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. 2007 Sep 10;52(1):24–36. doi: 10.1128/AAC.00133-06

TABLE 2.

Physical and chemical properties of the antibiotics investigated

Antibiotic Protein binding (%) PC (log) Mol wt Ka Referencesb
Amoxicillin 20 0.614 365.41 0.82 70a, S
Cefdinir 60-73 −0.725 395.42 0.39 69, S
Meropenem 2 −0.6 383.46 0.56 70a, M
Azithromycin 7.1-50 3.329 748.98 1.36 70a, S
Clarithromycin 80 3.159 747.95 1.32 70a, S
Cethromycin 90 5.24 765.93 1.76 65, S
Telithromycin 70 5.093 812 1.72 2, S
Ciprofloxacin 30 1.308 331.34 0.97 70a, S
Clinafloxacin 2-7 1.63 365.79 1.03 12, S
Garenoxacin 75 1.615 426.41 1.02 42, S
Gatifloxacin 20 1.586 375.39 1.02 69, S
Levofloxacin 30-40 1.485 361.37 1.00 70a, S
Lomefloxacin 10 2.334 351.35 1.18 12, S
Moxifloxacin 39-52 1.974 401.43 1.10 69, S
Pefloxacin 25 2.164 333.36 1.15 70a, S
Rufloxacin 60 1.894 363.41 1.09 12, S
Sparfloxacin 40 2.866 392.4 1.29 12, S
Trovafloxacin 87 1.566 416.35 1.01 12, S
Grepafloxacin 50 2.261 359.39 1.17 12, S
Pyrazinamide 50 −0.368 123.11 0.66 70a, S
Ethionamide 30 1.220 166.24 0.98 70a, S
Linezolid 31 −0.923 337.35 0.50 69, S
Itraconazole 99.8 3.291 705.63 1.35 70a, S
Tigecycline 79-89 2.09 585.65 1.11 23, M
Rifampin 80 0.486 822.94 0.76 70a, S
Ethambutol 10-40 −0.053 204.31 0.71 70a, S
Isoniazid 0 −0.887 137.14 0.55 70a, S
Rifapentine 97.7 1.981 877.03 1.07 55, S
a

Constant K = 0.96 + 0.091·ln (PC·MW−1/2).

b

S, SciFinder Scholar database (American Chemical Society; 2004); M, MDL quantitative structure-activity relationship (Elsevier Science, Inc.; 2004).