Beta Lactam Antibiotic Flashcards

(32 cards)

1
Q

It impede bacterial cell wall synthesis through their distinctive beta-lactam ring structure.

A

Penicillins and cephalosporins

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2
Q

It also inhibit cell wall synthesis

A

Vancomycin, fosfomycin, and bacitracin

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3
Q

It directly disrupting the bacterial cell membrane.

A

Daptomycin

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4
Q

All penicillins are derived from?

A

6-aminopenicillanic acid

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5
Q

Beta-lactam antibiotics bind to
__________________________and
inhibit_____________________, the finalstep in cell wall synthesis.
• Also activate autolytic enzy

A

penicillin-binding proteins , transpeptidation

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6
Q

Penicillins are generally polar compounds with limited metabolic processing, often excreted unchanged in urine through ?

A

glomerular filtration and tubular secretion

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7
Q

nafcillin and ampicillin, which are primarily excreted in

A

Bile

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8
Q

The plasma half-lives of most penicillins typically range from

A

30 minutes to 1 hour

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9
Q

Beta-lactam antibiotics are bactericidal drugs that disrupt bacterial cell wall synthesis
through binding to

A

penicillin-binding proteins (PBPs)

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10
Q

Very-narrow-spectrum .This subclass includes ______,_______,______primarily used for treating staphylococcal infections.

A

methicillin, nafcillin, and oxacillin,

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11
Q

Wider-spectrum. have a broader antibacterial spectrum but are
susceptible to penicillinases. They treat infections caused by enterococci, E. coli, L. monocytogenes, P. mirabilis, H. influenzae, and M. catarrhalis and can be enhanced by penicillinase inhibitors.

A

Ampicillin and amoxicillin

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12
Q

Cephalosporin drug that is excreted in bile

A

Cefoperazone, ceftriaxone

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13
Q

Cephalosporin first generation drug

A

Cefazolin,caphalexin

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14
Q

Cephalosporin second generation

A

Cefaclor,cefuroxime ,cefprozil

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15
Q

Cephalosporin third generation

A

Ceftrazidime,cefoperazone,ceforaxime

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16
Q

Cephalosporin fourth generation

A

Cefepime,ceftaroline

17
Q

Ceftaroline is effective in treating infections caused by

A

methicillin-resistant staphylococci

18
Q

Beta lactamase inhibitor

A

Clavulanic acid, sulbactam, and tazobactam

19
Q

is a bactericidal glycoprotein that disrupts bacterial cell wall synthesis by binding to the d-Ala-d-Ala terminal of peptidoglycan, inhibiting elongation and
cross-linking.

20
Q

acts as an antimetabolite inhibitor, targeting cytosolic
enolpyruvate transferase.

21
Q

common side effect of fosfomycin

22
Q

a peptide antibiotic, disrupts the final stages of cell wall synthesis
in Gram-positive bacteria.

23
Q

acts as an antimetabolite, inhibiting the incorporation of d-Ala into the pentapeptide side chain of peptidoglycan in bacterial cell walls.

24
Q

Its use is restricted to treating drug-resistant tuberculosis due to the potential
for neurotoxic side effects, which may include

A

tremors, seizures, and
psychosis.

25
is a unique cyclic lipopeptide antibiotic, offering a spectrum of activity similar to vancomycin but with effectiveness against vancomycin- resistant strains of enterococci and staphylococci.
Daptomycin
26
Chloramphenicol ribosomal sub unit target
50
27
Macrolides ribosomal subunit target
50
28
Tetracycline ribosomal subunit target
30S
29
serve as alternative drugs for treating syphilis.
Tetracycline
30
is employed in the treatment of gastrointestinal ulcers caused by Helicobacter pylori.
Tetracycline
31
is used for Lyme disease, malaria prevention, and the treatment of amebiasis.
Doxycycline
32
Backup drug for Gram-positive cocci, including methicillin-resistant S aureus, and is recommended for endocarditis prophylaxis in penicillin-allergic valvular disease patients.
Clindamycin