Chloramphenicol [56-75-7]

Cat# NB-64-03387-10g

Size : 10g

Brand : Neo Biotech


Chloramphenicol (Synonyms: Levomycetin, Chloromycetin, Chlornitromycin)

Catalog No. T1205 Copy Product Info
Purity: 99.90%
Chloramphenicol (Chloromycetin) is a broad-spectrum antibiotic that inhibits the biosynthesis of bacterial proteins. Chloramphenicol acts primarily on the 50S subunit of the bacterial 70S ribosome and is active against peptidyltransferases, inhibiting the formation of peptide bonds.

Chloramphenicol

Copy Product Info
Synonyms Levomycetin, Chloromycetin, Chlornitromycin

Chloramphenicol (Chloromycetin) is a broad-spectrum antibiotic that inhibits the biosynthesis of bacterial proteins. Chloramphenicol acts primarily on the 50S subunit of the bacterial 70S ribosome and is active against peptidyltransferases, inhibiting the formation of peptide bonds.

Chloramphenicol
Cas No. 56-75-7
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Purity:99.90%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Chloramphenicol (Chloromycetin) is a broad-spectrum antibiotic that inhibits the biosynthesis of bacterial proteins. Chloramphenicol acts primarily on the 50S subunit of the bacterial 70S ribosome and is active against peptidyltransferases, inhibiting the formation of peptide bonds.
Targets&IC50
protozoan motility:2.95 ± 0.25 mM
In vitro
METHODS: Human lung cancer cells A549 and H1299 were treated with Chloramphenicol (1-100 µg/mL) for 3-24 h. Cell viability was detected by MTT assay.
RESULTS: In the 3 h treatment group, the viability of A549 and H1299 cells at 100 µg/mL was 97.0±3.9% and 98.1±5.0%, respectively, and no cytotoxicity was observed. A significant reduction in cell viability was observed in the 24 h treatment group. [1]
METHODS: Mouse T cell lines A1.1 and IE5 and human T cell lines Jurkat and Jcam were stimulated with Chloramphenicol (100 nmol/L), and the DNA content was measured by Flow cytometry.
RESULTS: Chloramphenicol clearly blocked activation-induced cell death (AICD) in all four cell lines, even though these cells were activated by different stimuli. [2]
In vivo
METHODS: To investigate the potential to induce aplastic anemia, Chloramphenicol (2000 mg/kg) and Thiamphenicol (850 mg/kg) were administered by gavage to BALB/c mice once daily for 17 days.
RESULTS: Administration of Chloramphenicol and Thiamphenicol at hematotoxic dose levels for 17 days in BALB/c mice was associated with the development of aplastic anemia in humans, inducing reversible anemia but not chronic bone marrow aplasia. [3]
SynonymsLevomycetin, Chloromycetin, Chlornitromycin
Chemical Properties
Molecular Weight323.13
FormulaC11H12Cl2N2O5
Cas No.56-75-7
Smiles[C@@H]([C@H](NC(C(Cl)Cl)=O)CO)(O)C1=CC=C(N(=O)=O)C=C1
Relative Density.1.547 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 1 mg/mL (3.09 mM), Sonication is recommended.
Ethanol: 60 mg/mL (185.68 mM), Sonication is recommended.
DMSO: 250 mg/mL (773.68 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (15.47 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
H2O/Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.0947 mL15.4736 mL30.9473 mL154.7365 mL
Ethanol/DMSO
1mg5mg10mg50mg
5 mM0.6189 mL3.0947 mL6.1895 mL30.9473 mL
10 mM0.3095 mL1.5474 mL3.0947 mL15.4736 mL
20 mM0.1547 mL0.7737 mL1.5474 mL7.7368 mL
50 mM0.0619 mL0.3095 mL0.6189 mL3.0947 mL
100 mM0.0309 mL0.1547 mL0.3095 mL1.5474 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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