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Pinus contorta

Pinus contorta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pinus contorta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pinus contorta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pinus contorta - 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 UUID64400220e5edc182403077
Scientific name Pinus contorta
Authority Douglas ex Loudon
First published in Arbor. Frutic. Brit. 4: 2292 (1838)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pinus inops Bong. Mém. Acad. Imp. Sci. St.-Pétersbourg, Sér. 6, Sci. Math. 2: 168 (1832)
Pinus macintoshiana P.Lawson Cat. 1855: 15 (1855)
Pinus contorta subsp. bolanderi (Parl.) A.E.Murray Kalmia 12: 22. 1982 [July 1982]
Pinus bolanderi Parl. Prodr. 16(2): 379 (1868)
Pinus contorta var. bolanderi (Parl.) Vasey Leafl. Dept. Agric. 18: 177 1876
Pinus contorta subsp. bolanderi (Parl.) Critchf. Publ. Maria Moors Cabot. Found. Bot. Res. no. 3: 106. 1957
Pinus contorta var. bolanderi Lemmon Erythea 2: 176. 1894
Pinus contorta var. bolanderi (Parl.) Koehne Deut. Dendrol. 37 1893

Common names Top

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Language Common/alternative name
English bolander beach pine
English lodgepole pine
English tamarack pine
English shore pine
English bolander's beach pine
Spanish pino contorto costero
Spanish pino contorto de hoja ancha
Spanish pino de murray
Spanish pino contorto
Catalan lodgepole pine
chy hoóxe'e
Czech borovice pokroucená
Czech borovice murrayova
Czech borovice tyčová
Welsh pinwydden gamfrig
Danish contorta-fyr
Danish klit-fyr
Danish klitfyr
German dreh-kiefer
German drehkiefer
German küstenkiefer
German küsten-kiefer
Esperanto tordopino
Estonian keerdokkaline mänd
Estonian keerdmänd
Estonian murray mänd
Persian کاج ساحلی
Finnish kontortamänty
Finnish murraynmänty
French pin tordu
Hebrew אורן מפותל
Upper Sorbian wjertawa chójna
Hungarian csavarttűjű fenyő
Indonesian tusam pesisir
Icelandic stafafura
Italian pino contorto
Japanese コントルタマツ
Japanese ロッジポールマツ
Japanese ロッジポール松の木
Japanese ロッジポールパイン
Lithuanian suktaspyglė pušis
Norwegian Bokmål contortafuru
Norwegian Bokmål vrifuru
Dutch draaiden
Polish sosna wydmowa
Russian Сосна скрученная широкохвойная
Slovak borovica pobrežná
Slovak borovica stočená
Swedish strandtall
Swedish contortatall
Swedish kontortatall
Swedish klipptall
Swedish contorta
Ukrainian Сосна скручена широкохвойна
Chinese 扭葉鬆
Chinese 扭叶松
Chinese 海灘松
Chinese 美国黑松
Chinese 扭葉松
Chinese 海灘鬆
Chinese 美國黑松
Chinese 美國黑鬆

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pinus contorta var. contorta
Pinus contorta var. latifolia Engelm. ex S.Watson Botany [Fortieth Parallel] : 331 (1871)
Pinus contorta var. murrayana (Balf.) Engelm. Trans. Acad. Sci. St. Louis 4: 177. 1880 (1880)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  • Europe
    • Middle Europe
      • Czechoslovakia
      • Germany
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Italy
      • Romania
  • Northern America
    • Mexico
      • Mexico Northwest
    • North-central U.S.A.
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • Southwestern U.S.A.
      • California
      • Nevada
      • Utah
    • Subarctic America
      • Alaska
      • Northwest Territorie
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481330
UNII 31725596TV
Canadensys 7184
USDA Plants PICO
Tropicos 24900183
INPN 458773
KEW urn:lsid:ipni.org:names:30000492-2
The Plant List kew-2561967
Open Tree Of Life 1044477
Observations.org 7193
NCBI Taxonomy 3339
NBN Atlas NBNSYS0000004786
Nature Serve 2.147775
IUCN Red List 42351
IPNI 30000492-2
iNaturalist 48934
GBIF 5285750
Freebase /m/02jpyz
EPPO PIUCN
EOL 1061758
Elurikkus 6285
Calflora (Californian flora) 6508
US Library of Congress sh85078053
USDA GRIN 28435
Wikipedia Pinus_contorta

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
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
Characterizing heterogeneous forest structure in ponderosa pine forests via UAS-derived structure from motion Hanna L, Tinkham WT, Battaglia MA, Vogeler JC, Ritter SM, Hoffman CM Environ Monit Assess 09-May-2024
PMCID:PMC11082040
doi:10.1007/s10661-024-12703-1
PMID:38724828
Tree growth potential and its relationship with soil moisture conditions across a heterogeneous boreal forest landscape Larson J, Vigren C, Wallerman J, Ågren AM, Appiah Mensah A, Laudon H Sci Rep 09-May-2024
PMCID:PMC11078985
doi:10.1038/s41598-024-61098-z
PMID:38719887
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
Functional diversity enhances dryland forest productivity under long-term climate change Hisano M, Ghazoul J, Chen X, Chen HY Sci Adv 24-Apr-2024
PMCID:PMC11042740
doi:10.1126/sciadv.adn4152
PMID:38657059
Variation in genomic vulnerability to climate change across temperate populations of eelgrass (Zostera marina) Jeffery NW, Vercaemer B, Stanley RR, Kess T, Dufresne F, Noisette F, O'Connor MI, Wong MC Evol Appl 21-Apr-2024
PMCID:PMC11033490
doi:10.1111/eva.13671
PMID:38650965
Insights into the molecular phylogeny and morphology of three novel Dothiora species, along with a worldwide checklist of Dothiora Senwanna C, Hongsanan S, Khuna S, Kumla J, Yarasheva M, Gafforov Y, Abdurazakov A, Suwannarach N Front Cell Infect Microbiol 19-Apr-2024
PMCID:PMC11067756
doi:10.3389/fcimb.2024.1367673
PMID:38707512
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
Globe-LFMC 2.0, an enhanced and updated dataset for live fuel moisture content research Yebra M, Scortechini G, Adeline K, Aktepe N, Almoustafa T, Bar-Massada A, Beget ME, Boer M, Bradstock R, Brown T, Castro FX, Chen R, Chuvieco E, Danson M, Değirmenci CÜ, Delgado-Dávila R, Dennison P, Di Bella C, Domenech O, Féret JB, Forsyth G, Gabriel E, Gagkas Z, Gharbi F, Granda E, Griebel A, He B, Jolly M, Kotzur I, Kraaij T, Kristina A, Kütküt P, Limousin JM, Martín MP, Monteiro AT, Morais M, Moreira B, Mouillot F, Msweli S, Nolan RH, Pellizzaro G, Qi Y, Quan X, Resco de Dios V, Roberts D, Tavşanoğlu Ç, Taylor AF, Taylor J, Tüfekcioğlu İ, Ventura A, Younes Cardenas N Sci Data 04-Apr-2024
PMCID:PMC10995118
doi:10.1038/s41597-024-03159-6
PMID:38575621
Postfire reproduction of a serotinous conifer, the giant sequoia, in the Nelder Grove, California Hanson CT, Chi TY, Baker BC, Khosla M, Dorsey MK Ecol Evol 03-Apr-2024
PMCID:PMC10990047
doi:10.1002/ece3.11213
PMID:38571806
Warming affects leaf light use efficiency and functional traits in alpine plants: evidence from a 4-year in-situ field experiment Zhou Z, Su P, Yang J, Shi R, Ding X Front Plant Sci 19-Mar-2024
PMCID:PMC10985207
doi:10.3389/fpls.2024.1353762
PMID:38567127
A case study on the early stage of Pinus nigra invasion and its impact on species composition and pattern in Pannonic sand grassland Bakacsy L, Szepesi Á Sci Rep 01-Mar-2024
PMCID:PMC10907687
doi:10.1038/s41598-024-55811-1
PMID:38429361
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
Tree adaptive growth (TAG) model: a life-history theory-based analytical model for post-thinning forest stand dynamics Roitberg B, Li C, Lalonde R Front Plant Sci 26-Feb-2024
PMCID:PMC11027167
doi:10.3389/fpls.2024.1344883
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3-(4-hydroxyphenyl)propyl Acetate 187242 Click to see CC(=O)OCCCC1=CC=C(C=C1)O 194.23 unknown https://doi.org/10.1016/0031-9422(77)84029-6
4-(4-Hydroxyphenyl)-2-butanone 21648 Click to see CC(=O)CCC1=CC=C(C=C1)O 164.20 unknown https://doi.org/10.1016/0031-9422(77)84029-6
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown https://doi.org/10.1016/0031-9422(77)84029-6
> Benzenoids / Phenols / Methoxyphenols
5-Methoxy-2-allylphenol 6424515 Click to see COC1=CC(=C(C=C1)CC=C)O 164.20 unknown https://doi.org/10.1016/0031-9422(77)84029-6
Dihydroconiferyl alcohol 16822 Click to see COC1=C(C=CC(=C1)CCCO)O 182.22 unknown https://doi.org/10.1016/S0031-9422(00)81488-0
Zingerone 31211 Click to see CC(=O)CCC1=CC(=C(C=C1)O)OC 194.23 unknown https://doi.org/10.1016/0031-9422(77)84029-6
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptane 8900 Click to see CCCCCCC 100.20 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(1R,4aR,5S,8aR)-5-[(Z)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-ol 162875863 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)O)C 292.50 unknown https://doi.org/10.1071/CH9732735
18-Norlabda-8(20),13-diene-4alpha,15-diol 101277956 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)O)C 292.50 unknown https://doi.org/10.1071/CH9732735
5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-ol 557145 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)O)C 292.50 unknown https://doi.org/10.1071/CH9732735
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1139/B89-189
(3R)-5-[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 12444400 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1071/CH9732735
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/10.1071/CH9732735
18-Hydroxymanool 349315 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1071/CH9732735
5-[5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-en-1-ol 557177 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1071/CH9732735
Agathadiol 15558517 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1071/CH9732735
CID 12444399 12444399 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1071/CH9732735
Manool 3034394 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown https://doi.org/10.1071/CH9732735
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
> 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/S0031-9422(00)88048-6
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)88048-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3R,4S,5S,6R)-2-[2-[(2S,5R)-5-[(1S,3R,6S,8S,9S,11R,12S,14S,15R,16R)-6-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,14-dihydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-methyloxolan-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162849626 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(CO9)(CO)O)O)C 947.10 unknown https://doi.org/10.1016/0031-9422(77)84029-6
> 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
L-ornithine 6262 Click to see C(CC(C(=O)O)N)CN 132.16 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 / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 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 / Phenylalanine and derivatives
D-phenylalanine 71567 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1016/S0021-9673(01)97854-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
(3S,4R,5R)-3,4,5-trihydroxycyclohexene-1-carboxylic acid 40970370 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/S0031-9422(00)86711-4
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/S0031-9422(00)86711-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
4-[(E)-3-hydroxyprop-1-enyl]-2-methoxycyclohexa-1,5-dien-1-ol 53302003 Click to see COC1=C(C=CC(C1)C=CCO)O 182.22 unknown https://doi.org/10.1016/S0031-9422(00)81488-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(3-methoxy-4-prop-2-enylphenoxy)oxane-3,4,5-triol 162898214 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)CC=C 326.34 unknown https://doi.org/10.1016/0031-9422(77)84029-6
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-prop-2-enylphenoxy)oxane-3,4,5-triol 162996739 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/0031-9422(77)84029-6
2-(Hydroxymethyl)-6-(3-methoxy-4-prop-2-enylphenoxy)oxane-3,4,5-triol 162898213 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)CC=C 326.34 unknown https://doi.org/10.1016/0031-9422(77)84029-6
3-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propyl acetate 163193504 Click to see CC(=O)OCCCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 356.40 unknown https://doi.org/10.1016/0031-9422(77)84029-6
3-[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propyl acetate 162956196 Click to see CC(=O)OCCCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 356.40 unknown https://doi.org/10.1016/0031-9422(77)84029-6
4-(4-Hydroxyphenyl)-2-butanone glucoside 22376357 Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown https://doi.org/10.1016/0031-9422(77)84029-6
4-[3-methoxy-4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-2-one 162990333 Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 356.40 unknown https://doi.org/10.1016/0031-9422(77)84029-6
4-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-2-one 162875484 Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown https://doi.org/10.1016/0031-9422(77)84029-6
Chavicol O-beta-glucopyranoside 44338426 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 296.31 unknown https://doi.org/10.1016/0031-9422(77)84029-6
Zingerone glucoside 74937233 Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 356.40 unknown https://doi.org/10.1016/0031-9422(77)84029-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] benzoate 162842905 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(C(O2)CO)O)O)O 284.26 unknown https://doi.org/10.1016/0031-9422(77)84029-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Dihydromyricetin 161557 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1007/BF02907158
> 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/10.3891/ACTA.CHEM.SCAND.03-0763
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
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/S0021-9673(01)81355-8
https://doi.org/10.1007/BF02907158
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1016/S0021-9673(01)81355-8
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0021-9673(01)81355-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0305-1978(91)90007-M
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163040191 Click to see CC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)94228-6
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0305-1978(91)90007-M

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