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Sicyos edulis

Sicyos edulis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffd3d05595743409436
Scientific name Sicyos edulis
Authority Jacq.
First published in Enum. Syst. Pl. : 32 (1760)

Description Top

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No description added yet. Help us by writing one.

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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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
br chouchou
Catalan xaiota
cdo hiŏng-iòng-guă
Czech Čajot
German schuschu
Esperanto Ĉajoto
Basque chaiote
Persian چایوت
Finnish kajottikurpitsa
French mirliton
French chouchou
French chayote
French sousou
French chouchoute
French christophine
Galician caioteira
gn chuchu
Hebrew צ'יוטה
Croatian meksički krastavac
ht militon
Indonesian labu siam
Japanese センナリウリ
Japanese 隼人瓜
Japanese 千成瓜
Japanese ハヤトウリ
jv labu siam
Georgian ჩაიოტი
Kazakh Мексикалық қияр
Kannada ಸೀಮೆಬದನೆ
Korean 차요테
lfn xaiote
mai स्कुस
Macedonian чајот
Macedonian максиканска краставица
Macedonian чоко
Malayalam ചൊച്ചക്ക ചെടി
Malayalam മൂടുമുളച്ചി
Malayalam ചൗചൗ
Malayalam ചച്ചിയ്ക്ക
Malayalam ചച്ചയ്ക്ക
Malay pokok labu siem
Burmese ဂေါ်ရခါးပင်
nah chayohtli
Norwegian Bokmål chayote
Nepali स्कुस
Norwegian Nynorsk chayote
pam sayote
sco chayote
Slovenian Čajota
su gamas
Telugu బెంగుళూరు వంకాయ
Thai ฟักแม้ว
Uzbek chayot
xmf ჩაიოტი
yi טשאיאטע
Chinese 洋瓜
Chinese 合掌瓜
Chinese 仙瓜
Chinese 佛手瓜

Subspecies (abbr. subsp./ssp.) Top

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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
    • 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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Cook Islands
    • Southwestern Pacific
      • New Caledonia
  • Southern America
    • 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
Name Level Submitter Released Coverage Size
GCA_036507275.1 ASM3650727v1 Chromosome Beijing Vegetable Research Center 2024-02-22 151.0x 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!
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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 CC12C3C(C45CC(CCC4C3(CC(C1O)O)COC2=O)C(=C)C5)C(=O)O 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 CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)COC2=O 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 CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O 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 CC12C(C=CC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O 330.40 unknown https://doi.org/10.1007/BF00399923
Gibberellin A8 5280607 Click to see CC12C3C(C45CC(=C)C(C4)(CCC5C3(CC(C1O)O)OC2=O)O)C(=O)O 364.40 unknown https://doi.org/10.1007/BF00399923
Gibberellin A9 5281984 Click to see CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O 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 CC1(C(CCC2(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)C(=O)O)O)C(=O)O 378.40 unknown https://doi.org/10.1007/BF00399923
gibberellin A17 5460657 Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C(=O)O)C(=O)O 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 CC12CCCC(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)(C)C(=O)O 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 CC(=CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO 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
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3beta-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester 10720804 Click to see COC1=C(C=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5)OC 522.50 unknown via CMAUP database
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 COC1=CC2=C(C(=C1)OC)C3(C(CC(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)O)O 448.50 unknown via CMAUP database
Aglafoline 393601 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5 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 COC1=C(C=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)O 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 COC1=C(C=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5)O 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 COC1=CC2=C(C(=C1)OC)C3(C(C(C(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC)OC=O)O 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 COC1=CC2=C(C(=C1)OC)C3(C(C(C(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC)O)O 506.50 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 COC1=CC=C(C=C1)C23C(CC(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=CC=C5 434.50 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
i-Pentenyladenine 69205258 Click to see CC(C)C=CC1=NC(=C2C(=N1)N=CN2)N 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
N-[4-(2-Methyl-4-hydroxy-2-butenoylamino)butyl]cinnamamide 10980024 Click to see CC(=CCO)C(=O)NCCCCNC(=O)C=CC1=CC=CC=C1 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 C1C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)(CO)O 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 C1C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)(CO)O 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 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
Vicenin-2 3084407 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 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
> 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-hydroxy-3-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 86573698 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)OC)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-rutinoside 14374725 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)OC)O)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1021/JF040214Q
Diosmin 5281613 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
Isorhoifolin 9851181 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
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
Luteolin 7-o-rutinoside 10461109 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

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