| MDL | - |
|---|---|
| Molecular Weight | 411.38 |
| Molecular Formula | C19H20F3N3O4 |
| SMILES | O=C(O)C1=CN(C2=C(C1=O)C=C(C(N3C[C@@H](NCC3)C)=C2OC(F)F)F)C4CC4 |
Cadrofloxacin against
M.tuberculosis
with a MIC
50
of 0.25 μg/mL
[1]
.
Cadrofloxacin against
Acinetobacter spp.
and
Stenotrophomonas (Xanthomonas) maltophilia
with MIC
90
s of 0.03 and 2 μg/ml, respectively
[2]
.
Cadrofloxacin against
Haemophilus influenzae
,
Moraxella catarrhalis
, and
Neisseria spp.
with MIC
90
s less than or equal to 0.06 μg/mL
[2]
.
Cadrofloxacin against members of the family
Enterobacteriaceae
with MIC
90
s of 0.015 to 16 μg/mL (median MIC
90
, 0.06 μg/mL)
[2]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cadrofloxacin (9 mg/kg; i.g.; once or twice daily for 14 consecutive days) increases the activity of hepatic CYP2E1 in rats [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
| Animal Model: | Male Sprague-Dawley rats weighing 180-220 g [2] |
| Dosage: | 9 mg/kg |
| Administration: | I.g. once or twice daily for 14 consecutive days |
| Result: |
Enhanced the expression of hepatic CYP2E1 mRNA, inducing a 1.6-fold increase compared with that of control rats.
The level of CYP2E1 protein in the hepatic microsomes was significantly higher than control group, 190% of that in control rats. |
Solid
Room temperature in continental US; may vary elsewhere.
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
DMSO : 10 mg/mL ( 24.31 mM ; ultrasonic and warming and adjust pH to 3 with HCl and heat to 80°C)
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.4308 mL | 12.1542 mL | 24.3084 mL |
| 5 mM | 0.4862 mL | 2.4308 mL | 4.8617 mL |
| 10 mM | 0.2431 mL | 1.2154 mL | 2.4308 mL |