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Pinus ponderosa

Pinus ponderosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Pinus ponderosa - 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 UUID6440022bdda69897416365
Scientific name Pinus ponderosa
Authority P.Lawson & C.Lawson
First published in Agric. Man. : 354 (1836)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pinus engelmannii Torr. Pacif. Railr. Rep. Whipple, Bot. 4(5; 4): 141 (1857)
Pinus sinclairiana Carrière Traité Gén. Conif. : 355 (1855)
Pinus nootkatensis Manetti ex Gord. Pinetum , Suppl.: 67 (1862)
Pinus resinosa Torr. Ann. Lyceum Nat. Hist. New York 2: 249. 1827 (1827)
Pinus ponderosa var. parryana (Gordon) Rob. Fl. & Sylva 3: 104. 1905
Pinus ponderosa var. pendula Hook.f. ex H.W.Sarg. Gard. Chron. n.s., 10: 236. 1878
Pinus jeffreyi var. nigricans Lemmon Bienn. Rep. Calif. State Board Forest. 2: 74, 100. 1888
Pinus ponderosa var. nigricans (Lemmon) Lemmon Bienn. Rep. Calif. State Board Forest. 7: 8 1889
Pinus ponderosa f. pendula (Hook.f. ex H.W.Sarg.) Rehder Man. Cult. Trees ed. 2: 44 1940

Common names Top

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Language Common/alternative name
English ponderosa pine
English yellow pine
English western yellow-pine
English bull pine
English western yellow pine

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Pinus ponderosa var. pacifica J.R.Haller & Vivrette Aliso 29: 55 (2011)
Pinus ponderosa var. ponderosa
Pinus ponderosa var. scopulorum Engelm. Bot. California 2: 126 (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

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Germany
      • Hungary
    • Northern Europe
      • Great Britain
      • Ireland
      • Sweden
    • Southeastern Europe
      • Greece
      • Italy
      • Romania
    • Southwestern Europe
      • Spain
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • North-central U.S.A.
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481903
UNII NZA8UU1441
Cornell Woody Plants 292
Canadensys 7191
USDA Plants PIPO
UConn 329
Tropicos 24900205
INPN 458771
KEW urn:lsid:ipni.org:names:307165-2
The Plant List kew-2562565
Missouri Botanical Garden 285000
Open Tree Of Life 736900
Observations.org 139173
NCBI Taxonomy 55062
NBN Atlas NHMSYS0000461723
Nature Serve 2.137495
IUCN Red List 42401
IPNI 307165-2
iNaturalist 81248
iNaturalist 48461
GBIF 5285053
Freebase /m/02md50
EPPO PIUPO
EOL 1061751
Elurikkus 6309
Calflora (Californian flora) 6521
US Library of Congress sh85104789
USDA GRIN 28530
Wikipedia Pinus_ponderosa
PaleoBotany 51333

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
Climate change could negate U.S. forest ecosystem service benefits gained through reductions in nitrogen and sulfur deposition Phelan JN, Van Houtven G, Clark CM, Buckley J, Cajka J, Hargrave A, Horn K, Thomas RQ, Sabo RD Sci Rep 10-May-2024
PMCID:PMC11087459
doi:10.1038/s41598-024-60652-z
PMID:38730011
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
The Chemical Landscape of Leaf Surfaces and Its Interaction with the Atmosphere Ossola R, Farmer D Chem Rev 23-Apr-2024
PMCID:PMC11082906
doi:10.1021/acs.chemrev.3c00763
PMID:38652704
Scaling approaches and macroecology provide a foundation for assessing ecological resilience in the Anthropocene Enquist BJ, Erwin D, Savage V, Marquet PA Philos Trans R Soc Lond B Biol Sci 08-Apr-2024
PMCID:PMC10999275
doi:10.1098/rstb.2023.0010
PMID:38583479
The importance of regeneration processes on forest biodiversity in old-growth forests in the Pacific Northwest Luu H, Ris Lambers JH, Lutz JA, Metz M, Snell RS Philos Trans R Soc Lond B Biol Sci 08-Apr-2024
PMCID:PMC10999264
doi:10.1098/rstb.2023.0016
PMID:38583471
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
Behaviour and landscape contexts determine the effects of artificial light on two crepuscular bird species Adams CA, Clair CC, Knight EC, Bayne EM Landsc Ecol 26-Mar-2024
PMCID:PMC10965584
doi:10.1007/s10980-024-01875-3
PMID:38550967
Pest categorisation of Pyrrhoderma noxium 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, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Assessing silvopasture management as a strategy to reduce fuel loads and mitigate wildfire risk Batcheler M, Smith MM, Swanson ME, Ostrom M, Carpenter-Boggs L Sci Rep 12-Mar-2024
PMCID:PMC10928111
doi:10.1038/s41598-024-56104-3
PMID:38467773
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
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
Xylem plasticity of root, stem, and branch in Cunninghamia lanceolata under drought stress: implications for whole-plant hydraulic integrity Li S, Huang X, Zheng R, Zhang M, Zou Z, Heal KV, Zhou L Front Plant Sci 19-Feb-2024
PMCID:PMC10910014
doi:10.3389/fpls.2024.1308360
PMID:38439985
Towards portable MRI in the plant sciences Blystone S, Nuixe M, Traoré AS, Cochard H, Picon-Cochard C, Pagés G Plant Methods 18-Feb-2024
PMCID:PMC10874549
doi:10.1186/s13007-024-01152-z
PMID:38369530

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 / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1021/JF00110A049
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1021/JF00110A049
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1002/JPS.3030450308
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
> 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/10.1016/0031-9422(91)85265-2
https://doi.org/10.1016/S0031-9422(00)85047-5
(1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(3S)-3-methyl-5-oxopentyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 14830084 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC=O 320.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
(1S,4Ar,5S,8aR)-5-[(3R)-4-carboxy-3-methylbutyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 12314310 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O 336.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
4-[(E)-5-[(1S,4aR,5S,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-4-oxobutanoic acid 101599455 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 406.60 unknown https://doi.org/10.1016/0031-9422(91)85265-2
4-[(E)-5-[(1S,4aR,5S,8aR)-5-formyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-4-oxobutanoic acid 101599454 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
4-[5-(5-formyl-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoxy]-4-oxobutanoic acid 162876777 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C=O)C 404.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
4-[5-[5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-4-oxobutanoic acid 162846334 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 406.60 unknown https://doi.org/10.1016/0031-9422(91)85265-2
5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carbaldehyde 73198319 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C=O)C 304.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
5-[5-(3-carboxypropanoyloxy)-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 78069534 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 420.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
8,13-Abietadien-18-oic acid 16040 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
https://doi.org/10.1016/0031-9422(91)85265-2
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
https://doi.org/10.1016/S0031-9422(00)85047-5
Agatholal 15559800 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C=O)C 304.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
Butanedioic acid, mono((2E)-5-((1S,4aR,5S,8aR)-5-carboxydecahydro-5,8a-dimethyl-2-methylene-1-naphthalenyl)-3-methyl-2-pentenyl) ester 6440366 Click to see CC(=CCOC(=O)CCC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 420.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
CID 15559751 15559751 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CCO 322.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
Dihydroagathic acid 578152 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O 336.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
Imbricatoloic acid 15559752 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CCO 322.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
Isocupressic Acid 6438138 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C 320.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
https://doi.org/10.1016/0031-9422(91)85265-2
https://doi.org/10.1021/JF960290W
https://doi.org/10.1021/JF00039A031
Isopimaric Acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/0031-9422(91)85265-2
https://doi.org/10.1016/S0031-9422(00)85047-5
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
https://doi.org/10.1016/0031-9422(91)85265-2
methyl (1R,4aR,4bR,6R,10aS)-6-acetyloxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate 162957920 Click to see CC(C)C1=CC2=CCC3C(C2CC1OC(=O)C)(CCCC3(C)C(=O)OC)C 374.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
methyl (1R,4S,5R,9S,10R,14S)-5,9-dimethyl-13-propan-2-yl-15-oxatetracyclo[8.5.0.01,14.04,9]pentadec-12-ene-5-carboxylate 162984026 Click to see CC(C)C1=CCC2C3(CCCC(C3CCC24C1O4)(C)C(=O)OC)C 332.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
methyl (1S,4aR,5S,8aR)-5-[(E)-5-acetyloxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14890264 Click to see CC(=CCOC(=O)C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 376.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
methyl (1S,4aR,5S,8aR)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14060410 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 334.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
methyl 5-(5-acetyloxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 163024837 Click to see CC(=CCOC(=O)C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 376.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
methyl 5-(5-hydroxy-3-methylpent-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 85146322 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 334.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
Methyl 6-acetyloxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate 14378720 Click to see CC(C)C1=CC2=CCC3C(C2CC1OC(=O)C)(CCCC3(C)C(=O)OC)C 374.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
Methyl 8,14-epoxyabiet-12-en-18-oate 286952 Click to see CC(C)C1=CCC2C3(CCCC(C3CCC24C1O4)(C)C(=O)OC)C 332.50 unknown https://doi.org/10.1016/0031-9422(73)80708-3
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
https://doi.org/10.1016/0031-9422(91)85265-2
Palustric acid 443613 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
https://doi.org/10.1016/0031-9422(91)85265-2
Sandaracopimaric Acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85047-5
> 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/10.1002/FFJ.2730040105
> 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/10.1007/BF02751105
https://doi.org/10.1002/FFJ.2730040105
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF02751105
https://doi.org/10.1002/FFJ.2730040105
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)80320-9
https://doi.org/10.1007/BF02751105
https://doi.org/10.1002/FFJ.2730040105
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1002/FFJ.2730040105
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)85875-6
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF02751105
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1007/BF02751105
https://doi.org/10.1002/FFJ.2730040105
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1002/JPS.3030431207
CID 16396350 16396350 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1007/BF02751105
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1007/BF02751105
https://doi.org/10.1002/JPS.3030431207
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
(2S)-2-(phenylazaniumyl)propanoate 6946449 Click to see CC(C(=O)[O-])[NH2+]C1=CC=CC=C1 165.19 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
https://doi.org/10.1016/S0021-9673(01)97854-9
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
D-alanine 71080 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> 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
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
Glutamine 5961 Click to see C(CC(=O)N)C(C(=O)O)N 146.14 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
L-ornithine 6262 Click to see C(CC(C(=O)O)N)CN 132.16 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
Asparagine 6267 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
Aspartic Acid 5960 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
D-Aspartic acid 83887 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
Glutamic Acid 33032 Click to see C(CC(=O)O)C(C(=O)O)N 147.13 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> 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/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
D-Methionine 84815 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
Methionine 6137 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> 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/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine 6057 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
Gamma-Aminobutyric Acid 119 Click to see C(CC(=O)O)CN 103.12 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
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/10.1021/JF00110A049
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1021/JF00110A049
> 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/10.1021/JF00110A049
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/JF00110A049
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1034/J.1399-3054.1990.790104.X
> Organoheterocyclic compounds / Piperidines
(-)-Pinidinone 11159443 Click to see CC1CCCC(N1)CC(=O)C 155.24 unknown https://doi.org/10.1002/(SICI)1099-1565(199911/12)10:6<322::AID-PCA468>3.0.CO;2-W
2-Methyl-6-prop-1-enylpiperidine 580067 Click to see CC=CC1CCCC(N1)C 139.24 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
2-Methylpiperidine 7974 Click to see CC1CCCCN1 99.17 unknown https://doi.org/10.1016/0031-9422(94)00928-M
Pinidine 5281689 Click to see CC=CC1CCCC(N1)C 139.24 unknown https://doi.org/10.1002/(SICI)1099-1565(199911/12)10:6<322::AID-PCA468>3.0.CO;2-W
https://doi.org/10.1016/0031-9422(94)00928-M
https://doi.org/10.1021/JO00070A014
Pinidinol 182960 Click to see CC1CCCC(N1)CC(C)O 157.25 unknown https://doi.org/10.1002/(SICI)1099-1565(199911/12)10:6<322::AID-PCA468>3.0.CO;2-W
https://doi.org/10.1016/0031-9422(94)00928-M
> 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/10.1002/(SICI)1099-1565(199911/12)10:6<322::AID-PCA468>3.0.CO;2-W
9-Aza-1-methylbicyclo[3.3.1]nonan-3-one 573579 Click to see CC12CCCC(N1)CC(=O)C2 153.22 unknown https://doi.org/10.1021/JO00070A014
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(2R)-1-[(2R)-6-methyl-2,3,4,5-tetrahydropyridin-2-yl]propan-2-ol 101651530 Click to see CC1=NC(CCC1)CC(C)O 155.24 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
1-(6-Methyl-2,3,4,5-tetrahydro-pyridin-2-yl)-propan-2-one 90878365 Click to see CC1=NC(CCC1)CC(=O)C 153.22 unknown https://doi.org/10.1021/JO00070A014
1-(6-Methyl-2,3,4,5-tetrahydropyridin-2-yl)propan-2-ol 130131525 Click to see CC1=NC(CCC1)CC(C)O 155.24 unknown https://doi.org/10.1016/S0031-9422(00)90645-9
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/10.1021/JO00070A014
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 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
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.05-0121
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxyflavanone; Dihydrogalangin 3519897 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-0763
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.03-0763
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/10.1021/JF00110A049
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1021/JF00110A049
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/JF00110A049
> Phenylpropanoids and polyketides / Stilbenes
5-Styrylresorcinol 100754 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.03-0763
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.05-0121

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