Results 131 to 140 of about 796 (189)

Natural Colorants for a Bio-Based Economy-Recovering a Lost Knowledge for Novel Applications of <i>Chrozophora tinctoria</i> Extracts as Paints Through a Multi-Analytical Approach. [PDF]

Molecules
Cleveland I, Beeby A, Vieira M, Pina F, Branco PS, Nabais P, Melo MJ.   +6 more
europepmc   +1 more source

Depsidon 核の合成

YAKUGAKU ZASSHI, 1944
openaire   +1 more source

Towards the Use of Lichens as a Source of Bioactive Substances for Topical Applications. [PDF]

Molecules
Baczewska I, Hawrylak-Nowak B, Zagórska-Dziok M, Ziemlewska A, Nizioł-Łukaszewska Z, Borowski G, Dresler S.   +6 more
europepmc   +1 more source

The lichen secondary metabolite lichesterinic acid exhibits antibiofilm activity against fungal pathogens. [PDF]

Front Cell Infect Microbiol
Odabas MN, Kainz K, Weinberger I, Schloffer K, Riedl S, Chollet-Krugler M, Zweytick D, Boustie J, Madeo F, Carmona-Gutierrez D.   +9 more
europepmc   +1 more source

Cytotoxicity of norstictic acid derivatives, a depsidone from Ramalina anceps Nyl. [PDF]

Turk J Chem
Bogo D, Alcântara IMC, Alcantara GB, Micheletti AC, Honda NK, de Fátima C Matos M.   +5 more
europepmc   +1 more source

The limitless endophytes: their role as antifungal agents against top priority pathogens. [PDF]

Microb Cell Fact
Moussa AY.
europepmc   +1 more source

Chemical Composition, Antioxidant, and Anti-Inflammatory Activity of the Antarctic Lichen <i>Leptogium puberulum</i>: A Combination of Metabolomic, In Vitro, and In Silico Approaches. [PDF]

Int J Mol Sci
Torres-Benítez A, Ortega-Valencia JE, Salazar JR, Monje K, Ley-Martínez J, Vargas-Arana G, Simirgiotis MJ.   +6 more
europepmc   +1 more source

Flavonora: a new genus of lecanoroid lichens (Ascomycota, lichenized fungi). [PDF]

Sci Rep
Mazur E, Malíček J, Weerakoon G, Śliwa L.   +3 more
europepmc   +1 more source

Depsidone synthesis. XII. Some exploratory synthetic routes to highly functionalized depsidones

Australian Journal of Chemistry, 1978
Attempts to synthesize the depsidones virensic acid (1), physciosporin (2), and pannarin (3) by routes based on the Ullmann ether condensation and the Hems reaction are described. Selective functionalization of highly substituted p-xylenes by photobromination is reported.
T Sala, MV Sargent
core   +3 more sources

Three New Lichen Depsidones

Australian Journal of Chemistry, 1987
The depsidones a- acetylconstictic acid (5-acetoxymethyl-1,4-dihydroxy-10-methoxy-8-methyl-3,7-dioxo-1,3-dihydro-7 H- isobenzofuro [4,5- b][l,4] benzodioxepin-ll-carbaldehyde ) (6), substictic acid (1,4-dihydroxy-10-methoxy-8-methy1-3,7-dioxo- 1,3-dihydro-7 H- isobenzofuro [4,5-b][1,4]benzodioxepin-11-carbaldehyde) (7) and conphysodalic acid (9 ...
JA Elix, KL Gaul, PW James, OW Purvis
openaire   +2 more sources