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Achillea ligustica

Achillea ligustica - 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 UUID643fc9b072865322939125
Scientific name Achillea ligustica
Authority All.
First published in Auct. Syn. Meth. Stirp. Hort. Regii Taur. : 17 (1773)

Description Top

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Synonyms Top

Scientific name Authority First published in
Achillea ligustica var. foliosa Ball
Achillea pinnatisecta Porta Nuovo Giorn. Bot. Ital. 11: 285 (1879)
Achillea sylvatica Ten. Fl. Napol. 4: 126 (1830)
Achillea magna Sm. Fl. Graec. Prodr. 2(1): 194 (1813)
Achillea nobilis subsp. ligustica (All.) Bonnier Bonnier. 1922. 106 1922
Achillea sicula Raf. Précis Decouv. Somiol. 40. Jun-Dec 1814; et in Journ. Bot. ii. (1814) 271.

Common names Top

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Language Common/alternative name
English ligurian yarrow
English southern yarrow
co erba santa
Welsh milddail casnewydd
Chinese 利古里亚蓍草

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Germany
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Sardegna
      • Spain
  • Northern America
    • Northeastern U.S.A.
      • Massachusetts
      • Michigan
      • New York
      • Vermont

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000032595
USDA Plants ACLI2
Tropicos 2701620
INPN 79903
Flora of Italy 5655
KEW urn:lsid:ipni.org:names:174075-1
The Plant List gcc-131521
Open Tree Of Life 921025
Observations.org 131993
NCBI Taxonomy 282745
NBN Atlas NBNSYS0000014099
Nature Serve 2.135113
IPNI 174075-1
iNaturalist 157925
GBIF 3120032
EPPO ACHLI
EOL 597492
Wikipedia Achillea_ligustica

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
The Orophilous Shrubby Vegetation of the Juniperetalia hemisphaericae Order in Sicily: A Refuge Habitat for Many Endemic Vascular Species Sciandrello S, Giusso del Galdo G Plants (Basel) 31-Jan-2024
PMCID:PMC10857485
doi:10.3390/plants13030423
PMID:38337957
Isolation of Secondary Metabolites from Achillea grandifolia Friv. (Asteraceae) and Main Compounds’ Effects on a Glioblastoma Cellular Model Tsiftsoglou OS, Krigas N, Gounaris C, Papitsa C, Nanouli M, Vartholomatos E, Markopoulos GS, Isyhou R, Alexiou G, Lazari D Pharmaceutics 30-Apr-2023
PMCID:PMC10224520
doi:10.3390/pharmaceutics15051383
PMID:37242625
Repellent activity against Anopheles gambiae of the leaves of nesting trees in the Sebitoli chimpanzee community of Kibale National Park, Uganda Lacroux C, Pouydebat E, Rossignol M, Durand S, Aleeje A, Asalu E, Chandre F, Krief S Malar J 27-Sep-2022
PMCID:PMC9513939
doi:10.1186/s12936-022-04291-7
PMID:36163024
Eugenol: A novel therapeutic agent for the inhibition of Candida species infection Didehdar M, Chegini Z, Shariati A Front Pharmacol 09-Aug-2022
PMCID:PMC9395595
doi:10.3389/fphar.2022.872127
PMID:36016558
Plants with Antimicrobial Activity Growing in Italy: A Pathogen-Driven Systematic Review for Green Veterinary Pharmacology Applications Piras C, Tilocca B, Castagna F, Roncada P, Britti D, Palma E Antibiotics (Basel) 08-Jul-2022
PMCID:PMC9311764
doi:10.3390/antibiotics11070919
PMID:35884173
Essential Oil Biodiversity of Achillea ligustica All. Obtained from Mainland and Island Populations Bader A, AlQathama A, Cioni PL, Ceccarini L, Abdelhady MI, Al-Shareef W, Ascrizzi R, Flamini G Plants (Basel) 13-Apr-2022
PMCID:PMC9027389
doi:10.3390/plants11081054
PMID:35448782
Traditional and Phytochemical Bases of Herbs, Shrubs, Climbers, and Trees from Ethiopia for Their Anticancer Response Abate L, Tadesse MG, Bachheti A, Bachheti RK Biomed Res Int 03-Feb-2022
PMCID:PMC8831057
doi:10.1155/2022/1589877
PMID:35155671
Interstitial Arabidopsis-Type Telomeric Repeats in Asteraceae Maravilla AJ, Rosato M, Álvarez I, Nieto Feliner G, Rosselló JA Plants (Basel) 17-Dec-2021
PMCID:PMC8705333
doi:10.3390/plants10122794
PMID:34961265
The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants Lawson SK, Satyal P, Setzer WN Plants (Basel) 25-May-2021
PMCID:PMC8229852
doi:10.3390/plants10061061
PMID:34070663
A Comparison Study on Traditional Mixtures of Herbal Teas Used in Eastern Mediterranean Area Obón C, Rivera D, Fonollá E, Alcaraz F, Attieh L Front Pharmacol 23-Apr-2021
PMCID:PMC8103161
doi:10.3389/fphar.2021.632692
PMID:33967769
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
Treating Hyperglycemia From Eryngium caeruleum M. Bieb: In-vitro α-Glucosidase, Antioxidant, in-vivo Antidiabetic and Molecular Docking-Based Approaches Sadiq A, Rashid U, Ahmad S, Zahoor M, AlAjmi MF, Ullah R, Noman OM, Ullah F, Ayaz M, Khan I, Islam ZU, Ali W Front Chem 26-Nov-2020
PMCID:PMC7737655
doi:10.3389/fchem.2020.558641
PMID:33335883
Antibacterial activity of essential oils from Ethiopian thyme (Thymus serrulatus and Thymus schimperi) against tooth decay bacteria Damtie D, Mekonnen Y PLoS One 09-Oct-2020
PMCID:PMC7546913
doi:10.1371/journal.pone.0239775
PMID:33036019
In Vitro and In Vivo Effectiveness of Carvacrol, Thymol and Linalool against Leishmania infantum Youssefi MR, Moghaddas E, Tabari MA, Moghadamnia AA, Hosseini SM, Farash BR, Ebrahimi MA, Mousavi NN, Fata A, Maggi F, Petrelli R, Dall’Acqua S, Benelli G, Sut S Molecules 30-May-2019
PMCID:PMC6600403
doi:10.3390/molecules24112072
PMID:31151304
The Genus Solanum: An Ethnopharmacological, Phytochemical and Biological Properties Review Kaunda JS, Zhang YJ Nat Prod Bioprospect 12-Mar-2019
PMCID:PMC6426945
doi:10.1007/s13659-019-0201-6
PMID:30868423

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Decene-4,6-diynoic acid, methyl ester, (Z)- 643924 Click to see CCCC#CC#CC=CC(=O)OC 176.21 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R,6S)-2,6-dimethylocta-1,7-diene-3,6-diol 154495976 Click to see CC(=C)C(CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
2,6-Dimethylocta-1,7-diene-3,6-diol 548927 Click to see CC(=C)C(CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Ethyl 3,7-dimethyl-3,6-octadienoate 12485235 Click to see CCOC(=O)CC(=CCC=C(C)C)C 196.29 unknown https://doi.org/10.1016/J.BSE.2007.11.006
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3R,3aS,8aS)-8a-methyl-8-oxo-3-propan-2-yl-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde 14446658 Click to see CC(C)C1CCC2(C1C=C(CCC2=O)C=O)C 234.33 unknown https://doi.org/10.1016/J.BSE.2007.11.006
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,2S,3R,5S,6R,8S)-6-hydroxy-8-methyl-3-[(2R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-2-yl]methyl 4-hydroxybenzoate 137704782 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O 496.50 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,5aR,6R,9S,9aS,9bS)-6-hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,9,9a,9b-octahydrobenzo[g][1]benzofuran-2,8-dione 12097072 Click to see CC1C2C3C(CCC2(C(CC1=O)O)C)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
(3aS,5aR,6R,9S,9bS)-6-hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,9,9a,9b-octahydrobenzo[g][1]benzofuran-2,8-dione 101245659 Click to see CC1C2C3C(CCC2(C(CC1=O)O)C)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1002/CHIN.200336154
6-Hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,9,9a,9b-octahydrobenzo[g][1]benzofuran-2,8-dione 14779597 Click to see CC1C2C3C(CCC2(C(CC1=O)O)C)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(12-Chloro-2,11-dihydroxy-2,6,11-trimethyl-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-4-yl) acetate 74318735 Click to see CC1C2C(CC(C34C(C2OC1=O)C(C(C3O4)Cl)(C)O)(C)O)OC(=O)C 374.80 unknown https://doi.org/10.1002/CHIN.200816191
(1S,2R,5S,9S,10S,11S,12S,13S)-12-chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one 132513624 Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)O)Cl)OC(=O)C2=C)O 314.76 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
(alphaS,1aalpha,3abeta,8aR)-2beta-Chloro-alpha,3alpha,8alpha-trimethyl-3,4beta,8-trihydroxy-6beta-acetoxyoctahydro-3H-azuleno[1,8a-b]oxirene-5alpha-acetic acid 5,4-lactone 24800039 Click to see CC1C2C(CC(C34C(C2OC1=O)C(C(C3O4)Cl)(C)O)(C)O)OC(=O)C 374.80 unknown https://doi.org/10.1002/CHIN.200816191
[(1R,2R,3R,5S,9S,10S,11S)-3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-2-yl] acetate 162901791 Click to see CC(=O)OC1(C(CC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O)C 336.30 unknown https://doi.org/10.1016/0031-9422(88)80466-7
[(1R,2R,4S,5S,6S,9S,10S,11S,12R,13R)-12-chloro-2,11-dihydroxy-2,6,11-trimethyl-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-4-yl] acetate 162855724 Click to see CC1C2C(CC(C34C(C2OC1=O)C(C(C3O4)Cl)(C)O)(C)O)OC(=O)C 374.80 unknown https://doi.org/10.1515/ZNB-2008-0116
[(1R,2S,8R,9R,10R,11S,12R,14R)-11-chloro-9,10-dihydroxy-9,14-dimethyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-8-yl] acetate 162817336 Click to see CC(=O)OC1CC2C(C3C4(C(O4)C(C3(C1(C)O)O)Cl)C)OC(=O)C2=C 372.80 unknown https://doi.org/10.1016/J.BSE.2007.11.006
[(1S,2R,3R,5S,9S,10S,11R)-3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-2-yl] acetate 162901792 Click to see CC(=O)OC1(C(CC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O)C 336.30 unknown https://doi.org/10.1016/0031-9422(88)80466-7
12-Chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one 75058626 Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)O)Cl)OC(=O)C2=C)O 314.76 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
Artecanin 442147 Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O 278.30 unknown https://doi.org/10.1016/0031-9422(88)80466-7
Canin 442175 Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O 278.30 unknown https://doi.org/10.1016/0031-9422(88)80466-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12303667 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.BSE.2007.11.006
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
7-(5-Ethyl-6-methylhept-3-en-2-yl)-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-ol 163054339 Click to see CCC(C=CC(C)C1CCCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1016/0031-9422(88)80466-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3E,6S)-2,6-dimethylocta-3,7-diene-2,6-diol 15241420 Click to see CC(C)(C=CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/0031-9422(88)80466-7
https://doi.org/10.1016/S0040-4020(03)00572-6
2,6-Dimethylocta-3,7-diene-2,6-diol 527050 Click to see CC(C)(C=CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
https://doi.org/10.1016/0031-9422(88)80466-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
4-((1R,4S)-4-(5-hydroxypent-1-en-2-yl)-2,2-dimethylcyclobutyl)butan-2-one 12097073 Click to see CC(=O)CCC1C(CC1(C)C)C(=C)CCCO 238.37 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R,6S,7aS,8R,8aR)-8-acetyl-5,7a-dihydroxy-6-methoxy-3,5-dimethyl-6,7,8,8a-tetrahydrocyclopenta[f][1]benzofuran-2-one 12097067 Click to see CC1=C2C=C3C(C(CC3(C(C2OC1=O)C(=O)C)O)OC)(C)O 308.33 unknown https://doi.org/10.1002/CHIN.200336154
https://doi.org/10.1016/S0040-4020(03)00572-6
8-Acetyl-5,7a-dihydroxy-6-methoxy-3,5-dimethyl-6,7,8,8a-tetrahydrocyclopenta[f][1]benzofuran-2-one 162897682 Click to see CC1=C2C=C3C(C(CC3(C(C2OC1=O)C(=O)C)O)OC)(C)O 308.33 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
Ligustolide A 12097235 Click to see CC1=C2C=C3C(C(CC3(C(C2OC1=O)C(=O)C)O)OC)(C)O 308.33 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
https://doi.org/10.1002/CHIN.200336154
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4R,5S)-4-[(1R)-1-hydroxy-3-oxobutyl]-5-[(3S)-3-methoxy-2-methyl-5-oxocyclopenten-1-yl]-3-methylideneoxolan-2-one 162890520 Click to see CC1=C(C(=O)CC1OC)C2C(C(=C)C(=O)O2)C(CC(=O)C)O 308.33 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
(4S,5S)-5-[(3S,4R)-4-chloro-3-hydroxy-2-methyl-5-oxocyclopenten-1-yl]-3-methylidene-4-(3-oxobutyl)oxolan-2-one 12097070 Click to see CC1=C(C(=O)C(C1O)Cl)C2C(C(=C)C(=O)O2)CCC(=O)C 312.74 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
3-Deoxy-11,13-dihydroisosecotanapartholide 12097068 Click to see CC1C(C(OC1=O)C2=C(CCC2=O)C)CCC(=O)C 264.32 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
3-Methyl-5-(2-methyl-5-oxocyclopenten-1-yl)-4-(3-oxobutyl)oxolan-2-one 162399469 Click to see CC1C(C(OC1=O)C2=C(CCC2=O)C)CCC(=O)C 264.32 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
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/10.1002/CHIN.200336154
https://doi.org/10.1016/0031-9422(88)80466-7
https://doi.org/10.1016/S0040-4020(03)00572-6
https://doi.org/10.1002/CHIN.200816191
4-(1-Hydroxy-3-oxobutyl)-5-(3-methoxy-2-methyl-5-oxocyclopenten-1-yl)-3-methylideneoxolan-2-one 12097069 Click to see CC1=C(C(=O)CC1OC)C2C(C(=C)C(=O)O2)C(CC(=O)C)O 308.33 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
4-Hydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 99114 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O 262.30 unknown https://doi.org/10.1002/CHIN.200816191
https://doi.org/10.1016/S0040-4020(03)00572-6
5-(4-Chloro-3-hydroxy-2-methyl-5-oxocyclopenten-1-yl)-3-methylidene-4-(3-oxobutyl)oxolan-2-one 162941040 Click to see CC1=C(C(=O)C(C1O)Cl)C2C(C(=C)C(=O)O2)CCC(=O)C 312.74 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
Austricin 6713966 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O 262.30 unknown https://doi.org/10.1016/S0040-4020(03)00572-6
https://doi.org/10.1002/CHIN.200336154
https://doi.org/10.1002/CHIN.200816191
Filifolide A 90472998 Click to see CC1=CC(C2CC1OC2=O)(C)C 166.22 unknown https://doi.org/10.1016/J.BSE.2007.11.006
Matricarin 3083923 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 304.34 unknown https://doi.org/10.1002/CHIN.200816191
https://doi.org/10.1002/CHIN.200336154
https://doi.org/10.1016/S0040-4020(03)00572-6
https://doi.org/10.1016/0031-9422(88)80466-7
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
1-Piperidin-1-yltetradeca-2,4,6,10-tetraen-8-yn-1-one 162891167 Click to see CCCC=CC#CC=CC=CC=CC(=O)N1CCCCC1 283.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown https://doi.org/10.1016/0031-9422(88)80466-7
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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/10.1016/0031-9422(88)80466-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/0031-9422(88)80466-7

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