Journal of Antibiotics p. 998 - 1005 (1996)
Update date:2022-08-29
Topics:
Chen, Choryu
Imamura, Nobutaka
Nishijima, Miyuki
Adachi, Kyoko
Sakai, Miho
Sano, Hiroshi
Novel antimicroalgal substances halymecins A (1), B (2) and C (3) were isolated from the fermentation broth of a Fusarium sp. and halymecins D (4) and E (5) from an Acremonium sp. The structures of these halymecins, Fig. 1, were determined based on extensive 2D NMR studies as well as mass spectral data. These chemical structures are conjugates of di- and trihydroxydecanoic acid. Halymecin A showed antimicroalgal activity against Skeletonema costatum.
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