Pallenis spinosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pallenis spinosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pallenis spinosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Pallenis spinosa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fce0f893e6938211240
Scientific name Pallenis spinosa
Authority (L.) Cass.
First published in Dict. Sci. Nat., ed. 2. 37: 276 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pallenis spinosa f. microcephala Halácsy Halácsy, Consp. Fl. Graec. 2. 1902. 18 1902
Pallenis spinosa var. sulfurea Braun-Blanq. & Maire
Pallenis spinosa var. pallida Bornm.
Pallenis spinosa subsp. microcephala (Halácsy) Rech.f. Rech. f. in Österr. Bot. Z. 85. 1936. 62 1936
Asteriscus spinosus var. intermedius Alleiz. Bull. Soc. Hist. Nat. Afrique N. 12: 95 (1921)
Pallenis spinosa var. eriophora Burnat
Asteriscus spinosus var. gussonii (Pasq.) Fiori Nuov. Fl. Italia 2: 688 (1927)
Asteriscus spinosus subsp. spinosus (L.) Sch.Bip.
Pallenis spinosa var. straminea Maire, Weiller & Wilczek
Pallenis spinosa var. crocea Webb & Heldr.

Common names Top

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Language Common/alternative name
Spanish pallenis spinosa subsp. spinosa
Spanish asteriscus spinosus
Spanish falsa arnica
Spanish pincho de las diarreas
Spanish pincho cuco
Spanish pincho amarillo
Spanish patagallo
Spanish pampilosa de espinas
Spanish pallenis spinosa subsp spinosa
Spanish malhijo
Spanish inguinaria
Spanish estrellada espinosa
Spanish cevadilla
Spanish arnica de secano
Spanish amelos duros
Spanish madre e hija
Arabic زباد شائك
Arabic بالينس شوكي
Azerbaijani dalar pallenis
Bulgarian Бодлив паленис
Catalan gravit
German stechendes sternauge
Persian ستاره طلایی
French astérolide épineux
French pallénis épineux
French buphthalme épineux
Turkish dikenotu
Ukrainian Паленіс колючий
Vietnamese asteriscus spinosus

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pallenis spinosa subsp. asteroidea (Viv.) Greuter Fl. Medit. 7: 47 (1997)
Pallenis spinosa subsp. aurea (Willk.) Nyman Consp. Fl. Eur. : 391 (1879)
Pallenis spinosa subsp. maroccana (Aurich & Podlech) Greuter Fl. Medit. 7: 47 (1997)
Pallenis spinosa subsp. spinosa (L.) Cass.

Varieties (abbr. var.) Top

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No variety added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000077986
Tropicos 2701100
INPN 112065
KEW urn:lsid:ipni.org:names:236401-1
The Plant List gcc-34594
Open Tree Of Life 245301
Observations.org 145518
NCBI Taxonomy 73981
IPNI 236401-1
iNaturalist 633980
GBIF 5385215
Freebase /m/0gx2j02
EPPO PNSSP
Wikipedia Pallenis_spinosa

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
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
Foraging Behavior of Two Pollen Wasp Species of the Genus Celonites Latreille, 1802 (Hymenoptera: Vespidae: Masarinae), from the Altai Mountains Fateryga AV, Mauss V, Proshchalykin MY Insects 24-Apr-2023
PMCID:PMC10231071
doi:10.3390/insects14050408
PMID:37233036
The Role of Lichens, Mosses, and Vascular Plants in the Biodeterioration of Historic Buildings: A Review Cozzolino A, Adamo P, Bonanomi G, Motti R Plants (Basel) 08-Dec-2022
PMCID:PMC9781475
doi:10.3390/plants11243429
PMID:36559541
Effects of Prickly Burnet (Sarcopoterium spinosum (L.) Spach.) Control and Sheep Grazing on Hay Yield and Quality on Gökçeada Island, Turkey Alatürk F, Gökkuş A, Özaslan Parlak A, Baytekin H, Tölü C Animals (Basel) 08-Nov-2022
PMCID:PMC9686760
doi:10.3390/ani12223073
PMID:36428300
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
Ecological and Biological Properties of Satureja cuneifolia Ten. and Thymus spinulosus Ten.: Two Wild Officinal Species of Conservation Concern in Apulia (Italy). A Preliminary Survey Perrino EV, Valerio F, Jallali S, Trani A, Mezzapesa GN Plants (Basel) 18-Sep-2021
PMCID:PMC8471076
doi:10.3390/plants10091952
PMID:34579485
Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A Plants (Basel) 01-Apr-2021
PMCID:PMC8065674
doi:10.3390/plants10040680
PMID:33916121
The Role of Botanical Families in Medicinal Ethnobotany: A Phylogenetic Perspective Gras A, Hidalgo O, D’Ambrosio U, Parada M, Garnatje T, Vallès J Plants (Basel) 15-Jan-2021
PMCID:PMC7830233
doi:10.3390/plants10010163
PMID:33467763
Potential anti-influenza effective plants used in Turkish folk medicine: A review Sargin SA J Ethnopharmacol 31-Aug-2020
PMCID:PMC7458060
doi:10.1016/j.jep.2020.113319
PMID:32882361
Local Factors Rather than the Landscape Context Explain Species Richness and Functional Trait Diversity and Responses of Plant Assemblages of Mediterranean Cereal Field Margins Pallavicini Y, Bastida F, Hernández-Plaza E, Petit S, Izquierdo J, Gonzalez-Andujar JL Plants (Basel) 22-Jun-2020
PMCID:PMC7356665
doi:10.3390/plants9060778
PMID:32580354
Traditional knowledge in semi-rural close to industrial areas: ethnobotanical studies in western Gironès (Catalonia, Iberian Peninsula) Gras A, Serrasolses G, Vallès J, Garnatje T J Ethnobiol Ethnomed 02-Apr-2019
PMCID:PMC6444684
doi:10.1186/s13002-019-0295-2
PMID:30940210
Ethnobotanical uses in the Ancona district (Marche region, Central Italy) Lucchetti L, Zitti S, Taffetani F J Ethnobiol Ethnomed 05-Feb-2019
PMCID:PMC6364442
doi:10.1186/s13002-019-0288-1
PMID:30722788
Sesquiterpenoids from Pallenis spinosa Giovanni Appendino, Jasmin Jakupovic, Sven Jakupovic Elsevier BV 01-May-2003
doi:10.1016/S0031-9422(97)00386-5
Flavonoids of Pallenis spinosa (Asteraceae) Ahmed A. Ahmed, Mark Spaller, Tom J. Mabry Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(92)90038-F
A germacrane derivative from Pallenis spinosa Juan F. Sanz, J.Alberto Marco Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85146-Q

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(5R)-5-[(1S,2R,3S,5S,6S)-2,3-dihydroxy-2-methyl-6-bicyclo[3.1.0]hexanyl]-6-methylheptan-2-one 162963995 Click to see CC(C)C(CCC(=O)C)C1C2C1C(C(C2)O)(C)O 254.36 unknown https://doi.org/10.1016/0031-9422(90)80215-3
(5S)-5-[(1S,2R,3S,5S,6S)-2,3-dihydroxy-2-methyl-6-bicyclo[3.1.0]hexanyl]-6-methylheptan-2-one 162963994 Click to see CC(C)C(CCC(=O)C)C1C2C1C(C(C2)O)(C)O 254.36 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
[(1S,2R,3S,5S,6S)-2-hydroxy-2-methyl-6-[(3S)-2-methyl-6-oxoheptan-3-yl]-3-bicyclo[3.1.0]hexanyl] acetate 101936579 Click to see CC(C)C(CCC(=O)C)C1C2C1C(C(C2)OC(=O)C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
[2-Hydroxy-2-methyl-6-(2-methyl-6-oxoheptan-3-yl)-3-bicyclo[3.1.0]hexanyl] acetate 163053704 Click to see CC(C)C(CCC(=O)C)C1C2C1C(C(C2)OC(=O)C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
5-(2,3-Dihydroxy-2-methyl-6-bicyclo[3.1.0]hexanyl)-6-methylheptan-2-one 14733718 Click to see CC(C)C(CCC(=O)C)C1C2C1C(C(C2)O)(C)O 254.36 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
https://doi.org/10.1016/0031-9422(90)80215-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1,4-Dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl) acetate 14830819 Click to see CC(C)C1=CCC2(C(CC(C(C2C1)(C)O)OC(=O)C)O)C 296.40 unknown https://doi.org/10.1016/0031-9422(90)80215-3
https://doi.org/10.1016/S0031-9422(97)00386-5
(1,8-Dihydroxy-2,8-dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecan-9-yl) acetate 162991394 Click to see CC(C)C1CCC2(C1C3C(C(CC2(O3)O)OC(=O)C)(C)O)C 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
(1R,2S,4R,4aR,8aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,8,8a-hexahydronaphthalene-1,2,4-triol 14733707 Click to see CC(C)C1=CCC2(C(CC(C(C2C1)(C)O)O)O)C 254.36 unknown https://doi.org/10.1016/0031-9422(90)80215-3
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(91)85146-Q
(3-Acetyl-7-hydroxy-7-methyl-4-propan-2-yl-1,2,3,3a,4,5,6,7a-octahydroinden-2-yl) acetate 14830821 Click to see CC(C)C1CCC(C2C1C(C(C2)OC(=O)C)C(=O)C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
[(1R,2S,4aR,8aR)-1-hydroxy-1,4a-dimethyl-4-oxo-7-propan-2-yl-3,5,8,8a-tetrahydro-2H-naphthalen-2-yl] acetate 162817198 Click to see CC(C)C1=CCC2(C(C1)C(C(CC2=O)OC(=O)C)(C)O)C 294.40 unknown https://doi.org/10.1016/0031-9422(90)80215-3
[(1R,2S,4R,4aR,8aR)-1,4-dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl] acetate 163056185 Click to see CC(C)C1=CCC2(C(CC(C(C2C1)(C)O)OC(=O)C)O)C 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
https://doi.org/10.1016/0031-9422(90)80215-3
[(1R,3S,4R,4aR,8aR)-3-acetyloxy-4-hydroxy-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] acetate 14733709 Click to see CC(C)C1=CCC2(C(CC(C(C2C1)(C)O)OC(=O)C)OC(=O)C)C 338.40 unknown https://doi.org/10.1016/0031-9422(90)80215-3
[(1S,2R,5S,6S,7S,8S,9S)-1,8-dihydroxy-2,8-dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecan-9-yl] acetate 101937128 Click to see CC(C)C1CCC2(C1C3C(C(CC2(O3)O)OC(=O)C)(C)O)C 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
[(2S,3R,3aR,4S,7R,7aR)-3-acetyl-7-hydroxy-7-methyl-4-propan-2-yl-1,2,3,3a,4,5,6,7a-octahydroinden-2-yl] acetate 162945465 Click to see CC(C)C1CCC(C2C1C(C(C2)OC(=O)C)C(=O)C)(C)O 296.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
1-(2,4-Dihydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl)ethanone 14733714 Click to see CC(C)C1CCC(C2C1C(C(C2)O)C(=O)C)(C)O 254.36 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
https://doi.org/10.1016/0031-9422(90)80215-3
1-[(1R,2S,3aR,4R,7S,7aR)-2,4-dihydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone 162909368 Click to see CC(C)C1CCC(C2C1C(C(C2)O)C(=O)C)(C)O 254.36 unknown https://doi.org/10.1016/0031-9422(90)80215-3
https://doi.org/10.1016/S0031-9422(97)00386-5
1-[(1R,2S,3aR,4R,7S,7aS)-2,4-dihydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone 23786455 Click to see CC(C)C1CCC(C2C1C(C(C2)O)C(=O)C)(C)O 254.36 unknown https://doi.org/10.1016/0031-9422(90)80215-3
1-[(1S,3aR,4R,7S,7aR)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone 14138891 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
1,4a-Dimethyl-7-propan-2-yl-2,3,4,5,8,8a-hexahydronaphthalene-1,2,4-triol 14733706 Click to see CC(C)C1=CCC2(C(CC(C(C2C1)(C)O)O)O)C 254.36 unknown https://doi.org/10.1016/0031-9422(90)80215-3
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane 539857 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(91)85146-Q
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 522266 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
Ent-Spathulenol 13854255 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,4S,6R,7R,8S,11S)-4,11-dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecan-7-ol 124708193 Click to see CC(C)C1CCC2(C(O2)CCC3(C(C1O)O3)C)C 254.36 unknown https://doi.org/10.1016/0031-9422(91)85146-Q
(1S,2R,3E,5S,8E)-2,8-dimethyl-5-propan-2-ylcyclodeca-3,8-diene-1,2-diol 14219406 Click to see CC1=CCC(C(C=CC(CC1)C(C)C)(C)O)O 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
(2-Hydroxy-2,8-dimethyl-5-propan-2-ylcyclodeca-3,8-dien-1-yl) acetate 78409639 Click to see CC1=CCC(C(C=CC(CC1)C(C)C)(C)O)OC(=O)C 280.40 unknown https://doi.org/10.1016/0031-9422(89)80127-X
https://doi.org/10.1016/S0031-9422(97)00386-5
(6Z)-6,10-dimethyl-3-propan-2-yl-11-oxabicyclo[8.1.0]undec-6-en-2-ol 101967027 Click to see CC1=CCCC2(C(O2)C(C(CC1)C(C)C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(91)85146-Q
(9-Hydroxy-3,7-dimethyl-10-propan-2-ylcyclodeca-3,7-dien-1-yl) acetate 162915059 Click to see CC1=CC(C(C(CC(=CCC1)C)OC(=O)C)C(C)C)O 280.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
[(1S,2R,3E,5S,8E)-2-hydroxy-2,8-dimethyl-5-propan-2-ylcyclodeca-3,8-dien-1-yl] acetate 14219404 Click to see CC1=CCC(C(C=CC(CC1)C(C)C)(C)O)OC(=O)C 280.40 unknown https://doi.org/10.1016/0031-9422(89)80127-X
https://doi.org/10.1016/S0031-9422(97)00386-5
2,8-Dimethyl-5-propan-2-ylcyclodeca-3,8-diene-1,2-diol 78409640 Click to see CC1=CCC(C(C=CC(CC1)C(C)C)(C)O)O 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
4,11-Dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecan-7-ol 45359817 Click to see CC(C)C1CCC2(C(O2)CCC3(C(C1O)O3)C)C 254.36 unknown https://doi.org/10.1016/0031-9422(91)85146-Q
8-Acetyltovarol 101936578 Click to see CC1=CC(C(C(CC(=CCC1)C)OC(=O)C)C(C)C)O 280.40 unknown https://doi.org/10.1016/S0031-9422(97)00386-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin 5281678 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 332.26 unknown https://doi.org/10.1016/0305-1978(92)90038-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Tricin 5-glucoside 49800176 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/0305-1978(92)90038-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Patuletin 3-O-beta-D-galactoside 5320434 Click to see COC1=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)O 494.40 unknown https://doi.org/10.1016/0305-1978(92)90038-F
Patuletin 3-O-beta-D-robinobioside 44575854 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C(=C(C(=C4)O)OC)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 640.50 unknown https://doi.org/10.1016/0305-1978(92)90038-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Patuletin 7-galactoside 44259803 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 494.40 unknown https://doi.org/10.1016/0305-1978(92)90038-F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-3,5,6,7,3'-pentamethoxyflavone 14376231 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)O 388.40 unknown https://doi.org/10.1016/0305-1978(92)90038-F
Hexamethylquercetagetin 386331 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC 402.40 unknown https://doi.org/10.1016/0305-1978(92)90038-F

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