N,N-bis-heteroaryl methylamines: Potent anti-mitotic and highly cytotoxic agents

The synthesis and evaluation of a series of N,N-bis-heterocyclic-methylamines 1 as isoazaerianin analogues are described. It was demonstrated that the replacement of the 3,4,5-trimethoxyphenyl A-ring present in CA-4, isoCA-4 and isoazaerianin by a quinoline or a quinazoline ring is possible and often beneficiary for a high level of cytotoxicity. We have also showed that a carbazole or an indole nucleus are very effective as B-rings in this series, leading to anti-cancer drugs 1 having a sub-nanomolar level of cytotoxicity (1a: IC50 = 70 pM against HCT116 cells). 1a also display a high level of cytotoxicity against four other human cancer cells and inhibited tubulin assembly at a micromolar level. Moreover, at a concentration of 5 nM, 1a arrested the cellular cycle in G2/M phase of the cellular cycle and induced apoptosis of HCT116 cells. It was also showed that after few hours 1a at a concentration of 10 nM totally disrupted endothelial network formation on Matrigel. [Display omitted] •Cytotoxic N,N-bis-heterocyclic methylamine derivatives were design and synthesized.•Best combinations associate, a quinaldine and a carbazole connected to the NMe group.•Compound 1a, arrested cellular cycle in the G2/M phase at a concentration of 5 nM.•1a is a strong apoptosis inducer and a potent vascular disrupting agent.