Tetrose
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A tetrose is a monosaccharide with 4 carbon atoms.
They either have an aldehyde functional group in position 1 (aldotetroses) or a ketone functional group in position 2 (ketotetroses).
The aldotetroses have two chiralatrial centres ("asymmetric carbon atoms") and so 4 different stereoisomers are possible.
The naturally occurring aldotetroses are:
The 2 D-aldotetroses are:
CH=O CH=O | | HC-OH HO-CH | | HC-OH HC-OH | | CH2OH CH2OH D-Erythrose D-Threose
The ketotetroses have 1 chiral centres and therefore 2 possible stereoisomers — Erythrulose (L- and D-form).
The D-ketotetrose is:
CH2OH | C=O | HC-OH | CH2OH D-Erythrulose
The only naturally occurring ketotetrose is D-erythrulose.
See also
de:Tetroseneo:TetrozoAcknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

