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.

Sicyos edulis (Jacq.)—better known as chayote or Sechium edule—has a long culinary presence in Mesoamerica and the Caribbean, and its leaves and shoots are still taken in simple teas. Among urban markets in Mexico, leaves and tender shoots are sold for home preparations that are thought to have diuretic effects (Morales-García et al., 2007). In coastal Puerto Rico, a leaf infusion is a common domestic remedy used “to calm” or for a light sedative effect before sleep (Oakes & Morris, 1956). In northeastern Brazil,，特别是在巴伊亚和塞尔希佩州的集市上，叶子和嫩芽经常被用于泡茶，作为促进排尿的保健茶饮用（Pinheiro et al., 2008）。A practical preparation is a mild, daily-use leaf tea: place 6–8 fresh leaves (about 12–15 g) in 1 L of just-boiled water, cover and steep for 10–15 minutes, then strain and sip warm throughout the day. People who are prone to hypotension or who take diuretics should use this tea cautiously and avoid high, repeated doses. Reliable phytochemistry for this species shows the leaves contain flavonoids such as quercetin and kaempferol glycosides, modest amounts of vitamin C, and saponins; these constituents plausibly underlie the gentle diuretic and calming actions noted in field reports (Deng et al., 2014). Recent work continues to explore its antioxidant and anti-inflammatory potential in vitro, while fresh leaves remain available in many Latin American markets and home gardens for tea and soup, underscoring ongoing cultural use alongside interest in its bioactive profile.

General Uses Top

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Food and beverages (non-medicinal):
The immature fruits are consumed as a vegetable; they are commonly boiled, sautéed, steamed, stir‑fried, or baked. Mature fruits with hardened shells are also cooked. Young shoots and tendrils are widely used as leafy greens and in soups and stir‑fries. The starchy, tuberous root is boiled and used as a starch staple; it may be sliced and fried or cooked in stews. Fruit, tuber, and shoots are also employed in traditional processing such as pickling, fermenting, and flavoring curries. Pectin content supports gelling in preserves when combined with sugar and acid.

Synonyms Top

Scientific name	Authority	First published in
Sechium edule	Sw.	Fl. Ind. Occid. 2: 1150 (1800)
Sechium americanum	Poir.	Encycl. 7: 50 (1806)
Chayota edulis	Jacq.	Select. Stirp. Amer. Hist. : t. 245 (1780)
Sechium edule subsp. sylvestre	Lira & J.Castrejón	Acta Bot. Mex. 49: 57 (1999)

Common names Top

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Filter by language:

Language	Common/alternative name
English	chayote
English	pear squash
Spanish	chayote
Arabic	شايوت
ban	waluh jepang
bcl	sayotes
Belarusian	Чаёт ядомы
Bulgarian	обикновен чайот
bi	susut
Bengali	স্কোয়াশ (সবজি)
br	chouchou
Catalan	xaiota
cdo	hiŏng-iòng-guă
Czech	Čajot
German	schuschu
Esperanto	Ĉajoto
Basque	chaiote
Persian	چایوت
Finnish	kajottikurpitsa
French	chayote
French	mirliton
French	christophine
French	chouchoute
French	sousou
French	chouchou
Galician	caioteira
gn	chuchu
Hebrew	צ'יוטה
Croatian	meksički krastavac
ht	militon
Indonesian	labu siam
Japanese	センナリウリ
Japanese	ハヤトウリ
Japanese	千成瓜
Japanese	隼人瓜
jv	labu siam
Georgian	ჩაიოტი
Kazakh	Мексикалық қияр
Kannada	ಸೀಮೆಬದನೆ
Korean	차요테
lfn	xaiote
Latvian	čajots
mai	स्कुस
Macedonian	чоко
Macedonian	максиканска краставица
Macedonian	чајот
Malayalam	ചച്ചയ്ക്ക
Malayalam	ചച്ചിയ്ക്ക
Malayalam	ചൗചൗ
Malayalam	മൂടുമുളച്ചി
Malayalam	ചൊച്ചക്ക ചെടി
Malay	pokok labu siem
Burmese	ဂေါ်ရခါးပင်
nah	chayohtli
Norwegian Bokmål	chayote
Nepali	स्कुस
Norwegian Nynorsk	chayote
pam	sayote
sco	chayote
Slovenian	Čajota
su	gamas
Swedish	sechium edule
Telugu	బెంగుళూరు వంకాయ
Thai	ฟักแม้ว
Turkish	sechium edule
Uzbek	chayot
xmf	ჩაიოტი
yi	טשאיאטע
Chinese	佛手瓜
Chinese	仙瓜
Chinese	合掌瓜
Chinese	洋瓜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Middle Atlantic Ocean
  - Ascension
  - Saint Helena
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Mauritius
  - Rodrigues
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - West Himalaya
- Indo-China
  - Thailand
  - Vietnam
- Malesia
  - Jawa

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Marianas
- South-central Pacific
  - Cook Islands
- Southwestern Pacific
  - New Caledonia

Southern America click to expand
- Caribbean
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Venezuelan Antilles
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
- Northern South America
  - Venezuela
- Southern South America
  - Argentina Northwest
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000441493
Tropicos	9200749
INPN	636548
Flora of Italy	3318
KEW	urn:lsid:ipni.org:names:293946-1
Plantarium	62153
NCBI Taxonomy	184140
IPNI	293946-1
GBIF	3625017
Freebase	/m/04_pd3
USDA GRIN	33882
Wikipedia	Chayote
CMAUP	NPO22318
Open Tree Of Life	854697

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_036507275.1	ASM3650727v1	Chromosome	Beijing Vegetable Research Center	2024-02-22	151	580.04 Mb

Scientific Literature Top

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

Title

Authors

Publication

Released

IDs

On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India

Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S

Sci Rep

10-May-2024

PMCID:	PMC11087530
doi:	10.1038/s41598-024-61428-1
PMID:	38730080

Synergistic Inhibition of Synbiotic Cultures among Lactobacilli and Plant Extracts against Vaginal Discharge Causing Candida albicans

Sookkhee S, Khamnoi P, Sastraruji T, Boonkum S, Wikan N, Nimlamool W

Nutrients

30-Apr-2024

PMCID:	PMC11085874
doi:	10.3390/nu16091372
PMID:	38732618

Evaluation of Sechium edule fruit attenuation impact on the cardiomyopathy of the STZ-induced diabetic rats

Mohammad FS, Das U, Samanta SK, Irfan Z, Gopinath SC, Mostafa MA, Al-Haidari RA, Abdellatif AA, Shehata AM, Gouda MM

Heliyon

27-Apr-2024

PMCID:	PMC11089326
doi:	10.1016/j.heliyon.2024.e30440
PMID:	38742087

Composite Coatings Applied to Fresh and Blanched Chayote (Sechium edule) and Modeling of the Drying Kinetics and Sorption Isotherms

Estrada-Girón Y, del Campo-Campos AM, Gutiérrez-García E, Fernández-Escamilla VV, Martínez-Chávez L, Jaime-Ornelas TJ

Foods

12-Apr-2024

PMCID:	PMC11049529
doi:	10.3390/foods13081178
PMID:	38672851

Genome-wide identification and expression analysis of the cryptochromes reveal the CsCRY1 role under low-light-stress in cucumber

Cao H, Wang R, Zhao J, Shi L, Huang Y, Wu T, Zhang C

Front Plant Sci

10-Apr-2024

PMCID:	PMC11040678
doi:	10.3389/fpls.2024.1371435
PMID:	38660445

The Cancer-Protective Potential of Protocatechuic Acid: A Narrative Review

Cadena-Iñiguez J, Santiago-Osorio E, Sánchez-Flores N, Salazar-Aguilar S, Soto-Hernández RM, Riviello-Flores MD, Macías-Zaragoza VM, Aguiñiga-Sánchez I

Molecules

23-Mar-2024

PMCID:	PMC11012759
doi:	10.3390/molecules29071439
PMID:	38611719

Green Extraction of Natural Colorants from Food Residues: Colorimetric Characterization and Nanostructuring for Enhanced Stability

Lauria VB, Silva LP

Foods

21-Mar-2024

PMCID:	PMC10970246
doi:	10.3390/foods13060962
PMID:	38540952

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

He Y, Xu Y, Chen X

Insects

31-Jan-2024

PMCID:	PMC10889426
doi:	10.3390/insects15020093
PMID:	38392559

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

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

EFSA J

25-Jan-2024

PMCID:	PMC10809878
doi:	10.2903/j.efsa.2024.8544
PMID:	38273989

Hydroalcoholic extract from Sechium edule (Jacq.) S.w. root reverses oleic acid-induced steatosis and insulin resistance in vitro

Aziel Alvarado-Ojeda Z, Zamilpa A, Costet-Mejia A, Méndez-Martínez M, Trejo-Moreno C, Jiménez-Ferrer JE, Salazar-Martínez AM, Cruz-Muñoz ME, Fragoso G, Rosas-Salgado G

Heliyon

17-Jan-2024

PMCID:	PMC10835324
doi:	10.1016/j.heliyon.2024.e24567
PMID:	38312619

Aquilaria sinensis: An Upstart Resource for Cucurbitacin Production Offers Insights into the Origin of Plant Bitter (Bi) Gene Clusters

Ding X, Yang Z, Wang H, Zeng J, Dai H, Mei W

Plants (Basel)

16-Jan-2024

PMCID:	PMC10819951
doi:	10.3390/plants13020260
PMID:	38256813

Plant mediated synthesis of flower-like Cu2O microbeads from Artimisia campestris L. extract for the catalyzed synthesis of 1,4-disubstituted 1,2,3-triazole derivatives

Abdelbaki H, Djemoui A, Souli L, Souadia A, Ouahrani MR, Djemoui B, Lahrech MB, Messaoudi M, Ben Amor I, Benarfa A, Alsalme A, Bechelany M, Barhoum A

Front Chem

16-Jan-2024

PMCID:	PMC10829102
doi:	10.3389/fchem.2023.1342988
PMID:	38298761

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Biocontrol potential of endophytic bacterium Bacillus altitudinis GS-16 against tea anthracnose caused by Colletotrichum gloeosporioides

Wu Y, Tan Y, Peng Q, Xiao Y, Xie J, Li Z, Ding H, Pan H, Wei L

PeerJ

09-Jan-2024

PMCID:	PMC10785793
doi:	10.7717/peerj.16761
PMID:	38223761

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

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

Foods

11-Dec-2023

PMCID:	PMC10742603
doi:	10.3390/foods12244439
PMID:	38137243

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
(1R,2R,5R,8R,9S,10S,11S,16S,17R)-16,17-dihydroxy-11-methyl-6-methylidene-12-oxo-13-oxapentacyclo[9.3.3.15,8.01,10.02,8]octadecane-9-carboxylic acid	101603109	Click to see	362.40	unknown	https://doi.org/10.1007/BF00399923
(1S,2R,5S,8S,9S,10S,11S)-11-methyl-6-methylidene-12-oxo-13-oxapentacyclo[9.3.3.15,8.01,10.02,8]octadecane-9-carboxylic acid	159696818	Click to see	330.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellic acid	6466	Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	346.40	unknown	https://doi.org/10.1016/S0031-9422(00)80147-8
Gibberellin A1	5280379	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	348.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A4	92109	Click to see	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)80147-8
Gibberellin A44	5460372	Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)COC2=O	346.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A7	92782	Click to see	330.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A8	5280607	Click to see	364.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A9	5281984	Click to see	316.40	unknown	https://doi.org/10.1016/S0031-9422(00)80147-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 20-carboxylic acids
Gibberellin A13	10883375	Click to see	378.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A17	5460657	Click to see	378.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A25	14464358	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)C(=O)O)C(=O)O	362.40	unknown	https://doi.org/10.1007/BF00399923
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
Gibberellin A12	443450	Click to see	332.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A19	5460209	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://doi.org/10.1007/BF00399923
Gibberellin A53	440914	Click to see CC12CCCC(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)(C)C(=O)O	348.40	unknown	https://doi.org/10.1007/BF00399923
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Zeatin riboside	6440982	Click to see	351.36	unknown	https://doi.org/10.1016/S0168-9452(97)00186-6 https://doi.org/10.1016/S0176-1617(88)80206-2
> Organoheterocyclic compounds / Benzofurans / Flavaglines
8bH-Cyclopenta[b]benzofuran-1,8b-diol, 3a-(1,3-benzodioxol-5-yl)-1,2,3,3a-tetrahydro-6,8-dimethoxy-3-phenyl-, (1R,3S,3aR,8bS)-	10623340	Click to see	448.50	unknown	via CMAUP database
Aglafolin	393601	Click to see	492.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-acetyloxy-3a-(1,3-benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10697870	Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC	548.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-formyloxy-8b-hydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10650033	Click to see	536.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1,8b-dihydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10815498	Click to see	508.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1-formyloxy-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10721063	Click to see	534.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	390507	Click to see	506.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(3,4-dimethoxyphenyl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10720804	Click to see	522.50	unknown	via CMAUP database
Methyl 1-Formyloxyrocaglate	10839697	Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5	520.50	unknown	via CMAUP database
Rocaglaol	393602	Click to see	434.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
i-Pentenyladenine	69205258	Click to see	203.24	unknown	https://doi.org/10.1016/S0168-9452(97)00186-6
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
trans-Zeatin	449093	Click to see CC(=CCNC1=NC=NC2=C1NC=N2)CO	219.24	unknown	https://doi.org/10.1016/S0176-1617(88)80206-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Dasyclamide	10980024	Click to see	316.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	11006262	Click to see	564.50	unknown	https://doi.org/10.1021/JF040214Q
8-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	74977461	Click to see	564.50	unknown	https://doi.org/10.1021/JF040214Q
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	5378180	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF040214Q
Vicenin 2	3084407	Click to see	594.50	unknown	https://doi.org/10.1021/JF040214Q
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/JF040214Q
Vitexin	5280441	Click to see	432.40	unknown	https://doi.org/10.1021/JF040214Q
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12315422	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/JF040214Q
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	5353588	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1021/JF040214Q
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one	5377847	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1021/JF040214Q
Chrysoeriol 7-O-rutinoside	86573698	Click to see	608.50	unknown	https://doi.org/10.1021/JF040214Q
Chrysoeriol 7-rutinoside	14374725	Click to see	608.50	unknown	https://doi.org/10.1021/JF040214Q
Diosmin	5281613	Click to see	608.50	unknown	https://doi.org/10.1021/JF040214Q
Isorhoifolin	9851181	Click to see	578.50	unknown	https://doi.org/10.1021/JF040214Q
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF040214Q
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF040214Q
Scolymoside	10461109	Click to see	594.50	unknown	https://doi.org/10.1021/JF040214Q

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Sicyos edulis

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