For research use only. Not for therapeutic Use.
2-Deoxy-L-ribose (Cat No.: R014003) is a five-carbon monosaccharide and the L-enantiomer of 2-deoxy-D-ribose, differing by its stereochemistry. It lacks a hydroxyl group at the 2-position, making it a “deoxy” sugar. Although not naturally incorporated into DNA like its D-form counterpart, 2-deoxy-L-ribose is used in biochemical research and synthetic chemistry for studying enantiomeric sugar behavior and designing nucleoside analogs. Its unique stereochemistry can impact molecular recognition, making it a valuable tool in exploring chirality-dependent biological and pharmacological interactions.
CAS Number | 18546-37-7 |
Synonyms | 2-Deoxy-L-erythro-pentose; L-2-Deoxyribose |
Molecular Formula | C5H10O4 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | (3R,4S)-3,4,5-trihydroxypentanal |
InChI | InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1 |
InChIKey | ASJSAQIRZKANQN-UHNVWZDZSA-N |
SMILES | C(C=O)C(C(CO)O)O |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |