Antibiotics Classification, Mechanism of Action, Brand Generics and Mnemonics
Table of Contents
Antibiotics Classification
Antibiotics are categorized based on their core chemical structure, which determines their mechanism of action, spectrum of activity, and resistance profiles.
The chemical structure of an antibiotic dictates its target interaction, spectrum, and resistance mechanisms. Understanding these structural classes helps in drug design, resistance management, and combination therapy strategies.
Below is a detailed breakdown of the primary classification systems:
The chemical structure of an antibiotic dictates its target interaction, spectrum, and resistance mechanisms. Understanding these structural classes helps in drug design, resistance management, and combination therapy strategies.
Below is a detailed breakdown of the primary classification systems:
1. Classification by Chemical Structure
Antibiotics with similar structures often share mechanisms of action and resistance profiles.
Chemical Class | Examples | Key Feature |
β-Lactams | Penicillins, Cephalosporins, Carbapenems | Contain a β-lactam ring; inhibit cell wall synthesis. |
Aminoglycosides | Gentamicin, Amikacin | Amino sugars; bind 30S ribosomal subunit. |
Tetracyclines | Doxycycline, Minocycline | Four-ring structure; block 30S ribosomal subunit. |
Macrolides | Azithromycin, Clarithromycin | Macrocyclic lactone ring; inhibit 50S subunit. |
Fluoroquinolones | Ciprofloxacin, Levofloxacin | Synthetic; inhibit DNA gyrase/topoisomerase. |
Sulfonamides | Sulfamethoxazole, Trimethoprim | Folate synthesis inhibitors (PABA analogs). |
Glycopeptides | Vancomycin, Teicoplanin | Large molecules; disrupt cell wall (Gram+). |
Oxazolidinones | Linezolid | Synthetic; bind 50S ribosomal subunit. |
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2. Classification by Mechanism of Action
Antibiotics target specific bacterial processes:Mechanism | Drug Classes | Effect |
Cell Wall Synthesis Inhibitors | β-Lactams, Glycopeptides, Fosfomycin | Cause bacterial lysis. |
Protein Synthesis Inhibitors | Aminoglycosides, Macrolides, Tetracyclines | Block ribosomes (30S/50S). |
Nucleic Acid Synthesis Inhibitors | Fluoroquinolones, Rifampin | Target DNA/RNA enzymes. |
Folate Pathway Inhibitors | Sulfonamides, Trimethoprim | Block nucleotide synthesis. |
Cell Membrane Disruptors | Polymyxins (e.g., Colistin) | Damage bacterial membranes. |
3. Classification by Bacterial Target (Gram Stain)
Target | Antibiotics | Coverage |
Gram-Positive | Vancomycin, Clindamycin, Oxacillin | Staphylococci, Streptococci |
Gram-Negative | Aztreonam, Polymyxins, Ceftazidime | E. coli, Pseudomonas |
Anaerobes | Metronidazole, Clindamycin | Bacteroides, Clostridium |
Atypicals | Macrolides, Tetracyclines | Mycoplasma, Legionella |
4. Classification by Spectrum of Activity
(a) Narrow-Spectrum
Target specific bacteria (Gram+ or Gram-).Examples:
- Penicillin G (Gram+ cocci).
- Vancomycin (Gram+ MRSA).
(b) Broad-Spectrum
Target both Gram+ and Gram- bacteria.Examples:
- Tetracyclines, Fluoroquinolones, Carbapenems.
(c) Extended-Spectrum
Cover Pseudomonas, anaerobes, or drug-resistant strains.Examples:
- Piperacillin-tazobactam (Pseudomonas + anaerobes).
- Ceftazidime (ESBLs).
5. Classification by Route of Administration
- Oral: Amoxicillin, Ciprofloxacin.
- IV/IM: Vancomycin, Meropenem.
- Topical: Neomycin, Mupirocin.
6. Classification by Origin
- Natural: Penicillin (from Penicillium mold), Streptomycin (from Streptomyces).
- Semi-synthetic: Amoxicillin, Ceftriaxone.
- Synthetic: Fluoroquinolones, Sulfonamides.
Penicillin Antibiotics
Chemical Class | Brand Name | Generic Name | Mechanism of Action | Mnemonics |
Penicillins |
Amoxil | Amoxicillin |
Inhibit cell wall synthesis (peptidoglycan cross-linking) |
“PENs Write On Bacteria Walls.”
PENicillins = inhibit cell wall synthesis |
Principen, Omnipen | Ampicillin | |||
Augmentin | Amoxicillin-clavulanate | |||
Pen V K | Penicillin V potassium | |||
Ending in ___cillin is a penicillin |
Macrolides Antibiotics
Chemical Class | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Macrolides |
Azithromycin | Zithromax, Z-Pak |
Inhibit protein synthesis (bind 50S ribosomal subunit) |
ACE your Macrolide exam!”
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Clarithromycin | Biaxin | |||
Erythromycin | Ery-Tab, Erythrocin, E.E.S. | |||
Ending in ___mycin is grouped as an Macrolides or Erythromycins |
Antibiotic Tetracycline
Chemical Class | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Tetracyclines (TCN) |
Doxycycline | Vibramycin |
Inhibit protein synthesis
(bind 30S ribosomal subunit) |
“Tetra = 4 wheels
= Stops protein machine.” |
Tetracycline | Sumycin, Tetracyn | |||
Minocycline | Minocin | |||
|
Quinolones Antibiotics
Antibiotic Class | Generation | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Quinolones | 1st Generation | Nalidixic acid | Discontinued |
Inhibit bacterial DNA gyrase
and topoisomerase IVBlocks DNA replication. |
“Fluoro = Flow of DNA stopped.”
Block DNA gyrase
(DNA replication) |
Fluoroquinolones |
2nd Generation |
Ciprofloxacin | Cipro, Ciproxin | ||
Ofloxacin | Floxin, Ocuflox | ||||
Norfloxacin | Noroxin | ||||
3rd Generation | Levofloxacin | Levaquin, Iquix | |||
4th Generation |
Moxifloxacin | Avelox, Vigamox | |||
Gemifloxacin | Factive |
- Take with water only
- Avoid dairy, antacids, or calcium-fortified juices
- Photosensitivity (sunburn risk)
Antibiotic Cephalosporin
Antibiotic Class | Generation | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Cephalosporins |
1st Generation |
Cefazolin | Ancef, Kefzol |
Inhibit cell wall synthesis,
similar to penicillins.
Bind to penicillin-binding proteins (PBPs) → disrupt bacterial cell wall synthesis → cause cell lysis |
“CEF the chef cooks in 5 generations.” All start with CEF (e.g., Ceftriaxone, Cephalexin) 5 generations: each with broader Gram-negative coverage. |
Cephalexin | Keflex | ||||
2nd Generation |
Cefuroxime | Ceftin, Zinacef | |||
Cefoxitin | Mefoxin | ||||
Cefaclor | Ceclor | ||||
3rd Generation |
Ceftriaxone | Rocephin | |||
Cefotaxime | Claforan | ||||
Ceftazidime | Fortaz, Tazicef | ||||
Cefdinir | Omnicef | ||||
4th Generation | Cefepime | Maxipime | |||
5th Generation |
Ceftaroline | Teflaro | |||
Ceftobiprole | Zevtera |
- Class: β-Lactam antibiotics (structurally similar to penicillins)
- All starts with Cef______
- Photosensitivity (sunburn risk)
Sulfonamides Antibiotics
Chemical Class | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Sulfonamides |
Sulfamethoxazole + Trimethoprim | Bactrim, Septra |
Inhibit folic acid synthesis (DNA synthesis) |
“Sulfa drugs STOP Folic acid.”
Inhibit folic acid → block DNA synthesis |
Sulfasalazine | Azulfidine | |||
sulfisoxazole | Gantrisin |
- Be hydrated, drink enough water, else Crystalluria (Kidney Damage)
- Risk of Sun Sensitivity (Photosensitivity)”
aminoglycosides antibiotics
Chemical Class | Generic Name | Brand Name | Mechanism of Action | Mnemonics |
Aminoglycosides |
Gentamicin | Garamycin, Genoptic |
Inhibit protein synthesis cause mRNA misreading |
“A Mean GNATS can’t hear.”
G = Gentamicin N = Neomycin A = Amikacin T = Tobramycin S = Streptomycin Side effect: ototoxicity + nephrotoxicity |
Neomycin | Neo-Fradin, Myciguent | |||
Amikacin | Amikin | |||
Tobramycin | Tobrex, Bethkis, TOBI | |||
Streptomycin | Streptomycin |
aminoglycosides antibiotics
Nitroimidazoles are a structurally distinct class of antimicrobials defined by their 5-nitroimidazole core, with selective toxicity against anaerobes and protozoa. Their mechanism relies on nitro group reduction, making them irreplaceable for treating certain infections.
Nitroimidazole Antibiotic (not a typical antibacterial like β-lactams or macrolides).
Mechanism of Action:
The nitro group is reduced in anaerobic bacteria/protozoa, producing toxic intermediates that damage DNA.
Only active against anaerobic bacteria & certain parasites (not aerobic bacteria).
Mechanism of Action:
The nitro group is reduced in anaerobic bacteria/protozoa, producing toxic intermediates that damage DNA.
Only active against anaerobic bacteria & certain parasites (not aerobic bacteria).
Antibiotic Class | Generic Name | Brand Name | Mechanism of Action | Important |
Nitroimidazoles | Metronidazole | Flagyl | The nitro (–NO₂) group on the imidazole ring is reduced by microbial enzymes (nitroreductases), Causes DNA strands to breaks, disrupts microbial nucleic acids, then cell death |
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