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Festuca arundinacea

Festuca arundinacea - Unknown
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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
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Details Top

Internal ID UUID64403066711db532984125
Scientific name Festuca arundinacea
Authority Schreb.
First published in Spic. Fl. Lips. : 57 (1771)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aira oryzetorum Spreng. Pl. Min. Cogn. Pug. 2: 18. 1815 (1815)
Avena secunda Salisb. Prodr. Stirp. Chap. Allerton : 22 (1796)
Brachypodium interruptum Roem. & Schult. Syst. Veg., ed. 15 bis 2: 747 (1817)
Bromus decolorans Rchb. Fl. Germ. Excurs. 1: 44 (1830)
Bromus elatior Koeler Descr. Gramin. : 214 (1802)
Bromus elatus Gueldenst. ex Ledeb. Fl. Ross. (Ledeb.) 4(13): 353. 1852 [Sep 1852]
Bromus littoreus Retz. Fl. Scand. Prodr. : 19 (1779)
Bucetum elatius Parn. Grass. Scotland : 107 (1842)
Bucetum elatius var. variegatum Parn. Grass. Scotland 108. 1842
Festuca articulata De Not. ex Parl. Fl. Ital. (Parlatore) 1(2): 455. 1850 [Oct-Nov 1850]
Festuca arundinacea f. baltica (Asch. & Graebn.) Beldie Fl. Republ. Socialist. România 12: 502 (1972)
Festuca arundinacea f. obtusiflora (Schur) Beldie Fl. Republ. Socialist. România 12: 505 (1972)
Festuca arundinacea f. pseudomairei (Lit. & Maire) Auquier Bull. Soc. Échange Pl. Vasc. Eur. Occid. Bassin Médit. 16: 142 (1976)
Festuca arundinacea subsp. atlantigena (St.-Yves) Auquier Bull. Soc. Échange Pl. Vasc. Eur. Occid. Bassin Médit. 16: 142 (1976)
Festuca arundinacea subsp. cirtensis (St.-Yves) Gamisans Cat. Pl. Vasc. Corse : 63 (1985)
Festuca arundinacea subsp. conferta (Hack.) Soják Cas. Nár. Mus., Odd. Prír. 151: 14 (1982)
Festuca arundinacea subsp. corsica (Hack.) Kerguélen Bull. Soc. Bot. France 123: 320 (1976)
Festuca arundinacea subsp. fenas (Lag.) Arcang. Comp. Fl. Ital. ed. 2: 61. 1894 (1894)
Festuca arundinacea subsp. interrupta (Desf.) Tzvelev Bot. Zhurn. (Moscow & Leningrad) 56: 1253 (1971)
Festuca arundinacea subsp. mediterranea (Hack.) Franco & Rocha Afonso Bol. Soc. Brot. , sér. 2.A, 54: 88 (1980)
Festuca arundinacea subsp. orientalis (Hack.) Tzvelev Spisok Rast. Gerb. Fl. S.S.S.R. Bot. Inst. Vsesojuzn. Akad. Nauk 18: 17. 1970 (1970)
Festuca arundinacea subsp. uechtritziana (Wiesb.) Hegi Ill. Fl. Mitt.-Eur. 1: 345. 1908 (1908)
Festuca arundinacea var. aspera (Mutel) Asch. & Graebn. Syn. Mitteleur. Fl. 2(1): 509 1900
Festuca arundinacea var. baltica Asch. & Graebn. Syn. Mitteleur. Fl. 2(1): 507 1900
Festuca arundinacea var. corsica (Hack.) Kerguélen Lejeunia , n.s., 142: 22 (1993)
Festuca arundinacea var. glaucescens Boiss. Voy. Bot. Espagne 2: 675 (1844)
Festuca arundinacea var. letourneuxiana (St.-Yves) Torrec. & Catalán Syst. Bot. 27: 243 (2002)
Festuca arundinacea var. mediterranea (Hack.) Asch. & Graebn. Syn. Mitteleur. Fl. 2(1): 509 1900
Festuca arundinacea var. obtusiflora Schur Enum. Pl. Transsilv. 798 1866
Festuca arundinacea var. podperae Soó Acta Bot. Acad. Sci. Hung. 17: 117 (1971 publ. 1972)
Festuca arundinacea var. uechtritziana (Wiesb.) Beck Fl. Nieder-Osterreich 1: 96. 1890
Festuca caerulescens Ten. Fl. Napol. 3: 81 (1824)
Festuca cretica Hack. ex Nyman Consp. Fl. Eur. : 825 (1882)
Festuca decolorans Mert. & W.D.J.Koch Deutschl. Fl. (Mertens & W. D. J. Koch), ed. 3. 1: 663. 1823
Festuca elatior L. Sp. Pl. : 75 (1753)
Festuca elatior f. pseudomairei Litard. & Maire Mém. Soc. Sci. Nat. Maroc 2: 43 1930
Festuca elatior subsp. arundinacea (Schreb.) Čelak. Prodr. Fl. Böhmen 1: 51. 1867
Festuca elatior var. aspera Mutel Fl. Franç. Herbor. 4: 110. 1837
Festuca elatior var. atlantigena St.-Yves Candollea 1: 36 (1922)
Festuca elatior var. cirtensis St.-Yves Candollea 1: 36 (1922)
Festuca elatior var. elbursiana Vetter Repert. Spec. Nov. Regni Veg. 48: 165 1940
Festuca elatior var. fenas (Lag.) Hack. Monogr. Festuc. Eur. : 156 (1882)
Festuca elatior var. letourneuxii St.-Yves Candollea 1: 34 1922
Festuca elatior var. minutiflora (St.-Yves) Litard. Candollea 10: 141 1945
Festuca elatior var. mutica Chevall. Fl. Gen. Env. Paris 2: 167. 1827
Festuca elatior var. uechtritziana Hack. Monogr. Festuc. Eur. 155. 1882
Festuca fenas Lag. Gen. Sp. Pl. : 4 (1816)
Festuca fenas subsp. atlantigena (St.-Yves) Cebolla & Rivas Ponce Candollea 58: 195 (2003)
Festuca interrupta Desf. Fl. Atlant. 1: 89 (1798)
Festuca laxa Gaudin Agrost. Helv. 1: 261 (1811)
Festuca littorea (Retz.) Lilj. Utkast Sv. Fl. , ed. 3: 699 (1816)
Festuca loliacea Lam. Encycl. 2: 462 (1788)
Festuca mediterranea Rouy Fl. France 14: 226 (1913)
Festuca orientalis (Hack.) Krecz. & Bobrov Fl. URSS 2: 531 1934
Festuca oryzetorum Pollini Hort. Veron. Pl. : 3 (1816)
Festuca pauneroi Cebolla, López Rodr. & Rivas Ponce Candollea 58: 195 (2003)
Festuca phoenix Vill. Prosp. Hist. Pl. Dauphiné : 17 (1779)
Festuca pseudololiacea Hack. Monogr. Festuc. Eur. : 151 (1882)
Festuca regelii Pavlov Sovetsk. Bot. 1934(1): 19 (1934)
Festuca simplex Boiss. & Balansa Diagn. Pl. Orient. , ser. 2, 4: 138 (1859)
Festuca tenax hort. ex Link Enum. Hort. Berol. Alt. 1: 87 (1821)
Festuca uechtritziana Wiesb. Oesterr. Bot. Z. 28: 218 (1878)
Gnomonia elatior (L.) Lunell Amer. Midl. Naturalist 4: 224 (1915)
Lolium festuca Raspail Ann. Sci. Observ. 2: 244 (1829)
Poa curvata Koeler Descr. Gramin. : 207 (1802)
Poa elatior Moench Enum. Pl. Hass. : 37 (1777)
Poa fenas Steud. Syn. Pl. Glumac. 1: 252 (1854)
Poa kunthii Lindm. Bot. Jahrb. Syst. 44: 45 (1909)
Poa phoenix Scop. Fl. Carniol. , ed. 2, 1: 74 (1771)
Poa remota Kunth Nov. Gen. Sp. 1: 163 (1816)
Poa tenax Link Enum. Hort. Berol. Alt. 1: 87 (1821)
Poa uliginosa Willd. ex Spreng. Syst. Veg. 1: 342 (1824)
Schedonorus elatior P.Beauv. Ess. Agrostogr. : 99 (1812)
Schedonorus interruptus (Desf.) Tzvelev Novosti Sist. Vyssh. Rast. 31: 259 (1998)
Schedonorus littoreus (Retz.) Tzvelev Novosti Sist. Vyssh. Rast. 31: 258 (1998)
Schedonorus phoenix (Scop.) Holub Preslia 70: 113 (1998)
Schedonorus uechtritzianus (Wiesb.) Holub Preslia 70: 113 (1998)
Tragus elatior Panz. Ideen Rev. Gräser : 49 (1813)
Tragus loliaceus Panz. Denkschr. Akad. Muench. 1813 (1814).
Schedonorus arundinaceus subsp. fenas (Lag.) H.Scholz Ber. Inst. Landschafts Pflanzenökol. Univ. Hohenheim Beih. 16: 74 (2003)
Schedonorus arundinaceus subsp. atlantigenus (St.-Yves) H.Scholz Ber. Inst. Landschafts Pflanzenökol. Univ. Hohenheim Beih. 16: 74 (2003)
Schedonorus arundinaceus subsp. uechtritzianus (Wiesb.) H.Scholz & Valdés Willdenowia 37: 442 (2007)
Schedonorus arundinaceus subsp. cirtensis (St.-Yves) H.Scholz & Valdés Willdenowia 35: 243 (2005)
Schedonorus pauneroi (Cebolla, López Rodr. & Rivas Ponce) H.Scholz Willdenowia 35: 243 (2005)
Schedonorus arundinaceus subsp. corsicus (Hack.) H.Scholz & Valdés Willdenowia 35(2): 243
Festuca uechtritziana var. aristata Podp. Spisy Přír. Fak. Masarykovy Univ. 12: 11. 1922
Festuca arundinacea var. decolorans (Rchb.) Mert. ex W.D.J.Koch Fl. Sicul. (Lojacona) 3: 347 1909
Festuca arundinacea subsp. fenas (Lag.) Bornm. Repert. Spec. Nov. Regni Veg. 25: 330. 1928
Festuca arundinacea var. interrupta (Desf.) Coss. & Durieu Expl. Sci. Algérie 2: 170 1855
Festuca decolorans Mert. & W.D.J.Koch Deutschl. Fl. , ed. 3, 1: 663 (1823)
Festuca elatior var. glaucescens (Boiss.) Hack. Monogr. Festuc. Eur. 156 1882
Festuca elatior var. interrupta (Desf.) Cout. Bol. Soc. Brot., sér. 2, 10: 59 1935
Festuca elatior var. littorea (Retz.) Lilj. Utkast Svensk Fl. 47 1798
Festuca fenas var. conferta (Hack.) K.Richt. Pl. Eur. 1: 102 1890
Festuca fenas var. corsica (Hack.) K.Richt. Pl. Eur. 1: 102. 1890 (1890)
Festuca elatior var. arundinacea Schreb.

Common names Top

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Language Common/alternative name
Arabic فستوكة قصبية
Czech kostřava rákosovitá
German rohr-schwingel
Estonian roog-aruhein
Persian علف بره نی مانند
Upper Sorbian sćinojta dornica
Hungarian nádképű csenkesz
Japanese オニウシノケグサ
Lithuanian fétuque roseau
Swedish fétuque roseau
Swedish rörsvingel
Chinese 苇状羊茅
Chinese 葦狀羊茅

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000869819
Canadensys 18810
Tropicos 25509613
The Plant List kew-414517
Open Tree Of Life 105576
Observations.org 6784
NBN Atlas NHMSYS0000458758
IPNI 89139-1
iNaturalist 77134
GBIF 2706232
Freebase /m/03d8qv_
EOL 1115745
Elurikkus 4745
Calflora (Californian flora) 3576
US Library of Congress sh85132106
USDA GRIN 16631

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)!
Title Authors Publication Released IDs
Characterization of Inhibitory Substances of Tall Fescue on Birdsfoot Trefoil K. T. Luu, A. G. Matches, C. J. Nelson, E. J. Peters, G. B. Garner Wiley 29-Jul-2010
doi:10.2135/CROPSCI1989.0011183X002900020034X
Detection of ergopeptine alkaloids in endophyte-infected, toxic Ky-31 tall fescue by mass spectrometry/mass spectrometry Shelly G. Yates, Ronald D. Plattner, George B. Garner American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JF00064A038
Isolation, Semi-Synthesis, and Nmr Spectral Studies of Loline Alkaloids R. J. Petroski, S. G. Yates, D. Weisleder, R. G. Powell American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50064A023
Analysis of ergopeptine alkaloids in endophyte-infected tall fescue Shelly G. Yates, Richard G. Powell American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF00080A023
Steroid metabolites of Acremonium coenophialum, an endophyte of tall fescue Norman D. Davis, Richard J. Cole, Joe W. Dorner, John D. Weete, Paul A. Backman, Edward M. Clark, Charles C. King, Stephen P. Schmidt, Urban L. Diener American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF00067A029
Volatile alkaloids of Kentucky 31 tall fescue seed (Festuca arundinancea) Joe D. Robbins, James G. Sweeny, Stanley R. Wilkinson, Donald Burdick American Chemical Society (ACS) 10-Mar-2005
doi:10.1021/JF60183A003
High performance liquid chromatographic determination of phenolic compounds in seed exudates of Festuca arundinacea and F. pratense Bo??ivoj Klejdus, Vlastimil Kub�?? Wiley 25-Aug-2002
doi:10.1002/1099-1565(200011/12)11:6<375::AID-PCA539>3.0.CO;2-0
Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the poaceae Richard G. Powell, Mark R. TePaske, Ronald D. Plattner, James F. White, Stephen L. Clement Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94759-9
Composition of essential oil of tall fescue Aldo Tava, Nicola Berardo, Miriam Odoardi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84185-U
Determination of the alkaloid perloline in grasses by high-performance liquid chromatography Peter Lepom, Klaus-Dieter Robowsky Elsevier BV 25-Jul-2002
doi:10.1016/S0021-9673(01)97683-6
Allelochemicals in tall fescue-abscisic and phenolic acids. Buta JG, Spaulding DW J Chem Ecol 01-May-1989
doi:10.1007/BF01012389
PMID:24272104

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
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Ergopeptines
(6aR,9S)-N-[(1S,4R,7S)-2-hydroxy-4-methyl-7-(2-methylpropyl)-5,8-dioxo-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide 5317170 Click to see CC(C)CC1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O 547.60 unknown https://doi.org/10.1021/JF00080A023
(6aS,9R)-N-[(1S,2S,4R,7S)-2-hydroxy-4-methyl-5,8-dioxo-7-propan-2-yl-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide 6451531 Click to see CC(C)C1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O 533.60 unknown https://doi.org/10.1021/JF00080A023
Ergonine 13274438 Click to see CCC1(C(=O)N2C(C(=O)N3CCCC3C2(O1)O)C(C)C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C 547.60 unknown https://doi.org/10.1021/JF00064A038
Ergovaline 104843 Click to see CC(C)C1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O 533.60 unknown https://doi.org/10.1021/JF00080A023
Ergovalinine 20841588 Click to see CC(C)C1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O 533.60 unknown https://doi.org/10.1021/JF00080A023
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Ergopeptines / Ergotamines, dihydroergotamines, and derivatives
Ergotamine 8223 Click to see CC1(C(=O)N2C(C(=O)N3CCCC3C2(O1)O)CC4=CC=CC=C4)NC(=O)C5CN(C6CC7=CNC8=CC=CC(=C78)C6=C5)C 581.70 unknown https://doi.org/10.1021/JF00080A023
https://doi.org/10.1021/JF00064A038
Ergotaminine 115248 Click to see CC1(C(=O)N2C(C(=O)N3CCCC3C2(O1)O)CC4=CC=CC=C4)NC(=O)C5CN(C6CC7=CNC8=CC=CC(=C78)C6=C5)C 581.70 unknown https://doi.org/10.1021/JF00080A023
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Lysergamides
Ergosine 105137 Click to see CC(C)CC1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O 547.60 unknown https://doi.org/10.1021/JF00080A023
https://doi.org/10.1021/JF00064A038
> Alkaloids and derivatives / Loline alkaloids and derivatives
N-Demethylloine 361058 Click to see C1CN2CC3C(C2C1O3)N 140.18 unknown https://doi.org/10.1021/NP50064A023
N-methyl-N-[(1R,3R,7S,8R)-2-oxa-6-azatricyclo[4.2.1.03,7]nonan-8-yl]acetamide 100985848 Click to see CC(=O)N(C)C1C2CN3C1C(O2)CC3 196.25 unknown https://doi.org/10.1021/JF60183A003
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl butyl phthalate 2347 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCC2=CC=CC=C2 312.40 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1002/1099-1565(200011/12)11:6<375::AID-PCA539>3.0.CO;2-0
> Benzenoids / Benzene and substituted derivatives / Benzonitriles
o-Tolunitrile 10721 Click to see CC1=CC=CC=C1C#N 117.15 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Benzenoids / Benzene and substituted derivatives / Xylenes / o-Xylenes
O-Xylene 7237 Click to see CC1=CC=CC=C1C 106.16 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Tridecane 12388 Click to see CCCCCCCCCCCCC 184.36 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Dibutylmaleat- 7774 Click to see CCCCOC(=O)C=CC(=O)OCCCC 228.28 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1016/0031-9422(91)84185-U
1-Octen-3-Ol 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Hexadecanal 984 Click to see CCCCCCCCCCCCCCCC=O 240.42 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Methyl elaidolinolenate 5367462 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1016/0031-9422(91)84185-U
Epoxy-beta-ionone 129689900 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C=O 206.28 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-Abscisic acid 5375200 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 264.32 unknown https://doi.org/10.1007/BF01012389
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosterol 444679 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 396.60 unknown https://doi.org/10.1021/JF00067A029
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hexyl Acetate 8908 Click to see CCCCCCOC(=O)C 144.21 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.2135/CROPSCI1989.0011183X002900020034X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone 8163 Click to see CCCCCCCCCC(=O)C 170.29 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Organoheterocyclic compounds / Benzofurans
Dihydroactinidiolide 6432173 Click to see CC1(CCCC2(C1=CC(=O)O2)C)C 180.24 unknown https://doi.org/10.1016/0031-9422(91)84185-U
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
6-(3,4-Dimethoxyphenyl)benzo[f][2,7]naphthyridin-4-one 420115 Click to see COC1=C(C=C(C=C1)N2C=C3C(=CC=NC3=O)C4=CC=CC=C42)OC 332.40 unknown https://doi.org/10.1016/S0021-9673(01)97683-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1002/1099-1565(200011/12)11:6<375::AID-PCA539>3.0.CO;2-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44258017 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 640.50 unknown https://doi.org/10.1021/JF00080A023
> Phenylpropanoids and polyketides / Stilbenes
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/S0031-9422(00)94759-9

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