Pseudotsuga menziesii - Unknown
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Internal ID UUID644001a7ab845660057346
Scientific name Pseudotsuga menziesii
Authority (Mirb.) Franco
First published in Conif. Duarum Nominibus : 4 (1950)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pinus taxifolia Lamb. Descr. Pinus [Lambert] 27. t. 33.
Pseudotsuga mucronata Sudw. ex Holz. Contr. U.S. Natl. Herb. 3(4): 266. 1895 [23 Nov 1895]
Abies californica hort. ex Steud. Nomencl. Bot. , ed. 2, 1: 1 (1840)
Abies menziesii Mirb. Mém. Mus. Hist. Nat. 13: 63, 70 (1825)
Abies taxifolia Poir. Encycl. 6: 523 (1804)
Abies douglasii var. taxifolia Lindl. Arbor. Frutic. Brit. 4: 2319 1838
Pinus douglasii var. taxifolia (Lindl.) Antoine Coniferen 85 1841
Pseudotsuga taxifolia subsp. mucronata (Raf.) Schwer. Mitt. Deutsch. Dendrol. Ges. 32: 59. 1922 (1922)
Pinus douglasii var. brevibracteata Antoine Coniferen 85. 1841
Pseudotsuga taxifolia var. brevibracteata (Antoine) Schwer. Mitt. Deutsch. Dendrol. Ges. 32: 60 1922
Abies taxifolia var. pendula Neumann Fl. Serres Jard. Eur. 8: 186. 1853
Pseudotsuga taxifolia var. pendula (Neumann) Sudw. Bull. Div. Forest. U.S.D.A. 14: 46 1897
Pseudotsuga taxifolia subsp. viridis (Schwer.) Asch. & Graebn. Syn. Mitteleur. Fl. ed. 2, 1: 287. 1913 (1913)
Pseudotsuga taxifolia var. viridis (Schwer.) C.K.Schneid. Uns. Freil.-Nadelhölzer 269. 1914
Pseudotsuga douglasii var. laeta Schwer. Mitt. Deutsch. Dendrol. Ges. 17: 219. 1908
Pseudotsuga douglasii var. viminalis Schwer. Mitt. Deutsch. Dendrol. Ges. 27: 325. 1919
Pseudotsuga taxifolia var. viminalis (Schwer.) Schwer. Mitt. Deutsch. Dendrol. Ges. 32: 59 1922
Pseudotsuga douglasii f. pendula (Neumann) Beissn. Handb. Nadelholzk. 417 1891
Pinus douglasii var. pendula (Neumann) Parl. Prodr. 16(2): 430 1868
Pseudotsuga mucronata var. elongata (Lemmon) Lemmon Erythea 5: 24. 1897
Pseudotsuga mucronata var. palustris (Raf.) Lemmon Erythea 5: 24. 1897
Pseudotsuga taxifolia f. fastigiata (Knight ex Carrière) C.K.Schneid. Uns. Freil.-Nadelhölzer 269 1913
Tsuga douglasii var. fastigiata Knight ex Carrière Traité Gén. Conif. 193. 1855
Abies douglasii var. fastigiata (Knight ex Carrière) Gordon Pinetum 17 1858
Pseudotsuga taxifolia f. pendula (Neumann) Beissn. Handb. Conif. 41 1887
Abies douglasii var. pendula (Neumann) J.Nelson Pinaceae 35, 178 1866
Tsuga douglasii var. pendula (Neumann) Beissn. Ziergehloze Gart. Park. ed. 2: 446 1884
Abietia douglasii var. pendula (Neumann) A.H.Kent Man. Conif. new ed.: 478 1900
Abietia douglasii var. fastigiata (Knight ex Carrière) A.H.Kent Man. Conif. new ed.: 479 1900
Pseudotsuga douglasii f. compacta Beissn. Handb. Nadelholzk. 419 1891
Pseudotsuga taxifolia f. compacta (Beissn.) C.K.Schneid. Uns. Freil.-Nadelhölzer 269 1913
Pseudotsuga douglasii f. globosa Beissn. Mitt. Deutsch. Dendrol. Ges. 14: 75: 1905
Pseudotsuga taxifolia f. globosa (Beissn.) Schwer. Mitt. Deutsch. Dendrol. Ges. 32: 61 1922

Common names Top

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Language Common/alternative name
English douglas-fir
English douglas fir
English pseudotsuga douglasii
English columbian pine
English oregon pine
English pseudotsuga taxifolia
Spanish abeto de douglas
Spanish pseudotsuga taxifolia
Spanish pseudotsuga douglasii
Spanish abeto douglas
Spanish abies menziesii
Spanish douglas de oregon
Spanish douglas de oregón
Spanish falsa tsuga verde de las rocosas
Spanish pino de oregon
Spanish pino de oregón
Spanish pino oregon
Spanish pino oregón
Spanish pinus douglasii
Spanish pinus taxifolia
Spanish pseudotsuga mucronata
Azerbaijani yalançı tsuqa
Belarusian Дугласія шэрая
Catalan pseudotsuga menziesii var. menziesii
Catalan sapin de douglas
Catalan pseudotsuga menziesii var. glauca
Czech douglaska tisolistá
Czech abies menziesii
Czech pseudotsuga douglasii
Czech pseudotsuga taxifolia
Welsh ffynidwydden douglas
Danish grøn douglasgran
Danish blå douglasgran
Danish oregon pine
Danish pseudotsuga menziesii var. glauca
Danish pseudotsuga menziesii var. menziesii
German douglasie
German grüne douglasie
German douglas-tanne
German douglasfichte
German douglaskiefer
German douglastanne
German sapin de douglas
German pseudotsuga lindleyana
German gewöhnliche douglasie
Esperanto menzies-pseŭdocugo
Esperanto duglasa pseŭdocugo
Estonian harilik ebatsuuga
Estonian douglase kuusk
Estonian pseudotsuga douglasii
Estonian ranniku-ebatsuuga
Estonian roheline ebatsuuga
Estonian sinihall ebatsuuga
Basque douglas izei
Persian صنوبر داگلاس
Finnish lännendouglaskuusi
Finnish douglaskuusi
Finnish oregoninmänty
Finnish oregonmänty
French sapin de douglas
French pin d'oregon
French pin de l'orégon
Irish giúis dhúghlais
Galician abeto de douglas
Hebrew אשוח דאגלס
Croatian obična američka duglazija
Upper Sorbian wšědna douglasija
Hungarian amerikai duglászfenyő
Armenian Կեղծթսուգա կենիատերև
Icelandic degli
Italian abete di douglas
Italian pseudotsuga douglasii
Italian douglasia
Italian pino dell'oregon
Japanese ベイマツ
Japanese アメリカトガサワラ
Japanese アメリカマツ
Japanese オレゴンパイン
Japanese オレゴン松
Japanese ダグラス・ファー
Japanese ダグラスファー
Japanese ダグラスモミ
Japanese メリケンマツ
Japanese 米松
Korean 미송
Lithuanian didžioji pocūgė
Lithuanian sapin de douglas
Macedonian Дуглазија
Macedonian дуглазија
Norwegian Bokmål blå douglasgran
Norwegian Bokmål colorado-douglasgran
Norwegian Bokmål grå douglasgran
Norwegian Bokmål grønn douglasgran
Norwegian Bokmål kyst-douglasgran
Norwegian Bokmål kystdouglasgran
Norwegian Bokmål oregon-douglasgran
Norwegian Bokmål rocky mountain douglasgran
Norwegian Bokmål rocky mountain-douglasgran
Norwegian Bokmål rocky mountains-douglasgran
Norwegian Bokmål douglasgran
Dutch douglasspar
Dutch douglas spar
Dutch douglas-spar
Dutch oregonhout
Dutch douglas
Polish daglezja zielona
Polish jedlica douglasa
Polish jedlica menziesa
Polish jedlica zielona
Polish pesudotsuga douglasii
Portuguese abeto de douglas
Russian Псевдотсуга Мензиса
Russian дугласия тиссолистная
Russian дугласова ель
Russian Дугласова пихта
Russian лжетсуга Мензиса
Russian орегонская сосна
Russian пихта Дугласа
Slovak douglaska tisolistá
Slovak duglaska tisolistá
Slovenian duglazija
Serbian Дуглазија
Serbian дуглазија
Swedish sapin de douglas
Swedish douglasgran
Tamil உயரமான மரம்
Ukrainian Псевдотсуга Мензіса
Vietnamese linh sam douglas duyên hải
Chinese 花旗松
Chinese 北美黃杉
Chinese 道格拉斯冷杉

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pseudotsuga menziesii var. glauca (Mayr) Franco Conif. Duarum Nominibus : 6 (1950)
Pseudotsuga menziesii var. menziesii

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000478194
UNII U64740SKWN
Cornell Woody Plants 198
Canadensys 7200
USDA Plants PSME
UConn 369
Tropicos 24900226
INPN 116216
Flora of Italy 8586
KEW urn:lsid:ipni.org:names:677141-1
The Plant List kew-2556763
Missouri Botanical Garden 285009
PFAF Pseudotsuga menziesii
PaleoBotany 20781
Open Tree Of Life 1075713
Observations.org 7274
NCBI Taxonomy 3357
NBN Atlas NHMSYS0000462103
Nature Serve 2.136725
IUCN Red List 42429
IPNI 211600-2
iNaturalist 48256
GBIF 2685796
Freebase /m/0dd7d
EPPO PSTME
EOL 1061712
Elurikkus 6611
Calflora (Californian flora) 10283
US Library of Congress sh85039200
USDA GRIN 30191
Wikipedia Douglas_fir

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_001517045.1 DougFir1.0 Scaffold TreeGenes Database 2015-12-22 60.0x 13.67 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The importance of regeneration processes on forest biodiversity in old-growth forests in the Pacific Northwest Luu H, Ris Lambers JH, Lutz JA, Metz M, Snell RS Philos Trans R Soc Lond B Biol Sci 08-Apr-2024
PMCID:PMC10999264
doi:10.1098/rstb.2023.0016
PMID:38583471
The influence of tree genus, phylogeny, and richness on the specificity, rarity, and diversity of ectomycorrhizal fungi Tedersoo L, Drenkhan R, Abarenkov K, Anslan S, Bahram M, Bitenieks K, Buegger F, Gohar D, Hagh‐Doust N, Klavina D, Makovskis K, Zusevica A, Pritsch K, Padari A, Põlme S, Rahimlou S, Rungis D, Mikryukov V Environ Microbiol Rep 04-Apr-2024
PMCID:PMC10994715
doi:10.1111/1758-2229.13253
PMID:38575147
Behaviour and landscape contexts determine the effects of artificial light on two crepuscular bird species Adams CA, Clair CC, Knight EC, Bayne EM Landsc Ecol 26-Mar-2024
PMCID:PMC10965584
doi:10.1007/s10980-024-01875-3
PMID:38550967
Comparison of ddRADseq and EUChip60K SNP genotyping systems for population genetics and genomic selection in Eucalyptus dunnii (Maiden) Aguirre NC, Villalba PV, García MN, Filippi CV, Rivas JG, Martínez MC, Acuña CV, López AJ, López JA, Pathauer P, Palazzini D, Harrand L, Oberschelp J, Marcó MA, Cisneros EF, Carreras R, Martins Alves AM, Rodrigues JC, Hopp HE, Grattapaglia D, Cappa EP, Paniego NB, Marcucci Poltri SN Front Genet 26-Mar-2024
PMCID:PMC11008695
doi:10.3389/fgene.2024.1361418
PMID:38606359
Tracking effects of extreme drought on coniferous forests from space using dynamic habitat indices Safaei M, Kleinebecker T, Weis M, Große-Stoltenberg A Heliyon 20-Mar-2024
PMCID:PMC10981029
doi:10.1016/j.heliyon.2024.e27864
PMID:38560251
Fuel types misrepresent forest structure and composition in interior British Columbia: a way forward Baron JN, Hessburg PF, Parisien MA, Greene GA, Gergel SE, Daniels LD Fire Ecol 07-Feb-2024
PMCID:PMC10847212
doi:10.1186/s42408-024-00249-z
PMID:38333107
Transcriptomic Insights into Abies koreana Drought Tolerance Conferred by Aureobasidium pullulans AK10 Park J, Mannaa M, Han G, Jung H, Jeon HS, Kim JC, Park AR, Seo YS Plant Pathol J 01-Feb-2024
PMCID:PMC10850533
doi:10.5423/PPJ.FT.11.2023.0161
PMID:38326956
Family matters inside the order Agaricales: systematic reorganization and classification of incertae sedis clitocyboid, pleurotoid and tricholomatoid taxa based on an updated 6-gene phylogeny Vizzini A, Alvarado P, Consiglio G, Marchetti M, Xu J Stud Mycol 31-Jan-2024
PMCID:PMC11003440
doi:10.3114/sim.2024.107.02
PMID:38600959
Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW J Fungi (Basel) 26-Jan-2024
PMCID:PMC10890244
doi:10.3390/jof10020105
PMID:38392777
Severe and frequent extreme weather events undermine economic adaptation gains of tree-species diversification Fuchs JM, Husmann K, Schick J, Albert M, Lintunen J, Paul C Sci Rep 25-Jan-2024
PMCID:PMC10810831
doi:10.1038/s41598-024-52290-2
PMID:38272940
Differential Etching of Rays at Wood Surfaces Exposed to an Oxygen Glow Discharge Plasma Cheng KJ, Ma W, Evans PD Materials (Basel) 22-Jan-2024
PMCID:PMC10818692
doi:10.3390/ma17020521
PMID:38276461
Predicted and Experimental Bending Behaviour of Glulam Bonded by RPF Adhesive Kytka T, Gašparík M, Sahula L, Novák D, Karami E, Das S, Sviták M Materials (Basel) 21-Jan-2024
PMCID:PMC10817475
doi:10.3390/ma17020514
PMID:38276452
Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review Rungjindamai N, Jones EB J Fungi (Basel) 15-Jan-2024
PMCID:PMC10820240
doi:10.3390/jof10010067
PMID:38248976
Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 Strickland LE, Thompson RS, Shafer SL, Bartlein PJ, Pelltier RT, Anderson KH, Schumann RR, McFadden AK Sci Data 12-Jan-2024
PMCID:PMC10786896
doi:10.1038/s41597-023-02616-y
PMID:38216580
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

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
> Lignans, neolignans and related compounds / Furanoid lignans
(2R,3R)-2-[3-[5-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-hydroxy-3-methoxyphenyl]-4,5-dihydroxyphenyl]-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 102404043 Click to see COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)C3C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)C5C6COC(C6CO5)C7=CC(=C(C=C7)O)OC 660.60 unknown https://doi.org/10.1039/C39890000217
2-[3,4-Dihydroxy-5-[2-hydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-3-methoxyphenyl]phenyl]-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 162955463 Click to see COC1=CC(=CC(=C1O)C2=C(C(=CC(=C2)C3C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)C5C6COC(C6CO5)C7=CC(=C(C=C7)O)OC 660.60 unknown https://doi.org/10.1039/C39890000217
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Methyl 16-hydroxyhexadecanoate 3496888 Click to see COC(=O)CCCCCCCCCCCCCCCO 286.40 unknown https://doi.org/10.1016/0031-9422(72)80112-2
Methyl 18-hydroxyoctadecanoate 13245692 Click to see COC(=O)CCCCCCCCCCCCCCCCCO 314.50 unknown https://doi.org/10.1016/0031-9422(72)80112-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
Gibberellic acid 6466 Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 346.40 unknown https://doi.org/10.1034/J.1399-3054.1992.850312.X
Gibberellin A1 5280379 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O 348.40 unknown https://doi.org/10.1034/J.1399-3054.1992.850312.X
Gibberellin A4 92109 Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O 332.40 unknown https://doi.org/10.1034/J.1399-3054.1992.850312.X
Gibberellin A7 92782 Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O 330.40 unknown https://doi.org/10.1034/J.1399-3054.1992.850312.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
> 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/10.3891/ACTA.CHEM.SCAND.22-0938
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
(+)-beta-Pinene 10290825 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373196/
https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
> 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/10.3891/ACTA.CHEM.SCAND.22-0938
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.22-0938
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
(E)-alpha-bisabolene 5315468 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
(Z)-alpha-Bisabolene 5352653 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(95)00033-Q
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,8aR)-8a-methyl-5-methylidene-3-propan-2-yl-1,2,3,6,7,8-hexahydronaphthalene 162940475 Click to see CC(C)C1CCC2(CCCC(=C)C2=C1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91291-3
8a-Methyl-5-methylidene-3-propan-2-yl-1,2,3,6,7,8-hexahydronaphthalene 14038481 Click to see CC(C)C1CCC2(CCCC(=C)C2=C1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)91291-3
> Lipids and lipid-like molecules / Saccharolipids
[6-Methyl-5-(2-methylpropanoyloxy)-2-[[4,5,23-trihydroxy-24-(hydroxymethyl)-6-methyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-26-yl]oxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 2-methylbutanoate 78412972 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC(=O)C(C)C)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C(C)CC)OC5C(C(C(OC5O1)C)O)O)CO)O 1009.20 unknown https://doi.org/10.1055/S-2006-957983
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Zeatin riboside 6440982 Click to see CC(=CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO 351.36 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1062468/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
CID 476785 476785 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(89)80217-1
https://doi.org/10.1016/0031-9422(92)80317-8
Phlorin 12314169 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(89)80217-1
https://doi.org/10.1016/0031-9422(92)80317-8
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine 92180 Click to see CC(=CCNC1=NC=NC2=C1NC=N2)C 203.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1062468/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4R,5R,6S)-2-[4-[(2S,3R)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 163007250 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3C(C4=C(O3)C(=CC(=C4)CCCO)OC)CO)OC)O)O)O 506.50 unknown https://doi.org/10.1055/S-2006-957983
2-[4-[7-Hydroxy-3-(hydroxymethyl)-5-(3-hydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 45782907 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)OC4C(C(C(C(O4)CO)O)O)O 508.50 unknown https://doi.org/10.1055/S-2006-957983
Dihydrodehydroconiferyl alcohol 4-O-glucoside 14681438 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1055/S-2006-957983
Massonianoside B 76311962 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3C(C4=C(O3)C(=CC(=C4)CCCO)O)CO)OC)O)O)O 492.50 unknown https://doi.org/10.1055/S-2006-957983
Massonianoside D 101165147 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)OC4C(C(C(C(O4)CO)O)O)O 508.50 unknown https://doi.org/10.1055/S-2006-957983
Massoniaside B 73157194 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3C(C4=C(O3)C(=CC(=C4)CCCO)O)CO)OC)O)O)O 492.50 unknown https://doi.org/10.1055/S-2006-957983
Urolignoside 10602086 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown https://doi.org/10.1055/S-2006-957983
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Arecatannin A1 13752000 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 https://doi.org/10.1016/0031-9422(92)80317-8
Arecatannin C1 9876038 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 https://doi.org/10.1016/0031-9422(92)80317-8
Endotelon 130556 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 https://doi.org/10.1016/0031-9422(92)80317-8
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 https://doi.org/10.1016/0031-9422(92)80317-8
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 https://doi.org/10.1016/0031-9422(92)80317-8
Procyanidin B3 146798 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 https://doi.org/10.1016/0031-9422(92)80317-8
Procyanidin B4 147299 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 https://doi.org/10.1016/0031-9422(92)80317-8
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 https://doi.org/10.1016/0031-9422(92)80317-8
Procyanidin trimer T2 13751990 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 https://doi.org/10.1016/0031-9422(92)80317-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(89)80217-1
https://doi.org/10.1016/0031-9422(92)80317-8
Procyanidin 107876 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4(C(C(C5=C(C=C(C=C5O4)O)O)O)O)C6=CC(=C(C=C6)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
https://doi.org/10.1039/C39890000217
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R,3S)-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol 14282772 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol 14282771 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
3,5,7-Trihydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 14282773 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
4H-1-Benzopyran-4-one, 2-(3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl)-3,5,7-trihydroxy- 5748594 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(97)00245-8
Taxifolin 3'-glucoside 14282774 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14282768 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
(2S,3R,4S,5S,6R)-2-[[(2R,3R)-3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14282770 Click to see COC1=C(C=CC(=C1)C2C(CC3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3253888 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
2-[[3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14282769 Click to see COC1=C(C=CC(=C1)C2C(CC3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 14282776 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Catechin 7-glucoside 14282767 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Catechin 7-O-beta-D-glucopyranoside 10789789 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Sinensin 10456395 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8
Taxifolin 7-glucoside 14282775 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(92)80317-8

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