Pinus monticola - Unknown
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Details Top

Internal ID UUID64400229dbfdd974733433
Scientific name Pinus monticola
Authority Douglas ex D.Don
First published in Descr. Pinus , ed. 3, 2: 144 bis (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pinus grozelieri Carrière Rev. Hort. (Paris) 41: 126 (1869)
Pinus strobus subsp. monticola (D.Don) A.E.Murray Kalmia 12: 23. 1982 [July 1982]
Pinus porphyrocarpa A.Murray bis in Ravenscr. Pinet. Brit. 1: 83 (1866)
Pinus monticola f. porphyrocarpa (A.Murray bis) P.Landry Bull. Soc. Bot. France 123: 58 (1976)
Strobus monticola (Douglas ex D.Don) Rydb. Fl. Rocky Mts. : 13 (1917)
Pinus strobus var. monticola (Douglas ex D.Don) Nutt. N. Amer. Sylv. 2: 118 1849
Pinus monticola var. minima Lemmon Bienn. Rep. Calif. State Board Forest. 2: 70. 1888
Pinus monticola var. digitata Lemmon Handb. W. Amer. Cone-bearers ed. 3: 22. 1895
Pinus monticola var. porphyrocarpa (A.Murray bis) Mast. J. Roy. Hort. Soc. 14: 235 1892

Common names Top

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Language Common/alternative name
English california mountain pine
English western white pine
English silver pine
Arabic صنوبر أليف الجبال
Czech borovice pohorská
German westliche weymouth-kiefer
Esperanto arĝenta pino
Estonian läänemänd
French pin argenté
Hebrew אורן לבן מערבי
Icelandic hvítfura
Japanese アメリカシロマツ
Japanese モンチコラマツ
koi Рытвыв чочком пожум
Lithuanian kalvinė pušis
Norwegian Bokmål vestlig hvitfuru
Norwegian Nynorsk vestleg kvitfuru
Polish sosna zachodnia
Russian Сосна белая западная
Russian Сосна горная веймутова
Russian Сосна айдахская белая
Swedish vittall
udm Шунды пуксён пал тӧдьы пужым
Ukrainian Сосна гірська веймутова
Vietnamese thông trắng miền tây
Chinese 加州五针松
Chinese 西部白松
Chinese 西部白鬆

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
  • Northern America
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
      • Nevada
    • Western Canada
      • Alberta
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000481790
UNII TJ19UP4W49
Canadensys 7187
USDA Plants PIMO3
Tropicos 24900034
INPN 458780
KEW urn:lsid:ipni.org:names:197032-2
The Plant List kew-2562442
Open Tree Of Life 568650
NCBI Taxonomy 3345
Nature Serve 2.136952
IUCN Red List 42383
IPNI 197032-2
iNaturalist 68084
GBIF 5285621
Freebase /m/0280pm
FEIS plants/tree/pinmot
EPPO PIUMO
EOL 999710
Elurikkus 6300
Calflora (Californian flora) 6519
USDA GRIN 28491
Wikipedia Western_white_pine
CMAUP NPO28895
PaleoBotany 15622

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
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
Fungal communities associated with early immature tubers of wild Gastrodia elata Li D, Jin X, Li Y, Wang Y, He H, Zhang H Ecol Evol 21-Feb-2024
PMCID:PMC10881901
doi:10.1002/ece3.11004
PMID:38389997
Current status of the cryopreservation of embryogenic material of woody species Ballesteros D, Martínez MT, Sánchez-Romero C, Montalbán IA, Sales E, Moncaleán P, Arrillaga I, Corredoira E Front Plant Sci 17-Jan-2024
PMCID:PMC10828030
doi:10.3389/fpls.2023.1337152
PMID:38298606
Genome-wide identification of rubber tree pathogenesis-related 10 (PR-10) proteins with biological relevance to plant defense Longsaward R, Viboonjun U Sci Rep 11-Jan-2024
PMCID:PMC10784482
doi:10.1038/s41598-024-51312-3
PMID:38212354
Contrasting Effects of Grazing in Shaping the Seasonal Trajectory of Foliar Fungal Endophyte Communities on Two Semiarid Grassland Species Dong X, Jiang F, Duan D, Tian Z, Liu H, Zhang Y, Hou F, Nan Z, Chen T J Fungi (Basel) 14-Oct-2023
PMCID:PMC10608051
doi:10.3390/jof9101016
PMID:37888272
Epigenetic architecture of Pseudotaxus chienii: Revealing the synergistic effects of climate and soil variables Su Y, Liu L, Deng Q, Lü Z, Wang Z, He Z, Wang T Ecol Evol 10-Sep-2023
PMCID:PMC10493196
doi:10.1002/ece3.10511
PMID:37701023
The amide derivative of anticopalic acid induces non-apoptotic cell death in triple-negative breast cancer cells by inhibiting FAK activation Chawengrum P, Luepongpatthana N, Thongnest S, Sirirak J, Boonsombat J, Lirdprapamongkol K, Keeratichamroen S, Kongwaen P, Montatip P, Kittakoop P, Svasti J, Ruchirawat S Sci Rep 18-Aug-2023
PMCID:PMC10439230
doi:10.1038/s41598-023-40669-6
PMID:37596365
On the limited consensus of mountain pine beetle impacts on wildfire Romualdi DC, Wilkinson SL, James PM Landsc Ecol 13-Jul-2023
PMCID:PMC10372117
doi:10.1007/s10980-023-01720-z
PMID:37521154
Leaf spectroscopy of resistance to Ceratocystis wilt of ‘Ōhi’a Seeley MM, Martin RE, Giardina C, Luiz B, Francisco K, Cook Z, Hughes MA, Asner GP PLoS One 23-Jun-2023
PMCID:PMC10289452
doi:10.1371/journal.pone.0287144
PMID:37352315
Complex relationships between climate and reproduction in a resident montane bird Whitenack LE, Welklin JF, Branch CL, Sonnenberg BR, Pitera AM, Kozlovsky DY, Benedict LM, Heinen VK, Pravosudov VV R Soc Open Sci 21-Jun-2023
PMCID:PMC10282579
doi:10.1098/rsos.230554
PMID:37351489
Fungicidal and plant growth-promoting traits of Lasiodiplodia pseudotheobromae, an endophyte from Andrographis paniculata Segaran G, Sathiavelu M Front Plant Sci 14-Jun-2023
PMCID:PMC10329105
doi:10.3389/fpls.2023.1125630
PMID:37426966
Fungal effectors versus defense-related genes of B. juncea and the status of resistant transgenics against fungal pathogens Rai P, Prasad L, Rai PK Front Plant Sci 08-Jun-2023
PMCID:PMC10285668
doi:10.3389/fpls.2023.1139009
PMID:37360735
Pest categorisation of Coleosporium eupatorii 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 24-May-2023
PMCID:PMC10208091
doi:10.2903/j.efsa.2023.8020
PMID:37234271
Halostachys caspica pathogenesis-related protein 10 acts as a cytokinin reservoir to regulate plant growth and development Feng Y, Ren Y, Zhang H, Heng Y, Wang Z, Wang Y Front Plant Sci 26-Apr-2023
PMCID:PMC10169677
doi:10.3389/fpls.2023.1116985
PMID:37180382
Too hot, too cold, or just right: Can wildfire restore dry forests of the interior Pacific Northwest? Greenler SM, Dunn CJ, Johnston JD, Reilly MJ, Merschel AG, Hagmann RK, Bailey JD PLoS One 27-Feb-2023
PMCID:PMC9970105
doi:10.1371/journal.pone.0281927
PMID:36848330

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
> Benzenoids / Phenols / Methoxyphenols
4-[(2S,5S,6S)-6-[(2S,5R,6R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 162921705 Click to see COC1=CC(=CC(=C1O)OC)C2C(COC(CO2)C(C3=CC(=C(C=C3)O)OC)O)C4COC(COC4C5=CC(=C(C(=C5)OC)O)OC)C(C6=CC(=C(C=C6)O)OC)O 810.80 unknown https://doi.org/10.1002/HLCA.19810640424
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1002/JPS.3080220906
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5aS,8aR)-5-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 134842228 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(=O)C3CC4=CC5=C(C=C24)OCO5 398.40 unknown https://doi.org/10.1002/HLCA.19810640424
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(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/S0031-9422(00)85875-6
(E)-5-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoic acid 38352641 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)89956-2
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/S0031-9422(00)85875-6
18-Nordehydroabiet-4(19)-ene 44268166 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C 254.40 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 300.40 unknown via CMAUP database
Abieta-8,11,13-trien-15-ol 101586702 Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C 286.50 unknown via CMAUP database
Abieta-8,11,13-trien-7alpha-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
Abietatriene 6432211 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Anticopalic acid methyl ester 11290126 Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C 318.50 unknown https://doi.org/10.1016/S0031-9422(00)89956-2
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C 272.50 unknown via CMAUP database
methyl 5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoate 575209 Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C 318.50 unknown https://doi.org/10.1016/S0031-9422(00)89956-2
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
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/10.1139/B90-317
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1139/B90-317
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080191108
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080191108
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/JPS.3080191108
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1139/B90-317
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(24S)-Lanosta-9(11)-ene-3beta,24,25-triol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown https://doi.org/10.1002/HLCA.19810640424
(2R,5S)-5-[(3R)-3-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-2,4,4-trimethyl-1,3-dioxolane 162959269 Click to see CC1OC(C(O1)(C)C)CCC(C)C2CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C 500.80 unknown https://doi.org/10.1002/HLCA.19810640424
(3S,5R,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 162911890 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1002/HLCA.19810640424
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-1-en-3-ol 163008701 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.19810640424
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 162939471 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 474.80 unknown https://doi.org/10.1002/HLCA.19810640424
(5R,6S)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,5-diol 162913104 Click to see CC(C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C)C(CCC(C)(C)O)O 474.80 unknown https://doi.org/10.1002/HLCA.19810640424
(6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-one 163021792 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.19810640424
16-Oxo-21-episerratenediol 101280208 Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
21-Episerratenediol 3-methyl ether 101280203 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
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 via CMAUP database
5-[3-(3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl]-2,4,4-trimethyl-1,3-dioxolane 162959268 Click to see CC1OC(C(O1)(C)C)CCC(C)C2CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C 500.80 unknown https://doi.org/10.1002/HLCA.19810640424
6-(3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-1-en-3-ol 163008700 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.19810640424
6-(3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptan-3-one 163021791 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.19810640424
6-(3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptane-2,5-diol 162913103 Click to see CC(C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C)C(CCC(C)(C)O)O 474.80 unknown https://doi.org/10.1002/HLCA.19810640424
Serratenediol 3-methyl ether 21672660 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
Serratenediol dimethyl ether 101280202 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C 470.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives
(5R)-5-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]hexan-2-one 162858868 Click to see CC(CCC(=O)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 428.70 unknown https://doi.org/10.1002/HLCA.19810640424
5-(3-methoxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)hexan-2-one 162858867 Click to see CC(CCC(=O)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C 428.70 unknown https://doi.org/10.1002/HLCA.19810640424
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,4R,5S,6S,8S,9R,10S,13R,14S,15S,16R,17R)-17-[(E,2R,5S)-5-[[(2R,3R,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3-[(2S,3R,4S,5R)-4,5-dihydroxy-3-methoxyoxan-2-yl]oxy-4-hydroxyoxolan-2-yl]oxymethyl]-6-methylhept-3-en-2-yl]-10,13-dimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,4,6,8,15,16-hexol 163088767 Click to see CC(C)C(COC1C(C(C(O1)C(CO)O)O)OC2C(C(C(CO2)O)O)OC)C=CC(C)C3C(C(C4C3(CCC5C4(CC(C6C5(CCC(C6O)O)C)O)O)C)O)O 805.00 unknown https://doi.org/10.1002/HLCA.19810640424
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
13-Vinyl-16,17-dinor-14-oxaabietane 102594798 Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C 276.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-6-methyl-2-phenyl-4-benzopyrone 114429 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-Hydroxy-4-oxo-2-phenylchromen-5-olate 25200543 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-] 253.23 unknown via CMAUP database
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-) 25203524 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)[O-] 299.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
Phenol, 3-methoxy-5-(2-phenylethyl)- 636980 Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2 228.29 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
Pinosylvin 5280457 Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O 212.24 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-1147

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