CAS 65444-12-4
:Cytidine 5'-(tetrahydrogen triphosphate), 2'-amino-2'-deoxy-
Description:
Cytidine 5'-(tetrahydrogen triphosphate), 2'-amino-2'-deoxy- is a nucleotide derivative that plays a crucial role in cellular metabolism and biochemistry. This compound is characterized by its structure, which includes a cytidine base linked to a triphosphate group. The presence of the 2'-amino-2'-deoxy modification indicates that it is a deoxyribonucleotide, distinguishing it from ribonucleotides. This molecule is involved in various biochemical processes, including energy transfer and the synthesis of nucleic acids. Its triphosphate group is a high-energy moiety, making it a key player in cellular energy metabolism and signaling pathways. Additionally, the compound can participate in enzymatic reactions, serving as a substrate for kinases and polymerases. The CAS number 65444-12-4 uniquely identifies this substance in chemical databases, facilitating its study and application in research and biotechnology. Overall, Cytidine 5'-(tetrahydrogen triphosphate), 2'-amino-2'-deoxy- is significant in molecular biology and biochemistry due to its structural and functional properties.
Formula:C9H17N4O13P3
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Found 1 products.
2'-Amino-2'-deoxycytidine-5'-triphosphate
CAS:<p>2'-Amino-2'-deoxycytidine-5'-triphosphate is an inhibitor of viral RNA polymerase. It is a nucleoside analogue that mimics the natural substrate for the enzyme, 2'-deoxycytidine-5'-triphosphate. This compound binds to the active site of viral RNA polymerases and blocks their ability to synthesize RNA. The compound has been shown to inhibit the replication of norovirus and HIV in cell culture. 2'-Amino-2'-deoxycytidine-5'-triphosphate binds to metal ions in the active site of the enzyme, which prevents its binding with the template strand and prevents elongation of RNA synthesis.</p>Formula:C9H17N4O13P3Purity:Min. 95%Molecular weight:482.17 g/mol
