Cinnamomum camphora - Unknown
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Internal ID UUID6440112c6f66d281982969
Scientific name Cinnamomum camphora
Authority (L.) J.Presl
First published in Prir. Rostlin 2: 36 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Laurus calycina Stokes Bot. Mat. Med. 2: 421 (1812)
Laurus camphora L. Sp. Pl. : 369 (1753)
Laurus camphorifera Salisb. Prodr. Stirp. Chap. Allerton : 343 (1796)
Cinnamomum camphora var. cyclophyllum Nakai J. Jap. Bot. 19: 369. 1943
Cinnamomum camphora var. linaloolifera Y.Fujita Bot. Mag. (Tokyo) 65: 245 1952
Cinnamomum camphora f. linaloolifera (Y.Fujita) Sugim. New Keys Jap. Trees 459 1961
Cinnamomum camphora f. parvifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 195 1866
Camphora camelliifolia Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora camphora (L.) H.Karst. Ill. Repert. Pharm.-Med. Bot. : 504 (1886)
Camphora decaisnei Lukman. Nomencl. Icon. Cannel. : 23 (1878)
Camphora decandollei Lukman. Nomencl. Icon. Cannel. : 23 (1878)
Camphora hahnemannii Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora hippocratei Lukman. Nomencl. Icon. Cannel. : 21 (1878)
Camphora humboldtii Lukman. Nomencl. Icon. Cannel. : 24 (1878)
Camphora microphylla Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora neesii Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora officinarum Nees Pl. Asiat. Rar. (Wallich). 2: 72. 1831
Camphora officinarum var. glaucescens A.Braun Verh. Preuss. Ver. Gartenb. 21: 77 1852
Camphora oldhamii Lukman. Nomencl. Icon. Cannel. : 23 (1878)
Camphora pharbitifolia Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora procera Lukman. Nomencl. Icon. Cannel. : 23 (1878)
Camphora rougierii Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora sieboldii Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora syringifolia Lukman. Nomencl. Icon. Cannel. : 24 (1878)
Camphora thouarsii Lukman. Nomencl. Icon. Cannel. : 24 (1878)
Camphora thunbergii Lukman. Nomencl. Icon. Cannel. : 22 (1878)
Camphora thwaitesii Lukman. Nomencl. Icon. Cannel. : 23 (1878)
Camphora vera Raf. Sylva Tellur. : 136 (1838)
Camphora wrightii Lukman. Nomencl. Icon. Cannel. : 24 (1878)
Camphora zollingeri Lukman. Nomencl. Icon. Cannel. : 24 (1878)
Camphorina camphora (L.) Farw. Druggists' Circ. 62: 535 (1918)
Cinnamomum camphora var. glaucescens (A.Braun) Meisn. Prodr. 15(1): 24 1864
Cinnamomum camphora var. hosyo (Hatus.) J.C.Liao Quart. J. Chin. Forest. 11(3): 83 (1978)
Cinnamomum camphora var. lanatum Nakai Fl. Sylv. Kor. 22: 32 1939
Cinnamomum camphora var. nominale Hatus. & Hayata J. Coll. Sci. Imp. Univ. Tokyo 22: 349 1906
Cinnamomum camphora var. rotundifolia Makino Makinoa 8: 150 1948
Cinnamomum camphoriferum St.-Lag. Ann. Soc. Bot. Lyon 7: 122 (1880)
Cinnamomum camphoroides Hayata Icon. Pl. Formosan. 3: 158 (1913)
Cinnamomum nominale (Hatus. & Hayata) Hayata Icon. Pl. Formosan. 3: 160 (1913)
Cinnamomum officinarum Nees ex Steud. Nomencl. Bot. , ed. 2, 1: 366 (1840)
Cinnamomum simondii Lecomte Nouv. Arch. Mus. Hist. Nat. , sér. 5, 5: 73 (1913)
Cinnamomum taquetii H.Lév. Repert. Spec. Nov. Regni Veg. 10: 370 (1912)
Persea camphora (L.) Spreng. Syst. Veg. 2: 268 1825
Cinnamomum henricii Saporta ex Staub Math. Termeszettud. Értes. 19: 421 (1901)
Camphora rougieri var. glandulifera Lukman. Nomencl. Icon. Cannel.: 22 (1878)
Cinnamomum camphora subvar. hosyo Hatus. Biol. Mag. 9: 13 (1972)
Cinnamomum camphora f. cyclophyllum (Nakai) M.Kim Korean Endemic Pl.: 290 (2004)

Common names Top

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Language Common/alternative name
English camphor laurel
English camphor tree
English camphortree
English camphorwood
Spanish laurus camphora
Spanish alcanforero
Spanish arbol del alcanfor
Spanish Árbol del alcanfor
Spanish camphora camphora
ab Акамфараҵла
Afrikaans kanferboom
Arabic كافور(نبات)
Arabic كافور
Azerbaijani kamfora ağacı
Azerbaijani kafur ağacı
Belarusian Камфоравае дрэва
Bulgarian камфорово дърво
Bengali কর্পূর গাছ
Catalan camphrier
Catalan camforer
Czech kafrovník
Czech skořicovník kafrovník
Czech kafrovník lékařský
Danish kamfertræ
German kampferbaum
German campherbaum
German camphrier
German kampherbaum
dv ކާފޫރު ގަސް
Greek Καμφορά
Esperanto kamforarbo
Basque kanforrondo
Persian درخت کافور
Finnish kamferipuu
French camphrier
French ravintsara
Galician alcanforeiro
Galician Árbore da cánfora
Galician Árbore do alcanfor
Galician canforeira
Galician alcanforeira
Hindi कपूर
Croatian kamforovac
Upper Sorbian kamferowy štom
Hungarian kámforfa
Armenian կամֆորայի ծառ
Italian albero della canfora
Italian canforo
Japanese クスノキ(樟、楠)
Japanese
Japanese ナンジャモンジャ
Japanese クス
Japanese くすのき
Japanese
Japanese クスノキ
Georgian ქაფურის ხე
Kazakh Камфора ағашы
Korean 녹나무
ku dara kamfûrê
Lithuanian camphrier
lzh
Malagasy ravintsara
Malayalam കർപ്പൂരം
Malay kapur barus
Malay kapur barus jepun
Malay kapur jepun
Burmese ပရုတ်ပင်
nan chiuⁿ-á-chhiū
nan chiuⁿ-chhiū
nan chiuⁿ-á
Norwegian Bokmål kamfertre
Nepali कपुरको रूख
Dutch camphor laurel
Dutch cinnamonum camphora
Dutch kamferboom
oc camfrièr
Oriya କର୍ପୁର
Punjabi ਕਪੂਰ
Polish cynamonowiec kamforowy
Polish drzewo kamforowe
Polish kamforowiec
Portuguese canforeiro
Portuguese cânfora
Portuguese canforeira
pwn drakes
Quechua alkachchu
Quechua alkachu
Russian Камфорное дерево
Russian камфорный лавр
Russian Камфорный лавр
Russian Коричник камфорный
Russian Лавр камфорный
Slovenian kafrovec
Swedish kamferträd
Swedish camphrier
Tamil கர்பூரம் மரம்ம்
Telugu సిన్నామోనం కాంఫొర
Thai การบูร
Turkish kafur ağacı
Turkish cinnamomun camphora
Turkish kafur
Turkish kafurağacı
Ukrainian Камфорне дерево
Ukrainian Камфорний коричник
Ukrainian Камфорний лавр
Vietnamese cây long não
Vietnamese long não
za gaucah
Chinese 黄樟
Chinese 臭樟
Chinese 走马胎
Chinese 樟木
Chinese 香樟
Chinese 油樟
Chinese 樟树
Chinese 樟木子
Chinese 本樟
Chinese 栳樟
Chinese 桉油
Chinese
Chinese 樟 (香樟)
Chinese 樟(樟树)
Chinese 樟仔
Chinese 樟树叶
Chinese 樟树皮
Chinese 樟梨子
Chinese 樟樹
Chinese 樟脑
Chinese 香樟根
Chinese 鸟樟
Chinese 乌樟
Chinese 瑶人柴
Chinese 芳樟
Chinese 香樟树

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Guinea
    • West-central Tropical Africa
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
      • Pakistan
    • Indo-China
      • Cambodia
      • Laos
      • Vietnam
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Queensland
      • Victoria
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • Mississippi
      • North Carolina
      • South Carolina
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Fiji
  • Southern America
    • Caribbean
      • Leeward Islands
      • Trinidad-Tobago
    • Central America
      • El Salvador
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000604955
UNII 0B27814T7X
Florida Plant Atlas 442
Flora of Alabama 2521
USDA Plants CICA
Tropicos 17805257
INPN 447271
KEW urn:lsid:ipni.org:names:463336-1
The Plant List kew-2721183
Open Tree Of Life 849188
Observations.org 457225
NCBI Taxonomy 13429
Nature Serve 2.132610
IUCN Red List 15441072
IPNI 463336-1
iNaturalist 76341
GBIF 3033991
Freebase /m/06kk_r
EPPO CINCA
EOL 596902
Elurikkus 353646
Calflora (Californian flora) 8626
USDA GRIN 10578
Wikipedia Camphora_officinarum
CMAUP NPO6701

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
Comparative transcriptional analysis of Persea americana MYB, WRKY and AP2/ERF transcription factors following Phytophthora cinnamomi infection Fick A, Swart V, Bombarely A, van den Berg N Mol Plant Pathol 08-Apr-2024
PMCID:PMC11002358
doi:10.1111/mpp.13453
PMID:38590150
Effects of species mixing on maximum size–density relationships in Chinese fir (Cunninghamia lanceolata (Lamb.) Hook.)-dominated mixed forests converted from even-aged pure stands Han Y, Wang B, Sun H Front Plant Sci 03-Apr-2024
PMCID:PMC11024540
doi:10.3389/fpls.2024.1342307
Agriculture along the upper part of the Middle Zarafshan River during the first millennium AD: A multi-site archaeobotanical analysis Mir-Makhamad B, Lurje P, Parshuto V, Pulotov A, Aminov F, Shenkar M, Saidov M, Semenov N, Kurbanov S, Mirzaakhmedov S, Rakhmanov K, dal Martello R, Spengler R III PLoS One 28-Mar-2024
PMCID:PMC10977675
doi:10.1371/journal.pone.0297896
PMID:38547085
Identification and variation analysis of the composition and content of essential oil and fragrance compounds in Phoebe zhennan wood at different tree ages Yang H, Zhang S, Gu Y, Peng J, Huang X, Guo H, Chen L, Jiang Y, Liu M, Luo X, Xie J, Wan X Front Plant Sci 26-Mar-2024
PMCID:PMC11002133
doi:10.3389/fpls.2024.1368894
PMID:38595765
Recent advances in the potential effects of natural products from traditional Chinese medicine against respiratory diseases targeting ferroptosis Chen T, Ding L, Zhao M, Song S, Hou J, Li X, Li M, Yin K, Li X, Wang Z Chin Med 22-Mar-2024
PMCID:PMC10958864
doi:10.1186/s13020-024-00918-w
PMID:38519984
Effects of Drying Methods on the Physicochemical and Functional Properties of Cinnamomum camphora Seed Kernel Protein Isolate Ye M, Wang Z, Yan X, Zeng Z, Peng T, Xia J, Zhao J, Wang W, Gong D, Yu P Foods 21-Mar-2024
PMCID:PMC10969709
doi:10.3390/foods13060968
PMID:38540958
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
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
The accumulation of active ingredients of Polygonatum cyrtonema Hua is associated with soil characteristics and bacterial community Zhang Q, Cai Y, Zhang L, Lu M, Yang L, Wang D, Jia Q Front Microbiol 15-Mar-2024
PMCID:PMC10978593
doi:10.3389/fmicb.2024.1347204
PMID:38559348
Integration of transcriptomics and metabolomics reveals toxicological mechanisms of ZhuRiHeng drop pill in the 180-day repeated oral toxicity study Zhang Q, Wang F, Liu J, Li J, Zhang W, Na S, Lu J, Wang Y Front Pharmacol 15-Mar-2024
PMCID:PMC10978746
doi:10.3389/fphar.2024.1333167
PMID:38560353
Nuclear Magnetic Resonance Fingerprints and Mini DNA Markers for the Authentication of Cinnamon Species Ingredients Used in Food and Natural Health Products Ragupathy S, Thirugnanasambandam A, Vinayagam V, Newmaster SG Plants (Basel) 14-Mar-2024
PMCID:PMC10975438
doi:10.3390/plants13060841
PMID:38592863
Urbanization-induced soil organic carbon loss and microbial-enzymatic drivers: insights from aggregate size classes in Nanchang city, China Zhang F, Zhong J, Zhao Y, Cai C, Liu W, Wang Q, Wang W, Wang H, Jiang X, Yuan R Front Microbiol 28-Feb-2024
PMCID:PMC10933064
doi:10.3389/fmicb.2024.1367725
PMID:38481789
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Integrative management of insomnia during cancer chemotherapy: A case report Arathi P, Sreejith K, Pavithran K, Soman D J Ayurveda Integr Med 19-Feb-2024
PMCID:PMC10885578
doi:10.1016/j.jaim.2024.100899
PMID:38377655

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
1,10-Dimethoxy-6a-alpha-noraporphine-2,9-diol 628557 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1248/YAKUSHI1947.84.4_365
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1248/YAKUSHI1947.84.4_365
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Anethole, (Z)- 1549040 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
malyngamide M 10623415 Click to see CCCCCCCC(CC=CCCC(=O)N(C)CC(=CCl)C1=CC=CC(=C1O)C)OC 450.10 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
CID 499033 499033 Click to see [CH]1[CH][C]2[CH][C]=[C][C]=[C][C]2[CH]1 124.14 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Octatriene, dimethyl- 6434062 Click to see CC(C)C=CC=C(C)C=C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698258
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Cyclic olefins / Azulenes
Azulene 9231 Click to see C1=CC=C2C=CC=C2C=C1 128.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Paulownin 13747828 Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6 370.40 unknown via CMAUP database
(-)-Sesamin 382073 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 5315338 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1002/JCCS.198400021
Paulownin 3084131 Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6 370.40 unknown via CMAUP database
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.198400021
Xanthoxylol 130679 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1002/JCCS.198400021
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3,4-Bis(3,4-dimethoxybenzyl)tetrahydrofuran-2-one 10894352 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC)OC)OC 386.40 unknown via CMAUP database
Kusunokinin 384876 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1246/BCSJ.50.2821
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl 9-octadecenoate 8123 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC 310.50 unknown https://doi.org/10.1002/PS.3961
Ethyl oleate 5363269 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC 310.50 unknown https://doi.org/10.1002/PS.3961
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R,6S)-2,6-dimethylocta-1,7-diene-3,6-diol 154495976 Click to see CC(=C)C(CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)89020-2
[(2R)-2,3-dihydroxypropyl] 24-hydroxytetracosanoate 162960853 Click to see C(CCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCO 458.70 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
[(2R)-2,3-dihydroxypropyl] 28-hydroxyoctacosanoate 163075659 Click to see C(CCCCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCCCO 514.80 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
2,3-Dihydroxypropyl 28-hydroxyoctacosanoate 71350505 Click to see C(CCCCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCCCO 514.80 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
2,6-Dimethylocta-1,7-diene-3,6-diol 548927 Click to see CC(=C)C(CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)89020-2
Tetracosanoic acid, 24-hydroxy-, 2,3-dihydroxypropyl ester 10072879 Click to see C(CCCCCCCCCCCC(=O)OCC(CO)O)CCCCCCCCCCCO 458.70 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoate 5867807 Click to see CCCCCC=CCC=CCCCCCCCC(=O)[O-] 279.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-ol 4458 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1246/NIKKASHI1921.64.1125
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698258
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1246/NIKKASHI1921.64.1125
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698258
https://doi.org/10.1590/S1516-89132000000300011
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698258
> 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 via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1246/NIKKASHI1921.64.1125
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1246/BCSJ.50.2821
(4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 23308299 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(R)-Fenchone; L-(-)-Fenchone; L-Fenchone; l-Fenchone 2794921 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698258
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1246/BCSJ.50.2821
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1093/JAT/9.1.24
https://doi.org/10.1080/10412905.1998.9700962
https://doi.org/10.1590/S1516-89132000000300011
https://doi.org/10.1080/10412905.1993.9698258
cis-Thujenol 91746682 Click to see CC1=CC(C2(C1C2)C(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1993.9698258
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
malyngamide I acetate 6440420 Click to see CCCCCCCC(CC=CCCC(=O)N(C)CC(=CCl)C12C(O1)CC(C(C2=O)C)OC(=O)C)OC 526.10 unknown via CMAUP database
Malyngamide N 10528184 Click to see CCCCCCCC(CC=CCCC(=O)N(C)CC(=CCl)C12C(O1)CC=C(C2=O)C)OC 466.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1993.9698258
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1246/NIKKASHI1921.64.1125
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698258
https://doi.org/10.1246/NIKKASHI1921.64.1125
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
gamma-Camphorene 5315649 Click to see CC(=CCCC1=CCCC(C1)C(=C)CCC=C(C)C)C 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1080/10412905.1993.9698258
(3S,4aS)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,4,4a,5,6,8a-octahydronaphthalene 5315586 Click to see CC1CCC2C(C1)C(CC=C2C)C(=C)C 204.35 unknown via CMAUP database
(5E)-10-hydroxy-2,6,10-trimethyldodeca-2,5,11-trien-4-one 5322107 Click to see CC(=CC(=O)C=C(C)CCCC(C)(C=C)O)C 236.35 unknown via CMAUP database
(6Z,10E)-12-hydroxy-2,6,10-trimethyldodeca-2,6,10-trien-4-one 5320326 Click to see CC(=CC(=O)CC(=CCCC(=CCO)C)C)C 236.35 unknown via CMAUP database
[(E)-3-methyl-4-(3-methyl-5-oxo-6-propan-2-ylidenecyclohex-2-en-1-yl)but-2-enyl] acetate 5320327 Click to see CC1=CC(C(=C(C)C)C(=O)C1)CC(=CCOC(=O)C)C 276.40 unknown via CMAUP database
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1246/BCSJ.41.234
alpha-Bulnesene 520826 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
alpha-Calacorene 12302243 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1246/BCSJ.41.234
alpha-Camphorene 101750 Click to see CC(=CCCC1=CCC(CC1)C(=C)CCC=C(C)C)C 272.50 unknown via CMAUP database
alpha-Corocalene 5316074 Click to see CC1=CC2=C(C=CC(=C2CC1)C)C(C)C 200.32 unknown https://doi.org/10.1246/BCSJ.41.234
alpha-Santalene 94164 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 204.35 unknown via CMAUP database
beta-Santalene 10889018 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1246/NIKKASHI1921.64.1125
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown via CMAUP database
Campherenone 5315646 Click to see CC(=CCCC1(C2CCC1(C(=O)C2)C)C)C 220.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698258
https://doi.org/10.1246/NIKKASHI1921.64.1125
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1993.9698258
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698258
delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698258
Norbornane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)- 10534 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
trans-Calamenene 6429022 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1246/BCSJ.41.234
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(3aR,4S,6R,7R,7aR)-4-acetyloxy-6-ethenyl-3-methylidene-2-oxo-7-(3-oxoprop-1-en-2-yl)-4,5,7,7a-tetrahydro-3aH-1-benzofuran-6-yl]methyl acetate 162930686 Click to see CC(=O)OCC1(CC(C2C(C1C(=C)C=O)OC(=O)C2=C)OC(=O)C)C=C 362.40 unknown https://doi.org/10.1246/BCSJ.41.234
> 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/JCCS.198400021
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.198400021
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.198400021
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.198400021
> Organic Polymers / Polypeptides
Cinnamomin 139584655 Click to see CCC(C)C(C(=O)NC(CC(C)C)C(=O)NC(CO)C(=O)NC(CCC(=O)O)C(=O)NC(CO)C(=O)NC(CO)C=O)NC(=O)C(CO)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(C(C)O)NC(=O)C(CCCCN)NC(=O)C(CC1=CC=C(C=C1)O)NC(=O)C(C)NC(=O)C(C)NC(=O)C(C(C)O)NC(=O)C(CCC(=O)N)NC(=O)C(CCC(=O)N)NC(=O)C(C(C)O)NC(=O)C(C)NC(=O)C(C(C)O)NC(=O)C(CS)NC(=O)C(C)NC(=O)C(C(C)O)N 2358.60 unknown https://doi.org/10.1002/(SICI)1099-0844(199609)14:3<157::AID-CBF667>3.3.CO;2-N
https://doi.org/10.1016/S0041-0101(99)00078-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
4-Methyl-2-pentanol 7910 Click to see CC(C)CC(C)O 102.17 unknown https://doi.org/10.1080/10412905.1993.9698258
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3E,6S)-2,6-Dimethylocta-3,7-diene-2,6-diol 15241420 Click to see CC(C)(C=CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)89020-2
(4R,5R)-5-dodecyl-4-hydroxy-4-methylcyclopent-2-en-1-one 163039676 Click to see CCCCCCCCCCCCC1C(=O)C=CC1(C)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)81896-8
2-[(1S,8S)-1,8-dimethyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl]propan-2-ol 5318906 Click to see CC1CCC=C2C1C(C(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
2,6-Dimethylocta-3,7-diene-2,6-diol 527050 Click to see CC(C)(C=CCC(C)(C=C)O)O 170.25 unknown https://doi.org/10.1016/S0031-9422(00)89020-2
5-Dodecanyl-4-hydroxy-4-meth-yl-2-cyclopentenone 129695700 Click to see CCCCCCCCCCCCC1C(=O)C=CC1(C)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)81896-8
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown via CMAUP database
CID 10487440 10487440 Click to see C=CCC1=CC2=C(C=C1)OCO2 174.14 unknown via CMAUP database
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown https://doi.org/10.1080/10412905.1993.9698258
https://doi.org/10.1246/NIKKASHI1921.64.1125
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown via CMAUP database
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
3-Dodec-11-enylidene-4-hydroxy-5-methylideneoxolan-2-one 71438578 Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
4-Hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one 76005700 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Isolinderanolide B 53308122 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Isomahubannolide-23 46237230 Click to see CCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 364.60 unknown via CMAUP database
Isooblusilactonc A 6442493 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Isoobtusilactone 5318618 Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Obtusilactone 6442495 Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Obtusilactone A 6442492 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
(3E)-3-dodec-11-enylidene-4-hydroxy-5-methylideneoxolan-2-one 14259080 Click to see C=CCCCCCCCCCC=C1C(C(=C)OC1=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamate 5957728 Click to see C1=CC=C(C=C1)C=CC(=O)[O-] 147.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Octacosyl (E)-ferulate 5743442 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 586.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1002/JCCS.198400021
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B8 474541 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3R)-2-(Benzo[d][1,3]dioxol-5-yl)-5,7-dimethoxychroman-3-ol 10336729 Click to see COC1=CC2=C(CC(C(O2)C3=CC4=C(C=C3)OCO4)O)C(=C1)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
3,4'-Dihydroxy-3',5,7-trimethoxyflavan 68795440 Click to see COC1=CC2=C(CC(C(O2)C3=CC(=C(C=C3)O)OC)O)C(=C1)OC 332.30 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
3',4'-Methylenedioxy-5,7-dimethylepicatechin 71307295 Click to see COC1=CC2=C(CC(C(O2)C3=CC4=C(C=C3)OCO4)O)C(=C1)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
Epicatechin 5,7,3'-trimethyl ether 6482487 Click to see COC1=CC2=C(CC(C(O2)C3=CC(=C(C=C3)O)OC)O)C(=C1)OC 332.30 unknown https://doi.org/10.1016/S0031-9422(00)89583-7
> Phenylpropanoids and polyketides / Macrolides and analogues
[(1R)-1-[(1S,3R,4S,5S,9R,13S,14R)-13-hydroxy-3-[(2S,5S)-5-(3-hydroxyphenyl)-5-methoxypentan-2-yl]-4,14,16,16-tetramethyl-7,11-dioxo-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadecan-9-yl]ethyl] acetate 21672112 Click to see CC1CC(C23CC(C(C(O2)C(C)CCC(C4=CC(=CC=C4)O)OC)C)OC(=O)CC(OC(=O)CC1(O3)O)C(C)OC(=O)C)(C)C 634.80 unknown via CMAUP database
Anhydrodebromaplysiatoxin 393063 Click to see CC1C2CC3(C(CC(=C(O3)CC(=O)OC(CC(=O)O2)C(C)O)C)(C)C)OC1C(C)CCC(C4=CC(=CC=C4)O)OC 574.70 unknown via CMAUP database
Aplysiatoxin 21672114 Click to see CC1CC(C23CC(C(C(O2)C(C)CCC(C4=C(C=CC(=C4)O)Br)OC)C)OC(=O)CC(OC(=O)CC1(O3)O)C(C)O)(C)C 671.60 unknown via CMAUP database
Debromoaplysiatoxin 5352033 Click to see CC1CC(C23CC(C(C(O2)C(C)CCC(C4=CC(=CC=C4)O)OC)C)OC(=O)CC(OC(=O)CC1(O3)O)C(C)O)(C)C 592.70 unknown via CMAUP database
Manauealide B 21672113 Click to see CC1CC(C23CC(C(C(O2)C(C)CCC(C4=CC(=C(C=C4)Br)O)OC)C)OC(=O)CC(OC(=O)CC1(O3)O)C(C)O)(C)C 671.60 unknown via CMAUP database

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