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Dictyoloma vandellianum

Dictyoloma vandellianum - 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 UUID644016f6da5d4679464074
Scientific name Dictyoloma vandellianum
Authority A.Juss.
First published in Mém. Mus. Hist. Nat. 12: 499 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Benjamina alata Vell. Fl. Flumin. 93. 1829 [1825 publ. 7 Sep-28 Nov 1829] ; see also Fl. Flumin. Icon. 2: t. 139. 1831. [1827 publ. 29 Oct 1831]
Benjamina peruviana (Planch.) Kuntze Revis. Gen. Pl. 1: 103. 1891 [5 Nov 1891]
Dictyoloma incanescens DC. Prodr. 2: 89 (1825)
Dictyoloma peruvianum Planch. London J. Bot. 5: 583 (1846)

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000646352
Tropicos 28101406
KEW urn:lsid:ipni.org:names:813702-1
The Plant List kew-2767029
Open Tree Of Life 909219
NCBI Taxonomy 68538
IUCN Red List 146074378
IPNI 813702-1
iNaturalist 544588
GBIF 3831395
EOL 5623708
CMAUP NPO28783

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
8-Methoxyflindersine-Induced Apoptosis and Cell Cycle Disorder Involving MAPK Signaling Activation in Human Colorectal Cancer Cells Zhang D, Fu Y, Liu Y, Wu Y, Chen J, Zhang L, Wang R, Chen Z, Liu T Int J Mol Sci 28-Apr-2023
PMCID:PMC10179151
doi:10.3390/ijms24098039
PMID:37175741
Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes Mucha P, Skoczyńska A, Małecka M, Hikisz P, Budzisz E Molecules 12-Aug-2021
PMCID:PMC8398118
doi:10.3390/molecules26164886
PMID:34443474
5-O-methylcneorumchromone K Exerts Antinociceptive Effects in Mice via Interaction with GABAA Receptors Opretzka LC, de Freitas HF, Espírito-Santo RF, Abreu LS, Alves IM, Tavares JF, Velozo ED, Castilho MS, Villarreal CF Int J Mol Sci 26-Mar-2021
PMCID:PMC8037321
doi:10.3390/ijms22073413
PMID:33810317
Evaluation of conservation status of plants in Brazil’s Atlantic forest: An ethnoecological approach with Quilombola communities in Serra do Mar State Park Conde BE, Aragaki S, Ticktin T, Surerus Fonseca A, Yazbek PB, Sauini T, Rodrigues E PLoS One 18-Sep-2020
PMCID:PMC7500697
doi:10.1371/journal.pone.0238914
PMID:32946472
Participatory methods on the recording of traditional knowledge about medicinal plants in Atlantic forest, Ubatuba, São Paulo, Brazil Sauini T, Stern da Fonseca-Kruel V, Baptistela Yazbek P, Matta P, Cassas F, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Angelica Silva Gomes M, José Francischetti Garcia R, Honda S, Felipe Domingues Passero L, Esteves Conde B, Rodrigues E PLoS One 07-May-2020
PMCID:PMC7205242
doi:10.1371/journal.pone.0232288
PMID:32379779
Antinociceptive compounds and LC-DAD-ESIMSn profile from Dictyoloma vandellianum leaves Abreu LS, Alves IM, do Espírito Santo RF, do Nascimento YM, Dantas CA, dos Santos GG, Le Hyaric M, Guedes ML, da Silva MS, Villarreal CF, Velozo ED, Tavares JF PLoS One 29-Oct-2019
PMCID:PMC6818767
doi:10.1371/journal.pone.0224575
PMID:31661523
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Identity and relationships of the Arboreal Caatinga among other floristic units of seasonally dry tropical forests (SDTFs) of north-eastern and Central Brazil Santos RM, Oliveira-Filho AT, Eisenlohr PV, Queiroz LP, Cardoso DB, Rodal MJ Ecol Evol 01-Feb-2012
PMCID:PMC3298952
doi:10.1002/ece3.91
PMID:22423333
Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights Appelhans MS, Smets E, Razafimandimbison SG, Haevermans T, van Marle EJ, Couloux A, Rabarison H, Randrianarivelojosia M, Keßler PJ Ann Bot 01-Jun-2011
PMCID:PMC3101142
doi:10.1093/aob/mcr076
PMID:21610209
2-Quinolone alkaloids from the rare species of Rutaceae Andreadoxa flava Kallunki Sandra Virgínia Alves Hohlemwerger, Waldir Tavares, André Maurício de Carvalho, Paulo Cézar Vieira, Eudes da Silva Velozo Elsevier BV 06-Feb-2004
doi:10.1016/J.BSE.2003.09.006
Alkaloids from Dictyoloma vandellianum: their chemosystematic significance. Sartor CF, da Silva MF, Fernandes JB, Vieira PC, Fo ER, Garcia Cortez DA Phytochemistry 01-May-2003
doi:10.1016/S0031-9422(03)00006-2
PMID:12711140
The chemosystematics of Dictyoloma Paulo C. Vieira, Ana R. Lázaro, Joāo B. Fernandes, M.Fátima Das G.F. Da Sllva Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(88)90060-9
Chromones from Dictyoloma incanescens Angela Martha Campos, Duc Do Khac, Marcel Fetizon Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83597-9
4-Quinolinone alkaloids from Dictyoloma peruviana. Lavaud C, Massiot G, Vasquez C, Moretti C, Sauvain M, Balderrama L Phytochemistry 01-Sep-1995
doi:10.1016/0031-9422(95)00265-9
PMID:7546553

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 / 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 / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
> 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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-2,8,8-trimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 13915671 Click to see CC1=CC(=O)C2=C(C(=C3C(=C2O1)C=CC(O3)(C)C)CC=C(C)C)O 326.40 unknown https://doi.org/10.1016/S0031-9422(00)83597-9
5-Methoxy-2,8,8-trimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 13915672 Click to see CC1=CC(=O)C2=C(C(=C3C(=C2O1)C=CC(O3)(C)C)CC=C(C)C)OC 340.40 unknown https://doi.org/10.1016/S0031-9422(00)83597-9
> 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
> Organoheterocyclic compounds / Naphthopyrans
methyl (Z)-3-[(1R,2S,3R,5S,6R,7R,10S,11S,14S)-11-(furan-3-yl)-3-hydroxy-2,3',3',6,10-pentamethyl-4,13-dioxospiro[12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-5,2'-oxirane]-6-yl]prop-2-enoate 163189234 Click to see CC1(C2(O1)C(=O)C(C3(C(C2(C)C=CC(=O)OC)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)O)C 500.50 unknown https://doi.org/10.1016/0305-1978(88)90060-9
methyl (Z)-3-[(1R,2S,5S,6R,7R,10S,11S,14S)-3-acetyloxy-11-(furan-3-yl)-2,3',3',6,10-pentamethyl-4,13-dioxospiro[12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-5,2'-oxirane]-6-yl]prop-2-enoate 163191167 Click to see CC(=O)OC1C(=O)C2(C(O2)(C)C)C(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=COC=C6)C)(C)C=CC(=O)OC 542.60 unknown https://doi.org/10.1016/0305-1978(88)90060-9
Methyl 3-[11-(furan-3-yl)-3-hydroxy-2,3',3',6,10-pentamethyl-4,13-dioxospiro[12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-5,2'-oxirane]-6-yl]prop-2-enoate 162820475 Click to see CC1(C2(O1)C(=O)C(C3(C(C2(C)C=CC(=O)OC)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)O)C 500.50 unknown https://doi.org/10.1016/0305-1978(88)90060-9
Methyl 3-[3-acetyloxy-11-(furan-3-yl)-2,3',3',6,10-pentamethyl-4,13-dioxospiro[12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-5,2'-oxirane]-6-yl]prop-2-enoate 162820378 Click to see CC(=O)OC1C(=O)C2(C(O2)(C)C)C(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=COC=C6)C)(C)C=CC(=O)OC 542.60 unknown https://doi.org/10.1016/0305-1978(88)90060-9
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroquinolines
2-(12-hydroxy-12-methyltridecyl)-3-methoxy-3H-quinolin-4-one 78070226 Click to see CC(C)(CCCCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1OC)O 387.60 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-(12-hydroxy-12-methyltridecyl)-3H-quinolin-4-one 163192248 Click to see CC(C)(CCCCCCCCCCCC1=NC2=CC=CC=C2C(=O)C1)O 357.50 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(2R)-2-[(Z)-hex-3-enyl]-8-methoxy-1,2,3,4-tetrahydrobenzo[c]quinolizin-6-one 643838 Click to see CCC=CCCC1CCC2=CC(=O)C3=C(N2C1)C=CC(=C3)OC 311.40 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
(2S)-2-[(Z)-hex-3-enyl]-8-methoxy-1,2,3,4-tetrahydrobenzo[c]quinolizin-6-one 162989957 Click to see CCC=CCCC1CCC2=CC(=O)C3=C(N2C1)C=CC(=C3)OC 311.40 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-(12-hydroxy-12-methyltridecyl)-1H-quinolin-4-one 90858764 Click to see CC(C)(CCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1)O 357.50 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-(12-Hydroxy-12-methyltridecyl)-3-methoxyquinolin-4(1H)-one 71441120 Click to see CC(C)(CCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 387.60 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-(14-hydroxy-14,15-dimethylhexadecyl)-3-methoxy-1H-quinolin-4-one 90982795 Click to see CC(C)C(C)(CCCCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 443.70 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-(14-Hydroxy-14,15-dimethylhexadecyl)quinoline-4(1H)-one 90766936 Click to see CC(C)C(C)(CCCCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1)O 413.60 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-[(14R)-14-hydroxy-14,15-dimethylhexadecyl]-3-methoxy-1H-quinolin-4-one 163185855 Click to see CC(C)C(C)(CCCCCCCCCCCCCC1=C(C(=O)C2=CC=CC=C2N1)OC)O 443.70 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-[(14S)-14-hydroxy-14,15-dimethylhexadecyl]-1H-quinolin-4-one 163187169 Click to see CC(C)C(C)(CCCCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1)O 413.60 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-[(Z)-hex-3-enyl]-1,2,3,4-tetrahydrobenzo[c]quinolizin-6-one 10401479 Click to see CCC=CCCC1CCC2=CC(=O)C3=CC=CC=C3N2C1 281.40 unknown https://doi.org/10.1016/0031-9422(95)00265-9
2-[(Z)-hex-3-enyl]-8-methoxy-1,2,3,4-tetrahydrobenzo[c]quinolizin-6-one 22298571 Click to see CCC=CCCC1CCC2=CC(=O)C3=C(N2C1)C=CC(=C3)OC 311.40 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
2-Hex-3-enyl-8-methoxy-1,2,3,4-tetrahydrobenzo[c]quinolizin-6-one 73880874 Click to see CCC=CCCC1CCC2=CC(=O)C3=C(N2C1)C=CC(=C3)OC 311.40 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
Casimiroin 124075 Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC 233.22 unknown https://doi.org/10.1016/0305-1978(88)90060-9
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
7-methoxy-2,2-dimethyl-6H-pyrano[3,2-c]quinolin-5-one 14166104 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)NC2=O)C 257.28 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
https://doi.org/10.1016/J.BSE.2003.09.006
7-Methoxyflindersine 101995295 Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C 257.28 unknown https://doi.org/10.1016/S0031-9422(03)00006-2
> 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
[(2R,3S,4S,5S)-5-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 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)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 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
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 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
[(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
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 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
coumaroyl(-1)[coumaroyl(-3)][coumaroyl(3-OMe)(-6)]Fruf(b2-1a)Glc 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
coumaroyl(-1)[coumaroyl(3-OMe)(-6)]Fruf(b2-1a)Glc 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 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
> 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-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
(2S,3R,4S,5S,6R)-2-[[(2R,3R)-3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-methyl-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 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
> 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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