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Beta-Lactams
A group of bacteria with a ring like structure disrupts cell wall synthesis example: Penicillin,Oxicillin
Natural Penicilin
Extracted from fungal cultures BUT vulnerable tp penciliases (super bug enzymes)
Semisynthetic penicillins
Contain chemically added side chains, are less vulnerable to deactivation (from penicillinases) more stable, more absorbable, ex: Oxacillin
Vancomycin
Disrupt NAM subunits bridges from linking to each other
Bacitracin
Blocks transport of NAG and NAM from cytoplasm
Isoniazid
Disrupt mycolic acid formation in mycobacterial species

Chloramphenicol
Inhibits peptide bond formation, binds to the 50S subunity of the 70S ribosome, synthetic
Aminoglycosides
Change the shape of the 30S subunit in the 70S ribosome
example: Streptomycin, neomycin, gentamicin
Tetracyclines
Made by Streptomyces spp, it interferes with the tRNA attachment to the ribosome, penetrate tissue, suppress normal intesntinal microbiota
Erthromycin
Preventing the movement of ribosomes
Polymyxin
Attatches to the lipopolysaccharide (G-) and disrupts cytoplasmic membrane, produced by BACILLUS POLYMYXA, used for UTI caused by pseudomonas
Polyenes (Amphotericin B)
Attaches to ergosterol in funal membranes which is problematic because humans have similar cholesterol. Bacteria lack sterols and are invulnerable.
Sulfanilamide
A competitive inhibitor for with with PABA (para-aminobenzoic acid), preventing production of folic acid which disrupts synthesis of DNA and RNA
Rifamycin
inhibits messenger RNA synthesis
Nalidixic acid
Effective against prokaryotic DNA, synthetic, INHIBITS DNA GYRASE