Solidago gigantea - Unknown
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Internal ID UUID643fd3440e5b8861586013
Scientific name Solidago gigantea
Authority Aiton
First published in Hort. Kew. [W. Aiton] 3: 211. 1789

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Synonyms Top

Scientific name Authority First published in
Solidago fragrans Hort.Par. ex A.Gray Syn. Fl. N. Amer. 1(2): 156 (1884)
Solidago glabra Desf. Tabl. École Bot. : 402 (1829)
Solidago dumetorum Lunell Amer. Midl. Naturalist 2: 57 (1911)
Solidago deflexa Moench Methodus : 599 (1794)
Doria pitcheri (Nutt.) Lunell Amer. Midl. Naturalist 5: 43 (1917)
Solidago shinnersii (Beaudry) Beaudry Naturaliste Canad. 101 (6): 932 (1974)
Solidago pitcheri Nutt. J. Acad. Nat. Sci. Philadelphia 7: 101 (1834)
Solidago gigantea subsp. serotina (Kuntze) McNeill Bot. J. Linn. Soc. 67: 280 (1973)
Solidago sera J.F.Gmel. Syst. Nat. ed. 13[bis] 2(2): 1236 (1792)
Solidago serotina var. gigantea (Aiton) A.Gray Proc. Amer. Acad. Arts 17: 196 (1882)
Solidago cleliae DC. Prodr. 5: 331 (1836)
Solidago somesii Rydb. Brittonia 1: 101 (1931)
Solidago gigantea var. pitcheri (Nutt.) Shinners Rhodora 55: 322 (1953)
Solidago gigantea var. shinnersii Beaudry Canad. J. Genet. Cytol. 5: 168 (1963)
Solidago gigantea var. serotina (Kuntze) Cronquist Vasc. Pl. Pacif. N.W. 5: 306 (1955)
Solidago serotina var. minor Hook. Fl. Bor.-Amer. 2: 2 (1834)
Aster latissimifolius var. serotinus Kuntze Revis. Gen. Pl. 1: 314 (1891)
Solidago serotinoides Á.Löve & D.Löve Taxon 31(2): 358 (1982), nom. nov.
Doria dumetorum (Lunell) Lunell Amer. Midl. Naturalist 5: 43 (1917)

Common names Top

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Language Common/alternative name
English giant goldenrod
English tall goldenrod
Bulgarian гигантска златна пръчка
Czech zlatobýl obrovský
Welsh eurwialen gynnar
German riesen-goldrute
Estonian sügis-kuldvits
Finnish isopiisku
French solidage glabre
French verge d’or géante
French solidage tardif
French solidage géant
Manx bossan mollagh
Hungarian magas aranyvessző
Japanese オオアワダチソウ
Korean 미국미역취
Dutch late guldenroede
Norwegian Nynorsk haustgullris
Norwegian Nynorsk kjempegullris
Polish nawłoć późna
Russian Золотарник гигантский
Slovak zlatobyľ obrovská
Serbian golema zlatica
Swedish höstgullris
szl nawłoć půźno

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

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Database ID/link to page
World Flora Online wfo-0000130517
UNII 2Y9N8J33MF
Florida Plant Atlas 4197
Flora of Alabama 987
Canadensys 3448
USDA Plants SOGI
Tropicos 2701324
INPN 124168
Flora of Italy 5408
KEW urn:lsid:ipni.org:names:249575-1
The Plant List gcc-91414
Plantarium 36185
Missouri Botanical Garden 277236
PFAF Solidago gigantea
Open Tree Of Life 1083535
Observations.org 7488
NCBI Taxonomy 330183
NBN Atlas NBNSYS0000004419
Nature Serve 2.151897
IPNI 240237-2
iNaturalist 83073
GBIF 5389017
Freebase /m/0bbw94t
WisFlora 5085
EPPO SOOGI
EOL 468370
Elurikkus 7305
Calflora (Californian flora) 7672
USDA GRIN 104551
Wikipedia Solidago_gigantea

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
Potential of Plant-Based Extracts to Alleviate Sorbitol-Induced Osmotic Stress in Cabbage Seedlings Pacyga K, Pacyga P, Boba A, Kozak B, Wolko Ł, Kochneva Y, Michalak I Plants (Basel) 14-Mar-2024
PMCID:PMC10974712
doi:10.3390/plants13060843
PMID:38592867
How to successfully improve the biodiversity of city grasslands? Mollashahi H, Szymura TH, Szymura M Heliyon 13-Mar-2024
PMCID:PMC10955310
doi:10.1016/j.heliyon.2024.e27810
PMID:38515666
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Disparate Effects of Two Clerodane Diterpenes of Giant Goldenrod (Solidago gigantea Ait.) on Bacillus spizizenii Bozsó Z, Lapat V, Ott PG, Móricz ÁM Int J Mol Sci 26-Jan-2024
PMCID:PMC10855248
doi:10.3390/ijms25031531
PMID:38338810
Involvement of Dynamic Adjustment of ABA, Proline and Sugar Levels in Rhizomes in Effective Acclimation of Solidago gigantea to Contrasting Weather and Soil Conditions in the Country of Invasion Bączek-Kwinta R, Janowiak F, Simlat M, Antonkiewicz J Int J Mol Sci 19-Oct-2023
PMCID:PMC10607263
doi:10.3390/ijms242015368
PMID:37895047
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Honey as a Natural Nutraceutical: Its Combinational Therapeutic Strategies Applicable to Blood Infections—Septicemia, HIV, SARS-CoV-2, Malaria Mackin C, Dahiya D, Nigam PS Pharmaceuticals (Basel) 14-Aug-2023
PMCID:PMC10459786
doi:10.3390/ph16081154
PMID:37631069
Effects of extracts from various parts of invasive Solidago species on the germination and growth of native grassland plant species Perera PC, Chmielowiec C, Szymura TH, Szymura M PeerJ 28-Jul-2023
PMCID:PMC10389070
doi:10.7717/peerj.15676
PMID:37529210
Influences of chemotype and parental genotype on metabolic fingerprints of tansy plants uncovered by predictive metabolomics Dussarrat T, Schweiger R, Ziaja D, Nguyen TT, Krause L, Jakobs R, Eilers EJ, Müller C Sci Rep 19-Jul-2023
PMCID:PMC10356770
doi:10.1038/s41598-023-38790-7
PMID:37468576
Strategies for the Management of Aggressive Invasive Plant Species Lorenzo P, Morais MC Plants (Basel) 28-Jun-2023
PMCID:PMC10346621
doi:10.3390/plants12132482
PMID:37447043
Hydrochorous Seed Transport in the Lower Traisen River before and after Riverbed Restoration Rasran L, Vogt K, Trattnig M, Bernhardt KG Plants (Basel) 22-Jun-2023
PMCID:PMC10347095
doi:10.3390/plants12132409
PMID:37446970
Pest categorisation of Coleosporium asterum, C. montanum and C. solidaginis 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, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Maiorano A, Pautasso M, Reignault PL EFSA J 16-Jun-2023
PMCID:PMC10273073
doi:10.2903/j.efsa.2023.8069
PMID:37333989
Phenolic compounds in Hungarian acacia, linden, milkweed and goldenrod honeys Farkas Á, Horváth G, Kuzma M, Mayer M, Kocsis M Curr Res Food Sci 02-Jun-2023
PMCID:PMC10276249
doi:10.1016/j.crfs.2023.100526
PMID:37333501
The Invasion of Alien Populations of Solanum elaeagnifolium in Two Mediterranean Habitats Modifies the Soil Communities in Different Ways Karmezi M, Krigas N, Papatheodorou EM, Argyropoulou MD Plants (Basel) 31-May-2023
PMCID:PMC10255462
doi:10.3390/plants12112193
PMID:37299172
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / 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/10.9734/EJMP/2013/4976
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.9734/EJMP/2013/4976
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
[[4-[(7-Methoxy-1,3-benzodioxol-5-yl)methyl]-2-oxooxolan-3-yl]-(3,4,5-trimethoxyphenyl)methyl] acetate 162876896 Click to see CC(=O)OC(C1C(COC1=O)CC2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 488.50 unknown https://doi.org/10.1016/0031-9422(88)83158-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4aS,7R,8R,8aS)-8-[2-(furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 162941811 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C(=O)O 316.40 unknown https://doi.org/10.1139/V73-200
(E)-5-[(1S,2R,4aR,5S,8aR)-1,2,4a,5-tetramethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpent-2-enal 162969283 Click to see CC1CCC2(C(C(=O)CCC2C1(C)CCC(=CC=O)C)C)C 304.50 unknown https://doi.org/10.1139/V74-293
(Z)-5-[(1S,2R,4aR,5S,8aR)-1,2,4a,5-tetramethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpent-2-enal 162969282 Click to see CC1CCC2(C(C(=O)CCC2C1(C)CCC(=CC=O)C)C)C 304.50 unknown https://doi.org/10.1139/V74-293
[(4aS,5R,6R,8aR)-5-[2-(furan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 162878516 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2CO)C 302.50 unknown https://doi.org/10.1139/V73-201
[(4aS,7R,8R,8aS)-8-[2-(furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl]methanol 11438096 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)CO 302.50 unknown https://doi.org/10.1139/V73-201
[5-[2-(Furan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 14057938 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2CO)C 302.50 unknown https://doi.org/10.1139/V73-201
[8-[2-(Furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalen-4a-yl]methanol 72961580 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)CO 302.50 unknown https://doi.org/10.1139/V73-201
3-[2-(1,2,4a,5-Tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)ethyl]furan 14166227 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C 286.50 unknown https://doi.org/10.1139/V74-293
3-[2-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]furan 10880686 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C 286.50 unknown https://doi.org/10.1139/V74-293
5-(1,2,4a,5-tetramethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpent-2-enal 162969281 Click to see CC1CCC2(C(C(=O)CCC2C1(C)CCC(=CC=O)C)C)C 304.50 unknown https://doi.org/10.1139/V74-293
8-[2-(Furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 12312682 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C(=O)O 316.40 unknown https://doi.org/10.1139/V73-200
> 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/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> 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/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
gamma-Gurjunene 90805 Click to see CC1CCC(C=C2C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Ledol 6431133 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
(1aS,4S,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 25089154 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
Cyclocolorenone 160491 Click to see CC1CCC2C(C2(C)C)C3=C(C(=O)CC13)C 218.33 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
5-Bromo-1-isopropyl-2,5a-dimethyl-decahydro-cyclopropa[a]inden-2-ol 42608144 Click to see CC(C)C1C2C1C3C(=C)CCC(C3(C2)C)O 220.35 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/1099-1026(200101/02)16:1<19::AID-FFJ940>3.0.CO;2-U
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4S,5R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101612331 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC4C(C(C(CO4)O)OC5C(C(C(C(O5)C)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)OC7C(C(C(CO7)O)O)O)O)OC(=O)C89CCC(CC8C1=CCC2C(C1(CC9)C)(CCC1C2(CC(C(C1(C)CO)OC1C(C(C(C(O1)CO)O)OC1C(C(C(C(O1)CO)O)OC1C(C(CO1)(CO)O)O)O)O)O)C)C)(C)C)C)O)O)O)O 1956.00 unknown https://doi.org/10.1016/S0040-4039(00)99331-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6aS,7R,8R,10aS)-5-hydroxy-7,8-dimethyl-7-[2-(5-oxo-2H-furan-3-yl)ethyl]-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 13994692 Click to see CC1CCC23COC(=O)C2=CC(CC3C1(C)CCC4=CC(=O)OC4)O 346.40 unknown https://doi.org/10.1016/0031-9422(88)83158-3
(5S,6aS,7R,8R,10aS)-7,8-dimethyl-7-[2-(5-oxo-2H-furan-3-yl)ethyl]-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 13994694 Click to see CC1CCC23COC(=O)C2=CC(CC3C1(C)CCC4=CC(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O 508.60 unknown https://doi.org/10.1016/0031-9422(88)83158-3
3-[2-(1,2,4a,5-tetramethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl)ethyl]-2H-furan-5-one 162911408 Click to see CC1CCC2(C(C(=O)CCC2C1(C)CCC3=CC(=O)OC3)C)C 318.40 unknown https://doi.org/10.1139/V74-293
3-[2-(5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)ethyl]-2H-furan-5-one 14109640 Click to see CC1CCC2(C(C1(C)CCC3=CC(=O)OC3)CCC(C2(C)O)O)C 336.50 unknown https://doi.org/10.1139/V74-293
3-[2-[(1S,2R,4aR,5R,6R,8aR)-5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 162996222 Click to see CC1CCC2(C(C1(C)CCC3=CC(=O)OC3)CCC(C2(C)O)O)C 336.50 unknown https://doi.org/10.1139/V74-293
3-[2-[(1S,2R,4aR,5S,8aR)-1,2,4a,5-tetramethyl-6-oxo-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 162911409 Click to see CC1CCC2(C(C(=O)CCC2C1(C)CCC3=CC(=O)OC3)C)C 318.40 unknown https://doi.org/10.1139/V74-293
6-Desoxysolidagolacton-IV-18,19-olid 13857180 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CCC4=CC(=O)OC4 330.40 unknown https://doi.org/10.1016/0031-9422(88)83158-3
7,8-dimethyl-7-[2-(5-oxo-2H-furan-3-yl)ethyl]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 13994693 Click to see CC1CCC23COC(=O)C2=CC(CC3C1(C)CCC4=CC(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O 508.60 unknown https://doi.org/10.1016/0031-9422(88)83158-3
Articulin 156833 Click to see CC1CCC23COC(=O)C2=CC(CC3C1(C)CCC4=CC(=O)OC4)O 346.40 unknown https://doi.org/10.1016/0031-9422(88)83158-3
> Organoheterocyclic compounds / Oxepanes
(E)-5-[(1aR,3aR,4S,5R,7aR,7bS)-4,5,7a,7b-tetramethyl-2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxiren-4-yl]-3-methylpent-2-enal 163083770 Click to see CC1CCC2(C(C1(C)CCC(=CC=O)C)CCC3C2(O3)C)C 304.50 unknown https://doi.org/10.1139/V74-293
(Z)-5-[(1aR,3aR,4S,5R,7aR,7bS)-4,5,7a,7b-tetramethyl-2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxiren-4-yl]-3-methylpent-2-enal 163083771 Click to see CC1CCC2(C(C1(C)CCC(=CC=O)C)CCC3C2(O3)C)C 304.50 unknown https://doi.org/10.1139/V74-293
5-(4,5,7a,7b-tetramethyl-2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxiren-4-yl)-3-methylpent-2-enal 163083769 Click to see CC1CCC2(C(C1(C)CCC(=CC=O)C)CCC3C2(O3)C)C 304.50 unknown https://doi.org/10.1139/V74-293

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