MOA Flashcards

(36 cards)

1
Q

Pens Cephs and Carbs

A

Activate PbPs

Or catalyze peptidoglycan cross-linkages via Transpeptidase (late step)

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2
Q

Vancomycin

A

Prevent peptidoglycan elongation via transglycosylase (early step)

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3
Q

Tetracycline

A

30s and blocks docking site of tRNA

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4
Q

AmiNOglycosides

A

Binds 30s and blocks initiation complex and inhibit translocation by inducing misreading

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5
Q

Macrolides (MAC) and Clindamycin

A

Binds to 50s and inhibits translocation

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6
Q

Sulfonamides

A

PABA analogs that compete with PABA for DIHYDROPHOLATE SYNTHASE to decrease folic acid

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7
Q

Trimethoprim

A

Inhibits dihydrofolate reductase to decrease purine and pyramidine and AA’s (all formed from tetrahydrofolic acid)

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8
Q

Metronidazole

A

Activated by feredoxin and binds to DNA molecules (inhibits Nucleic acid synthesis)

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9
Q

Fluoroquinolones

A

Inhibits DNA Gyrase/topoisomerase II
Prevents DNA from unwinding and duplicating
(PREVENTS RELAXATION OF POSITIVE SUPERCOILS)

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10
Q

Fusion inhibitors

A

Blocks gp41 and CCR5 on T-cell to prevent viral entry

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11
Q

Reverse transcriptase inhibitors

A

NRTI: nucleoSide that must be phosphorylated to 5’ to 3’ to terminate DNA elongation
NtRTI: nucleotide that has 1 phosphate and must be furtherphosphorylated
NNRTI: already active/ not a prodrug…actively bind to RT (allosterically)

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12
Q

Integrase inhibitor

A

Inhibits HIV enzyme integrase, blocking genetic material into human chromosomes

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13
Q

Protease inhibitors

A

Inhibits HIV-1 protease, blocking release/ budding for infected cells

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14
Q

-Ovirs (HSV)

A

Inhibits DNA polymerase via acyclovir triphosphate (herpes puts on first P we put on the other 2)

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15
Q

Foscarnet (HSV)

A

Inhibits phosphate binding site on DNA polymerase (decrease viral DNA replication)

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16
Q

-ivirs (Flu)

A

Inhibits NEURAMINIDASE, decrease budding/release from the cell

17
Q

Isoniazid

A

Prodrug that is activated to decrease MYCOLIC ACID synthesis (required for mycobacterial cell wall)

18
Q

Rifampin (TB) and Rifabutin (MAC)

A

Blocks DNA-dependent RNA polymerase, decrease transcription

19
Q

Pyrazinamide (TB)

A

Activated to pyrazinoic acid (competes with Uric acid)

Changing pH and decreasing FA synthesis

20
Q

Ethambutol (TB)

A

inhibits synthesis of Mycobacterial cell wall component

21
Q

Streptomycin (TB)

A

Inhibits bacterial protein synthesis by binding 30s (inhibiting translocation)

22
Q

-bendazoles (pinworm/ Nematodes)

A

Inhibit microtubule synthesis

23
Q

Pyrantel (Nematodes)

A

Constantly stimulates nicotinic receptors, causes spastic paralysis of the worm (succinylcholine)

24
Q

Ivermectin (nematodes)

A

GABA agonist that causes hyperpolarization of worms nerves/muscle cells, killing the worm

25
Praziquantel (tapeworms and flukes)
Increase membrane permeability to Ca2+ causing muscle contraction and muscle paralysis
26
Amphotericin B
Binds to ERGOSTEROL to form pores and leak cell components
27
Flucytosine
Converted to 5-FU then 5-F DUMP to inhibit THYMIDYLATE SYNTHASE, to decrease fungal DNA synthesis
28
Azole (-conazoles)
Inhibits ergosterol membrane synthesis by blocking (14-alpha demthylase)
29
Echinocardins (fungins)
Inhibits B 1,2 glucan synthesis, FUNGAL CELL WALL COMPONENT!!
30
Terbenafine (fungal)
Inhibits squalene epoxide, Increases squalene which is toxic to fungal cells
31
Chloroquine (blood schizonticide)
Accumulates in food vacuoles of plasmodium and increased intracellular heme (increases toxicity to Vivax parasite)
32
Primequine (tissue schizonticide)
Forms the cellular oxidants “quinolone-quinone metabolites” which is lethal to vivax parasite
33
Quinine (blood schizonticide)
Complexes with falciparum parasitic DNA to block replication and transcription
34
Mefloquine
Alternative to quinone for falciparum prevention
35
Metronidazole (giardia and histolytica)
Activated by ferredoxin which decreases binding to DNA
36
TMP SMX (toxoplasmosis)
Inhibits DIHYDROFOLATE REDUCTASE