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Carindacillin sodium

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Catalog No. T40295Cas No. 26605-69-6
Alias CP-15464-2, Carindacillin sodium, Carbenicillin indanyl sodium

Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized in urinary tract infection research.

Carindacillin sodium

Carindacillin sodium

😃Good
Catalog No. T40295Alias CP-15464-2, Carindacillin sodium, Carbenicillin indanyl sodiumCas No. 26605-69-6
Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized in urinary tract infection research.
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2 mg$535 days
5 mg$975 days
10 mg$1875 days
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Product Introduction

Bioactivity
Description
Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized in urinary tract infection research.
In vitro
Carindacillin sodium exhibits broad-spectrum antibacterial activity in vitro[1].
In vivo
Carindacillin sodium, when administered orally (p.o.), effectively safeguards mice from deadly infections caused by various pathogens including Escherichia coli, Salmonella choleraesuis, Pasteurella multocida, Proteus vulgaris, Staphylococcus aureus, and Streptococcus pyogenes. The protective doses (PD 95) required to prevent 95% of such infections range from 30.4 mg/kg to 220.4 mg/kg[1].
AliasCP-15464-2, Carindacillin sodium, Carbenicillin indanyl sodium
Chemical Properties
Molecular Weight516.54
FormulaC26H25N2NaO6S
Cas No.26605-69-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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