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. 1999 Dec;43(12):2904–2909. doi: 10.1128/aac.43.12.2904

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
a

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). 

b

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. 

c

ND, not determined.