Details Top

Internal ID UUID643fe2387d65f263778637
Scientific name Magnolia kobus
Authority DC.
First published in Syst. Nat. 1: 456 (1817)

Ethnobotanical Use Top

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General Uses Top

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Wood and fiber:
The light-colored, fine-grained wood of Magnolia kobus is used for furniture, veneer, interior joinery, and carving. Logs and residuals also supply pulpwood chips to the kraft and mechanical pulp industries for printing and writing papers. The species is suitable for high-grade fiberboard and plywood. Moderate density and low shrinkage characteristics influence these applications.

Industrial and craft applications:
Plywood and fiberboard panels are made from veneer or reconstituted wood. Softwood pulpwood chips contribute to the bleached and unbleached kraft grades used in paper manufacture. Bark has been evaluated for fiberboard adhesives in East Asian studies, but commercial adoption remains limited.

Fragrance and cosmetics:
Flowers yield essential oil and absolute by steam distillation or solvent extraction. These extracts are used by perfumery and soap manufacturers for their sweet-floral note. They are not widely commercialized but are listed in ingredient resources and cited for their constituent aromatics, including phenylpropanoids such as estragole.

Scientific/model use:
Magnolia kobus is a research subject in woody plant biology, phenology, developmental genetics, and evolutionary studies. It is a reference species for phylogenetic and population-genetics work within Magnolia. Genomic resources (e.g., genome assemblies and transcriptomes) are available through public databases, and the species is used for protocol development, phenotyping pipelines, and comparative genomics.

Standards and regulation:
Forest products and timber must meet national grading, processing, and CITES export rules where applicable. Cosmetic uses of essential oil/absolutes are subject to INCI naming and IFRA fragrance safety guidelines; no health or medicinal claims are made for cosmetic applications.

Sustainability and sourcing:
Supply is regional. If harvested from wild populations, follow sustainable management and any applicable CITES controls for Magnoliaceae. Plantation-grown or mixed hardwood-origin chips for pulping may reduce pressure on wild stocks.

Synonyms Top

Scientific name Authority First published in
Magnolia borealis Kudô Medic. Pl. Hokkaido : 47 (1922)
Magnolia kobus var. borealis Sarg. Trees & Shrubs 2: 57. 1908
Magnolia kobushi Mayr Fremdländ. Wald-Parkbäume : 484 (1906)
Magnolia praecocissima Koidz. Bot. Mag. (Tokyo) 43: 386 (1929)
Magnolia pseudokobus Abe & Akasawa Bull. Kochi Women's Coll. 2: 104, 110 (1954)
Magnolia thurberi hort. ex Gard. Kew i. Polypet. (1894) 17.
Michelia gracilis Kostel. Allg. Med.-Pharm. Fl. 5: 1701 (1836)
Yulania kobus (DC.) Spach Hist. Nat. Vég. 7: 467. 1839 (1839)
Buergeria obovata Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 187 (1845)
Talauma obovata (Siebold & Zucc.) Benth. & Hook.f. ex Hance J. Bot. 20: 2 (1882)
Magnolia kobus f. horisontalidivaricata V.V.Byalt & Firsov Hortus Botanicus 14: 43 (2019)

Common names Top

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Language Common/alternative name
English northern japanese magnolia
English kobushi magnolia
English kobus magnolia
Spanish yulania kobus
Spanish talauma obovata
Spanish magnolia thurberi
Spanish magnolia pseudokobus
Spanish magnolia borealis
Spanish buergeria obovata
Spanish michelia gracilis
Arabic مغنولية كوبوس
Azerbaijani kobus maqnoliyası
Czech magnólie japonská
Czech šácholan japonský
German baummagnolie
German kobushi-magnolie
Estonian hondo magnoolia
Finnish japaninmagnolia
Hungarian fehér liliomfa
Hungarian japán liliomfa
Armenian մագնոլիա կոբուս
Japanese コブシ
Japanese 辛夷
Japanese
Japanese シンイ
Japanese キタコブシ
Korean 목련
koi Кобуши магнолия
Norwegian Bokmål snømagnolia
Russian Магнолия кобус
Russian Магнолия кобуси
Russian Магнолия Кобуси
Slovenian kobuši magnolija
Swedish japansk magnolia
udm Кобуши магнолия
Chinese 日本辛夷

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
remove pulpy coat with detergent washes; germination unlikely if dried by just 20%, store seeds @ 4°C

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Ontario
    • Northeastern U.S.A.
      • New York
      • Pennsylvania

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000233225
UNII K1XWN9D74Y
Canadensys 32638
USDA Plants MAKO
UConn 275
Tropicos 19300152
INPN 107143
Flora of Italy 10277
KEW urn:lsid:ipni.org:names:332100-2
The Plant List kew-117662
Missouri Botanical Garden 282534
PFAF Magnolia kobus
PaleoBotany 6955
Open Tree Of Life 664531
NCBI Taxonomy 54732
IUCN Red List 193954
IPNI 332100-2
iNaturalist 143787
GBIF 3153260
Freebase /m/02ph16r
EPPO MAGKO
EOL 1154977
Elurikkus 5620
USDA GRIN 23113
Wikipedia Magnolia_kobus
CMAUP NPO1918

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Pharmacological potential of micheliolide: A focus on anti-inflammatory and anticancer activities Uddin J, Fatima M, Riaz A, Kamal GM, Muhsinah AB, Ahmed AR, Iftikhar R Heliyon 05-Mar-2024
PMCID:PMC10944196
doi:10.1016/j.heliyon.2024.e27299
PMID:38496875
Adjuvant Novel Nanocarrier-Based Targeted Therapy for Lung Cancer Sarma K, Akther MH, Ahmad I, Afzal O, Altamimi AS, Alossaimi MA, Jaremko M, Emwas AH, Gautam P Molecules 29-Feb-2024
PMCID:PMC10934468
doi:10.3390/molecules29051076
PMID:38474590
Bimetallic nanoparticle production using Cannabis sativa and Vitis vinifera waste extracts Michailidu J, Miškovská A, Jarošová I, Čejková A, Mat’átková O RSC Adv 09-Feb-2024
PMCID:PMC10854393
doi:10.1039/d3ra07134k
PMID:38343999
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Fine-Root Distribution and Soil Physicochemical Property Variations in Four Contrasting Urban Land-Use Types in South Korea Tran LT, An JY, Carayugan MB, Hernandez JO, Rahman SA, Youn WB, Carvalho JI, Jo MS, Han SH, Nguyen HH, Park BB Plants (Basel) 07-Jan-2024
PMCID:PMC10821101
doi:10.3390/plants13020164
PMID:38256718
Disruptive Effects of Two Curcuminoids (Demethoxycurcumin and Bisdemethoxycurcumin) on the Larval Development of Drosophila melanogaster Jeon JH, Jeong SA, Park DS, Park HH, Shin SW, Oh HW Insects 18-Dec-2023
PMCID:PMC10744261
doi:10.3390/insects14120959
PMID:38132632
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Biological Synthesis of Copper Nanoparticles Using Edible Plant Allium monanthum: Characterization of Antibacterial, Antioxidant, and Anti-Inflammatory Properties Using In Silico Molecular Docking Analysis Han HS, Jung JS, Jeong YI, Choi KC Materials (Basel) 12-Oct-2023
PMCID:PMC10608194
doi:10.3390/ma16206669
PMID:37895651
A comprehensive review on potential applications of metallic nanoparticles as antifungal therapies to combat human fungal diseases Madkhali OA Saudi Pharm J 06-Aug-2023
PMCID:PMC10463261
doi:10.1016/j.jsps.2023.101733
PMID:37649674
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095

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
> Alkaloids and derivatives / Aporphines
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1007/BF01170231
1-Methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol 12308663 Click to see 267.32 unknown https://doi.org/10.1007/BF02234867
1,2-Methylenedioxynoraporphine 3462225 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1007/BF02234867
Asimilobine 25774982 Click to see 267.32 unknown https://doi.org/10.11110/KJPT.1985.15.3.145
https://doi.org/10.1007/BF02234867
https://doi.org/10.1007/BF01170231
Lanuginosine 97622 Click to see 305.30 unknown https://doi.org/10.1007/BF02234867
Lauterine 73104 Click to see COC1=CC2=C(C=C1)C(=O)C3=NC=CC4=CC5=C(C2=C43)OCO5 305.30 unknown https://doi.org/10.11110/KJPT.1985.15.3.145
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1007/BF01170231
R-(-)-asimilobine 160875 Click to see 267.32 unknown https://doi.org/10.1007/BF01170231
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1007/BF01170231
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Ethylstyrene 18940 Click to see CCC1=CC=C(C=C1)C=C 132.20 unknown https://doi.org/10.5650/JOS.60.591
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-Hydroxy-4-methoxy-N,N,N-trimethylbenzeneethanaminium 160877 Click to see 210.29 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1,3,5,5-Tetramethyl-1,3-cyclohexadiene 78453 Click to see 136.23 unknown via CMAUP database
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Fargesin 10926754 Click to see 370.40 unknown via CMAUP database
(+)-Epimagnolin A 21722943 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown via CMAUP database
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1016/S0031-9422(97)00458-5
https://doi.org/10.1002/HLCA.200890256
(3R,3aS,6R,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 325601 Click to see 386.40 unknown via CMAUP database
(3R,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 7299790 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
(3S,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 11870582 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1016/0031-9422(82)83163-4
https://doi.org/10.1002/HLCA.200890256
1,4-Bis(3,4,5-trimethoxyphenyl)tetrahydro-1H,3H-furo(3,4-c)furan 99091 Click to see 446.50 unknown https://doi.org/10.1002/HLCA.200890256
https://doi.org/10.1007/S10600-008-9093-0
2,3-Dimethoxy-5-[6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenol 162912276 Click to see 432.50 unknown https://doi.org/10.1002/HLCA.200890256
3-(3,4-Dimethoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 5319210 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1016/J.PHYMED.2008.04.012
https://doi.org/10.1002/HLCA.200890256
4-[(3S,3aS,6S,6aS)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 12314159 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
5-[(3R,3aS,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 7059611 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
5-[(3R,3aS,6S,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 162875204 Click to see 370.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
5-[(3S,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 102034302 Click to see 386.40 unknown https://doi.org/10.1002/HLCA.200890256
5-[(3S,3aR,6S,6aR)-3-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 162901384 Click to see 402.40 unknown https://doi.org/10.1007/S10600-008-9093-0
5-[(3S,3aR,6S,6aR)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,3-dimethoxyphenol 102034301 Click to see 432.50 unknown https://doi.org/10.1002/HLCA.200890256
5-[3-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 163020895 Click to see 386.40 unknown https://doi.org/10.1002/HLCA.200890256
5-[3-(3,4-Dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,3-dimethoxyphenol 162901383 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)O)OC 402.40 unknown https://doi.org/10.1007/S10600-008-9093-0
Epimagnolin A 10454576 Click to see 416.50 unknown via CMAUP database
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/10.1080/00021369.1975.10861682
https://doi.org/10.1002/HLCA.200890256
https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1016/0031-9422(82)83163-4
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1002/HLCA.200890256
Medioresinol dimethyl ether 169234 Click to see 416.50 unknown https://doi.org/10.1016/J.PHYMED.2008.04.012
https://doi.org/10.1002/HLCA.200890256
Methylpiperitol;O-Methylpiperitol; Spinescin 12697524 Click to see 370.40 unknown via CMAUP database
Npc268574 5320622 Click to see 370.40 unknown https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1016/0031-9422(82)83163-4
https://doi.org/10.1002/HLCA.200890256
Phillygenol; Epipinoresinol methyl ether; (+)-Phillygenin 4166098 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1016/0031-9422(82)83163-4
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/10.1080/00021369.1975.10861682
https://doi.org/10.1007/S10600-008-9093-0
https://doi.org/10.1002/HLCA.200890256
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1007/BF01170231
https://doi.org/10.1007/BF02234867
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1007/BF01170231
https://doi.org/10.11110/KJPT.1985.15.3.145
https://doi.org/10.1007/BF02234867
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/HLCA.200890256
https://doi.org/10.1007/S10600-008-9093-0
> 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
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
Citronellol 8842 Click to see 156.26 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.5650/JOS.60.591
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(-)-Fenchone 82229 Click to see 152.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown via CMAUP database
(+-)-Fenchone 14525 Click to see 152.23 unknown via CMAUP database
(+)-4-Carene 71351627 Click to see 136.23 unknown via CMAUP database
(+)-Bornyl acetate 6950274 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-Fenchone 1201521 Click to see 152.23 unknown via CMAUP database
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate 443131 Click to see 196.29 unknown via CMAUP database
(1R)-Camphor 230921 Click to see 152.23 unknown via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate 442460 Click to see 196.29 unknown via CMAUP database
(1s)-1,3,3-Trimethyl-norbornan-2-one 12049113 Click to see 152.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-one 16213045 Click to see 152.23 unknown via CMAUP database
(R)-Fenchone; L-(-)-Fenchone; L-Fenchone; l-Fenchone 2794921 Click to see 152.23 unknown via CMAUP database
4-[1-(1,3-Benzodioxol-5-yl)-1-oxopropan-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 14130915 Click to see 370.40 unknown via CMAUP database
4-Carene, (1S,3R,6R)-(-)- 530422 Click to see 136.23 unknown via CMAUP database
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
alpha-Thujene 17868 Click to see 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown via CMAUP database
Camphor 2537 Click to see 152.23 unknown via CMAUP database
D-Camphor 159055 Click to see 152.23 unknown via CMAUP database
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
Npc54264 9543187 Click to see 152.23 unknown via CMAUP database
Sabinene 18818 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
beta-Terpinene 66841 Click to see CC(C)C1=CCC(=C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene 12306052 Click to see 204.35 unknown via CMAUP database
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(+)-alpha-Muurolene 12306049 Click to see 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see 204.35 unknown via CMAUP database
(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal 5280598 Click to see 220.35 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(5R)-3,8-dimethyl-5-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene 91748288 Click to see 204.35 unknown via CMAUP database
(6S,7E,10S)-6-hydroperoxy-10-hydroxy-2,6,10-trimethyldodeca-2,7,11-trien-4-one 163024742 Click to see 268.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
(7S,10S)-7-hydroperoxy-10-hydroxy-2,10-dimethyl-6-methylidenedodeca-2,11-dien-4-one 162895197 Click to see 268.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
(Z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one 5356787 Click to see CC1=CCCC(C1C=C(C)C(=O)C)(C)C 206.32 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see 204.35 unknown via CMAUP database
1-epi-Bicyclosesquiphellandrene 521496 Click to see 204.35 unknown via CMAUP database
1-Isopropyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydro-4a(2H)-naphthalenol 519857 Click to see 222.37 unknown via CMAUP database
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown via CMAUP database
10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one 71364441 Click to see 236.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one 5372174 Click to see 206.32 unknown via CMAUP database
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown via CMAUP database
3,7-Dimethyl-4-(propan-2-yl)-3a,3b,4,5,6,7-hexahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzene 86609 Click to see 204.35 unknown via CMAUP database
6-Hydroperoxy-10-hydroxy-2,6,10-trimethyldodeca-2,7,11-trien-4-one 129686024 Click to see 268.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
7-Hydroperoxy-10-hydroxy-2,10-dimethyl-6-methylidenedodeca-2,11-dien-4-one 14021431 Click to see 268.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
9-Oxonerolidol 73331190 Click to see 236.35 unknown https://doi.org/10.1016/0031-9422(82)83163-4
alpha-Panasinsene 578929 Click to see 204.35 unknown via CMAUP database
alpha-Patchoulene 521710 Click to see 204.35 unknown via CMAUP database
beta-Cadinene 10657 Click to see 204.35 unknown via CMAUP database
Cadin-4-en-10-ol 519662 Click to see 222.37 unknown via CMAUP database
Calamenene 6429077 Click to see 202.33 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown via CMAUP database
Elixene 94254 Click to see 204.35 unknown via CMAUP database
gamma-Cadinene 6432404 Click to see 204.35 unknown via CMAUP database
Isocadinene 595385 Click to see 204.35 unknown https://doi.org/10.5650/JOS.60.591
Npc109838 6427091 Click to see 204.35 unknown via CMAUP database
Npc57877 6431302 Click to see 222.37 unknown via CMAUP database
tau-Muurolol 6432221 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
trans-Muurola-4(14),5-diene 91747125 Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C 204.35 unknown via CMAUP database
Tricyclo[4.4.0.0(2,7)]dec-3-ene, 8-isopropyl-1,3-dimethyl-, (1S,2R,6R,7R,8S)-(+)- 6432119 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown via CMAUP database
Npc30025 6432176 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1H-Cycloprop(e)azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, (1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha))- 6432640 Click to see 220.35 unknown via CMAUP database
1H-Cycloprop(e)azulene, 1a,2,3,4,4a,5,6,7b-octahydro-1,1,4,7-tetramethyl-, (1aR,4R,4aR,7bS)- 521243 Click to see 204.35 unknown via CMAUP database
beta-Spathulenol 522266 Click to see 220.35 unknown via CMAUP database
Npc143639 6432706 Click to see 220.35 unknown via CMAUP database
Spathulenol 92231 Click to see 220.35 unknown via CMAUP database
Spathulenol, (-)- 13854255 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
15-Demethyl plumieride 453214 Click to see 456.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
alpha-Linalool 69016 Click to see 154.25 unknown via CMAUP database
Linalool oxide (5-ring) 102611 Click to see 170.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Nystose 166775 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)COC3(C(C(C(O3)CO)O)O)COC4(C(C(C(O4)CO)O)O)CO)O)O)O)O 666.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
1,10-Epoxy-4-methoxy-7-methyl-8-(3,4-methylenedioxyphenyl)-spiro(5,5)undeca-1,4-dien-3-one 596172 Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5 340.40 unknown https://doi.org/10.1016/J.JCHROMB.2011.10.023
Fargesone A 442838 Click to see 372.40 unknown https://doi.org/10.1016/J.JCHROMB.2011.10.023
Futoenone 9819306 Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5 340.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(1S,8R,10S,11R)-3-methoxy-11-methyl-10-(3,4,5-trimethoxyphenyl)-7-oxatricyclo[6.3.1.01,6]dodeca-2,5-dien-4-one 91895474 Click to see 386.40 unknown via CMAUP database
CID 21723002 21723002 Click to see 386.40 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Cocculin 6473767 Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O 602.60 unknown via CMAUP database
Picrotoxin 31304 Click to see CC(=C)C1C2C3C4(C(C1C(=O)O2)(CC5C4(O5)C(=O)O3)O)C.CC12C3C4C(C(C1(CC5C2(O5)C(=O)O3)O)C(=O)O4)C(C)(C)O 602.60 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Magnoline 362563 Click to see 596.70 unknown https://doi.org/10.1016/J.JCHROMB.2011.10.023
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown via CMAUP database
Rose oxide 27866 Click to see 154.25 unknown https://doi.org/10.5650/JOS.60.591
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Hydrazinonicotinic acid 585323 Click to see 153.14 unknown https://doi.org/10.5650/JOS.60.591
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide 22310 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
Linalool oxide, cis- 6428573 Click to see 170.25 unknown via CMAUP database
trans-Linalool oxide 6432254 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database

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