DNA-PK INHIBITORS

摘要

The invention relates to the use of compounds of formula (I) and isomers, salts, solvates, chemically protected forms, and prodrugs thereof, in the preparation of a medicament for inhibiting the activity of DNA-PK, wherein R 1 and R2 are independently hydrogen, an optionally substituted C1-7 alkyl grou p, C3-20 heterocyclyl group, or C5-20 aryl group, or may together form, along with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring having from 4 to 8 ring atoms; X and Y are selected from C R4 and O, O and CR'4 and NR"4 and N, where the unsaturation is in the appropria te place in the ring, and where one of R3 and R4 or R'4 is an optionally substituted C3-20 heteroaryl or C5-20 aryl group, and the other of R3 and R4 or R'4 is H, or R3 and R4 or R"4 together are -A-B-, which collectively represent a fused optionally substituted aromatic ring. The compounds also selectively inhibit the activity of DNA-PK compared to PI 3-kinase and/or AT M.