1 oxime (DAMO)-thiosemicarbazide (TSC) or DAMO-antipyrine.

2  did not alter the absorption rate for (14)C-antipyrine.

3 tructurally characterized lower rim 1,3-di{4-antipyrine}amide conjugate of calix[4]arene (L) exhibits

4 ption of (3)H-D-glucose, (3)H-leucine, (14)C-antipyrine, and (51)Cr-EDTA were investigated by monitor

5 tic drugs such as acetaminophen, phenacetin, antipyrine, and dipyrone, and is potently inhibited by s

6         Caffeine elimination rate (k(elim)), antipyrine (AP) clearance (Cl), MEGX concentration, meth

7 icities of halogen acceptor substrates (RHs) antipyrine (ap), NADH, 2-chlorodimedone (2cd), and barbi

8 to an isolated jejunal segment together with antipyrine as a marker for absorption.

9 compared with that of freely diffusible 125I-antipyrine, membrane-excluded 125I-bovine serum albumin

10 low (CBF) with the autoradiographic Iodo-14C-antipyrine methodology in four groups of animals: Toxin

11 5I-ODN are 2 times more radiotoxic than 125I-antipyrine, which is freely diffusible into cells, and 8

12 7-0.8) was determined to be superior to DAMO-antipyrine (Z'-factors 0.5-0.6) with significantly less