Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel R. Mulholland"'
Autor:
Melissa M. Cadelis, Hugo Gordon, Alex Grey, Soeren Geese, Daniel R. Mulholland, Bevan S. Weir, Brent R. Copp, Siouxsie Wiles
Publikováno v:
Molecules, Vol 26, Iss 11, p 3235 (2021)
Fungi have become an invaluable source of bioactive natural products, with more than 5 million species of fungi spanning the globe. Fractionation of crude extract of Neodidymelliopsis sp., led to the isolation of a novel polyketide, (2Z)-cillifuranon
Externí odkaz:
https://doaj.org/article/cbf72b4f88c14309bef97dcc8db690e4
Autor:
Melissa M. Cadelis, Soeren Geese, Benedict B. Uy, Daniel R. Mulholland, Shara J. van de Pas, Alex Grey, Bevan S. Weir, Brent R. Copp, Siouxsie Wiles
Publikováno v:
Molecules, Vol 26, Iss 4, p 1094 (2021)
Antimicrobial bioassay-guided fractionation of the endophytic fungi Neofusicoccum australe led to the isolation of a new unsymmetrical naphthoquinone dimer, neofusnaphthoquinone B (1), along with four known natural products (2–5). Structure elucida
Externí odkaz:
https://doaj.org/article/14ea11c5a5d24bd5beca23385830f016
Autor:
Daniel R. Mulholland, Melissa M. Cadelis, Brent R. Copp, Alex Grey, Soeren Geese, Hugo Gordon, Siouxsie Wiles, Bevan S. Weir
Publikováno v:
Molecules
Volume 26
Issue 11
Molecules, Vol 26, Iss 3235, p 3235 (2021)
Volume 26
Issue 11
Molecules, Vol 26, Iss 3235, p 3235 (2021)
Fungi have become an invaluable source of bioactive natural products, with more than 5 million species of fungi spanning the globe. Fractionation of crude extract of Neodidymelliopsis sp., led to the isolation of a novel polyketide, (2Z)-cillifuranon
Autor:
Shara J. van de Pas, Brent R. Copp, Daniel R. Mulholland, Melissa M. Cadelis, Bevan S. Weir, Siouxsie Wiles, Soeren Geese, Benedict Uy, Alex Grey
Publikováno v:
Molecules
Volume 26
Issue 4
Molecules, Vol 26, Iss 1094, p 1094 (2021)
Volume 26
Issue 4
Molecules, Vol 26, Iss 1094, p 1094 (2021)
Antimicrobial bioassay-guided fractionation of the endophytic fungi Neofusicoccum australe led to the isolation of a new unsymmetrical naphthoquinone dimer, neofusnaphthoquinone B (1), along with four known natural products (2–5). Structure elucida