TABLE 3.
Stabilities of THF carbapenems to hydrolysis by serine β-lactamases
| β-Lactam | Relative hydrolysis rate (%) by the following enzyme (functional group)a:
|
|||
|---|---|---|---|---|
| P99 (1) | PC1 (2a) | TEM-2 (2b) | TEM-26 (2be) | |
| Cephaloridineb | 100 | NDc | ND | ND |
| Benzylpenicillin | ND | 100 | 100 | 100 |
| Imipenem | 0.01 | ≤0.01 | 0.03 | 0.28 |
| CL 188,624 | 0.12 | ≤0.01 | 0.02 | 0.27 |
| CL 190,294 | 0.01 | ≤0.01 | 0.01 | 0.29 |
| CL 191,121 | 0.29 | ≤0.01 | 0.16 | 0.60 |
Relative hydrolysis rate was calculated on the basis of 100% hydrolysis of the reference β-lactam. Functional groups are those of Bush et al. (6).
Cephaloridine was selected as the reference compound for the group 1 β-lactamase P99; benzylpenicillin was selected as reference compound for the group 2 β-lactamases.
ND, not determined.