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CAS 130036-23-6

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Cytidine 5′-(trihydrogen diphosphate), 2′,3′-dideoxy-, P′-(2-aminoethyl) ester

Description:
Cytidine 5′-(trihydrogen diphosphate), 2′,3′-dideoxy-, P′-(2-aminoethyl) ester, commonly referred to as a nucleotide analog, is a chemical compound that plays a significant role in biochemical research, particularly in studies related to nucleic acid metabolism and enzyme interactions. This compound features a cytidine base linked to a diphosphate moiety, which is essential for its function in biological systems. The presence of the 2′,3′-dideoxy modification indicates that it lacks hydroxyl groups at these positions, which can influence its ability to act as a substrate for nucleic acid polymerases, making it a useful tool in antiviral and anticancer research. The P′-(2-aminoethyl) ester group enhances its solubility and may facilitate cellular uptake. Overall, this compound is characterized by its structural modifications that impact its biological activity, making it a valuable compound in the study of nucleotides and their derivatives in various biochemical applications.
Formula:C11H20N4O9P2
InChI:InChI=1S/C11H20N4O9P2/c12-4-6-21-25(17,18)24-26(19,20)22-7-8-1-2-10(23-8)15-5-3-9(13)14-11(15)16/h3,5,8,10H,1-2,4,6-7,12H2,(H,17,18)(H,19,20)(H2,13,14,16)/t8-,10+/m0/s1
InChI key:InChIKey=GBUOFJVOGQHJIM-WCBMZHEXSA-N
SMILES:O=C1N([C@@H]2O[C@H](COP(OP(OCCN)(=O)O)(=O)O)CC2)C=CC(N)=N1
Synonyms:
  • Cytidine 5′-(trihydrogen diphosphate), 2′,3′-dideoxy-, P′-(2-aminoethyl) ester
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