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Tanacetum balsamita

Tanacetum balsamita - 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 UUID643fc7484419a526395283
Scientific name Tanacetum balsamita
Authority L.
First published in Sp. Pl. : 845 (1753)

Description Top

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is a perennial temperate herb with a variety of names, including costmary, alecost, balsam herb, bible leaf, and mint geranium. It can grow up to 2 meters tall and has serrated oval leaves. During the summer, it produces small yellow flowers in clusters. The plant is believed to have originated in the Mediterranean and has been used for medicinal purposes since ancient times. It was commonly grown in herb gardens during the medieval period, but has since disappeared in Europe. However, it is still widely used in southwest Asia. The leaves of the plant contain essential oils, with carvone being the main component. It has been traditionally used to treat menstruation problems, stomach issues, and as an astringent. In the 17th century, herbalist Nicholas Culpeper recommended it for various ailments, including chronic headaches and digestive issues. It is also known for its ability to heal old ulcers when made into a salve.

Synonyms Top

Scientific name Authority First published in
Chrysanthemum grandiflorum (Desf.) Dum.Cours. Bot. Cult. 2: 467. 1802 [Jul 1802]
Chrysanthemum majus Asch. Fl. Brandenburg : 329
Pyrethrum tanaceum DC. Prodr. 6: 63 (1838)
Balsamita suaveolens Pers. Syn. Pl. 2(2): 408 (1807)
Matricaria apetala Hort.Erf. ex DC. Prodr. 6: 63 (1838)
Balsamita vulgaris Willd. Sp. Pl., ed. 4 , 3: 1802 (1803)
Balsamita major Desf. Actes Soc. Hist. Nat. Paris 1: 8 (1792)
Chrysanthemum balsamita var. tanacetoides Boiss.
Chrysanthemum balsamita Baill. Hist. Pl. 8: 311 (1882)
Matricaria balsamita Desr. Encycl. 3: 733 (1792)
Leucanthemum balsamita Over Fl. S. Dakota 108. 1932 as Balsomita
Tanacetum ovatifolium Stokes Bot. Mat. Med. iv. 180 (1812)
Balsamita balsamita Rydb. N. Amer. Fl. 34(3): 238 (1916)
Pyrethrum majus (Desf.) Tzvelev Fl. URSS xxvi. 198 (1961)
Tanacetum simplicifolium Salisb. Prodr. Stirp. Chap. Allerton : 190 (1796)
Pyrethrum balsamita Willd. Sp. Pl., ed. 4 , 3: 2153 (1803)
Chamaemelum balsamita E.H.L.Krause Deutschl. Fl. (Sturm), ed. 2. 13: 208 (1905)

Common names Top

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Language Common/alternative name
English mint geranium
English bible leaf
English balsam herb
English alecost
English costmary
English alecost or balsam herb
Spanish hoja romana
Spanish costo de los huertos
Spanish costo hortense
Spanish hierba buena romana
Spanish hierba de huerto
Spanish hierba santa romana
Spanish hoja de romana
Spanish hojicas de santa maria
Spanish chrysanthemum tanacetum
Spanish hojicas de santa maría
Spanish menta greca
Spanish menta sarracena
Spanish menta sarracenica
Spanish menta sarracénica
Spanish pyrethrum balsamita var. tanacetoides
Spanish pyrethrum balsamitoides
Spanish yerba buena romana
Spanish yerba romana
Spanish yerba santa romana
Spanish chrysanthemum grande
Spanish chrysanthemum balsamitoides
Spanish balsamita olorosa
Spanish balsamita major var. tanacetoides
Spanish balsamita major var tanacetoides
Spanish balsamita major subsp. balsamitoides
Spanish chrysanthemum tanacetifolium
Spanish balsamita balsamitoides
Afrikaans balsemwormkruid
Arabic غرديب
Arabic حشيشة الملكة
Arabic إهلال قسطا
Belarusian кануфер
Belarusian пінавея
Belarusian півоня
Belarusian калуфар
Belarusian піжма
Bulgarian калоферче
Czech maří list balšámový
Welsh tansi mair
German balsamkraut
German marienblatt
German frauenminze
Estonian palsam-neitsikummel
Persian شاهسپرغم
Finnish palsamipietaryrtti
Finnish palsamipäivänkakkara
French menthe-coq
French grande balsamite
Irish gormshúileach
Croatian balzamski vratić
Armenian սուսամբար
Italian menta greca
Italian fritola
Italian balsamita
Italian balsamita odorosa
Italian erba amara
Georgian სუსამბარი
Cornish kosta maria
Lithuanian balzaminė bitkrėslė
Lithuanian balzamita
Lithuanian vaistinė balzamita
Macedonian балзамска вратика
Macedonian калофер
Dutch balsemwormkruid
Dutch vrouwenmunt
Russian Пижма бальзамическая
Russian Калуфер
Russian Канупер
Russian Кануфер
Russian Колуфер
Russian Мята сарацинская
Russian Пижма пахучая
Russian Ромашка шпанская
Slovak vratič balzamový
Swedish balsamblad
Chinese 流香艾菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Belgium
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Kansas
      • Missouri
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • Southeastern U.S.A.
      • Delaware
      • Maryland
    • Southwestern U.S.A.
      • California
      • Nevada
      • Utah
    • Western Canada
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000013170
UNII UL54A923JV
Canadensys 3599
USDA Plants TABA
Tropicos 2711176
INPN 125457
Flora of Italy 5701
KEW urn:lsid:ipni.org:names:249302-2
The Plant List gcc-112746
PFAF Tanacetum balsamita
Open Tree Of Life 616342
Observations.org 311229
NCBI Taxonomy 301877
NBN Atlas NBNSYS0000034008
IPNI 249302-2
iNaturalist 181875
GBIF 3118254
Freebase /m/0cb1hv
WisFlora 13446
EPPO CHYBA
EOL 405000
Elurikkus 214959
Calflora (Californian flora) 10411
USDA GRIN 317329
Wikipedia Tanacetum_balsamita

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
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Research status of indole-modified natural products Duan SF, Song L, Guo HY, Deng H, Huang X, Shen QK, Quan ZS, Yin XM RSC Med Chem 17-Oct-2023
PMCID:PMC10718587
doi:10.1039/d3md00560g
PMID:38107170
Brahma-related gene 1 acts as a profibrotic mediator and targeting it by micheliolide ameliorates peritoneal fibrosis Li S, Luo C, Chen S, Zhuang Y, Ji Y, Zeng Y, Zeng Y, He X, Xiao J, Wang H, Chen X, Long H, Peng F J Transl Med 19-Sep-2023
PMCID:PMC10510267
doi:10.1186/s12967-023-04469-w
PMID:37726857
Anthelmintic Activity of Tanacetum vulgare L. (Leaf and Flower) Extracts against Trichostrongylidae Nematodes in Sheep In Vitro Kļaviņa A, Keidāne D, Ganola K, Lūsis I, Šukele R, Bandere D, Kovalcuka L Animals (Basel) 02-Jul-2023
PMCID:PMC10339931
doi:10.3390/ani13132176
PMID:37443974
Posters N/A FEBS Open Bio 28-Jun-2023
PMCID:PMC10300527
doi:10.1002/2211-5463.13646
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
The Leaf Essential Oil of Myrtus communis subsp. tarentina (L.) Nyman: From Phytochemical Characterization to Cytotoxic and Antimigratory Activity in Human Prostate Cancer Cells Giuliani C, Moretti RM, Bottoni M, Santagostini L, Fico G, Montagnani Marelli M Plants (Basel) 13-Mar-2023
PMCID:PMC10056649
doi:10.3390/plants12061293
PMID:36986980
Interaction between gut microbiota and sex hormones and their relation to sexual dimorphism in metabolic diseases Santos-Marcos JA, Mora-Ortiz M, Tena-Sempere M, Lopez-Miranda J, Camargo A Biol Sex Differ 07-Feb-2023
PMCID:PMC9903633
doi:10.1186/s13293-023-00490-2
PMID:36750874
Volatile Oils Discrepancy between Male and Female Ochradenus arabicus and Their Allelopathic Activity on Dactyloctenium aegyptium Abd-ElGawad AM, Assaeed AM, El Gendy AE, Dar BA, Elshamy AI Plants (Basel) 26-Dec-2022
PMCID:PMC9824887
doi:10.3390/plants12010110
PMID:36616238
Antiviral Activity of Selected Essential Oils against Cucumber Mosaic Virus Paduch-Cichal E, Mirzwa-Mróz E, Wojciechowska P, Bączek K, Kosakowska O, Węglarz Z, Szyndel MS Plants (Basel) 20-Dec-2022
PMCID:PMC9823813
doi:10.3390/plants12010018
PMID:36616147
An In-Depth Study of Metabolite Profile and Biological Potential of Tanacetum balsamita L. (Costmary) Gevrenova R, Zengin G, Sinan KI, Zheleva-Dimitrova D, Balabanova V, Kolmayer M, Voynikov Y, Joubert O Plants (Basel) 20-Dec-2022
PMCID:PMC9824382
doi:10.3390/plants12010022
PMID:36616151
Chemical Composition and Biological Activity of Tanacetum balsamita Essential Oils Obtained from Different Plant Organs Vukic MD, Vukovic NL, Obradovic AD, Galovičová L, Čmiková N, Kačániová M, Matic MM Plants (Basel) 12-Dec-2022
PMCID:PMC9783112
doi:10.3390/plants11243474
PMID:36559586
Traditional Ethnobotanical Knowledge of the Central Lika Region (Continental Croatia)—First Record of Edible Use of Fungus Taphrina pruni Vitasović-Kosić I, Hodak A, Łuczaj Ł, Marić M, Juračak J Plants (Basel) 16-Nov-2022
PMCID:PMC9693171
doi:10.3390/plants11223133
PMID:36432861
Biological Activity of Picrorhiza kurroa: A Source of Potential Antimicrobial Compounds against Yersinia enterocolitica Thapa A, Kaushik R, Arora S, Jaglan S, Jaswal V, Yadav VK, Singh M, Bains A, Chawla P, Khan A, Fogarasi M, Fogarasi S Int J Mol Sci 15-Nov-2022
PMCID:PMC9694339
doi:10.3390/ijms232214090
PMID:36430568
Natural Active Ingredients for Poly (Lactic Acid)-Based Materials: State of the Art and Perspectives Lombardi A, Fochetti A, Vignolini P, Campo M, Durazzo A, Lucarini M, Puglia D, Luzi F, Papalini M, Renzi M, Cavallo A, Bernini R Antioxidants (Basel) 20-Oct-2022
PMCID:PMC9598241
doi:10.3390/antiox11102074
PMID:36290797

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
> Alkaloids and derivatives / Lupin alkaloids / Aloperine and related alkaloids / Ormosia-type alkaloids
(-)-Ormosanine 442959 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/J.FOODCHEM.2010.03.064
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Decene-4,6,8-triynoic acid, methyl ester, (Z)- 5281309 Click to see CC#CC#CC#CC=CC(=O)OC 172.18 unknown https://doi.org/10.1002/CBER.19751080503
Methyl 2-decene-4,6,8-triynoate 75958 Click to see CC#CC#CC#CC=CC(=O)OC 172.18 unknown https://doi.org/10.1002/CBER.19751080503
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.2002.9699741
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.2002.9699741
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
1H-Naphtho[1,8a-c]furan-3(5H)-one, 7-[2-(acetyloxy)-2-(3-furanyl)ethyl]-6,6a,7,8,9,10-hexahydro-7,8-dimethyl- 368920 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C 372.50 unknown https://doi.org/10.1246/CL.1996.441
Tanabalin 10667003 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C 372.50 unknown https://doi.org/10.1246/CL.1996.441
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3S,3aS,5aR,6S,9bS)-6-hydroxy-3,5a,9-trimethyl-3a,4,5,6,7,9b-hexahydro-3H-benzo[g][1]benzofuran-2,8-dione 13944244 Click to see CC1C2CCC3(C(CC(=O)C(=C3C2OC1=O)C)O)C 264.32 unknown https://doi.org/10.1135/CCCC19791468
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,3S,4R,6S,9E,11R)-3-hydroxy-4,9-dimethyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one 162971583 Click to see CC1=CC2C(CC(C3(C(O3)CC1)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
(3aS,5S,6R,7R,10E,11aR)-5,7-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,6,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 163012677 Click to see CC1C(CCC(=CC2C(CC1O)C(=C)C(=O)O2)C)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)80269-1
https://doi.org/10.1016/0031-9422(89)80194-3
(4,9-Dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl) 2-methylbutanoate 162889014 Click to see CCC(C)C(=O)OC1CC2C(C=C(CCC3C1(O3)C)C)OC(=O)C2=C 348.40 unknown https://doi.org/10.1016/S0031-9422(00)80269-1
https://doi.org/10.1016/0031-9422(89)80194-3
(4,9-Dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl) 2-methylpropanoate 163017566 Click to see CC1=CC2C(CC(C3(C(O3)CC1)C)OC(=O)C(C)C)C(=C)C(=O)O2 334.40 unknown https://doi.org/10.1016/S0031-9422(00)80269-1
https://doi.org/10.1016/0031-9422(89)80194-3
(4,9-Dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl) propanoate 162888300 Click to see CCC(=O)OC1CC2C(C=C(CCC3C1(O3)C)C)OC(=O)C2=C 320.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl) 2-methylpropanoate 162990183 Click to see CC1=CC2C(CC(C(=CCC1)C)OC(=O)C(C)C)C(=C)C(=O)O2 318.40 unknown https://doi.org/10.1016/S0031-9422(00)80269-1
https://doi.org/10.1016/0031-9422(89)80194-3
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl) propanoate 163075530 Click to see CCC(=O)OC1CC2C(C=C(CCC=C1C)C)OC(=O)C2=C 304.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
[(1S,3S,4S,6S,9E,11R)-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl] (2R)-2-methylbutanoate 162889015 Click to see CCC(C)C(=O)OC1CC2C(C=C(CCC3C1(O3)C)C)OC(=O)C2=C 348.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
[(1S,3S,4S,6S,9E,11R)-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl] 2-methylpropanoate 163017567 Click to see CC1=CC2C(CC(C3(C(O3)CC1)C)OC(=O)C(C)C)C(=C)C(=O)O2 334.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
[(1S,3S,4S,6S,9E,11R)-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-3-yl] propanoate 162888301 Click to see CCC(=O)OC1CC2C(C=C(CCC3C1(O3)C)C)OC(=O)C2=C 320.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
[(3aS,5S,6E,10E,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-methylpropanoate 14286998 Click to see CC1=CC2C(CC(C(=CCC1)C)OC(=O)C(C)C)C(=C)C(=O)O2 318.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
[(3aS,5S,6E,10E,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] propanoate 14286996 Click to see CCC(=O)OC1CC2C(C=C(CCC=C1C)C)OC(=O)C2=C 304.40 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
3-Hydroxy-4,9-dimethyl-14-methylidene-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-13-one 162971581 Click to see CC1=CC2C(CC(C3(C(O3)CC1)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1016/S0031-9422(00)80269-1
https://doi.org/10.1016/0031-9422(89)80194-3
5,7-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,6,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 163012676 Click to see CC1C(CCC(=CC2C(CC1O)C(=C)C(=O)O2)C)O 266.33 unknown https://doi.org/10.1016/0031-9422(89)80194-3
https://doi.org/10.1016/S0031-9422(00)80269-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic 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/10.1016/J.FOODCHEM.2010.03.064
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/10.1016/J.FOODCHEM.2010.03.064
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/10.1016/J.FOODCHEM.2010.03.064
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(2R,3S,4S)-2,3,4-trimethyl-3-(3-methylidenepent-4-enyl)cyclohexan-1-one 101277331 Click to see CC1CCC(=O)C(C1(C)CCC(=C)C=C)C 220.35 unknown https://doi.org/10.1002/CBER.19751080503
2,3,4-Trimethyl-3-(3-methylidenepent-4-enyl)cyclohexan-1-one 14313695 Click to see CC1CCC(=O)C(C1(C)CCC(=C)C=C)C 220.35 unknown https://doi.org/10.1002/CBER.19751080503
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(E)-tetradec-6-en-8,10,12-triyn-3-one 6244989 Click to see CCC(=O)CCC=CC#CC#CC#CC 198.26 unknown https://doi.org/10.1002/CBER.19751080503
Tetradec-6-en-8,10,12-triyn-3-one 100451 Click to see CCC(=O)CCC=CC#CC#CC#CC 198.26 unknown https://doi.org/10.1002/CBER.19751080503
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1515/ZNC-1997-3-401
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown https://doi.org/10.1016/J.FOODCHEM.2010.03.064
5,7,4'-Trihydroxy-8,3'-dimethoxyflavone 14825849 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O 330.29 unknown https://doi.org/10.1016/J.FOODCHEM.2010.03.064

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