P10801
Perinaphthenon
97%
Synonym(e):
1H-Benzonaphthen-1-one, 7-Perinaphthenone, Phenalenone, Phenalone
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Alle Fotos(1)
About This Item
Empfohlene Produkte
Assay
97%
Form
powder
mp (Schmelzpunkt)
153-156 °C (lit.)
SMILES String
O=C1C=Cc2cccc3cccc1c23
InChI
1S/C13H8O/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8H
InChIKey
WWBGWPHHLRSTFI-UHFFFAOYSA-N
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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The marine-derived fungus Coniothyrium cereale was isolated from the green alga Enteromorpha sp. and found to produce the new phenalenone derivatives 1-7 as well as the known compounds lactone 8, (-) sclerodin (9), lamellicolic anhydride (10), (-) scleroderolide (11), and
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Magnetic resonance in chemistry : MRC, 45(5), 439-441 (2007-03-21)
The complete (1)H and (13)C NMR assignments are reported for the novel natural product Bacillosporin D together with the known compound Bacillosporin C. These compounds containing seven rings were isolated from the mangrove endophytic fungus SBE-14 from the South China
Accounts of chemical research, 39(5), 293-300 (2006-05-17)
Plants defend themselves from pathogen infections or mechanical injury by a number of mechanisms, including the induced biosynthesis of antimicrobial secondary metabolites. These compounds, termed phytoalexins, represent a very economical way to counteract hazard, because the carbon and energy resources
Journal of agricultural and food chemistry, 57(16), 7417-7421 (2009-07-28)
The levels of native fungitoxic perinaphthenone phytoalexins in susceptible Musa varieties (banana), which are commercially grown in large plantations, are too low to provide plants with long-lasting protection against highly pathogenic fungi. Novel strategies for plant protection are necessary to
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