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Tanacetum coccineum

Tanacetum coccineum - 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 UUID643fd254a2bc7591893443
Scientific name Tanacetum coccineum
Authority (Willd.) Grierson
First published in Notes Roy. Bot. Gard. Edinburgh 33(2): 262 (1974)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Chrysanthemum roseum Adams Beitr. Naturk. (Weber & Mohr) 1: 70. [15 Nov 1805-1806]
Pyrethrum roseum var. adamii Trautv. Trudy Imperatorskago S.-Peterburgskago Botanicheskago Sada 5(2): 443 1878

Common names Top

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Language Common/alternative name
English pyrethrum
English pyrethum daisy
Arabic الأقحوان القرمزي
Arabic أقحوان قرمزي
Azerbaijani pyrethrum
Azerbaijani birəotu
Bulgarian червена пижма
Catalan piretre
Catalan tanacetum cinerariifolium
Catalan chrysanthemum cinerariifolium
Catalan pyrethrum
Greek Πύρεθρο
Esperanto piretro
Estonian pyrethrum roseum
Estonian roosa püreeter
Estonian roosa neitsikummel
Basque chrysanthemum cinerariaefolium
Basque chrysanthemum cinerariifolium
Basque piretro
Persian پیرتروم
Persian گل حشرهکش
Persian گل حشره کش
Finnish punapäivänkakkara
Finnish punapietaryrtti
French pyrèthre rose
Irish pioratram
Armenian լվածաղիկ մուգ կարմիր
Indonesian piretrum
io piretro
Italian piretro
Japanese アカバナムシヨケギク
Japanese ペルシアジョチュウギク（波斯除虫菊）
Japanese アカムシヨケギク
Japanese アカバナジョチュウギク
Malayalam പൈറിത്രം
Malayalam pyrethrum
Norwegian Bokmål pyrethrum
Polish pyretrum
Portuguese piretro
Russian Пиретрум
Russian pyrethrum
Kinyarwanda ibireti
Kinyarwanda tanacetum cinerariifolium
Slovenian bolhač
Swedish rosenkrage
Chinese 除蟲菊
Chinese 红花除虫菊
Chinese 除虫菊

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Tanacetum coccineum subsp. carneum (M.Bieb.) Grierson Notes Roy. Bot. Gard. Edinburgh 33(2): 262 (1974)
Tanacetum coccineum subsp. chamaemelifolium (Sommier & Levier) Grierson Notes Roy. Bot. Gard. Edinburgh 33(2): 262 (1974)
Tanacetum coccineum subsp. coccineum

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • East European Russia
    • Middle Europe
      • Germany
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Norway
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • France
  • Northern America
    • Mexico
      • Mexico Southeast
    • Northeastern U.S.A.
      • New York

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000122722
UNII UH9RT2A2WE
Canadensys 32867
USDA Plants TACO6
Tropicos 2732023
INPN 162467
KEW urn:lsid:ipni.org:names:252277-1
The Plant List gcc-83879
Missouri Botanical Garden 277669
PFAF Tanacetum coccineum
Open Tree Of Life 1040269
NCBI Taxonomy 301880
NBN Atlas NBNSYS0200003285
IPNI 252277-1
iNaturalist 135202
GBIF 3118616
Freebase /m/01nc_z
EPPO CHYCC
EOL 486898
Elurikkus 7656
USDA GRIN 317328
CMAUP NPO13754

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_026074375.1 Tcoc_v1.0 Scaffold Research & development laboratory, DAINIHON JOCHUGIKU Co.,Ltd. 2022-11-02 137.0x 8.81 Gb

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
Tanacetum species: Bridging empirical knowledge, phytochemistry, nutritional value, health benefits and clinical evidence Khatib S, Sobeh M, Faraloni C, Bouissane L Front Pharmacol 20-Apr-2023
PMCID:PMC10157496
doi:10.3389/fphar.2023.1169629
PMID:37153781
Key Amino Acids for Transferase Activity of GDSL Lipases Yamashiro T, Shiraishi A, Nakayama K, Satake H Int J Mol Sci 01-Dec-2022
PMCID:PMC9736205
doi:10.3390/ijms232315141
PMID:36499468
Draft Genome of Tanacetum Coccineum: Genomic Comparison of Closely Related Tanacetum-Family Plants Yamashiro T, Shiraishi A, Nakayama K, Satake H Int J Mol Sci 24-Jun-2022
PMCID:PMC9267051
doi:10.3390/ijms23137039
PMID:35806039
Sorting out the plants responsible for a contamination with pyrrolizidine alkaloids in spice seeds by means of LC-MS/MS and DNA barcoding: Proof of principle with cumin and anise spice seeds Willocx M, Van der Beeten I, Asselman P, Delgat L, Baert W, Janssens SB, Leliaert F, Picron JF, Vanhee C Food Chem (Oxf) 01-Jan-2022
PMCID:PMC8991971
doi:10.1016/j.fochms.2021.100070
PMID:35415703
Transcriptional Responses and GCMS Analysis for the Biosynthesis of Pyrethrins and Volatile Terpenes in Tanacetum coccineum Zeng T, Li JW, Zhou L, Xu ZZ, Li JJ, Hu H, Luo J, Zheng RR, Wang YY, Wang CY Int J Mol Sci 30-Nov-2021
PMCID:PMC8657971
doi:10.3390/ijms222313005
PMID:34884809
Fabrication and characterization of noble crystalline silver nanoparticles from Pimenta dioica leave extract and analysis of chemical constituents for larvicidal applications Kumar D, Kumar P, Vikram K, Singh H Saudi J Biol Sci 20-Sep-2021
PMCID:PMC8865016
doi:10.1016/j.sjbs.2021.09.052
PMID:35241964
Plant Extracts as Alternative Additives for Sperm Preservation Ros-Santaella JL, Pintus E Antioxidants (Basel) 13-May-2021
PMCID:PMC8152457
doi:10.3390/antiox10050772
PMID:34068069
Pyrethroid-Induced Organ Toxicity and Anti-Oxidant-Supplemented Amelioration of Toxicity and Organ Damage: The Protective Roles of Ascorbic Acid and α-Tocopherol Al-Omar MS, Naz M, Mohammed SA, Mansha M, Ansari MN, Rehman NU, Kamal M, Mohammed HA, Yusuf M, Hamad AM, Akhtar N, Khan RA Int J Environ Res Public Health 25-Aug-2020
PMCID:PMC7503327
doi:10.3390/ijerph17176177
PMID:32854455
The complete chloroplast genome of Tanacetum coccineum Zeng T, Li J, Wang C, He J Mitochondrial DNA B Resour 01-Jun-2020
PMCID:PMC7510654
doi:10.1080/23802359.2020.1768915
PMID:33366986
The changing face of farmers’ home gardens: a diachronic analysis from Sillian (Eastern Tyrol, Austria) Vogl-Lukasser B, Vogl CR J Ethnobiol Ethnomed 29-Oct-2018
PMCID:PMC6205796
doi:10.1186/s13002-018-0262-3
PMID:30373655
Factors Influencing in Vitro Organogenesis of Chrysanthemum morifolium cv. ‘Resomee Splendid’ Kazeroonian R, Mousavi A, Jari SK, Tohidfar M Iran J Biotechnol 15-May-2018
PMCID:PMC6371633
doi:10.21859/ijb.1454
PMID:30805383
Fischer’s Lexicon of Slavic beliefs and customs: a previously unknown contribution to the ethnobotany of Ukraine and Poland Kujawska M, Łuczaj Ł, Typek J J Ethnobiol Ethnomed 24-Dec-2015
PMCID:PMC4690239
doi:10.1186/s13002-015-0073-8
PMID:26704421
Morphological and Molecular Revision of the Genus Ozirhincus (Diptera: Cecidomyiidae)—Long-Snouted Seed-Feeding Gall Midges on Asteraceae Dorchin N, Astrin JJ, Bodner L, Harris KM PLoS One 02-Jul-2015
PMCID:PMC4489628
doi:10.1371/journal.pone.0130981
PMID:26134526
Chrysanthemyl Diphosphate Synthase Operates in Planta as a Bifunctional Enzyme with Chrysanthemol Synthase Activity Yang T, Gao L, Hu H, Stoopen G, Wang C, Jongsma MA J Biol Chem 05-Nov-2014
PMCID:PMC4276892
doi:10.1074/jbc.M114.623348
PMID:25378387
Adaptive evolution of the chrysanthemyl diphosphate synthase gene involved in irregular monoterpene metabolism Liu PL, Wan JN, Guo YP, Ge S, Rao GY BMC Evol Biol 08-Nov-2012
PMCID:PMC3518182
doi:10.1186/1471-2148-12-214
PMID:23137178

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 / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)O)C=CC=C3O 494.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4-hydroxy-9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(oxalooxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 11972451 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 518.40 unknown via CMAUP database
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
Rhein-8-glucoside 5320961 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 446.40 unknown via CMAUP database
Sennidin A 92826 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C(=O)O)C=C(C=C3O)C(=O)O 538.50 unknown via CMAUP database
Sennoside A 73111 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O 862.70 unknown via CMAUP database
Sennoside C 46173829 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)CO 848.80 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
8-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-1-hydroxy-3-methoxy-6-methylanthraquinone 5320543 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(=O)C5=C(C2=O)C=C(C=C5O)OC 608.50 unknown via CMAUP database
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Aloe-emodin-glucoside 147295 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)COC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
Chrysophanein 6324923 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Rheochrysin 168938 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
6-O-galloyl-beta-D-glucose 5317463 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Pyrethroids
Cinerin I 5281547 Click to see CC=CCC1=C(C(CC1=O)OC(=O)C2C(C2(C)C)C=C(C)C)C 316.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
Cinerin II 5281548 Click to see CC=CCC1=C(C(CC1=O)OC(=O)C2C(C2(C)C)C=C(C)C(=O)OC)C 360.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Pyrethroids / Pyrethrins
[2-Methyl-4-oxo-3-[(2Z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1R,3R)-3-[(E)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate 12314789 Click to see CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C(=O)OC)CC=CC=C 372.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
Jasmolin I 12304687 Click to see CCC=CCC1=C(C(CC1=O)OC(=O)C2C(C2(C)C)C=C(C)C)C 330.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
Jasmolin II 12304690 Click to see CCC=CCC1=C(C(CC1=O)OC(=O)C2C(C2(C)C)C=C(C)C(=O)OC)C 374.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
Pyrethrin I 5281045 Click to see CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C)CC=CC=C 328.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
Pyrethrin II 5281555 Click to see CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C(=O)OC)CC=CC=C 372.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21607580 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)CO)C(=O)O)C)C)C)O)O)O)O)O 751.00 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-5-amino-2-ammonio-5-oxopentanoate 6992086 Click to see C(CC(=O)N)C(C(=O)[O-])[NH3+] 146.14 unknown via CMAUP database
> 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/10.1007/BF00565061
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/10.1007/BF00565061
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O 378.40 unknown via CMAUP database
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)O 394.40 unknown via CMAUP database
2-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-5-carboxylic acid 5315687 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 382.30 unknown via CMAUP database
4-[(6-O-Galloyl-beta-D-glucopyranosyl)oxy]-4-deoxygallic acid 11972354 Click to see C1=C(C=C(C(=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)C(=O)O 484.40 unknown via CMAUP database
Ethanone, 1-[8-[[6-O-(carboxycarbonyl)-beta-D-glucopyranosyl]oxy]-1-hydroxy-6-methoxy-3-methyl-2-naphthalenyl]- 5321979 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)OC 480.40 unknown via CMAUP database
Raspberryketone glucoside 5320521 Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 11972309 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2O)CO)O)O 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-[(2S)-2-Hydroxypropyl]-5-methyl-7-hydroxy-4H-1-benzopyran-4-one 45272307 Click to see CC1=CC(=CC2=C1C(=O)C=C(O2)CC(C)O)O 234.25 unknown via CMAUP database
2H-1-Benzopyran-5-acetic acid, 3,4-dihydro-7-hydroxy-2-methyl-4-oxo-, (S)- 5319543 Click to see CC1CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 236.22 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-acetyl-7-hydroxy-2-methyl- 5315891 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid 14429402 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 234.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-carboxylic acid 5315688 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)O 220.18 unknown via CMAUP database
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Chrysanthin 12314793 Click to see CC1=CC(C2C(CC3(C(O3)CC1)C)OC(=O)C2=C)OC(=O)C 306.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(3S,3aS,6aS,9S,10R,10aR)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3a,6,6a,8,9,10-hexahydro-3H-benzo[d][2]benzofuran-9-yl] (2R)-2-hydroxydecanoate 139584079 Click to see CCCCCCCCC(C(=O)OC1CC(C2CC=C(C3C2(C1O)C(=O)OC3O)C=O)(C)C)O 466.60 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.38B-0902
> 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/10.1007/BF00565061
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00565061
> 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
procyanidin B1 3-O-gallate 12795888 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)O 730.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin 5-O-beta-D-glucopyranoside 6324898 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 / Stilbenes
Rhapontigenin 5320954 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 5322088 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 542.50 unknown via CMAUP database
Resveratrol 4'-O-beta-D-(2''-O-galloyl)-glucopyranoside 10325054 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 542.50 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Rhapontin 637213 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1-O,6-O-Digalloyl-2-O-cinnamoyl-beta-D-glucopyranose 6325082 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 614.50 unknown via CMAUP database
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown via CMAUP database
2-Cinnamoyl-1-galloylglucose 5315898 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O 462.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database

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