Table 7.2 Examples of drugs that inhibit the formation of cell wall synthesis
Compound/Active against Structure Mode of action
D-Cycloserine. A broad spectrum
antibiotic.
N
H
O C O
H
H
H
NH 3
D-Cycloserine
O
H C O
H
H
H
NH 3
D-Alanine
Inhibits the enzymes alanine racemase and
D-alanyl-D-alanyl synthetase that are
responsible for producing the dipeptide
D-alanyl-D-alanine, a precursor of the
pentapeptide chain in cell wall formation. It
is believed that the rigid structure of the
isoxazole ring gives the drug a better chance
of binding to the enzyme than the more
flexible structure of D-alanine.
Fosomycin. Active against Gram-positive
and Gram-negative bacteria.
O
H 3 C
H H
O
P
O−
O−
Fosomycin
Inhibits enol-pyruvate transferase, which
catalyses the incorporation of
phosphoenolpyruvic acid (PEP) into uridine
diphospho-N-acetylglucoamine
(UDPNAG), a precursor involved in the
formation of bacterial cell walls.
Bacitracin A. Active against Gram-positive
bacteria. The configurations of the amino
acid residues are given in the brackets.
Believed to inhibit a number of the stages in
the biosynthesis of the peptidoglycan
chains. (Letter key, see Table 1.1.)
Bacitracin A
L
(L)
E
(D)
I
(L)
K
(L)
D
(L)
CH 3
CH 3
NH 2
N
S
OC
N
H (D)
(L)
F
(D)
Orn
(D)
I
(L)
b-Lactam group of antibiotics. More
effective against Gram-positive than Gram-
negative bacteria but some cephalosporins,
such as ceftazidime, are very effective
against Gram-negative bacteria.
Theb-lactam group of antibiotics inhibit
cell wall synthesis by inhibiting the
formation of the transpeptidases responsible
for the cross linking between the
peptidoglycan chains.
N
O
RCONH
H H
S
X
COOH
Penicillins
Cephalosporins
R−
R− X−
Benzylpenicillin
(Penicillin G)
Ampicillin (X = H)
Amoxicillin (X = OH)
CH 2
NH 2
X
(D)
Cephalothin
Ceftazidime
S CH^2
−CH 2 N
HOOCC(CH 3 ) 2 O
N
S
H 2 N
N
−OCOCH 3
S
N
O
RCONH
H H
CH 3
CH 3
HCOOH
EXAMPLES OF DRUGS THAT DISRUPT CELL MEMBRANES AND WALLS 137