An anomer is a type of stereoisomer and epimer found in carbohydrate chemistry. While an epimer is a stereoisomer that differs in configuration at any single stereogenic center, an anomer is a cyclic saccharide and an epimer that differs in configuration, specifically at the hemiacetal/acetal carbon, also called the anomeric carbon. The anomeric carbon is the carbon derived from the carbonyl carbon (the ketone or aldehyde functional group) of the open-chain form of the carbohydrate molecule. Anomerization is the process of conversion of one anomer to the other.
Two anomers are designated alpha (α) or beta (β), according to the configurational relationship between the anomeric centre and the anomeric reference atom, hence they are relative stereodescriptors. The anomeric centre in hemiacetals is the anomeric carbon C-1. In hemiketals it is the carbon derived from the carbonyl of the ketone (e.g. C-2 in D-fructose). In aldohexoses the anomeric reference atom is the stereocenter that is farthest from anomeric carbon in the ring (the configurational atom, defining the sugar as D or L). In α-D-glucopyranose the reference atom is C-5.
Dark thoughts rise up
Deep in your mind
The killing of hope
The end has begun
The locked psycho-door breaks down
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Blows bloody thoughts into your mind
Demons whisper, "commit suicide"
Weak is your body, helpless your soul, The beast destroyed your will
Left nothing but an empty shell
Self-destruction leads its way
Your wepons turn against yourself
Cutting through, killing you
A downward spiral, the shadowbeast has won
The shadowbeast calls
A vulture of life
Your worst enemy dwells