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Tectona grandis

Tectona grandis - 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 UUID643feec021af9507424560
Scientific name Tectona grandis
Authority L.f.
First published in Suppl. Pl. : 151 (1782)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Jatus grandis Kuntze Revis. Gen. Pl. 2: 508 (1891)
Tectona grandis f. canescens Moldenke Phytologia 31: 28 (1975)
Tectona grandis f. pilosula Moldenke Phytologia 31: 28 (1975)
Tectona grandis f. punctata Moldenke Phytologia 31: 28 (1975)
Tectona grandis f. tomentella Moldenke Phytologia 31: 28 (1975)
Tectonia theca Lour. Fl. Cochinch. 1: 137. 1790 [Sep 1790]
Theka grandis Lam. Tabl. Encycl. 2: 111 (1797)
Tectona grandis f. abludens Koord. & Valeton Bijdr. Boomsoort. Java 7: 171 1900

Common names Top

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Language Common/alternative name
English teak
English common teak
English teak tree
Spanish teca
ace jatoë
Arabic شجر التيك
Arabic ساج كبير
Arabic ساج
Arabic الدلب الهندي
Arabic شجرة الساج
ban jati
bho सागौन
Bengali সেগুন
Catalan teca
Czech teak
Czech týk
Czech teka obrovská
Danish teaktræ
dag aluura
German teakbaum
German teak
German teakholz
German teakbäume
German thekholz
Greek τικ
Esperanto granda tektono
Estonian suur tiikpuu
Basque teka
Persian چوب ساج
Persian ساج
Finnish tiikki
French teck
Irish téac
Galician teca
Gujarati સાગ
Hebrew טיק
Hindi साग
Hindi सागवान
Hindi टीकवुड
Hindi सागौन
Croatian obični tik
Upper Sorbian hoberski teakowc
Hungarian indiaitölgy
Hungarian tikfa
Hungarian tíkfa
Hungarian teakfa
Armenian կաղնի հնդկական
Armenian տեքի
Indonesian kayu jati
Indonesian pohon jati
Indonesian jati
io teko
Italian teak
Italian teck
Italian legno teak
Japanese チーク材
Japanese チーク
jv jati
Georgian ტექის ხე
Kazakh Тик
Kannada ತೇಗ
Kannada ಸಾಗುವಾನಿ
Korean 티크
Lithuanian tikmedis
mad jhâtè
Macedonian тик
Macedonian тиково дрво
Malayalam തേക്ക്
Malayalam ടെക്റ്റോണ ഗ്രാൻഡിസ്
mnw တၞံဆုကၠ
Marathi साग
Marathi सागवान
Marathi टेक्टोना
Malay pokok jati
Burmese ကျွန်းသစ်
Burmese ကျွန်း(အပင်)
Norwegian Bokmål teak
Dutch djati
Dutch teakboom
Norwegian Nynorsk teaktre
Norwegian Nynorsk teak
oc tèc
Punjabi ਟੀਕ
Polish dąb indyjski
Polish teczyna wyniosła
Punjab ٹیک
Punjab ساگوان
Punjab ساگواݨ
Portuguese teca
Romanian tec
Russian Тиковое дерево
Sinhala sinhala languages
Slovak teak
Slovak tíkové drevo
Slovak tík
Slovenian pravi tikovec
Slovenian tikovina
Slovenian tikovec
su jati
Swedish teak
Tamil தேக்கு
tcy ತೆಕ್ಕಿದಮರ
Telugu టెక్టోనా
Telugu టేకు చెట్టు
Telugu టేకు చెట్లు
Telugu టేకు
Thai สัก
Thai ต้นสัก
Thai ไม้สัก
Turkish tik ağacı
Turkish tikağacı
Ukrainian Тік
Urdu ساگوان
Vietnamese giá tị
Vietnamese giá tỵ
Vietnamese tếch
Chinese 柚木
Chinese 紫油木
Chinese 紫柚木
Chinese 脂树

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Gambia
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Comoros
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
  • Southern America
    • Caribbean
      • Southwest Caribbean
      • Trinidad-Tobago
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000321229
UNII 0L0OS9IILV
USDA Plants TEGR
Tropicos 33700544
INPN 447682
KEW urn:lsid:ipni.org:names:864923-1
The Plant List kew-202018
Missouri Botanical Garden 287459
PFAF Tectona grandis
Open Tree Of Life 738848
Observations.org 455796
NCBI Taxonomy 41396
Nature Serve 2.159429
IUCN Red List 62019830
IPNI 864923-1
iNaturalist 62887
GBIF 2925649
Freebase /m/01s5tq
EPPO TCTGR
EOL 579742
Elurikkus 7850
USDA GRIN 80123
Wikipedia Teak
CMAUP NPO18640

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
New Understanding of Meta-Topolin Riboside Metabolism in Micropropagated Woody Plants Grira M, Prinsen E, Werbrouck S Plants (Basel) 06-May-2024
PMCID:PMC11085518
doi:10.3390/plants13091281
PMID:38732496
A concise review on waste biomass valorization through thermochemical conversion Joshi NC, Sinha S, Bhatnagar P, Nath Y, Negi B, Kumar V, Gururani P Curr Res Microb Sci 23-Apr-2024
PMCID:PMC11067365
doi:10.1016/j.crmicr.2024.100237
PMID:38706494
Comparative physiological, biochemical, metabolomic, and transcriptomic analyses reveal the formation mechanism of heartwood for Acacia melanoxylon Zhang R, Zhang Z, Yan C, Chen Z, Li X, Zeng B, Hu B BMC Plant Biol 22-Apr-2024
PMCID:PMC11034122
doi:10.1186/s12870-024-04884-1
PMID:38644502
Allopolyploid origin and diversification of the Hawaiian endemic mints Tomlin CM, Rajaraman S, Sebesta JT, Scheen AC, Bendiksby M, Low YW, Salojärvi J, Michael TP, Albert VA, Lindqvist C Nat Commun 10-Apr-2024
PMCID:PMC11006916
doi:10.1038/s41467-024-47247-y
PMID:38600100
Use of Residual Malt from an Artisanal Beer Brewing Process in the Biosynthesis of Silver Nanoparticles Mediated by Nucleating and Structure-Directing Agents Dueñas-Bolaños CA, Cid-Hernández M, Velázquez-Juárez G, García-Casillas LA, González-Ortiz LJ, Sánchez-Peña MJ, Herrera-González A, Zúñiga-González OG, López-Naranjo EJ Molecules 07-Apr-2024
PMCID:PMC11013108
doi:10.3390/molecules29071660
PMID:38611939
Chemical Composition and Mechanical Properties of Wood after Thermal Modification in Closed Process under Pressure in Nitrogen Grinins J, Sosins G, Brazdausks P, Zicans J Materials (Basel) 22-Mar-2024
PMCID:PMC11012288
doi:10.3390/ma17071468
PMID:38611982
Assessing the cadmium content of cacao crops in Arauca, Colombia Bravo D, Quiroga-Mateus R, López-Casallas M, Torres S, Contreras R, Otero AC, Araujo-Carrillo GA, González-Orozco CE Environ Monit Assess 21-Mar-2024
PMCID:PMC10954870
doi:10.1007/s10661-024-12539-9
PMID:38509267
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
Comprehensive genomic analysis of Bacillus subtilis and Bacillus paralicheniformis associated with the pearl millet panicle reveals their antimicrobial potential against important plant pathogens Ashajyothi M, Mahadevakumar S, Venkatesh YN, Sarma PV, Danteswari C, Balamurugan A, Prakash G, Khandelwal V, Tarasatyavathi C, Podile AR, Mysore KS, Chandranayaka S BMC Plant Biol 18-Mar-2024
PMCID:PMC10946124
doi:10.1186/s12870-024-04881-4
PMID:38500040
Exploring research trends and priorities of genus Melia S SR, Arunachalam A, Sahoo UK, Upadhyaya K Sci Rep 15-Mar-2024
PMCID:PMC10943012
doi:10.1038/s41598-024-53736-3
PMID:38490998
Experimental and computational studies of crystal violet removal from aqueous solution using sulfonated graphene oxide Oluwasina OO, Adelodun AA, Oluwasina OO, Duarte HA, Olusegun SJ Sci Rep 14-Mar-2024
PMCID:PMC10940666
doi:10.1038/s41598-024-54499-7
PMID:38485952
Chromosome-level genome of Thymus mandschuricus reveals molecular mechanism of aroma compounds biosynthesis Jia L, Xu N, Xia B, Gao W, Meng Q, Li Q, Sun Y, Xu S, He M, Gu H Front Plant Sci 13-Mar-2024
PMCID:PMC10965588
doi:10.3389/fpls.2024.1368869
PMID:38545395
Rich specialized insect damage on Pliocene leaves from the Mahuadanr Valley (India) growing under a warm climate with weak seasonality Adroit B, Hazra T, Denk T, Kumar Sarkar S, Khan MA Ecol Evol 11-Mar-2024
PMCID:PMC10927363
doi:10.1002/ece3.11114
PMID:38469042
Influence of Shade in Cocoa Agroforestry Systems on Physicochemical and Functional Characteristics of Cocoa Beans in Bonon, Central-West Côte d'Ivoire Kouassi AT, Boko AC, Blei SH, Angaman DM, Barima YS Int J Food Sci 06-Mar-2024
PMCID:PMC10937077
doi:10.1155/2024/1543904
PMID:38481613
Water, starch, and nuclear behavior in ray parenchyma during heartwood formation of Catalpa bungei ‘Jinsi’ Guo P, Zhao X, Yang Z, Wang Y, Li H, Zhang L Heliyon 27-Feb-2024
PMCID:PMC10937695
doi:10.1016/j.heliyon.2024.e27231
PMID:38486779

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Munjistin 160476 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C(=O)O)O 284.22 unknown https://doi.org/10.1055/S-0028-1097561
> Benzenoids / Anthracenes / Anthraquinones
1,4-Dihydroxy-2-methylanthraquinone 99300 Click to see CC1=CC(=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1016/S0031-9422(98)00478-6
https://doi.org/10.1007/BF00602933
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see CC1=CC2C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 256.25 unknown via CMAUP database
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1016/0031-9422(89)80224-9
https://doi.org/10.1055/S-0028-1097561
https://doi.org/10.1055/S-2006-946676
9,10-Dimethoxy-2-methylanthracene-1,4-dione 14283285 Click to see CC1=CC(=O)C2=C(C3=CC=CC=C3C(=C2C1=O)OC)OC 282.29 unknown https://doi.org/10.1016/0031-9422(89)80224-9
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Chrysophanol 8-(6-O-galloyl-beta-D-glucopyranoside) 5315852 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 568.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
15-Oxolaurene 23426957 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)C=O 214.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
15-Hydroxylaurene 23426955 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)CO 216.32 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]phenyl]methyl acetate 23426956 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)COC(=O)C 258.35 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Cyperine 182142 Click to see CC1=CC(=CC(=C1)OC2=C(C=C(C=C2C)OC)O)O 260.28 unknown https://doi.org/10.1080/14786410902951088
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]-4-methylbenzene 11790230 Click to see CC1C(=C)CCC1(C)C2=CC=C(C=C2)C 200.32 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
5-Hydroxylapachol 5318245 Click to see CC(=CCC1=C(C2=C(C=CC=C2O)C(=O)C1=O)O)C 258.27 unknown https://doi.org/10.1016/S0031-9422(98)00478-6
Lapachol 3884 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=O)C1=O)O)C 242.27 unknown https://doi.org/10.1111/J.1600-0536.1996.TB02217.X
https://doi.org/10.1016/0031-9422(89)80224-9
https://doi.org/10.1016/S0031-9422(98)00478-6
https://doi.org/10.1016/S0031-9422(98)00478-6
https://doi.org/10.1055/S-0028-1097561
> Benzenoids / Phenols / Cresols / Meta cresols
2-[(1R,2R,3E)-3-(bromomethylidene)-1,2-dimethylcyclopentyl]-5-methylphenol 12305606 Click to see CC1C(=CBr)CCC1(C)C2=C(C=C(C=C2)C)O 295.21 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1080/14786410902951088
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]-4-methylcyclohexa-1,4-diene 14865952 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)C 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
20-Hydroxyicosyl octadeca-9,12-dienoate 162964713 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCO 577.00 unknown https://doi.org/10.1080/14786410902951088
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(7S)-7-hydroxyoctadecyl] decanoate 163037509 Click to see CCCCCCCCCCCC(CCCCCCOC(=O)CCCCCCCCC)O 440.70 unknown https://doi.org/10.1080/14786410902951088
7-Hydroxyoctadecyl decanoate 163037508 Click to see CCCCCCCCCCCC(CCCCCCOC(=O)CCCCCCCCC)O 440.70 unknown https://doi.org/10.1080/14786410902951088
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3Z,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol 23424689 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
(6R,7R,9Z,12E)-3,9,12-Pentadecatriene-1-yne-6,7-diol 11264813 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(18R)-18-hydroxyhexacosyl] decanoate 162982818 Click to see CCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCC(CCCCCCCC)O 553.00 unknown https://doi.org/10.1080/14786410902951088
18-Hydroxyhexacosyl decanoate 91482539 Click to see CCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCC(CCCCCCCC)O 553.00 unknown https://doi.org/10.1080/14786410902951088
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(Z)-2-[2-[(1R,4aS,6R,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethyl]but-2-ene-1,4-diol 101967034 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)CCC(=CCO)CO)C 322.50 unknown https://doi.org/10.1515/ZNC-1977-9-1009
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enyl] acetate 92973629 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)C)C 338.60 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
1-[(3R,5S,9S,10R)-10-hydroxy-6,9,10-trimethylspiro[4.5]dec-6-en-3-yl]ethanone 23427059 Click to see CC1CC=C(C2(C1(C)O)CCC(C2)C(=O)C)C 236.35 unknown via CMAUP database
Laurenon A 23427058 Click to see CC1CC=C(C2(C1(C)O)CCC(C2)C(=O)C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6,6-Trimethylocta-2,7-dien-1-ol 163046637 Click to see CC(=CCCC(C)(C)C=C)CO 168.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Deoxylapachol 97448 Click to see CC(=CCC1=CC(=O)C2=CC=CC=C2C1=O)C 226.27 unknown https://doi.org/10.1111/J.1600-0536.1996.TB02217.X
https://doi.org/10.1002/CBER.19630960830
https://doi.org/10.1055/S-2006-946676
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R)-3-[(3S)-3-hydroxybutyl]-2,2,4-trimethylcyclohex-3-en-1-ol 102026252 Click to see CC1=C(C(C(CC1)O)(C)C)CCC(C)O 212.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
(1R)-4-[(3S)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-3-en-1-ol 11298813 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)O 212.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
2-Cyclohexen-1-one, 3-(3-hydroxybutyl)-2,4,4-trimethyl- 520295 Click to see CC1=C(C(CCC1=O)(C)C)CCC(C)O 210.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
3-[(3S)-3-hydroxybutyl]-2,4,4-trimethylcyclohex-2-en-1-one 14086374 Click to see CC1=C(C(CCC1=O)(C)C)CCC(C)O 210.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
3-Hydroxy-7,8-dihydro-beta-ionone 91747289 Click to see CC1=C(C(C(CC1)O)(C)C)CCC(C)O 212.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
4-(3-Hydroxybutyl)-3,5,5-trimethylcyclohex-3-en-1-ol 15406338 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)O 212.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
4-(4-Hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)butan-2-one 14135407 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(=O)C 210.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
4-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-one 10878432 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(=O)C 210.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
9-Epiblumenol B 14135401 Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
blumenol B 14135402 Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
gamma-BISABOLENE, (E)- 5352437 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown via CMAUP database
Merrillianone 10564833 Click to see CC1CC=C2C13CC4(C(C2(COC(C3O)O4)C)(C)O)O 282.33 unknown https://doi.org/10.1016/0031-9422(93)85309-F
Selin-4,7(11)-diene 23425324 Click to see CC1=C2CC(=C(C)C)CCC2(CCC1)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(1R,1'S,2'S,5R,6S)-2',3-dibromo-1'-chloro-1',4,4,6-tetramethylspiro[7-oxabicyclo[4.1.0]hept-2-ene-5,4'-cyclohexane] 14371607 Click to see CC1(C(=CC2C(C13CCC(C(C3)Br)(C)Cl)(O2)C)Br)C 412.59 unknown via CMAUP database
(1R,1'S,4'S,5R,5'S,6S)-3,4'-dibromo-5'-chloro-4,4,5',6-tetramethylspiro[7-oxabicyclo[4.1.0]hept-2-ene-5,2'-cyclohexane]-1'-ol 15385746 Click to see CC1(C(=CC2C(C13CC(C(CC3O)(C)Cl)Br)(O2)C)Br)C 428.58 unknown via CMAUP database
(1R,3R,6S,8R,11R)-8-bromo-4,11,12,12-tetramethyl-7-oxatricyclo[6.3.1.01,6]dodeca-4,9-diene-3,11-diol 21637490 Click to see CC1=CC2C3(CC1O)C(C(O2)(C=CC3(C)O)Br)(C)C 329.23 unknown via CMAUP database
(1R,6S,8R,11R)-3,8-dibromo-4,11,12,12-tetramethyl-7-oxatricyclo[6.3.1.01,6]dodeca-3,9-dien-11-ol 21773247 Click to see CC1=C(CC23C(C1)OC(C2(C)C)(C=CC3(C)O)Br)Br 392.13 unknown via CMAUP database
(1S,1'S,2R,2'S,4R,6R)-2',4-dibromo-1'-chloro-1,1',3,3-tetramethylspiro[7-oxabicyclo[4.1.0]heptane-2,4'-cyclohexane] 21634305 Click to see CC1(C(CC2C(C13CCC(C(C3)Br)(C)Cl)(O2)C)Br)C 414.60 unknown via CMAUP database
(2R,4R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-2-ol 23424644 Click to see CC1(C(CC(C(=C)C12CCC(C(C2)Br)(C)Cl)O)Br)C 414.60 unknown via CMAUP database
(2R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-3-en-2-ol 23426577 Click to see CC1(C(=CC(C(=C)C12CCC(C(C2)Br)(C)Cl)O)Br)C 412.59 unknown via CMAUP database
(4R,6S,9S,10S)-4,10-dibromo-1,5,5,9-tetramethylspiro[5.5]undec-1-en-9-ol 23424645 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)O)(C)C)Br 380.16 unknown via CMAUP database
(4R,6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane 23424643 Click to see CC1(C(CCC(=C)C12CCC(C(C2)Br)(C)Cl)Br)C 398.60 unknown via CMAUP database
(4S,6R,9R,10R)-4,9-dibromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane 21675022 Click to see CC1(C(CCC(=C)C12CCC(C(C2)Cl)(C)Br)Br)C 398.60 unknown via CMAUP database
(6S,9S,10S)-4,10-dibromo-9-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-3-en-2-one 23426578 Click to see CC1(C(=CC(=O)C(=C)C12CCC(C(C2)Br)(C)Cl)Br)C 410.57 unknown via CMAUP database
(6S)-1,5,5,9-Tetramethyl-4beta,8alpha-dibromo-9beta-chlorospiro[5.5]undeca-1-ene 14108781 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)Cl)(C)C)Br 398.60 unknown via CMAUP database
10-Bromo-beta-chamigrene 21675030 Click to see CC1=CCC2(CC1)C(=C)CCC(C2(C)C)Br 283.25 unknown via CMAUP database
2,10-Dibromo-3-hydroxy-alpha-chamigrene 101356858 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)O)(C)C)Br 380.16 unknown via CMAUP database
CID 636451 636451 Click to see CC1(C23CC(C(CC2OC1(C=CC3(C)O)Br)(C)Cl)Br)C 428.58 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,8aR)-8a-methyl-5-methylidene-3-propan-2-yl-2,3,4,6,7,8-hexahydro-1H-naphthalen-4a-ol 23426660 Click to see CC(C)C1CCC2(CCCC(=C)C2(C1)O)C 222.37 unknown via CMAUP database
Cycloeudesmol 442362 Click to see CC1CCCC2(C13CC3(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Deoxyloganin 440906 Click to see CC1CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410902951088
https://doi.org/10.1016/J.FITOTE.2010.03.019
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.03.019
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 https://doi.org/10.1016/J.FITOTE.2010.03.019
https://doi.org/10.1080/14786410902951088
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1080/14786410902951088
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1080/14786410902951088
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/10.1016/S0031-9422(98)00478-6
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/10.1016/S0031-9422(98)00478-6
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.03.019
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroid glucuronide conjugates
4-oxotridecyl (2S,3S,4R,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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]-4,5-dihydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]oxyoxane-2-carboxylate 162994908 Click to see CCCCCCCCCC(=O)CCCOC(=O)C1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC 1047.60 unknown https://doi.org/10.1080/14786410902951088
4-oxotridecyl 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]-4,5-dihydroxy-3-octadeca-9,12,15-trienoyloxyoxane-2-carboxylate 162994907 Click to see CCCCCCCCCC(=O)CCCOC(=O)C1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC 1047.60 unknown https://doi.org/10.1080/14786410902951088
> 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/10.1016/J.FITOTE.2010.03.019
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/10.1016/J.FITOTE.2010.03.019
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/10.1016/J.FITOTE.2010.03.019
https://doi.org/10.1080/14786410902951088
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/10.1016/J.FITOTE.2010.03.019
https://doi.org/10.1080/14786410902951088
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]cyclohexa-1,4-dien-1-yl]methyl acetate 23426954 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)COC(=O)C 260.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(2-Butoxy-2-oxoethyl)-2-hydroxysuccinic acid 14134171 Click to see CCCCOC(=O)CC(CC(=O)O)(C(=O)O)O 248.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
[4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]cyclohexa-1,4-dien-1-yl]methanol 23426953 Click to see CC1C(=C)CCC1(C)C2=CCC(=CC2)CO 218.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R,3R,5R)-5-[(E,1R)-1-bromohex-3-enyl]-2-[(E)-pent-2-en-4-ynyl]oxolan-3-ol 11758790 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)O)Br 313.23 unknown via CMAUP database
[(2R,3R,5R)-5-[(E,1S)-1-bromohex-3-enyl]-2-[(E)-pent-2-en-4-ynyl]oxolan-3-yl] acetate 11772642 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
trans-Kumausyne 10882777 Click to see CCC=CCC(C1CC(C(O1)CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,5-Dibromo-4-Hydroxybenzaldehyde 18100 Click to see C1=C(C=C(C(=C1Br)O)Br)C=O 279.91 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Isoaplysin 11822545 Click to see CC1CCC2(C1(OC3=C2C=CC(=C3)C)CBr)C 295.21 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Aminopyrimidines and derivatives
Heteromine H 10774848 Click to see CNC1=C(C(=NC(=N1)N)OC)N(C)C=O 211.22 unknown https://doi.org/10.1016/S0031-9422(98)00478-6
> Organoheterocyclic compounds / Dioxepanes / 1,3-dioxepanes
(1S,3R,5S,7R)-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-8-en-10-one 23426796 Click to see CC(=C)C1CC23C(O1)OC2(C=CC(=O)C3(C)C)C 248.32 unknown via CMAUP database
(1S,3R,5S,7S,8S)-10-bromo-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-en-8-ol 23425344 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)O)C 329.23 unknown via CMAUP database
(1S,3R,5S,7S,8S)-10-bromo-8-chloro-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-ene 23426795 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)Cl)C 347.67 unknown via CMAUP database
(1S,3R,5S,7S,8S)-8,10-dibromo-7,11,11-trimethyl-3-prop-1-en-2-yl-4,6-dioxatricyclo[5.4.0.01,5]undec-9-ene 23426794 Click to see CC(=C)C1CC23C(O1)OC2(C(C=C(C3(C)C)Br)Br)C 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
(+)-Z-Isolaureatin 16062462 Click to see CCC(C1CC2C(CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,2S,4R,6S,7S)-7-bromo-4-[(1S)-1-bromopropyl]-2-[(E)-pent-2-en-4-ynyl]-3,9-dioxabicyclo[4.2.1]nonane 11101244 Click to see CCC(C1CC2C(CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
2,2-Dimethyl-2H-naphtho[1,2-b]pyran-5,6-dione 24991545 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3C(=O)C2=O)C 240.25 unknown https://doi.org/10.1016/0031-9422(89)80224-9
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(5E)-5-(2,2-dimethyl-5-oxobenzo[g]chromen-10-ylidene)-2,2-dimethylbenzo[g]chromen-10-one 14283286 Click to see CC1(C=CC2=C(O1)C(=O)C3=CC=CC=C3C2=C4C5=CC=CC=C5C(=O)C6=C4OC(C=C6)(C)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(89)80224-9
5-(2,2-Dimethyl-5-oxobenzo[g]chromen-10-ylidene)-2,2-dimethylbenzo[g]chromen-10-one 162997582 Click to see CC1(C=CC2=C(O1)C(=O)C3=CC=CC=C3C2=C4C5=CC=CC=C5C(=O)C6=C4OC(C=C6)(C)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(89)80224-9
alpha-Lapachone 72732 Click to see CC1(CCC2=C(O1)C(=O)C3=CC=CC=C3C2=O)C 242.27 unknown via CMAUP database
beta-Lapachone 3885 Click to see CC1(CCC2=C(O1)C3=CC=CC=C3C(=O)C2=O)C 242.27 unknown via CMAUP database
Xyloidone 72734 Click to see CC1(C=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)C 240.25 unknown https://doi.org/10.1016/0031-9422(89)80224-9
https://doi.org/10.1016/S0031-9422(98)00478-6
> Organoheterocyclic compounds / Oxanes
(1R,3R,4S,6S,8R,10S)-4,10-dibromo-3-ethyl-8-[(E)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.2]decane 14731401 Click to see CCC1C(CC2C(CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,5S,6R,8R,9R)-2,5,6,8-tetramethyl-7-oxatricyclo[6.2.2.01,6]dodec-2-en-9-ol 23424606 Click to see CC1CC=C(C23C1(OC(CC2)(C(C3)O)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(1R,3R,5R,6R,8R)-5-bromo-3-[(1S)-1-bromopropyl]-8-[(Z)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.1]nonane 101599860 Click to see CCC(C1CC(C2CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(1S,3R,5S,6S,8S)-5-bromo-3-[(1S)-1-bromopropyl]-8-[(Z)-pent-2-en-4-ynyl]-2,7-dioxabicyclo[4.2.1]nonane 11326787 Click to see CCC(C1CC(C2CC(O1)C(O2)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
4-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-3-buten-2-one 181574 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C 224.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
Annuionone D 14605579 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C 224.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
Laurencial 11086786 Click to see CC1(C(=CC2(C13CCC(C(C3)O2)(C)Cl)C)C=O)C 268.78 unknown via CMAUP database
> Organoheterocyclic compounds / Oxetanes
(1S,2S,4R,6R,7R)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(Z)-pent-2-en-4-ynyl]-3,8-dioxabicyclo[5.1.1]nonane 11101243 Click to see CCC(C1CC(C2CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
(3E)-Laureatin 102095592 Click to see CCC(C1CC(C2CC(O2)C(O1)CC=CC#C)Br)Br 392.13 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
2H-Oxocin-2-methanol, 7-bromo-8-ethyl-3,6,7,8-tetrahydro-alpha-2-penten-4-ynyl-, acetate, (E)-(alphaR,2R,7S,8R)- 6436276 Click to see CCC1C(CC=CCC(O1)C(CC=CC#C)OC(=O)C)Br 355.30 unknown via CMAUP database
Prelaureatin 10870702 Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)O)Br 313.23 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
Notoryne 23427873 Click to see CCC1C(CC(O1)C2CC(C(O2)CC=CC#C)Cl)Br 347.67 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
(2R,5S,6R,8R)-2,6,10,10-tetramethyl-1-oxaspiro[4.5]decane-6,8-diol 163050409 Click to see CC1CCC2(O1)C(CC(CC2(C)O)O)(C)C 228.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
2,6,10,10-Tetramethyl-1-oxaspiro[4.5]decane-6,8-diol 163050408 Click to see CC1CCC2(O1)C(CC(CC2(C)O)O)(C)C 228.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.FITOTE.2010.03.019
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.FITOTE.2010.03.019
> Phenylpropanoids and polyketides / Isochromanequinones / Benzoisochromanequinones
Tecomaquinone I 3574508 Click to see CC(=CC1C2=C(C3=C(O1)C4=CC=CC=C4C5=C3C=CC(O5)(C)C)C(=O)C6=CC=CC=C6C2=O)C 448.50 unknown https://doi.org/10.1016/0031-9422(89)80224-9

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