Results 51 to 60 of about 1,481 (197)

The isolation, analytical characterization by HPLC-UV and NMR spectroscopy, cytotoxic and antioxidant activities of baeomycesic acid from Thamnolia vermicularis var. subuliformis [PDF]

open access: yesHemijska Industrija, 2011
The aim of this work was the analytical characterization of the β-orcinol depside, baeomycesic acid in lichens extracts. The extract of Thamnolia vermicularis var.
Manojlović Nedeljko T.   +5 more
doaj   +1 more source

Influence of the Solvent on the Extraction of Phenolic Com-pounds from the Coffee Grounds by Soxhlet Leaching

open access: yesIngeniería e Investigación, 2022
In this study, phenolic compounds were extracted from the essential oil of coffee grounds originated in the coffee industry in the city of Guayaquil, Ecuador.
Rafael Norberto Calle Chumo   +3 more
doaj   +1 more source

The Role of Secondary Metabolites and Bark Chemistry in Shaping Diversity and Abundance of Epiphytic Lichens

open access: yesFrontiers in Forests and Global Change, 2022
Diversity of secondary lichen metabolites was studied in epiphytic lichens on six phorophytes—spruce, pine, birch, alder, aspen and poplar in the Middle Urals of Russia. Atranorin, usnic, fumarprotocetraric acid, zeorin, and gyrophoric acid were found in
Alexander Paukov   +4 more
doaj   +1 more source

New Depsides From Erioderma Lichens

open access: yes, 1987
A chemosyndrome of para- depsides based on methyl 4-O-demethylbarbatate (3) has been detected in Erioderma lichens and the structures of the metabolites have been established by unambiguous syntheses.
JA Elix   +4 more
core   +1 more source

Caffeic Acid Derivatives from Eupatorium perfoliatum L.

open access: yesMolecules, 2008
From the ethyl acetate soluble fraction of a methanol/water extract of the herb Eupatorium perfoliatum L. (Asteraceae) six caffeic acid derivatives have been isolated and identified by 1D- and 2D-NMR spectroscopic data.
Andreas Hensel   +2 more
doaj   +1 more source

Characterization of the depsidone gene cluster reveals etherification, decarboxylation and multiple halogenations as tailoring steps in depsidone assembly

open access: yesActa Pharmaceutica Sinica B, 2023
Depsides and depsidones have attracted attention for biosynthetic studies due to their broad biological activities and structural diversity. Previous structure‒activity relationships indicated that triple halogenated depsidones display the best anti ...
Jiafan Yang   +4 more
doaj   +1 more source

Redirecting a Fungal Quercetin 2,3‐Dioxygenase Toward Artificial Flavonols

open access: yesChemCatChem, Volume 18, Issue 6, 27 March 2026.
A novel quercetin 2,3‐dioxygenase was engineered to reshape its substrate‐binding cavity and redirect its specificity toward artificial flavonols. One variant with a larger substrate‐binding cavity exhibited 20‐ to 1750‐fold higher activity toward bulky flavonols with phenyl‐based substitutions at position C‐8.
Michael Kotik   +9 more
wiley   +1 more source

Synthesis of Lichen para-Sphaerophorol Depsides

open access: yes, 1987
The total synthesis of the lichen depsides sphaerophorin (I), 4-O-demethylsphaerophorin (2),isosphaeric acid (3), hyperlatolic acid (4) and isohyperlatolic acid (5) is described.
JA Elix, JH Wardlaw
core   +1 more source

Dereplicative Combination of HPLC/DAD/MS and 2D NMR to Identify Lichexanthone Isomers in Lichen Extracts

open access: yesPhytochemical Analysis, Volume 37, Issue 2, Page 330-343, March 2026.
ABSTRACT Introduction Lichexanthones are the major xanthones found in lichens. They present a high degree of isomerism, which makes their identification tedious. Xanthones are known to occur in lichens according to chemosyndromes, and these compounds act as chemotaxonomic markers.
Solenn Ferron   +5 more
wiley   +1 more source

New Depsides From the Lichen Biatora sorediosa

open access: yes, 1991
The new depsides 2′-O-methylisohyperlatolic acid (4) and 2′-O-methylsuperlatolic acid (5) have been detected in the lichen Biatora sorediosa, and the structure of these metabolites has been established by unambiguous synthesis.
F David, JA Elix
core   +1 more source

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