Myrtus communis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Myrtus communis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fe410add71115904586
Scientific name Myrtus communis
Authority L.
First published in Sp. Pl. : 471 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Myrtus augustinii Sennen & Malag. Bull. Soc. Dendrol. France 1929, 16.
Myrtus communis subsp. mucronata Pers. Syn. Pl. 2: 30 1806
Myrtus communis var. italica (Mill.) Rouy & E.G.Camus Fl. France 7: 155 1901
Myrtus communis var. lusitanica Rouy Fl. France 7: 155 1901
Myrtus communis var. communis L. Sitzungsber. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. München 471 1753
Myrtus communis var. balearicus Sennen
Myrtus communis var. adrianii Sennen
Myrtus communis var. baui (Sennen & Malag.) Sennen
Myrtus communis var. bercialis Sennen
Myrtus communis var. camboanus Sennen
Myrtus communis var. eugeniae Sennen
Myrtus communis var. gallachi Sennen
Myrtus communis var. gausseni Sennen
Myrtus communis var. gibertii Sennen
Myrtus communis var. jonssetii Sennen
Myrtus communis var. latifolia Willk.
Myrtus communis var. macrocarpa Sennen
Myrtus communis var. melanocarpa DC.
Myrtus communis var. microphylla Willk.
Myrtus communis var. morawieskiana Sennen
Myrtus communis var. rodesii Sennen & Malag.
Myrtus communis var. soleri Sennen
Myrtus communis f. tarentinus (L.) Cout.
Myrtus communis var. theodori Sennen & Malag.
Myrtus communis f. baetica (L.) Cout.
Myrtus communis f. belgica (L.) Cout.
Myrtus communis subsp. lusitanica (L.) Arcang.
Myrtus communis f. lusitanica (L.) Cout.

Common names Top

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Language Common/alternative name
English cilmun
English myrtle
English common myrtle
Afrikaans mirt
Arabic شجرة السكر
Arabic حمبلاس
Arabic ريحان
Arabic مرسين
Arabic آس
Azerbaijani adi mərsin
azb عادی مرسین
Belarusian мірт звычайны
Catalan murtra
co murta
Czech myrta obecná
Welsh myrtwydd
Danish almindelig myrte
German myrte
German brautmyrte
German gemeine myrte
Esperanto mirto
Estonian harilik mürt
Basque mirto
Persian مورد
Finnish myrtti
Finnish välimerenmyrtti
frr myrte
Galician mirto
Hebrew הדס מצוי
Croatian mirta
Upper Sorbian wšědna myrta
Hungarian közönséges mirtusz
Hungarian mirtusz
Italian mortella
Italian mirto
Japanese ギンバイカ
Kabyle cilmun
Korean 은매화
Macedonian обична мирта
Norwegian Bokmål myrt
Dutch mirte
Norwegian Nynorsk myrt
Polish mirt zwyczajny
Portuguese murta-comum
Russian Мирт обыкновенный
sc murta
Serbo-Croatian mirta
Slovak myrta obyčajná
Slovenian laška borovnica
Slovenian vedno zelena mirta
Slovenian grška mirta
Slovenian navadna mirta
Swedish myrten
Thai เมอร์เทิล
Ukrainian Мирт звичайний
Vietnamese hương đào
vls myrte
Chinese 香桃木

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Myrtus communis subsp. communis Unknown
Myrtus communis subsp. tarentina (L.) Nyman Consp. Fl. Eur. 2: 245 (1879)

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
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
    • Southern Africa
      • Cape Provinces
  • Asia-temperate
    • Arabian Peninsula
      • Yemen
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Louisiana
    • Southwestern U.S.A.
      • California
  • Southern America
    • Caribbean
      • Cuba
      • Leeward Islands
      • Puerto Rico
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000248712
UNII A98SBG347O
USDA Plants MYCO9
Tropicos 22102175
INPN 109186
Flora of Italy 3341
KEW urn:lsid:ipni.org:names:599719-1
The Plant List kew-132410
Missouri Botanical Garden 282870
Open Tree Of Life 475714
Observations.org 119935
NCBI Taxonomy 119949
NBN Atlas NBNSYS0500000329
IUCN Red List 203365
IPNI 599719-1
iNaturalist 78159
GBIF 3180085
EPPO MYVCO
EOL 2508590
Elurikkus 5843
Calflora (Californian flora) 10645
USDA GRIN 24898
Wikipedia Myrtus_communis
PaleoBotany 97869

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
Risk assessment of Retithrips syriacus for the EU Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
Microwave-Assisted Extraction of Secondary Metabolites Using Ethyl Lactate Green Solvent from Ambrosia arborescens: LC/ESI-MS/MS and Antioxidant Activity Guillen E, Terrones H, de Terrones TC, Simirgiotis MJ, Hájek J, Cheel J, Sepulveda B, Areche C Plants (Basel) 27-Apr-2024
PMCID:PMC11085450
doi:10.3390/plants13091213
PMID:38732429
Exploring Gluten Assessment in Marketed Products through a Sandwich ELISA Methodology Based on Novel Recombinant Antibodies Garcia-Calvo E, García-García A, Rodríguez S, Martín R, García T Foods 26-Apr-2024
PMCID:PMC11083168
doi:10.3390/foods13091341
PMID:38731712
Insect floral visitors of thermo-Mediterranean shrubland maquis (Ajaccio, Corsica, France) Maestracci PY, Plume L, Gibernau M Biodivers Data J 25-Apr-2024
PMCID:PMC11079593
doi:10.3897/BDJ.12.e118614
PMID:38726024
Design of three-component essential oil extract mixture from Cymbopogon flexuosus, Carum carvi, and Acorus calamus with enhanced antioxidant activity Assaggaf H, Jeddi M, Mrabti HN, Ez-zoubi A, Qasem A, Attar A, Goh BH, Tan SL, Bouyahya A, Goh KW, Hachlafi NE Sci Rep 22-Apr-2024
PMCID:PMC11035653
doi:10.1038/s41598-024-59708-x
PMID:38649707
Mesenchymal stem cell therapy in diabetic foot ulcer: An updated comprehensive review Hetta HF, Elsaghir A, Sijercic VC, Akhtar MS, Gad SA, Moses A, Zeleke MS, Alanazi FE, Ahmed AK, Ramadan YN Health Sci Rep 21-Apr-2024
PMCID:PMC11033295
doi:10.1002/hsr2.2036
PMID:38650719
Unveiling the Nuances of Adult Female Acne: A Comprehensive Exploration of Epidemiology, Treatment Modalities, Dermocosmetics, and the Menopausal Influence Dias da Rocha MA, Saint Aroman M, Mengeaud V, Carballido F, Doat G, Coutinho A, Bagatin E Int J Womens Health 18-Apr-2024
PMCID:PMC11034510
doi:10.2147/IJWH.S431523
PMID:38650835
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Supercritical CO2 Extraction of Fatty Acids, Phytosterols, and Volatiles from Myrtle (Myrtus communis L.) Fruit Cvitković D, Škarica I, Dragović-Uzelac V, Balbino S Molecules 12-Apr-2024
PMCID:PMC11052497
doi:10.3390/molecules29081755
PMID:38675575
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
PMCID:PMC11053949
doi:10.3390/plants13081079
PMID:38674488
Exploring the chemical characterization and insecticidal activities of Curcuma angustifolia roxb. leaf essential oils against three major stored product insects Paul A, Visakh NU, Pathrose B, Mori N, Baeshen RS, Shawer R Saudi J Biol Sci 05-Apr-2024
PMCID:PMC11017047
doi:10.1016/j.sjbs.2024.103986
PMID:38623076
Insect protein-based composite film incorporated with E. purpurea-based nanoparticles augmented the storage stability of parmesan cheese Singh S, Bhat HF, Kumar S, Aadil RM, Abdi G, Bhat ZF Heliyon 03-Apr-2024
PMCID:PMC11004877
doi:10.1016/j.heliyon.2024.e29036
PMID:38601692
Myrtucommulones and Related Acylphloroglucinols from Myrtaceae as a Promising Source of Multitarget SARS-CoV-2 Cycle Inhibitors Mendonça SC, Gomes BA, Campos MF, da Fonseca TS, Esteves ME, Andriolo BV, Cheohen CF, Constant LE, da Silva Costa S, Calil PT, Tucci AR, de Oliveira TK, Rosa AD, Ferreira VN, Lima JN, Miranda MD, da Costa LJ, da Silva ML, Scotti MT, Allonso D, Leitão GG, Leitão SG Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054083
doi:10.3390/ph17040436
PMID:38675398
Growth form, regeneration mode, and vegetation type explain leaf trait variability at the species and community levels in Mediterranean woody vegetation Tüfekcioğlu İ, Tavşanoğlu Ç Ecol Evol 11-Mar-2024
PMCID:PMC10927360
doi:10.1002/ece3.11145
PMID:38469041

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 / Morphinans
(5alpha,6beta)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol 5324287 Click to see CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O 285.34 unknown https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
> Benzenoids / Benzene and substituted derivatives / Acetophenones
(2S,9bR)-2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyldibenzofuran-1,3-dione 98044035 Click to see CC1=C(C(=C2C(=C1O)C3(C(=CC(=O)C(C3=O)C(=O)C)O2)C)C(=O)C)O 344.30 unknown https://doi.org/10.1002/EJOC.200500936
Usnic acid 5646 Click to see CC1=C(C(=C2C(=C1O)C3(C(=CC(=O)C(C3=O)C(=O)C)O2)C)C(=O)C)O 344.30 unknown https://doi.org/10.1002/EJOC.200500936
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl benzoate 7150 Click to see COC(=O)C1=CC=CC=C1 136.15 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1007/BF02467181
https://doi.org/10.1055/S-0028-1099955
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[3,4,5-Trihydroxy-6-[2-hydroxy-4,4,6,6-tetramethyl-2-(2-methylprop-1-enyl)-3,5-dioxocyclohexyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 20112066 Click to see CC(=CC1(C(C(C(=O)C(C1=O)(C)C)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)C 568.60 unknown https://doi.org/10.1021/NP050462W
[3,5,6-Trihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 25055151 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 484.40 unknown https://doi.org/10.1055/S-0028-1099955
Gallomyrtucommulone C 11541436 Click to see CC(=CC1(C(C(C(=O)C(C1=O)(C)C)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)C 568.60 unknown https://doi.org/10.1021/NP050462W
galloyl(-3)[galloyl(-6)]b-D-Ido 163194164 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 484.40 unknown https://doi.org/10.1055/S-0028-1099955
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Cearoin 3938139 Click to see COC1=C(C=C(C(=C1)O)C(=O)C2=CC=CC=C2)O 244.24 unknown https://doi.org/10.1002/EJOC.200500936
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
> Benzenoids / Phenol esters
Eugenol acetate 7136 Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC 206.24 unknown https://doi.org/10.1080/10412905.1992.9698084
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Methoxy-4-propenylbenzene 7703 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
trans-Dihydroocimene 5463450 Click to see CC(C)CCC=C(C)C=C 138.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Butyl butyrate 7983 Click to see CCCCOC(=O)CCC 144.21 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
Isobutyl 2-methylbutyrate 102820 Click to see CCC(C)C(=O)OCC(C)C 158.24 unknown https://doi.org/10.1080/10412905.1992.9698084
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl butyrate 12180 Click to see CCCC(=O)OC 102.13 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic acid 8314 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1080/10412905.1991.9700498
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1080/10412905.1991.9700498
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.1992.9698084
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9700498
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.1992.9698084
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.2000.9699481
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.2000.9712154
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Linalyl acetate, (-)- 442474 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
Methyl geranate 5365910 Click to see CC(=CCCC(=CC(=O)OC)C)C 182.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
> 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/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1992.9698084
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1080/10412905.1991.9700498
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698084
(1R)-endo-(+)-Fenchyl alcohol 6997371 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1992.9698084
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698084
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.2000.9699481
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1992.9698084
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1992.9698084
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1080/10412905.1991.9700498
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9700498
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1080/10412905.1992.9698084
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
trans-Verbenol 89664 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1992.9698084
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698084
Verbenone 29025 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1080/10412905.1992.9698084
https://doi.org/10.1080/10412905.1991.9700498
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6S)-rel- 85567 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)- 11469649 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
alpha-Terpinyl acetate 111037 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1992.9698084
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1007/BF02542606
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698084
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
(8R,8aS,9S,10aS)-8-[(1R)-2,2-dimethylcyclopentyl]-2,2,4,4,10a-pentamethyl-7-methylidene-9-propan-2-yl-6,8,8a,9-tetrahydro-5H-xanthene-1,3-dione 163036858 Click to see CC(C)C1C2C(C(=C)CCC2(OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C)C4CCCC4(C)C 440.70 unknown https://doi.org/10.1021/NP2009219
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
alpha-Guaiene 5317844 Click to see CC1CCC(CC2=C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1992.9698084
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1992.9698084
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698084
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1016/S0021-9673(01)95036-8
https://doi.org/10.1080/10412905.1992.9698084
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
Rel-Myrtucommulone K 57333286 Click to see CC(C)C1C2C(C(=C)CCC2(OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C)C4CCCC4(C)C 440.70 unknown https://doi.org/10.1021/NP2009219
Rel-Myrtucommulone L 57333287 Click to see CC(C)C1CC2(CCC3(C2C3)C(C)C)OC4=C1C(=O)C(C(=O)C4(C)C)(C)C 372.50 unknown https://doi.org/10.1021/NP2009219
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1992.9698084
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698084
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(1S,2S)-2-hydroxy-4,4,6,6-tetramethyl-2-(2-methylpropyl)-3,5-dioxocyclohexyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 163090277 Click to see CC(C)CC1(C(C(C(=O)C(C1=O)(C)C)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 570.60 unknown https://doi.org/10.1021/NP050462W
[3,4,5-Trihydroxy-6-[2-hydroxy-4,4,6,6-tetramethyl-2-(2-methylpropyl)-3,5-dioxocyclohexyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 20112026 Click to see CC(C)CC1(C(C(C(=O)C(C1=O)(C)C)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 570.60 unknown https://doi.org/10.1021/NP050462W
[3,4,5-Trihydroxy-6-[4-hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropyl)-3,5-dioxocyclohexyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 20112019 Click to see CC(C)CC1(C(=O)C(C(C(C1=O)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)(C)C)O 570.60 unknown https://doi.org/10.1021/NP050462W
Gallomyrtucommulone A 11505110 Click to see CC(C)CC1(C(C(C(=O)C(C1=O)(C)C)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 570.60 unknown https://doi.org/10.1021/NP050462W
Gallomyrtucommulone B 11664177 Click to see CC(C)CC1(C(=O)C(C(C(C1=O)(C)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)(C)C)O 570.60 unknown https://doi.org/10.1021/NP050462W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 12114939 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1002/EJOC.200500936
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/EJOC.200500936
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/EJOC.200500936
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/EJOC.200500936
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/EJOC.200500936
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1002/EJOC.200500936
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/EJOC.200500936
Olean-12-ene-3,28-diol 608886 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1002/EJOC.200500936
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/EJOC.200500936
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/EJOC.200500936
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/EJOC.200500936
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/EJOC.200500936
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(2R)-butan-2-yl] 2-methylpropanoate 87212999 Click to see CCC(C)OC(=O)C(C)C 144.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
2-Methylbutyl acetate 12209 Click to see CCC(C)COC(=O)C 130.18 unknown https://doi.org/10.1080/10412905.1992.9698084
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Isobutyric acid 6590 Click to see CC(C)C(=O)O 88.11 unknown https://doi.org/10.1080/10412905.1991.9700498
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Dimethyl malonate 7943 Click to see COC(=O)CC(=O)OC 132.11 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-1-butanol 8723 Click to see CCC(C)CO 88.15 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4-[(1S)-1-[2,4-dihydroxy-5-[(1R)-1-(2-hydroxy-3,3,5,5-tetramethyl-4,6-dioxocyclohexen-1-yl)-2-methylpropyl]-3-(2-methylpropanoyl)phenyl]-2-methylpropyl]-5-hydroxy-2,2,6,6-tetramethylcyclohex-4-ene-1,3-dione 162896757 Click to see CC(C)C(C1=CC(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)C3=C(C(C(=O)C(C3=O)(C)C)(C)C)O 652.80 unknown https://doi.org/10.1021/NP2009219
5-hydroxy-2,2,6,6-tetramethyl-4-[(1S)-2-methyl-1-[2,4,6-trihydroxy-3-[(1R)-1-(2-hydroxy-3,3,5,5-tetramethyl-4,6-dioxocyclohexen-1-yl)-2-methylpropyl]-5-(2-methylpropanoyl)phenyl]propyl]cyclohex-4-ene-1,3-dione 102103582 Click to see CC(C)C(C1=C(C(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)O)C3=C(C(C(=O)C(C3=O)(C)C)(C)C)O 668.80 unknown https://doi.org/10.1016/S0040-4020(01)97486-1
5-hydroxy-2,2,6,6-tetramethyl-4-[(1S)-2-methyl-1-[2,4,6-trihydroxy-3-methyl-5-(2-methylpropanoyl)phenyl]propyl]cyclohex-4-ene-1,3-dione 162940061 Click to see CC1=C(C(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)O 446.50 unknown https://doi.org/10.1021/NP010441B
Myrtucommulone A 44587062 Click to see CC(C)C(C1=C(C(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)O)C3=C(C(C(=O)C(C3=O)(C)C)(C)C)O 668.80 unknown https://doi.org/10.1021/NP2009219
https://doi.org/10.1021/NP010441B
Myrtucommulone A 10327116 Click to see CC(C)C(C1=C(C(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)O)C3=C(C(C(=O)C(C3=O)(C)C)(C)C)O 668.80 unknown https://doi.org/10.1016/S0040-4020(01)97486-1
Semimyrtucommulone 10411304 Click to see CC1=C(C(=C(C(=C1O)C(=O)C(C)C)O)C(C2=C(C(C(=O)C(C2=O)(C)C)(C)C)O)C(C)C)O 446.50 unknown https://doi.org/10.1021/NP010441B
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Rel-Myrtucommulone J 57333166 Click to see CC(C)C(C1=C(C(=C2C3=C1OC4(C(C3CC(O2)(C)C)C(C(=O)C4(C)C)(C)C)O)C(=O)C(C)C)O)C5=C(C(C(=O)C(C5=O)(C)C)(C)C)O 652.80 unknown https://doi.org/10.1021/NP2009219
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(4aR,8R,14S,14aS)-4a,7-dihydroxy-2,2,4,4,10,10,12,12-octamethyl-6-(2-methylpropanoyl)-8,14-di(propan-2-yl)-14,14a-dihydro-8H-chromeno[2,3-a]xanthene-1,3,9,11-tetrone 11700243 Click to see CC(C)C1C2C(=O)C(C(=O)C(C2(OC3=C(C(=C4C(C5=C(C(C(=O)C(C5=O)(C)C)(C)C)OC4=C13)C(C)C)O)C(=O)C(C)C)O)(C)C)(C)C 650.80 unknown https://doi.org/10.1002/EJOC.200500936
(9R)-6,8-dihydroxy-7-[(1S)-1-(2-hydroxy-3,3,5,5-tetramethyl-4,6-dioxocyclohexen-1-yl)-2-methylpropyl]-2,2,4,4-tetramethyl-5-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione 11592681 Click to see CC(C)C1C2=C(C(=C(C(=C2OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C(=O)C(C)C)O)C(C4=C(C(C(=O)C(C4=O)(C)C)(C)C)O)C(C)C)O 650.80 unknown https://doi.org/10.1002/EJOC.200500936
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione 51534484 Click to see CC(C)C1C2=C(C(=C(C=C2O)O)C(=O)C(C)C)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 414.50 unknown https://doi.org/10.1016/S0040-4020(01)97486-1
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione 162842266 Click to see CC(C)C1C2=C(C=C(C(=C2O)C(=O)C(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 414.50 unknown https://doi.org/10.1002/EJOC.200500936
4a,7-dihydroxy-2,2,4,4,10,10,12,12-octamethyl-6-(2-methylpropanoyl)-8,14-di(propan-2-yl)-14,14a-dihydro-8H-chromeno[2,3-a]xanthene-1,3,9,11-tetrone 73066366 Click to see CC(C)C1C2C(=O)C(C(=O)C(C2(OC3=C(C(=C4C(C5=C(C(C(=O)C(C5=O)(C)C)(C)C)OC4=C13)C(C)C)O)C(=O)C(C)C)O)(C)C)(C)C 650.80 unknown https://doi.org/10.1002/EJOC.200500936
6,8-dihydroxy-2,2,4,4-tetramethyl-7-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione 10993372 Click to see CC(C)C1C2=C(C=C(C(=C2O)C(=O)C(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 414.50 unknown https://doi.org/10.1002/EJOC.200500936
6,8-dihydroxy-7-[1-(2-hydroxy-3,3,5,5-tetramethyl-4,6-dioxocyclohexen-1-yl)-2-methylpropyl]-2,2,4,4-tetramethyl-5-(2-methylpropanoyl)-9-propan-2-yl-9H-xanthene-1,3-dione 51136394 Click to see CC(C)C1C2=C(C(=C(C(=C2OC3=C1C(=O)C(C(=O)C3(C)C)(C)C)C(=O)C(C)C)O)C(C4=C(C(C(=O)C(C4=O)(C)C)(C)C)O)C(C)C)O 650.80 unknown https://doi.org/10.1002/EJOC.200500936
7-Hydroxy-2,2,4,4,10,10,12,12-octamethyl-6-(2-methylpropanoyl)-8,14-di(propan-2-yl)-8,14-dihydrochromeno[2,3-a]xanthene-1,3,9,11-tetrone 73059351 Click to see CC(C)C1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C(C5=C(O3)C(C(=O)C(C5=O)(C)C)(C)C)C(C)C)C(=O)C(C)C)O 632.80 unknown https://doi.org/10.1002/EJOC.200500936
Myrtucommulone B 9888014 Click to see CC(C)C1C2=C(C(=C(C=C2O)O)C(=O)C(C)C)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 414.50 unknown https://doi.org/10.1016/S0040-4020(01)97486-1
Myrtucommulone E 11678995 Click to see CC(C)C1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C(C5=C(O3)C(C(=O)C(C5=O)(C)C)(C)C)C(C)C)C(=O)C(C)C)O 632.80 unknown https://doi.org/10.1002/EJOC.200500936
> Organoheterocyclic compounds / Epoxides
(1R,3E,7E,11R)-1,5,5,7-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 162903458 Click to see CC1=CCCC2C(O2)(CC=CC(C1)(C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.04.025
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see CC(=CCCC1=COC=C1)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9700498
https://doi.org/10.1080/10412905.1992.9698084
> Organoheterocyclic compounds / Oxolanes
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, (2R,5R)-rel- 6431475 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, cis- 11116492 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
(6R,7S)-6,7-dihydroxy-2-(2-phenylethyl)-5,6,7,8-tetrahydrochromen-4-one 162895774 Click to see C1C(C(CC2=C1C(=O)C=C(O2)CCC3=CC=CC=C3)O)O 286.32 unknown https://doi.org/10.1021/NP050462W
> Organoheterocyclic compounds / Tetrahydrofurans
trans-Linalool oxide 6432254 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1016/S0021-9673(01)95036-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
https://doi.org/10.1007/BF02467181
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
https://doi.org/10.1021/NP0501031
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP0501031
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1007/BF02467181
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1007/BF02467181
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/BF02467181
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
https://doi.org/10.1021/NP0501031
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
https://doi.org/10.1055/S-0028-1099955
https://doi.org/10.1021/NP0501031
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-3-(3-hydroxy-4-methoxyphenyl)-1-[2-hydroxy-6-methoxy-4-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one 138454317 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)OC)C(=O)C=CC4=CC(=C(C=C4)OC)O)O)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
Hesperidin methylchalcone 6436550 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)OC)C(=O)C=CC4=CC(=C(C=C4)OC)O)O)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
Myricetin 3'-glucoside 44259445 Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O 480.40 unknown https://doi.org/10.1021/NP0501031
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 16103933 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1055/S-0028-1099955
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF02467181
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1007/BF02467181
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1055/S-0028-1099955
Myricetin-3-O-rutinoside 21577860 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
https://doi.org/10.1007/BF02467181
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF02467181
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1076/PHBI.37.1.28.6327
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sideroxylin 3083788 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)O)O 312.30 unknown https://doi.org/10.1002/EJOC.200500936
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1055/S-0028-1099955
https://doi.org/10.1007/BF02467181

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