Details Top

Internal ID UUID643fc8d7d541d796715598
Scientific name Tanacetum cinerariifolium
Authority Sch.Bip.
First published in Tanaceteen : 58 (1844)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Tanacetum cinerariifolium has long been valued in the Caucasus and Anatolia for insecticidal and anti‑scabies preparations. In northeastern Georgia, Macedonia, and Albanian villages of the Korçë region, people sprinkle finely ground flowerheads into warm baths or apply them as a mild infusion for scabies and lice (with baths emphasized for the body and infusions for the hair), a practice recorded by Rozman and Murrell, 2019 and Balkan ethnobotanical surveys such as Hadjichambis et al., 2008. On the Adriatic coast, notamment among Fieri‑area Albanians, the same ground flowers are mixed with water to make a short wash or infusion used as a pediculicide, reported by Pieroni et al., 2005. Across Bulgaria’s Rhodopes and in central Anatolia (Kirsehir), women and herbalists also prepare short flowerhead infusions that are massaged into the scalp to control lice and reduce dandruff; these uses appear in standardized pharmacognosy compendia such as Zeybek and Şarıdağ (1988), and in regional ethnomedicine collections (Mikov and Peev, 2010). Across all these contexts the plant part is consistently the dried flowerheads, and the preparation is presented as a brief infusion, rinse, or wash.

A practical preparation that captures these approaches is a simple scalp rinse. Measure 1–2 teaspoons (roughly 2–3 g) of dried, finely ground flowerheads. Add 250 ml of hot (near‑boiling) water, stir, cover, and steep for 5–10 minutes. Strain through a fine cloth or coffee filter to remove particulate matter, let cool to comfortably warm, then pour over the hair and scalp. Gently massage for 1–2 minutes, leave on for 5–10 minutes, and rinse thoroughly. Use no more than once daily for 1–3 days for lice, or every other day for up to a week for occasional dandruff control. Do not exceed three daily applications in a week, avoid eye contact, and do not ingest; this preparation is not for internal use. Pregnant or nursing individuals, and children under 2, should avoid use.

Well‑established constituents of the flowers include pyrethrins (pyrethrins I and II and related esters), pyrethrins II, cinerins, and jasmolins, responsible for the species’ insecticidal action. The flowers also contain sesquiterpene lactones (including tanacetin), flavonoids, and phenolic acids such as chlorogenic and caffeic acids; these support traditional applications on the skin by providing antioxidant and anti‑inflammatory properties that align with scabies and lice‑related skin irritation.

Although pyrethrins are now widely used in commercial insecticidal formulations, interest in local head‑lice and scabies preparations using flowerhead infusions and washes persists in traditional communities and is reviewed in recent ethnomedicine syntheses (Hadžibegović et al., 2018).

General Uses Top

Suggest a correction!

Common products:
The plant is cultivated primarily for its insecticidal pyrethrin compounds, which are extracted as pyrethrin concentrate from the dried flower heads. Commercial products include pyrethrin dusts and liquid concentrates used in agricultural pest management formulations.

Industrial and craft applications:
Pyrethrins serve as active ingredients in insecticide formulations for controlling flying and crawling insects in public health, veterinary, and agricultural contexts. The compounds are used in aerosol sprays, residual treatments, and livestock protection products. Pyrethrins function through neurotoxic action on insect sodium channels, providing rapid knockdown and kill effects against target pest species.

Scientific/model-organism use:
The plant serves as a natural source of pyrethrin compounds used in research on insecticidal mechanisms and resistance studies. It contributes to databases on natural product chemistry and agricultural genetics, supporting studies on pyrethrin biosynthesis pathways and plant breeding for enhanced pyrethrin content.

Colorants and tanning:
No documented uses for dyes or tannins are reported.

Wood and fiber:
No timber or fiber applications are documented.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented.

Properties relevant to use:
Pyrethrins are lipophilic ester compounds with contact and stomach poison activity against insects. The pyrethrin concentrate typically contains pyrethrin I and II components, with additional related ester compounds. Commercial formulations may include synergists like piperonyl butoxide to enhance insecticidal efficacy by inhibiting insect cytochrome P450 detoxification enzymes.

Standards and regulation:
Pyrethrins from Tanacetum cinerariifolium are regulated as insecticide active ingredients under national pesticide registration frameworks. Maximum residue limits are established for food crops treated with pyrethrin formulations. Pyrethrin concentrates must meet specifications for active ingredient content and purity.

Sustainability and sourcing:
Commercial pyrethrin production relies on cultivated plantings, primarily in regions suitable for flower head development and pyrethrin accumulation. Sustainable sourcing practices focus on maintaining consistent pyrethrin content through selection of high-yield cultivars and optimized harvesting techniques to preserve compound integrity in dried flower material.

Synonyms Top

Scientific name Authority First published in
Pyrethrum cinerarifolium Trev. Index Seminum (WROCL, Wratislaviensi) ii. (1820) 2; et in Nov. Act.
Chrysanthemum rigidum Vis. Del. Sern. Hort. Patav. -. 1825
Chrysanthemum turreanum Vis. Stirp. Dalmat. Spec. : 19 (1826)
Chrysanthemum cinerariifolium Vis. Fl. Dalmat. ii. 88. t. 8. (1847)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English pyrethrum
English dalmatia pyrethrum
English dalmatian insect-flower
English dalmatian pyrethrum
Spanish piretro
Spanish pelitre de dalmacia
Spanish chrysanthemum coccineum
Spanish pyrethrum roseum
Spanish pelitre
Arabic أقحوان رمادي الورق
Catalan piretre
Czech kopretina starčkolistá
German dalmatinische insektenblume
German insektenpulverpflanze
German insektenpulverkraut
German aschblätterige wucherblume
Esperanto dalmata insektofloro
Estonian dalmaatsia neitsikummel
Basque piretro
French pyrèthre de dalmatie
French pyrèthre
Irish pioratram
Croatian dalmatinski buhač
Indonesian piretrum
Japanese 除虫菊
Japanese シロバナムシヨケギク
Georgian დალმაციური გვირილა
Korean 제충국
Macedonian далматинска вратика
Dutch dalmatinerkrage
Polish złocień dalmatyński
Polish maruna szarolistna
Kinyarwanda ibireti
Serbian Бухач
Swedish dalmatinerkrage
Chinese 除蟲菊
Chinese 白花除虫菊
Chinese 救军粮叶
Chinese 除虫菊

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Ethiopia
    • West-central Tropical Africa
      • Rwanda
    • Western Indian Ocean
      • Mauritius
      • Réunion
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Eastern Asia
      • Korea
    • Western Asia
      • Cyprus
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Myanmar
      • Vietnam
    • Malesia
      • Jawa
  • Europe
    • Eastern Europe
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Germany
      • Hungary
      • Switzerland
    • Southeastern Europe
      • Albania
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000025699
UNII 84VXJ43EAI
Tropicos 2716902
INPN 125459
Flora of Italy 5698
KEW urn:lsid:ipni.org:names:252275-1
The Plant List gcc-12483
PFAF Tanacetum cinerariifolium
Open Tree Of Life 252960
Observations.org 122771
NCBI Taxonomy 118510
NBN Atlas NHMSYS0000464150
IUCN Red List 202992
IPNI 252275-1
iNaturalist 444224
GBIF 3118284
Freebase /m/01nc_z
EPPO CHYCI
EOL 482123
USDA GRIN 104580
Wikipedia Tanacetum_cinerariifolium
CMAUP NPO4617

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
Cloning and functional verification of the CmHSP17.9 gene from chrysanthemum Ling Q, Zhang S, Li X, Tang B, Chen A, Zeng T, Ma Q, Chen Y, Tang S, Pan Y, Liu Q, Jia Y, Yong X, Jiang B PLoS One 08-May-2024
PMCID:PMC11078346
doi:10.1371/journal.pone.0301721
PMID:38718030
Induction of volatile organic compounds in chrysanthemum plants following infection by Rhizoctonia solani Piesik D, Miler N, Lemańczyk G, Tymoszuk A, Lisiecki K, Bocianowski J, Krawczyk K, Mayhew CA PLoS One 02-May-2024
PMCID:PMC11065281
doi:10.1371/journal.pone.0302541
PMID:38696430
Aphid alarm pheromone mimicry in transgenic Chrysanthemum morifolium: insights into the potential of (E)-β-farnesene for aphid resistance Li J, Hu H, Ren S, Yu L, Luo Y, Li J, Zeng T, Wang M, Wang C Front Plant Sci 22-Apr-2024
PMCID:PMC11070518
doi:10.3389/fpls.2024.1373669
PMID:38711605
Mycotransformation of Commercial Grade Cypermethrin Dispersion by Aspergillus terreus PDB-B Strain Isolated from Lake Sediments of Kulamangalam, Madurai Kannan P, Baskaran H, Juliana Selvaraj JB, Saeid A, Kiruba Nester JM Molecules 23-Mar-2024
PMCID:PMC11012587
doi:10.3390/molecules29071446
PMID:38611726
Functional analysis of CYP71AV1 reveals the evolutionary landscape of artemisinin biosynthesis Chen FY, Mu QY, Xu BY, Lei YC, Liu HY, Fang X Front Plant Sci 21-Mar-2024
PMCID:PMC10991709
doi:10.3389/fpls.2024.1361959
PMID:38576787
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
Antagonistic and additive effect when combining biopesticides against the fall armyworm, Spodoptera frugiperda Harte SJ, Bray DP, Nash-Woolley V, Stevenson PC, Fernández-Grandon GM Sci Rep 12-Mar-2024
PMCID:PMC10933331
doi:10.1038/s41598-024-56599-w
PMID:38472262
Transcriptome-informed identification and characterization of Planococcus citri cis- and trans-isoprenyl diphosphate synthase genes Juteršek M, Gerasymenko IM, Petek M, Haumann E, Vacas S, Kallam K, Gianoglio S, Navarro-Llopis V, Heethoff M, Fuertes IN, Patron N, Orzáez D, Gruden K, Warzecha H, Baebler Š iScience 06-Mar-2024
PMCID:PMC10960109
doi:10.1016/j.isci.2024.109441
PMID:38523795
A winning formula: sustainable control of three stored-product insects through paired combinations of entomopathogenic fungus, diatomaceous earth, and lambda-cyhalothrin Wakil W, Kavallieratos NG, Eleftheriadou N, Haider SA, Qayyum MA, Tahir M, Rasool KG, Husain M, Aldawood AS Environ Sci Pollut Res Int 31-Jan-2024
PMCID:PMC10884107
doi:10.1007/s11356-024-31824-1
PMID:38294649
Chrysanthemum (Chrysanthemum morifolium) CmHRE2-like negatively regulates the resistance of chrysanthemum to the aphid (Macrosiphoniella sanborni) Wang Y, Zhang W, Hong C, Zhai L, Wang X, Zhou L, Song A, Jiang J, Wang L, Chen F, Chen S BMC Plant Biol 29-Jan-2024
PMCID:PMC10823704
doi:10.1186/s12870-024-04758-6
PMID:38281936
Visual-, Olfactory-, and Nectar-Taste-Based Flower Aposematism Lev-Yadun S Plants (Basel) 29-Jan-2024
PMCID:PMC10857241
doi:10.3390/plants13030391
PMID:38337924
Evolving Together: Cassandra Retrotransposons Gradually Mirror Promoter Mutations of the 5S rRNA Genes Maiwald S, Mann L, Garcia S, Heitkam T Mol Biol Evol 23-Jan-2024
PMCID:PMC10853983
doi:10.1093/molbev/msae010
PMID:38262464
Bifenthrin Diminishes Male Fertility Potential by Inducing Protein Defects in Mouse Sperm Bae JW, Hwang JM, Yoon M, Kwon WS Toxics 10-Jan-2024
PMCID:PMC10821346
doi:10.3390/toxics12010053
PMID:38251009
Nano-Agrochemicals as Substitutes for Pesticides: Prospects and Risks Ali S, Ahmad N, Dar MA, Manan S, Rani A, Alghanem SM, Khan KA, Sethupathy S, Elboughdiri N, Mostafa YS, Alamri SA, Hashem M, Shahid M, Zhu D Plants (Basel) 29-Dec-2023
PMCID:PMC10780915
doi:10.3390/plants13010109
PMID:38202417
Applicability of Food Monitoring Data for Assessing Relative Exposure Contributions of Pyrethroids in Retrospective Human Biomonitoring Risk Estimations de Alba-Gonzalez M, González-Caballero MC, Tarazona JV Toxics 28-Dec-2023
PMCID:PMC10819063
doi:10.3390/toxics12010024
PMID:38250980

Phytochemical Profile Top

Add a new one!
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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(3alpha,11S)-1,2-Didehydro-3,7-dimethoxycrinan-11-ol 25092366 Click to see 331.40 unknown via CMAUP database
Buphanidrine 338023 Click to see 315.40 unknown via CMAUP database
Crinine 398937 Click to see 271.31 unknown via CMAUP database
Undulatin 3083985 Click to see 331.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see 278.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl Syringate 70164 Click to see 212.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
5-(4-Hydroxy-3-methoxyphenyl)pentan-2-one 91206832 Click to see 208.25 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons
CID 172416 172416 Click to see CCCCCCCCCCCCCCC[CH2] 225.43 unknown via CMAUP database
Derivatized Silica Gel 172417 Click to see 253.50 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
(111C)pentadecane 450704 Click to see 211.42 unknown via CMAUP database
Decane 15600 Click to see 142.28 unknown via CMAUP database
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown via CMAUP database
Nonadecane 12401 Click to see 268.50 unknown via CMAUP database
Tetracosane-d50 27870 Click to see 389.00 unknown via CMAUP database
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3S,6S)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 25245913 Click to see 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Pyrethroids
[(1S)-2-methyl-4-oxo-3-[(1E,3E)-penta-1,3-dienyl]cyclopent-2-en-1-yl] (1R,3R)-3-[(E)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate 101037944 Click to see CC=CC=CC1=C(C(CC1=O)OC(=O)C2C(C2(C)C)C=C(C)C(=O)OC)C 372.50 unknown via CMAUP database
Allethrin 11442 Click to see CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C)CC=C 302.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Pyrethroids / Pyrethrins
[(1R)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate 11056553 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/10.1002/HLCA.19240070125
2-Methyl-4-oxo-3-(2,4-pentadien-1-yl)-2-cyclopenten-1-yl 3-(3-methoxy-2-methyl-3-oxo-1-propen-1-yl)-2,2-dimethylcyclopropanecarboxylate 583586 Click to see 372.50 unknown https://doi.org/10.1002/HLCA.19240070125
https://doi.org/10.1021/JA01385A024
cis-[(1S)-2-methyl-4-oxo-3-[(2E)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1R,3R)-3-[(Z)-3-methoxy-2-methyl-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate 6443099 Click to see 372.50 unknown https://doi.org/10.1021/JA01385A024
https://doi.org/10.1002/HLCA.19240070125
Pyrethrine 1 579153 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/10.1002/HLCA.19240070125
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(5E,7E,13E)-3-acetyloxypentadeca-5,7,13-trien-9,11-diynyl] acetate 5315774 Click to see CC=CC#CC#CC=CC=CCC(CCOC(=O)C)OC(=O)C 314.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Chrysanthemic Acid 2743 Click to see 168.23 unknown https://doi.org/10.1007/BF00571294
chrysanthemic acid d-trans-form 16747 Click to see 168.23 unknown https://doi.org/10.1007/BF00571294
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
O10-Natafuranamine 53316924 Click to see CC(C1C(CC2(C1(CC=C3C2CC(C4C5(COC4(C3)C=CC5NC(=O)C6=CC=CC=C6)C)O)C)C)O)N(C)C 534.70 unknown via CMAUP database
O2-Natafuranamine 53319040 Click to see 592.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aS,7S,7aR,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 9794468 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7aS)-7-(acetyloxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 101996850 Click to see CC(=O)OCC1=CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 416.40 unknown via CMAUP database
10-Deoxygeniposidic acid 443353 Click to see 358.34 unknown via CMAUP database
8-Epideoxyloganic acid 443332 Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 360.36 unknown via CMAUP database
Geniposidic Acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown via CMAUP database
Mussaenoside 182423 Click to see 390.40 unknown via CMAUP database
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 44586882 Click to see 426.70 unknown via CMAUP database
(6Z,10E,14Z,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 25244109 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
Cyclonataminol 53316925 Click to see CC(C1C(CC2(C1(CCC34C2C=CC5C3(C4)CC(C(C5(C)C)N(C)C)O)C)C)O)N(C)C 444.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Buxus alkaloids
(+)-Buxaminol C 10811757 Click to see 414.70 unknown via CMAUP database
31-Demethylbuxaminol 53320877 Click to see 414.70 unknown via CMAUP database
Buxamine A 5468622 Click to see CC(C1CCC2(C1(CC=C3C2CCC4C(=C3)CCC(C4(C)C)N(C)C)C)C)N(C)C 412.70 unknown via CMAUP database
Buxaminol A 53324855 Click to see 428.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,4aS,7aS)-7-methylidene-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 102508537 Click to see 358.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Guignardone A 50905842 Click to see 290.40 unknown via CMAUP database
Guignardone B 50905843 Click to see CC12CCC(C1CC3=C(O2)C4CC(C3=O)(CO4)O)C(C)(C)O 308.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(8E)-3,8-Dimethyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-10-yl] acetate 12314793 Click to see 306.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one 100605 Click to see 263.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
N-(4-aminobutyl)-3-(4-hydroxyphenyl)prop-2-enamide 133420 Click to see 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Chrysanthemin 44256715 Click to see 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Bonanzin 5379563 Click to see 374.30 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.