A triazole compound of the formula (I) or a pharmacologically salt thereof:
1
wherein X represents a group of formula X—OH which has antifungal activity, L represents an -(adjacently substituted C
6
-C
10
aryl)-CH
2
group and R represents a —P(═O)(OH)
2
group.
This invention includes oxazolidinone prodrug compounds of Formula (I) and Formula (II) as defined herein. The prodrugs are convertible by natural biological processes into an active ingredient possessed of antimicrobial properties useful in treating bacterial infections in mammals.