| 摘要 |
<p>6-phenylpyrrolopyrimidinedione derivatives of the formula (I), and pharmaceutically acceptable salts thereof, wherein R?1,R2,R3,R4 and R5¿ are organic residues, L¿1? is a spacer group and R?6¿ is C(O)NR10R11, -S(O)¿2?NR?10R11,-ON=CR 12R13¿, or a heterocyclyl, arylor heteroaryl group, where R?10, R11, R12 and R13¿ are organic residues, have therapeutic potential as A2 adenosine receptor inhibitors.</p> |
