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Achillea fragrantissima

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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 UUID643fd02145064414690089
Scientific name Achillea fragrantissima
Authority Sch.Bip.
First published in Flora 38: 13 (1855)

Description Top

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Synonyms Top

Scientific name Authority First published in
Santolina simplicifolia L'Hér. ex DC. Prodr. 6: 37 (1838)
Santolina fragrantissima Forssk. Fl. Aegypt.-Arab. : 147 (1775)

Common names Top

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Language Common/alternative name
Arabic بعيثران
Arabic حزمبل
Arabic قيصوم جبلي (نبات)

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
  • Asia-temperate
    • Arabian Peninsula
      • Kuwait
      • Saudi Arabia
    • Western Asia
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000096460
Tropicos 50146780
KEW urn:lsid:ipni.org:names:173984-1
The Plant List gcc-52604
Open Tree Of Life 245230
NCBI Taxonomy 282738
IPNI 173984-1
iNaturalist 628054
GBIF 3120394
EPPO ACHFR
USDA GRIN 469093

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
Prevention and treatment of anthracycline-induced cardiotoxicity: A bibliometric analysis of the years 2000–2023 Kong Y, Wei X, Zhang D, Lin H, Peng M, Shang H Heliyon 21-Apr-2024
PMCID:PMC11064157
doi:10.1016/j.heliyon.2024.e29926
PMID:38698971
Endophytic Alternaria and Fusarium species associated to potato plants (Solanum tuberosum L.) in Iran and their capability to produce regulated and emerging mycotoxins Alijani Mamaghani N, Masiello M, Somma S, Moretti A, Saremi H, Haidukowski M, Altomare C Heliyon 15-Feb-2024
PMCID:PMC10907534
doi:10.1016/j.heliyon.2024.e26385
PMID:38434378
Chemotaxonomy, antibacterial and antioxidant activities of selected aromatic plants from Tabuk region-KSA Elbalola AA, Abbas ZK Heliyon 16-Dec-2023
PMCID:PMC10772130
doi:10.1016/j.heliyon.2023.e23641
PMID:38192876
Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE Biomolecules 21-Nov-2023
PMCID:PMC10742071
doi:10.3390/biom13121683
PMID:38136556
The Potential Gastro-Protective Effect of Qaysum (Achillea fragrantissima) Against Ethanol-Induced Gastric Ulcer in Wistar Albino Rats Alhejaily TB, Alamri ZZ, ALaryani FS, Shareef SH Cureus 26-Oct-2023
PMCID:PMC10676238
doi:10.7759/cureus.47696
PMID:38021520
Evaluation of the Insecticidal Potential of Heterotheca inuloides Acetonic and Methanolic Extracts against Spodoptera frugiperda and Their Ecotoxicological Effect on Poecilia reticulata Hernández-Caracheo K, Guerrero-López L, Rodríguez-Sánchez B, Rodríguez-Núñez E, Rodríguez-Chávez JL, Delgado-Lamas G, Campos-Guillén J, Amaro-Reyes A, Monroy-Dosta MD, Zavala-Gómez CE, Chaparro-Sánchez R, Rodríguez-Morales JA, Pérez-Moreno V, Ramos-López MA Plants (Basel) 13-Oct-2023
PMCID:PMC10610112
doi:10.3390/plants12203555
PMID:37896019
Chemical Characterization and Chemotaxonomic Significance of Essential Oil Constituents of Matricaria aurea Grown in Two Different Agro-Climatic Conditions Khan M, Khan M, Alshareef E, Alaqeel SI, Alkhathlan HZ Plants (Basel) 12-Oct-2023
PMCID:PMC10610148
doi:10.3390/plants12203553
PMID:37896017
Nutritional values of wild edible freshwater macrophytes Zakaria MH, Ramaiya SD, Bidin N, Syed NN, Bujang JS PeerJ 11-Jul-2023
PMCID:PMC10348304
doi:10.7717/peerj.15496
PMID:37456903
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Predicting phytochemical diversity of medicinal and aromatic plants (MAPs) across eco-climatic zones and elevation in Uttarakhand using Generalized Additive Model Tiwari D, Kewlani P, Gaira KS, Bhatt ID, Sundriyal RC, Pande V Sci Rep 05-Jul-2023
PMCID:PMC10322824
doi:10.1038/s41598-023-37495-1
PMID:37407604
Eco-Efficient Systems Based on Nanocarriers for the Controlled Release of Fertilizers and Pesticides: Toward Smart Agriculture Fincheira P, Hoffmann N, Tortella G, Ruiz A, Cornejo P, Diez MC, Seabra AB, Benavides-Mendoza A, Rubilar O Nanomaterials (Basel) 29-Jun-2023
PMCID:PMC10343595
doi:10.3390/nano13131978
PMID:37446494
Medicinal plants of Jordan: Scoping review Abu-Odeh A, Fino L, Al-Absi G, Alnatour D, Al-Darraji M, Shehadeh M, Suaifan G Heliyon 07-Jun-2023
PMCID:PMC10276232
doi:10.1016/j.heliyon.2023.e17081
PMID:37332946
Effect of Achillea fragrantissima Extract on Excision Wound Biofilms of MRSA and Pseudomonas aeruginosa in Diabetic Mice Almuhanna Y, Alqasmi MH, AlSudais H, Alrouji M, Kuriri FA, Alissa M, Alsuwat MA, Asad M, Joseph B Int J Mol Sci 05-Jun-2023
PMCID:PMC10253793
doi:10.3390/ijms24119774
PMID:37298725
Alzheimer’s disease and neuroinflammation: will new drugs in clinical trials pave the way to a multi-target therapy? Melchiorri D, Merlo S, Micallef B, Borg JJ, Dráfi F Front Pharmacol 02-Jun-2023
PMCID:PMC10272781
doi:10.3389/fphar.2023.1196413
PMID:37332353
Translational Research on Bee Pollen as a Source of Nutrients: A Scoping Review from Bench to Real World Kacemi R, Campos MG Nutrients 22-May-2023
PMCID:PMC10221365
doi:10.3390/nu15102413
PMID:37242296

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-3-Nonanol 6999725 Click to see CCCCCCC(CC)O 144.25 unknown https://doi.org/10.1002/JPS.2600531215
3-Hexen-1-ol 10993 Click to see CCC=CCCO 100.16 unknown https://doi.org/10.1002/JPS.2600531215
3-Nonanol 12216 Click to see CCCCCCC(CC)O 144.25 unknown https://doi.org/10.1002/JPS.2600531215
trans-3-Hexen-1-ol 5284503 Click to see CCC=CCCO 100.16 unknown https://doi.org/10.1002/JPS.2600531215
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/JPS.2600531215
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/JPS.2600531215
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698204
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/JPS.2600531215
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698204
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/JPS.2600531215
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/JPS.2600531215
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698204
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0378-8741(91)90177-F
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(9-acetyloxy-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl)methyl acetate 73188872 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)CCC(=C)C(=O)CC1OC(=O)C 362.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
(9R,10E,11aR)-9-hydroxy-3-(hydroxymethyl)-10-methyl-6-methylidene-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-2,7-dione 162920444 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1O 278.30 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(7R,9R,10Z,11aR)-7-hydroxy-3-(hydroxymethyl)-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 162844067 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(CC1OC(=O)C)O 322.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(7R,9R,10Z,11aR)-9-acetyloxy-7-hydroxy-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-3-yl]methyl acetate 162956889 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)CCC(=C)C(CC1OC(=O)C)O 364.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(7S,9R,10E,11aR)-7-acetyloxy-3-(hydroxymethyl)-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 163085907 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(CC1OC(=O)C)OC(=O)C 364.40 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
[(7S,9R,10Z,11aR)-7-hydroxy-3-(hydroxymethyl)-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 162844069 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(CC1OC(=O)C)O 322.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(7S,9R,10Z,11aR)-9-acetyloxy-7-hydroxy-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-3-yl]methyl acetate 162956888 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)CCC(=C)C(CC1OC(=O)C)O 364.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(7S,9S,10E,11aR)-7-acetyloxy-3-(hydroxymethyl)-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 13895749 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(CC1OC(=O)C)OC(=O)C 364.40 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
[(9R,10E,11aS)-3-(hydroxymethyl)-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 13895746 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1OC(=O)C 320.30 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
[(9R,10Z,11aR)-3-(hydroxymethyl)-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 162951084 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1OC(=O)C 320.30 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(9R,10Z,11aR)-9-acetyloxy-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl]methyl acetate 162998885 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)CCC(=C)C(=O)CC1OC(=O)C 362.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(9S,10E,11aR)-3-(hydroxymethyl)-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 13895747 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1OC(=O)C 320.30 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(9S,10E,11aR)-9-acetyloxy-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl]methyl acetate 13895752 Click to see CC1=CC2C(=C(C(=O)O2)COC(=O)C)CCC(=C)C(=O)CC1OC(=O)C 362.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[3-(hydroxymethyl)-10-methyl-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 73188870 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1OC(=O)C 320.30 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
https://doi.org/10.1016/0031-9422(89)80381-4
[7-Acetyloxy-3-(hydroxymethyl)-10-methyl-6-methylidene-2-oxo-4,5,7,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 73188871 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(CC1OC(=O)C)OC(=O)C 364.40 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
9-hydroxy-3-(hydroxymethyl)-10-methyl-6-methylidene-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-2,7-dione 162920442 Click to see CC1=CC2C(=C(C(=O)O2)CO)CCC(=C)C(=O)CC1O 278.30 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1S,1'S,3'R,5R,6S,7S,9S)-7-hydroxy-3'-(hydroxymethyl)-4',4'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl] acetate 13919289 Click to see CC(=O)OC1CCC(C(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)CO)(C)C 406.50 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Judaicin 118701072 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(90)85454-N
Vulgarin 94253 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(5Z,7S,9R,10Z,11aR)-7-hydroxy-3-(hydroxymethyl)-6,10-dimethyl-2-oxo-7,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 162921905 Click to see CC1=CCC2=C(C(=O)OC2C=C(C(CC1O)OC(=O)C)C)CO 322.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(5Z,7S,9R,10Z,11aR)-9-acetyloxy-7-hydroxy-6,10-dimethyl-2-oxo-7,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-3-yl]methyl acetate 101501874 Click to see CC1=CCC2=C(C(=O)OC2C=C(C(CC1O)OC(=O)C)C)COC(=O)C 364.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,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-yl] acetate 137704689 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1R,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-Tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 17750996 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
9,19-Cyclolanost-24-en-3-ol, acetate, (3beta)- 518616 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
Cycloartenol acetate 13023741 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3,3,6-Trimethylhepta-1,5-dien-4-ol 100197 Click to see CC(=CC(C(C)(C)C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698204
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,4S)-4-ethenyl-2,5-dimethylhexane-2,3,5-triol 162860351 Click to see CC(C)(C(C=C)C(C(C)(C)O)O)O 188.26 unknown https://doi.org/10.1016/0031-9422(90)85454-N
(3S,4R)-4-ethenyl-2,5-dimethylhexane-2,3,5-triol 162860352 Click to see CC(C)(C(C=C)C(C(C)(C)O)O)O 188.26 unknown https://doi.org/10.1016/0031-9422(90)85454-N
3-Ethyl-2,5-dimethylhexane-2,5-diol 148344119 Click to see CCC(CC(C)(C)O)C(C)(C)O 174.28 unknown https://doi.org/10.1016/0031-9422(89)80381-4
4-Ethenyl-2,5-dimethyl-2,3,5-hexanetriol 14589058 Click to see CC(C)(C(C=C)C(C(C)(C)O)O)O 188.26 unknown https://doi.org/10.1016/0031-9422(90)85454-N
Santolina alcohol 519843 Click to see CC(=CC(C=C)C(C)(C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698204
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(2E,4S)-4-(2-hydroxypropan-2-yl)-2-methylhexa-2,5-dienal 162993263 Click to see CC(=CC(C=C)C(C)(C)O)C=O 168.23 unknown https://doi.org/10.1016/0031-9422(90)85454-N
(2Z,4R)-4-(2-hydroxypropan-2-yl)-2-methylhexa-2,5-dienal 162993264 Click to see CC(=CC(C=C)C(C)(C)O)C=O 168.23 unknown https://doi.org/10.1016/0031-9422(90)85454-N
4-(2-Hydroxypropan-2-yl)-2-methylhexa-2,5-dienal 162993262 Click to see CC(=CC(C=C)C(C)(C)O)C=O 168.23 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
3,3,6-Trimethylhepta-1,5-dien-4-one 68346 Click to see CC(=CC(=O)C(C)(C)C=C)C 152.23 unknown https://doi.org/10.1080/10412905.1993.9698204
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-[(1R,2R)-2-acetyl-1-propan-2-ylcyclopropyl]acetic acid 12444318 Click to see CC(C)C1(CC1C(=O)C)CC(=O)O 184.23 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
[(9R,10E,11aS)-3-(hydroxymethyl)-6-methylidene-2,7-dioxo-5,8,9,11a-tetrahydro-4H-cyclodeca[b]furan-9-yl] acetate 132580937 Click to see CC(=O)OC1CC(=O)C(=C)CCC2=C(C(=O)OC2C=C1)CO 306.31 unknown https://doi.org/10.1016/S0040-4020(01)83452-9
> Organoheterocyclic compounds / Naphthofurans
(8-acetyloxy-6-hydroxy-5a-methyl-9-methylidene-2-oxo-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-3-yl)methyl acetate 14021351 Click to see CC(=O)OCC1=C2CCC3(C(CC(C(=C)C3C2OC1=O)OC(=O)C)O)C 364.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
(8-acetyloxy-6,9-dihydroxy-5a,9-dimethyl-2-oxo-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-3-yl)methyl acetate 15627979 Click to see CC(=O)OCC1=C2CCC3(C(CC(C(C3C2OC1=O)(C)O)OC(=O)C)O)C 382.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(5aR,6R,8S,9S,9aS,9bR)-6,9-dihydroxy-3-(hydroxymethyl)-5a,9-dimethyl-2-oxo-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-8-yl] acetate 15627978 Click to see CC(=O)OC1CC(C2(CCC3=C(C(=O)OC3C2C1(C)O)CO)C)O 340.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(5aR,6R,8S,9S,9aS,9bR)-8-acetyloxy-6,9-dihydroxy-5a,9-dimethyl-2-oxo-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-3-yl]methyl acetate 15627980 Click to see CC(=O)OCC1=C2CCC3(C(CC(C(C3C2OC1=O)(C)O)OC(=O)C)O)C 382.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(6R,8S,9aR,9bR)-8-acetyloxy-6-hydroxy-9-methylidene-2-oxo-4,5,5a,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-3-yl]methyl acetate 162817326 Click to see CC(=O)OCC1=C2CCC3C(CC(C(=C)C3C2OC1=O)OC(=O)C)O 350.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(6R,8S,9S,9aS,9bR)-6,9-dihydroxy-3-(hydroxymethyl)-9-methyl-2-oxo-4,5,5a,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-8-yl] acetate 162817328 Click to see CC(=O)OC1CC(C2CCC3=C(C(=O)OC3C2C1(C)O)CO)O 326.34 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[(6R,8S,9S,9aS,9bR)-8-acetyloxy-6,9-dihydroxy-9-methyl-2-oxo-4,5,5a,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-3-yl]methyl acetate 163009019 Click to see CC(=O)OCC1=C2CCC3C(CC(C(C3C2OC1=O)(C)O)OC(=O)C)O 368.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
[6,9-dihydroxy-3-(hydroxymethyl)-5a,9-dimethyl-2-oxo-5,6,7,8,9a,9b-hexahydro-4H-benzo[g][1]benzofuran-8-yl] acetate 15627977 Click to see CC(=O)OC1CC(C2(CCC3=C(C(=O)OC3C2C1(C)O)CO)C)O 340.40 unknown https://doi.org/10.1016/0031-9422(89)80381-4
> Organoheterocyclic compounds / Oxolanes
(2S,3R,4S)-4-ethenyl-2-(hydroxymethyl)-2,5,5-trimethyloxolan-3-ol 14589060 Click to see CC1(C(C(C(O1)(C)CO)O)C=C)C 186.25 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> Organoheterocyclic compounds / Tetrahydrofurans
4-Ethenyl-2-(hydroxymethyl)-2,5,5-trimethyloxolan-3-ol 14589059 Click to see CC1(C(C(C(O1)(C)CO)O)C=C)C 186.25 unknown https://doi.org/10.1016/0031-9422(90)85454-N
> 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/10.1080/10412905.1993.9698204
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
4H-1-Benzopyran-4-one, 6-(2-O-arabinosyl-beta-D-glucopyranosyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy- 101422754 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O 578.50 unknown https://doi.org/10.1021/NP50059A028
6-[(2S,3S,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 163078799 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O 578.50 unknown https://doi.org/10.1021/NP50059A028
Swertisin 2''-O-arabinoside 44258322 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(CO5)O)O)O 578.50 unknown https://doi.org/10.1021/NP50059A028
> 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/10.1080/10412905.1993.9698204
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/10412905.1993.9698204
Scolymoside 5282152 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/10412905.1993.9698204

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