Achillea nobilis, also known as the noble yarrow, is a flowering plant found in Eurasia, with a wide distribution across Europe, Turkey, the Caucasus, and Central Asia. It has also been reported in western China, although this is based on a single specimen collected in the 19th century. This species is commonly cultivated and has become naturalized in North America and other parts of the world. It has creamy-white or yellow flowers and is similar to common yarrow, but with smaller flower heads and more of them. The leaves are finely dissected and form a low-growing clump in early spring, with flowering stems reaching up to 75 cm tall in late spring. The plant is covered in soft hairs and has a medium green color.

Synonyms Top

No known synonyms.

Common names Top

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Language	Common/alternative name
English	noble yarrow
Spanish	achillea punctata
Spanish	achillea pectinata
Spanish	achillea nobilis subsp nobilis
Spanish	achillea hispanica
Spanish	achillea grata
Spanish	achillea gerberi var. angustifolia
Spanish	achillea corymbifera
Spanish	chamaemelum gerberi
Spanish	achillea eridania
Spanish	achillea fruticulosa
Spanish	achillea odorata
Spanish	achillea camphorata
Spanish	achillea decipiens
Spanish	achillea nobilis subsp. nobilis
Spanish	chamaemelum achilleum
Arabic	قيصوم نبيل
Azerbaijani	nəcib boymadərən
Belarusian	Крываўнік дабрародны
Bulgarian	благороден равнец
Czech	řebříček sličný
German	edel-schafgarbe
German	edle schafgarbe
Estonian	lõhnav raudrohi
Persian	بومادران نجیبزاده
Finnish	jalokärsämö
French	achillee noble
French	achillée noble
Latvian	dižais pelašķis
Polish	krwawnik szlachetny
Russian	Тысячелистник благородный
Turkish	ayvadana
Ukrainian	Деревій благородний
Chinese	壮观蓍

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Achillea nobilis subsp. densissima	(O.Schwarz ex Bässler) Hub.-Mor.	Notes Roy. Bot. Gard. Edinburgh 33(3): 427 (1975)
Achillea nobilis subsp. kurdica	Hub.-Mor.	Notes Roy. Bot. Gard. Edinburgh 33(2): 209 (1974)
Achillea nobilis subsp. neilreichii	(A.Kern.) Velen.	263 1891

Varieties (abbr. var.) Top

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No variety added yet.

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Russian Far East
  - Khabarovsk
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Switzerland
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- North-central U.S.A.
  - Minnesota
- Northeastern U.S.A.
  - New York
- Northwestern U.S.A.
  - Montana

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000092435
USDA Plants	ACNO
Tropicos	2700016
INPN	79914
Flora of Italy	5651
KEW	urn:lsid:ipni.org:names:2332-2
The Plant List	gcc-48678
Open Tree Of Life	395150
Observations.org	135853
NCBI Taxonomy	282753
NBN Atlas	NBNSYS0000004455
Nature Serve	2.148514
IPNI	2332-2
iNaturalist	157927
GBIF	3120024
Freebase	/m/02qjfs1
EPPO	ACHNO
EOL	509736
Elurikkus	2510
USDA GRIN	103752
Wikipedia	Achillea_nobilis

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

Phytochemical analysis and allelopathic potential of essential oil of yarrow (Achillea spp.) ecotypes against redroot pigweed (Amaranthus retroflexus L.)

Niazipoor G, AghaAlikhani M, Mokhtassi-Bidgoli A, Iriti M, Vitalini S

Heliyon

14-Feb-2024

PMCID:	PMC10881850
doi:	10.1016/j.heliyon.2024.e26101
PMID:	38390126

Lanthanide-Doped ZnO Nanoparticles: Unraveling Their Role in Cytotoxicity, Antioxidant Capacity, and Nanotoxicology

Mejía-Méndez JL, Navarro-López DE, Sanchez-Martinez A, Ceballos-Sanchez O, Garcia-Amezquita LE, Tiwari N, Juarez-Moreno K, Sanchez-Ante G, López-Mena ER

Antioxidants (Basel)

08-Feb-2024

PMCID:	PMC10886043
doi:	10.3390/antiox13020213
PMID:	38397812

Phenolic Compounds of the Medicinal Plants in an Anthropogenically Transformed Environment

Vinogradova N, Vinogradova E, Chaplygin V, Mandzhieva S, Kumar P, Rajput VD, Minkina T, Seth CS, Burachevskaya M, Lysenko D, Singh RK

Molecules

29-Aug-2023

PMCID:	PMC10488847
doi:	10.3390/molecules28176322
PMID:	37687151

Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications

Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD

Molecules

18-Jun-2023

PMCID:	PMC10301071
doi:	10.3390/molecules28124838
PMID:	37375393

Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats

Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z

Plants (Basel)

31-May-2023

PMCID:	PMC10255522
doi:	10.3390/plants12112184
PMID:	37299162

Synthesis, biomedical applications, and toxicity of CuO nanoparticles

Naz S, Gul A, Zia M, Javed R

Appl Microbiol Biotechnol

13-Jan-2023

PMCID:	PMC9838533
doi:	10.1007/s00253-023-12364-z
PMID:	36635395

Syntheses Based on 3,4α-Epoxy-1,5,7α,6β(H)-guai-10(14),11(13)-dien-6,12-olide

Adekenov S

Molecules

13-Mar-2022

PMCID:	PMC8949978
doi:	10.3390/molecules27061862
PMID:	35335225

UHPLC-MS Characterization and Biological Insights of Different Solvent Extracts of Two Achillea Species (A. aleppica and A. santolinoides) from Turkey

Gevrenova R, Zengin G, Sinan KI, Yıldıztugay E, Zheleva-Dimitrova D, Picot-Allain C, Mahomoodally MF, Imran M, Dall’Acqua S

Antioxidants (Basel)

24-Jul-2021

PMCID:	PMC8388973
doi:	10.3390/antiox10081180
PMID:	34439428

A Systematic Review of Traditionally Used Herbs and Animal-Derived Products as Potential Analgesics

Rengasamy KR, Mahomoodally MF, Joaheer T, Zhang Y

Curr Neuropharmacol

01-Apr-2021

PMCID:	PMC8206464
doi:	10.2174/1570159X18666200808151522
PMID:	32781962

Achillea Species as Sources of Active Phytochemicals for Dermatological and Cosmetic Applications

Strzępek-Gomółka M, Gaweł-Bęben K, Kukula-Koch W

Oxid Med Cell Longev

25-Mar-2021

PMCID:	PMC8018854
doi:	10.1155/2021/6643827
PMID:	33833853

Maternal Reproductive Toxicity of Some Essential Oils and Their Constituents

Dosoky NS, Setzer WN

Int J Mol Sci

27-Feb-2021

PMCID:	PMC7956842
doi:	10.3390/ijms22052380
PMID:	33673548

Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece

Musarella CM, Brullo S, del Galdo GG

Plants (Basel)

30-Nov-2020

PMCID:	PMC7760968
doi:	10.3390/plants9121678
PMID:	33266088

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

Analysis of flavonoids in Achillea nobilis L. bv capillarv electrophoresis

Elke Marchart, Almut Hattenberger, Liselotte Krenn, Brigitte Kopp

MDPI AG

03-May-2019

doi:	10.3797/SCIPHARM.AUT-03-15

The Natural Sesquiterpene Lactones Arglabin, Grosheimin, Agracin, Parthenolide, and Estafiatin Inhibit T Cell Receptor (TCR) Activation

Schepetkin IA, Kirpotina LN, Mitchell PT, Kishkentaeva AS, Shaimerdenova ZR, Atazhanova GA, Adekenov SM, Quinn MT

Phytochemistry

22-Dec-2017

PMCID:	PMC5750123
doi:	10.1016/j.phytochem.2017.11.010
PMID:	29216473

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
[(1R,3S)-3-[(1R)-1-hydroperoxy-2-methylprop-2-enyl]-2,2-dimethylcyclopropyl]methyl acetate	163063607	Click to see CC(=C)C(C1C(C1(C)C)COC(=O)C)OO	228.28	unknown	https://doi.org/10.1055/S-2006-958010
[(1S,3S)-3-[(1R)-1-hydroperoxy-2-methylprop-2-enyl]-2,2-dimethylcyclopropyl]methyl acetate	163063608	Click to see CC(=C)C(C1C(C1(C)C)COC(=O)C)OO	228.28	unknown	https://doi.org/10.1055/S-2006-958010
[3-(1-Hydroperoxy-2-methylprop-2-enyl)-2,2-dimethylcyclopropyl]methyl acetate	163063606	Click to see CC(=C)C(C1C(C1(C)C)COC(=O)C)OO	228.28	unknown	https://doi.org/10.1055/S-2006-958010
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,5R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-6-ene-2,5-diol	162916044	Click to see CC1=CCC(CC1)C(C)(CCC(C(=C)C)O)O	238.37	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
(8-Acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate	163040517	Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C	338.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
(8,10-Dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate	92012847	Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)OC(=O)C)C	296.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
[(4S,6E,8S,10R)-8-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate	14707122	Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C	338.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
[(4S,6E,8S,10R)-8,10-dihydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate	14167377	Click to see CC(=CC(CC(=CC(CC(C)(C=C)O)O)C)OC(=O)C)C	296.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
2-Methyl-6-(4-methylcyclohex-3-en-1-yl)hept-3-ene-2,6-diol	71364069	Click to see CC1=CCC(CC1)C(C)(CC=CC(C)(C)O)O	238.37	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
achilleol B	24873746	Click to see CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC3C(=C)CCC(C3(C)C)O	426.70	unknown	https://doi.org/10.1016/S0040-4020(01)81472-1
Levomenol	442343	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
4,10-Dimethylidene-7-(propan-2-yl)cyclodec-5-en-1-ol	71370041	Click to see CC(C)C1CCC(=C)C(CCC(=C)C=C1)O	220.35	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,6E,9S,10E,11aS)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	162918394	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1007/BF00580067
(3aS,6Z,9S,10Z,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	101316778	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1016/0031-9422(88)80466-7 https://doi.org/10.1007/BF00580067
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl) acetate	71437691	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C	290.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
[(3aS,6E,9S,10E,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate	13895556	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)OC(=O)C	290.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
9-Hydroxy-6,10-dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one	5377194	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1007/BF00580067
9-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	281981	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1007/BF00580067
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,2R,5S,9S,10S,11S)-2-hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	10588629	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1055/S-2006-958010
(1R,2S,6S,9R,10R,11R,13R,14S)-9,14-dihydroxy-9,14-dimethyl-5-methylidene-3,12-dioxatetracyclo[8.4.0.02,6.011,13]tetradecan-4-one	163190277	Click to see CC1(CCC2C(C3C1C4C(C3(C)O)O4)OC(=O)C2=C)O	280.32	unknown	https://doi.org/10.1007/BF00580067
(1S,2S,10S,12R,14S)-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one	15559180	Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4	246.30	unknown	https://doi.org/10.1007/BF00580067
(1S,2S,6S,9R,10S,11R,13R,14S)-9,14-dihydroxy-9,14-dimethyl-5-methylidene-3,12-dioxatetracyclo[8.4.0.02,6.011,13]tetradecan-4-one	162898461	Click to see CC1(CCC2C(C3C1C4C(C3(C)O)O4)OC(=O)C2=C)O	280.32	unknown	https://doi.org/10.1007/BF00580067
(2-Hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-3-yl) 3-methylbutanoate	14682839	Click to see CC(C)CC(=O)OC1CC2C(C3C4(C=CC3(C1(C)O)OO4)C)OC(=O)C2=C	378.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
(3aS,6aR,8R,9R,9aS,9bS)-8,9-dihydroxy-9-methyl-3,6-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one	15690511	Click to see CC1(C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)O)O	264.32	unknown	https://doi.org/10.1007/BF00630399
[(1S,2R,3R,5S,9S,10R,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-3-yl] acetate	163188542	Click to see CC(=O)OC1CC2C(C3C4(C=CC3(C1(C)O)OO4)C)OC(=O)C2=C	336.30	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
2-Hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	14219460	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1055/S-2006-958010
5,8-Dihydroxy-5,8-dimethyl-1-methylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one	60198108	Click to see CC1(CCC2C1CC3C(CC2(C)O)OC(=O)C3=C)O	266.33	unknown	https://doi.org/10.1007/BF00630399
Anobin	538430	Click to see CC1(CCC2C(C3C1C4C(C3(C)O)O4)OC(=O)C2=C)O	280.32	unknown	https://doi.org/10.1007/BF00580067
Canin	442175	Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1007/BF02238225
Estafiatin	566474	Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4	246.30	unknown	https://doi.org/10.1007/BF00580067
Estafietin	11118339	Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4	246.30	unknown	https://doi.org/10.1007/BF00580067
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/0031-9422(88)80466-7
2,2-Dimethyl-4-methylidene-3-(3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl)cyclohexan-1-ol	78180739	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC1C(=C)CCC(C1(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1016/S0040-4039(00)99242-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3S,5S,8R,9S,10S,13S,14S,17R)-17-[(5S)-5,6-dimethylhept-1-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	163194932	Click to see CC(C)C(C)CCC(=C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C	442.70	unknown	https://doi.org/10.1007/S10600-010-9709-Z
[17-(5,6-dimethylhept-1-en-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	162972662	Click to see CC(C)C(C)CCC(=C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C	442.70	unknown	https://doi.org/10.1007/S10600-010-9709-Z
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
4-[(1R,2R)-3,3-dimethyl-2-(3-oxobutyl)cyclobutyl]pent-4-enyl acetate	14682851	Click to see CC(=O)CCC1C(CC1(C)C)C(=C)CCCOC(=O)C	280.40	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Phthalazines
Hydralazine	3637	Click to see C1=CC=C2C(=C1)C=NN=C2NN	160.18	unknown	https://doi.org/10.1016/0031-9422(88)80466-7
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3,6,9-trimethyl-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl acetate	627631	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C	304.34	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
Matricarin	3083923	Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C	304.34	unknown	https://doi.org/10.1016/0031-9422(90)80187-L
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-6,7,8-trimethoxyflavone	5379262	Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=CC=C3)O)OC)OC	344.30	unknown	https://doi.org/10.1007/BF00580067
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-[(2S,3R,4S,5S,6S)-3-[(2S,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	163105241	Click to see C1C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)(CO)O	580.50	unknown	https://doi.org/10.3797/SCIPHARM.AUT-03-15
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	https://doi.org/10.1515/ZNC-2003-1-202
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1515/ZNC-2003-1-202
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1515/ZNC-2003-1-202
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1515/ZNC-2003-1-202
> 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/10.1016/0305-1978(88)90033-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3,6,7,4'-tetramethoxyflavone	5318355	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC	358.30	unknown	https://doi.org/10.1055/S-2006-958010
chrysoplenol D	5280699	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC	360.30	unknown	https://doi.org/10.1016/0305-1978(88)90033-6
Cirsimaritin	188323	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC	314.29	unknown	https://doi.org/10.1016/0305-1978(88)90033-6
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/10.1016/0305-1978(88)90033-6

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Achillea nobilis

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