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Macrolide erythromycin

The results showed that the compounds studied with more frequency in the aquatic environment, and of which, logically, there is more information, are the antibiotics, analgesics and anti-inflammatories (like diclofenac, ibuprofen, naproxen, acetylsalicylic acid, and paracetamol), as well as the p-blocker atenolol. In the category of antibiotics, several families are included, like the macrolides (erythromycin), the fluoroquinolones (ofloxacin and ciprofloxacin), sulfonamides (sulfamethoxazole), penicillins (amoxicillin), the metronidazol, and trimethoprim. Other therapeutic groups also widely studied and frequently found in the environmental waters are the lipid regulators (gemfibrozil and bezafibrat), antiepileptic carbamaze-pine, and antidepressants (diazepam, fluoxetine, paroxetine) (see Table 3). [Pg.213]

The macrolide erythromycin inhibits protein synthesis and resistance is induced by N -dimethyl-ation of adenine within the 23S rRNA, which results in reduced affinity of ribosomes for antibiotics related to erythromcin (Skinner et al. 1983). Sulfonamides function by binding tightly to chromosomal dihydropteroate synthetase and resistance to sulfonamides is developed in the resistance plasmid through a form of the enzyme that is resistant to the effect of sulfonamides. [Pg.171]

The complete degradation of sulfamethoxazole was also reported within 14 days with P. chrysosporium, Bjerkandera sp. R1 and B. adusta [4], although, contrary to the reports of enzymatic transformation, metabolites were not identified. Partial removal (from 30% to 55%) of sulfamethoxazole from activated-sludge-mixed liquor and the effluent of a WWTP was demonstrated at bench scale within 5 days with P. chrysosporium propagules entrapped in a granular bioplastic formulation [25]. This approach was also successful in the partial elimination of other kinds of antibiotics, eg., ciprofloxacin (see below) and the macrolide erythromycin. [Pg.178]

Macrolides Erythromycin Inhibits protein synthesis by binding Gram-positive cocci, mycoplasma,... [Pg.12]

Azalides azithromycin Azoles fluconazole, itraconazole, ketoconazole, and voriconazole Macrolides erythromycin, clarithromycin Protease inhibitors amprenavir, indinavir, lopinavir/ritonavir, nelfinavir, ritonavir, and saquinavir Quinolones ciprofloxacin, gatifloxacin, levofloxacin, moxifloxacin. [Pg.396]

Other key classes of antibacterials include the tetracyclines (Aureomycin, Terramycin), macrolides (erythromycin, Zithromax, Biaxin), and aminoglycosides (streptomycin, amikacin, neomycin). These antibacterials are protein synthesis inhibitors. [Pg.329]

Alvarez-Elleoro S and Enzler MJ. Symposium on antimicrobial agents Part IX. The macrolides Erythromycin, clarithromycin, and azithromycin. Mayo CUn Proc 1999 74 613-634. [Pg.551]

Drugs that have been shown, or would be expected, to increase plasma carbamazepine levels include cimetidine, danazol, diltiazem, macrolides, erythromycin, troleandomycin, clarithromycin, fluoxetine, fluvoxamine, nefazodone, loratadine, terfenadine, isoniazid, niacinamide, nicotinamide, propoxyphene, azoles (e.g., ketaconazole, itraconazole, and fluconazole), acetazolamide, verapamil, grapefruit juice, ... [Pg.266]

Macrolides Erythromycin useful in diabetic gastroparesis but tolerance develops... [Pg.1331]

Alternative treatment for cellulitis in a patient hypersensitive to penicillins is the macrolide erythromycin. [Pg.310]

CLOZAPINE MACROLIDES- ERYTHROMYCIN t clozapine levels with risk of clozapine toxicity Clozapine is metabolized by CYPIA2, which is moderately inhibited by erythromycin. Erythromycin is a potent inhibitor of CYP3A4, which has a minor role in the metabolism of clozapine. This may lead to 1 clearance and therefore t levels of clozapine Cautious use advised... [Pg.254]

MIDAZOLAM, TRIAZOLAM, POSSIBLY ALPRAZOLAM MACROLIDES -ERYTHROMYCIN, CLARITHROMYCIN, TELITHROMYCIN t BZD levels Inhibition of CYP3A4-mediated metabolism 1 dose of BZD by 50% warn patients not to perform skilled tasks such as driving for at least 10 hours after the dose of BZD... [Pg.264]

CIMETIDINE MACROLIDES- ERYTHROMYCIN t efficacy and adverse effects of erythromycin, including hearing loss t bioavailability Consider an alternative antibiotic, e.g. clarithromycin. Deafness has been reversible with cessation of erythromycin... [Pg.639]

CANNABIS ANTIBIOTICS -MACROLIDES -erythromycin Unpredictable changes in plasma concentration. Risk of toxicity or therapeutic failure, particularly of drugs with a narrow therapeutic index Induction or inhibition of CYP3A4-mediated metabolism by cannabis. It is not yet known whether the effects are dependent on the degree of cannabis consumption Be aware. Watch for signs of toxicity especially when cannabis use abruptly changes... [Pg.693]

It may be argued that this unusual biosynthetic sequence is due to the unique composition and organization of the dps (dauno- or doxorubicin polyketide synthase) genes of Streptomyces peucetius [88]. But, also in more typical biosyntheses of polyketide oligodeoxysaccharides, for example, the macrolides erythromycin A (14) [24, 58, 89] in Saccharopolyspora erythraea and tylosin in Streptomyces fradiae [90], or urdamycin biosynthesis in Streptomyces fradiae TU2717 [77,91,... [Pg.19]

Chlomydio pneumonioe (TWAR strain) tetracycline a macrolide erythromycin... [Pg.211]

Which macrolide (erythromycin, clarithromycin, or azithromycin) may cause drug interactions with his current medications ... [Pg.113]

Figure 6.8. The structures of the macrolides erythromycin, clarithromycin, and azithromycin. Figure 6.8. The structures of the macrolides erythromycin, clarithromycin, and azithromycin.
Azithromycin is a macrolide (erythromycin, clarithromycin, and azithromycin) that interferes with microbial protein synthesis. It is indicated in the following conditions. Adults treatment of infections of the respiratory tract, acute bacterial sinusitis, acute bacterial exacerbations of COPD, community-acquired pneumonia, Mycobacterium avium complex, pelvic inflammatory disease, pharyngitis/tonsilli-tis, skin and skin structure infections, and sexually transmitted diseases caused by susceptible organisms. Children treatment of acute bacterial sinusitis, acute otitis media caused by susceptible organisms, community-acquired pneumonia, pharyngitis/tonsillitis caused by S. pyogenes in patients who cannot use first-line therapy. [Pg.97]

Adapted in part from Alvarez-Elcoro, S., and Enzler, M. J. (1999). The macrolides Erythromycin, clarithromycin, and azythromycin. Mayo Clin. Proc. 74, 613-634. [Pg.363]

Figure 14 Representative structures of the macrolide (erythromycin and tylosin) and ketolide subclass of the macrolides (telithromycin). Figure 14 Representative structures of the macrolide (erythromycin and tylosin) and ketolide subclass of the macrolides (telithromycin).
Macrolides (erythromycin, 1 azithromycin, clarithromycin, j etc.) and clindamycin Formation of methyltransferases that alter drug binding sites on the SOS ribosomal subunit Active transport out of cells... [Pg.182]


See other pages where Macrolide erythromycin is mentioned: [Pg.311]    [Pg.361]    [Pg.31]    [Pg.165]    [Pg.102]    [Pg.138]    [Pg.402]    [Pg.311]    [Pg.438]    [Pg.2]    [Pg.3365]    [Pg.382]    [Pg.222]    [Pg.80]    [Pg.110]    [Pg.159]    [Pg.300]    [Pg.314]    [Pg.364]    [Pg.480]    [Pg.487]    [Pg.384]    [Pg.769]    [Pg.389]   
See also in sourсe #XX -- [ Pg.191 ]




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