| 摘要 |
The present invention is directed to substituted spiro-azacyclic derivatives of the formula (I):(wherein R1, R2, R3, R4, R5, R6, R9, R10, X, Y, p and q are defined herein) which are tachykinin antagonists and are useful, for example, in the treatment or prevention of pain, inflammation, migraine, emesis and postherpetic neuralgia. |
