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Pinus flexilis

Pinus flexilis - 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 UUID64400224ad46a994194821
Scientific name Pinus flexilis
Authority E.James
First published in Narrat. Exp. St. Peter's River 2: 35 (1824)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pinus flexilis var. megalocarpa Sudw. Bull. Div. Forest. U.S.D.A. 14: 16 (1897)
Pinus flexilis var. macrocarpa Engelm. Rep. U.S. Geogr. Surv., Wheeler 6(Botany): 258 (1878 publ. 1879)
Pinus flexilis var. serrulata Engelm. Rep. U.S. Geogr. Surv., Wheeler 6(Botany): 258 (1878 publ. 1879)
Pinus flexilis var. alpina Silba J. Int. Conifer Preserv. Soc. 7: 30 (2000)
Pinus flexilis var. callahanii Silba J. Int. Conifer Preserv. Soc. 7: 30 (2000)
Pinus novaemexicana P.Landry Phytologia 65: 479 (1989)
Apinus flexilis Rydb. Bull. Torrey Bot. Club 32: 598 (1905)
Pinus lambertiana var. brevifolia Hook. Fl. Bor.-Amer. 2: 162. 1838
Pinus flexilis subsp. alpina (Silba) Silba J. Int. Conifer Preserv. Soc. 16: 22 (2009)
Pinus flexilis subsp. callahanii (Silba) Silba J. Int. Conifer Preserv. Soc. 16: 22 (2009)

Common names Top

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Language Common/alternative name
English rocky mountain white pine
English limber pine
Spanish pino torcido
Arabic صنوبر منحني
Bulgarian мек бор
Catalan pi limber
Czech borovice ohebná
German biegsame kiefer
Esperanto fleksebla pino
Estonian kalju-seedermänd
Estonian kalifornia seedermänd
Estonian kaljumänd
Persian کاج نرمسوزن
French pin flexible
Hebrew אורן גמיש
Hungarian nevadai cirbolyafenyő
Icelandic sveigfura
Japanese フレキシマツ
koi Лунвыв-рытвыв чочком пожум
nv naatsisʼáán bińdíshchííʼ
Polish sosna giętka
Russian Сосна мягкая
Vietnamese thông limber
Chinese 柔枝松
Chinese 软叶五针松

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pinus flexilis var. reflexa Engelm. Rep. U.S. Geogr. Surv., Wheeler 6(Botany): 258 (1878 publ. 1879)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Nebraska
      • North Dakota
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481474
Cornell Woody Plants 290
Canadensys 7186
USDA Plants PIFL2
UConn 323
Tropicos 24900193
INPN 717412
KEW urn:lsid:ipni.org:names:262945-1
The Plant List kew-2562108
Missouri Botanical Garden 284996
Open Tree Of Life 799605
Observations.org 211196
NCBI Taxonomy 151559
Nature Serve 2.140758
IUCN Red List 42363
IPNI 262945-1
iNaturalist 78585
GBIF 5285551
Freebase /m/02cm9b
FEIS plants/tree/pinfle
EPPO PIUFL
EOL 1061756
Elurikkus 6290
Calflora (Californian flora) 6514
US Library of Congress sh91004253
USDA GRIN 28449
Wikipedia Pinus_flexilis
CMAUP NPO23108
PaleoBotany 80161

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
Frequent and strong cold‐air pooling drives temperate forest composition Pastore MA, Classen AT, D'Amato AW, English ME, Rand K, Foster JR, Adair EC Ecol Evol 01-Apr-2024
PMCID:PMC10985370
doi:10.1002/ece3.11126
PMID:38571787
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
A Pinus strobus transcription factor PsbHLH1 activates the production of pinosylvin stilbenoids in transgenic Pinus koraiensis calli and tobacco leaves Kim YR, Han JY, Choi YE Front Plant Sci 18-Jan-2024
PMCID:PMC10830828
doi:10.3389/fpls.2024.1342626
PMID:38304739
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
Stone Pine (Pinus pinea L.) High-Added-Value Genetics: An Overview Simões AS, Borges MM, Grazina L, Nunes J Genes (Basel) 10-Jan-2024
PMCID:PMC10815827
doi:10.3390/genes15010084
PMID:38254973
Annual (2023) taxonomic update of RNA-directed RNA polymerase-encoding negative-sense RNA viruses (realm Riboviria: kingdom Orthornavirae: phylum Negarnaviricota) Kuhn JH, Abe J, Adkins S, Alkhovsky SV, Avšič-Županc T, Ayllón MA, Bahl J, Balkema-Buschmann A, Ballinger MJ, Kumar Baranwal V, Beer M, Bejerman N, Bergeron É, Biedenkopf N, Blair CD, Blasdell KR, Blouin AG, Bradfute SB, Briese T, Brown PA, Buchholz UJ, Buchmeier MJ, Bukreyev A, Burt F, Büttner C, Calisher CH, Cao M, Casas I, Chandran K, Charrel RN, Kumar Chaturvedi K, Chooi KM, Crane A, Dal Bó E, Carlos de la Torre J, de Souza WM, de Swart RL, Debat H, Dheilly NM, Di Paola N, Di Serio F, Dietzgen RG, Digiaro M, Drexler JF, Duprex WP, Dürrwald R, Easton AJ, Elbeaino T, Ergünay K, Feng G, Firth AE, Fooks AR, Formenty PB, Freitas-Astúa J, Gago-Zachert S, Laura García M, García-Sastre A, Garrison AR, Gaskin TR, Gong W, Gonzalez JP, de Bellocq J, Griffiths A, Groschup MH, Günther I, Günther S, Hammond J, Hasegawa Y, Hayashi K, Hepojoki J, Higgins CM, Hongō S, Horie M, Hughes HR, Hume AJ, Hyndman TH, Ikeda K, Jiāng D, Jonson GB, Junglen S, Klempa B, Klingström J, Kondō H, Koonin EV, Krupovic M, Kubota K, Kurath G, Laenen L, Lambert AJ, Lǐ J, Li JM, Liu R, Lukashevich IS, MacDiarmid RM, Maes P, Marklewitz M, Marshall SH, Marzano SY, McCauley JW, Mirazimi A, Mühlberger E, Nabeshima T, Naidu R, Natsuaki T, Navarro B, Navarro JA, Neriya Y, Netesov SV, Neumann G, Nowotny N, Nunes MR, Ochoa-Corona FM, Okada T, Palacios G, Pallás V, Papa A, Paraskevopoulou S, Parrish CR, Pauvolid-Corrêa A, Pawęska JT, Pérez DR, Pfaff F, Plemper RK, Postler TS, Rabbidge LO, Radoshitzky SR, Ramos-González PL, Rehanek M, Resende RO, Reyes CA, Rodrigues TC, Romanowski V, Rubbenstroth D, Rubino L, Runstadler JA, Sabanadzovic S, Sadiq S, Salvato MS, Sasaya T, Schwemmle M, Sharpe SR, Shi M, Shimomoto Y, Kavi Sidharthan V, Sironi M, Smither S, Song JW, Spann KM, Spengler JR, Stenglein MD, Takada A, Takeyama S, Tatara A, Tesh RB, Thornburg NJ, Tian X, Tischler ND, Tomitaka Y, Tomonaga K, Tordo N, Tu C, Turina M, Tzanetakis IE, Maria Vaira A, van den Hoogen B, Vanmechelen B, Vasilakis N, Verbeek M, von Bargen S, Wada J, Wahl V, Walker PJ, Waltzek TB, Whitfield AE, Wolf YI, Xia H, Xylogianni E, Yanagisawa H, Yano K, Ye G, Yuan Z, Zerbini FM, Zhang G, Zhang S, Zhang YZ, Zhao L, Økland AL J Gen Virol 25-Aug-2023
PMCID:PMC10721048
doi:10.1099/jgv.0.001864
PMID:37622664
Presence of p25alpha-Domain in Seed Plants (Spermatophyta): Microbial/Animal Contaminations and/or Orthologs Orosz F Life (Basel) 30-Jul-2023
PMCID:PMC10455874
doi:10.3390/life13081664
PMID:37629521
Lost in the bloom: DNA-PKcs in green plants Kumar KR Front Plant Sci 28-Jul-2023
PMCID:PMC10419180
doi:10.3389/fpls.2023.1231678
PMID:37575944
What matters most? Assessment of within-canopy factors influencing the needle microbiome of the model conifer, Pinus radiata Addison S, Armstrong C, Wigley K, Hartley R, Wakelin S Environ Microbiome 30-May-2023
PMCID:PMC10230745
doi:10.1186/s40793-023-00507-8
PMID:37254222
Growth, drought response, and climate‐associated genomic structure in whitebark pine in the Sierra Nevada of California van Mantgem PJ, Milano ER, Dudney J, Nesmith JC, Vandergast AG, Zald HS Ecol Evol 17-May-2023
PMCID:PMC10191741
doi:10.1002/ece3.10072
PMID:37206686
Bioclimatic Characterisation of Specific Native Californian Pinales and Their Future Suitability under Climate Change González-Pérez A, Álvarez-Esteban R, Penas Á, del Río S Plants (Basel) 12-May-2023
PMCID:PMC10224251
doi:10.3390/plants12101966
PMID:37653883
Presence and activity of nitrogen-fixing bacteria in Scots pine needles in a boreal forest: a nitrogen-addition experiment Bizjak T, Sellstedt A, Gratz R, Nordin A Tree Physiol 18-Apr-2023
PMCID:PMC10423461
doi:10.1093/treephys/tpad048
PMID:37073466
Genomic clines across the species boundary between a hybrid pine and its progenitor in the eastern Tibetan Plateau Guo JF, Zhao W, Andersson B, Mao JF, Wang XR Plant Commun 11-Mar-2023
PMCID:PMC10363505
doi:10.1016/j.xplc.2023.100574
PMID:36906801
Identification of Seven Additional Genome Segments of Grapevine-Associated Jivivirus 1 Candresse T, Svanella-Dumas L, Marais A, Depasse F, Faure C, Lefebvre M Viruses 22-Dec-2022
PMCID:PMC9862270
doi:10.3390/v15010039
PMID:36680079
Western Spruce Budworm Effects on Forest Resilience Polinko AD, Rapp MA, Sánchez Meador AJ, Graves AD, Ryerson DE, Waring KM Plants (Basel) 28-Nov-2022
PMCID:PMC9736256
doi:10.3390/plants11233266
PMID:36501306

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 / Benzene and substituted derivatives
1-Phenyl-5-heptene-1,3-diyne 5281154 Click to see CC=CC#CC#CC1=CC=CC=C1 166.22 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
Phenylheptatriyne 77981 Click to see CC#CC#CC#CC1=CC=CC=C1 164.20 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Butoxyethyl oleate 6436064 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCCOCCCC 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-1-hydroxytrideca-5,7,9,11-tetrayn-2-yl]oxyoxane-3,4,5-triol 54671425 Click to see CC#CC#CC#CC#CCCC(CO)OC1C(C(C(C(O1)CO)O)O)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(5E)-1-Phenyl-5-heptene-1,3-diyn-7-ol acetate 23274467 Click to see CC(=O)OCC=CC#CC#CC1=CC=CC=C1 224.25 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyne-1-ol acetate 11644243 Click to see CC(=O)OCC#CC#CC#CC1=CC=CC=C1 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-7-Phenyl-4,6-heptadiyne-1,2-diol 101808987 Click to see C1=CC=C(C=C1)C#CC#CCC(CO)O 200.23 unknown via CMAUP database
(S)-7-Phenyl-4,6-heptadiyne-2-ol 101395939 Click to see CC(CC#CC#CC1=CC=CC=C1)O 184.23 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyn-1-ol 3085176 Click to see C1=CC=C(C=C1)C#CC#CC#CCO 180.20 unknown via CMAUP database
7-Phenylhept-2-en-4,6-diyn-1-ol 114662 Click to see C1=CC=C(C=C1)C#CC#CC=CCO 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
2-Butoxyethyl linoleate 87553426 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCCOCCCC 380.60 unknown via CMAUP database
2-Butoxyethyl linolenate 87552578 Click to see CCCCOCCOC(=O)CCCCCCCC=CCC=CCC=CCC 378.60 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
Ethyl linolenate 5367460 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC 306.50 unknown via CMAUP database
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Rrr-alpha-tocopherylquinone 46183941 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoic acid 42433537 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CC(=O)O)C 310.50 unknown via CMAUP database
[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl] heptanoate 101918983 Click to see CCCCCCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C 408.70 unknown via CMAUP database
> 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(93)90029-Q
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
beta-Thujene 520384 Click to see CC1C=CC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/0305-1978(93)90029-Q
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 460890 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[[2-O-Acetyl-6-O-[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-beta-D-glucopyranosyl]oxy]benzeneacrylic acid 15071014 Click to see CC(=O)OC1C(C(C(OC1OC2=CC=C(C=C2)C=CC(=O)O)COC(=O)C=CC3=CC=C(C=C3)O)O)O 514.50 unknown via CMAUP database
4-[[6-O-[3-(4-Hydroxyphenyl)-1-oxo-2-propenyl]-beta-D-glucopyranosyl]oxy]benzeneacrylic acid 15071011 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C=CC(=O)O)O)O)O)O 472.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylthiophene 6920 Click to see CC(=O)C1=CC=CS1 126.18 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-[(2R)-6-methyl-2,3,4,5-tetrahydropyridin-2-yl]propan-2-one 101663292 Click to see CC1=NC(CCC1)CC(=O)C 153.22 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(Phenylethynyl)thiophene-2-methanol 2822242 Click to see C1=CC=C(C=C1)C#CC2=CC=C(S2)CO 214.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(Z)-7-[[beta-D-Glucopyranosyl]oxy]-3',4',6-trihydroxyaurone 15071008 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester 66883 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(4E)-1,7-Bis(3,4-dihydroxyphenyl)-4-hepten-3-one; 1,7-Bis-(3,4-dihydroxyphenyl)-4-hepten-3-one; Hirsutanone 66954880 Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O 328.40 unknown https://doi.org/10.1021/NP9801460
(r)-1,7-Diphenyl-3-heptanol 129821339 Click to see C1=CC=C(C=C1)CCCCC(CCC2=CC=CC=C2)O 268.40 unknown https://doi.org/10.1021/NP9801460
1,7-Bis-(3,4-dihydroxyphenyl)-heptane-5-ol 21672146 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)O)O)O 332.40 unknown https://doi.org/10.1021/NP9801460
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 14707657 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.1021/NP9801460
1,7-Diphenylheptan-3-ol 11076452 Click to see C1=CC=C(C=C1)CCCCC(CCC2=CC=CC=C2)O 268.40 unknown https://doi.org/10.1021/NP9801460
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75168353 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1021/NP9801460
Hirsutanonol 9928190 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1021/NP9801460
Hirsutenone 637394 Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O 328.40 unknown https://doi.org/10.1021/NP9801460
Oregonin 14707658 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O 478.50 unknown https://doi.org/10.1021/NP9801460
Rubranol 10088141 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)O)O)O 332.40 unknown https://doi.org/10.1021/NP9801460
Rubranoside A 10097263 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1021/NP9801460
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2,3-Dihydroxy-4-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]phenyl 4-O,6-O-diacetyl-beta-D-glucopyranoside 10840030 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)OC(=O)C 534.50 unknown via CMAUP database
2',3,3',4-Tetrahydroxy-4'-(6-O-acetyl-beta-D-glucopyranosyloxy)-trans-chalcone 14213555 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 492.40 unknown via CMAUP database
3',4'-Di(beta-D-glucopyranosyloxy)-2',3,4-trihydroxychalcone 102149400 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 612.50 unknown via CMAUP database
4'-(3-O,4-O,6-O-Triacetyl-beta-D-glucopyranosyloxy)-2',3,3',4-tetrahydroxychalcone 14861259 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)OC(=O)C)OC(=O)C 576.50 unknown via CMAUP database
4'-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-2',3,3',4-tetrahydroxychalcone 14213552 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O)O)O 612.50 unknown via CMAUP database
chrysosplenosid-C 118856019 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC4C(C(C(C(O4)CO)O)O)O)O)OC)O 522.50 unknown via CMAUP database
Marein 6441269 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
(2Z)-2-(3,4-Dihydroxybenzylidene)-6-[(4-O,6-O-diacetyl-beta-D-glucopyranosyl)oxy]-7-hydroxybenzofuran-3(2H)-one 101669623 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)O)OC(=O)C 532.40 unknown via CMAUP database
(Z)-6-[[6-O-[3-(4-Hydroxyphenyl)-1-oxo-2-propenyl]-beta-D-glucopyranosyl]oxy]-3',4',7-trihydroxyaurone 15071009 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)C(=O)C(=CC5=CC(=C(C=C5)O)O)O4)O)O)O)O)O 594.50 unknown via CMAUP database
(Z)-6-[[6-O-Acetyl-beta-D-glucopyranosyl]oxy]-3',4',7-trihydroxyaurone 15071010 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)O)O 490.40 unknown via CMAUP database
2-[(alphaZ)-3,4-Dihydroxybenzylidene]-6-(2-O,4-O,6-O-triacetyl-beta-D-glucopyranosyloxy)-7-hydroxybenzofuran-3(2H)-one 10674637 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)OC(=O)C)O)OC(=O)C 574.50 unknown via CMAUP database
2-[(alphaZ)-3,4-Dihydroxybenzylidene]-6-(3-O,4-O,6-O-triacetyl-beta-D-glucopyranosyloxy)-7-hydroxybenzofuran-3(2H)-one 10603216 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)OC(=O)C)OC(=O)C 574.50 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 / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,3'-Dimethoxy-4',5-dihydroxy-7-(beta-D-glucopyranosyloxy)flavone 13344657 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC)O 492.40 unknown via CMAUP database
3,3'-Dimethoxy-4',5-dihydroxy-7-[(6-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl)oxy]flavone 102316697 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5495545 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
Axillaroside 101243893 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown via CMAUP database
Centaurein 5489090 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Jacein 11577257 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Okanin 5281294 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)O)O)O)O)O 288.25 unknown via CMAUP database

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