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Cedrus libani

Cedrus libani - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cedrus libani - 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 UUID64401002d9986234257133
Scientific name Cedrus libani
Authority A.Rich.
First published in Dict. Class. Hist. Nat. 3: 299 (1823)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Peuce cedrus Rich. Ann. Mus. Hist. Nat. 16: 298 (1810)
Larix patula Salisb. Trans. Linn. Soc. London 8: 314 (1807)
Larix cedrus Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Pinus effusa Salisb. Prodr. Stirp. Chap. Allerton : 399 (1796)
Pinus cedrus L. Sp. Pl. : 1001 (1753)
Abies cedrus (L.) Poir. Encycl. [J. Lamarck & al.] 6(2): 510. 1805 [28 Aug 1805]
Cedrus cedrus Huth Helios 11: 133 (1893)
Cedrus effusa Voss Mitt. Deutsch. Dendrol. Ges. 16: 92 (1907)
Cedrus libani var. argentea Antoine & Kotschy Conif. Cilic. Taurus 417 1855
Cedrus libani var. pendula Carrière Traité Gén. Conif. 294 1855
Cedrus libanitica Trew ex Pilg. Nat. Pflanzenfam. ed. 2 , 13: 329 (1926)
Cedrus libanotica subsp. libani (A.Rich.) Holmboe Stud. Veg. Cyprus 30. 1914 (1914)
Cedrus patula K.Koch Dendrologie 2(2): 268 (1873)
Cedrus libani var. pendula-sargentii Hornibr. Dwarf Conifers 26 1923
Cedrus libanitica var. pendula (Carrière) L.H.Bailey Cult. Conif. 130 1933
Cedrus libanotica var. pendula (Carrière) Rehder Man. Cult. Trees 53 1927
Cedrus libani var. nana Loudon Arbor. Frutic. Brit. 4: 2403 1838
Cedrus libani f. nana (Loudon) Beissn. Handb. Conif. 32 1887
Cedrus libani f. pendula (Carrière) Beissn. Handb. Conif. 32 1887
Cedrus libanotica f. pendula (Carrière) Rehder J. Arnold Arbor. 6: 205 1925
Cedrus libani subsp. stenocoma (O.Schwarz) P.H.Davis J. Roy. Hort. Soc. 74: 113 1949
Picea cedrus (L.) Peterm. Pflanzenreich : 236 (1838-1845)

Common names Top

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Language Common/alternative name
English cedar of lebanon
English lebanon cedar
English lebanese cedar
Spanish cedro del líbano
Spanish cedro de salomon
Spanish cedro de salomón
Spanish cedro del libano
Spanish cedrus libanotica
Spanish larix cedrus
Spanish peuce cedrus
Spanish pinus cedrus
Arabic أرز لبناني
Arabic أرز لبنان
Arabic شجرة القطران
Arabic شربين
Arabic أرز
Azerbaijani livan sidri
azb لوبنان سیدری
Belarusian Кедр ліванскі
Bulgarian ливански кедър
Catalan cedre del líban
Czech cedr libanonský
Welsh cedrwydden libanus
Danish libanon-ceder
German cedrus cedrus
German cedrus libanensis
German cedrus libanitica
German cedrus libanotica
German cedrus patula
German libanonzeder
German libanon-zeder
Greek Κέδρος του Λιβάνου
Esperanto lebanona cedro
Estonian liibanoni seeder
Basque cedrus libani subsp. stenocoma
Basque cedrus libani var. stenocoma
Basque taurus zedro
Basque turkiako zedro
Basque libanoko zedro
Persian سدر
Finnish libanoninsetri
French cèdre du liban
French cedre du liban
French cédre du liban
French cédres du liban
French cèdres du liban
Galician cedro do líbano
Hebrew ארז הלבנון
Croatian libanonski cedar
Upper Sorbian libanonska cedra
Hungarian libanoni cédrus
Armenian Մայրի լիբանանական
hyw Լիբանանեան Մայրի
Indonesian aras lebanon
Icelandic líbanonsedrus
Italian cedro del libano
Italian cedri del libano
Italian pinus cedrus
Japanese レバノンシーダー
Japanese レバノン杉
Japanese レバノンスギ
Georgian ლიბანის კედარი
Korean 레바논시다
koi Сыспу
koi Любнанісь сыспу
Lithuanian libano kedras
Latvian libānas ciedrs
Malagasy sedera libàna
Macedonian либански кедар
Malayalam ലെബനൻ ദേവദാരു
Malayalam സെഡ്രസ് ലിബാനി
Norwegian Bokmål libanonseder
Dutch libanese ceder
Dutch libanon ceder
Dutch libanonceder
Polish cedr libański
Punjab لبنانی سیڈر
Portuguese cedro da turquia
Portuguese cedro do atlas
Portuguese cedro do chipre
Portuguese cedro do líbano
Portuguese cedro turco
Portuguese cedro-da-turquia
Portuguese cedro-do-chipre
Portuguese cedro-turco
Portuguese cedrus brevifolia
Portuguese cedrus libani atlantica
Portuguese cedrus libani brevifolia
Portuguese cedrus libani libani
Portuguese cedrus libani stenocoma
Portuguese cedro-do-líbano
Portuguese cedro libanês
Russian Ливанский кедр
Russian Кедр ливанский
Serbo-Croatian libanonski cedar
Slovenian libanonska cedra
Somali geedka cedar
Swedish libanonceder
Swahili mti wa mwerezi
Swahili mwerezi
Tamil லெபனான் தேவதாரு
Turkish lübnan sediri
Turkish toros sediri
Ukrainian Ліванський кедр
Vietnamese tuyết tùng liban
Walloon cede do liban
Chinese 黎巴嫩雪松

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Cedrus libani var. brevifolia Hook.f. J. Linn. Soc., Bot. 17(104-105): 518. 1880
Cedrus libani var. libani Unknown

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
  • Europe
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Bulgaria

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000592537
UNII 9G0JE54296
Cornell Woody Plants 300
USDA Plants CELI6
Tropicos 24900697
INPN 89455
KEW urn:lsid:ipni.org:names:676705-1
The Plant List kew-2707327
Missouri Botanical Garden 285042
Open Tree Of Life 608496
Observations.org 131969
NCBI Taxonomy 93692
NBN Atlas NHMSYS0000457003
IUCN Red List 46191675
IPNI 676705-1
iNaturalist 136150
GBIF 5284682
Freebase /m/023jks
EPPO CEULI
EOL 1061705
Elurikkus 3520
Calflora (Californian flora) 10524
USDA GRIN 9695
Wikipedia Cedrus_libani
CMAUP NPO11882

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
Latitude or altitude as the future refugium? A case for the future of forests in Asia Minor and its surroundings Ekberzade B, Yetemen O, Ezber Y, Sen OL, Dalfes HN Ecol Evol 12-Apr-2024
PMCID:PMC11009660
doi:10.1002/ece3.11131
PMID:38617103
Antioxidant Activity of Essential Oils from Pinaceae Species Ancuceanu R, Anghel AI, Hovaneț MV, Ciobanu AM, Lascu BE, Dinu M Antioxidants (Basel) 26-Feb-2024
PMCID:PMC10967544
doi:10.3390/antiox13030286
PMID:38539820
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
Paeoniflorin Induces ER Stress-Mediated Apoptotic Cell Death by Generating Nox4-Derived ROS under Radiation in Gastric Cancer Kim TW Nutrients 13-Dec-2023
PMCID:PMC10745742
doi:10.3390/nu15245092
PMID:38140352
An arrangement of secretory cells involved in the formation and storage of resin in tracheid-based secondary xylem of arborescent plants Tulik M, Jura-Morawiec J Front Plant Sci 05-Sep-2023
PMCID:PMC10508844
doi:10.3389/fpls.2023.1268643
PMID:37731990
Near-complete de novo assembly of Tricholoma bakamatsutake chromosomes revealed the structural divergence and differentiation of Tricholoma genomes Ichida H, Murata H, Hatakeyama S, Yamada A, Ohta A G3 (Bethesda) 02-Sep-2023
PMCID:PMC10627285
doi:10.1093/g3journal/jkad198
PMID:37659058
Biomolecular characterization of 3500-year-old ancient Egyptian mummification balms from the Valley of the Kings Huber B, Hammann S, Loeben CE, Jha DK, Vassão DG, Larsen T, Spengler RN, Fuller DQ, Roberts P, Devièse T, Boivin N Sci Rep 31-Aug-2023
PMCID:PMC10471619
doi:10.1038/s41598-023-39393-y
PMID:37652925
Simultaneous Hydrodistillation of Healthy Cedrus atlantica Manetti and Infected by Trametes pini and Ungulina officinalis: Effect on Antibacterial Activity Utilizing a Mixture-Design Method Moustaid W, Saffaj T, Annemer S, Assouguem A, Ullah R, Ali EA, Ercisli S, Marc RA, Farah A ACS Omega 22-Aug-2023
PMCID:PMC10483654
doi:10.1021/acsomega.3c03555
PMID:37692238
Antioxidant, Volatile Compounds; Antimicrobial, Anti-Inflammatory, and Dermatoprotective Properties of Cedrus atlantica (Endl.) Manetti Ex Carriere Essential Oil: In Vitro and In Silico Investigations El Hachlafi N, Mrabti HN, Al-Mijalli SH, Jeddi M, Abdallah EM, Benkhaira N, Hadni H, Assaggaf H, Qasem A, Goh KW, AL-Farga A, Bouyahya A, Fikri-Benbrahim K Molecules 06-Aug-2023
PMCID:PMC10421490
doi:10.3390/molecules28155913
PMID:37570883
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
Pest categorisation of Hoplolaimus galeatus 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, Migheli Q, Vloutoglou I, Maiorano A, Pautasso M, Reignault PL EFSA J 20-Jul-2023
PMCID:PMC10357347
doi:10.2903/j.efsa.2023.8117
PMID:37485256
Commodity risk assessment of Acer campestre 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 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Fungal Planet description sheets: 1478–1549 Crous PW, Osieck ER, Shivas RG, Tan YP, Bishop-Hurley SL, Esteve-Raventós F, Larsson E, Luangsa-ard JJ, Pancorbo F, Balashov S, Baseia IG, Boekhout T, Chandranayaka S, Cowan DA, Cruz RH, Czachura P, De la Peña-Lastra S, Dovana F, Drury B, Fell J, Flakus A, Fotedar R, Jurjević Ž, Kolecka A, Mack J, Maggs-Kölling G, Mahadevakumar S, Mateos A, Mongkolsamrit S, Noisripoom W, Plaza M, Overy DP, Piątek M, Sandoval-Denis M, Vauras J, Wingfield MJ, Abell SE, Ahmadpour A, Akulov A, Alavi F, Alavi Z, Altés A, Alvarado P, Anand G, Ashtekar N, Assyov B, Banc-Prandi G, Barbosa KD, Barreto GG, Bellanger JM, Bezerra JL, Bhat DJ, Bilański P, Bose T, Bozok F, Chaves J, Costa-Rezende DH, Danteswari C, Darmostuk V, Delgado G, Denman S, Eichmeier A, Etayo J, Eyssartier G, Faulwetter S, Ganga KG, Ghosta Y, Goh J, Góis JS, Gramaje D, Granit L, Groenewald M, Gulden G, Gusmão LF, Hammerbacher A, Heidarian Z, Hywel-Jones N, Jankowiak R, Kaliyaperumal M, Kaygusuz O, Kezo K, Khonsanit A, Kumar S, Kuo CH, Læssøe T, Latha KP, Loizides M, Luo SM, Maciá-Vicente JG, Manimohan P, Marbach PA, Marinho P, Marney TS, Marques G, Martín MP, Miller AN, Mondello F, Moreno G, Mufeeda KT, Mun HY, Nau T, Nkomo T, Okrasińska A, Oliveira JP, Oliveira RL, Ortiz DA, Pawłowska J, Pérez-De-Gregorio MÀ, Podile AR, Portugal A, Privitera N, Rajeshkumar KC, Rauf I, Rian B, Rigueiro-Rodríguez A, Rivas-Torres GF, Rodriguez-Flakus P, Romero-Gordillo M, Saar I, Saba M, Santos CD, Sarma PV, Siquier JL, Sleiman S, Spetik M, Sridhar KR, Stryjak-Bogacka M, Szczepańska K, Taşkın H, Tennakoon DS, Thanakitpipattana D, Trovão J, Türkekul İ, van Iperen AL, van ’t Hof P, Vasquez G, Visagie CM, Wingfield BD, Wong PT, Yang WX, Yarar M, Yarden O, Yilmaz N, Zhang N, Zhu YN, Groenewald JZ Persoonia 29-Jun-2023
PMCID:PMC10983837
doi:10.3767/persoonia.2023.50.05
PMID:38567263
Long-term fungal inoculation of Ficus sycomorus and Tectona grandis woods with Aspergillus flavus and Penicillium chrysogenum Mansour MM, Mohamed WA, El-Settawy AA, Böhm M, Salem MZ, Farahat MG Sci Rep 28-Jun-2023
PMCID:PMC10307807
doi:10.1038/s41598-023-37479-1
PMID:37380674
Quartet Fiduccia–Mattheyses revisited for larger phylogenetic studies Mim SA, Zarif-Ul-Alam M, Reaz R, Bayzid MS, Rahman MS Bioinformatics 07-Jun-2023
PMCID:PMC10260390
doi:10.1093/bioinformatics/btad332
PMID:37285316

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
3,5,5,9-Tetramethyl-6,7-dihydro-5H-benzo[7]annulene 6428454 Click to see CC1=CCCC(C2=C1C=CC(=C2)C)(C)C 200.32 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Bergenin 66065 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown via CMAUP database
Norbergenin 90476206 Click to see C1=C2C(=C(C(=C1O)O)O)C3C(C(C(C(O3)CO)O)O)OC2=O 314.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
11-o-Galloylbergenin 56680102 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)OC2=O)O 480.40 unknown via CMAUP database
5-Galloylshikimic acid 460897 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 326.25 unknown via CMAUP database
6-O-(3,4,5-Trihydroxybenzoyl)-alpha-D-glucopyranose 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
3'-(3-Acetyl-2,4-dihydroxy-5-methyl-6-methoxybenzyl)-2',4',6'-trihydroxy-5'-(3-methyl-2-butenyl)butyrophenone 5315573 Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)CC=C(C)C)O 472.50 unknown via CMAUP database
Mallotojaponin 122659 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C)O)O)C(=O)C)O 444.50 unknown via CMAUP database
Mallotophenone 179090 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)C(=O)C)O 404.40 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rhodiocyanoside A 6442274 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)C#N 259.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/0031-9422(88)83057-7
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83057-7
(1S,4aR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 6552012 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/0031-9422(88)83057-7
(3R)-5-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 154496976 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(4aR,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene 162854594 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
(4aS,4bR,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene 60077691 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
1,4a-Dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 90895 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83057-7
https://doi.org/10.1016/S0031-9422(00)97289-3
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 15618 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/0031-9422(88)83057-7
https://doi.org/10.1016/S0031-9422(00)97289-3
7-Isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene 86869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
Abieta-7,13-diene 443470 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C 272.50 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83057-7
https://doi.org/10.1016/S0031-9422(00)97289-3
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
Manool 3034394 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown https://doi.org/10.1080/10412905.2000.9712210
https://doi.org/10.1016/J.PHYMED.2007.03.013
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
phenanthrene, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS,4bR,10aS)- 14241160 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- 221064 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)97289-3
Sandaracopimaric acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83057-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
https://doi.org/10.1080/10412905.2000.9712210
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,2S,7S,8R,9R)-2,6,6,9-tetramethyltricyclo[5.4.0.02,9]undecan-8-ol 101637059 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1r,3s,5r)-6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol 88302 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1S,2R,7S,8S,9S)-2,6,6,9-Tetramethyltricyclo[5.4.0.02,9]undecan-8-ol 12304755 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.2000.9712210
(S)-cis-Verbenol 87839 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
https://doi.org/10.1080/10412905.2000.9712210
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
https://doi.org/10.1080/10412905.2000.9712210
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
cis-Verbenol 164888 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Longiborneol 521200 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.2000.9712210
https://doi.org/10.1016/J.PHYMED.2007.03.013
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(4R)-4-[(2R)-4-oxopentan-2-yl]cyclohexene-1-carboxylic acid 96019538 Click to see CC(CC(=O)C)C1CCC(=CC1)C(=O)O 210.27 unknown https://doi.org/10.1016/0031-9422(88)83057-7
(4S)-4-[(2R)-4-oxopentan-2-yl]cyclohexene-1-carboxylic acid 96019540 Click to see CC(CC(=O)C)C1CCC(=CC1)C(=O)O 210.27 unknown https://doi.org/10.1016/0031-9422(88)83057-7
4-(4-Oxopentan-2-yl)cyclohex-1-ene-1-carboxylic acid 14192386 Click to see CC(CC(=O)C)C1CCC(=CC1)C(=O)O 210.27 unknown https://doi.org/10.1016/0031-9422(88)83057-7
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
https://doi.org/10.1080/10412905.2000.9712210
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol 83218 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C 631.10 unknown via CMAUP database
Ficaprenol 10 12866490 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C 699.20 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
Ficaprenol 12 14380582 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C)C 835.40 unknown via CMAUP database
Ficaprenol 9 12442866 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C 631.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-alpha-Bulgarene 12306053 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-Epicubenol 11831045 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-gamma-Bulgarene 12313023 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,2S,6S,7S,8R)-1-methyl-3-methylidene-8-propan-2-yltricyclo[4.4.0.02,7]decane 162867026 Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene 12313021 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1S,2R,7S,9R)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.02,9]undecane 12304749 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 101607926 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1S,4S,4aR)-1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene 13966509 Click to see CC1CCC(C2C1=CCC(=C2)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(4R)-4-[(Z)-6-methyl-4-oxohept-2-en-2-yl]cyclohexene-1-carboxylic acid 162929118 Click to see CC(C)CC(=O)C=C(C)C1CCC(=CC1)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(88)83057-7
(E,R)-alpha-bisabolene 13252682 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
1-Cyclohexene-1-carboxylic acid, 4-(1,5-dimethyl-3-oxohexyl)- 28809 Click to see CC(C)CC(=O)CC(C)C1CCC(=CC1)C(=O)O 252.35 unknown https://doi.org/10.1016/0031-9422(88)83057-7
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
2-Hepten-4-one, 2-methyl-6-(4-methyl-3-cyclohexen-1-ylidene)-, (6Z)- 91698329 Click to see CC1=CCC(=C(C)CC(=O)C=C(C)C)CC1 218.33 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
4-(6-Methyl-4-oxohept-2-en-2-yl)cyclohex-1-ene-1-carboxylic acid 71339703 Click to see CC(C)CC(=O)C=C(C)C1CCC(=CC1)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(88)83057-7
9-Oxo-2,7-bisaboladien-15-oic acid 91885239 Click to see CC(C)CC(=O)C=C(C)C1CCC(=CC1)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(88)83057-7
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Epitodomatuic acid 12444430 Click to see CC(C)CC(=O)CC(C)C1CCC(=CC1)C(=O)O 252.35 unknown https://doi.org/10.1016/0031-9422(88)83057-7
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Ylangene 20055075 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(-)-alpha-Himachalene 11830551 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1080/10412905.2000.9712210
https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,6R)-alpha-himachalene 11367721 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(1R,6R)-gamma-himachalene 24798697 Click to see CC1=CC2C(CC1)C(=CCCC2(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(4aR,5R,9aR)-2,5,9,9-tetramethyl-4,4a,6,7,8,9a-hexahydro-3H-benzo[7]annulen-5-ol 6335141 Click to see CC1=CC2C(CC1)C(CCCC2(C)C)(C)O 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
(4aR)-3,5,5-trimethyl-9-methylidene-2,4a,6,7,8,9a-hexahydro-1H-benzo[7]annulene 163188687 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene 15095 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1080/10412905.2000.9712210
https://doi.org/10.1016/J.PHYMED.2007.03.013
beta-Himachalene 11586487 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1080/10412905.2000.9712210
https://doi.org/10.1016/J.PHYMED.2007.03.013
gamma-Himachalene 577062 Click to see CC1=CC2C(CC1)C(=CCCC2(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Himachalol 121536 Click to see CC1=CC2C(CC1)C(CCCC2(C)C)(C)O 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3R,4R,4aS,10bS)-8,10-dihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-3-yl] 3,4,5-trihydroxybenzoate 71571588 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
1beta,2-O-(4,6-Dihydroxy-5-methoxy-1,2-phenylenecarbonyl)-3-O,6-O-bis(3,4,5-trihydroxybenzoyl)-1-deoxy-beta-D-glucopyranose 102314951 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(4aR,9R,9aS)-4,4,6,9a-tetramethyl-2,3,4a,7,8,9-hexahydro-1H-benzo[7]annulen-9-ol 12305940 Click to see CC1=CC2C(CCCC2(C(CC1)O)C)(C)C 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
Allohimachalol 10585158 Click to see CC1=CC2C(CCCC2(C(CC1)O)C)(C)C 222.37 unknown https://doi.org/10.1016/J.PHYMED.2007.03.013
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Rhodiocyanoside D 6442230 Click to see CC=C(COC1C(C(C(C(O1)CO)O)O)O)C#N 259.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-Methoxy-4-hydroxyphenyl 6-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside 102442447 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 454.40 unknown via CMAUP database
2,6-Dimethoxy-4-hydroxyphenyl 6-O-galloyl-beta-D-glucopyranoside 25262417 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC)O 484.40 unknown via CMAUP database
3-Methoxy-4-hydroxyphenyl 6-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside 102442448 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 454.40 unknown via CMAUP database
3,4,5-Trimethoxyphenyl 2-O,6-O-bis(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside 102469980 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 650.50 unknown via CMAUP database
4-Hydroxy-3-methoxyphenyl 2-O,6-O-bis(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside 102147465 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 606.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)ethanone 14602300 Click to see CC1=C(C=C(C(=C1O)C(=O)C)O)OC 196.20 unknown via CMAUP database
Butyrylmallotochromene 189457 Click to see CCCC(=O)C1=C2C(=C(C(=C1O)CC3=C(C(=C(C(=C3O)C(=O)C)O)C)OC)O)C=CC(O2)(C)C 470.50 unknown via CMAUP database
Isomallotochromene 10433453 Click to see CC1=C(C(=C(C(=C1OC)CC2=C3C(=C(C(=C2O)C(=O)C)O)C=CC(O3)(C)C)O)C(=O)C)O 442.50 unknown via CMAUP database
Mallophenone 14602301 Click to see CC1=C(C(=C(C(=C1OC)C)O)C(=O)C)O 210.23 unknown via CMAUP database
Mallotochromene 126969 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C)O)O)C(=O)C)O 442.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide 936 Click to see C1=CC(=CN=C1)C(=O)N 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin gallate 5276454 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin 15559735 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O 334.23 unknown via CMAUP database
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin 128861 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Peonidin 441773 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O 301.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic acid, (-)- 23757219 Click to see C1=CC(=CC=C1CC(CC(=O)O)(C(=O)O)O)O 240.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1S,19R,21S,22R,23R)-6,7,8,11,12,13,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-22-yl] 3,4,5-trihydroxybenzoate 14284664 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)O 786.60 unknown via CMAUP database
2-[[(1R,7R,8S,26R,28S,29R,38R)-1,14,15,18,19,20,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 16201525 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)OC1=C(C(=C(C=C1C(=O)O)O)O)O 1120.70 unknown via CMAUP database
2-[[(1S,19R,21S,22R,23R)-6,7,8,11,12,22,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 46905124 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O)O)O)O)O)O 802.60 unknown via CMAUP database
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose 11754973 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O 482.30 unknown via CMAUP database
3,4,4'-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)OC)C(=O)O2)O 330.24 unknown via CMAUP database
Casuarictin 73644 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown via CMAUP database
Giadmmrdajabjm-oaqcrpkasa- 21668995 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C(C(C(OC8OC(=O)C9=CC(=C(C(=C9)O)O)O)CO)OC5=O)O)O)O)O)O)O)O 808.60 unknown via CMAUP database
Mahtabin A 10557787 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Mallotinic acid 10056140 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O 802.60 unknown via CMAUP database
Mallotusinin 514180 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 918.60 unknown via CMAUP database
Nobotanin D 14429414 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)O 786.60 unknown via CMAUP database
Pariin M 14284542 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 786.60 unknown via CMAUP database
Pmgvhtaltibnie-gloqphdasa- 21668994 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)OC1=C(C(=C(C=C1C(=O)O)O)O)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O 1278.90 unknown via CMAUP database
Punicafolin 5320800 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O 1110.80 unknown via CMAUP database

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