Antimicrobial and cytotoxic activity of agelasine and agelasimine analogs.

Agelasine and agelasimine derivatives with substantially less complicated terpenoid side chains compared to the naturally occurring compounds have been synthesized and their ability to inhibit growth of microorganisms and cancer cells has been studied. Compounds with excellent activity against cancer cell lines (MIC ca. 1 microM for the most potent compounds), including a drug resistant renal cell line, have been identified.

Microporous organic crystals: an unusual case for L-leucyl-L-serine.

Cocrystallized acetonitrile solvent molecules located inside 5.2 A channels in the crystal structure of L-leucyl-L-serine have been replaced by I2 molecules with full retention of the peptide scaffold.