Photo-​control of cancer cell growth by benzodiazo N-​substituted pyrrole derivatives

In order to expand the class of diazocompounds able to act as photo-​activable microtubule inhibitors the potential of azo-​heteroarenes has been explored. In this paper we focus on the synthesis, phys. properties and biol. effects of Me rac-​2-​(2-​((E)​-​(4-​((R)​-​2,​3-​dihydroxypropoxy)​phenyl) diazenyl)​-​1H-​pyrrol-​1-​yl)​-​3-​hydroxypropanoate (1a) and Me rac-​2-​(2-​((E)​-​(4-​((S)​-​2,​3-​dihydroxypropoxy)​phenyl) diazenyl)​-​1H-​pyrrol-​1-​yl)​-​3-​hydroxypropanoate (1b)​. Preliminary biol. studies on the HCT-​116 p53-​/- cancer cell line have shown that the weak antiproliferative action of the trans isomers of these mols., esp. of 1a, is enhanced upon LED light irradn. at 435 nm. On A375 cells the mols. have not shown any effect on cell viability either in the dark or under irradn. Moreover, the two diastereomeric components of 1a as pure stereomers have been synthesized and characterized for their chem.-​phys. properties. Interestingly, upon irradn., 1a has shown an antiproliferative activity on the HCT-​116 p53-​/- cells greater than that of the pure stereomers, 1RR and 1RS. Tubulin polymn. assay has also demonstrated that 1a, 1RR and 1RS inhibit tubulin aggregation mostly after exposure of the samples to LED light irradn.