Title : Chloramphenicol is a potent inhibitor of cytochrome P450 isoforms CYP2C19 and CYP3A4 in human liver microsomes.

Pub. Date : 2003 Nov

PMID : 14576103






4 Functional Relationships(s)
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1 Chloramphenicol is a potent inhibitor of cytochrome P450 isoforms CYP2C19 and CYP3A4 in human liver microsomes. Chloramphenicol cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 Chloramphenicol had a potent inhibitory effect on CYP2C19-catalyzed S-mephytoin 4"-hydroxylation and CYP3A4-catalyzed midazolam 1-hydroxylation, with apparent 50% inhibitory concentrations (inhibitory constant [K(i)] values are shown in parentheses) of 32.0 (7.7) and 48.1 (10.6) microM, respectively. Chloramphenicol cytochrome P450 family 3 subfamily A member 4 Homo sapiens
3 In conclusion, inhibition of CYP2C19 and CYP3A4 is the probable mechanism by which chloramphenicol decreases the clearance of coadministered drugs, which manifests as a drug interaction with chloramphenicol. Chloramphenicol cytochrome P450 family 3 subfamily A member 4 Homo sapiens
4 In conclusion, inhibition of CYP2C19 and CYP3A4 is the probable mechanism by which chloramphenicol decreases the clearance of coadministered drugs, which manifests as a drug interaction with chloramphenicol. Chloramphenicol cytochrome P450 family 3 subfamily A member 4 Homo sapiens