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Transcript
Tutorial aminoglycosides
1.
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6.
What are the building blocks (composition) of ribosome?
Why drug interaction with rRNA is less specific than with proteins
Mention 3 types of tetracyclines obtained from bacterial cell culture
Mention 3 types of tetracyclines semisynthesized
Why tetracycline molecule is regarded amphoteric?
How tetracycline undergo inactivation in aqueous medium (give representative
drawing)
7. Why tetracycline is unstable in acidic medium? And how it can be overcomed in
molecular design?
8. How the di-methyl amino group at ring A affects the interaction of tetracycline with
the ribosome?
9. How many keto-enol systems are available in tetracycline?
10. There are two keto-enol systems in tetracyclines, please point to them in the
structure.
11. Why is it prohibited to substitute other than hydrogen at C4a ?
12. Which of the following groups at C4 gives inactive compound (H, OH, CH3)?
13. Why doxycycline is more acid stable than tetracycline?
14. Why doxycycline is taken twice daily while tetracycline is taken 4 times daily?
15. Why the administration of chlortetracycline is causing photoxicity upon explore to
sun light?
16. Mention 3 possible sites of metabolism in tetracycline
17. Which mechanism of resistance the bacteria can use to resist tetracycline without
undergoing mutations, or inactivation of antibiotic?
18. How bacteria can inactivate tetracycline by TetX
19. Does methacycline is acid stable?
20. Correct the error in the following name of tetracycline (4-dimethylamino1,4,4a,5,5a,6,11,12aoctahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2anthracenecarboxamide
21. Mention name of 2 tetracyclines that are associated with phototoxic effect.
22. Give name for one tetracycline available as prodrug.
23. What is the functional group difference between tetracycline and doxycycline?
24. What is the functional group difference between tetracycline and minocycline?
25. Highlight the functional groups of tetracycline which should not be changed in the
newly designed analogues.