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CJZ-3

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Catalog No. T201940Cas No. 766508-73-0
Alias CJZ3, CJZ 3

CJZ-3, a derivative of Lomefloxacin, exhibits significant in vitro inhibition of P-gp function. It enhances the intracellular accumulation of Rh123 in a time-dependent manner and markedly reduces Rh123 efflux from cells.

CJZ-3

CJZ-3

😃Good
Catalog No. T201940Alias CJZ3, CJZ 3Cas No. 766508-73-0
CJZ-3, a derivative of Lomefloxacin, exhibits significant in vitro inhibition of P-gp function. It enhances the intracellular accumulation of Rh123 in a time-dependent manner and markedly reduces Rh123 efflux from cells.
Pack SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
CJZ-3, a derivative of Lomefloxacin, exhibits significant in vitro inhibition of P-gp function. It enhances the intracellular accumulation of Rh123 in a time-dependent manner and markedly reduces Rh123 efflux from cells.
AliasCJZ3, CJZ 3
Chemical Properties
Molecular Weight447.35
FormulaC24H22Cl2F2N2
Cas No.766508-73-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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