Cedronella canariensis - Unknown
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Internal ID UUID64402be5be42d988602755
Scientific name Cedronella canariensis
Authority (L.) Webb & Berthel.
First published in Hist. Nat. Iles Canaries 3(2; 3): 87 (1845)

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Synonyms Top

Scientific name Authority First published in
Brittonastrum triphyllum (Moench) A.Lyons Pl. Nam. , ed. 2: 81 (1907)
Cedronella madrensis M.E.Jones Contr. W. Bot. 12: 70 (1908)
Cedronella triphylla Moench Methodus : 411 (1794)
Dracocephalum balsamicum Salisb. Prodr. Stirp. Chap. Allerton : 87 (1796)
Dracocephalum canariense L. Sp. Pl. : 594 (1753)
Dracocephalum ternatifolium Stokes Bot. Mat. Med. 3: 329 (1812)

Common names Top

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Language Common/alternative name
English herb of gilead
Spanish algaritope
Czech cedronela kanárská
German balsamstrauch
French cédronelle
Dutch cédronelle

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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Maintain seeds at a constant 10°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Southern Africa
      • Cape Provinces
  • Australasia
    • Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000824856
USDA Plants CECA
Tropicos 17601951
KEW urn:lsid:ipni.org:names:445603-1
The Plant List kew-36239
Open Tree Of Life 248831
Observations.org 105129
NCBI Taxonomy 260595
NBN Atlas NHMSYS0000456999
Nature Serve 2.136563
IPNI 445603-1
iNaturalist 160257
GBIF 2926887
Freebase /m/09xfjr
EPPO CDNCA
EOL 579626
Calflora (Californian flora) 8613
USDA GRIN 414420
CMAUP NPO14449

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
Chemical profile, antimicrobial activity, and leaf anatomy of Adenophyllum porophyllum var. cancellatum Aguilar-Rodríguez S, López-Villafranco ME, Jácquez-Ríos MP, Hernández-Delgado CT, Mata-Pimentel MF, Estrella-Parra EA, Espinosa-González AM, Nolasco-Ontiveros E, Avila-Acevedo JG, García-Bores AM Front Pharmacol 11-Oct-2022
PMCID:PMC9592750
doi:10.3389/fphar.2022.981959
PMID:36304152
Lamiaceae Essential Oils, Phytochemical Profile, Antioxidant, and Biological Activities Ramos da Silva LR, Ferreira OO, Cruz JN, de Jesus Pereira Franco C, Oliveira dos Anjos T, Cascaes MM, Almeida da Costa W, Helena de Aguiar Andrade E, Santana de Oliveira M Evid Based Complement Alternat Med 14-Dec-2021
PMCID:PMC8692021
doi:10.1155/2021/6748052
PMID:34950215
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Phenylalkanoid Glycosides (Non-Salicinoids) from Wood Chips of Salix triandra × dasyclados Hybrid Willow Noleto-Dias C, Wu Y, Bellisai A, Macalpine W, Beale MH, Ward JL Molecules 23-Mar-2019
PMCID:PMC6470679
doi:10.3390/molecules24061152
PMID:30909533
Chavicol β-d-glucoside, a phenylpropanoid heteroside, benzyl-β-d-glucoside and glycosidically bound volatiles from subspecies of Cedronella canariensis Matthias Coen, Ralf Engel, Adolf Nahrstedt Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00241-X
A dimer of d-pinocarvone from Cedronella canariensis María C. Carreiras, Benjamín Rodríguez, Rosario E. López-Garcia, Rosa M. Rabanal Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82506-6

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
1-Phenylethanol 7409 Click to see CC(C1=CC=CC=C1)O 122.16 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / m-Hydroxybenzoic acid esters
Methyl 2,3-dihydroxybenzoate 75484 Click to see COC(=O)C1=C(C(=CC=C1)O)O 168.15 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzyl salicylate 8363 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O 228.24 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown via CMAUP database
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic acid 7424 Click to see C1=C(C=C(C=C1O)O)C(=O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 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 https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
(3-Ethylphenyl)methanol 104659 Click to see CCC1=CC(=CC=C1)CO 136.19 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> 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 https://doi.org/10.1016/0031-9422(95)00241-X
2-Phenyl-2-propanol 12053 Click to see CC(C)(C1=CC=CC=C1)O 136.19 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Vinylphenol 62453 Click to see C=CC1=CC=C(C=C1)O 120.15 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / Cresols / Meta cresols
M-Cresol 342 Click to see CC1=CC(=CC=C1)O 108.14 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / Cresols / Ortho cresols
o-Cresol 335 Click to see CC1=CC=CC=C1O 108.14 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol 2879 Click to see CC1=CC=C(C=C1)O 108.14 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
Chavibetol 596375 Click to see COC1=C(C=C(C=C1)CC=C)O 164.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(+)-Secoisolariciresinol 6336781 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
alpha-(beta-D-Glucopyranosyloxy)-trans-cinnamic acid 53385591 Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptanol 8129 Click to see CCCCCCCO 116.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1016/0031-9422(95)00241-X
1-Octen-3-Ol 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1016/0031-9422(95)00241-X
2-Ethylhexan-1-ol 7720 Click to see CCCCC(CC)CO 130.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
2-Heptanol 10976 Click to see CCCCCC(C)O 116.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,1'R,5R,5'R,9R)-6',6',10,10-tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one 12305215 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
(1R,5R)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-one 10012081 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
(1S,1'S,5R,5'S,9S)-6',6',10,10-tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one 163009492 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
(1S,3S,5R)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol 6427126 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
6',6',10,10-Tetramethylspiro[6-oxatricyclo[7.1.1.02,7]undec-2(7)-ene-5,2'-bicyclo[3.1.1]heptane]-3'-one 5320137 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
Cedronellone 11722355 Click to see CC1(C2CC1C3=C(C2)OC4(CC3)C5CC(C5(C)C)CC4=O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Pinocarveol, cis-(+/-)- 10931630 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
https://doi.org/10.1016/0031-9422(95)00241-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Perillyl alcohol 10819 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3-Hydroxy-beta-damascenone 129845667 Click to see CC1=C(C(CC=C1)(C)C)C(=CC(=O)C)O 206.28 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Neophytadiene 10446 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C 278.50 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)82506-6
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 https://doi.org/10.1016/S0031-9422(00)82506-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Prenol 11173 Click to see CC(=CCO)C 86.13 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Butoxy-2-propanol 21210 Click to see CCCCOCC(C)O 132.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
2-Hexanol 12297 Click to see CCCCC(C)O 102.17 unknown https://doi.org/10.1016/0031-9422(95)00241-X
3-Heptanol 11520 Click to see CCCCC(CC)O 116.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
3-Methyl-2-pentanol 11261 Click to see CCC(C)C(C)O 102.17 unknown https://doi.org/10.1016/0031-9422(95)00241-X
4-Heptanol 11513 Click to see CCCC(CCC)O 116.20 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
4-Methylcyclohexanol 11524 Click to see CC1CCC(CC1)O 114.19 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclopentanols
2-Methylcyclopentanol 32205 Click to see CC1CCCC1O 100.16 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-(4-prop-2-enylphenoxy)oxan-2-yl]methyl acetate 59800843 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)CC=C)OC(=O)C)OC(=O)C)OC(=O)C 464.50 unknown https://doi.org/10.1016/0031-9422(95)00241-X
[3,4,5-Triacetyloxy-6-(4-prop-2-enylphenoxy)oxan-2-yl]methyl acetate 59800844 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)CC=C)OC(=O)C)OC(=O)C)OC(=O)C 464.50 unknown https://doi.org/10.1016/0031-9422(95)00241-X
4-(2-Propenyl)phenyl-beta-d-glucopyranoside 44390556 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Chavicol O-beta-glucopyranoside 44338426 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/0031-9422(95)00241-X
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Organoheterocyclic compounds / Benzofurans
Dihydroactinidiolide 6432173 Click to see CC1(CCCC2(C1=CC(=O)O2)C)C 180.24 unknown https://doi.org/10.1016/0031-9422(95)00241-X
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 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
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 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
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
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
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
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
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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
Isoquercetin 5280804 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-robinobioside 10371536 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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