Panapophenanthrin, a Rare Oligocyclic Diterpene from <i>Panus strigellus</i>
Natalia A. Llanos-López,
Sherif Saeed Ebada,
Aída M. Vasco-Palacios,
Laura M. Sánchez-Giraldo,
Lina López,
Luisa F. Rojas,
Attila Mándi,
Tibor Kurtán,
Yasmina Marin-Felix
Affiliations
Natalia A. Llanos-López
Department of Microbial Drugs, Helmholtz Centre for Infection Research (HZI) and German Centre for Infection Research (DZIF), DZIF Partner Site Hannover-Braunschweig, Inhoffenstrasse 7, 38124 Braunschweig, Germany
Sherif Saeed Ebada
Department of Microbial Drugs, Helmholtz Centre for Infection Research (HZI) and German Centre for Infection Research (DZIF), DZIF Partner Site Hannover-Braunschweig, Inhoffenstrasse 7, 38124 Braunschweig, Germany
Aída M. Vasco-Palacios
Grupo de Microbiología Ambientaland Grupo BioMicro, Escuela de Microbiología, Universidad de Antioquia, Calle 70 No. 52-21, 050010 Medellin, Colombia
Laura M. Sánchez-Giraldo
Grupo de Investigación de Biotecnología Industrial, Facultad de Ciencias, Universidad Nacional de Colombia Sede Medellín, Calle 59A No. 63-20, 050034 Medellin, Colombia
Lina López
Grupo de Biotransformación, Escuela de Microbiología, Universidad de Antioquia, Calle 70 No. 52-21, 050010 Medellin, Colombia
Luisa F. Rojas
Grupo de Biotransformación, Escuela de Microbiología, Universidad de Antioquia, Calle 70 No. 52-21, 050010 Medellin, Colombia
Attila Mándi
Department of Organic Chemistry, University of Debrecen, P.O. Box 400, 4002 Debrecen, Hungary
Tibor Kurtán
Department of Organic Chemistry, University of Debrecen, P.O. Box 400, 4002 Debrecen, Hungary
Yasmina Marin-Felix
Department of Microbial Drugs, Helmholtz Centre for Infection Research (HZI) and German Centre for Infection Research (DZIF), DZIF Partner Site Hannover-Braunschweig, Inhoffenstrasse 7, 38124 Braunschweig, Germany
During the course of our search for biologically active secondary metabolites from fungal cultures, a new oligocyclic diterpenoidal derivative, panapophenanthrin (1), was isolated from Panus strigellus. In addition, two known metabolites, panepophenanthrin (2) and dihydrohypnophilin (3), were also obtained. The chemical structures of the isolated compounds were elucidated based on extensive 1D and 2D NMR spectral analyses together with high-resolution electrospray ionization mass spectrometry (HR-ESI-MS). The absolute configuration was determined through TDDFT-ECD calculations. All of the compounds were assessed for their antimicrobial and cytotoxic activities. Compounds 1 and 3 showed moderate to weak activities in the performed antimicrobial assays, while compound 1 exhibited potent cytotoxic activity against the mammalian cell lines mouse fibroblast (L929) and human endocervical adenocarcinoma (KB3.1).