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Ephedra aphylla

Ephedra aphylla - 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 UUID644028c17a42c747042919
Scientific name Ephedra aphylla
Authority Forssk.
First published in Fl. Aegypt.-Arab. : 170 (1775)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic علندى عديمة الأوراق
Hebrew שרביטן ריסני
Chinese 无叶麻黄

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
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Saudi Arabia
    • Western Asia
      • Cyprus
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000794308
Tropicos 100185186
KEW urn:lsid:ipni.org:names:383356-1
The Plant List kew-332875
Open Tree Of Life 626696
NCBI Taxonomy 191304
IUCN Red List 201678
IPNI 383356-1
iNaturalist 135592
GBIF 2653283
EPPO EPEAP
EOL 1156305
CMAUP NPO1897

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
Ecological aspects and relationships of the emblematic Vachellia spp. exposed to anthropic pressures and parasitism in natural hyper-arid ecosystems: ethnobotanical elements, morphology, and biological nitrogen fixation Vincent B, Bourillon J, Gotty K, Boukcim H, Selosse MA, Cambou A, Damasio C, Voisin M, Boivin S, Figura T, Nespoulous J, Galiana A, Maurice K, Ducousso M Planta 25-Apr-2024
PMCID:PMC11045644
doi:10.1007/s00425-024-04407-0
PMID:38662123
Assessment of the anti-cancer potential of Ephedra foeminea leaf extract on MDA-MB-231, MCF-7, 4 T1, and MCF-10 breast cancer cell lines: Cytotoxic, apoptotic and oxidative assays Abdulkarim Alharbi S, Eldin Ahmed Abdelsalam K, Asad M, Alrouji M, Ahmed Ibrahim M, Almuhanna Y Saudi Pharm J 19-Jan-2024
PMCID:PMC10847678
doi:10.1016/j.jsps.2024.101960
PMID:38328794
Bio-Guided Assay of Ephedra foeminea Forssk Extracts and Anticancer Activities: In Vivo, In Vitro, and In Silico Evaluations Nazeam JA, Boshra SA, Mohammed EZ, El Gizawy HA Molecules 29-Dec-2023
PMCID:PMC10780881
doi:10.3390/molecules29010199
PMID:38202783
Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula Alrajhi K, Bibi S, Abu-Dieyeh M Saudi J Biol Sci 25-Dec-2023
PMCID:PMC10805673
doi:10.1016/j.sjbs.2023.103911
PMID:38268781
A review on synthesis and antibacterial potential of bio-selenium nanoparticles in the food industry Ao B, Du Q, Liu D, Shi X, Tu J, Xia X Front Microbiol 13-Jul-2023
PMCID:PMC10373938
doi:10.3389/fmicb.2023.1229838
PMID:37520346
Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK Biomolecules 25-Jun-2023
PMCID:PMC10377637
doi:10.3390/biom13071038
PMID:37509074
Biogenic Selenium Nanoparticles in Biomedical Sciences: Properties, Current Trends, Novel Opportunities and Emerging Challenges in Theranostic Nanomedicine Zambonino MC, Quizhpe EM, Mouheb L, Rahman A, Agathos SN, Dahoumane SA Nanomaterials (Basel) 19-Jan-2023
PMCID:PMC9921003
doi:10.3390/nano13030424
PMID:36770385
Limoniastrum monopetalum–Mediated Nanoparticles and Biomedicines: In Silico Study and Molecular Prediction of Biomolecules Mohammed AE, Alghamdi SS, Alharbi NK, Alshehri F, Suliman RS, Al-Dhabaan F, Alharbi M Molecules 18-Nov-2022
PMCID:PMC9693928
doi:10.3390/molecules27228014
PMID:36432115
Significance of Arbuscular Mycorrhizal Fungi in Mitigating Abiotic Environmental Stress in Medicinal and Aromatic Plants: A Review Israel A, Langrand J, Fontaine J, Lounès-Hadj Sahraoui A Foods 26-Aug-2022
PMCID:PMC9455813
doi:10.3390/foods11172591
PMID:36076777
Microbial Natural Products with Antiviral Activities, Including Anti-SARS-CoV-2: A Review Frediansyah A, Sofyantoro F, Alhumaid S, Al Mutair A, Albayat H, Altaweil HI, Al-Afghani HM, AlRamadhan AA, AlGhazal MR, Turkistani SA, Abuzaid AA, Rabaan AA Molecules 05-Jul-2022
PMCID:PMC9268554
doi:10.3390/molecules27134305
PMID:35807550
Importance of Zinc Nanoparticles for the Intestinal Microbiome of Weaned Piglets Baholet D, Skalickova S, Batik A, Malyugina S, Skladanka J, Horky P Front Vet Sci 02-Jun-2022
PMCID:PMC9201420
doi:10.3389/fvets.2022.852085
PMID:35720843
Broad-Spectrum Theranostics and Biomedical Application of Functionalized Nanomaterials Alshamrani M Polymers (Basel) 17-Mar-2022
PMCID:PMC8956086
doi:10.3390/polym14061221
PMID:35335551
Control of Staphylococcus aureus methicillin resistant isolated from auricular infections using aqueous and methanolic extracts of Ephedra alata Dbeibia A, Taheur FB, Altammar KA, Haddaji N, Mahdhi A, Amri Z, Mzoughi R, Jabeur C Saudi J Biol Sci 01-Oct-2021
PMCID:PMC8848002
doi:10.1016/j.sjbs.2021.09.071
PMID:35197771
Biotransformation ability of endophytic fungi: from species evolution to industrial applications Liu X, Zhou ZY, Cui JL, Wang ML, Wang JH Appl Microbiol Biotechnol 09-Sep-2021
PMCID:PMC8426592
doi:10.1007/s00253-021-11554-x
PMID:34499202
Antioxidants: Classification, Natural Sources, Activity/Capacity Measurements, and Usefulness for the Synthesis of Nanoparticles Flieger J, Flieger W, Baj J, Maciejewski R Materials (Basel) 25-Jul-2021
PMCID:PMC8347950
doi:10.3390/ma14154135
PMID:34361329

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
> Benzenoids / Benzene and substituted derivatives
Phenylacetic Acid 999 Click to see C1=CC=C(C=C1)CC(=O)O 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
sphaeropsidin C 10544575 Click to see CC1(CCCC2(C1CC(=O)C3=CC(CCC32O)(C)C=C)C(=O)O)C 332.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Hydroxyoleic acid 5312773 Click to see C(CCCCO)CCCC=CCCCCCCCC(=O)O 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(5S)-5-[(1S,2Z,4E)-1-hydroxyhexa-2,4-dienyl]oxolan-2-one 10631273 Click to see CC=CC=CC(C1CCC(=O)O1)O 182.22 unknown via CMAUP database
sapinofuranone B 11665504 Click to see CC=CC=CC(C1CCC(=O)O1)O 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Arjunglucoside II 52951052 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one 14465806 Click to see CC1=C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 440.70 unknown via CMAUP database
(4R,4aS,6aR,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 7067822 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-2,3-dione 15081673 Click to see CC1C(=O)C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
[(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate 14465799 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Cerin 21596125 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Cerin acetate 14465798 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C 484.80 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
4-Hydroxymellein, (3S-trans)- 119025905 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
5-Methylmellein 14807789 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C 192.21 unknown via CMAUP database
cis-4-Hydroxymellein 10420140 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sphaeropsidin A 51361447 Click to see CC1(CCCC23C1C(C(=O)C4=CC(CCC42O)(C)C=C)(OC3=O)O)C 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(4aR,6S,8aS)-6-[(1S)-1-hydroxyethyl]-6,8a-dihydro-4aH-pyrano[3,2-b]pyran-2-one 637192 Click to see CC(C1C=CC2C(O1)C=CC(=O)O2)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
7-Methoxy-4-oxo-1,4-dihydroquinoline-2-carboxylic acid 13223157 Click to see COC1=CC2=C(C=C1)C(=O)C=C(N2)C(=O)O 219.19 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,4'-Trihydroxy-7,8-dimethoxyflavone 14034221 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)OC 330.29 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
Herbacetin 5280544 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
Pollenitin 44259965 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see CC(=O)OC1C(C(OC(C1OC(=O)C)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 824.70 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 14162295 Click to see CC(=O)OC1C(OC(C(C1O)O)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O 636.60 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10439992 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O)O 740.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see CC(=O)OC1C(OC(C(C1OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC(=O)C=CC6=CC=C(C=C6)O 824.70 unknown via CMAUP database
Kaempferol-3-O-(2',6'-di-O-trans-p-coumaroyl)-beta-D-glucopyranoside 10439991 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O)O 740.70 unknown via CMAUP database
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
6,8-bis[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 101714435 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)C6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O 918.80 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
6,8-Bis[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 163038059 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)C6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O 918.80 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
8-[(3S,4S,5S)-3-[(2S,3S)-2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3S,4S,5S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(3S,4S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 162817294 Click to see C1C(CC(C(C1O)O)OC2C(C(C(OC2C3=C4C(=C(C(=C3O)C5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C(=O)C=C(O4)C7=CC=C(C=C7)O)CO)O)O)CO 900.80 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
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/10.1016/S0031-9422(97)00092-7
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/10.1016/S0031-9422(97)00092-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 6442291 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O 594.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 101714436 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162942335 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162942334 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978534 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(97)00092-7
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1R,2R,20R,42S,46S)-46-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 16167199 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
CID 12302513 12302513 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown via CMAUP database
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown via CMAUP database

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