Rubia argyi - Unknown
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Internal ID UUID643feb4516a59983093208
Scientific name Rubia argyi
Authority (H.Lév. & Vaniot) H.Hara
First published in Notes Roy. Bot. Gard. Edinburgh 32: 114 (1972)

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Synonyms Top

Scientific name Authority First published in
Rubia akane Nakai J. Jap. Bot. 13: 783 (1937)
Rubia akane var. erecta Masam. Trans. Nat. Hist. Soc. Formosa 29: 63. 1939
Rubia chekiangensis Deb Bull. Bot. Soc. Bengal 24: 166 (1970 publ. 1971)
Rubia cordifolia var. pubescens Nakai Enum. Pl. Corea : 326 (1922)
Rubia nankotaizana Masam. Hokuriku J. Bot. 2: 40 (1953)
Rubia pubescens (Nakai) Nakai J. Jap. Bot. 13: 783 (1937)
Galium argyi H.Lév. & Vaniot Bull. Soc. Bot. France 55: 58 (1908)

Common names Top

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Language Common/alternative name
Japanese アカネ
Chinese 红叶藤
Chinese 东南茜草
Chinese 主线草

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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 South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000298386
Tropicos 100252581
KEW urn:lsid:ipni.org:names:765187-1
The Plant List kew-180192
Open Tree Of Life 3872638
NCBI Taxonomy 1531356
IPNI 765187-1
iNaturalist 702071
GBIF 2892230
EPPO RBIAK
EOL 1106131
Wikipedia Rubia_argyi
CMAUP NPO28159

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
The impact of selected xanthophylls on oil hydrolysis by pancreatic lipase: in silico and in vitro studies Dąbrowski G, Czaplicki S, Szustak M, Korkus E, Gendaszewska-Darmach E, Konopka I Sci Rep 01-Feb-2024
PMCID:PMC10834431
doi:10.1038/s41598-024-53312-9
PMID:38302772
Optimizing the Droplet-Vitrification Procedure by Balancing the Cryoprotection and Cytotoxicity of Alternative Plant Vitrification Solutions Based on the Nature of Donor Plant Vigor Kim H Plants (Basel) 30-Nov-2023
PMCID:PMC10707743
doi:10.3390/plants12234040
PMID:38068674
Cyclic Hexapeptide from Bouvardia ternifolia (Cav.) Schltdl. and Neuroprotective Effects of Root Extracts Lopera YM, Trejo-Tapia G, González-Cortazar M, Herrera-Ruiz M, Zamilpa A, Jiménez-Ferrer E Plants (Basel) 10-Jul-2023
PMCID:PMC10416155
doi:10.3390/plants12142600
PMID:37514215
Anthraquinone Production from Cell and Organ Cultures of Rubia Species: An Overview Murthy HN, Joseph KS, Paek KY, Park SY Metabolites 26-Dec-2022
PMCID:PMC9861034
doi:10.3390/metabo13010039
PMID:36676964
In Vitro Multiplication and Cryopreservation of Penthorum chinense Shoot Tips Zilani RA, Lee H, Popova E, Kim H Life (Basel) 01-Nov-2022
PMCID:PMC9694001
doi:10.3390/life12111759
PMID:36362913
Effects of various Agrobacterium rhizogenes strains on hairy root induction and analyses of primary and secondary metabolites in Ocimum basilicum Sathasivam R, Choi M, Radhakrishnan R, Kwon H, Yoon J, Yang SH, Kim JK, Chung YS, Park SU Front Plant Sci 17-Oct-2022
PMCID:PMC9619037
doi:10.3389/fpls.2022.983776
PMID:36325544
Mass spectrometry data on specialized metabolome of medicinal plants used in East Asian traditional medicine Kang KB, Jeong E, Son S, Lee E, Lee S, Choi SY, Kim HW, Yang H, Shim SH Sci Data 27-Aug-2022
PMCID:PMC9420114
doi:10.1038/s41597-022-01662-2
PMID:36030263
In Vitro Technologies for American Chestnut (Castanea dentata (Marshall) Borkh) Conservation Liu Z, Bi WL, Shukla MR, Saxena PK Plants (Basel) 08-Feb-2022
PMCID:PMC8840129
doi:10.3390/plants11030464
PMID:35161445
The Natural Products Targeting on Allergic Rhinitis: From Traditional Medicine to Modern Drug Discovery Lim S, Jeong I, Cho J, Shin C, Kim KI, Shim BS, Ko SG, Kim B Antioxidants (Basel) 26-Sep-2021
PMCID:PMC8532887
doi:10.3390/antiox10101524
PMID:34679659
Design and synthesis of analogues of RA-VII—an antitumor bicyclic hexapeptide from Rubiae radix Hitotsuyanagi Y J Nat Med 10-Jul-2021
PMCID:PMC8397687
doi:10.1007/s11418-021-01542-w
PMID:34244894
Complex evolution in Aphis gossypii group (Hemiptera: Aphididae), evidence of primary host shift and hybridization between sympatric species Lee Y, Thieme T, Kim H PLoS One 04-Feb-2021
PMCID:PMC7861460
doi:10.1371/journal.pone.0245604
PMID:33539375
Crystal structure of death-associated protein kinase 1 in complex with the dietary compound resveratrol Yokoyama T, Suzuki R, Mizuguchi M IUCrJ 01-Jan-2021
PMCID:PMC7792996
doi:10.1107/S2052252520015614
PMID:33520249
Modern Trends in the In Vitro Production and Use of Callus, Suspension Cells and Root Cultures of Medicinal Plants Babich O, Sukhikh S, Pungin A, Ivanova S, Asyakina L, Prosekov A Molecules 09-Dec-2020
PMCID:PMC7763305
doi:10.3390/molecules25245805
PMID:33316965
Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention) Alamgir AN Therapeutic Use of Medicinal Plants and their Extracts: Volume 2 24-Jun-2018
PMCID:PMC7123938
doi:10.1007/978-3-319-92387-1_7
Targeting phosphatases of regenerating liver (PRLs) in cancer Wei M, Korotkov KV, Blackburn JS Pharmacol Ther 05-Jun-2018
PMCID:PMC6192704
doi:10.1016/j.pharmthera.2018.05.014
PMID:29859177

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
2-Ethoxycarbonyl-1-hydroxyanthraquinone 15139061 Click to see CCOC(=O)C1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 296.27 unknown https://doi.org/10.1016/0031-9422(90)85382-P
Munjistin 160476 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C(=O)O)O 284.22 unknown via CMAUP database
Pseudopurpurin 442765 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3O)C(=O)O)O)O 300.22 unknown https://doi.org/10.5511/PLANTBIOTECHNOLOGY1984.9.220
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.1021/NP50104A020
https://doi.org/10.1016/0031-9422(90)85382-P
Anthraquinone 6780 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O 208.21 unknown via CMAUP database
Lucidin primeveroside 160180 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1021/NP50104A020
Lucidin-3-O-primveroside 148037 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown via CMAUP database
Ruberythric acid 92101 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)C(=O)C5=CC=CC=C5C4=O)O)O)O)O)O)O)O 534.50 unknown via CMAUP database
Xanthopupurin 3-O-beta-D-glucoside 44575697 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 402.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
[6-(4,7-Dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate 14539982 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)COC(=O)C)O)O)O)O)O 620.60 unknown https://doi.org/10.1007/S12272-010-1106-4
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown https://doi.org/10.1021/NP50104A020
1,3,6-trihydroxy-2-methyl-9,10-anthraquinone-3-O-(6'-O-acetyl)-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 70698136 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)COC(=O)C)O)O)O)O)O 620.60 unknown https://doi.org/10.1007/S12272-010-1106-4
1,3,6-Trihydroxy-2-methylanthracene-9,10-dione 5319801 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C=C(C=C3)O)O 270.24 unknown https://doi.org/10.1007/S12272-010-1106-4
2-(Methoxymethyl)-1,3-dihydroxyanthraquinone 149782 Click to see COCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 284.26 unknown via CMAUP database
Alizarin 6293 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)O)O 240.21 unknown https://doi.org/10.1271/BBB.61.1743
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Nordamnacanthal 160712 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 268.22 unknown via CMAUP database
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2,3,4-Trimethoxybenzoic acid 11308 Click to see COC1=C(C(=C(C=C1)C(=O)O)OC)OC 212.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
(2R,3S,4S)-2,3-diethyl-4-(4-hydroxy-3-methoxy-phenyl)-7-methoxy-tetralin-6-ol 486613 Click to see CCC1CC2=CC(=C(C=C2C(C1CC)C3=CC(=C(C=C3)O)OC)O)OC 356.50 unknown https://doi.org/10.1021/NP2002918
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)- 160521 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1007/BF02856539
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 101855692 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(4aR,6aR,6aS,6bR,8aR,12aR,14aR,14bR)-6a,7-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-13-oxo-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 138114013 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(=O)C4(C3(C(CC5(C4CC(CC5)(C)C)C)O)C)O)C)C 516.80 unknown https://doi.org/10.1021/NP50104A020
[(4aR,6aR,6aS,6bS,8aR,12aS,14aS,14bR)-6a-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-13-oxo-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 138114012 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC(=O)C4(C3(CCC5(C4CC(CC5)(C)C)C)C)O)C)C 500.80 unknown https://doi.org/10.1021/NP50104A020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50104A020
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50104A020
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid 222656 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown via CMAUP database
D-malate 92824 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown via CMAUP database
Hydron;2-hydroxybutanedioate 20130941 Click to see [H+].[H+].C(C(C(=O)[O-])O)C(=O)[O-] 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(-)-Quinate 1560034 Click to see C1C(C(C(CC1(C(=O)[O-])O)O)O)O 191.16 unknown via CMAUP database
(+)-Quinic acid 37439 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown via CMAUP database
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 9549179 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
6-O-beta-D-glucopyranosyl-D-glucose 5460026 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
alpha-Cellobiose 441014 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
beta-D-Fructofuranosyl alpha-D-glucopyranoside 91692850 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
beta-D-Glucopyranose, 4-O-beta-D-galactopyranosyl- 294 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
beta-Gentiobiose 441422 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
beta-Maltose 6255 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Cellobiose 10712 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
CID 24802156 24802156 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
D-Cellobiose 439178 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gentiobiose, alpha- 12302012 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
L-Glc(a1-4)a-Ido 46936190 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose NF 46782954 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Methyl 1,4-bisglucosyloxy-3-prenyl-2-naphthoate 10031663 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=C1C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 610.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
D-Ribose 10975657 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown via CMAUP database
D-Xylose 135191 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown via CMAUP database
DL-Arabinose 854 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown via CMAUP database
DL-Xylose 644160 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Raffinose 439242 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O 504.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Mollugin 124219 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3C(=C2C(=O)OC)O)C 284.31 unknown https://doi.org/10.1021/NP50104A020
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
(2S)-6-Geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Geranyl-2,4-dihydroxy-6-phenethylbenzoate 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

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