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Corymbia citriodora

Corymbia citriodora - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644035fbe988e365737392
Scientific name Corymbia citriodora
Authority (Hook.) K.D.Hill & L.A.S.Johnson
First published in Telopea 6: 388 (1995)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Corymbia citriodora subsp. variegata (F.Muell.) A.R.Bean & M.W.McDonald Austrobaileya 5: 735 (2000)
Corymbia variegata (F.Muell.) K.D.Hill & L.A.S.Johnson Telopea 6: 389 (1995)
Eucalyptus citriodora Hook. J. Exped. Trop. Australia : 235 (1848)
Eucalyptus maculata var. citriodora (Hook.) F.M.Bailey Syn. Queensl. Fl. : 181 (1883)
Eucalyptus melissiodora Lindl. J. Exped. Trop. Australia : 235 (1848)
Eucalyptus variegata F.Muell. J. Proc. Linn. Soc., Bot. 3: 88 (1858)

Common names Top

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Language Common/alternative name
English lemon eucalyptus
English lemonscented gum
Spanish eucalyptus maculata var citriodora
Spanish eucalyptus maculata var. citriodora
Spanish eucalipto con olor a limon
Spanish eucalipto con olor a limón
Spanish eucaliptus maculata var citriodora
Spanish eucaliptus maculata var. citriodora
Spanish eucaliptus melissiodora
Spanish eucalyptus citriodora
Spanish eucalyptus melissiodora
Azerbaijani limonu evkalipt
Azerbaijani eucalyptus melissiodora
Azerbaijani eucalyptus maculata var. citriodora
Azerbaijani eucalyptus citriodora
azb لیمونو ائوکالیپت
Bulgarian лимонов евкалипт
Bengali মহা কর্পূর
Czech blahovičník citroníkový
Czech citrónový eukalyptus
German zitroneneukalyptus
Persian اکالیپتوس لیمویی
French eucalyptus citriodora
French eucalyptus citronné
Hebrew אקליפטוס לימוני
Italian eucalyptus citriodora
Japanese レモンユーカリ
Portuguese eucalyptus citriodora
Chinese 柠檬桉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Morocco
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Gambia
      • Guinea-Bissau
    • West-central Tropical Africa
      • Rwanda
    • Western Indian Ocean
      • Comoros
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Wake Island
    • South-central Pacific
      • Easter Island
      • Society Islands
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • El Salvador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000925431
UNII 434834630Z
USDA Plants COCI4
Tropicos 100172588
INPN 966732
KEW urn:lsid:ipni.org:names:986336-1
The Plant List kew-47992
Missouri Botanical Garden 368798
Open Tree Of Life 409369
NCBI Taxonomy 34329
IUCN Red List 61905636
IPNI 986336-1
iNaturalist 334772
GBIF 5418431
Freebase /m/0fpwxk
EPPO EUCCI
EOL 301375
USDA GRIN 404658
Wikipedia Corymbia_citriodora
CMAUP NPO15538
CMAUP NPO31132

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014858505.1 Ccitriodora_v2_1 Chromosome DOE Joint Genome Institute 2020-10-21 405.0x 518.98 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The effect of ginger (Zingiber officinale L.) liquid extract on growth, immune response, antioxidant defence mechanism, and general health of Holstein calves Özkaya S, Pigamov F, Erbaş S, Mutlucan M, Arın UE, Şanlı ER Trop Anim Health Prod 11-Apr-2024
PMCID:PMC11008059
doi:10.1007/s11250-024-03972-6
PMID:38602560
Evolution of the WRKY Family in Angiosperms and Functional Diversity under Environmental Stress Wu W, Yang J, Yu N, Li R, Yuan Z, Shi J, Chen J Int J Mol Sci 21-Mar-2024
PMCID:PMC10971295
doi:10.3390/ijms25063551
PMID:38542523
Pest categorisation of Pyrrhoderma noxium 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, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Identification of m6A RNA methylation genes in Oryza sativa and expression profiling in response to different developmental and environmental stimuli Hasan M, Nishat ZS, Hasan MS, Hossain T, Ghosh A Biochem Biophys Rep 12-Mar-2024
PMCID:PMC10950732
doi:10.1016/j.bbrep.2024.101677
PMID:38511186
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Adulticidal synergy of two plant essential oils and their major constituents against the housefly Musca domestica and bioassay on non-target species Soonwera M, Moungthipmalai T, Puwanard C, Sittichok S, Sinthusiri J, Passara H Heliyon 27-Feb-2024
PMCID:PMC10920383
doi:10.1016/j.heliyon.2024.e26910
PMID:38463861
Exploring the Efficacy of Four Apiaceae Essential Oils against Nine Stored-Product Pests in Wheat Protection Kavallieratos NG, Eleftheriadou N, Boukouvala MC, Skourti A, Filintas CS, Gidari DL, Maggi F, Rossi P, Drenaggi E, Morshedloo MR, Ferrati M, Spinozzi E Plants (Basel) 15-Feb-2024
PMCID:PMC10893152
doi:10.3390/plants13040533
PMID:38498519
Study of the antimicrobial activity of zinc oxide nanostructures mediated by two morphological structures of leaf extracts of Eucalyptus radiata Droepenu EK, Amenyogbe E, Boatemaa MA, Opoku E Heliyon 07-Feb-2024
PMCID:PMC10869787
doi:10.1016/j.heliyon.2024.e25590
PMID:38370246
Chemical composition of four essential oils and their adulticidal, repellence, and field oviposition deterrence activities against Culex pipiens L. (Diptera: Culicidae) Farag SM, Moustafa MA, Fónagy A, Kamel OM, Abdel-Haleem DR Parasitol Res 25-Jan-2024
PMCID:PMC10808171
doi:10.1007/s00436-024-08118-z
PMID:38267697
Meloidogyne spp. in Eucalypts - Reproduction and Damage to Seedling Growth Lopes Vieira JO Júnior, Cunha Pereira R, Mangeiro MZ, Moreira Souza R J Nematol 23-Jan-2024
PMCID:PMC10805518
doi:10.2478/jofnem-2023-0059
PMID:38264460
Understanding Phakopsora pachyrhizi in soybean: comprehensive insights, threats, and interventions from the Asian perspective Hossain MM, Sultana F, Yesmin L, Rubayet MT, Abdullah HM, Siddique SS, Bhuiyan MA, Yamanaka N Front Microbiol 11-Jan-2024
PMCID:PMC10808435
doi:10.3389/fmicb.2023.1304205
PMID:38274768
Phytochemical screening, antioxidant activity of selected methanolic plant extracts and their detoxification capabilities against AFB1 toxicity Kongolo Kalemba MR, Makhuvele R, Njobeh PB Heliyon 11-Jan-2024
PMCID:PMC10835242
doi:10.1016/j.heliyon.2024.e24435
PMID:38312698
Preliminary Study on Total Component Analysis and In Vitro Antitumor Activity of Eucalyptus Leaf Residues Wu J, Wang Z, Cheng X, Lian Y, An X, Wu D Molecules 05-Jan-2024
PMCID:PMC10820358
doi:10.3390/molecules29020280
PMID:38257193
Exploring the versatility of sesquiterpene biosynthesis in guava plants: a comparative genome-wide analysis of two cultivars Canal D, dos Santos PH, de Avelar Carpinetti P, Silva MA, Fernandes M, Brustolini OJ, Ferreira A, da Silva Ferreira MF Sci Rep 05-Jan-2024
PMCID:PMC10770072
doi:10.1038/s41598-023-51007-1
PMID:38182724
The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M Sci Rep 21-Dec-2023
PMCID:PMC10739867
doi:10.1038/s41598-023-49696-9
PMID:38129458

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1002/JCCS.200000074
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1002/JCCS.200000074
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698428
> Lignans, neolignans and related compounds / Furanoid lignans
1,4-Bis(3,4,5-trimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 99091 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1002/JCCS.200000074
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JCCS.200000074
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JCCS.200000074
Yangambin 443028 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1002/JCCS.200000074
> 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/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/10412905.1994.9698428
https://doi.org/10.1080/10412905.1992.9698059
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/JCCS.200000074
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1002/JCCS.200000074
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/00128325.1980.11663072
https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/10412905.1994.9698428
https://doi.org/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.1080/10412905.1992.9698059
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.2000.9712194
https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.1080/10412905.1994.9698428
https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/00128325.1980.11663072
Citronellic acid 10402 Click to see CC(CCC=C(C)C)CC(=O)O 170.25 unknown https://doi.org/10.1080/10412905.1992.9698059
D-Citronellol 101977 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1994.9698428
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,3E,5S,7S)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)-1-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 10031531 Click to see CC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC(CC=C(C)C)C(=C)C)C 602.80 unknown via CMAUP database
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/10.1080/10412905.1994.9698428
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697921
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698428
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(-)-Isopulegone 10534862 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown via CMAUP database
(+)-Neoisopulegol 6553885 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.4314/BCSE.V11I1.21012
(1S,2S,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-ol 11126484 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
1alpha,3beta,4beta-p-Menthane-3,8-diol 22214620 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697921
Isopulegol 24585 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown https://doi.org/10.4314/BCSE.V11I1.21012
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.1080/10412905.1994.9698428
Menthoglycol 19100 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown https://doi.org/10.1271/BBB1961.46.319
https://doi.org/10.1016/0031-9422(84)83014-9
Neomenthoglycol 9920491 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown https://doi.org/10.1271/BBB1961.46.319
https://doi.org/10.1016/0031-9422(84)83014-9
p-Menthane-3,8-diol 556998 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown https://doi.org/10.1271/BBB1961.46.319
https://doi.org/10.1016/0031-9422(84)83014-9
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698428
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 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/10.1002/JCCS.200000074
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/10.1002/JCCS.200000074
DL-alpha-Tocopherol 2116 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/10.1002/JCCS.200000074
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,4aR,7S,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalene-1,7-diol 12304867 Click to see CC1=CC2C(CCC(C2CC1O)(C)O)C(C)C 238.37 unknown https://doi.org/10.1002/JCCS.200000074
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JCCS.200000074
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1002/JCCS.200000074
1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalene-1,7-diol 12304866 Click to see CC1=CC2C(CCC(C2CC1O)(C)O)C(C)C 238.37 unknown https://doi.org/10.1002/JCCS.200000074
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JCCS.200000074
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JCCS.200000074
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698428
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698428
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JCCS.200000074
trans-Calamenene 6429022 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1002/JCCS.200000074
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698428
(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/10.1080/10412905.1994.9698428
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698428
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698428
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a-tetradecahydropicene-4a-carboxylic acid 5319898 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/JCCS.200000074
3-Oxolup-20(29)-en-28-oic acid 289985 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/JCCS.200000074
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/JCCS.200000074
Erythrodiol 101761 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/JCCS.200000074
Morolic acid 489944 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/JCCS.200000074
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/JCCS.200000074
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1002/JCCS.200000074
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1002/JCCS.200000074
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] (Z)-11-[(2R,3R)-3-pentyloxiran-2-yl]undec-9-enoate 162872523 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)OC2CCC34CC35CCC6(C(CCC6(C5CCC4C2C)C)C(C)CCC(=C)C(C)C)C 705.10 unknown https://doi.org/10.1002/JCCS.200000074
[7,12,16-Trimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] 11-(3-pentyloxiran-2-yl)undec-9-enoate 162872522 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)OC2CCC34CC35CCC6(C(CCC6(C5CCC4C2C)C)C(C)CCC(=C)C(C)C)C 705.10 unknown https://doi.org/10.1002/JCCS.200000074
3-Epicycloeucalenol 543796 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1002/JCCS.200000074
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1002/JCCS.200000074
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
[3,4,5-triacetyloxy-6-[[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-yl]oxy]oxan-2-yl]methyl acetate 12895762 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 unknown https://doi.org/10.1002/JCCS.200000074
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/JCCS.200000074
24-Ethylcholest-5-en-3beta-ol 22012 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/JCCS.200000074
beta-Sitostenone 60123241 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1002/JCCS.200000074
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/JCCS.200000074
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.200000074
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/JCCS.200000074
Sitostenone 579897 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1002/JCCS.200000074
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1002/JCCS.200000074
Tetraacetyldaucosterol 12895763 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 unknown https://doi.org/10.1002/JCCS.200000074
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
H-gGlu-DL-Cys(1)-Gly-OH.H-gGlu-DL-Cys(1)-Gly-OH 44630308 Click to see C(CC(=O)NC(CSSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)C(=O)NCC(=O)O)C(C(=O)O)N 612.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Glutaric acid 743 Click to see C(CC(=O)O)CC(=O)O 132.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1071/CH9570093
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1071/CH9570093
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
5,11-dimethyl-6H-pyrido[4,3-b]carbazol-2-ium 5288156 Click to see CC1=C2C=C[NH+]=CC2=C(C3=C1NC4=CC=CC=C43)C 247.31 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
Rose oxide 27866 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698059
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-6-[(1R)-1-(4-hydroxyphenyl)ethyl]-7-methoxy-2,3-dihydrochromen-4-one 162946913 Click to see CC(C1=CC=C(C=C1)O)C2=C(C=C3C(=C2O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)OC 422.40 unknown https://doi.org/10.1002/MRC.1929
(2R,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(1R)-1-(4-hydroxyphenyl)ethyl]-2,3-dihydrochromen-4-one 163077411 Click to see CC(C1=CC=C(C=C1)O)C2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC=C(C=C4)O)O 408.40 unknown https://doi.org/10.1002/MRC.1929
3,5-Dihydroxy-2-(4-hydroxyphenyl)-6-[1-(4-hydroxyphenyl)ethyl]-7-methoxy-2,3-dihydrochromen-4-one 162946912 Click to see CC(C1=CC=C(C=C1)O)C2=C(C=C3C(=C2O)C(=O)C(C(O3)C4=CC=C(C=C4)O)O)OC 422.40 unknown https://doi.org/10.1002/MRC.1929
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-[1-(4-hydroxyphenyl)ethyl]-2,3-dihydrochromen-4-one 163077410 Click to see CC(C1=CC=C(C=C1)O)C2=C(C3=C(C=C2O)OC(C(C3=O)O)C4=CC=C(C=C4)O)O 408.40 unknown https://doi.org/10.1002/MRC.1929
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,4',7-Trihydroxyflavanone 3512634 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown via CMAUP database
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-3,4'-Dihydroxy-5,7-dimethoxyflavone 10403456 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(C(O2)C3=CC=C(C=C3)O)O 316.30 unknown via CMAUP database
Aromadendrin 7-methyl ether 181132 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown via CMAUP database
Eucalyptin 76573 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)OC)O 326.30 unknown via CMAUP database
Folerogenin 5319509 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Chlorophenyl)pentanedioic acid 607276 Click to see C1=CC(=CC=C1C(CC(=O)O)CC(=O)O)Cl 242.65 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Castalagin 3002104 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown via CMAUP database
CID 12302513 12302513 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown via CMAUP database
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 via CMAUP database

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