Five novel extracellular metabolites with an unprecedented diterpenoid skel
eton, 5-[(5-carboxy-2-hydroxy)benzyl]-11-hydroxymethyl-2,5,6,8a,11-pentamet
hyldodecahydrocyclopenta[a]naphthalene (1), 5-[(5-carboxy-2-hydroxy)benzyl]
-11-formyl-2,5,6,8a,11-pentamethyl-dodecahydrocyclopenta[a]naphthalene (2),
5-[(5-carboxy-2-hydroxy)benzyl]-11-carboxy-2,5,6,8a,11-pentamethyl-dodecah
ydrocyclopenta[a]naphthalene (3), 5-[(5-carboxy-2-hydroxy)benzyl]-11-dihydr
oxymethyl-2,5,6,8a,11-pentamethyldodecahydrocyclopenta[a]naphthalene (4), a
nd 5-[(5-carboxy-2-hydroxy)benzyl]-11-acetyl-2,5,6,8a-tetramethyldodecahydr
ocyclopenta[a]naphthalene (5), have been isolated from the culture medium o
f the terrestrial cyanobacterium Nostoc commune by means of bioguided isola
tion. The molecules were designated as comnostins A-E. The structures were
determined by spectroscopic methods, mainly NMR and mass spectrometry. The
relative stereochemistry of comnostin A was confirmed by single-crystal X-r
ay structure analysis. All comnostins showed antibacterial activities. Addi
tionally, cytotoxic and molluscicidal activities were found for comnostin B
.