M C Castle
Index: Xenobiotica 19(1) , 115-21, (1989)
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1. Hydrolysis of the drug esters procaine, chloramphenicol succinate, and prednisolone succinate was studied. Addition of soman to guinea pig liver microsomes caused a dose-dependent inhibition of hydrolysis of all three substrates; at the highest soman concentration (1 microM), ester hydrolysis was totally abolished. 2. Ester hydrolysis was also measured in liver microsomes from guinea pigs pretreated with soman at a low dose (10% of LD50) or at a high dose (90% of LD50) either 1 h or 12 h before killing. Plasma-cholinesterase activity was decreased in all pretreated animals. Liver carboxylesterase activity, measured with the three drug substrates and by hydrolysis of 4-nitrophenyl acetate was increased by all pretreatments. 3. This enhancing effect varies with the substrate and increases with dose of soman. The 12 h pretreatment produced a greater increase in activity than did the 1 h pretreatment. 4. These studies indicate that soman is a potent inhibitor of carboxylesterase activity in vitro but increases the activity of the liver enzyme when administered in vivo.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Chloramphenicol sodium succinate
CAS:982-57-0 |
C15H15Cl2N2NaO8 |
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Chloramphenicol succinate, a competitive substrate and inhib...
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1993-05-01 [J. Clin. Microbiol. 31(5) , 1303-7, (1993)] |
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2000-08-01 [Eur. J. Clin. Pharmacol. 56(5) , 405-9, (2000)] |
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