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QuickView for Roxithromycin (compound)


PubChem
Name: Roxithromycin
PubChem Compound ID: 444037
Description: Semisynthetic derivative of erythromycin. It is concentrated by human phagocytes and is bioactive intracellularly. While the drug is active against a wide spectrum of pathogens, it is particularly effective in the treatment of respiratory and genital tract infections.
Molecular formula: C41H76N2O15
Molecular weight: 837.047 g/mol
Synonyms:
NINDS_000382; KBioGR_000779; DivK1c_000382; Spectrum3_001159; Spectrum4_000200; SPBio_001422; Spectrum2_001551; Spectrum_001653; KBio1_000382; KBio3_002217.
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DrugBank
Identification
Name: Roxithromycin
Name (isomeric): DB00778
Drug Type: small molecule
Description: Semisynthetic derivative of erythromycin. It is concentrated by human phagocytes and is bioactive intracellularly. While the drug is active against a wide spectrum of pathogens, it is particularly effective in the treatment of respiratory and genital tract infections.
Brand: Rulide, Rulid, ROX, Surlid
Category: Anti-Bacterial Agents, Macrolides
CAS number: 80214-83-1
Pharmacology
Indication: Used to treat respiratory tract, urinary and soft tissue infections.
Pharmacology:
Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin has the following antibacterial spectrum in vitro: Streptococcus agalactiae, Streptococcus pneumoniae (Pneumococcus), Neisseria ...
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Mechanism of Action:
Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly ...
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Absorption: Very rapidly absorbed and diffused into most tissues and phagocytes.
Protein binding: 96%, mainly to alpha1-acid glycoproteins
Biotransformation: Hepatic. Roxithromycin is only partially metabolised, more than half the parent compound being excreted unchanged. Three metabolites have been identified in urine and faeces: the major metabolite is descladinose roxithromycin, with N-mono and N-di-demethyl roxithromycin as minor metabolites. The respective percentage of roxithromycin and these three metabolites is similar in urine and faeces.
Half Life: 12 hours
Toxicity: Most common side-effects are gastrointestinal; diarrhoea, nausea, abdominal pain and vomiting. Less common side-effects include headaches, rashes, abnormal liver function values and alteration in senses of smell and taste.
Affected organisms: Enteric bacteria and other eubacteria
Interactions
Drug interaction:
CyclosporineThe macrolide, roxithromycin, may increase the effect of cyclosporine.

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