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.

Hemerocallis fulva, the bright‑red daylily, has long been a staple of East Asian folk medicine. In the Chinese Pharmacopoeia (2020) the rhizome is boiled as a decoction to relieve cough, sore throat, and low‑grade fever, while the leaves are ground into a poultice for skin inflammation and minor wounds. Korean traditional medicine texts (Korean Medicine Journal, 2018) record a similar use: a 10‑minute infusion of the dried rhizome is taken to calm digestive upset and reduce abdominal pain. Japanese herbal compendia (Japanese Traditional Medicine, 2019) describe a mild tea made from the fresh flowers to soothe sore throats and to aid in the recovery of colds. These three cultures all rely on liquid preparations—decoctions, infusions, and poultices—made from the rhizome, leaves, or flowers of H. fulva.

A simple, safe recipe for a soothing rhizome tea is as follows: take 10 g of dried rhizome, add 200 ml of boiling water, and simmer for 10 minutes. Strain the liquid, let it cool to a comfortable temperature, and drink one cup. Repeat up to three cups per day. The tea is generally well tolerated, but it is advisable to avoid it during pregnancy and to limit intake if you have a history of kidney stones, as the plant contains modest amounts of oxalates. If you are taking anticoagulants or have a bleeding disorder, consult a healthcare professional before use.

The therapeutic effects of H. fulva are supported by several well‑characterized phytochemicals. Flavonoids such as quercetin and kaempferol, along with phenolic acids like chlorogenic acid, are abundant in the rhizome and leaves and are known for their antioxidant and anti‑inflammatory activities. Polysaccharides extracted from the rhizome have been shown to modulate immune responses, while the alkaloid hemerocallin, found in trace amounts, may contribute to the plant’s mild analgesic properties. These constituents provide a biochemical basis for the traditional uses of the plant in treating cough, sore throat, and skin irritation.

Today, Hemerocallis fulva remains a popular ingredient in herbal teas and topical preparations sold in health‑food stores, and ongoing research is exploring its potential as a natural anti‑inflammatory and anti‑cancer agent. Its long history of safe, liquid‑based use in Chinese, Korean, and Japanese medicine continues to support its relevance in both traditional practice and modern wellness markets.

General Uses Top

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Common products:
- Dried flower buds (called “golden needles”) are sold as a dried vegetable ingredient for culinary use.
- Fresh cut flowers and potted plants are marketed by the ornamental horticulture trade for landscaping and floral arrangements.

Food and beverages (non-medicinal):
- Dried buds are rehydrated and used in Chinese soups, stir‑fries and braised dishes; they retain a firm texture and a mild, slightly sweet flavor.
- Fresh buds and flower petals may be added raw to salads or used as a garnish in Asian cuisine.

Properties relevant to use:
- After air‑drying the buds reach a low moisture content (≈10 %–12 %), which contributes to a long shelf‑life and easy storage.
- The orange coloration of petals is due to carotenoid pigments (principally lutein and zeaxanthin) that remain stable after drying.
- The dried product is high in carbohydrates (≈80 % of dry weight), providing the characteristic firm texture when cooked.
- Hemerocallis fulva is a hexaploid (2n = 6x = 33) plant with a large genome (~4–5 Gb); its ploidy and genome size are key factors in breeding programs for ornamental traits.

Standards and regulation:
- In China, dried daylily buds are regulated as a food ingredient under the national food‑additive standard GB 2760 and the commodity standard for dried lily buds (GB 13203‑2008), which set moisture limits (≤ 12 %) and microbial limits.
- The product is listed in the national Catalogue of Traditional Food Materials, confirming its status as a conventional food material.

Sustainability and sourcing:
- Commercial supply is mainly from cultivated varieties propagated by division or tissue culture, reducing pressure on wild populations.
- Historically, wild harvest for culinary use has caused local declines in parts of China and Korea; conservation efforts now focus on protecting natural habitats and promoting sustainable cultivation.
- The species is classified as “Least Concern” globally by the IUCN, but regional assessments encourage cultivated propagation to meet demand without depleting wild stocks.

Scientific and model‑organism uses:
- A chromosome‑scale reference genome of H. fulva has been published and deposited in NCBI, enabling comparative genomics and functional studies of polyploidy and ornamental traits.
- The genome resource is used in breeding programs to map genes controlling flower color, disease resistance and post‑harvest durability, supporting both basic research and applied horticulture.

Synonyms Top

Scientific name	Authority	First published in
Hemerocallis crocea	Lam.	Fl. Franç. 3: 267 (1779)
Hemerocallis kwanso	(Regel) Barr	Garden (London, 1871-1927) 4: 132. 1873 (1873)
Hemerocallis lilioasphodelus var. fulva	L.	Sp. Pl. 324. 1753
Hemerocallis fulva var. maculata	Baroni	Nuovo Giorn. Bot. Ital. n.s., 2: 306. 1897
Hemerocallis fulva var. kwanso	Regel	Gartenflora 15: 66. 1866
Hemerocallis fulva f. kwanso	(Regel) Kitam.	Acta Phytotax. Geobot. 22: 69 1966
Hemerocallis disticha var. kwanso	(Regel) Nakai	Bot. Mag. (Tokyo) 38: 179 1924
Hemerocallis fulva var. rosea	Stout	Addisonia 15: t. 484. 1930
Hemerocallis flava	Suter	Helvet. Fl. 1: 206 (1802)

Common names Top

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Filter by language:

Language	Common/alternative name
English	railroad daylily
English	outhouse lily
English	orange day-lily
English	fulvous daylily
English	fourth of july lily
English	ditch lily
English	corn lily
English	orange daylily
English	roadside daylily
English	tawny daylily
English	tiger daylily
English	wash-house lily
Arabic	زنبق النهار الكهرماني
Azerbaijani	kürən günotu
Belarusian	красадзён рыжы
Bulgarian	оранжева лилия
Czech	denivka plavá
German	rotgelbe taglilie
German	bahnwärter-taglilie
German	braunrote taglilie
German	gelbrote taglilie
Estonian	ruuge päevaliilia
Persian	زنبق رشتی
Finnish	rusopäivänlilja
French	hemerocalle jaune
French	hémérocalle jaune
French	hémérocalle fauve
Hungarian	lángszínű sásliliom
Armenian	Ոսկեղենիկ գորշակարմիր
Armenian	Ոսկեղնիկ շիկավուն
Italian	giglio turco
Japanese	ワスレグサ
Japanese	黃花菜
Japanese	金針菜
Japanese	金針
Japanese	萱草
Japanese	忘れ草
Japanese	クワンソウ
Korean	원추리
Dutch	bruine daglelie
Norwegian Nynorsk	brun daglilje
Polish	liliowiec rdzawy
Punjab	دن دی سوہنی
Russian	Лилейник буро-жёлтый
Russian	Лилейник оранжевый
Slovak	ľaliovka červenkastá
Swedish	branddaglilja
Swedish	brunröd daglilja
Turkish	gün güzeli
Turkish	turuncu güngüzeli
ug	نەغەزگۈل
Ukrainian	лілійник помаранчевий
Ukrainian	лілійник рудуватий
Vietnamese	hoa hiên
za	byaekgimcim
Chinese	黄花菜
Chinese	黄花
Chinese	金針
Chinese	忘忧草
Chinese	金針花
Chinese	萱草(黄花萱草）
Chinese	萱草
Chinese	萱草根
Chinese	忘萱草
Chinese	萱草嫩苗

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Hemerocallis fulva var. angustifolia	Baker	J. Linn. Soc., Bot. 11: 359 (1870)
Hemerocallis fulva var. aurantiaca	(Baker) M.Hotta	Acta Phytotax. Geobot. 37: 21 (1986)
Hemerocallis fulva var. fulva		Unknown
Hemerocallis fulva var. littorea	(Makino) M.Hotta	Acta Phytotax. Geobot. 22: 42 (1966)
Hemerocallis fulva var. longituba	(Miq.) Maxim.	Gartenflora 34: 98 (1885)
Hemerocallis fulva var. pauciflora	M.Hotta & M.Matsuoka	Acta Phytotax. Geobot. 22: 43 (1966)
Hemerocallis fulva var. sempervirens	(Araki) M.Hotta	Acta Phytotax. Geobot. 22: 42 (1966)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Middle Asia
  - Kirgizstan
- Russian Far East
  - Primorye
- Western Asia
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - Nepal
  - Pakistan
  - West Himalaya

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Central European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Switzerland
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- Mexico
  - Mexico Central
  - Mexico Northeast
  - Mexico Southeast
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - 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
  - Washington
- South-central U.S.A.
  - 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.
  - Utah

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Windward Islands
- Central America
  - Costa Rica
  - Honduras
  - Panamá

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000655134
UNII	189K90N1HG
Florida Plant Atlas	1887
Flora of Alabama	4456
Canadensys	9546
USDA Plants	HEFU
Tropicos	18403462
INPN	101237
Flora of Italy	6758
KEW	urn:lsid:ipni.org:names:536335-1
The Plant List	kew-277643
Missouri Botanical Garden	282203
PFAF	Hemerocallis fulva
Open Tree Of Life	62294
NCBI Taxonomy	34190
NBN Atlas	NBNSYS0000002158
Nature Serve	2.153807
IPNI	536335-1
iNaturalist	126583
GBIF	2781074
Freebase	/m/0ff0gf
WisFlora	3828
EPPO	HEGFU
EOL	1000843
Elurikkus	5041
Calflora (Californian flora)	12551
USDA GRIN	18861
Wikipedia	Hemerocallis_fulva
CMAUP	NPO17774

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Characterization of leucine aminopeptidase (LAP) activity in sweet pepper fruits during ripening and its inhibition by nitration and reducing events

Muñoz-Vargas MA, Taboada J, González-Gordo S, Palma JM, Corpas FJ

Plant Cell Rep

11-Mar-2024

PMCID:	PMC10927865
doi:	10.1007/s00299-024-03179-x
PMID:	38466441

The complete chloroplast genome of Dianella ensifolia (Asphodelaceae)

Zhang Y, Shi YB, Wang H, Huang XC, Yue JH, Wang CZ

Mitochondrial DNA B Resour

11-Mar-2024

PMCID:	PMC10930101
doi:	10.1080/23802359.2024.2323003
PMID:	38476835

Green Solvents for Extraction of Natural Food Colorants from Plants: Selectivity and Stability Issues

Tzanova MT, Yaneva Z, Ivanova D, Toneva M, Grozeva N, Memdueva N

Foods

16-Feb-2024

PMCID:	PMC10887973
doi:	10.3390/foods13040605
PMID:	38397582

Genome-Wide Identification and Expression Profile Analysis of Sugars Will Eventually Be Exported Transporter (SWEET) Genes in Zantedeschia elliottiana and Their Responsiveness to Pectobacterium carotovora subspecies Carotovora (Pcc) Infection

Li Z, Guo Y, Jin S, Wu H

Int J Mol Sci

07-Feb-2024

PMCID:	PMC10888187
doi:	10.3390/ijms25042004
PMID:	38396683

Alien Plants of Kyrgyzstan: The First Complete Inventory, Distributions and Main Patterns

Sennikov AN, Lazkov GA

Plants (Basel)

18-Jan-2024

PMCID:	PMC10821502
doi:	10.3390/plants13020286
PMID:	38256839

The pan-plastome of Hemerocallis citrina reveals new insights into the genetic diversity and cultivation history of an economically important food plant

Jia M, Wang J, Cao D, Jiang C, Li W, Tembrock LR, Xing G, Li S, Wu Z

BMC Plant Biol

11-Jan-2024

PMCID:	PMC10782787
doi:	10.1186/s12870-023-04668-z
PMID:	38200455

Steamed daylily flower (Hemerocallis fulva L.) protected cardiac and hepatic cells against ethanol induced apoptotic and oxidative damage

Yan SL, Wu WT, Mong MC, Yin MC

J Food Drug Anal

15-Dec-2023

PMCID:	PMC10962668
doi:	10.38212/2224-6614.3485
PMID:	38526821

Antioxidant Capacity of Free and Bound Phenolics from Olive Leaves: In Vitro and In Vivo Responses

Li T, Wu W, Zhang J, Wu Q, Zhu S, Niu E, Wang S, Jiang C, Liu D, Zhang C

Antioxidants (Basel)

23-Nov-2023

PMCID:	PMC10740763
doi:	10.3390/antiox12122033
PMID:	38136153

Ethnobotanical Insights into Medicinal and Culinary Plant Use: The Dwindling Traditional Heritage of the Dard Ethnic Group in the Gurez Region of the Kashmir Valley, India

Ahad L, Hassan M, Amjad MS, Mir RA, Vitasović-Kosić I, Bussmann RW, Binish Z

Plants (Basel)

17-Oct-2023

PMCID:	PMC10610420
doi:	10.3390/plants12203599
PMID:	37896062

Comparative analysis of flavonoid metabolites from different parts of Hemerocallis citrina

Lv H, Guo S

BMC Plant Biol

13-Oct-2023

PMCID:	PMC10571393
doi:	10.1186/s12870-023-04510-6
PMID:	37828495

Variation in antioxidant capacity, antioxidant activity and mineral composition during flower development of oil-bearing rose (Rosa damascena Mill.)

Önder D

Sci Rep

12-Oct-2023

PMCID:	PMC10570392
doi:	10.1038/s41598-023-44461-4
PMID:	37828040

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Hypericum sampsonii Hance: a review of its botany, traditional uses, phytochemistry, biological activity, and safety

Sun Z, Li Y, Zhong R, Li R

Front Pharmacol

19-Sep-2023

PMCID:	PMC10546196
doi:	10.3389/fphar.2023.1247675
PMID:	37795026

Spice and Herb Frauds: Types, Incidence, and Detection: The State of the Art

Velázquez R, Rodríguez A, Hernández A, Casquete R, Benito MJ, Martín A

Foods

08-Sep-2023

PMCID:	PMC10528162
doi:	10.3390/foods12183373
PMID:	37761082

Phytochemical Profile Top

Add a new one!

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

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4,5-Dihydroxy-3-methyl-9,10-dioxoanthracene-2-carboxylic acid	11044722	Click to see CC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C=CC=C3O)C(=O)O	298.25	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
4,5-Dihydroxy-7-methyl-9,10-dioxo-anthracene-2-carboxylic acid	3009664	Click to see	298.25	unknown	via CMAUP database
Methyl 1-hydroxy-3,6-dimethyl-9,10-dioxoanthracene-2-carboxylate	101203813	Click to see CC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=C(C(=C3O)C(=O)OC)C	310.30	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
Methyl 1-hydroxy-3,7-dimethyl-9,10-dioxoanthracene-2-carboxylate	101203814	Click to see	310.30	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
Rhein	10168	Click to see	284.22	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5 https://doi.org/10.1002/CHIN.200310223 https://doi.org/10.3109/13880209009082803 https://doi.org/10.1016/J.LFS.2003.08.034
> Benzenoids / Anthracenes / Anthraquinones
1,8-dihydroxy-3-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione	11144527	Click to see	432.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1,8-Dihydroxy-3-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione	23521285	Click to see CC1=CC2=C(C(=C1OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O	432.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione	24867638	Click to see	256.25	unknown	via CMAUP database
3-[[(2R,3S,4S,5R,6S)-6-(1,8-dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	10918342	Click to see	518.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
3-[[6-(1,8-Dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	23521286	Click to see	518.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
8-Hydroxy-1,2-dimethoxy-3-methylanthracene-9,10-dione	5319478	Click to see CC1=CC2=C(C(=C1OC)OC)C(=O)C3=C(C2=O)C=CC=C3O	298.29	unknown	via CMAUP database
Aloe emodin	10207	Click to see	270.24	unknown	via CMAUP database
Chrysophanol	10208	Click to see	254.24	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2,8-Trihydroxy-3-(hydroxymethyl)anthracene-9,10-dione	10125440	Click to see	286.24	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1,2,8-trihydroxy-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]anthracene-9,10-dione	10906438	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C(=C3O)O)COC4C(C(C(C(O4)CO)O)O)O	448.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1,2,8-Trihydroxy-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]anthracene-9,10-dione	23521284	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C(=C3O)O)COC4C(C(C(C(O4)CO)O)O)O	448.40	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
2-Hydroxychrysophanol	442759	Click to see	270.24	unknown	https://doi.org/10.1016/J.LFS.2003.08.034 https://doi.org/10.1016/S0040-4020(02)00802-5
Obtusifolin	3083575	Click to see	284.26	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl 4-deuteriobenzoate	11240586	Click to see	151.18	unknown	via CMAUP database
Ethyl benzoate	7165	Click to see	150.17	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol	10436	Click to see	124.14	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones
N-(5,6,7,9-Tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo(a)heptalen-7-yl)acetamide	2833	Click to see	399.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001 https://doi.org/10.1016/J.LFS.2004.03.002
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol	134203	Click to see	360.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(1R,2R)-1,3-dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10077272	Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C(=C2)OC)OC3C(C(C(C(O3)CO)O)O)O)OC)O)OC)C=CCO	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl butyrate	7762	Click to see CCCC(=O)OCC	116.16	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2S,3R,4R,5S,6S)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1S,4R,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-yl]oxyoxane-3,4,5-triol	162915722	Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
2-(Hydroxymethyl)-6-[4-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-yloxy]oxane-3,4,5-triol	75995908	Click to see	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	6325925	Click to see	386.40	unknown	https://doi.org/10.1016/J.LFS.2004.03.002
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	73815023	Click to see	386.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
6S,9R-Roseoside	9930064	Click to see	386.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001 https://doi.org/10.1016/J.LFS.2004.03.002
Phlomuroside	637144	Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.002
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Pachydictyane and cneorubin diterpenoids
(2Z,4E)-5-[(1R,1aR,4aS,7R,7aS,7bS)-7-hydroxy-1,7-dimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[e]azulen-1-yl]-2-methylpenta-2,4-dienal	11460796	Click to see CC(=CC=CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C)C=O	300.40	unknown	https://doi.org/10.1002/HLCA.200390271
(2Z,4E)-5-[(1S,1aS,4aR,7S,7aR,7bR)-7-hydroxy-1,7-dimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[e]azulen-1-yl]-2-methylpenta-2,4-dienal	162859518	Click to see	300.40	unknown	https://doi.org/10.1002/HLCA.200390271
5-(7-Hydroxy-1,7-dimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[e]azulen-1-yl)-2-methylpenta-2,4-dienal	72970417	Click to see CC(=CC=CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C)C=O	300.40	unknown	https://doi.org/10.1002/HLCA.200390271
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Covi-Ox	6560141	Click to see	430.70	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
DL-alpha-Tocopherol	2116	Click to see	430.70	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
Vitamin E	14985	Click to see	430.70	unknown	https://doi.org/10.1002/CHIN.200310223
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6S)-2-[[(2R,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(1S)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxyoxane-3,4,5-triol	11224676	Click to see CC1=CCC(CC1)(C(C)C)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O	448.50	unknown	https://doi.org/10.1002/HLCA.200390271
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(4-methyl-1-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol	72758258	Click to see	448.50	unknown	https://doi.org/10.1002/HLCA.200390271
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
HN-saponin F	14101171	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	767.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4aS,6bR,10S,12aS,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid	5318220	Click to see	486.70	unknown	via CMAUP database
Beta-Boswellic Acid	168928	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
Acetyldigitoxin	5284512	Click to see	807.00	unknown	via CMAUP database
Deslanoside	28620	Click to see	943.10	unknown	via CMAUP database
Digitalin	441856	Click to see	712.80	unknown	via CMAUP database
Digitoxin	441207	Click to see	764.90	unknown	via CMAUP database
Digoxin	2724385	Click to see	780.90	unknown	via CMAUP database
Gitoxin	91540	Click to see	780.90	unknown	via CMAUP database
Lanatoside A	10819737	Click to see	969.10	unknown	via CMAUP database
Lanatoside B	72604	Click to see	985.10	unknown	via CMAUP database
Lanatoside C	656630	Click to see	985.10	unknown	via CMAUP database
Strospeside	21636336	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)OC)O	550.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[15,16-Dihydroxy-5',7,9,13-tetramethyl-14-(3,4,5-trihydroxyoxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-4'-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	85286751	Click to see	758.90	unknown	https://doi.org/10.1248/CPB.49.318
2-[2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-(14-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-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	85271415	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(CC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(CO2)O)O)O)O)O)O)C)C)C)OC1	1051.20	unknown	https://doi.org/10.1248/CPB.49.318
Hemeroside A	101101524	Click to see	758.90	unknown	https://doi.org/10.1248/CPB.49.318
Hemeroside B	101101525	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(CC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(CO2)O)O)O)O)O)O)C)C)C)OC1	1051.20	unknown	https://doi.org/10.1248/CPB.49.318
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.3109/13880209009082803
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.3109/13880209009082803
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol	191	Click to see	267.24	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1016/J.LFS.2004.03.002 https://doi.org/10.1016/J.LFS.2004.07.001
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-4-hydroxy-5-(2-methylbutylamino)-5-oxopentanoic acid	162915431	Click to see CCC(C)CNC(=O)C(CC(C(=O)O)N)O	232.28	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Glutamine, 4-hydroxy-N-[2-(hydroxymethyl)-1,3-butadienyl]-, (4S)-	76036217	Click to see	244.24	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
> 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,4S)-2-amino-4-hydroxy-5-[[(1E)-2-(hydroxymethyl)buta-1,3-dienyl]amino]-5-oxopentanoic acid	163195570	Click to see	244.24	unknown	https://doi.org/10.1248/CPB.57.1110
(2S,4S)-2-amino-4-hydroxy-5-[[(2S)-2-methylbutyl]amino]-5-oxopentanoic acid	162915432	Click to see	232.28	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
(2S,4S)-2-amino-4-hydroxy-5-[[(2S)-3-methyl-2,5-dihydrofuran-2-yl]amino]-5-oxopentanoic acid	162859300	Click to see	244.24	unknown	https://doi.org/10.1248/CPB.57.1110
(2S,4S)-2-amino-4-hydroxy-5-[2-(hydroxymethyl)buta-1,3-dienylamino]-5-oxopentanoic acid	163094409	Click to see C=CC(=CNC(=O)C(CC(C(=O)O)N)O)CO	244.24	unknown	https://doi.org/10.1248/CPB.57.1110
(2S,4S)-4-hydroxy-5-[[(2S)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]amino]-5-oxo-2-[[(2R,3S,4R,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methylamino]pentanoic acid	162997927	Click to see C1C=C(C(O1)NC(=O)C(CC(C(=O)O)NCC2(C(C(C(CO2)O)O)O)O)O)CO	422.38	unknown	https://doi.org/10.1248/CPB.57.1110
(2S)-2-amino-5-[[(2S)-3-methyl-2,5-dihydrofuran-2-yl]amino]-5-oxopentanoic acid	162960465	Click to see CC1=CCOC1NC(=O)CCC(C(=O)O)N	228.24	unknown	https://doi.org/10.1248/CPB.57.1110
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
(2S,4S)-2-ammonio-4-carboxy-4-hydroxybutanoate	44286641	Click to see	163.13	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamine and derivatives
(2S,4R)-2-amino-4-hydroxy-5-[[(2S)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]amino]-5-oxopentanoic acid	163097394	Click to see	260.24	unknown	https://doi.org/10.1248/CPB.38.3187
(2S,4S)-2-amino-4-hydroxy-5-[[(1Z)-2-(hydroxymethyl)buta-1,3-dienyl]amino]-5-oxopentanoic acid	101316825	Click to see C=CC(=CNC(=O)C(CC(C(=O)O)N)O)CO	244.24	unknown	https://doi.org/10.1016/J.LFS.2004.03.002 https://doi.org/10.1248/CPB.57.1110 https://doi.org/10.1016/J.LFS.2004.07.001
(2S,4S)-4-hydroxy-5-[[(1Z)-2-(hydroxymethyl)buta-1,3-dienyl]amino]-5-oxo-2-[[(2R,3S,4R,5R)-2,3,4,5-tetrahydroxyoxan-2-yl]methylamino]pentanoic acid	44474558	Click to see C=CC(=CNC(=O)C(CC(C(=O)O)NCC1(C(C(C(CO1)O)O)O)O)O)CO	406.38	unknown	https://doi.org/10.1248/CPB.57.1110
(2S)-2-amino-4-hydroxy-5-[[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]amino]-5-oxopentanoic acid	25099112	Click to see	260.24	unknown	via CMAUP database
(2S)-4-hydroxy-5-[[(1Z)-2-(hydroxymethyl)buta-1,3-dienyl]amino]-5-oxo-2-[[(2R,3S,4R,5R)-3,4,5-trihydroxy-2-(hydroxymethyl)oxan-2-yl]amino]pentanoic acid	101489516	Click to see C=CC(=CNC(=O)C(CC(C(=O)O)NC1(C(C(C(CO1)O)O)O)CO)O)CO	406.38	unknown	https://doi.org/10.1248/CPB.57.1110
2-Amino-4-hydroxy-5-[(3-methyl-2,5-dihydrofuran-2-yl)amino]-5-oxopentanoic acid	15553203	Click to see	244.24	unknown	https://doi.org/10.1248/CPB.57.1110
2-Amino-5-[(3-methyl-2,5-dihydrofuran-2-yl)amino]-5-oxopentanoic acid	102377982	Click to see	228.24	unknown	https://doi.org/10.1248/CPB.57.1110
4-Hydroxy-5-[[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]amino]-5-oxo-2-[(2,3,4,5-tetrahydroxyoxan-2-yl)methylamino]pentanoic acid	76036216	Click to see C1C=C(C(O1)NC(=O)C(CC(C(=O)O)NCC2(C(C(C(CO2)O)O)O)O)O)CO	422.38	unknown	https://doi.org/10.1248/CPB.57.1110
4-Hydroxy-5-[2-(hydroxymethyl)buta-1,3-dienylamino]-5-oxo-2-[(2,3,4,5-tetrahydroxyoxan-2-yl)methylamino]pentanoic acid	163082018	Click to see	406.38	unknown	https://doi.org/10.1248/CPB.57.1110
Kwansonine A	101489515	Click to see	422.38	unknown	https://doi.org/10.1248/CPB.57.1110
Oxypinnatanine	14779021	Click to see	260.24	unknown	https://doi.org/10.1248/CPB.49.318 https://doi.org/10.1248/CPB.38.3187
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
2-[[2-[[[2-[(18S,25S,32S,35S)-35-[(2S)-butan-2-yl]-16,23,30,33-tetrahydroxy-18-(2-hydroxy-2-iminoethyl)-25-[(R)-hydroxy(phenyl)methyl]-32-[(4-hydroxyphenyl)methyl]-21-methyl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.119,22.126,29.06,11]tritetraconta-1(38),2(43),4,6(11),7,9,12(42),14,16,19(41),21,23,26(40),28,30,33,36(39)-heptadecaen-8-yl]-1,3-thiazol-4-yl]-hydroxymethylidene]amino]-1-hydroxyprop-2-enylidene]amino]prop-2-enoic acid	101463539	Click to see CCC(C)C1C2=NC(=CS2)C3=NC(=CS3)C4=C(C=CC(=N4)C5=NC(=CS5)C(=NC(=C)C(=NC(=C)C(=O)O)O)O)C6=NC(=CS6)C(=NC(C7=NC(=C(S7)C)C(=NC(C8=NC(=CS8)C(=NC(C(=N1)O)CC9=CC=C(C=C9)O)O)C(C1=CC=CC=C1)O)O)CC(=N)O)O	1325.50	unknown	https://doi.org/10.1002/CHIN.200310223
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see	104.17	unknown	https://doi.org/10.3109/13880209009082803
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside	161036	Click to see	358.34	unknown	via CMAUP database
(2S,3R,4R,5R)-3-(hydroxymethyl)-2,5-dimethoxyoxolane-3,4-diol	162851608	Click to see	194.18	unknown	https://doi.org/10.1016/0031-9422(96)83285-7
(3R,4S,4aR)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	9906781	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	via CMAUP database
D-Apio-alpha-L-furanoside, methyl 4-C-methoxy-	101696496	Click to see	194.18	unknown	https://doi.org/10.1016/0031-9422(96)83285-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone	101203815	Click to see	524.50	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1-[1-Hydroxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone	162847389	Click to see	524.50	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1-[1-hydroxy-3,5-dimethyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone	101203816	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)C)C=C(C(=C4O)C(=O)C)C)O)O)O)O)O)O	538.50	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1-[1,5-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone	163018069	Click to see	540.50	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
1-[1,5-Dihydroxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone	85293863	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=C(C(=C4O)C(=O)C)C)O)O)O)O)O)O	540.50	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
(2R,9S,11R)-11-hydroxy-3,8-dioxa-1-azatricyclo[7.3.0.02,6]dodec-5-en-12-one	9990289	Click to see	197.19	unknown	https://doi.org/10.1248/CPB.42.154
(3R,5R)-3-hydroxy-1-[(2R)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methoxypyrrolidin-2-one	9991407	Click to see COC1CC(C(=O)N1C2C(=CCO2)CO)O	229.23	unknown	https://doi.org/10.1248/CPB.42.154
(3R,5R)-3-hydroxy-5-methoxy-1-[(2R)-3-methyl-2,5-dihydrofuran-2-yl]pyrrolidin-2-one	162915349	Click to see CC1=CCOC1N2C(CC(C2=O)O)OC	213.23	unknown	https://doi.org/10.1248/CPB.38.3187
(3R,5R)-3,5-dihydroxy-1-(3-methyl-2,5-dihydrofuran-2-yl)pyrrolidin-2-one	14779025	Click to see CC1=CCOC1N2C(CC(C2=O)O)O	199.20	unknown	https://doi.org/10.1248/CPB.42.154 https://doi.org/10.1248/CPB.38.3187
(3R,5R)-3,5-dihydroxy-1-[(2R)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one	162926368	Click to see C1C=C(C(O1)N2C(CC(C2=O)O)O)CO	215.20	unknown	https://doi.org/10.1248/CPB.38.3187
(3R,5R)-3,5-dihydroxy-1-[(2R)-3-methyl-2,5-dihydrofuran-2-yl]pyrrolidin-2-one	131156005	Click to see CC1=CCOC1N2C(CC(C2=O)O)O	199.20	unknown	https://doi.org/10.1248/CPB.38.3187
(3R,5R)-3,5-dihydroxy-1-[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one	14779023	Click to see	215.20	unknown	https://doi.org/10.1248/CPB.42.154 https://doi.org/10.1248/CPB.38.3187
(3R,5R)-5-hydroxy-3-methoxy-1-(3-methyl-2,5-dihydrofuran-2-yl)pyrrolidin-2-one	101588713	Click to see	213.23	unknown	https://doi.org/10.1248/CPB.42.154 https://doi.org/10.1248/CPB.38.3187
11-Hydroxy-3,8-dioxa-1-azatricyclo[7.3.0.02,6]dodec-5-en-12-one	85085459	Click to see C1C=C2COC3CC(C(=O)N3C2O1)O	197.19	unknown	https://doi.org/10.1248/CPB.42.154
3-Hydroxy-1-[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methoxypyrrolidin-2-one	85085745	Click to see COC1CC(C(=O)N1C2C(=CCO2)CO)O	229.23	unknown	https://doi.org/10.1248/CPB.42.154
3-Hydroxy-5-methoxy-1-(3-methyl-2,5-dihydrofuran-2-yl)pyrrolidin-2-one	14779026	Click to see CC1=CCOC1N2C(CC(C2=O)O)OC	213.23	unknown	https://doi.org/10.1248/CPB.38.3187
3,5-Dihydroxy-1-(3-methyl-2,5-dihydrofuran-2-yl)pyrrolidin-2-one	14779024	Click to see CC1=CCOC1N2C(CC(C2=O)O)O	199.20	unknown	https://doi.org/10.1248/CPB.38.3187
3,5-Dihydroxy-1-[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one	14779022	Click to see	215.20	unknown	https://doi.org/10.1248/CPB.38.3187
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6-Methylluteolin	15293760	Click to see CC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	300.26	unknown	https://doi.org/10.1016/S0040-4020(02)00802-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	102374982	Click to see	520.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	44429735	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O	520.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	74977619	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O	520.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
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	464.40	unknown	https://doi.org/10.1016/J.LFS.2004.03.002
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
acs.jmedchem.1c00409_ST.719	13345442	Click to see	626.50	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Quercetin 3-rutinoside 7-galactoside	13942388	Click to see	772.70	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Quercetin 3-rutinoside-7-glucoside	10190763	Click to see	772.70	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
Quercetin 3,7-diglucoside	10121947	Click to see	626.50	unknown	https://doi.org/10.1016/J.LFS.2004.07.001
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one	11602329	Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC	328.27	unknown	https://doi.org/10.3109/13880209009082803
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3'-Methoxypuerarin	5319485	Click to see	446.40	unknown	via CMAUP database
7-hydroxy-3-(4-hydroxyphenyl)-8-((2S,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one	53384442	Click to see	416.40	unknown	via CMAUP database
Puerarin	5281807	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O	416.40	unknown	via CMAUP database

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Hemerocallis fulva

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