| 8448346 |
Berkman CE, Ryu S, Quinn DA, Thompson CM: Kinetics of the postinhibitory reactions of acetylcholinesterase poisoned by chiral isomalathion: a surprising nonreactivation induced by the RP stereoisomers. Chem Res Toxicol. 1993 Jan-Feb;6(1):28-32.
Inhibitory (ki), spontaneous (k0), and oxime-mediated reactivation (k (oxime)) reaction kinetics for the four stereoisomers of isomalathion (SPRC,SPSC,RPRC, and RPSC) were determined against rat brain acetylcholinesterase (AChE). (SPRC)-Isomalathion was the most potent anticholinesterase agent and RPSC-isomalathion the least potent with racemic material approximately midway in activity. |
2(0,0,0,2) |
Details |