Knightia excelsa - Unknown
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Internal ID UUID643ff3b01b0c8530983459
Scientific name Knightia excelsa
Authority R.Br.
First published in Trans. Linn. Soc. London 10: 194 (1810)

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Synonyms Top

Scientific name Authority First published in
Rymandra excelsa Knight Cult. Prot. : 124 (1809)

Common names Top

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Language Common/alternative name
Spanish new zealand honeysuckle
Spanish rewarewa
French chèvrefeuille de nouvelle-zélande
French rewarewa
mi rewarewa
Chinese 蜜汁树

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000356860
Tropicos 26500850
KEW urn:lsid:ipni.org:names:704692-1
The Plant List kew-2334761
PFAF Knightia excelsa
Open Tree Of Life 541974
NCBI Taxonomy 35944
IPNI 704692-1
iNaturalist 366632
GBIF 5638587
Freebase /m/05072q
EPPO KNGEX
Elurikkus 561123
USDA GRIN 21184
Wikipedia Knightia_excelsa
CMAUP NPO26211

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
Diversity of Methylobacterium species associated with New Zealand native plants Jahan R, McDonald IR FEMS Microbiol Lett 20-Nov-2023
PMCID:PMC10699869
doi:10.1093/femsle/fnad124
PMID:37985695
Proteomic Analysis of Honey: Peptide Profiling as a Novel Approach for New Zealand Mānuka (Leptospermum scoparium) Honey Authentication Bong J, Middleditch M, Stephens JM, Loomes KM Foods 12-May-2023
PMCID:PMC10217132
doi:10.3390/foods12101968
PMID:37238786
Exploring the Chemical Properties and Biological Activity of Four New Zealand Monofloral Honeys to Support the Māori Vision and Aspirations Zucchetta C, Tangohau W, McCallion A, Hardy DJ, Clavijo McCormick A Molecules 20-May-2022
PMCID:PMC9143981
doi:10.3390/molecules27103282
PMID:35630758
A field test of forest canopy structure measurements with the CanopyCapture smartphone application Lusk CH PeerJ 13-May-2022
PMCID:PMC9109689
doi:10.7717/peerj.13450
PMID:35586134
A Comprehensive Survey of Phenolic Constituents Reported in Monofloral Honeys around the Globe Lawag IL, Lim LY, Joshi R, Hammer KA, Locher C Foods 15-Apr-2022
PMCID:PMC9025093
doi:10.3390/foods11081152
PMID:35454742
An investigation of the suitability of melissopalynology to authenticate Jarrah honey Islam MK, Lawag IL, Green KJ, Sostaric T, Hammer KA, Lim LY, Locher C Curr Res Food Sci 26-Feb-2022
PMCID:PMC8904405
doi:10.1016/j.crfs.2022.02.014
PMID:35281336
Assessing Two Different Aerial Toxin Treatments for the Management of Invasive Rats O’Malley TD, Stanley MC, Russell JC Animals (Basel) 27-Jan-2022
PMCID:PMC8833531
doi:10.3390/ani12030309
PMID:35158633
Metabolomic Profiling of Malaysian and New Zealand Honey Using Concatenated NMR and HRMS Datasets Yusoff YM, Abbott G, Young L, Edrada-Ebel R Metabolites 17-Jan-2022
PMCID:PMC8781004
doi:10.3390/metabo12010085
PMID:35050207
Putative Anticancer Compounds from Plant-Derived Endophytic Fungi: A Review Hridoy M, Gorapi MZ, Noor S, Chowdhury NS, Rahman MM, Muscari I, Masia F, Adorisio S, Delfino DV, Mazid MA Molecules 04-Jan-2022
PMCID:PMC8746379
doi:10.3390/molecules27010296
PMID:35011527
Chemical Elements and the Quality of Mānuka (Leptospermum scoparium) Honey Meister A, Gutierrez-Gines MJ, Maxfield A, Gaw S, Dickinson N, Horswell J, Robinson B Foods 20-Jul-2021
PMCID:PMC8303644
doi:10.3390/foods10071670
PMID:34359540
Optimisation of Bee Pollen Extraction to Maximise Extractable Antioxidant Constituents Lawag IL, Yoo O, Lim LY, Hammer K, Locher C Antioxidants (Basel) 12-Jul-2021
PMCID:PMC8301099
doi:10.3390/antiox10071113
PMID:34356345
Monofloral Honeys as a Potential Source of Natural Antioxidants, Minerals and Medicine Mărgăoan R, Topal E, Balkanska R, Yücel B, Oravecz T, Cornea-Cipcigan M, Vodnar DC Antioxidants (Basel) 25-Jun-2021
PMCID:PMC8300703
doi:10.3390/antiox10071023
PMID:34202118
An exploration of assembly strategies and quality metrics on the accuracy of the rewarewa (Knightia excelsa) genome McCartney AM, Hilario E, Choi S, Guhlin J, Prebble JM, Houliston G, Buckley TR, Chagné D Mol Ecol Resour 19-Jun-2021
PMCID:PMC8362059
doi:10.1111/1755-0998.13406
PMID:33955186
Reflections on Menisporopsis, Multiguttulispora and Tainosphaeria Using Molecular and Morphological Data Réblová M, Nekvindová J, Hernández-Restrepo M J Fungi (Basel) 31-May-2021
PMCID:PMC8227749
doi:10.3390/jof7060438
PMID:34072784
Alignment of ordinal and quantitative species abundance and size indices for the detection of shifting baseline syndrome Lyver PO, Timoti P, Richardson SJ, Gormley AM Ecol Appl 05-May-2021
PMCID:PMC8244062
doi:10.1002/eap.2301
PMID:33560524

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
cis-3-Hexenyl benzoate 5367706 Click to see CCC=CCCOC(=O)C1=CC=CC=C1 204.26 unknown via CMAUP database
Ethyl benzoate 7165 Click to see CCOC(=O)C1=CC=CC=C1 150.17 unknown via CMAUP database
Hexyl benzoate 23235 Click to see CCCCCCOC(=O)C1=CC=CC=C1 206.28 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2-Phenylphenol 7017 Click to see C1=CC=C(C=C1)C2=CC=CC=C2O 170.21 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide 20488062 Click to see [H+].C1=CC=C(C=C1)[O-] 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see C1=CC(=CC=C1O)O 110.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol 6992244 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown via CMAUP database
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
cis-3-Hexen-1-ol 5281167 Click to see CCC=CCCO 100.16 unknown via CMAUP database
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(2S)-2-[(1R)-4-methylcyclohex-3-en-1-yl]propanal 76958477 Click to see CC1=CCC(CC1)C(C)C=O 152.23 unknown via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 11788398 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown via CMAUP database
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl Acetate 8857 Click to see CCOC(=O)C 88.11 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
(R)-3-Hydroxy-2-oxobutanoicacid 15284009 Click to see CC(C(=O)C(=O)O)O 118.09 unknown via CMAUP database
4-Hydroxy-2-oxobutanoic acid 11963036 Click to see C(CO)C(=O)C(=O)O 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(S)-(-)-2-Methyl-1-butanol 2723602 Click to see CCC(C)CO 88.15 unknown via CMAUP database
1-Butanol 263 Click to see CCCCO 74.12 unknown via CMAUP database
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(S)-(+)-2-Pentanol 2724896 Click to see CCCC(C)O 88.15 unknown via CMAUP database
3-Methyl-3-buten-2-ol, (R)- 10678185 Click to see CC(C(=C)C)O 86.13 unknown via CMAUP database
3-Pentanol 11428 Click to see CCC(CC)O 88.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5315597 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 434.40 unknown via CMAUP database
4-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]phenol 11968602 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 434.40 unknown via CMAUP database
Pyroside 5315513 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)O)O)O)O 314.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Valeraldehyde 8063 Click to see CCCCC=O 86.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(E,Z)-2,4-heptadienal 11788274 Click to see CCC=CC=CC=O 110.15 unknown via CMAUP database
2-Decenal 5283345 Click to see CCCCCCCC=CC=O 154.25 unknown via CMAUP database
2-Heptenal 5283316 Click to see CCCCC=CC=O 112.17 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
2,4-Heptadienal 5283321 Click to see CCC=CC=CC=O 110.15 unknown via CMAUP database
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown via CMAUP database
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
Octanal 454 Click to see CCCCCCCC=O 128.21 unknown via CMAUP database
trans-2,cis-6-Nonadienal 643731 Click to see CCC=CCCC=CC=O 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Octadecanone 81844 Click to see CCCCCCCCCCCCCCCCC(=O)C 268.50 unknown via CMAUP database
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Alpha-diketones
2,3-Butanedione 650 Click to see CC(=O)C(=O)C 86.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
Excelsione 16109859 Click to see CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C(=C4C(=C3C)COC4=O)O)CO)O 358.30 unknown https://doi.org/10.1021/NP060202U
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters / O-cinnamoyl glycosides
1-O-trans-Cinnamoyl-beta-D-glucopyranose 5280653 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O 310.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
Cinnamtannin B1 475277 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Cinnamtannin B2 16130973 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Epicatechin-(4beta->8)-epicatechin-(2beta->7,4beta->8)-catechin 10350652 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=C(C(=CC(=C45)O)O)C6C(C(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B6 474540 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B8 474541 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
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 O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 11972444 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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 26202188 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercitin 10813969 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercetin-3-o-alpha-d-arabinofuranoside 11968848 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 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

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