Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors.

摘要

In search for a novel chemotype to develop topoisomerase I (Top1) inhibitors, the pyrazolo[1,5-a]quinazoline\udnucleus, structurally related to the indenoisoquinoline system precursor of well-known Top1 poisons, was variously decorated\ud(i.e., a substituted phenyl ring at 2- or 3-position, a protonable side chain at 4- or 5-position), affording a number of Top1\udinhibitors with cleavage patterns common to CPT and MJ-III-65. SARs data were rationalized by means of an advanced docking\udprotocol.