Picea sitchensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Picea sitchensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Picea sitchensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644002459da8c781791625
Scientific name Picea sitchensis
Authority (Bong.) Carrière
First published in Traité Gén. Conif. : 260 (1855)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sequoia rafinesquei Carrière Traité Gén. Conif. , ed. 2: 213 (1867)
Pinus sitchensis Bong. Mém. Acad. Imp. Sci. St.-Pétersbourg, Sér. 6, Sci. Math. 2: 164 (1832)
Pinus menziesii Douglas ex Lamb. Descr. Pinus [Lambert], ed. 2. 3: 161, t. 71.
Picea menziesii Carrière Traité Gén. Conif. 237. 1855
Picea grandis Gordon Pinetum : 155 (1858)
Picea falcata (Raf.) J.V.Suringar Meded. Landbouwhoogeschool 30(2): 49 1927
Abies falcata Raf. Atlantic J. 1: 119 (1832)
Abies merkiana Fisch. ex Parl. Prodr. 16(2): 418 (1868)
Abies sitchensis Lindl. & Gord. J. Hort. Soc. London 5: 212 (1850)
Abies trigona Raf. Atlantic J. 1: 119 (1832)
Abies menziesii Lindl. Penny Cyclop. 1: 32. 1833
Pinus menziesii var. crispa Antoine Coniferen 86. 1841
Picea menziesii var. crispa (Antoine) Carrière Traité Gén. Conif. 237 1855
Picea sitchensis f. speciosa Beissn. Handb. Nadelholzk. 293 1891

Common names Top

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Language Common/alternative name
English sitka spruce
Spanish pícea de sitka
Arabic تنوب سيتكي
Arabic راتنج سيتكي
Azerbaijani sitxin küknarı
azb سیتکین کوکناری
Catalan pícea de sitka
Czech smrk sitka
Welsh sbriwsen sitca
Danish sitka-gran
Danish sitkagran
German sitka-fichte
German sitkafichte
Esperanto sitka-piceo
Estonian sitka kuusk
Persian نوئل سیتکایی
Finnish sitkakuusi
Finnish sitkankuusi
French Épicéa de sitka
French épinette de sitka
Irish sprús sitceach
Hebrew אשוחית סיטקה
Croatian sitkanska smreka
Upper Sorbian sitkowy šmrěk
Hungarian szitka luc
Icelandic sitkagreni
Italian peccio di sitka
Japanese シトカトウヒ
koi Ситкаись кӧз
lb sitkafiicht
Lithuanian sitkinė eglė
Macedonian ситканска смрча
Norwegian Bokmål sitkagran
Dutch sitka spar
Dutch sitkaspar
Norwegian Nynorsk sitkagran
Polish Świerk sitkajski
Portuguese sitka spruce
Russian Ель ситхинская
Slovak smrek sitkanský
Serbian Ситканска смрча
Serbian Смрча ситканска
Serbian Смрека ситканска
Serbian Ситканска смрека
Swedish sitkagran
Swedish sitkatall
Turkish sitka ladini
udm Ситкаысь кыз
vep sithine kuz'
Chinese 西加雲杉
Chinese 北美雲杉
Chinese 西加云杉
Chinese 阿拉斯加云杉
Chinese 巨云杉

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Netherlands
      • Poland
    • Northern Europe
      • Denmark
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • Newfoundland
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Subarctic America
      • Alaska
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000482639
UNII 8L4384H6HG
Canadensys 7178
USDA Plants PISI
INPN 113444
KEW urn:lsid:ipni.org:names:676986-1
The Plant List kew-2563578
Open Tree Of Life 771664
Observations.org 7185
NCBI Taxonomy 3332
NBN Atlas NHMSYS0000461257
Nature Serve 2.137451
IUCN Red List 42337
IPNI 676986-1
iNaturalist 68131
GBIF 5284827
Freebase /m/035762
FEIS plants/tree/picsit
EPPO PIESI
EOL 1033696
Elurikkus 6233
Calflora (Californian flora) 6495
US Library of Congress sh85123029
USDA GRIN 28327
Wikipedia Picea_sitchensis
CMAUP NPO13296
PaleoBotany 103419

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_010110895.2 Q903_v1 Scaffold BC Cancer Agency 2020-01-09 90.7x 19.05 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
Identifying the generalizable controls on insect associations of native and non‐native trees Gougherty AV, Klapwijk M, Liebhold AM, Mech A, Trombik J, Fei S Ecol Evol 12-May-2024
PMCID:PMC11089089
doi:10.1002/ece3.11265
PMID:38742186
Co-located ecological data for exploring top- and subsoil carbon dynamics across grassland-woodland contrasts Reinsch S, Lebron I, Brentegani M, Brooks M, Busi SB, Cagnarini C, Cooper D, Day J, Emmett BA, Fitos E, Goodall T, Griffiths R, Jones B, Keenan P, Keith A, Lopes-Mazzetto JM, Mason KE, Pallett D, Pereira MG, Pinder A, Robinson DA, Smart SM, Thomas A, Benham S, Vanguelova E, Cosby BJ Sci Data 09-May-2024
PMCID:PMC11081944
doi:10.1038/s41597-024-03333-w
PMID:38724554
A dataset of 40’000 trees with section-wise measured stem diameter and branch volume from across Switzerland Didion M, Herold A, Thürig E, Topuz S, Vulovic Z, Abegg M, Nitzsche J, Stillhard J, Glatthorn J Sci Data 09-May-2024
PMCID:PMC11082132
doi:10.1038/s41597-024-03336-7
PMID:38724536
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
Snow avalanches are a primary climate-linked driver of mountain ungulate populations White KS, Hood E, Wolken GJ, Peitzsch EH, Bühler Y, Wikstrom Jones K, Darimont CT Commun Biol 29-Apr-2024
PMCID:PMC11058775
doi:10.1038/s42003-024-06073-0
PMID:38684895
The origin, connectivity, and individual specialization of island wolves after deer extirpation Eriksson CE, Roffler GH, Allen JM, Lewis A, Levi T Ecol Evol 16-Apr-2024
PMCID:PMC11021858
doi:10.1002/ece3.11266
PMID:38633525
Comparative genomics analysis of pheophorbide a oxygenase (PAO) genes in eight pyrus genomes and their regulatory role in multiple stress responses in Chinese pear (Pyrus bretschneideri) Ma Y, Sun J, Zhang X, Sadaqat M, Tahir Ul Qamar M, Liu T Front Genet 16-Apr-2024
PMCID:PMC11058654
doi:10.3389/fgene.2024.1396744
PMID:38689648
Assembly and comparative analysis of the complete multichromosomal mitochondrial genome of Cymbidium ensifolium, an orchid of high economic and ornamental value Shen B, Shen A, Liu L, Tan Y, Li S, Tan Z BMC Plant Biol 09-Apr-2024
PMCID:PMC11003039
doi:10.1186/s12870-024-04962-4
PMID:38594641
Complete organelle genomes of Korean fir, Abies koreana and phylogenomics of the gymnosperm genus Abies using nuclear and cytoplasmic DNA sequence data Park S, Kwak M, Park S Sci Rep 01-Apr-2024
PMCID:PMC10985005
doi:10.1038/s41598-024-58253-x
PMID:38561351
Integrated transcriptomic and WGCNA analyses reveal candidate genes regulating mainly flavonoid biosynthesis in Litsea coreana var. sinensis Xie N, Guo Q, Li H, Yuan G, Gui Q, Xiao Y, Liao M, Yang L BMC Plant Biol 01-Apr-2024
PMCID:PMC10985888
doi:10.1186/s12870-024-04949-1
PMID:38561656
Development and laboratory validation of a plant-derived repellent blend, effective against Aedes aegypti [Diptera: Culicidae], Anopheles gambiae [Diptera: Culicidae] and Culex quinquefasciatus [Diptera: Culicidae] Wood MJ, Bull JC, Kanagachandran K, Butt TM PLoS One 21-Mar-2024
PMCID:PMC10956804
doi:10.1371/journal.pone.0299144
PMID:38512948
All tidal wetlands are blue carbon ecosystems Adame MF, Kelleway J, Krauss KW, Lovelock CE, Adams JB, Trevathan-Tackett SM, Noe G, Jeffrey L, Ronan M, Zann M, Carnell PE, Iram N, Maher DT, Murdiyarso D, Sasmito S, Tran DB, Dargusch P, Kauffman JB, Brophy L Bioscience 18-Mar-2024
PMCID:PMC11075650
doi:10.1093/biosci/biae007
PMID:38720908
Physiological responses to drought stress of three pine species and comparative transcriptome analysis of Pinus yunnanensis var. pygmaea Xiao F, Zhao Y, Wang X, Jian X, Yang Y BMC Genomics 16-Mar-2024
PMCID:PMC10944613
doi:10.1186/s12864-024-10205-5
PMID:38493093
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
2-Methyl-6-propylpiperidine 566623 Click to see CCCC1CCCC(N1)C 141.25 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Capillin 10321 Click to see CC#CC#CC(=O)C1=CC=CC=C1 168.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3S)-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 12312736 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown https://doi.org/10.1139/V70-170
1-Naphthalenepropanol, alpha-ethenyldecahydro-alpha,5,5,8a-tetramethyl-2-methylene- 238792 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown https://doi.org/10.1139/V70-170
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
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/10.1007/BF00193007
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/10.1111/J.1399-3054.1989.TB05975.X
Gibberellin A9 5281984 Click to see CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O 316.40 unknown https://doi.org/10.1111/J.1399-3054.1989.TB05975.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1002/JPS.3080200111
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1002/JPS.3080200111
> 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/10.1002/JPS.3080200111
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080200111
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1002/JPS.3080200111
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080200111
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1002/JPS.3080200111
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080200111
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epi-alpha-bisabolol 1201551 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophylla-4,8-dien-5-ol 14524924 Click to see CC1(CC2C1CCC(=C)C(CCC2=C)O)C 220.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Fgpdtarjoxrwjd-rrfjbimhsa- 11435962 Click to see CC(C)C1=CCC2(C(CCC(=C)C2C1)O)C 220.35 unknown via CMAUP database
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,3S,6S)-3-ethenyl-3-methyl-6-propan-2-yl-2-prop-1-en-2-ylcyclohexan-1-ol 102012174 Click to see CC(C)C1CCC(C(C1O)C(=C)C)(C)C=C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,5R,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,5-diol 10729639 Click to see CC12CCC(C(C1C(=C)CCC2O)O)C(C)(C)O 254.36 unknown via CMAUP database
2-[(2R,4aR)-4a,8-dimethyl-3,4,5,6-tetrahydro-2H-naphthalen-2-yl]propan-2-ol 10632752 Click to see CC1=CCCC2(C1=CC(CC2)C(C)(C)O)C 220.35 unknown via CMAUP database
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Pygmol 14167388 Click to see CC12CCCC(C1C(C(CC2)C(C)(C)O)O)(C)O 256.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,7S)-4beta,5alpha-Epoxygermacr-1(10)-en-2beta,6beta-diol 101014201 Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)O 254.36 unknown via CMAUP database
(1R,2E,6E,10S)-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-ol 71608919 Click to see CC1=CCCC(=CC(C(CC1)C(C)C)O)C 222.37 unknown via CMAUP database
(1R,2E,6R,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol 15479893 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O 254.36 unknown via CMAUP database
(1R,2E,6S,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol 15479892 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O 254.36 unknown via CMAUP database
(1R,2R,3S,6E,10S)-6,10-dimethyl-3-propan-2-yl-11-oxabicyclo[8.1.0]undec-6-en-2-ol 14109689 Click to see CC1=CCCC2(C(O2)C(C(CC1)C(C)C)O)C 238.37 unknown via CMAUP database
(1R,2R,3S,7R,10S)-10-methyl-6-methylidene-3-propan-2-yl-11-oxabicyclo[8.1.0]undecane-2,7-diol 10610977 Click to see CC(C)C1CCC(=C)C(CCC2(C(C1O)O2)C)O 254.36 unknown via CMAUP database
(1R,4S,5E,7S)-4-methyl-10-methylidene-7-propan-2-ylcyclodec-5-ene-1,4-diol 9991811 Click to see CC(C)C1CCC(=C)C(CCC(C=C1)(C)O)O 238.37 unknown via CMAUP database
(1S,2R,3S,6E)-6-methyl-10-methylidene-3-propan-2-ylcyclodec-6-ene-1,2-diol 100982186 Click to see CC1=CCCC(=C)C(C(C(CC1)C(C)C)O)O 238.37 unknown via CMAUP database
(1S,4E,6R,7S)-4-Methyl-7-isopropyl-10-methylene-4-cyclodecene-1,6-diol 100982187 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)C)O 238.37 unknown via CMAUP database
(4aR,11E,12aR)-2,2,4,4,11-pentamethyl-7-methylidene-4a,5,6,9,10,12a-hexahydrocyclodeca[d][1,3]dioxin-8-one 10732427 Click to see CC1=CC2C(CCC(=C)C(=O)CC1)C(OC(O2)(C)C)(C)C 292.40 unknown via CMAUP database
(4E,6R,7R)-6-hydroxy-7-(2-hydroxypropan-2-yl)-4-methyl-10-methylidenecyclodec-4-en-1-one 10729506 Click to see CC1=CC(C(CCC(=C)C(=O)CC1)C(C)(C)O)O 252.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
tatridin B 14191260 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 12299961 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,11R,12S,15S,16S,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-one 162939212 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown https://doi.org/10.1139/V70-170
(1S,6R,8R,11R,12S,15S,16R,19R,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280204 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
(1S,6R,8R,11S,15S,16R,19R,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3(12)-en-8-ol 102118065 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4C(C3)(CCC5C4(CCC(C5(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
(1S,6S,11R,12R,15S,16R,19S,21R)-19-hydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-one 163026501 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1O)C)C)(C)C)C)C 440.70 unknown https://doi.org/10.1139/V70-170
(1S,6S,11R,12S,15S,16R,19R,21S)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-one 162939211 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown https://doi.org/10.1139/V70-170
(3S,6R,8R,11R,12S,15S,16R,19R,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 101280205 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C 470.80 unknown https://doi.org/10.1139/V70-170
(3S,6R,8S,11R,12S,15S,16R,19S,21S)-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene-8,19-diol 163195079 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1139/V70-170
11-Methoxy-4,4,7a,10,10,13a,15b-heptamethyl-1,2,4,4a,5,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-3h-cyclohepta[1,2-a:5,4-a']dinaphthalen-3-one 279466 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown https://doi.org/10.1139/V70-170
https://doi.org/10.1016/S0040-4020(01)82906-9
11-Methoxy-4,4,7a,10,10,13a,15b-heptamethyl-2,3,4,4a,5,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-1h-cyclohepta[1,2-a:5,4-a']dinaphthalen-3-ol 279464 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
19-Hydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-one 73816206 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1O)C)C)(C)C)C)C 440.70 unknown https://doi.org/10.1139/V70-170
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
8,19-Dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 14830064 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C 470.80 unknown https://doi.org/10.1139/V70-170
Arnidiol 10478550 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CCC1=C)C)O)C)C)(C)C)O)C 442.70 unknown via CMAUP database
C(14a)-Homo-27-norgammacer-13-en-21beta-ol, 3alpha-methoxy- 550210 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4C(C3)(CCC5C4(CCC(C5(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1016/S0040-4020(01)82906-9
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
CID 634946 634946 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown https://doi.org/10.1139/V70-170
https://doi.org/10.1016/S0040-4020(01)82906-9
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown via CMAUP database
Dammaradienyl acetate 14137680 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)C 468.80 unknown via CMAUP database
Faradiol 9846222 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CC=C1C)C)O)C)C)(C)C)O)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1016/S0031-9422(00)81127-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
(3R,5S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 13475124 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O 448.70 unknown https://doi.org/10.1016/S0031-9422(00)81127-9
Typhasterol 13475120 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O 448.70 unknown https://doi.org/10.1016/S0031-9422(00)81127-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> 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://doi.org/10.1016/S0015-3796(17)30130-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,4R,5R,9S,10S,12R,15S)-4,9,15-triacetyloxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] benzoate 162817241 Click to see CC1CC23C(=O)C(C4(C5C(C5(C)C)C(C(C4=CC2(C1OC(=O)C)O3)OC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 580.60 unknown https://doi.org/10.1016/S0031-9422(00)81127-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(4S)-2-METHYL-2,4-pentanediol 5288834 Click to see CC(CC(C)(C)O)O 118.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2E,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 44575221 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown via CMAUP database
(2Z,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 44575223 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown via CMAUP database
[(2E,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92269932 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
[(2E,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92269933 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
[(2Z,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92973365 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
[(2Z,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92973366 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
Indole-3-acetic acid 802 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)O 175.18 unknown https://doi.org/10.1007/BF00387138
Methyl indole-3-acetate 74706 Click to see COC(=O)CC1=CNC2=CC=CC=C21 189.21 unknown https://doi.org/10.1007/BF00387138
> Organoheterocyclic compounds / Piperidines
(-)-Pinidinone 11159443 Click to see CC1CCCC(N1)CC(=O)C 155.24 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
> Organoheterocyclic compounds / Piperidines / Piperidinones
(1s,5r)-1-Methyl-9-azabicyclo[3.3.1]nonan-3-one 161131 Click to see CC12CCCC(N1)CC(=O)C2 153.22 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dracunculin 5319474 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2 220.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838451/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786330/
https://doi.org/10.1007/S00253-015-6691-1
https://doi.org/10.1002/HON.2122
https://doi.org/10.1016/J.JNUTBIO.2015.07.005
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1021/JF5050266
https://doi.org/10.3892/MMR.2015.4156
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-{3-[2-(3,4-Dihydroxyphenyl)ethenyl]-5-hydroxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol 5089891 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)88881-0
Astringin 5281712 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/0031-9422(91)83610-W
https://doi.org/10.1016/S0031-9422(00)88881-0
https://doi.org/10.1111/J.1365-3059.1992.TB02555.X
Isorhapontin 5281716 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://doi.org/10.1016/0031-9422(91)83610-W
https://doi.org/10.1111/J.1365-3059.1992.TB02555.X

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