a large, cosmopolitan genus of Ascomycota is in the focus of our current poly-thetic taxonomic studies, and served as an excellent source for bioactive secondary metabolites at the same time. The present work concerns a survey of the species complex based on specimens from Iran and Europe by morphological studies and high performance liquid chromatography coupled to mass spectrometry and diode array detection (HPLC-MS-DAD). Apart from known chemotaxonomic markers like binaphthalene tetrol (BNT) and daldinin F, two unprece-dented molecules were detected and subsequently isolated to purity by semi preparative HPLC. Their structures were established by nuclear-magnetic resonance (NMR) spectroscopy as 3'-malonyl-daldinin F () and pseudofuscochalasin A (). The new daldinin derivative showed weak cytotoxicity towards mammalian cells but bactericidal activity. The new cytochalasin was compared to cytochalasin C in an actin disruption assay using fluorescence microscopy of human osteo-sarcoma U2OS cells, revealing comparable activity towards F-actin but being irreversible compared to cytochalasin C. Concurrently, a multilocus molecular phylogeny based on ribosomal and proteinogenic nucleotide sequences of species resulted in a well-supported clade for and its allies. From a comparison of morphological, chemotaxonomic and phylogenetic evidence, we introduce the new species and .

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916920PMC
http://dx.doi.org/10.3390/jof7020131DOI Listing

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