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Chrysanthemum morifolium

Chrysanthemum morifolium - 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 UUID643fc983de41b618624146
Scientific name Chrysanthemum morifolium
Authority Ramat.
First published in J. Hist. Nat. 2: 240. 1792

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English florist's daisy
Afrikaans krisant
Arabic أقحوان زهرة الغريب
Bengali মালীর চন্দ্রমল্লিকা
Czech listopadka zahradní
German garten-chrysantheme
Esperanto Ĝarden-krizantemo
Persian داودی
Hebrew חרצית הגננים
Japanese 和菊
Japanese 洋菊
Japanese 菊
Japanese キク
Korean 국화 (식물)
lzh 菊
Macedonian Хризантема - морифолиум
Dutch chrysanthemum ×hortorum hort. fide
Dutch tuinchrysant
Dutch dendranthema × grandiflorum
Dutch chrysanthemum ×indicum hort.
Dutch chrysanthemum ×grandiflorum
Dutch bolchrysant
Polish złocień wielkokwiatowy
Russian Хризантема садовая
sd گل دائودي
Swedish krysantemum
Turkish krizantem × morifolium
Chinese 菊
Chinese 秋菊
Chinese 鞠
Chinese 菊花

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000031162
UNII BEI52721UI
USDA Plants CHMO14
Tropicos 2700550
INPN 91060
Flora of Italy 11800
The Plant List gcc-130137
NCBI Taxonomy 41568
IPNI 193607-1
iNaturalist 53806
GBIF 3150767
Freebase /m/0n4bx_w
EOL 483963
USDA GRIN 10373
Wikipedia Chrysanthemum_%C3%97_morifolium
CMAUP NPO30745

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
Phylogenomic profiles of whole-genome duplications in Poaceae and landscape of differential duplicate retention and losses among major Poaceae lineages Zhang T, Huang W, Zhang L, Li DZ, Qi J, Ma H Nat Commun 17-Apr-2024
PMCID:PMC11024178
doi:10.1038/s41467-024-47428-9
PMID:38632270
Research progress on optimization of in vitro isolation, cultivation and preservation methods of dental pulp stem cells for clinical application Wang X, Li F, Wu S, Xing W, Fu J, Wang R, He Y Front Bioeng Biotechnol 03-Apr-2024
PMCID:PMC11021638
doi:10.3389/fbioe.2024.1305614
PMID:38633667
The traditional uses, pharmacology, and phytochemistry of Peucedanum praeruptorum Dunn Wang Q, Sun Q, Huang Q, Qin L, Zhu B Front Pharmacol 03-Apr-2024
PMCID:PMC11021687
doi:10.3389/fphar.2024.1352657
PMID:38633612
CmDOF18 positively regulates salinity tolerance in Chrysanthemum morifolium by activating the oxidoreductase system Li P, Fang T, Chong X, Chen J, Yue J, Wang Z BMC Plant Biol 01-Apr-2024
PMCID:PMC10985857
doi:10.1186/s12870-024-04914-y
PMID:38561659
Photoperiodic and lighting treatments for flowering control and its genetic regulation in sugarcane breeding Wickramasinghe KP, Kong CY, Lin XQ, Zhao PF, Mehdi F, Li XJ, Liu XL, Mao J, Lu X Heliyon 26-Mar-2024
PMCID:PMC10998108
doi:10.1016/j.heliyon.2024.e28531
PMID:38586380
Phylogeny and expression patterns of ERF genes that are potential reproductive inducers in hybrid larch Hao J, Xu D, Wang C, Cao Q, Zhao Q, Xie M, Zhang H, Zhang L BMC Genomics 18-Mar-2024
PMCID:PMC10946173
doi:10.1186/s12864-024-10188-3
PMID:38500084
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
A GASA Protein Family Gene, CmGEG, Inhibits Petal Growth in Chrysanthemum He Z, Jiang R, Wang X, Wang Y Int J Mol Sci 16-Mar-2024
PMCID:PMC10970651
doi:10.3390/ijms25063367
PMID:38542341
Editorial: Quantum dots for biological applications, volume II Hussain S, Packirisamy G, Misra K, Tariq M, Sk MP Front Bioeng Biotechnol 13-Mar-2024
PMCID:PMC10966111
doi:10.3389/fbioe.2024.1389974
PMID:38544978
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
Abscisic-acid-responsive StlncRNA13558 induces StPRL expression to increase potato resistance to Phytophthora infestans infection Shang K, Wang R, Cao W, Wang X, Wang Y, Shi Z, Liu H, Zhou S, Zhu X, Zhu C Front Plant Sci 05-Mar-2024
PMCID:PMC10948444
doi:10.3389/fpls.2024.1338062
PMID:38504894
Neurodegeneration in Cognitive Impairment and Mood Disorders for Experimental, Clinical and Translational Neuropsychiatry Battaglia S, Avenanti A, Vécsei L, Tanaka M Biomedicines 05-Mar-2024
PMCID:PMC10968650
doi:10.3390/biomedicines12030574
PMID:38540187
Adsorption Characteristics of Ball Milling-Modified Chinese Medicine Residue Biochar Toward Quercetin Li L, Xie Y, Chen K, Zhou J, Wang M, Wang W, Zhang Z, Lu F, Du Y, Feng Y ACS Omega 29-Feb-2024
PMCID:PMC10938329
doi:10.1021/acsomega.3c09016
PMID:38496992
Multi-Omics Analysis Reveals That Anthocyanin Degradation and Phytohormone Changes Regulate Red Color Fading in Rapeseed (Brassica napus L.) Petals Huang L, Lin B, Hao P, Yi K, Li X, Hua S Int J Mol Sci 23-Feb-2024
PMCID:PMC10931936
doi:10.3390/ijms25052577
PMID:38473825
Plant-Microbe Interactions under the Extreme Habitats and Their Potential Applications Tiwari P, Bose SK, Park KI, Dufossé L, Fouillaud M Microorganisms 22-Feb-2024
PMCID:PMC10972407
doi:10.3390/microorganisms12030448
PMID:38543499

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives
Ethyl phenylacetate 7590 Click to see CCOC(=O)CC1=CC=CC=C1 164.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1055/S-2005-873181
> Benzenoids / Benzene and substituted derivatives / Cumenes
4-Isopropyl-3-methylphenol 18597 Click to see CC1=C(C=CC(=C1)O)C(C)C 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
3-tert-Butylphenol 11450 Click to see CC(C)(C)C1=CC(=CC=C1)O 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
4-sec-Butylphenol 7453 Click to see CCC(C)C1=CC=C(C=C1)O 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Phenol, isobutylenated 110629 Click to see CC(=C)CC1=CC=C(C=C1)O 148.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
o-Isopropenyltoluene 81886 Click to see CC1=CC=CC=C1C(=C)C 132.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Butylphenol 15420 Click to see CCCCC1=CC=C(C=C1)O 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Hydrocarbons / Polycyclic hydrocarbons
4-Camphen 129848108 Click to see CC1(C2=CCC1(CC2)C)C 136.23 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
3-Methylheptane 11519 Click to see CCCCC(C)CC 114.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Hydrocarbons / Unsaturated hydrocarbons / Acetylenes / Alkynes / Terminal alkynes
2-Decyne 75424 Click to see CCCCCCCC#CC 138.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
3-Ethylidene-1-methylcyclopentene 44005 Click to see CC=C1CCC(=C1)C 108.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Cyclic olefins / Cycloalkenes
4-Methylcyclohexene 11572 Click to see CC1CCC=CC1 96.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Octene 8125 Click to see CCCCCCC=C 112.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Methylbutyl 2-methylbutyrate 17129 Click to see CCC(C)COC(=O)C(C)CC 172.26 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
3-Hexenyl 2-methylbutyrate 61467 Click to see CCC=CCCOC(=O)C(C)CC 184.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Hexyl valerate 70694 Click to see CCCCCCOC(=O)CCCC 186.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Pentyl 2-methylbutyrate 107059 Click to see CCCCCOC(=O)C(C)CC 172.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Pentyl 3-methylbutanoate 95978 Click to see CCCCCOC(=O)CC(C)C 172.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Pentyl valerate 62433 Click to see CCCCCOC(=O)CCCC 172.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
4-[(Dimethylazaniumyl)amino]-4-oxobutanoate 72200802 Click to see C[NH+](C)NC(=O)CCC(=O)[O-] 160.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Tetradecanal 31291 Click to see CCCCCCCCCCCCCC=O 212.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
5-Hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid 4632016 Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 332.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079367/
Gibberellin 20 439635 Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 332.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079367/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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
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
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
2-Methylenebornane 123425 Click to see CC1(C2CCC1(C(=C)C2)C)C 150.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
beta-Terpinene 66841 Click to see CC(C)C1=CCC(=C)CC1 136.23 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
Isoterpinolene 102443 Click to see CC1CCC(=C(C)C)C=C1 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
5-Isopropenyl-2-methylcyclopent-1-enecarboxaldehyde 572089 Click to see CC1=C(C(CC1)C(=C)C)C=O 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
Cyclohexene, 1-methyl-3-(1-methylethenyl)- 10354 Click to see CC1=CC(CCC1)C(=C)C 136.23 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Dictyopterol 10059334 Click to see CC(=C)C1CCC2(C(CCC(=C)C2C1)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(96)00690-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
[(1R,5S,7S)-7-acetyloxy-2,8-dimethylidene-5-prop-1-en-2-ylcyclodecyl] acetate 102066425 Click to see CC(=C)C1CCC(=C)C(CCC(=C)C(C1)OC(=O)C)OC(=O)C 320.40 unknown https://doi.org/10.1016/S0031-9422(96)00690-5
[(1S,5S,7S)-7-acetyloxy-2,8-dimethylidene-5-prop-1-en-2-ylcyclodecyl] acetate 11688333 Click to see CC(=C)C1CCC(=C)C(CCC(=C)C(C1)OC(=O)C)OC(=O)C 320.40 unknown https://doi.org/10.1016/S0031-9422(96)00690-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Chamazulene 10719 Click to see CCC1=CC2=C(C=CC2=C(C=C1)C)C 184.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3-Epicabraleadiol 21575463 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 460.70 unknown https://doi.org/10.1021/JF010164E
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Alantolactone 72724 Click to see CC1CCCC2(C1=CC3C(C2)OC(=O)C3=C)C 232.32 unknown https://doi.org/10.1111/J.1600-0536.1978.TB03741.X
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
9-cis-Lutein 131801655 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.038
9'-cis-Lutein 131801656 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.038
Lutein 5281243 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.038
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5R,7S,10R,11R,14R,15S,16S,17R,19R,21S,22S)-1,2,6,6,10,16,17,21-octamethyl-18-oxahexacyclo[12.9.0.02,11.05,10.015,21.017,19]tricosane-7,22-diol 101121171 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CC6C1(O6)C)C)O)C)C)(C)C)O)C 458.70 unknown https://doi.org/10.1021/JF010164E
(3S,6aR,6bS,8S,8aS,12aS,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol 23641100 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)C 458.70 unknown https://doi.org/10.1021/JF010164E
12-Ursene-3b,16b-diol 12302049 Click to see CC1CCC2(C(CC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)O)C 442.70 unknown https://doi.org/10.1021/JF010164E
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,8,9-triol 74344353 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C=C1C)O)C)O)C)C)(C)C)O)C 458.70 unknown https://doi.org/10.1021/JF010164E
https://doi.org/10.1016/S0944-7113(98)80031-7
Arnidiol 10478550 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CCC1=C)C)O)C)C)(C)C)O)C 442.70 unknown https://doi.org/10.1021/JF010164E
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown https://doi.org/10.1021/JF010164E
CID 9890381 9890381 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO 458.70 unknown via CMAUP database
Dammarenediol 122880 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C 444.70 unknown https://doi.org/10.1021/JF010164E
Dammarenediol II 10895555 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C 444.70 unknown https://doi.org/10.1021/JF010164E
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1021/JF010164E
Faradiol 9846222 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CC=C1C)C)O)C)C)(C)C)O)C 442.70 unknown https://doi.org/10.1021/JF010164E
https://doi.org/10.1016/S0944-7113(98)80031-7
Heliantriol C 397879 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C=C1C)O)C)O)C)C)(C)C)O)C 458.70 unknown https://doi.org/10.1021/JF010164E
https://doi.org/10.1016/S0944-7113(98)80031-7
Maniladiol 397934 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1021/JF010164E
Ursadiol 5273648 Click to see CC1(CCC2(C(CC3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)C)C 442.70 unknown https://doi.org/10.1021/JF010164E
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Octen-3-yl acetate 17121 Click to see CCCCCC(C=C)OC(=O)C 170.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
Octen-1-ol acetate 520583 Click to see CCCCCCC=COC(=O)C 170.25 unknown https://doi.org/10.1093/CHROMSCI/46.2.127
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 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 https://doi.org/10.1055/S-2005-873181
3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 3802778 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1055/S-2005-873181
3,4-Di-O-caffeoylquinic acid methyl ester 10392218 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 530.50 unknown https://doi.org/10.1055/S-2005-873181
3,5-Dicaffeoyl-epi-quinic acid 60150332 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1055/S-2005-873181
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1055/S-2005-873181
Chlorogenic Acid 1794427 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 https://doi.org/10.1055/S-2005-873181
Chlorogensaure 12310830 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
Methyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 73412063 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1055/S-2005-873181
Methyl 3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylate 460892 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 530.50 unknown https://doi.org/10.1055/S-2005-873181
Methyl 3,5-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4-dihydroxycyclohexane-1-carboxylate 460893 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 530.50 unknown https://doi.org/10.1055/S-2005-873181
Methyl chlorogenate 6476139 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1055/S-2005-873181
Neochlorogenic acid 5280633 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 https://doi.org/10.1055/S-2005-873181
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://doi.org/10.1055/S-2005-873181
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
3-Methylcyclohex-3-en-1-one 520546 Click to see CC1=CCCC(=O)C1 110.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dihydroxyacetophenone 14530 Click to see CC(=O)C1=CC(=C(C=C1)O)O 152.15 unknown via CMAUP database
Resacetophenone 6990 Click to see CC(=O)C1=C(C=C(C=C1)O)O 152.15 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1055/S-2005-873181
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown https://doi.org/10.1055/S-2005-873181
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown https://doi.org/10.1055/S-2005-873181
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2005-873181
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-2005-873181
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2005-873181
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-2005-873181
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-Buten-2-ol, 4-phenyl- 15172 Click to see CC(C=CC1=CC=CC=C1)O 148.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272594/
> 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 https://doi.org/10.1021/NP50103A006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1055/S-2005-873181
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/NP50103A006
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1055/S-2005-873181
Flavanone 10251 Click to see C1C(OC2=CC=CC=C2C1=O)C3=CC=CC=C3 224.25 unknown https://doi.org/10.1021/NP50103A006
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/NP50103A006
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,8-Dihydroxyflavone 1880 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3)O)O 254.24 unknown https://doi.org/10.1021/NP50103A006
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1055/S-2005-873181
https://doi.org/10.1055/S-2003-43207
https://doi.org/10.1271/BBB.67.2091
https://doi.org/10.1021/NP50103A006
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1021/NP50103A006
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown https://doi.org/10.1021/NP50103A006
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 https://doi.org/10.1080/10286020903128470
https://doi.org/10.1055/S-2005-873181
https://doi.org/10.1055/S-2003-43207
https://doi.org/10.1271/BBB.67.2091
https://doi.org/10.1021/NP50103A006
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxyflavone 11349 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)O 238.24 unknown https://doi.org/10.1021/NP50103A006
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50103A006
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP50103A006
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown https://doi.org/10.1021/NP50103A006
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1021/NP50103A006
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 https://doi.org/10.1271/BBB.67.2091
https://doi.org/10.1021/NP50103A006
https://doi.org/10.1055/S-2003-43207
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-(6-O-malonyl-beta-D-glucoside) 443915 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O)O)O 535.40 unknown https://doi.org/10.1016/0031-9422(88)80697-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1055/S-2003-43207
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1021/NP50103A006
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272765/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 5-glucoside 5317471 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50103A006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2003-43207
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 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 https://doi.org/10.1055/S-2003-43207
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5R,6R)-3,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-4-yl] acetate 155541096 Click to see CC(=O)OC1C(C(OC(C1O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)CO)O 488.40 unknown https://doi.org/10.1055/S-2005-873181
[3,5-Dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-4-yl] acetate 162929505 Click to see CC(=O)OC1C(C(OC(C1O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)CO)O 488.40 unknown https://doi.org/10.1055/S-2005-873181
4-{5-(acetyloxy)-4-oxo-7-[(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)oxy]-4H-chromen-2-yl}benzene-1,2-diyl diacetate 16396576 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C(=C2)OC(=O)C)C(=O)C=C(O3)C4=CC(=C(C=C4)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 742.60 unknown https://doi.org/10.1021/NP50103A006
5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44559598 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1021/NP50103A006
7-(beta-D-Galactopyranosyloxy)-5-hydroxy-2-(4-Methoxyphenyl)- 5291487 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1055/S-2005-873181
https://doi.org/10.1248/CPB.39.3346
Acacetin-7-O-beta-D-galactopyranoside 5480899 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1021/NP50103A006
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP50103A006
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1021/NP50103A006
Luteolin 7-galactoside 5291488 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 https://doi.org/10.1055/S-2005-873181
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 https://doi.org/10.1021/NP50103A006
https://doi.org/10.1248/CPB.39.3346
https://doi.org/10.1055/S-2005-873181
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272765/
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1055/S-2005-873181
https://doi.org/10.1248/CPB.39.3346
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-methyltricetin 11267045 Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 316.26 unknown https://doi.org/10.1055/S-2005-873181
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 https://doi.org/10.1055/S-2005-873181
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-3',4',5'-trimethoxyflavone 5379265 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 344.30 unknown https://doi.org/10.1055/S-2005-873181
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1055/S-2005-873181
https://doi.org/10.1271/BBB.67.2091
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2005-873181
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone 5496475 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown https://doi.org/10.1055/S-2005-873181
6-Methoxytricin 14034284 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown https://doi.org/10.1055/S-2005-873181
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1055/S-2005-873181
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown https://doi.org/10.1055/S-2005-873181
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/J.PHYMED.2013.10.019
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Angeloylgomisin P 13844273 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC 514.60 unknown https://doi.org/10.1055/S-2005-873181

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