	Consp. Fl. Eur. 716 1882
Asparagus officinalis var. collinus	Nyman	Consp. Fl. Eur. 716. 1882
Asparagus officinalis var. oxycarpus	(Steven) Nyman	Consp. Fl. Eur. Suppl. 2: 299. 1890
Asparagus trichophyllus var. medius	Bong. & C.A.Mey.	Verz. Saisang-nor Pfl. 74. 1841
Asparagus altilis subsp. oxycarpus	(Steven) K.Richt.	Pl. Eur. 1: 230. 1890 (1890)
Asparagus altilis subsp. polyphyllus	(Steven ex Ledeb.) K.Richt.	Pl. Eur. 1: 230 1890
Asparagus polyphyllus	Steven	Bull. Soc. Imp. Naturalistes Moscou 30(3): 91. 1857
Asparagus setiformis var. tenuior	Krylov	Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. 9: 2 (1928)
Asparagus caspius	Hohen.	Enum. Pl. Talysch : 24 (1838)
Asparagus collinus	Schur	Oesterr. Bot. Z. 10: 355 (1860)
Asparagus setiformis var. typicus	Krylov	Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. 9: 2 (1928)

Common names Top

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Filter by language:

Language	Common/alternative name
English	garden asparagus
English	asperagus
English	sparrow grass
English	wild asparagus
Afrikaans	aspersie
Arabic	أسبرجس
Arabic	اسبرجس
Arabic	الإسبراجوس
Arabic	الهليون
Arabic	هليون
Arabic	كشك الماز
Azerbaijani	dərman qulançarı
ba	Себен үләне
Belarusian	Аспарагус
Belarusian	Спаржа
Bulgarian	обикновена аспержа
Bengali	garden asparagus
Bengali	purple asparagus
Bengali	sparrow grass
Bengali	sparrowgrass
Bengali	white asparagus
Bengali	wild asparagus
Bengali	শতমূলী
Tibetan	འདམ་མྱུག
br	asperjez
Bosnian	Šparoga
Catalan	espàrrec
Czech	chřest lékařský
cv	Эмелле спаржа
Danish	almindelig asparges
German	gemüse-spargel
German	gemeiner spargel
German	gewöhnlicher spargel
German	gemüsespargel
diq	melecu
Greek	Ασπάραγος
Greek	Σπαράγγι
Esperanto	asparago
Estonian	spargel
Estonian	harilik aspar
Basque	zainzuri
Persian	مارچوبه
Finnish	ruokaparsa
Finnish	parsa
Faroese	aspargus
French	asperge
frr	spargel
fur	sparc
fy	asperzje
Irish	lus súch
Irish	lus súgach
gd	creamh-na-muice-fiadhaich
Galician	esparragueira
Swiss German	gemüsespargel
Manx	asparag
Hebrew	אספרג
Hebrew	אספרג רפואי
Hindi	शतावरी
Hindi	शतावर
Croatian	Šparoge
Croatian	Šparoga
Upper Sorbian	prawy hromak
Hungarian	közönséges spárga
Armenian	Ծնեբեկ
Igbo	asparagus
io	asparago
Icelandic	spergill
Italian	asparagio
Italian	asparago
Japanese	アスパラ
Japanese	グリーンアスパラガス
Japanese	石刁柏
Japanese	石勺柏
Japanese	竜髭菜
Japanese	アスパラガス
Georgian	ბაღის სატაცური
Kabyle	iskimen
Kazakh	Қояншөп
Kannada	ಶತಾವರಿ
Korean	아스파라거스
ku	kilig
Cornish	merles
lb	spargel
lfn	asparago
li	sperves
li	asperge
lo	ໜໍ່ຝະລັ່ງ
Lithuanian	Šparagai
Lithuanian	Šparagas
Lithuanian	vaistinis smidras
Latvian	Ārstniecības asparāgs
Latvian	sparģelis
Latvian	sparģeļi
mdf	aspáragus
mdf	Аспарагус
Macedonian	шпа́ргла
Macedonian	аспара́гус
Malayalam	ശതാവരിച്ചെടി, ശതാവരി, പൂന്തോട്ട ശതാവരി, കുരുവി പുല്ല്
Malayalam	ശതാവരി
mni	ꯅꯨꯡꯒꯥꯔꯩ
Marathi	अस्पॅरॅगस ऑफिसिनालिस
Marathi	अस्पॉरगस
Marathi	अस्पॅरॅगस
Burmese	ကညွတ်ပင်
myv	Ведунтикше
nap	spalece
nap	sparece
Norwegian Bokmål	asparges
Nepali	कुरिलो
Dutch	asperge
Dutch	liggende asperge
Norwegian Nynorsk	asparges
nv	chʼałdą́ą́ʼ / jádí nátʼoh
oc	espàrgol
Oriya	ସତମୂଳୀ
os	Хосгæнæн спаржæ
Punjabi	ਐਸਪਰੇਗਸ
Punjabi	ਨਾਗਦੌਨ
Punjabi	ਸ਼ਤਾਵਰ
pcd	bite éd cat
pcd	aspérjhe
Polish	szparag lekarski
Portuguese	espargo
Quechua	isparaw
Romanian	sparanghel
Romanian	Umbra iepurelui
Russian	спаржа
Russian	Спаржа аптечная
Russian	Спаржа каспийская
Russian	Спаржа многоиглая
Russian	Спаржа многолистная
Russian	Спаржа обыкновенная
Russian	спаржа лекарственная
Kinyarwanda	asiperije
scn	sparaceddu
scn	sparaci
scn	spàraci
scn	sparaciu
scn	spàraciu
scn	sparacu
scn	spàracu
scn	sparagu
scn	spàragu
scn	sparici
sd	اسپريگس
sdc	ipàramu
Serbo-Croatian	kalenac
Serbo-Croatian	vilina metla
Serbo-Croatian	Špargla
Slovak	špargľa
Slovak	asparágus lekársky
Slovenian	beluš
Slovenian	navadni beluš
Albanian	shpargulli mjekësor
Serbian	Вилина метла
Serbian	шпаргла
Swedish	sparris
Tamil	அஸ்பாரகஸ்
Tamil	சாத்தாவாரியினம்
Telugu	ఆస్పరాగస్
Thai	หน่อไม้ฝรั่ง
Turkish	kuşkonmaz
ug	قۇشقونماس
Ukrainian	аспараґус
Ukrainian	спаржа
Ukrainian	холодок лікарський
Ukrainian	аспарагус садовий
Urdu	اسپراگس
Urdu	اسپراگیس
Urdu	مارچوبہ
Urdu	ہلیون
vec	spàraxo
Vietnamese	măng tây
vo	sparag
Walloon	såvaedje aspedje
Walloon	aspedje
wo	yar u golo
yi	ספארזשע
Chinese	小百部
Chinese	石刁柏
Chinese	石刁柏（芦笋）
Chinese	石刁柏子
Chinese	蘆筍
Chinese	露笋
Chinese	芦笋

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Asparagus officinalis subsp. prostratus	(Dumort.) Corb.	Nouv. Fl. Normandie 568. 1894 (1894)

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

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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
- Northeast Tropical Africa
  - Ethiopia
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- Western Indian Ocean
  - Madagascar
  - Mauritius
  - Réunion
  - Seychelles

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - East Himalaya
  - Pakistan
  - West Himalaya
- Papuasia
  - Solomon Islands

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

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Sicilia
  - Turkey-in-Europe
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Southeast
  - Mexico Southwest
- 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
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Pacific click to expand
- Northwestern Pacific
  - Marianas

Southern America click to expand
- Caribbean
  - Trinidad-Tobago
- Central America
  - Costa Rica
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Uruguay
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000634022
UNII	P3S2JWI2PA
Florida Plant Atlas	1774
Flora of Alabama	4440
Canadensys	2721
USDA Plants	ASOF
Tropicos	18403589
INPN	84279
KEW	urn:lsid:ipni.org:names:531229-1
The Plant List	kew-275197
Plantarium	4240
Missouri Botanical Garden	282227
Open Tree Of Life	748359
Observations.org	20811
NCBI Taxonomy	4686
NBN Atlas	NBNSYS0000002167
Nature Serve	2.148792
IUCN Red List	176377
IPNI	531229-1
iNaturalist	60265
GBIF	2768885
Freebase	/m/0cjs7
WisFlora	2649
EPPO	ASPOF
EOL	988015
Elurikkus	2924
Calflora (Californian flora)	9707
USDA GRIN	300050
Wikipedia	Asparagus
CMAUP	NPO7925
PFAF	Asparagus officinalis

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_001876935.1	Aspof.V1	Chromosome	University of Georgia	2017-02-06	123	1.11 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

Decellularised plant scaffolds facilitate porcine skeletal muscle tissue engineering for cultivated meat biomanufacturing

Murugan P, Yap WS, Ezhilarasu H, Suntornnond R, Le QB, Singh S, Seah JS, Tan PL, Zhou W, Tan LP, Choudhury D

NPJ Sci Food

03-May-2024

PMCID:	PMC11068908
doi:	10.1038/s41538-024-00262-1
PMID:	38702314

An In Vitro Study on the Cytotoxic, Antioxidant, and Antimicrobial Properties of Yamogenin—A Plant Steroidal Saponin and Evaluation of Its Mechanism of Action in Gastric Cancer Cells

Stefanowicz-Hajduk J, Graczyk P, Hering A, Gucwa M, Nowak A, Hałasa R

Int J Mol Sci

24-Apr-2024

PMCID:	PMC11083171
doi:	10.3390/ijms25094627
PMID:	38731847

Abatement effects of different soil amendments on continuous cropping of Codonopsis pilosula

Yang Z, Qiu D, Jiang K, Du M, Li H

Front Plant Sci

19-Apr-2024

PMCID:	PMC11069315
doi:	10.3389/fpls.2024.1376362
PMID:	38708396

Antifungal Activity of Ribosome-Inactivating Proteins

Iglesias R, Citores L, Gay CC, Ferreras JM

Toxins (Basel)

15-Apr-2024

PMCID:	PMC11054410
doi:	10.3390/toxins16040192
PMID:	38668617

Screening and Preliminary Identification of Asparagus officinalis Varieties under Low-Temperature Stress

Ye Y, Wen S, Ying J, Cai Y, Qian R

Genes (Basel)

12-Apr-2024

PMCID:	PMC11050096
doi:	10.3390/genes15040486
PMID:	38674420

Wild Edible Plants Used in Dalmatian Zagora (Croatia)

Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł

Plants (Basel)

11-Apr-2024

PMCID:	PMC11053949
doi:	10.3390/plants13081079
PMID:	38674488

Composition and Functional Properties of the Edible Spear and By-Products from Asparagus officinalis L. and Their Potential Prebiotic Effect

Goñi I, García-Alonso A, Alba C, Rodríguez JM, Sánchez-Mata MC, Guillén-Bejarano R, Redondo-Cuenca A

Foods

10-Apr-2024

PMCID:	PMC11049112
doi:	10.3390/foods13081154
PMID:	38672827

Research Progress of Small Plant Peptides on the Regulation of Plant Growth, Development, and Abiotic Stress

Ren G, Zhang Y, Chen Z, Xue X, Fan H

Int J Mol Sci

08-Apr-2024

PMCID:	PMC11012589
doi:	10.3390/ijms25074114
PMID:	38612923

The complete chloroplast genome of Eremurus zoae Vved. (Asphodelaceae), an endemic species of Kyrgyz Republic

Jang JE, Jeong HJ, Kim AL, Choi YR, Lazkov GA, Jang CG, Choi HJ, Gil HY

Mitochondrial DNA B Resour

03-Apr-2024

PMCID:	PMC10993749
doi:	10.1080/23802359.2024.2336003
PMID:	38586509

Inhibition of Proliferation and Induction of Apoptosis in Prostatic Carcinoma DU145 Cells by Polysaccharides from Yunnan Rosa roxburghii Tratt

Yang Z, Chen G

Molecules

01-Apr-2024

PMCID:	PMC11013296
doi:	10.3390/molecules29071575
PMID:	38611854

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

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

BMC Genomics

28-Mar-2024

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

Identification and characterization of the critical genes encoding Cd-induced enhancement of SOD isozymes activities in Zhe-Maidong (Ophiopogon japonicus)

Hou R, Wang Z, Zhu Q, Wang J, Zhou Y, Li Y, Liu H, Zhao Q, Huang J

Front Plant Sci

28-Mar-2024

PMCID:	PMC11007131
doi:	10.3389/fpls.2024.1355849
PMID:	38606075

Phytosulfokine alpha enhances regeneration of transformed and untransformed protoplasts of Brassica oleracea

Vogrinčič V, Kastelec D, Murovec J

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004253
doi:	10.3389/fpls.2024.1379618
PMID:	38601308

Breaking boundaries: a novel role for CUC genes in sex determination in cucurbits

Pelayo MA, Wellmer F

J Exp Bot

27-Mar-2024

PMCID:	PMC10967247
doi:	10.1093/jxb/erae056
PMID:	38534185

Transcriptome analysis of Gossypium reveals the molecular mechanisms of Ca2+ signaling pathway on arsenic tolerance induced by arbuscular mycorrhizal fungi

Gong M, Bai N, Su J, Wang Y, Wei Y, Zhang Q

Front Microbiol

25-Mar-2024

PMCID:	PMC11000422
doi:	10.3389/fmicb.2024.1362296
PMID:	38591035

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine, (-)-	978315	Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6	353.40	unknown	via CMAUP database
CID 24201226	24201226	Click to see	389.80	unknown	via CMAUP database
> Benzenoids / Indanes / Indanones
(2S,3s)-2,3-dihydro-3-hydroxy-6-(2-hydroxyethyl)-5-hydroxymethyl-2,7-dimethyl-1h-inden-1-one	21670042	Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)CO)CCO)C)O	250.29	unknown	via CMAUP database
(2S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one	169739	Click to see	234.29	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
1-methoxy-4-[(E)-5-(4-methoxyphenoxy)pent-3-en-1-ynyl]benzene	9994590	Click to see COC1=CC=C(C=C1)C#CC=CCOC2=CC=C(C=C2)OC	294.30	unknown	https://doi.org/10.1021/JF0305229 https://doi.org/10.1248/CPB.43.564
1-Methoxy-4-[5-(4-methoxyphenoxy)pent-3-en-1-ynyl]benzene	85086644	Click to see	294.30	unknown	https://doi.org/10.1021/JF0305229 https://doi.org/10.1248/CPB.43.564
4-[(E)-5-(4-methoxyphenoxy)pent-3-en-1-ynyl]phenol	10107705	Click to see	280.30	unknown	https://doi.org/10.1248/BPB.18.1472 https://doi.org/10.1248/CPB.43.564 https://doi.org/10.1021/JF0305229
4-[5-(4-Methoxyphenoxy)pent-3-en-1-yn-1-yl]phenol	54097411	Click to see	280.30	unknown	https://doi.org/10.1248/BPB.18.1472 https://doi.org/10.1248/CPB.43.564 https://doi.org/10.1021/JF0305229
Asparenyol	131753100	Click to see	280.30	unknown	https://doi.org/10.1248/BPB.22.561
> Benzenoids / Phenols / 4-alkoxyphenols
4-[5-(4-Hydroxyphenoxy)pent-3-en-1-ynyl]phenol	53862888	Click to see	266.29	unknown	https://doi.org/10.1248/CPB.43.564
Asparenydiol	10084256	Click to see C1=CC(=CC=C1C#CC=CCOC2=CC=C(C=C2)O)O	266.29	unknown	https://doi.org/10.1248/CPB.43.564
> Benzenoids / Phenols / Methoxyphenols
2-methoxy-5-[(E)-5-(4-methoxyphenoxy)pent-3-en-1-ynyl]phenol	11243832	Click to see	310.30	unknown	https://doi.org/10.1021/JF0305229
2-Methoxy-5-[5-(4-methoxyphenoxy)pent-3-en-1-yn-1-yl]phenol	71374502	Click to see	310.30	unknown	https://doi.org/10.1021/JF0305229
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane	11636	Click to see	380.70	unknown	via CMAUP database
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol	234817	Click to see	358.40	unknown	https://doi.org/10.1021/JF0305229
Epipinoresinol	637584	Click to see	358.40	unknown	https://doi.org/10.1021/JF0305229
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Benzenepropanoic acid, 4-hydroxy-, methyl ester	79706	Click to see	180.20	unknown	https://doi.org/10.1271/BBB1961.46.821
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids
(2R)-2-(acetylsulfanylmethyl)-3-sulfanylpropanoic acid	154497388	Click to see	194.30	unknown	https://doi.org/10.1016/S0040-4039(01)84871-1
3-(Acetylthio)-2-(mercaptomethyl)propanoic acid	85798858	Click to see	194.30	unknown	https://doi.org/10.1016/S0040-4039(01)84871-1
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid	3931	Click to see	280.40	unknown	https://doi.org/10.1021/JF0305229
Linoleic Acid	5280450	Click to see	280.40	unknown	https://doi.org/10.1021/JF0305229
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Monopalmitin	14900	Click to see	330.50	unknown	https://doi.org/10.1021/JF0305229
3-Palmitoyl-sn-glycerol	11359451	Click to see CCCCCCCCCCCCCCCC(=O)OCC(CO)O	330.50	unknown	https://doi.org/10.1021/JF0305229
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
15-Hydroxydehydroabietic Acid	14487943	Click to see	316.40	unknown	via CMAUP database
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione	46183941	Click to see	446.70	unknown	via CMAUP database
Imbricatolic Acid	70688370	Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CCO	322.50	unknown	via CMAUP database
Junicedric acid	38347252	Click to see	336.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4R)-4-hydroxy-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	25755218	Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C	226.31	unknown	https://doi.org/10.1021/JF0305229
9-Epiblumenol B	14135401	Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C	226.31	unknown	https://doi.org/10.1021/JF0305229
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4R,5R,6S)-6-[(3S)-5-[(1S,2R,4S,4aR,8aR)-4-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	10509989	Click to see	907.00	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	24882166	Click to see	614.80	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	16109823	Click to see CC1CC(C2(C(C1(C)CCC(=CCO)C)CCC=C2C)C)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)CO)O)O)O)O)O	614.80	unknown	via CMAUP database
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(3S)-3-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-methylpent-4-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	10724564	Click to see CC1CC(C2(C(C1(C)CCC(C)(C=C)OC3C(C(C(C(O3)C)OC4C(C(C(C(O4)C)O)O)O)O)O)CCC=C2C)C)OC5C(C(C(C(O5)C)OC6C(C(C(C(O6)COC(=O)C)O)O)O)O)O	949.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(2E,4E,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one	25243952	Click to see	584.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25R)-5alpha-Spirostan-3beta-ol	219836	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
Glutinol	9932254	Click to see	426.70	unknown	via CMAUP database
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.021
Sarsasapogenin	92095	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1	416.60	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
Spirost-5-en-3-ol	234096	Click to see	414.60	unknown	https://doi.org/10.1016/0031-9422(88)80057-8 https://doi.org/10.1016/J.STEROIDS.2005.09.005
Yamogenin	441900	Click to see	414.60	unknown	https://doi.org/10.1016/0031-9422(88)80057-8 https://doi.org/10.1016/J.STEROIDS.2005.09.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
17-(5-ethylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	76808560	Click to see	400.70	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-5-ethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	139376850	Click to see CCC(CC)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-5-ethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162997538	Click to see	562.80	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
2-[[17-(5-ethylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85042281	Click to see	562.80	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
Capsicastrine	21575044	Click to see	577.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25r)-5alpha-spirostan-3beta-ol 3-O-beta-d-galactopyranoside	11050123	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	578.80	unknown	via CMAUP database
(2R,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163030671	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	871.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
(2R,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6R,7S,8S,9S,12S,13S,16S,18R)-8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163044386	Click to see	887.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1S,2R,4S,6R,7S,8R,9S,12R,13S,16S,18R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162854276	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1215.30	unknown	https://doi.org/10.1007/BF00565519
(2R,3R,4S,5S,6R)-2-[4-[(18R)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	6325818	Click to see	1023.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7R,8R,9S,12S,13R,16S)-7-(hydroxymethyl)-5',9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162970191	Click to see	885.00	unknown	https://doi.org/10.1016/J.FITOTE.2009.09.002
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162997663	Click to see	1049.20	unknown	https://doi.org/10.1055/S-2006-957667
(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R,6R)-3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163034205	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)OC9C(C(C(CO9)O)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)C)C)C)OC1	1035.20	unknown	https://doi.org/10.1007/BF00565519
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4R,5'S,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162984179	Click to see	873.00	unknown	https://doi.org/10.1080/00021369.1990.10870343
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'S,6R,7S,8S,9S,12S,13S,16S,18R)-8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11204972	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)O)C)OC1	756.90	unknown	https://doi.org/10.1021/NP040128K https://doi.org/10.1016/J.STEROIDS.2005.09.005
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(1R,2S,4S,8S,9S,12S,13S,16S,18R)-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-16-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162963987	Click to see	903.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5320488	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)C)C)C)OC1	887.10	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(3R,4R,5R,6S)-6-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5320480	Click to see	873.00	unknown	via CMAUP database
(3I(2),5I(2),25S)-Spirostan-3-yl O-I(2)-D-glucopyranosyl-(1a2)-O-[I(2)-D-xylopyranosyl-(1a4)]-I(2)-D-glucopyranoside	101591768	Click to see	873.00	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	271916	Click to see	869.00	unknown	https://doi.org/10.1016/J.FITOTE.2009.09.002
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	3640213	Click to see	871.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	158680	Click to see	887.10	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
2-[4-Hydroxy-2-(hydroxymethyl)-6-(8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163044385	Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)O)C)OC1	887.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
2-[4-Hydroxy-2-(hydroxymethyl)-6-[7-(hydroxymethyl)-5',9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162970190	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)CO)OC1	885.00	unknown	https://doi.org/10.1016/J.FITOTE.2009.09.002
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(8-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	72750002	Click to see	756.90	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[7,9,13-trimethyl-6-[3-methyl-4-(3,4,5-trihydroxy-6-methoxyoxan-2-yl)oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-16-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162963986	Click to see	903.10	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
3-O-[alpha-L-ramnopyranosyl(1 to 2)]-O-[alpha-L-ramnopyranosyl(1 to 4)]-O-beta-D-galactopyranosid(1)]-(25S)-spirost-5-ene-3beta-ol	10653210	Click to see	869.00	unknown	https://doi.org/10.1016/J.FITOTE.2009.09.002
Aspafilioside A	44445743	Click to see	710.90	unknown	via CMAUP database
Aspafilioside B	44445744	Click to see	827.00	unknown	via CMAUP database
Asparagoside C	24833885	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)OC1	740.90	unknown	https://doi.org/10.1007/BF00564989
Asparagoside E	131751196	Click to see	921.10	unknown	https://doi.org/10.1007/BF00564989
asparagoside F	131750849	Click to see	1035.20	unknown	https://doi.org/10.1007/BF00565519
Asparagoside H	3042723	Click to see	1215.30	unknown	https://doi.org/10.1007/BF00565519
Asparanin A	21575007	Click to see	740.90	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
Asparanin B	441896	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
beta-D-Glucopyranoside, (3beta,25R)-26-(beta-D-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1->2)-O-(6-deoxy-alpha-L-mannopyranosyl-(1->4))-	500375	Click to see	1049.20	unknown	https://doi.org/10.1055/S-2006-957667 https://doi.org/10.1271/BBB.120143 https://doi.org/10.1111/J.1750-3841.2010.01824.X https://doi.org/10.1021/JF401462W
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	https://doi.org/10.1111/J.1750-3841.2010.01824.X https://doi.org/10.1021/JF401462W https://doi.org/10.1021/JF0344587 https://doi.org/10.1271/BBB.120143
Sarsasapogenin 3-O-[beta-D-Glucopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->4)]-beta-D-glucopyranoside]	73802021	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	873.00	unknown	https://doi.org/10.1080/00021369.1990.10870343 https://doi.org/10.1016/J.STEROIDS.2005.09.005
Schidigerasaponin D5	3272925	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	740.90	unknown	https://doi.org/10.1016/J.STEROIDS.2005.09.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8S,9R,10R,13R,14S,17R)-17-[(2R,5R)-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	122411787	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	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	https://doi.org/10.1016/0031-9422(88)80057-8
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/10.1016/0031-9422(88)80057-8
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/10.1016/0031-9422(88)80057-8
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80057-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(2S)-4-amino-2-ammonio-4-oxobutanoate	6992089	Click to see	132.12	unknown	via CMAUP database
CID 6991971	6991971	Click to see C(C(C(=O)[O-])[NH3+])C(=O)N	132.12	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
(2R,2'S)-Isobuteine	14889929	Click to see CC(CSCC(C(=O)O)N)C(=O)O	207.25	unknown	https://doi.org/10.1021/JA00294A051
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives / L-cysteine-S-conjugates
(2R)-3-[(2R)-2-amino-2-carboxyethyl]sulfanyl-2-methylpropanoic acid	162911496	Click to see CC(CSCC(C(=O)O)N)C(=O)O	207.25	unknown	https://doi.org/10.1021/JA00294A051
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids
2-Acetamido-3-hydroxypropanoic acid	352294	Click to see CC(=O)NC(CO)C(=O)O	147.13	unknown	https://doi.org/10.1271/BBB1961.45.1483
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids / N-acyl-L-alpha-amino acids
Acetylserine	65249	Click to see	147.13	unknown	https://doi.org/10.1271/BBB1961.45.1483
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-Gln-OH	11308921	Click to see	846.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC38796/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S)-N-[(1S)-1-[[(1S)-1-(acetylcarbamoyl)-4-guanidino-butyl]carbamoyl]-4-guanidino-butyl]-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-[[(2S)-5-guanidino-2-hydroxy-pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanoyl]amino]pentanamide	49769220	Click to see	1465.70	unknown	via CMAUP database
Npc168718	44630308	Click to see	612.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Dihydroasparagusic acid	440312	Click to see C(C(CS)C(=O)O)S	152.20	unknown	https://doi.org/10.1016/S0040-4039(01)84871-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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/10.1093/OXFORDJOURNALS.PCP.A078100
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(2,4-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	102392053	Click to see	316.30	unknown	via CMAUP database
Arbutin	440936	Click to see	272.25	unknown	via CMAUP database
Isotachioside	15098566	Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	302.28	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal	3037556	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1021/JA02215A010
L-Galactose	24749	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1021/JA02215A010
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,3R,4S,5S,6R)-2-((2R,3S,4S,5R)-2-(((2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl)oxymethyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy-6-(((2R,3S,4S,5R)-2-(((2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl)oxymethyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)oxymethyl)oxane-3,4,5-triol	21582504	Click to see	828.70	unknown	https://doi.org/10.1271/BBB1961.43.1375
(2R,3S,4S,5R,6R)-2-(((2R,3S,4S,5R)-2-(((2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl)oxymethyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)oxymethyl)-6-((2S,3S,4S,5R)-2-(((2R,3S,4S,5R)-2-(((2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl)oxymethyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)oxymethyl)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl)oxyoxane-3,4,5-triol	91861965	Click to see	990.90	unknown	https://doi.org/10.1016/0031-9422(81)83099-3
1-O-beta-D-Fructofuranosyl-beta-D-fructofuranosyl 6-O-(1-O-(1-O-(beta-D-fructofuranosyl)-beta-D-fructofuranosyl)-beta-D-fructofuranosyl)-alpha-D-glucopyranoside	91854243	Click to see	990.90	unknown	https://doi.org/10.1016/0031-9422(81)83099-3
2-[[2-[[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-[[2-[[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxyoxane-3,4,5-triol	162977507	Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)COC5(C(C(C(O5)CO)O)O)COC6(C(C(C(O6)CO)O)O)CO)O)O)O)O)O)O	990.90	unknown	https://doi.org/10.1016/0031-9422(81)83099-3
2-[2-[[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-[[2-[[2-[[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol	163013463	Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3(C(C(C(O3)CO)O)O)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)COC6(C(C(C(O6)CO)O)O)CO)O)O)O)O)O)O	990.90	unknown	https://doi.org/10.1016/0031-9422(81)83099-3
beta-D-Fructofuranosyl-(2->1)-beta-D-fructofuranosyl-(2->6)-alpha-D-glucopyranosyl-(1->2)-beta-D-fructofuranosyl beta-D-fructofuranoside	73805521	Click to see C(C1C(C(C(O1)(CO)OCC2(C(C(C(O2)CO)O)O)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)COC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O	828.70	unknown	https://doi.org/10.1271/BBB1961.43.1375
Neokestose	14282017	Click to see	504.40	unknown	https://doi.org/10.1016/0008-6215(89)80044-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Nonacosan-10-one	441490	Click to see	422.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Dithiolanes / 1,2-dithiolanes
methyl (1S,4R)-1-oxodithiolane-4-carboxylate	163082546	Click to see	180.20	unknown	https://doi.org/10.1021/JF0305229
Methyl 1-oxodithiolane-4-carboxylate	163082545	Click to see	180.20	unknown	https://doi.org/10.1021/JF0305229
> Organoheterocyclic compounds / Dithiolanes / Dithiolanecarboxylic acids / 1,2-dithiolanecarboxylic acids / 1,2-dithiolane-4-carboxylic acids
(1S,4S)-1-oxodithiolane-4-carboxylic acid	162801170	Click to see	166.20	unknown	https://doi.org/10.1016/S0040-4039(01)95907-6 https://doi.org/10.1016/S0040-4039(01)84871-1
1,2-Dithiolane-4-carboxylic acid	16682	Click to see	150.20	unknown	https://doi.org/10.1021/JA00294A051 https://doi.org/10.1021/JA00369A057 https://doi.org/10.1016/S0040-4039(01)84871-1
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
5-{[5-(2-Amino-2-carboxyethyl)-1-methyl-1H-imidazol-4-yl]sulfanyl}-6,8-dihydroxy-1-[(4-hydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid	360123	Click to see	514.60	unknown	https://doi.org/10.1016/S0040-4039(01)95907-6 https://doi.org/10.1016/S0040-4039(01)84871-1
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Chelidonic acid	7431	Click to see	184.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Trithianes
1,2,3-Trithiane-5-carboxylic acid	54323246	Click to see	182.30	unknown	https://doi.org/10.1271/BBB1961.46.821
Methyl trithiane-5-carboxylate	162938406	Click to see	196.30	unknown	https://doi.org/10.1271/BBB1961.46.821
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl-	8784	Click to see	148.16	unknown	https://doi.org/10.1271/BBB1961.46.821
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1271/BBB1961.46.821
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[2-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	67283061	Click to see	444.40	unknown	https://doi.org/10.1021/JF0305229
[3-Hydroxy-2-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	72727916	Click to see	444.40	unknown	https://doi.org/10.1021/JF0305229
1,2-Diferuloyl-sn-glycerol	76967301	Click to see	444.40	unknown	https://doi.org/10.1021/JF0305229
Glyceryl 1,3-diferulate	14135369	Click to see	444.40	unknown	https://doi.org/10.1021/JF0305229
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives / Coumaric acids
cis-2-Coumarate	54714352	Click to see C1=CC=C(C(=C1)C=CC(=O)O)[O-]	163.15	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R)-2-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxypropyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	25768379	Click to see	414.40	unknown	https://doi.org/10.1021/JF0305229
[2-Hydroxy-3-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxyphenyl)prop-2-enoate	72727917	Click to see	414.40	unknown	https://doi.org/10.1021/JF0305229
[2-Hydroxy-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]propyl] 3-(4-hydroxyphenyl)prop-2-enoate	90833706	Click to see	384.40	unknown	https://doi.org/10.1021/JF0305229
1,3-o-Di-p-coumaroylglycerol	14034127	Click to see	384.40	unknown	https://doi.org/10.1021/JF0305229
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid	709	Click to see	194.18	unknown	https://doi.org/10.1021/JF0305229
Ferulic Acid	445858	Click to see	194.18	unknown	https://doi.org/10.1021/JF0305229
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	via CMAUP database
Thamnosmonin	312089	Click to see	276.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-4-benzopyrone	442396	Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O	300.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1021/JF001497Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4S,5R,6S)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	154496406	Click to see	595.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.021
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1021/JF001497Z
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	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
quercetin 3-O-alpha-L-fucopyranoside	5359430	Click to see	448.40	unknown	https://doi.org/10.1021/JF001497Z
Quercitrin	5280459	Click to see	448.40	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.21273/HORTSCI.40.5.1221 https://doi.org/10.1021/JF0344587 https://doi.org/10.1021/JF001497Z
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.21273/HORTSCI.40.5.1221 https://doi.org/10.1021/JF001497Z
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-chroman-4-one	49770782	Click to see	314.30	unknown	via CMAUP database

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Asparagus officinalis

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