| 摘要 |
Neurofibromatosis in a human is treated by administration of a pharmaceutical compsn. contg. a therapeutically effective amount of a combination of a phenylacetylglutamine cpd. of formula (A) and a phenylacetic acid cpd. of formula (B) in a wt. ratio (A:B) of 1:1 to 1:10. Salts of (A) and (B) may also be used. R = H, OH, NH2 or OW; X = H, F, Cl, Br, I, OH, OW, NO2 or NH2; Y = H, F, Cl, Br or I; W = -C(=O)-Z or 1-12C aliphatic gp.; and Z = 1-12C aliphatic or aromatic gp.. X and Y can both vary within the cpd. |
