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Cefprozil monohydrate

🥰Excellent
Catalog No. T1118Cas No. 121123-17-9
Alias Cefprozil hydrate, Cefprozil

Cefprozil monohydrate (Cefprozil) is a second-generation cephalosporin-type antibiotic.

Cefprozil monohydrate

Cefprozil monohydrate

🥰Excellent
Purity: 960u/mg
Catalog No. T1118Alias Cefprozil hydrate, CefprozilCas No. 121123-17-9
Cefprozil monohydrate (Cefprozil) is a second-generation cephalosporin-type antibiotic.
Pack SizePriceAvailabilityQuantity
10 mg$37In Stock
25 mg$51In Stock
50 mg$70In Stock
100 mg$103In Stock
200 mg$148In Stock
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Purity:960u/mg
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Product Introduction

Bioactivity
Description
Cefprozil monohydrate (Cefprozil) is a second-generation cephalosporin-type antibiotic.
In vitro
Cefprozil is particularly active against the Gram-positive organisms Streptococcus pyogenes, pneumoniae and agalactiae and against methicillin-susceptible Staphylococcus aureus. Cefprozil is also moderately active against Haemophilus influenzae, Moraxella catarrhalis, Neisseria gonorrhoeae, many Enterobacteriaceae and certain anaerobic organisms, and is relatively stable to hydrolysis by a number of beta-lactamases. [1] Cefprozil is a newer oral Cephalosporin with a spectrum of activity against organisms that include gram-positive and gram-negative pathogens. Cefprozil is active (susceptibility, less than or equal to 8 mg /mL; moderate susceptibility, 16 mg/mL; resistance, greater than or equal to 32 mg/mL) against gram-positive species such as streptococci, methicillin-susceptible staphylococci, and Listeria monocytogenes. [2] Cefprozil is at least as active as cefuroxime, cefaclor, and cephalexin against all organisms tested, but is fourfold less active than doxycycline against E coli and 16-fold less active than clarithromycin versus S pneumoniae. Cefprozil is as active as amoxicillin/clavulanate against K pneumoniae and E coli. [3]
In vivo
Cefprozil results in the mean peak concentration (Cmax) in infant dogs (21.2 mg/mL) and adult dogs (27.8 mg/mL). Cefprozil results in the areas under the concentration-time curve (AUC, in infant dogs: 121 mg.hr/mL, in adult dogs: 130 mg.hr/mL), half-lives (T 1/2, in infant dogs: 4.7 hours, in adult dogs: 4.7 hours) or urinary recovery rates (UR, in infant dogs: 36.3%, in adult dogs: 34.7%) between the 2 groups. [4]
AliasCefprozil hydrate, Cefprozil
Chemical Properties
Molecular Weight407.44
FormulaC18H21N3O6S
Cas No.121123-17-9
SmilesO.CC=CC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](N)c1ccc(O)cc1)C2=O)C(O)=O
Relative Density.1.534g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 55 mg/mL (134.99 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4543 mL12.2717 mL24.5435 mL122.7175 mL
5 mM0.4909 mL2.4543 mL4.9087 mL24.5435 mL
10 mM0.2454 mL1.2272 mL2.4543 mL12.2717 mL
20 mM0.1227 mL0.6136 mL1.2272 mL6.1359 mL
50 mM0.0491 mL0.2454 mL0.4909 mL2.4543 mL
100 mM0.0245 mL0.1227 mL0.2454 mL1.2272 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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