b-Lactamase Inhibitors

Slides:



Advertisements
Similar presentations
Beta-Lactamase Inhibitors
Advertisements

Antimicrobials: Drugs that Weaken the Cell Wall
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 84 Drugs That Weaken the Bacterial Cell Wall I: Penicillins.
1 © Patrick An Introduction to Medicinal Chemistry 3/e Chapter 16 ANTIBACTERIAL AGENTS Part 3: Other lactams.
Antibiotics.
 Cefixime is quickly establishing in Western countries as a potent broad-spectrum antibiotic with a variety of indications. A multinational, nonrandomized.
Bacterial Physiology (Micr430) Lecture 10 Macromolecular Synthesis: Cell Wall (Text Chapter: 11)
Cephalosporins B-Lactam antibiotics ( similar to penicillins) Broad spectrum Act by inhibition of cell wall synthesis Bactericidal Inactive against :
PHL 424 Antimicrobials 6 th Lecture By Abdelkader Ashour, Ph.D. Phone:
Antibiotics By Dr. Humodi A. Saeed Associate Prof. of Medical Microbiology College of Medical Lab. Science Sudan University of Science and Technology E.
Sorting Out Antibiotics: A systematic approach to antibiotic selection Kenneth Alexander, M.D., Ph.D. Associate Professor of Pediatrics and Microbiology.
Gram-positive bacteria: Staphylococci
CEPHALOSPORINS First used clinically in the early 1960’s. First used clinically in the early 1960’s. They have an important role in the modern treatment.
Cephalosporins.
Antibiotics Review 10 August :39 AM.
Bacterial Cell Wall Inhibitors
Beta-lactam antibiotics - Cephalosporins
Β-Lactam antibiotics. Classification Penicillins Cephalosporins Other β-Lactam drugs Cephamycins (头霉素类) Carbapenems (碳青霉烯类) Oxacephalosporins (氧头孢烯类)
Gram Negative Gram Positive
Drugs acting on bacterial protein biosynthesis
Vancomycin Vancomycin is called a ‘glycopeptide’, meaning that it is a cyclic peptide, with sugar residues attached to it.
Antibiotics 101 Puja Van Epps 1/20/14.
Antibacterial Inhibitors of Cell Wall Synthesis –Very high therapeutic index Low toxicity with high effectiveness β- lactam Drugs –Inhibit peptidoglycan.
Beta lactam antibiotics & Other cell wall synthesis inhibitors
Definitions Bacteremia: Presence of bacteria in the blood Under normal circumstances, the blood is a sterile environment.
Clinical Cases Beta-Lactam Answers. Case 1 What antibiotic would you recommend for intravenous therapy in a 40yo BM with a Staphylococcus aureus (MSSA)
Staphylococcus aureus…………quickly posed a problem
CELL WALL SYNTHESIS INHIBITORS
Penicillin and Cephalosprin: Beta- Lactam Antibiotics and Other Inhibitors of Cell Wall Synthesis by Dena Nguyen
CEPHALOSPORINS.
Definitions Bacteremia: Presence of bacteria in the blood Under normal circumstances, the blood is a sterile environment.
Cephalosporins First Generation Cephalosporins
AMINOGLYCOSIDES The different members of this group share many properties in common. The different members of this group share many properties in common.
Antibiotics.
Beta lactams. INHIBITORS OF CELL WALL SYNTHESIS Natural: Pencillinase Resistant: (Anti staph) 1)Benzyl pencillin (G) k+ Na+1) oxcillin 2)Procaine pencillin.
An Introduction to Medicinal Chemistry 3/e
Vancomycin Vancomycin is called a ‘glycopeptide’, meaning that it is a cyclic peptide, with sugar residues attached to it.
DENS 521 Clinical Dental Therapeutics
β-lactamase inhibitors
أ. م. د. وحدة اليوزبكي Head of Department of Pharmacology- College of Medicine- University of Mosul-2014 Cephalosporins 3.
Antimicrobial drugs. Antimicrobial drugs are effective in the treatment of infections because of their selective toxicity (that is, they have the ability.
4 th Lecture By Abdelkader Ashour, Ph.D. Phone: DENS 521 Clinical Dental Therapeutics.
1 Drugs that Inhibit Cell wall synthesis Beta-lactams –Penicillin family –Cephalosporin family –Carbapenems and Monobactams –Β-lactamase inhibitors Vancomycin.
Antimicrobial Agents & Mechanisms of Resistance BY Prof. DR. Zainalabideen A. Abdulla, DTM&H., MRCPI, Ph.D., FRCPath. (U.K.)
CLINICAL PHARMACOLOGY OF ANTIBACTERIAL AND ANTIVIRAL AGENTS
Treatment Of Respiratory Tract infections. Prof. Azza ELMedany Department of Pharmacology Ext
 At the end of the lecture, students should :  Describe briefly common types of meningitis  Describe the principles of treatment  List the name of.
N.meningitidis Ceftriaxone- children and adults Cefotaxime- neonates Ampicillin Chloramphenicol N. gonorrhea Ceftriaxone Cefotaxime Ciprofloxacin Spectinomycin.
Dr. Laila M. Matalqah Ph.D. Pharmacology
Although it is less potent than cephalothin against Gram-positive bacteria and cefamandole against most of the Enterobacteriaceae, cefoxitin is effective.
Treatment of Respiratory Tract infections. Prof. Azza EL-Medany.
Lecture 23-Antibiotic Therapy-2-Lecture Objectives
Principles of Medical Science Pharmacology Review
Cephalosporins Four Generations! Bactericidal & Time-Dependent!
Protein Synthesis Inhibitors
Cephalosporins B-Lactam antibiotics ( similar to penicillins)
Cell wall inhibitor Cephalosporins Dr. Naza M. Ali Lec D
Interior Health Pharmacy Resident Kootenay Lake Hospital
By :Lecturer Nabeel Ahmed Al anbagi
Drugs /Agents Inhibitors of cell wall synthesis
An Introduction to Medicinal Chemistry 3/e
Cephalosporin and Other Cell Wall Synthesis Inhibitors
Pharmacology of Cephalosporins: General Overview
Overview of Antimicrobials
b-Lactamase Inhibitors
Cephalosporin and Cell Wall Synthesis Inhibitors
CEPHALOSPORINS.
Β-LACTAM ANTIBIOTICS THIENAMYCIN MONOBACTAMS β-LACTAM INHIBITORS.
Cephalosporin and Cell Wall Synthesis Inhibitors
Other β-lactam A. Carbapenems:
Presentation transcript:

b-Lactamase Inhibitors Clavulanic acid (Beecham 1976)(from Streptomyces clavuligerus) Weak, unimportant antibacterial activity Powerful irreversible inhibitor of b-lactamases - suicide substrate Used as a sentry drug for ampicillin Augmentin = amoxicillin+ clavulanic acid Allows less amoxicillin per dose and an increased activity spectrum Timentin = ticarcillin + clavulanic acid

Augmentin = Amoxicillin + Clavulanic Acid b-Lactamase Inhibitors Augmentin = Amoxicillin + Clavulanic Acid

b-Lactamase Inhibitors Penicillanic acid sulfone derivatives Sulbactam Tazobactam Suicide substrates for b-lactamase enzymes Sulbactam has a broader spectrum of activity vs b-lactamases than clavulanic acid, but is less potent Unasyn = ampicillin + sulbactam Tazobactam has a broader spectrum of activity vs b-lactamases than clavulanic acid, and has similar potency Tazocin or Zosyn = piperacillin + tazobactam

The aminopenicillins + b-lactamase inhibitor combinations include ampicillin-sulbactam (parenteral) and amoxicillin-clavulanate (oral) Gram-positive bacteria Some Staphylococcus aureus, Streptococcus pyogenes, Viridans streptococci, Some Streptoocus pneumoniae, Some enterococci Listeria monocytogenes Gram-negative bacteria Neisseria spp. Haemophilus influenzae, Many Enterobacteriaceae Anaerobic bacteria Clostridia spp. (except C. difficile), Actinomyces israellii, Bacteroides spp. Spirochetes Borrelia burgdorferi

Problem 3 - Range of Activity Examples of Broad Spectrum Penicillins Class 2 - CO2H at the a-position (carboxypenicillins) Examples R = H CARBENICILLIN R = Ph CARFECILLIN Carfecillin = prodrug for carbenicillin Active over a wider range of Gram -ve bacteria than ampicillin Active vs. Pseudomonas aeruginosa Resistant to most b-lactamases Less active vs Gram + bacteria (note the hydrophilic group) Acid sensitive and must be injected Stereochemistry at the a-position is important CO2H at the a-position is ionised at blood pH

Problem 3 - Range of Activity Examples of Broad Spectrum Penicillins Class 2 - CO2H at a-position (carboxypenicillins) Examples TICARCILLIN Administered by injection Identical antibacterial spectrum to carbenicillin Smaller doses required compared to carbenicillin More effective against P. aeruginosa Fewer side effects Can be administered with clavulanic acid

Problem 3 - Range of Activity Examples of Broad Spectrum Penicillins Class 3 - Urea group at the a-position (ureidopenicillins) Examples Azlocillin Mezlocillin Piperacillin Administered by injection Generally more active than carboxypenicillins vs. streptococci and Haemophilus species Generally have similar activity vs Gram - aerobic rods Generally more active vs other Gram - bacteria Azlocillin is effective vs P. aeruginosa Piperacillin can be administered alongside tazobactam

The Extended Spectrum Penicillins include Piperacillin and Ticarcillin (parenteral) as well as Carbenicillin (oral) Gram-positive bacteria Streptococcus pyogenes, Viridans streptococci, Some Streptococcus pneumoniae, Some enterococci Gram-negative bacteria Neisseria meningitidis, Some Haemophilus influenzae, Some Enterobacteriaceae, Pseudomonas aeruginosa Anaerobic bacteria Clostridia spp. (except C. difficile), Some Bacteroides spp.

Extended-Spectrum Penicillin + b-Lactamase Inhibitor Combinations include:Piperacillin-tazobactam as well as ticarcillin-clavulanate (both pairs are parenteral) Gram-positive bacteria Some Staphylococcus aureus, Streptocosoccus pyogenes, Viridans streptococci, Some Streptococcus pneumoniae, Some enterococci Listeria monocytogenes Gram-negative bacteria Neisseria spp. Haemophilus influenzae, Most Enterobacteriaceae, Pseudomonas aeruginosa Anaerobic bacteria Clostridia spp. (except C. difficile), Bacteroides spp.

CEPHALOSPORINS

1. Introduction Antibacterial agents which inhibit bacterial cell wall synthesis Discovered from a fungal colony in Sardinian sewer water (1948) Cephalosporin C identified in 1961

Giussepe Brotzu noticed that the substance cultured from the sewer water had activity against Salmonella typhi, the active cause of typhoid fever Typhoid fever is transmitted human to human by contact with contaminated feces.

6. Mechanism of Action The acetoxy group acts as a good leaving group and aids the mechanism

The Cephalosporins Generation Parenteral Agents Oral Agents First-generation Cefazolin Cefadroxil, cephalexin Second-generation Cefotetan, cefoxitin, cefuroxime Cefaclor, cefprozil, cefuroxime axetil, loracarbef Third-generation Cefotaxime, ceftazidime, ceftizoxime, ceftriaxone Cefdinir, cefditoren, cefpodoxime proxetil, ceftibuten, cefixime Fourth-generation Cefepime

8. First Generation Cephalosporins Cephalothin First generation cephalosporin More active than penicillin G vs. some Gram - bacteria Less likely to cause allergic reactions Useful vs. penicillinase producing strains of S. aureus Not active vs. Pseudonomas aeruginosa Poorly absorbed from GIT Administered by injection Metabolised to give a free 3-hydroxymethyl group (deacetylation) Metabolite is less active

8. First Generation Cephalosporins Cephalothin - drug metabolism Metabolism Less active OH is a poorer leaving group Strategy Replace the acetoxy group with a metabolically stable leaving group

8. First Generation Cephalosporins Cephaloridine The pyridine ring is stable to metabolism The pyridine ring is a good leaving group (neutralisation of charge) Exists as a zwitterion and is soluble in water Poorly absorbed through the gut wall Administered by injection

8. First Generation Cephalosporins Cefalexin The methyl group at position 3 is not a good leaving group The methyl group is bad for activity but aids oral absorption - mechanism unknown Cefalexin can be administered orally A hydrophilic amino group at the a-carbon of the side chain helps to compensate for the loss of activity due to the methyl group

First Generation Cephalosporins Cefazolin Cefadroxil Cefalexin

First Generation Cephalosporins include Cefazolin (parenteral) as well as cefadroxil and cefalexin (oral). Gram-positive bacteria Streptococcus pyogenes, Some virdans streptococci, Some Staphylococcus aureus, Some Streptococcus pneumoniae Gram-negative bacteria Some Eschericia coli, Some Klebsiella pneumoniae, Some Proteus mirabilis

9. Second Generation Cephalosporins 9.1 Cephamycins Cephamycin C Isolated from a culture of Streptomyces clavuligerus First b-lactam to be isolated from a bacterial source Modifications carried out on the 7-acylamino side chain

9. Second Generation Cephalosporins 9.1 Cephamycins Cefoxitin Broader spectrum of activity than most first generation cephalosporins Greater resistance to b-lactamase enzymes The 7-methoxy group may act as a steric shield The urethane group is stable to metabolism compared to the ester Introducing a methoxy group to the equivalent position of penicillins (position 6) eliminates activity.

9. Second Generation Cephalosporins 9.2 Oximinocephalosporins Cefuroxime Much greater stability against some b-lactamases Resistant to esterases due to the urethane group Wide spectrum of activity Useful against organisms that have gained resistance to penicillin Not active against P. aeruginosa Used clinically against respiratory infections

Second generation The second-generation cephalosporins have a greater Gram-negative spectrum while retaining some activity against Gram-positive cocci. They are also more resistant to beta-lactamase. Cefaclor (Ceclor, Distaclor, Keflor, Raniclor) Cefonicid (Monocid) Cefprozil (cefproxil; Cefzil) Cefuroxime (Zinnat, Zinacef, Ceftin, Biofuroksym) Cefuzonam

Forms of Cefuroxime (2nd generation cephalosporin) Cefuroxime axetil (CEFTIN) Cefuroxime sodium (ZINACEF)

More second generation cephalosporins: Loracarbef (Lorabid)

The Second-generation cephalosporins include Cefotetan, cefoxitin, and cefuroxime (all parenteral) as well as Cefaclor, cefprozil, cefuroxime axetil, and loracarbef (all oral). Gram-positive bacteria True cephalosporins have activity equivalent to first-generation agents. Cefoxitin and cefotetan have little activity Gram-negative bacteria Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Haemophilus influenzae, Neisseria spp. Anaerobic bacteria Cefoxitin and cefotetan have moderate anaerobic activity.

10. Third Generation Cephalosporins Oximinocephalosporins Aminothiazole ring Aminothiazole ring enhances penetration of cephalosporins across the outer membrane of Gram - bacteria May also increase affinity for the transpeptidase enzyme Good activity against Gram - bacteria Variable activity against Gram + cocci Variable activity vs. P. aeruginosa Lack activity vs MRSA Generally reserved for troublesome infections

It is the drug of choice for bacterial meningitis Ceftriazone (Rocephin) is a popular third generation cephalosporin It is the drug of choice for bacterial meningitis

10. Third Generation Cephalosporins Oximinocephalosporins Ceftazidime Injectable cephalosporin Excellent activity vs. P. aeruginosa and other Gram - bacteria Can cross the blood brain barrier Used to treat meningitis

The Third-generation Cephalosporins include Cefotaxime, ceftazidime, ceftizoxime, and ceftriaxone (all parenteral) as well as Cefdinir, cefditoren, cefpodoxime proxetil, ceftibuten, and cefixime (all oral). Gram-positive bacteria Streptococcus pyogenes, Viridans streptococci, Many Streptococcus pneumoniae, Modest activity against Staphylococcus aureus Gram-negative bacteria Escherichia coli, Klebsiella pneumoniae, Proteus spp. Haemophilus influenzae, Neisseria spp. Some Enterobacteriaceae. Anaerobic bacteria Atypical bacteria Spirochetes Borrelia burgorferi

11. Fourth Generation Cephalosporins Oximinocephalosporins Zwitterionic compounds Enhanced ability to cross the outer membrane of Gram negative bacteria Good affinity for the transpeptidase enzyme Low affinity for some b-lactamases Active vs. Gram + cocci and a broad array of Gram - bacteria Active vs. P. aeruginosa

Fourth Generation Cephalosporins include cefepime (parenteral). Gram-positive bacteria Streptococcus pyogenes, Viridans streptococci, Many Streptocossus pneumoniae. Modest activity against Staphylococcus aureus Gram-negative bacteria Escherichia coli, Klebsiella pneumoniae, Proteus spp. Haemophilus influenzae, Neisseria spp. Many other Enterobacteriaceae, Pseudomonas aeruginosa. Anaerobic bacteria Atypical bacteria

Newer b-Lactam Antibiotics Thienamycin (Merck 1976)(from Streptomyces cattleya) Potent and wide range of activity vs Gram + and Gram - bacteria Active vs. Pseudomonas aeruginosa Low toxicity High resistance to b-lactamases Poor stability in solution (ten times less stable than Pen G)

Newer b-Lactam Antibiotics Thienamycin analogues used in the clinic Imipenem Ertapenem(2002) Meropenem

Primaxin = Imipenem + Cilastatin Cilastatin is an inhibitor of a human enzyme, renal dehydropeptidase, which degrades carbapenems

Meropenem, Merrem, AstraZeneca Ertapenem, Invanz, Merck

The Carbapenems include Imipenem/cilstatin, Meropenem, and Ertapenem (all parenteral) Gram-positive bacteria Streptococcus pyogenes, Viridans group streptococci, Streptococcus pneumoniae, Modest activity against Staphylococcus aureus, Some enterococci, Listeria monocytogenes Gram-negative bacteria Haemophilus influenzae, Neisseria spp., Enterobacteriaceae, Pseudomonas aeruginosa Anaerobic bacteria Bacteroides fragilis, Most other anaerobes.

Newer b-Lactam Antibiotics Clinically useful monobactam Aztreonam Administered by intravenous injection Can be used for patients with allergies to penicillins and cephalosporins No activity vs. Gram + or anaerobic bacteria Active vs. Gram - aerobic bacteria

The Monobactams include only Aztreonam, which is parenteral Gram-positive bacteria Gram-negative bacteria Haemophilus influenzae, Neisseria spp. Most Enterobacteriaceae, Many Pseudomonas aeruginosa. Anaerobic bacteria Atypical bacteria

Vancomycin

Mechanism of Action of Vancomycin Vancomycin binds to the D-alanyl-D-alanine dipeptide on the peptide side chain of newly synthesized peptidoglycan subunits, preventing them from being incorporated into the cell wall by penicillin-binding proteins (PBPs). In many vancomycin-resistant strains of enterococci, the D-alanyl-D-alanine dipeptide is replaced with D-alanyl-D-lactate, which is not recognized by vancomycin. Thus, the peptidoglycan subunit is appropriately incorporated into the cell wall.

http://student. ccbcmd http://student.ccbcmd.edu/courses/bio141/lecguide/unit2/control/vanres.html LINK

Antimicrobial Activity of Vancomycin Gram-positive bacteria Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pyogenes. Viridans group streptococci, Streptococcus pneumoniae, Some enterococci. Gram-negative bacteria Anaerobic bacteria Clostridium spp. Other Gram-positive anaerobes. Atypical bacteria

Daptomycin Daptomycin is a lipopeptide antibiotic Approved for use in 2003 Lipid portion inserts into the bacterial cytoplasmic membrane where it forms an ion-conducting channel.

Antimicrobial Activity of Daptomycin Gram-positive bacteria Streptococcus pyogenes, Viridans group streptococci, Streptococcus pneumoniae, Staphylococci, Enterococci. Gram-negative bacteria Anaerobic bacteria Some Clostridium spp. Atypical

Rifamycins Rifampin is the oldest and most widely used of the rifamycins Rifampin is also the most potent inducer of the cytochrome P450 system Therefore, Rifabutin is favored over rifampin in individual who are simultaneously being treated for tuberculosis and HIV infection, since it will not result in oxidation of the antiviral drugs the patient is taking Rifaximin is a poorly absorbed rifamycin that is used for treatment of travelers’ diarrhea.

The Rifamycins include Rifampin, Rifabutin, Rifapentine, and Rifaximin, all of which can be administered orally. Rifampin can also be administered parenterally. Gram-positive bacteria Staphylococci Gram-negative bacteria Haemophilus influenzae, Neisseria meningitidis Anaerobic bacteria Mycobacteria Mycobacterium tuberculosis, Mycobacterium avium complex, Mycobacteriumleprae.

Aminoglycosides The structure of the aminoglycoside amikacin. Features of aminoglycosides include amino sugars bound by glycosidic linkages to a relatively conserved six-membered ring that itself contains amino group substituents.

Bacterial resistance to aminoglycosides occurs via one of three mechanisms that prevent the normal binding of the antibiotic to its ribosomal target: Efflux pumps prevent accumulation of the aminoglycoside in the cytosol of the bacterium. Modification of the aminoglycoside prevents binding to the ribosome. Mutations within the ribosome prevent aminoglycoside binding.

The Aminoglycosides include Streptomycin, Gentamicin, Tobramycin, and Amikacin (all parenteral), as well as Neomycin (oral). Gram-positive bacteria Used synergistically against some: Staphylococci, Streptococci, Enterococci, and Listeria monocytogenes Gram-negative bacteria Haemophilus influenzae, Enterobacteiaceae, Pseudomonas aeruginosa Anaerobic bacteria Atypical bacteria Mycobacteria Mycobacterium tuberculosis, Mycobacterium avium complex.

Macrolides and Ketolides The structures of erythromycin and telithromycin Circled substituents and distinguish telithromycin from the macrolides. Substituent allows telithromycin to bind to a second site on the bacterial ribosome.

The macrolide group consists of Erythromycin, Clarithromycin, and Azithromycin (all oral, with erythromycin and azithromycin also being available parenterally). Gram-positive bacteria Some Streptococcus pyogenes. Some viridans streptococci, Some Streptococcus pneumoniae. Some Staphylococcus aureus. Gram-negative bacteria Neiseria spp. Some Haemophilus influenzae. Bordetella pertussis Anaerobic bacteria Atypical bacteria Chlamydia spp. Mycoplasma spp. Legionella pneumophila, Some Rickettsia spp. Mycobacteria Mycobacterium avium complex, Mycobacterium leprae. Spirochetes Treponema pallidum, Borrelia burgdorferi.

The related ketolide class consists of Telithromycin (oral). Gram-positive bacteria Streptococcus pyogenes, Streptococcus pneumoniae, Some Staphylococcus aureus Gram-negative bacteria Some Haemophilus influenzae, Bordetella pertussis Anaerobic bacteria Atypical bacteria Chlamydia spp. Mycoplasma spp. Legionella pneumophila

The Tetracycline Antibiotics The structure of tetracycline

The Tetracycline Class of Antibiotics consists of Doxycycline and Tigecycline (parenteral) as well as Tetracycline, Doxycycline and Minocycline (oral) Gram-positive bacteria Some Streptococcus pneumoniae Gram-negative bacteria Haemophilus influenzae, Neisseria meningitidis Anaerobic bacteria Some Clostridia spp. Borrelia burgdorferi, Treponema pallidum Atypical bacteria Rickettsia spp. Chlamydia spp.

Tigecycline

The antimicrobial activity of Tigecycline (parenteral) Gram-positive bacteria Streptococcus pyogenes. Viridans group streptococci, Streptococcus pneumoniae, Staphylococci, Enterococci, Listeria monocytogenes Gram-negative bacteria Haemophilus influenzae, Neisseria spp. Enterobacteriaceae Anaerobic bacteria Bacteroides fragilis, Many other anaerobes Atypical bacteria Mycoplasma spp.

Chloramphenicol

The Antimicrobial Activity of Chloramphenicol Gram-positive bacteria Streptococcus pyogenes, Viridans group streptococci. Some Streptococcus pneumoniae Gram-negative bacteria Haemophilus influenzae, Neisseria spp. Salmonella spp. Shigella spp. Anaerobic bacteria Bacteroides fragilis. Some Clostridia spp. Other anaerobic Gram-positive and Gram negative bacteria Atypical bacteria Rickettsia spp. Chlamydia trachomatis, Mycoplasma spp.

Clindamycin

The Antimicrobial Activity of Clindamycin (both oral and parenteral) Gram-positive bacteria Some Streptococcus pyogenes, Some viridans group streptococci. Some Streptococcus pneumoniae, Some Staphylococcus aureus Gram-negative bacteria Anaerobic bacteria Some Bacteroides fragilis, Some Clostridium spp. Most other anaerobes. Atypical bacteria

Streptogramins

The Antimicrobial Activity of Quinupristin/Dalfopristin (parenteral) Gram-positive bacteria Streptococcus pyogenes, Viridans group streptococci, Streptococcus pneumoniae, Staphylococcus aureus, Some enterococci. Gram-negative bacteria Anaerobic bacteria Atypical bacteria

The structure of Linezolide The Oxazolidinones The structure of Linezolide

The Antimicrobial Activity of Linezolid (both oral and parenteral) Gram-positive bacteria Streptococcus pyogenes. Viridans group streptococci, Streptococcus pneumoniae, Staphylococci, Enterococci. Gram-negative bacteria Anaerobic bacteria Atypical bacteria