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1 eability and active efflux of ampicillin and benzylpenicillin.
2 of beta-lactamase from Escherichia coli with benzylpenicillin.
3 yperbolic dependence on the concentration of benzylpenicillin.
4 -Ala-D-Ala-carboxypeptidase interacting with benzylpenicillin.
5 The limit of quantitation was 10mug/kg for benzylpenicillin, 20mug/kg for cloxacillin, 25mug/kg dic
7 attached to the cleaved beta-lactam rings of benzylpenicillin and cephaloridine are located in a simi
8 a-lactam ring, when the rigid fused rings of benzylpenicillin and cephaloridine each form different i
10 complexes with the traditional beta-lactams benzylpenicillin and cephalosporin C were determined for
11 ed in 90 (12%) infants who received procaine benzylpenicillin and gentamicin (reference), 76 (10%) of
12 a day for 7 days; or intramuscular procaine benzylpenicillin and gentamicin once a day for 2 days fo
13 ned infants to either intramuscular procaine benzylpenicillin and gentamicin once a day for 7 days (r
14 r 7 days (group B) or intramuscular procaine benzylpenicillin and gentamicin once per day for 2 days,
15 tandard treatment was intramuscular procaine benzylpenicillin and gentamicin once per day for 7 days
16 assigned the reference treatment of procaine benzylpenicillin and gentamicin, 816 (751 per protocol)
18 sequently, the kcat values for hydrolysis of benzylpenicillin and nitrocefin have been reduced by 10(
19 uctures of two acyl-enzyme adducts, one with benzylpenicillin and the other with cephaloridine, have
20 ree and substrate-bound forms of TEM-1 (with benzylpenicillin) and PSE-4 (with carbenicillin) were re
21 It exhibits no detectable activity toward benzylpenicillin, and 10(5)-fold reduction of kcat for n
23 in the literature and (with the exception of benzylpenicillin) are less than the maximum residue limi
25 d BcII, the pH dependence of k(cat)/K(m) for benzylpenicillin, cephalexin, and cefoxitin similarly in
26 tion of four penicillin antibiotic residues (benzylpenicillin, cloxacillin, dicloxacillin and oxacill
29 ctive efflux by AcrAB was more effective for benzylpenicillin due to the stronger affinity and high d
31 and 99 (13%) of those treated with procaine benzylpenicillin, gentamicin, and amoxicillin (risk diff
33 1170 infants to receive injectable procaine benzylpenicillin-gentamicin and 1163 infants to receive
34 was as efficacious as an injectable procaine benzylpenicillin-gentamicin combination for 7 days for s
35 in for 7 days (group B); injectable procaine benzylpenicillin-gentamicin for 2 days, then oral amoxic
36 cated infants to receive injectable procaine benzylpenicillin-gentamicin for 7 days (group A, referen
37 ens were as effective as injectable procaine benzylpenicillin-gentamicin for 7 days on an outpatient
38 dequate follow-up in the injectable procaine benzylpenicillin-gentamicin group and 1145 (98%) infants
40 pital, to receive either injectable procaine benzylpenicillin-gentamicin once per day or oral amoxici
45 in the k2/Kd value as compared with that of benzylpenicillin is mostly attributable to the decreased
46 ly, product complex structures of hydrolyzed benzylpenicillin-, methicillin-, and oxacillin-bound NDM
47 affected by prior acylation of the enzyme by benzylpenicillin; nor did it inhibit reaction at that si
48 ith psr did not modify the susceptibility to benzylpenicillin or the growth and cell autolysis rates.
49 how a trend that explains the preference for benzylpenicillin over cephaloridine in the class A beta-
50 e beta-lactam antibiotics, ampicillin (AMP), benzylpenicillin (PEG), cephalexin (CFX), cefazolin (CFL
51 alyses the cleavage of the amide bond in the benzylpenicillin (penicillin G) side-chain to produce ph
52 tine sputum culture, and that treatment with benzylpenicillin remains appropriate for clinical failur
53 GSH restores defective swarming motility and benzylpenicillin sensitivity in a cydD mutant and also b
54 cillin sensitivity in a cydD mutant and also benzylpenicillin sensitivity in a gshA mutant defective
55 er rate constants (ka) of PBP2a acylation by benzylpenicillin showed a hyperbolic dependence on the c
56 (+) ) CD4(+) T lymphocytes showed that these benzylpenicillin-specific CD4(+) T lymphocytes belonged
58 this study was to evaluate the frequency of benzylpenicillin-specific CD4(+) T lymphocytes in health
61 own number of bacteria radiolabeled with [3H]benzylpenicillin were separated by sodium dodecyl sulfat
62 th pneumococci of intermediate resistance to benzylpenicillin, which comprised 28% of pneumococcal is
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