CPI-613, an inhibitor of pyruvate dehydrogenase (PDH) and -ketoglutarate dehydrogenase (KGDH) enzymes, is currently in development for the treatment of pancreatic cancer, acute myeloid leukemia, and other cancers. CPI-613 is an analog of lipoic acid, an essential cofactor for both PDH and KGDH. Metabolism and mass balance studies were conducted in rats after intravenous administration of [C]-CPI-613.
View Article and Find Full Text PDFTaranabant (N-[(1S,2S)-3-(4-chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]-2-methyl-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanamide or MK-0364) is an orally active inverse agonist of the cannabinoid 1 (CB-1) receptor that was under development for the management of obesity. The metabolism and excretion of taranabant were investigated following a single oral dose of 5 mg/201 μCi [14C]taranabant to six healthy male subjects. The overall excretion recovery of the administered radioactivity was nearly quantitative (∼92%), with the majority of the dose (∼87%) excreted into faeces and a much smaller fraction (∼5%) into urine.
View Article and Find Full Text PDFMicrobiology (Reading)
July 1997
We have examined the degradation of C ring- and side-chain-labelled 2,4,5-trichlorophenoxyacetic acid by and The effects of Mn on the degradation of these radiolabeled substrates by D. squalens and the effect of nitrogen limitation on their degradation by suggested that in both fungi, side-chain cleavage was catalysed by a mechanism independent of the lignin degradation system, whereas the degradation of the aromatic ring was dependent on the lignin degradative system. Using unlabelled substrates, a pathway for the degradation of chlorophenoxyacetic acids was elucidated in Time courses for the degradation of unlabelled chlorophenoxyacetic acids by demonstrated that the corresponding chlorophenol was the initial product formed.
View Article and Find Full Text PDF