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Euonymus sachalinensis

Euonymus sachalinensis - Unknown
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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 UUID64401bcd0ac04876655845
Scientific name Euonymus sachalinensis
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 27: 446 (1882)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Euonymus macropterus var. miniatus (Tolm.) Vorosch. Byull. Glavn. Bot. Sada 84: 33 (1972)
Euonymus maximowiczianus (Prokh.) Vorosch. Index Seminum (Acad. Sci. URSS) 9: 64 (1954)
Euonymus miniatus Tolm. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 18: 159 (1957)
Euonymus oxyphyllus var. kuenbuergia Honda Bot. Mag. (Tokyo) 47: 297 1933
Euonymus planipes (Koehne) Koehne Mitt. Deutsch. Dendrol. Ges. 15: 62 (1906 publ. 1907)
Euonymus robustus Nakai Bot. Mag. (Tokyo) 28: 307 (1914)
Euonymus tricarpus Koidz. Icon. Pl. Koisikav. 3: 77 (1916)
Euonymus latifolius var. sachalinensis F.Schmidt Reis. Amur-Land., Bot. 121 1868
Euonymus sachalinensis var. tricarpus (Koidz.) Kudô Rep. Exp. Forest. Agric. Kyusk. Univ. 1: 76 1931
Euonymus latifolius var. planipes Koehne Gartenflora 53(2): 29 (1904)
Kalonymus maximowiczianus Prokh. Fl. URSS 14: 744 (1949)
Kalonymus miniata (Tolm.) Prokh. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 20: 412 (1960)
Kalonymus sachalinensis (F.Schmidt) Prokh. Fl. URSS 14: 571 (1949)
Turibana planipes (Koehne) Nakai J. Jap. Bot. 24: 13 (1949)
Turibana sachalinensis (Fr.Schmidt) Nakai J. Jap. Bot. 24: 13 (1949)
Turibana tricarpa (Koidz.) Nakai J. Jap. Bot. 24: 13 (1949)
Euonymus planipes subsp. maximowiczianus (Prokh.) Nedol.

Common names Top

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Language Common/alternative name
Korean 회나무
Russian Бересклет сахалинский
Chinese 东北卫矛
Chinese 库页卫矛

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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Sow seeds directly at 4°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000682052
UNII 2RBY15E1QD
Tropicos 6600005
KEW urn:lsid:ipni.org:names:161105-1
The Plant List kew-2803604
Plantarium 15444
Open Tree Of Life 598270
Observations.org 142178
NCBI Taxonomy 749925
IPNI 161105-1
GBIF 3794098
EPPO EUOSA
EOL 2880510
Elurikkus 415494
USDA GRIN 104666
Wikipedia Euonymus_sachalinensis
CMAUP NPO29362

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
Euonymus sachalinensis Induces Apoptosis by Inhibiting the Expression of c-Myc in Colon Cancer Cells Park SM, Jee W, Park YR, Kim H, Na YC, Jung JH, Jang HJ Molecules 14-Apr-2023
PMCID:PMC10140968
doi:10.3390/molecules28083473
PMID:37110707
Disjunction and Vicariance Between East and West Asia: A Case Study on Euonymus sect. Uniloculares Based on Plastid Genome Analysis Jamshed S, Kim JH Front Plant Sci 11-Mar-2022
PMCID:PMC8963480
doi:10.3389/fpls.2022.825209
PMID:35360330
Analysis of traditional knowledge of medicinal plants from residents in Gayasan National Park (Korea) Song MJ, Kim H, Lee BY, Brian H, Park CH, Hyun CW J Ethnobiol Ethnomed 21-Oct-2014
PMCID:PMC4216341
doi:10.1186/1746-4269-10-74
PMID:25336281
Screening of Korean Medicinal Plant Extracts for α-Glucosidase Inhibitory Activities Sancheti S, Sancheti S, Lee SH, Lee JE, Seo SY Iran J Pharm Res 01-Mar-2011
PMCID:PMC3828923
PMID:24250352
New Sesquiterpene Polyesters from Euonymus Species Judit Hohmann, Gábor Nagy, Zuber Dini, Gábor Günther, István Pelczer, Gyula Jerkovich, László Varjas American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50122A006
Isolation and structure elucidation of four new dihydro-β-agarofuran polyesters from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther, Gyula Argay, Alajos Kálmán, Gábor Czira Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19940003281
A sesquiterpene polyol ester from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85549-7
Two sesquiterpene pyridine alkaloids from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther, Lászlò Varjas Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85382-2

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
> Alkaloids and derivatives
[(1R,3S,13R,14R,17R,18R,19R,20S,21R,23S,24R,25S)-18,19,21,24-tetraacetyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15,22-trioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 163087610 Click to see CC1C(C(=O)OC2C(C(C3(C(C(=O)C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C 761.70 unknown https://doi.org/10.1021/NP50122A006
[(1S,3S,13S,14S,17R,18R,19S,20R,21S,24R,25R)-18,19,21,24-tetraacetyloxy-3,13,14,25-tetramethyl-6,15,22-trioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 101593037 Click to see CC1C(C(=O)OC2C(C34C(C(C(=O)C(C3(C(C2OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)C(O4)(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)C)C 745.70 unknown https://doi.org/10.1016/0031-9422(93)85382-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2R,3R,4S,5R,6S,7S,9R,10R,12R)-3,4,5,7,12-pentaacetyloxy-6-(acetyloxymethyl)-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 10259204 Click to see CC1C(C(C(C2(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)COC(=O)C4=CC=CC=C4)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 704.70 unknown https://doi.org/10.1039/P19940003281
[3,4,5,7,12-Pentaacetyloxy-6-(acetyloxymethyl)-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 163045380 Click to see CC1C(C(C(C2(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)COC(=O)C4=CC=CC=C4)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 704.70 unknown https://doi.org/10.1039/P19940003281
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7,12-tetraacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-3-[(2R)-2-methylbutanoyl]-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162848272 Click to see CCC(C)C(=O)C1C(C(C2(C(C(=O)C3C(C2(C1(C)O)OC3(C)COC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 746.70 unknown https://doi.org/10.1039/P19940003281
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7,12-tetraacetyloxy-6-(acetyloxymethyl)-3-(furan-3-carbonyl)-2-hydroxy-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162913916 Click to see CC(=O)OCC12C(C(C(C(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)COC(=O)C4=CC=CC=C4)OC(=O)C)(C)O)C(=O)C5=COC=C5)OC(=O)C)OC(=O)C 756.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7,12-Tetraacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-3-(2-methylbutanoyl)-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162848271 Click to see CCC(C)C(=O)C1C(C(C2(C(C(=O)C3C(C2(C1(C)O)OC3(C)COC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 746.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7,12-Tetraacetyloxy-6-(acetyloxymethyl)-3-(furan-3-carbonyl)-2-hydroxy-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162913915 Click to see CC(=O)OCC12C(C(C(C(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)COC(=O)C4=CC=CC=C4)OC(=O)C)(C)O)C(=O)C5=COC=C5)OC(=O)C)OC(=O)C 756.70 unknown https://doi.org/10.1039/P19940003281
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2S,4R,5S,6R,7R,9S,12S)-4,7,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162938304 Click to see CC1CC(C(C2(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C4=CC=CC=C4)OC(=O)C 588.60 unknown https://doi.org/10.1016/0031-9422(93)85549-7
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7-triacetyloxy-6-(acetyloxymethyl)-2,12-dihydroxy-2,10-dimethyl-3-[(2R)-2-methylbutanoyl]-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162907097 Click to see CCC(C)C(=O)C1C(C(C2(C(C(=O)C3C(C2(C1(C)O)OC3(C)COC(=O)C4=CC=CC=C4)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 704.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7-Triacetyloxy-6-(acetyloxymethyl)-2,12-dihydroxy-2,10-dimethyl-3-(2-methylbutanoyl)-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162907096 Click to see CCC(C)C(=O)C1C(C(C2(C(C(=O)C3C(C2(C1(C)O)OC3(C)COC(=O)C4=CC=CC=C4)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 704.70 unknown https://doi.org/10.1039/P19940003281
[5,12-Diacetyloxy-6-(acetyloxymethyl)-4-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162960481 Click to see CC(=O)OCC12C(CC3C(C1(C(CC(C2OC(=O)C)OC(=O)C4=CC=CC=C4)(C)O)OC3(C)C)OC(=O)C)OC(=O)C5=CC=CC=C5 652.70 unknown https://doi.org/10.1021/NP50122A006
5,7,10-Triacetoxy-5a-(acetoxymethyl)-6-(benzoyloxy)-3,4,5,5a,6,7,8,9-octahydro-2,2,9-trimethyl-2H-3,9a-methano-1-benzooxepin-4-one 75012107 Click to see CC1CC(C(C2(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C4=CC=CC=C4)OC(=O)C 588.60 unknown https://doi.org/10.1016/0031-9422(93)85549-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-(3,5-Dihydroxy-phenyl)-2-(4-hydroxy-phenyl)-2,3-dihydro-benzofuran-5-carbaldehyde 636845 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=O)C4=CC(=CC(=C4)O)O)O 348.30 unknown via CMAUP database
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 242.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-O-(6-O-Acetyl-alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11092923 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)O)CO)O)O)O 560.50 unknown via CMAUP database
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown via CMAUP database
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
helonioside A 16745274 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(CO)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O 694.60 unknown via CMAUP database
Helonioside B 21636195 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)O)O)O 736.70 unknown via CMAUP database
Smilaside L 24862701 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 870.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-2,5-bis[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11593148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O 882.80 unknown via CMAUP database
1-O-(4-Hydroxy-trans-cinnamoyl)-2-O-(alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11735009 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 664.60 unknown via CMAUP database
Smilaside C 10919948 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 840.80 unknown via CMAUP database
Smilaside G 24862591 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 810.70 unknown via CMAUP database
Smilaside H 24862644 Click to see CC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)CO)O)O 852.80 unknown via CMAUP database
Smilaside I 24862642 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 852.80 unknown via CMAUP database
Smilaside J 24850451 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 840.80 unknown via CMAUP database
Smilaside K 24862643 Click to see CC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)COC(=O)C=CC5=CC=C(C=C5)O)CO)O)O 882.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 C-glycosides
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-2alpha-(3-Hydroxy-4-methoxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 11081337 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
(2R)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 10885307 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 5320854 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown via CMAUP database
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database

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