TY - JOUR T1 - Metabolism and Disposition of the Antifolate LY231514 in Mice and Dogs JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 693 LP - 700 VL - 25 IS - 6 AU - J. M. Woodland AU - C. J. Barnett AU - D. E. Dorman AU - J. M. Gruber AU - C. Shih AU - L. A. Spangle AU - T. M. Wilson AU - W. J. Ehlhardt Y1 - 1997/06/01 UR - http://dmd.aspetjournals.org/content/25/6/693.abstract N2 - The metabolism and disposition of LY231514 was studied in mice and dogs. LY231514 is a novel pyrrolopyrimidine-based multi-target antifolate (MTA) showing broad in vivo antitumor activity in mouse models and is currently in phase II human clinical trials. Doses (iv) of the compound showed high plasma levels, resulting in AUC values of 30–33 μg-hr/ml for mice and dogs after 20 and 7.5 mg/kg doses, respectively. The compound was eliminated rapidly. Half-life values for mice and dogs were about 7 and 2 hr, respectively. In vitro plasma binding measured 56% in mice, 46% in dogs, and 81% in humans. Fecal elimination was the major excretion pathway in mice after single iv doses of [14C]LY231514. Urine constituted the major route of excretion in dogs. Parent LY231514 accounted for the majority of urinary radiocarbon in mice (90%) and dogs (68%). Minor metabolites were found in urine, but the amounts were too small to isolate or identify. Based on an earlier observation that LY231514 photodegraded to produce reaction products having similar retention times as these minor urinary isolates, a photo-oxidation system was developed which in fact produced these metabolites. Subsequently, these photolytically-produced materials were used as standards to identify two novel in vivo metabolites formed by oxidation of the pyrrolo-pyrimidine ring system of LY231514. The oxidative transformations are similar to those observed for tryptophan and other indoles in that the pyrrole ring is oxidized to give an amide; further oxidation cleaves this ring, one ring carbon is lost, and a ketone is formed. The American Society for Pharmacology and Experimental Therapeutics ER -