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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H17N9O5S3
Molecular Weight 511.558
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFMENOXIME

SMILES

CO\N=C(/C(=O)N[C@H]1[C@H]2SCC(CSC3=NN=NN3C)=C(N2C1=O)C(O)=O)C4=CSC(N)=N4

InChI

InChIKey=HJJDBAOLQAWBMH-YCRCPZNHSA-N
InChI=1S/C16H17N9O5S3/c1-24-16(20-22-23-24)33-4-6-3-31-13-9(12(27)25(13)10(6)14(28)29)19-11(26)8(21-30-2)7-5-32-15(17)18-7/h5,9,13H,3-4H2,1-2H3,(H2,17,18)(H,19,26)(H,28,29)/b21-8-/t9-,13-/m1/s1

HIDE SMILES / InChI

Description

Cefmenoxime is a semisynthetic beta-lactam cephalosporin antibiotic with activity similar to that of cefotaxime. Like other 'third-generation' cephalosporins it is active in vitro against most common Gram-positive and Gram-negative pathogens, is a potent inhibitor of Enterobacteriaceae (including beta-lactamase-producing strains), and is resistant to hydrolysis by beta-lactamases. Cefmenoxime has a high rate of clinical efficacy in many types of infection and is at least equal in clinical and bacteriological efficacy to several other cephalosporins in urinary tract infections, respiratory tract infections, postoperative infections and gonorrhoea. The bactericidal activity of cefmenoxime results from the inhibition of cell wall synthesis via affinity for penicillin-binding proteins (PBPs). Cefmenoxime is stable in the presence of a variety of b-lactamases, including penicillinases and some cephalosporinases. Cefmenoxime is marketed in Japan under the brand name Bestron, indicated for the treatment of otitis externa, otitis media, and sinusitis. Cefmenoxime hydrochloride was approved by the U.S. Food and Drug Administration (FDA) on Dec 30, 1987. It was developed and marketed as Cefmax®, but it has being discontinued.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
BESTRON
Curative
BESTRON
Curative
BESTRON

Cmax

ValueDoseCo-administeredAnalytePopulation
88.3 μg/mL
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens
95.5 μg/mL
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
84 μg × h/mL
15 mg/kg bw single, intravenous
CEFMENOXIME serum
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
1.06 h
15 mg/kg bw single, intravenous
CEFMENOXIME serum
Homo sapiens
1.34 h
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens
8.14 h
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens

Funbound

ValueDoseCo-administeredAnalytePopulation
23%
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens
23%
10 mg/kg bw single, intravenous
CEFMENOXIME plasma
Homo sapiens

Doses

PubMed

Sample Use Guides

In Vivo Use Guide
Dissolve the powder in the attached solvent at a final concentration of 10 mg (potency)/1 mL as cefmenoxime hydrochloride, and used as follows: For otitis externa and otitis media, usually instill 6 to 10 drops into the ear and keep the same position for about 10 minutes twice daily. For sinusitis, usually inhale nasally by a nebulizer 2 to 4 mL every other day, 3 times per week or inject 1 mL into the maxillary sinus once per week. The frequency of administration may be adjusted depending on the patient’s symptoms.
Route of Administration: Topical
In Vitro Use Guide
Cefmenoxime showed the most potent activity, the MIC of this drug against all of the 92 strains of Haemophilus influenzae was 0.063 ug/ml.