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Therapeutic utility and medicinal chemistry of cathepsin C inhibitors.
[papillon-lefèvre syndrome]
The
lysosomal
cysteine
protease
cathepsin
C
(
Cat
C
)
,
also
known
as
dipeptidyl
peptidase
I
,
activates
a
number
of
granule-associated
serine
proteases
with
pro-
inflammatory
and
immune
functions
by
removal
of
their
inhibitory
N-
terminal
dipeptides
.
Thus
,
Cat
C
is
a
therapeutic
target
for
the
treatment
of
a
number
of
inflammatory
and
autoimmune
diseases
.
Cathepsin
C
null
mice
and
humans
with
Cat
C
loss
of
function
mutations
(
Papillon-
Lefèvre
syndrome
)
show
deficiencies
in
disease-relevant
proteases
including
neutrophil
elastase
,
cathepsin
G
,
chymases
and
granzymes
and
the
Cat
C
mice
are
protected
in
a
number
of
disease
models
.
Several
methodologies
have
been
recently
reported
for
assessing
the
effects
of
Cat
C
inhibitors
on
serine
protease
activities
in
cellular
assays
and
prolonged
treatment
of
rats
with
a
reversible
,
selective
Cat
C
inhibitor
reduced
the
activity
of
three
leukocyte
serine
proteases
.
Nearly
all
potent
and
selective
Cat
C
inhibitors
described
are
based
on
the
preferred
dipeptide
substrates
bearing
either
irreversible
(
e
.
g
.
diazomethylketone
,
acyloxymethyl
ketone
,
o-acyl
hydroxamic
acid
and
vinyl
sulfone
)
or
reversible
(
e
.
g
.
semicarbazide
,
nitrile
and
cyanamide
)
electrophilic
warheads
.
While
potent
and
highly
selective
,
the
best
inhibitors
described
to
date
still
have
poor
stability
and
/
or
rodent
pharmacokinetics
,
likely
resulting
from
their
peptidic
nature
.
The
lack
of
selective
compounds
with
appropriate
rodent
pharmacokinetic
properties
has
hampered
the
assessment
of
the
effects
of
Cat
C
inhibitors
on
the
activation
of
disease-relevant
proteases
in
vivo
and
the
full
evaluation
of
the
therapeutic
utility
of
Cat
C
inhibitors
.
Diseases
Validation
Diseases presenting
"loss of function mutations"
symptom
child syndrome
familial hypocalciuric hypercalcemia
hirschsprung disease
kallmann syndrome
krabbe disease
papillon-lefèvre syndrome
pendred syndrome
werner syndrome
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