2005 Volume 53 Issue 4 Pages 453-455
New 3-amino-5-ethenylcyclopentenones, myrothenones A (4) and B (5), were isolated together with known 6-n-pentyl-α-pyrone (1), trichodenone A (2), and cyclonerodiol (3) from the marine algicolous fungus of genus of Myrothecium. The structure and absolute stereochemistry of the new compounds were established by spectral interpretation and X-ray analysis. Compounds 1 and 4 exhibited a tyrosinase inhibitory activity with IC50 value of 0.8 and 6.6 μM, respectively, which are more active than kojic acid (IC50, 7.7 μM) currently being used as a functional personal-care compound.