Chamaemelum nobile - Unknown
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Details Top

Internal ID UUID643fc76d2b507239757044
Scientific name Chamaemelum nobile
Authority All.
First published in Fl. Pedem. i. 185. 1785

Description Top

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Synonyms Top

Scientific name Authority First published in
Ormenis nobilis (L.) J.Gay ex Coss. & Germ. Fl. Descr. Anal. Paris : 398 (1845)
Chamaemelum nobile f. discoideum (Boiss. ex Willk.) Benedí Collect. Bot. (Barcelona) 17(1): 59 (1988)
Anthemis nobilis L. Sp. Pl. : 894 (1753)
Anthemis santolinoides Munby Bull. Soc. Bot. France 2: 284 (1855)
Chamaemelum nobile var. discoideum (Boiss.) P.Silva
Ormenis nobilis subsp. aurea (L.) Maire Cat. Pl. Maroc 3: 764 (1934)
Chamomilla nobilis Godr. Fl. Lorraine 2: 19 (1843)
Anacyclus aureus L. Mant. Pl. : 287 (1771)

Common names Top

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Language Common/alternative name
English roman chamomile
English chamomile
English matricaria recutita
English garden dog-fennel
Spanish camamilla romana
Spanish camomila comun
Spanish camomila común
Spanish camomila de jardin
Spanish camomila oficinal
Spanish camomila romana
Spanish manzanilla comun
Spanish manzanilla oficial
Spanish manzanilla verdadera
Spanish matricaria nobilis
Spanish rosa de manzanilla
Spanish camamila de moncayo
Spanish anthemis odorata
Arabic زهرة السباع
Arabic فراخ أم علي
Arabic البابونج الألماني
Arabic بابونج
Arabic قراص
Arabic مشرف
Arabic أقحوان شريف
Azerbaijani roma çobanyastığı
Azerbaijani anthemis aurea
Azerbaijani anacyclus nobilis
Belarusian пупок дабрародны
Belarusian валовае вочка
br mammlouzoù
Catalan camamilla romana
Czech heřmánek římský
Czech rmen římský
Czech rmen sličný
Czech rmenec sličný
Welsh camri
German römische kamille
Greek Χαμομήλι
Greek Χαμομήλι το ευγενές
Basque kamamila erromatar
Basque erromatar kamamila
Persian بابونهٔ رومی
Persian بابونه رومی
Finnish jalosauramo
French camomille romaine
Galician macela dourada
Hungarian római kamilla
Japanese ローマンカモミール
Korean 캐모마일
Lithuanian kilnioji blezdingūnė
Latvian smaržīgā kumelīte
Norwegian Nynorsk romersk kamille
oc camomilha romana
Polish rumian rzymski
Polish rumian szlachetny
Portuguese camomila-de-paris
Portuguese camomila-romana
Romanian musetel
Russian римская ромашка
Russian ромашка римская
Russian хамемелюм благородный
Russian пупавка благородная
Samogitian rīma ramonė
Slovak ruman rímsky
Slovenian rimska kamilica
Serbian Римска камилица
Swedish romersk kamomill
Urdu بابونہ رومی
Chinese 白花春黄菊
Chinese 罗马揩暮米辣
Chinese 果香菊
Chinese 羅馬洋甘菊
Chinese 罗马洋甘菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Africa
    • Macaronesia
      • Azores
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • Krym
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • New Jersey
      • New York
      • Ohio
    • Southeastern U.S.A.
      • Delaware
      • Maryland
      • North Carolina
    • Southwestern U.S.A.
      • California
  • Southern America
    • Caribbean
      • Haiti
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000014359
USDA Plants CHNO3
Tropicos 2741158
INPN 90470
Flora of Italy 5625
KEW urn:lsid:ipni.org:names:192489-1
The Plant List gcc-113893
Missouri Botanical Garden 277709
Open Tree Of Life 472684
Observations.org 199497
NCBI Taxonomy 99037
NBN Atlas NBNSYS0000004450
Nature Serve 2.150142
IUCN Red List 202952
IPNI 192489-1
iNaturalist 143243
GBIF 5391599
Freebase /m/05cmcg
EPPO ANTNO
EOL 488414
Elurikkus 730454
Calflora (Californian flora) 1918
US Library of Congress sh99005120
USDA GRIN 104133
Wikipedia Chamaemelum_nobile
PFAF Chamaemelum nobile

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
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
Plant-Mediated Synthesis of Magnetite Nanoparticles with Matricaria chamomilla Aqueous Extract Paut A, Guć L, Vrankić M, Crnčević D, Šenjug P, Pajić D, Odžak R, Šprung M, Nakić K, Marciuš M, Prkić A, Mitar I Nanomaterials (Basel) 22-Apr-2024
PMCID:PMC11053587
doi:10.3390/nano14080729
PMID:38668223
Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J Pathogens 13-Apr-2024
PMCID:PMC11054384
doi:10.3390/pathogens13040320
PMID:38668275
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Phytotherapeutic Approaches in Canine Pediatrics Quintavalla F Vet Sci 20-Mar-2024
PMCID:PMC10974738
doi:10.3390/vetsci11030133
PMID:38535867
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Antibacterial and antibiofilm activities of protocatechualdehyde and its synergy with ampicillin against methicillin-resistant Staphylococcus aureus Wang Y, Liu X, Song L, Chen K, Shi C, Peng C, Yang Q, Li Z Front Microbiol 28-Feb-2024
PMCID:PMC10932990
doi:10.3389/fmicb.2024.1366400
PMID:38481792
High-Quality Assembly and Analysis of the Complete Mitogenomes of German Chamomile (Matricaria recutita) and Roman Chamomile (Chamaemelum nobile) Yang J, Zhang X, Hua Z, Jia H, Li K, Ling C Genes (Basel) 26-Feb-2024
PMCID:PMC10970603
doi:10.3390/genes15030301
PMID:38540360
Chitosan-Based Nanoencapsulated Essential Oils: Potential Leads against Breast Cancer Cells in Preclinical Studies Tan WN, Samling BA, Tong WY, Chear NJ, Yusof SR, Lim JW, Tchamgoue J, Leong CR, Ramanathan S Polymers (Basel) 08-Feb-2024
PMCID:PMC10891598
doi:10.3390/polym16040478
PMID:38399856
Recent Advances in the Management of Rosacea through Natural Compounds Semenescu I, Similie D, Diaconeasa Z, Danciu C Pharmaceuticals (Basel) 06-Feb-2024
PMCID:PMC10892689
doi:10.3390/ph17020212
PMID:38399428
Importance of phytotherapy for oral health care and quality of life in adults: A scoping review Shinkai RS, Azevedo CL, de Campos TT, Michel-Crosato E, Biazevic MG J Dent Sci 24-Jan-2024
PMCID:PMC11010713
doi:10.1016/j.jds.2024.01.002
PMID:38618093
Antifungal Activity of Thirty Essential Oils to Control Pathogenic Fungi of Postharvest Decay Allagui MB, Moumni M, Romanazzi G Antibiotics (Basel) 28-Dec-2023
PMCID:PMC10812670
doi:10.3390/antibiotics13010028
PMID:38247587
In silico screening of herbal phytochemicals to develop a Rasayana for immunity against Nipah virus Debroy B, De A, Bhattacharya S, Pal K J Ayurveda Integr Med 03-Dec-2023
PMCID:PMC10746367
doi:10.1016/j.jaim.2023.100825
PMID:38048723
The effects of precipitation change on urban meadows in different design models and substrates Jiang Y, Yuan T Sci Rep 23-Nov-2023
PMCID:PMC10667351
doi:10.1038/s41598-023-44974-y
PMID:37996501
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
4-(Prop-1-en-2-yl)benzaldehyde 14597914 Click to see CC(=C)C1=CC=C(C=C1)C=O 146.19 unknown https://doi.org/10.1002/HLCA.19810640746
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown https://doi.org/10.1039/CT9140501829
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2-Hydroperoxy-2-methylbut-3-enyl) 2-methylbut-2-enoate 163020171 Click to see CC=C(C)C(=O)OCC(C)(C=C)OO 200.23 unknown https://doi.org/10.1002/ARDP.19893221109
(3-Hydroperoxy-2-methylidenebutyl) 2-methylbut-2-enoate 163046037 Click to see CC=C(C)C(=O)OCC(=C)C(C)OO 200.23 unknown https://doi.org/10.1002/ARDP.19893221109
(3-Hydroxy-2-methylidenebutyl) 2-methylbut-2-enoate 162955700 Click to see CC=C(C)C(=O)OCC(=C)C(C)O 184.23 unknown https://doi.org/10.1002/HLCA.19810640739
(3-Methylidene-4-oxopentyl) 2-methylbut-2-enoate 162866176 Click to see CC=C(C)C(=O)OCCC(=C)C(=O)C 196.24 unknown https://doi.org/10.1002/HLCA.19810640739
[(2R)-2-hydroperoxy-2-methylbut-3-enyl] (Z)-2-methylbut-2-enoate 163020172 Click to see CC=C(C)C(=O)OCC(C)(C=C)OO 200.23 unknown https://doi.org/10.1002/ARDP.19893221109
[(2R)-2-hydroxy-2-methylbut-3-enyl] (Z)-2-methylbut-2-enoate 163039512 Click to see CC=C(C)C(=O)OCC(C)(C=C)O 184.23 unknown https://doi.org/10.1002/HLCA.19810640739
[(3S)-3-hydroperoxy-2-methylidenebutyl] (Z)-2-methylbut-2-enoate 163046038 Click to see CC=C(C)C(=O)OCC(=C)C(C)OO 200.23 unknown https://doi.org/10.1002/ARDP.19893221109
[(3S)-3-hydroxy-2-methylidenebutyl] (Z)-2-methylbut-2-enoate 162955701 Click to see CC=C(C)C(=O)OCC(=C)C(C)O 184.23 unknown https://doi.org/10.1002/HLCA.19810640739
2-Hydroxy-2-methylbut-3-en-1-yl 2-methylbut-2-enoate 557909 Click to see CC=C(C)C(=O)OCC(C)(C=C)O 184.23 unknown https://doi.org/10.1002/HLCA.19810640739
2-methylpropyl (3S)-3-hydroperoxy-2-methylidenebutanoate 163063699 Click to see CC(C)COC(=O)C(=C)C(C)OO 188.22 unknown https://doi.org/10.1002/ARDP.19893221109
2-Methylpropyl 3-hydroperoxy-2-methylidenebutanoate 14446951 Click to see CC(C)COC(=O)C(=C)C(C)OO 188.22 unknown https://doi.org/10.1002/ARDP.19893221109
3-Methylidene-4-oxopentyl angelate 157009897 Click to see CC=C(C)C(=O)OCCC(=C)C(=O)C 196.24 unknown https://doi.org/10.1002/HLCA.19810640739
Isoamyl angelate 5366155 Click to see CC=C(C)C(=O)OCCC(C)C 170.25 unknown https://doi.org/10.1055/S-2006-960081
Isobutyl angelate 5367807 Click to see CC=C(C)C(=O)OCC(C)C 156.22 unknown https://doi.org/10.1080/10412905.1998.9700974
Pentyl 2-methylisocrotonate 6430804 Click to see CCCCCOC(=O)C(=CC)C 170.25 unknown https://doi.org/10.1016/S0367-326X(03)00195-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3,7-Dimethylocta-2,6-dienyl 3-methylbutanoate 19802 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00993-X
Geranyl isovalerate 5362830 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00993-X
Neryl isobutyrate 5365991 Click to see CC(C)C(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1080/10412905.1991.9697949
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Pentadecanal 17697 Click to see CCCCCCCCCCCCCCC=O 226.40 unknown https://doi.org/10.1080/10412905.1991.9697949
Tridecanal 25311 Click to see CCCCCCCCCCCCC=O 198.34 unknown https://doi.org/10.1080/10412905.1991.9697949
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/J.FITOTE.2003.07.007
https://doi.org/10.1016/S0367-326X(03)00195-3
> 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/10.1055/S-2006-960081
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3R,5S)-3-hydroperoxy-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptane 13819205 Click to see CC1(C2CC1C(=C)C(C2)OO)C 168.23 unknown https://doi.org/10.1002/ARDP.19893221109
(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/J.FITOTE.2003.07.007
6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptane-3-peroxol 13819203 Click to see CC1(C2CC1C(=C)C(C2)OO)C 168.23 unknown https://doi.org/10.1002/ARDP.19893221109
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(03)00195-3
https://doi.org/10.1016/J.FITOTE.2003.07.007
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-2006-960081
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(03)00195-3
https://doi.org/10.1016/J.FITOTE.2003.07.007
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1016/J.FITOTE.2003.07.007
https://doi.org/10.1016/S0367-326X(03)00195-3
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0367-326X(03)00195-3
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1016/J.FITOTE.2003.07.007
https://doi.org/10.1016/S0367-326X(03)00195-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(7-hydroperoxy-9-hydroxy-10-methyl-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 78410382 Click to see CC=C(C)C(=O)OC1CC(=C)C(CC(C(=CC2C1C(=C)C(=O)O2)C)O)OO 378.40 unknown https://doi.org/10.1002/ARDP.19873200408
https://doi.org/10.1002/ARDP.19893221109
[(3aR,4S,7R,9S,10Z,11aR)-7-hydroperoxy-9-hydroxy-10-methyl-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 163081822 Click to see CC=C(C)C(=O)OC1CC(=C)C(CC(C(=CC2C1C(=C)C(=O)O2)C)O)OO 378.40 unknown https://doi.org/10.1002/ARDP.19873200408
https://doi.org/10.1002/ARDP.19893221109
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
CID 12305204 12305204 Click to see CC12CCC3C(C1C(C=CC2=O)(C)O)OC(=O)C3=C 262.30 unknown https://doi.org/10.1080/10412905.1998.9700974
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,8,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 75050460 Click to see CC=C(C)C(=O)OC1CC(=CCC(=O)C(=CC2C1C(=C)C(=O)O2)C)C 344.40 unknown https://doi.org/10.1135/CCCC19771053
[(1R,2S,4S,6R,8R,11S)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] 2-methylbut-2-enoate 163080153 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1135/CCCC19771053
[(1R,2S,4S,6R,8R,9Z,11S)-8-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.04,6]tetradec-9-en-2-yl] (E)-2-methylbut-2-enoate 163187366 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1135/CCCC19771053
[(3aR,4S,6E,10Z,11aR)-6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,8,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 162899340 Click to see CC=C(C)C(=O)OC1CC(=CCC(=O)C(=CC2C1C(=C)C(=O)O2)C)C 344.40 unknown https://doi.org/10.1135/CCCC19771053
[(3aR,4S,6E,10Z,11aS)-6,10-dimethyl-3-methylidene-2,9-dioxo-4,5,8,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162899339 Click to see CC=C(C)C(=O)OC1CC(=CCC(=O)C(=CC2C1C(=C)C(=O)O2)C)C 344.40 unknown https://doi.org/10.1135/CCCC19771053
[(3aR,4S,6E,9R,10Z,11aS)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 163094455 Click to see CC=C(C)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1135/CCCC19771053
[(3aR,4S,6E,9S,10Z,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 5320178 Click to see CC=C(C)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1135/CCCC19771053
CID 11953937 11953937 Click to see CC=C(C)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1135/CCCC19643096
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(9-Hydroperoxy-9-methyl-3,6-dimethylidene-2-oxo-3a,4,5,6a,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl) 2-methylbut-2-enoate 162886112 Click to see CC=C(C)C(=O)OC1CC(=C)C2C=CC(C2C3C1C(=C)C(=O)O3)(C)OO 360.40 unknown https://doi.org/10.1002/ARDP.19893221109
[(3aR,4S,6aR,9R,9aS,9bS)-9-hydroperoxy-9-methyl-3,6-dimethylidene-2-oxo-3a,4,5,6a,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 163186286 Click to see CC=C(C)C(=O)OC1CC(=C)C2C=CC(C2C3C1C(=C)C(=O)O3)(C)OO 360.40 unknown https://doi.org/10.1002/ARDP.19893221109
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1039/CT9140501829
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1039/CT9140501829
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,3S,5Z,7R,8E,11S,12S,13E,15R,17R,21R,23R,25S)-12-acetyloxy-1,11,21-trihydroxy-17-[(1R)-1-hydroxyethyl]-5,13-bis(2-methoxy-2-oxoethylidene)-10,10,26,26-tetramethyl-19-oxo-18,27,28,29-tetraoxatetracyclo[21.3.1.13,7.111,15]nonacos-8-en-25-yl] 3-methylbutanoate 44559609 Click to see CC(C)CC(=O)OC1CC2CC(CC(=O)OC(CC3CC(=CC(=O)OC)C(C(O3)(C(C=CC4CC(=CC(=O)OC)CC(O4)CC(C1(C)C)(O2)O)(C)C)O)OC(=O)C)C(C)O)O 867.00 unknown https://doi.org/10.1135/CCCC19643096
[(1S,3S,5Z,7R,8E,11S,12S,13E,15R,17R,21R,23R,25S)-12-butanoyloxy-1,11,21-trihydroxy-17-[(1R)-1-hydroxyethyl]-5,13-bis(2-methoxy-2-oxoethylidene)-10,10,26,26-tetramethyl-19-oxo-18,27,28,29-tetraoxatetracyclo[21.3.1.13,7.111,15]nonacos-8-en-25-yl] 3-methylbutanoate 44559608 Click to see CCCC(=O)OC1C(=CC(=O)OC)CC2CC(OC(=O)CC(CC3CC(C(C(O3)(CC4CC(=CC(=O)OC)CC(O4)C=CC(C1(O2)O)(C)C)O)(C)C)OC(=O)CC(C)C)O)C(C)O 895.00 unknown https://doi.org/10.1135/CCCC19643096
[(1S,3S,5Z,7R,8Z,11S,12S,13E,15S,17R,21R,23R,25S)-12-acetyloxy-1,11,21-trihydroxy-17-[(1R)-1-hydroxyethyl]-5,13-bis(2-methoxy-2-oxoethylidene)-10,10,26,26-tetramethyl-19-oxo-18,27,28,29-tetraoxatetracyclo[21.3.1.13,7.111,15]nonacos-8-en-25-yl] butanoate 22610414 Click to see CCCC(=O)OC1CC2CC(CC(=O)OC(CC3CC(=CC(=O)OC)C(C(O3)(C(C=CC4CC(=CC(=O)OC)CC(O4)CC(C1(C)C)(O2)O)(C)C)O)OC(=O)C)C(C)O)O 853.00 unknown https://doi.org/10.1135/CCCC19643096
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(S)-(-)-3-Hydroxy-2-methylen-butyric Acid Butyl Ester 86587837 Click to see CCCCOC(=O)C(=C)C(C)O 172.22 unknown https://doi.org/10.1002/HLCA.19810640739
[(2S)-2-methylbutyl] (3S)-3-hydroxy-2-methylidenebutanoate 163002337 Click to see CCC(C)COC(=O)C(=C)C(C)O 186.25 unknown https://doi.org/10.1002/HLCA.19810640739
2-Methylbutyl 3-hydroxy-2-methylidenebutanoate 101412557 Click to see CCC(C)COC(=O)C(=C)C(C)O 186.25 unknown https://doi.org/10.1002/HLCA.19810640739
2-methylpropyl (3S)-3-hydroxy-2-methylidenebutanoate 162973646 Click to see CC(C)COC(=O)C(=C)C(C)O 172.22 unknown https://doi.org/10.1002/HLCA.19810640739
2-Methylpropyl 3-hydroxy-2-methylidenebutanoate 546207 Click to see CC(C)COC(=O)C(=C)C(C)O 172.22 unknown https://doi.org/10.1002/HLCA.19810640739
3-methylbutyl (3S)-3-hydroxy-2-methylidenebutanoate 163031140 Click to see CC(C)CCOC(=O)C(=C)C(C)O 186.25 unknown https://doi.org/10.1002/HLCA.19810640739
3-Methylbutyl 3-hydroxy-2-methylidenebutanoate 551273 Click to see CC(C)CCOC(=O)C(=C)C(C)O 186.25 unknown https://doi.org/10.1002/HLCA.19810640739
Butyl 3-hydroxy-2-methylidenebutanoate 568158 Click to see CCCCOC(=O)C(=C)C(C)O 172.22 unknown https://doi.org/10.1002/HLCA.19810640739
> Organic oxygen compounds / Organic hydroperoxides
2-methylprop-2-enyl (2R)-2-hydroperoxypropanoate 163062158 Click to see CC(C(=O)OCC(=C)C)OO 160.17 unknown https://doi.org/10.1002/ARDP.19893221109
2-Methylprop-2-enyl 2-hydroperoxypropanoate 14446952 Click to see CC(C(=O)OCC(=C)C)OO 160.17 unknown https://doi.org/10.1002/ARDP.19893221109
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1039/CT9140501829
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
Lepalone 535169 Click to see CC(=C)C(=O)CCC1=COC=C1 164.20 unknown https://doi.org/10.1002/HLCA.19810640746
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1002/HLCA.19810640746
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Methyl-5-(fur-3-yl)-pent-1-en-3-ol 557594 Click to see CC(=C)C(CCC1=COC=C1)O 166.22 unknown https://doi.org/10.1002/HLCA.19810640746
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3,4-Dihydroxy cinnamic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1039/CT9140501829
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1039/CT9140501829
> 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/10.1039/CT9140501829
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1515/ZNC-2003-1-202
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(3R)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid 163007176 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(95)00487-4
https://doi.org/10.1055/S-2006-957532
(3S)-3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid 163007175 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(95)00487-4
3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 101482793 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 740.70 unknown https://doi.org/10.1039/CT9140501829
3-hydroxy-3-methyl-5-oxo-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid 101688668 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1055/S-2006-957532
https://doi.org/10.1016/0031-9422(95)00487-4
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/S0021-9673(01)88492-2
https://doi.org/10.1515/ZNC-2003-1-202
Chamaemeloside 59492121 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O 576.50 unknown https://doi.org/10.1055/S-2006-957532
https://doi.org/10.1016/0031-9422(95)00487-4
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/10.1515/ZNC-2003-1-202
https://doi.org/10.1016/S0021-9673(01)88492-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one 638205 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)OC)OC 342.30 unknown https://doi.org/10.1039/CT9140501829
> Phenylpropanoids and polyketides / Macrolides and analogues
3,13,15,25,35,37-Hexahydroxy-11,33-bis[3-hydroxy-6-(4-methoxy-6-methyloxan-2-yl)-4-methylhexan-2-yl]-17,39-dimethoxy-6,12,16,28,34,38-hexamethyl-10,32,45,46-tetraoxatricyclo[39.3.1.119,23]hexatetraconta-5,7,21,27,29,43-hexaene-9,31-dione 73309078 Click to see CC1CC(CC(O1)CCC(C)C(C(C)C2C(C(CC(C(C(CC3CC=CC(O3)CC(CC=C(C=CC(=O)OC(C(C(CC(C(C(CC4CC=CC(O4)CC(CC=C(C=CC(=O)O2)C)O)OC)C)O)O)C)C(C)C(C(C)CCC5CC(CC(O5)C)OC)O)C)O)OC)C)O)O)C)O)OC 1389.90 unknown https://doi.org/10.1135/CCCC19771053
https://doi.org/10.1039/CT9140501829

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