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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 66592-87-8 Chemical Structure| 66592-87-8

Structure of Cefadroxil hydrate
CAS No.: 66592-87-8

Chemical Structure| 66592-87-8

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Cefadroxil is a pan cephalosporin type antibiotic.

Synonyms: BL-S 578 hydrate; Cefadroxil hydrate; Bidocel

4.5 *For Research Use Only !

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Product Details of Cefadroxil hydrate

CAS No. :66592-87-8
Formula : C16H19N3O6S
M.W : 381.40
SMILES Code : O=C(C(N12)=C(C)CS[C@]2([H])[C@H](NC([C@H](N)C3=CC=C(O)C=C3)=O)C1=O)O.[H]O[H]
Synonyms :
BL-S 578 hydrate; Cefadroxil hydrate; Bidocel
MDL No. :MFCD01682047
InChI Key :NBFNMSULHIODTC-CYJZLJNKSA-N
Pubchem ID :47964

Safety of Cefadroxil hydrate

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H317-H334
Precautionary Statements:P261-P280-P342+P311
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Rat brain slices 0.8 μM 2 h To study the distribution of cefadroxil in brain cells and its transport mechanisms. Results showed that PEPT2 substrates Ala-Ala and GlySar reduced cefadroxil accumulation in brain cells, while probenecid increased its accumulation. Fluids Barriers CNS. 2014 Nov 14;11(1):25

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Swiss-Webster mice Experimental infection model Oral 25-200 mg/kg Twice administration Evaluate the therapeutic efficacy of cefadroxil in experimental infections of mice, showing superior efficacy against Streptococcus pyogenes and comparable efficacy against other strains compared to cephalexin. Antimicrob Agents Chemother. 1977 Feb;11(2):324-30
Mice LPS-induced acute inflammation model Intravenous injection 1 nmol/g Single dose, observed for 120 minutes To investigate the impact of LPS-induced inflammation on the disposition of cefadroxil. Results showed that LPS treatment significantly increased cefadroxil concentrations in blood, cerebrospinal fluid, and tissues, while decreasing tissue-to-blood concentration ratios in the kidneys and choroid plexus. Additionally, LPS treatment significantly reduced the renal clearance of cefadroxil (3-fold). Antimicrob Agents Chemother. 2013 Dec;57(12):6171-8
Mice Wild-type (WT) and humanized PepT1 (huPepT1) mice Oral 5, 15, and 30 mg/kg Single dose To evaluate the systemic exposure of cefadroxil during dose escalation, drug-drug interaction study, and multiple dosing study Drug Metab Dispos. 2019 Mar;47(3):173-183
Mice Pept2 knockout mice Intracerebroventricular injection 80 pmol Single injection, observed for 60 minutes To investigate the effect of PEPT2 knockout on the distribution of cefadroxil in CSF and choroid plexus, results showed that PEPT2 knockout significantly reduced the uptake of cefadroxil in choroid plexus and its clearance from CSF J Cereb Blood Flow Metab. 2011 Jan;31(1):250-61
Sprague-Dawley rats Normal rats Intravenous injection 0.3 mg/kg/min for 20 min followed by 0.15 mg/kg/min for 160 min Single dose, total duration 180 min To investigate the effect of probenecid on the distribution of cefadroxil in rat blood, brain extracellular fluid, and cerebrospinal fluid. Results showed that probenecid increased cefadroxil concentrations in blood and brain ECF but had no significant effect on CSF concentrations. Fluids Barriers CNS. 2014 Nov 14;11(1):25

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.62mL

0.52mL

0.26mL

13.11mL

2.62mL

1.31mL

26.22mL

5.24mL

2.62mL

 

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