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Silicon,
right below carbon on the periodic table, shares many of the same attributes,
such as bonds to four tetrahedrally arrayed substituents and strong bonds
to carbon. Silicon is far more abundant than carbon, but mostly in
the form of silica, with bonds only to oxygen, earth's most abundant element.
Organic derivatives of silicon do not occur naturally.[1] Dialkyl
and diarylsilanediols are best known as unstable precursors of silicones,
which form by dehydrative polymerization. Silicones are well known
for their outstanding thermal stability, fluid properties and low toxicity.[2]
The notion that silanediols are unstable is reinforced by the huge annual
production of dimethylsilanediol. This smallest of the dialkylsilanediols
is intrinsically unstable and spontaneously yields permethylsilicone.
As the organic substituents increase in bulk, polymerization is inhibited,
and highly stable examples are also well known. More than 100 silanediols
have been characterized.[3]
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Unlike
hydrated carbonyls (carbondiols) that readily dehydrate and form carbon–oxygen
double bonds, silanes form silicon–oxygen double bonds only under forcing
conditions. The intrinsic tetrahedral stability of silanediols, along
with their close relationship to carbon and low toxicity, makes them good
candidates for mimics (bioisosteres) of hydrated carbonyls. Hydrated
carbonyl analogs are central to designed inhibitors of proteolytic enzymes
(proteases).[4] Substitution of a silanediol into the backbone of
a polypeptide would result in a molecule that can be recognized by a protease,
bind to its active site, and inhibit it. Silanediols are outstanding
hydrogen bond donators (better than alcohols) and at the same time equivalent
in their abilities to accept hydrogen bonds. This excellent hydrogen
bonding can be seen in the X-ray structures of silanediols, and also in
properties such as the liquid crystallinity of diisobutylsilanediol.
One such crystal structure for diphenylsilanediol is shown. Good
hydrogen bonding will promote binding at the active site of the aspartic
proteases, one of the four classes of proteases. The HIV protease
is the best known aspartic protease.
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Metalloproteases
are another important class of protease, with a zinc ion at the active
site that is critical to hydrating and cleaving the peptide bond.
Captopril was the first drug designed as a protease inhibitor, targeting
the metalloprotease angiotensin-converting enzyme (ACE). Could silanediols
act as metalloprotease inhibitors? The precedent for metal chelation
by silanediols is sparse. To test silanediols as metalloprotease
inhibitors, we prepared a silanediol analog of a known ketone inhibitor.[5]
Ketones can act as analogs of amides and are generally thought to bind
to a protease active site as the hydrate. Two types of silanols were
prepared, a silanediol and a methylsilanol. Both were prepared as
a mixture of diastereomers. The silanediol was a very good inhibitor,
with an IC50 of 14 nM (the concentration needed to inhibit 50%
of the enzyme, the lower this value the better).[6] It is likely
that most of the inhibition is derived from only one of the four diastereomers.
The methylsilane was a very poor inhibitor, suggesting that the silanediol
acts by chelating the active site zinc. Note that in this exercise
we prepared the silanediol with an isobutyl group between silicon and nitrogen.
The results from testing a silanediol with the ‘correct’ benzyl group
and control of stereochemistry are expected very soon.
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To test the silanediol as an inhibitor
of the HIV protease, an aspartic protease, a C2 symmetric silanediol
was prepared, modeled on a known, nearly C2 symmetric, carbinol.
The silanediol proved to be quite potent, with a Ki value of 2.7 nM.
The carbinol and indinavir (one of the currently marketed HIV treatments)
are more potent against the enzyme, but only by a factor of about 7.
This relative potency holds true in whole cell protection assays as well,
where the drug candidate must cross cell membranes in order to demonstrate
its inhibitory properties. [7]
We are continuing the work described above, and expanding it to other
enzymes and other enzyme classes.
Last
modified: October 2001