- chain.
Aldoses with
alcohol groups on the
right of the
Fischer projection are D-
aldoses, and
those with
alcohols on the left are L-
aldoses. D-
aldoses are...
- groups: the
aldoses,
which have an
aldehyde group, and the ketoses,
which have a
ketone group.
Ketoses must
first tautomerize to
aldoses before they can...
-
principle that, when heated,
ketoses are more
rapidly dehydrated than
aldoses. It is
named after Theodor Seliwanoff, the
chemist who
devised the test...
-
monosaccharide ketoses are
reducing sugars,
because they can
tautomerize into
aldoses via an
enediol intermediate, and the
resulting aldehyde group can be oxidised...
- In enzymology,
aldose reductase (or
aldehyde reductase) (EC 1.1.1.21) is an
enzyme in
humans encoded by the gene AKR1B1. It is an
cytosolic NADPH-dependent...
-
Aldose reductase inhibitors are a
class of
drugs being studied as a way to
prevent eye and
nerve damage in
people with diabetes.
Their target,
aldose...
-
monosaccharide with
chemical formula C3H6O3. It is the
simplest of all
common aldoses. It is a sweet, colorless,
crystalline solid that is an
intermediate compound...
-
carbons (tri-, tetr-, pent-, hex-, etc.) with the
suffixes "-ose" for
aldoses and "-ulose" for ketoses. In the
latter case, if the
carbonyl is not at...
-
direct access to
aldoses,
whereas some
sugars of
interest may
instead be ketoses. Some
ketoses may be
accessible from
similar aldoses by isomerization...
-
glucose condensation reactions intramolecular bonding isomerization of
aldoses to
ketoses dehydration reactions fragmentation reactions unsaturated polymer...
