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Antibiotics I: Antimetabolites

ljjepson Pharmacology B English 21 cards

Antibiotics I: Antimetabolites

Cards in this deck (21)

  1. 1What did Ehrlich discover about altering structure of compounds?Related compounds may have curative action increase independent of toxicity
  2. 2What are the two types of effect antibiotics can have?Bactericidal= kills bacteria
    bacteriostatic= stops growth
  3. 3what are the 4 main sites of antibiotic action-metabolism (antimetabolites)
    -cell wall synthesis
    -protein synthesis
    -nucleic acid synthesis
  4. 4what was the first sulphonamide antibacterialwhat was the first sulphonamide antibacterial
  5. 5what is prontosil structurewhat is prontosil structure
  6. 6What are the functional groups of a sulphonamide-amino terminus (cannot be changed or modified)
    -benzene ring (more active than other aromatics)
    -sulphonamide terminus (can be modified- swap hydrogens for other groups)
  7. 7what molecule are sulphonamides similar to? what is this similarity called?pAB (para-amino benzoic acid)
    isosterism
  8. 8what is pAB used forfolate synthesis
  9. 9how do sulphonamides workincorporated instead of pAB, creates a false product, prevents folate synthesis
  10. 10why does incorporation of a sulphonamide prevent folate synthesis-next step after pAB is glutamate addition
    -glutamate can't be added to sulphonamide group
  11. 11what is folic acid used for'one-carbon metabolism'- transfer of methyl groups (e.g. dUMP-->dTMP)
  12. 12why are sulphonamides selectively toxic to bacteria?Humans do not synthesise folate, sulphonamides block a pathway that is present in bacteria but not humans
  13. 13what is the sulphonamide general structurewhat is the sulphonamide general structure
  14. 14why do sulphonamides work so well?-they generate a false product- prevents a build up before the block (competition=overcome block)
    -bacteria have no uptake mechanisms for end-product
    -we don't synthesise folate- pAB not present in our cells
  15. 15what blocks the action of sulphonamidesend products of folate metabolism (serine, thymine etc)
  16. 16what effect do sulphonamides have on bacteriausually bacteriostatic (become bacteriocidal in absence of thymine- 'thymineless death')
  17. 17how is sulphonamide resistance achieved-inc pAB levels
    -inc folate uptake
    -reduced uptake of drug
    -metabolism of drug
  18. 18what are sulphonamides used forUTIs, meningitis, and in veterinary medicine
  19. 19what types of bacteria do sulphonamides affectbroad spectrum- Gram -ve and +ve
  20. 20what are 2 related drugs that act by the same mechanism-dapsone (used in combi therapy for leprosy)
    -p-amino salicyclic acid (tuberculosis)
  21. 21what are some other drugs which target folate synthesisdihydrofolate reductase inhibitors (enzyme also present in humans so toxic):
    -methotrexate (anticancer)
    -trimethoprim - selective for bacterial enzyme (bacterial IC50=0.01µM, mammalian IC50=300µM)

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sulphonamides
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