Penicillin antibiotics Flashcards

1
Q

Natural Penicillins

A

Penicillin G - the prototype, requires injection
Penicillin V - the most acid-stable, taken orally

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2
Q

Narrow spectrum Penicillin

A

Beta-lactamases break the beat-lactam ring
good against Gram + organisms such as Staphylococcus, streptococcus, and some Spirochetes

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3
Q

Semi-synthetic Penicillin

A

Oxacillin - narrow-spectrum, Gram+ but resistant to penicillinase
Ampicillin - Extended-spectrum, many gram-

more resistant to stomach acid

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4
Q

Semi-synthetic with Potassium clavulanate
Penicillin

A

Product of Streptomyces (non-competitive inhibitor of penicillinase)
Augmentin when combined with amoxicillin

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5
Q

Semi-synthetic with a C in place of the S
Penicillin

A

Carbapenems
inhibits cell wall synthesis
good against 98% of the hospital isolates nosocomial
infections
Good broad-spectrum activity

Primaxin- Combination of imipenem and cilastin (Protects from degradation in the kidneys)

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6
Q

Semi-synthetic - with only one ring
Penicillin

A

Monobactams
Newer synthetic antibiotic - Aztreonam
no beta-lactam ring
not affected by penicillinases
low toxicity to host
good for Pseudomonas and Escherichia

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7
Q

Cephalosporins (over 70 versions) Synthetic

A

Inhibits cell wall synthesis
more resistant to penicillinases than natural penicillins
“Cephalo-wonderful”
more expensive than penicillin
broader spectrum & originally injected now some oral
Ex. Keflex

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8
Q

Polypeptides (from the genus Bacillus)

A

Bacitracin -
inhibits cell wall synthesis
restricted to topical use only
Vancomycin (VRSA & VRE) -
inhibits cell wall synthesis
Narrow spectrum: good against penicillinase-
producing Staphylococci
Can be toxic to the host - careful administration

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9
Q

Antimycobacterial Antibiotics

A

rifamycin -
inhibits the synthesis of mRNA
good for mycobacterium
concentrates in the CSF and abscesses
Isoniazid (INH) -
Inhibits synthesis of mycolic acid in acid-fast
organisms
good synthetic against mycobacterium
Ethambutol -
synthetic against mycobacterium
Inhibits synthesis of mycolic acid incorporation into
cell wall; therefore used as a secondary drug
because it is a weaker drug

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