Results 131 to 140 of about 911 (189)

Genome Mining-Guided Discovery of Two New Depsides from <i>Talaromyces</i> sp. HDN1820200. [PDF]

Mar Drugs
Zhang X, Liu L, Huang J, Ren X, Zhang G, Che Q, Li D, Zhu T.   +7 more
europepmc   +1 more source

Computational Exploration of Phenolic Compounds from Endophytic Fungi as α-Glucosidase Inhibitors for Diabetes Management. [PDF]

ACS Omega
Kannakazhi Kantari SA, Kanchi S, Patnaik B, Agraharam A.   +3 more
europepmc   +1 more source

Extracting Value from Marine and Microbial Natural Product Artifacts and Chemical Reactivity. [PDF]

Mar Drugs
Butler MS, Capon RJ.
europepmc   +1 more source

A Comprehensive Review on Chemical Structures and Bioactivities of <i>Ostropomycetidae</i> Lichens. [PDF]

J Fungi (Basel)
Wang Y, Hao C, Jiang S, Ju Y, Li W, Jia Z.   +5 more
europepmc   +1 more source

Chemical Profiling and In Vitro Evaluation of Bioactive Properties of Evernia prunastri Extract: Implications for Therapeutic Applications. [PDF]

Plants (Basel)
Stojković D, Živković J, Bolevich S, Bolevich S, Zengin G, Gašić U, Soković M.   +6 more
europepmc   +1 more source

Elevational microhabitats influence some endolichenic traits of Umbilicaria aprina, an alpine lichen species. [PDF]

Sci Rep
Rahimi-Rizi M, Norouzi H, Sohrabi M, Dashtipoor S, Omidi Nasab M, Boustie J.   +5 more
europepmc   +1 more source

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A new depsidone from Usnea diffracta

Chinese Chemical Letters, 2009
Abstract A new depsidone, diffractione A ( 1 ), as well as six known phenolic compounds ( 2 – 7 ) were isolated from Usnea diffracta . Their structures were elucidated by 1D and 2D NMR spectroscopy together with HRESIMS analysis. All components were obtained for the first time from U. diffracta.
Huan Yang Qi, Yuan Peng Jin, Yan Ping Shi   +2 more
exaly   +2 more sources

Depsidone synthesis. Part 19. Some β-orcinol depsidones

J. Chem. Soc., Perkin Trans. 1, 1981
The synthesis of the lichen depsidones 3,8-dihydroxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo[b,e][1,4]-dioxepin-7-carboxylic acid (hypoprotocetraric acid)(4), 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylic acid (O-methylhyprprotocetraric acid)(5), 4-formyl-3,8-dihydroxy-1,6,9-trimethyl-11-oxo-11H-dibenzo[b,e][1,
Tony Sala, Melvyn V. Sargent
openaire   +2 more sources

Depsidone synthesis. Part 11. Synthesis of some fungal depsidones related to nidulin

Journal of the Chemical Society, Perkin Transactions 1, 1978
The synthesis of 3-hydroxy-8-methoxy-1,9-dimethyl-6-(s-butyl)dibenzo[b,e][1,4]dioxepin-11-one (tridechlorodihydronidulin)(34), a derivative of the fungal depsidone nidulin (1), and of 3,8-dihydroxy-1,9-dimethyl-6-(s-butyl)dibenzo[b,e][1,4]dioxepin-11-one (tridechlorodihydro-O-nornidulin)(39), a derivative of the fungal depsidone tridechloro-O ...
Peter Djura, Melvyn V. Sargent
openaire   +2 more sources

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
openaire   +2 more sources