FK-448 Free base 

The rates of hydrolysis of TAME by trypsin (0.5 μg/mL), plasmin (0.1 U/mL), plasma kallikrein (0.9 U/mL), pancreatic kallikrein (4 U/mL), and thrombin (6 U/mL), and that of ATEE by chymotrypsin (2 μg/mL), are determined at a substrate concentration of 10 mM. Caseinolysis of chymotrypsin is determined. The final concentration of casein is 1%. For measurement of inhibitory effects, mixtures of enzyme solution and inhibitor are preincubated at 37°C for 10 min and then the residual enzyme activity is determined. Km and Ki values are determined^[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Rats^[2]
Rats are anaesthetized with ethylcarbamate (0.9 g/kg, intraperitoneally), and a front midline incision is made to expose the viscera. A hypodermic needle attached to a syringe containing the test solution is then carefully inserted into the lumen of the jejunum 2cm under the pylons. Insulin is dissolved in saline (and 0.1 M HCl if necessary) and injected at 2 mL/kg. Although most inhibitors tested are soluble in water, chymostatin is insoluble, and so it is dissolved in DMSO (final concentration, 10%). For measurement of blood glucose, samples of 0.2 mL of blood are drawn from the inferior vena cava of rats before, and 1 h after treatment or before, 0.5, 1, 1.5,2, 3 and 4 h after that, and are centrifuged at 3000 rev/min for 10 min. The plasma glucose concentration of samples is determined, and indicated as relative percents of the blood glucose level at each period compared with that before administration (as 100%).
Dogs^[2]
Enteric-coated gelatin capsules containing insulin and FK-448 are administered orally to the dogs and samples of 1 mL of blood are drawn from the median cubital vein before, and 0.5, 1, 1.5, 2, 2.5, 3, 4 and 5 h after treatment, are centrifuged at 3000 rev/min for 10min. The plasma glucose concentration of samples is also determined and indicated. Plasma IRI level is determined by double antibody radioimmunoassay using the Insulin-RIA kit^[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

• [1]. Fujii S, et al. New synthetic inhibitors of chymotrypsin. J Biochem. 1984 Feb;95(2):319-22.  [Content Brief]

  [2]. Fujii S, et al. Promoting effect of the new chymotrypsin inhibitor FK-448 on the intestinal absorption of insulin in rats and dogs. J Pharm Pharmacol. 1985 Aug;37(8):545-9.  [Content Brief]