Mechanism of Action and class Flashcards

1
Q

inhibitors of murein monomer synthesis

A

varies by drug

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2
Q

fosfomycin

A

inhibitors of murein monomer synthesis - phosphoenolpyruvate analog that inhibits bacterial enol pyruvate transferase by covalent modification of enzymes active site to inhibit UDP-NAM -> UDP-NAG

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3
Q

fosmidomycin

A

inhibitors of murein monomer synthesis - phosphoenolpyruvate analog that inhibits bacterial enol pyruvate transferase by covalent modification of enzymes active site to inhibit UDP-NAM -> UDP-NAG

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4
Q

cycloserine

A

inhibitors of murein monomer synthesis - inhibits both alanine racemase and D-ala-d-ala ligase

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5
Q

bacitracin

A

inhibitors of murein monomer synthesis - inhibits dephosphorylation of bactoprenyl diphosphate

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6
Q

what is the MoA of inhibitors of murein polymer synthesis

A

bind to the D-ala-d-ala terminus of the murein monomer unit and inhibit peptidoglycan glycosyltransferase (PGT) to prevent addition of murein units to growing polymer chain

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7
Q

vancomycin

A

inhibits murein polymer synthesis

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8
Q

telavancin

A

inhibits murein polymer synthesis

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9
Q

teicoplanin

A

inhibits murein polymer synthesis

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10
Q

what is the MoA of inhibitors of polymer crosslinking penicillins

A

beta-lactams inhibit transpeptidase by forming a covelent dead-end acyl enzyme intermediate; PCN have a 5 member accesory ring attached to the beta-lactam ring

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11
Q

penicillin G

A

penicillin, IV form

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12
Q

penicillin V

A

penicillin, oral form

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13
Q

oxacillin

A

penicillin (beta-lactamase resistant)

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14
Q

cloxacillin

A

penicillin (beta-lactamase resistant)

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15
Q

dicloxacillin

A

penicillin (beta-lactamase resistant)

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16
Q

nafcillin

A

penicillin (beta-lactamase resistant)

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17
Q

ampicillin

A

penicillin, broad spectrum

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18
Q

amoxicillin

A

penicillin, broad spectrum

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19
Q

amoxicillin/clavulanic acid

A

penicllin, broad spectrum/beta lactamase inhibitor

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20
Q

ampicillin/sulbactam

A

penicllin, broad spectrum/beta lactamase inhibitor

21
Q

carbenicillin

A

penicillin, broad spectrum

22
Q

ticarcillin

A

penicillin, broad spectrum

23
Q

piperacillin

A

penicillin, broad spectrum

24
Q

mezlocillin

A

penicillin, broad spectrum

25
what is the MoA of inhibitors of polymer crosslinking cephalosporins?
beta-lactams inhibit transpeptidase by formin covalent dead end acyl enzyme intermediate; cephalosporins have a 6 member accessory ring attached to beta lactam ring
26
cefazolin
cephalosporin, 1st generation
27
cephalexin
cephalosporin, 1st generation
28
cefuroxime
cephalosporin, 2nd generation
29
cefotetan
cephalosporin, 2nd generation
30
cefoxitin
cephalosporin, 2nd generation
31
cefotaxime
cephalosporin, 3rd generation
32
cefrizoxime
cephalosporin, 3rd generation
33
ceftriaxone
cephalosporin, 3rd generation
34
cefoperazone
cephalosporin, 3rd generation
35
ceftazidime
cephalosporin, 3rd generation
36
cefepime
cephalosporin, 4th generation
37
ceftaroline
cephalosporin, 5th generation
38
what is the MoA of inhibitors of polymer cross linking monobactams/carbapenems
beta lactams inhibit transpeptidase forming covalent dead end acyl enzyme intermediate
39
aztreonam
inhibits polymer crosslinking; monobactam
40
imipenem/cilastatin
inhibits polymer crosslinking; carbapenem
41
meropenem
inhibits polymer crosslinking; carbapenem
42
doripenem
inhibits polymer crosslinking; carbapenem
43
ertapenem
inhibits polymer crosslinking; carbapenem
44
what is the MoA of inhibitors of cell membrane stability
integrates in Gram pos bacterial membranes; leading to formation of pores that cause K+ efflux, membrane depolarization and cell death
45
daptomycin
inhibits cell membrane stability
46
ethambutol
antimycobacterial; decreases arabinogalactan synthesis by inhibiting arabinosyl transferase that adds arabinose units to end of growing arabinogalactan chain
47
pyrazinamide
antimycobacterial; inhibits fatty acid synthetase 1
48
isoniazid
antimycobacterial; inhibits mycolic acid synthesis by targeting fatty acid synthetase 2
49
ethionamide
antimycobacterial; inhibits mycolic acid synthesis by targeting fatty acid synthetase 2