azithromycin

Azithromycin (CP 62993) is a macrolide antibiotic that primarily targets the 50S subunit of bacterial ribosomes. Azithromycin is commonly used in studies of bacterial infections.

Azithromycin hydrate (CP-62993 dihydrate) is a semi-synthetic macrolide antibiotic structurally related to ERYTHROMYCIN. It has been used in the treatment of Mycobacterium avium intracellulare infections, toxoplasmosis, and cryptosporidiosis.

Azithromycin B is primarily used for the treatment of specific bacterial infections.

Azathramycin (Desmethyl Azithromycin) is an antibiotic derived from erythromycin, binding to the 50S subunit of the bacterial ribosome, and thus inhibits translation of mRNA.

Descladinose 6-N-Desmethyl Azithromycin is an impurity of Teramycin.

Azithromycin-d3 is the deuterated form of Azithromycin. Azithromycin (CP-62993) is a macrolide antibiotic frequently utilized in bacterial infection research.

Azithromycin-13C,d3 is the deuterated form of Azithromycin labeled with 13C.

Descladinose Azithromycin (Standard) is the standard substance of Descladinose Azithromycin, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Descladinose azithromycin is a natural product that can be used in related research in the field of life sciences. Its product number is TN8501.

Descladinose azithromycin is a natural product that can be used in related research in the field of life sciences. Its product number is TN8501.

Azithromycin-13C-d3 the 13C and deuterated compound of Azithromycin. Azithromycin has a CAS number of 83905-01-5. Azithromycin is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections.

FPL-64170XX is a selective inhibitor of the enzyme 5-lipoxygenase.

SpHistin, an antimicrobial peptide (AMP), binds to lipopolysaccharide (LPS) and permeabilizes the bacterial membrane. In combination with Rifampicin and Azithromycin, it facilitates increased intracellular uptake of these antibiotics, thereby enhancing their collective bactericidal efficacy against Pseudomonas aeruginosa [1].