摘要 |
<p>The invention provides a hydroxamate or hydroxamic acid compound of general formula (Ia) or (Ib): HONH-[linker]-X1R1R2 or (Ic): R1R2X1-[linker]-X1R1R2, in which X1 is a polar group selected from the group consisting of -C=O; -COR1; -CF2; -CNH2; -CNR1; -SO2-; -P(O)(OH)-; -C=S; -CSR1; -C-COR1; -C-CONR1R2 and -C-CH¿2?OH; R?1 and R2¿ are the same or different, and each is independently selected from the group consisting of H; OH; NH¿2?; NHOH; substituted or unsubstituted, branched or unbranched alkyl, alkenyl, alkylamino, alkyloxy or arylalkyloxy; substituted or unsubstituted aryl, aryloxy or pyridino; substituted or unsubstituted arylamino, piperidino, cycloalkyl, cycloalkylamino, pyridineamino, 9-purine-6-amine, and thiazoleamino; or either R?1 or R2¿ is absent; and the linker is a group having a backbone of 5 to 9 atoms, which may comprise 1, 2 or 3 amino acids, or a pharmaceutically acceptable salt, ester or derivative thereof. The compounds have the ability to selectively prevent the growth of a variety of human tumour cell types, without affecting growth of normal cells. The compounds of the invention also inhibit the growth of protozoan parasites.</p> |