Abstract. Effects of methazole [2-(3,4-dichlorophenyl)-4-methyl-l,2,4-oxadiazolidine-3,5-dione] and of its plant degradation products, DCPMU [3-(3,4-dichlorophenyl)-l-methylurea] and DCPU [3-(3,4-dichlorophenyl)urea], on photosynthesis, protein synthesis, ribonucleic acid (RNA) synthesis, and lipid synthesis of enzymatically isolated leaf cells of velvetleaf (Abutilon theophrasti Medic) were compared. Photosynthesis and protein, RNA, and lipid synthesis were assayed by the incorporation of NaH14CO3, [~4C]-leucine, [14C]-uracil, and [14C]-acetate, respectively, into the isolated cells. Time-course and concentration studies included incubation times of 30, 60, and 120 rain and concentrations of 0.1, 1, 10, and 100 /zM of all three chemicals. DCPMU was a more potent inhibitor of the four metabolic processes examined than either the parent herbicide methazole or DCPU. The sensitivity of the four metabolic processes to DCPMU decreased in the order: photosynthesis > lipid > RNA > protein synthesis. Inhibition of all metabolic processes by methazole was time-dependent, increasing in magnitude with concomitant increases in incubation time. It is probable that the observed effects of methazole were caused by DCPMU, formed through metabolism of methazole by the iso-* Contribution No. 470,