Lespedeza cyrtobotrya - Unknown
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Internal ID UUID643fd955b6896798730489
Scientific name Lespedeza cyrtobotrya
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi3: 48 (1867)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lespedeza cyrtobotrya var. kawachiana (Nakai) Ohwi J. Jap. Bot.26: 234 (1951)
Lespedeza cyrtobotrya var. longiramea Nakai
Lespedeza cyrtobotrya var. patens H.Koidz.
Lespedeza cyrtobotrya var. pedunculata Nakai
Lespedeza kawachiana Nakai Lespedeza Japan Korea: 47 (1927)
Lespedeza anthobotrya Ricker Amer. J. Bot.33: 257 (1946)
Campylotropis virgata Miq. Fl. Ned. Ind.1(1): 230 (1855)
Lespedeza cyrtobotrya f. virginea H.Ohashi J. Jap. Bot.84: 360 (2009)
Lespedeza cyrtobotrya f. alba Ohwi Bull. Natl. Sci. Mus. Tokyo33: 77 (1953)
Lespedeza cyrtobotrya f. semialba Nakai Bull. Seoul Natl. Univ. Forests2: 11 (1965)

Common names Top

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Language Common/alternative name
English leafy lespedeza
Korean 참싸리
Chinese 短梗胡枝子
Chinese 籽条
Chinese 铁扫帚
Chinese 圆叶胡枝子
Chinese 短序胡枝子

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185058
USDA Plants LECY80
Tropicos 13021817
KEW urn:lsid:ipni.org:names:502433-1
The Plant List ild-31196
Open Tree Of Life 1077029
Observations.org 119326
NCBI Taxonomy 701533
Nature Serve 2.131022
IPNI 502433-1
iNaturalist 164567
GBIF 2955621
EPPO LESCY
EOL 643224
USDA GRIN 21858
CMAUP NPO11451

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
Cladosporium—Insect Relationships Nicoletti R, Russo E, Becchimanzi A J Fungi (Basel) 19-Jan-2024
PMCID:PMC10820778
doi:10.3390/jof10010078
PMID:38276024
Lignin Extraction by Using Two-Step Fractionation: A Review Tanis MH, Wallberg O, Galbe M, Al-Rudainy B Molecules 22-Dec-2023
PMCID:PMC10779531
doi:10.3390/molecules29010098
PMID:38202680
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Development of a system for the automated identification of herbarium specimens with high accuracy Shirai M, Takano A, Kurosawa T, Inoue M, Tagane S, Tanimoto T, Koganeyama T, Sato H, Terasawa T, Horie T, Mandai I, Akihiro T Sci Rep 16-May-2022
PMCID:PMC9110755
doi:10.1038/s41598-022-11450-y
PMID:35577859
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Nocturnal ambush predators and their potential impact on flower‐visiting moths Sakagami K, Funamoto D, Sugiura S Ecology 16-Oct-2021
PMCID:PMC9286552
doi:10.1002/ecy.3482
PMID:34289091
GPNMB Extracellular Fragment Protects Melanocytes from Oxidative Stress by Inhibiting AKT Phosphorylation Independent of CD44 Wang Q, Kuroda Y, Yang L, Lai S, Mizutani Y, Iddamalgoda A, Guo J, Yamamoto A, Murase D, Takahashi Y, Xiang L, Inoue S, Tsuruta D, Katayama I Int J Mol Sci 07-Oct-2021
PMCID:PMC8509362
doi:10.3390/ijms221910843
PMID:34639184
Zebrafish as a Useful Model to Study Oxidative Stress-Linked Disorders: Focus on Flavonoids Abbate F, Maugeri A, Laurà R, Levanti M, Navarra M, Cirmi S, Germanà A Antioxidants (Basel) 25-Apr-2021
PMCID:PMC8147052
doi:10.3390/antiox10050668
PMID:33922976
Historical migration and taxonomic entity of Korean endemic shrub Lespedeza maritima (Fabaceae) based on microsatellite loci Jin DP, Park JS, Choi BH AoB Plants 18-Feb-2021
PMCID:PMC7983312
doi:10.1093/aobpla/plab009
PMID:33767807
Exploring the metabolomic diversity of plant species across spatial (leaf and stem) components and phylogenic groups Lee S, Oh DG, Singh D, Lee JS, Lee S, Lee CH BMC Plant Biol 28-Jan-2020
PMCID:PMC6986006
doi:10.1186/s12870-019-2231-y
PMID:31992195
Pest categorisation of the non‐EU phytoplasmas of Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Ribes L., Rubus L. and Vitis L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 13-Jan-2020
PMCID:PMC7008834
doi:10.2903/j.efsa.2020.5929
PMID:32626484
Nestedness in Arbuscular Mycorrhizal Fungal Communities in a Volcanic Ecosystem: Selection of Disturbance-tolerant Fungi along an Elevation Gradient Atunnisa R, Ezawa T Microbes Environ 14-Aug-2019
PMCID:PMC6759341
doi:10.1264/jsme2.ME19073
PMID:31413228
Extraction of Kaempferol and Its Glycosides Using Supercritical Fluids from Plant Sources: A Review Cid-Ortega S, Monroy-Rivera JA Food Technol Biotechnol 01-Dec-2018
PMCID:PMC6399721
doi:10.17113/ftb.56.04.18.5870
PMID:30923445
A Zebrafish Embryo as an Animal Model for the Treatment of Hyperpigmentation in Cosmetic Dermatology Medicine Lajis AF Medicina (Kaunas) 25-May-2018
PMCID:PMC6122095
doi:10.3390/medicina54030035
PMID:30344266

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 / Naphthalenes / Phenylnaphthalenes
6,8-dihydroxy-2-(4-hydroxyphenyl)-4H-naphthalen-1-one 45052307 Click to see C1C=C(C(=O)C2=C1C=C(C=C2O)O)C3=CC=C(C=C3)O 268.26 unknown https://doi.org/10.1248/CPB.28.1172
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2R,3S)-2,3-bis(1,3-benzodioxol-5-ylmethyl)butane-1,4-diol 11428305 Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 358.40 unknown via CMAUP database
Dihydrocubebin 193042 Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Asarinin 101612 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Horsfieldin 101389128 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trimyristin 11148 Click to see CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC 723.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(E)-N-[(2R,3R,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide 163039527 Click to see CC=C(C)C(=O)NC1CC2CCC3C4CCC(C4(CCC3C2(CC1O)C)C)C(C)N(C)C 444.70 unknown https://doi.org/10.1021/NP800535G
> 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,4,6-Trihydroxyphenyl)dodecan-1-one 11771258 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C=C1O)O)O 308.40 unknown via CMAUP database
1-(2,6-Dihydroxyphenyl)dodecan-1-one 365016 Click to see CCCCCCCCCCCC(=O)C1=C(C=CC=C1O)O 292.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2-(6-phenylhexyl)-gamma-chromene-4-one 101219429 Click to see C1=CC=C(C=C1)CCCCCCC2=CC(=O)C3=C(C=C(C=C3O2)O)O 338.40 unknown via CMAUP database
5,7-Dihydroxy-2-nonyl-chromen-4-one 5378621 Click to see CCCCCCCCCC1=CC(=O)C2=C(C=C(C=C2O1)O)O 304.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(6aR,11aR)-6a,11a-Dihydro-8-[5-hydroxy-2-(2,4-dihydroxy-5-prenylphenyl)-7,7-dimethyl-7H-furo[2,3-f][1]benzopyran-3-ylcarbonyl]-2,10-diprenyl-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol 25208601 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C7C=CC(OC7=C(C=C56)O)(C)C)C8=C(C=C(C(=C8)CC=C(C)C)O)O)O)CC=C(C)C)C 810.90 unknown https://doi.org/10.1021/NP800535G
(6aR,11aR)-8-[[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 25208759 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=C(C(=C4CC=C(C)C)O)CC5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)C 799.00 unknown https://doi.org/10.1021/NP800535G
(6aR,11aR)-8-[1-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]ethenyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 162842380 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=C)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C 811.00 unknown https://doi.org/10.1021/NP800535G
[(6aR,11aR)-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-(2,4-dihydroxyphenyl)-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone 25208600 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C=C7)O)O)O)CC=C(C)C)C 744.80 unknown https://doi.org/10.1021/NP800535G
[(6aR,11aR)-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[5,6-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone 25208908 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C8C(=C7)C=CC(O8)(C)C)O)O)CC=C(C)C)C 810.90 unknown https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-7,7-dimethylfuro[2,3-f]chromen-3-yl]methanone 74429465 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C7C=CC(OC7=C(C=C56)O)(C)C)C8=C(C=C(C(=C8)CC=C(C)C)O)O)O)CC=C(C)C)C 810.90 unknown https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone 56664386 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C 812.90 unknown https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[5,6-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone 74429595 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C8C(=C7)C=CC(O8)(C)C)O)O)CC=C(C)C)C 810.90 unknown https://doi.org/10.1021/NP800535G
2-(2,4-Dihydroxyphenyl)-6-hydroxybenzofuran 15480861 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=C(C=C(C=C3)O)O 242.23 unknown https://doi.org/10.1248/CPB.28.1172
8-[1-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]ethenyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 162842379 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=C)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C 811.00 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin H1 45269771 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C(C(=C3O2)CC=C(C)C)O)O)CC4=CC5C(C(=C4O)CC=C(C)C)OC6=C5C(=O)OC7=C6C=C(C(=C7)O)CC=C(C)C)C 812.90 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin H2 45273188 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C(C(=C3O2)CC=C(C)C)O)O)C(=O)C4=CC5C(C(=C4O)CC=C(C)C)OC6=C5C(=O)OC7=C6C=C(C(=C7)O)CC=C(C)C)C 826.90 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin H3 45272315 Click to see CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4C3C=C(C(=C4CC=C(C)C)O)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C8C(=C7)C=CC(O8)(C)C)O)C 824.90 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin H4 45273189 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C4C(=C3O2)C=CC(O4)(C)C)O)C(=O)C5=CC6C(C(=C5O)CC=C(C)C)OC7=C6C(=O)OC8=C7C=C(C(=C8)O)CC=C(C)C)C 824.90 unknown https://doi.org/10.1021/NP800535G
lespeflorin J3 25243394 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C 812.90 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-1-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163076397 Click to see CC(C)(C1CC2=C(C=CC(=C2O1)C(=O)C=CC3=CC=C(C=C3)O)O)O 340.40 unknown https://doi.org/10.1021/NP800535G
1-(5-Hydroxy-2,2-dimethylchromen-8-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one 74429466 Click to see CC1(C=CC2=C(C=CC(=C2O1)C(=O)C=CC3=CC=C(C=C3)O)O)C 322.40 unknown https://doi.org/10.1021/NP800535G
1-[4-Hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 74429379 Click to see CC(C)(C1CC2=C(C=CC(=C2O1)C(=O)C=CC3=CC=C(C=C3)O)O)O 340.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin B2 25208602 Click to see CC1(C=CC2=C(C=CC(=C2O1)C(=O)C=CC3=CC=C(C=C3)O)O)C 322.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
Abssinone II 7330517 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
abyssinone II 10064832 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
ent-abyssinone II 7330518 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 26436537 Click to see CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 5321775 Click to see CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
Bavachin 14236566 Click to see CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
2',4',5,7-Tetrahydroxy-8-(3-methyl-2-butenyl)flavanone 11810419 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C 356.40 unknown https://doi.org/10.1021/NP800535G
3,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 24175339 Click to see CC(=CCC1=C(C=CC2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1021/NP800535G
7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11609510 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
Isobavachin 193679 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
Leachianone G 5275227 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C 356.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin A1 25208280 Click to see CC(=CCC1=C(C=CC2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1021/NP800535G
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1021/NP800535G
> 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 https://doi.org/10.1021/NP800535G
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1021/NP800535G
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP800535G
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1021/NP800535G
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-2,3-dihydrochromen-4-one 163042844 Click to see CC1=CC2=C(C=C1O)OC(C(C2=O)O)C3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1021/NP800535G
3,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methyl-2,3-dihydrochromen-4-one 163042843 Click to see CC1=CC2=C(C=C1O)OC(C(C2=O)O)C3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Lespecyrtin G1 25208599 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)O)OC3=O)C 352.30 unknown https://doi.org/10.1021/NP800535G
Lespeflorin I2 25243392 Click to see CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C 420.50 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,14R)-3-methoxy-7,7,20,20-tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene 101316460 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C(=C6C=CC(OC6=C5)(C)C)OC)C 418.50 unknown https://doi.org/10.1021/NP800535G
(1S,14S)-3-methoxy-7,7,20,20-tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene 163011000 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C(=C6C=CC(OC6=C5)(C)C)OC)C 418.50 unknown https://doi.org/10.1021/NP800535G
(6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 5117820 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
2-(3-hydroxy-3-methylbutyl)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 56674233 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C(C(=C4)O)CCC(C)(C)O)O)C 410.50 unknown https://doi.org/10.1021/NP800535G
4-Prenylphaseollidin 21141346 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1021/NP800535G
6,6-Dimethyl-10,16-bis(3-methylbut-2-enyl)-7,12,20-trioxapentacyclo[11.8.0.02,11.03,8.014,19]henicosa-2,4,8,10,14(19),15,17-heptaene-9,17-diol 56680953 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C5C(=C34)C=CC(O5)(C)C)O)CC=C(C)C)C 474.60 unknown https://doi.org/10.1021/NP800535G
7-Methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4,6,8,14,20-hexaene-6,18-diol 56657021 Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=CC(=C(C=C45)OC)O)O)C 370.40 unknown https://doi.org/10.1021/NP800535G
7,17,17-Trimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol 56671417 Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C 404.50 unknown https://doi.org/10.1021/NP800535G
7,7,19,19-Tetramethyl-23-(3-methylbut-2-enyl)-8,12,20,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.016,21]pentacosa-2(11),3,5,9,15,17,21,23-octaen-22-ol 56665483 Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C4COC5=C(C4O2)C=C6C=CC(OC6=C5)(C)C)C 472.60 unknown https://doi.org/10.1021/NP800535G
7,7,20,20-Tetramethyl-16-(3-methylbut-2-enyl)-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15,17,21,23-octaen-17-ol 56670902 Click to see CC(=CCC1=C2C3COC4=C(C3OC2=C5C=CC(OC5=C1O)(C)C)C=C6C=CC(OC6=C4)(C)C)C 472.60 unknown https://doi.org/10.1021/NP800535G
7,7,20,20-Tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene 56681660 Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C 388.50 unknown https://doi.org/10.1021/NP800535G
Anhydroglycinol 442667 Click to see C1C2=C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O 254.24 unknown https://doi.org/10.1248/CPB.28.1172
CID 10408212 10408212 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP800535G
Erybraedin A 362562 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C 392.50 unknown https://doi.org/10.1021/NP800535G
Erybreadin C 21147013 Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP800535G
Erythrabyssin II 5086400 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1021/NP800535G
Gangetinin 44257472 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C(=C6C=CC(OC6=C5)(C)C)OC)C 418.50 unknown https://doi.org/10.1021/NP800535G
Lespebuergine G4 56657670 Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C(C(=C4)O)CC=C(C)C 406.50 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E1 25195062 Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C 388.50 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E2 25208755 Click to see CC(=CCC1=C2C3COC4=C(C3OC2=C5C=CC(OC5=C1O)(C)C)C=C6C=CC(OC6=C4)(C)C)C 472.60 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E3 25208431 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C5C(=C34)C=CC(O5)(C)C)O)CC=C(C)C)C 474.60 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E4 25208756 Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C4COC5=C(C4O2)C=C6C=CC(OC6=C5)(C)C)C 472.60 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E5 25208432 Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C 404.50 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E6 25208757 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C(C(=C4)O)CCC(C)(C)O)O)C 410.50 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin E7 25208433 Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=CC(=C(C=C45)OC)O)O)C 370.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin F1 25208435 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)O)OC3)C 338.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin F2 25208758 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C 406.50 unknown https://doi.org/10.1021/NP800535G
lespeflorin G4 25243081 Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C(C(=C4)O)CC=C(C)C 406.50 unknown https://doi.org/10.1021/NP800535G
Phaseolin 91572 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1021/NP800535G
Phaseolin; Phaseolin (phytoalexin) 4063834 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.1021/NP800535G
Phaseollidin 119268 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
Haginin D 14077819 Click to see C1C(=CC2=C(O1)C=C(C=C2)O)C3=C(C=C(C=C3)O)O 256.25 unknown https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6-Methylgenistein 45273092 Click to see CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1021/NP800535G
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1248/CPB.28.1172
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1021/NP800535G
https://doi.org/10.1248/CPB.28.1172
Neobavaisoflavone 5320053 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)C 322.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 132988548 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=C(C=C(C=C3)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP800535G
(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 124300749 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1248/CPB.28.1172
Dalbergioidin 181994 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
Haginin B 14077816 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(C=C(C=C3)O)OC2 270.28 unknown https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
(3S)-5,7-dihydroxy-3-(4-hydroxy-2,3-dimethoxyphenyl)-2,3-dihydrochromen-4-one 163018343 Click to see COC1=C(C=CC(=C1OC)O)C2COC3=CC(=CC(=C3C2=O)O)O 332.30 unknown https://doi.org/10.1021/NP800535G
(3S)-7-hydroxy-3-(4-hydroxy-2,3-dimethoxyphenyl)-2,3-dihydrochromen-4-one 162887796 Click to see COC1=C(C=CC(=C1OC)O)C2COC3=C(C2=O)C=CC(=C3)O 316.30 unknown https://doi.org/10.1248/CPB.28.1172
4-[7-hydroxy-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]-6-methoxybenzene-1,3-diol 56679475 Click to see CC(=CCC1=C(C=C2C(=C1)CC(CO2)C3=CC(=C(C=C3O)O)OC)O)C 356.40 unknown https://doi.org/10.1021/NP800535G
7,4'-Dihydroxy-2',3'-dimethoxyisoflavanone 14077832 Click to see COC1=C(C=CC(=C1OC)O)C2COC3=C(C2=O)C=CC(=C3)O 316.30 unknown https://doi.org/10.1248/CPB.28.1172
Haginin A 338286 Click to see COC1=C(C=CC(=C1OC)O)C2=CC3=C(C=C(C=C3)O)OC2 300.30 unknown https://doi.org/10.1248/CPB.28.1172
Haginin C 44257525 Click to see COC1=C(C=CC(=C1O)C2=CC3=C(C=C(C=C3)O)OC2)O 286.28 unknown https://doi.org/10.1248/CPB.28.1172
Lespecyrtin D1 25208603 Click to see CC(=CCC1=C(C=C2C(=C1)CC(CO2)C3=CC(=C(C=C3O)O)OC)O)C 356.40 unknown https://doi.org/10.1021/NP800535G
Parvisoflavanone 44257394 Click to see COC1=C(C=CC(=C1OC)O)C2COC3=CC(=CC(=C3C2=O)O)O 332.30 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(5-Hydroxy-2,2-dimethyl-chromen-6-yl)-3-(4-hydroxyphenyl)propan-1-one 9973521 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
3-(4-hydroxyphenyl)-1-[(2S)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]propan-1-one 163032239 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)O 324.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin C1 25195061 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)O 324.40 unknown https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(3E)-1-[(S)-5-Hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)-2-propene-1-one 101505024 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown https://doi.org/10.1248/CPB.28.1172
https://doi.org/10.1021/NP800535G
5-Hydroxy-6-(4-hydroxycinnamoyl)-2-methyl-2-(4-methyl-3-pentenyl)-2h-1-benzopyran 74037136 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown https://doi.org/10.1248/CPB.28.1172
https://doi.org/10.1021/NP800535G
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/CPB.28.1172
Lespeol 23259405 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C 390.50 unknown https://doi.org/10.1021/NP800535G
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 124949 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown https://doi.org/10.1248/CPB.28.1172
https://doi.org/10.1021/NP800535G
Isobavachalcone 5281255 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown https://doi.org/10.1021/NP800535G
Xanthoangelol 643007 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown https://doi.org/10.1248/CPB.28.1172
https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Furanochalcones
(E)-3-(4-hydroxyphenyl)-1-[(2R)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-one 163084794 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O 322.40 unknown https://doi.org/10.1021/NP800535G
3-(4-Hydroxyphenyl)-1-(4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl)prop-2-en-1-one 74429302 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O 322.40 unknown https://doi.org/10.1021/NP800535G
Lespecyrtin B1 25208281 Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O 322.40 unknown https://doi.org/10.1021/NP800535G

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