CAS NO:1032-65-1 2'-Deoxycytidine-5'-monophosphoric acid
CAS NO:1032-65-1 NAME:2'-Deoxycytidine-5'-monophosphoric acid MF: C9H14N3O7P APPEARANCE:White powder Purity:98%min Souble:Soluble in water COA:Provide
Categories:
Life Science Chemicals
Biochemicals
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Product introduction
| PRODUCT NAME | 2'-Deoxycytidine-5'-monophosphoric acid |
| CAS NO | 1032-65-1 |
| MW | 307.2 |
| MP | 169-172 °C (dec.) |
| BP | 633.8±65.0 °C(Predicted) |
| EINECS | 213-849-9 |
| DENSITY | 2.01±0.1 g/cm3(Predicted) |
| STORAGE | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:1032-65-1 2'-Deoxycytidine-5'-monophosphoric acid
2'-Deoxycytidine-5'-monophosphate (dCMP) CAS NO:1032-65-1 is a nucleotide that is synthesized by the enzyme cytidine monophosphate synthetase. It has been shown to inhibit the activity of many enzymes, including those involved in DNA synthesis and repair. The incorporation of dCMP into DNA can be used as a probe for studying various biological processes, such as radiation damage and cellular physiology. In addition, it has been shown that dCMP inhibits the growth of human osteosarcoma cells. This drug is also used in combination preparations with other drugs, such as with 5-fluorouracil and doxorubicin, to treat cancer tumors.
2'-Deoxycytidine-5'-monophosphate (dCMP) is a nucleotide that plays a crucial role in the structure and function of DNA. It is a component of the genetic material in cells and participates in various biological processes, including DNA replication and repair. The molecule consists of a cytosine base, a deoxyribose sugar, and a phosphate group, which are essential for the formation of the DNA backbone and base pairing

Applications of CAS NO:1032-65-1 2'-Deoxycytidine-5'-monophosphoric acid
1)Radioactive Labeling in Biological Experiments
2'-Deoxycytidine-5'-monophosphate (dCMP) is utilized in the preparation of radioactive monophosphates;
2)Biosynthesis in DNA
dCMP serves as a basic component of DNA and finds wide usage in medicine, as well as chemical and biochemical reagents. Its biosynthesis is crucial;
3)Structural and Protonation Analysis
The electron density distribution and protonation of dCMP have been analyzed using quantum chemistry methods;
4)Chromatographic Analysis
High-performance liquid chromatography has been employed to optimize the separation of dCMP and its methylated form;
5)Gas-Phase Conformational Studies
The gas-phase structures of deprotonated dCMP and other deoxymononucleotides have been examined using infrared multiple photon dissociation spectroscopy;
6)Enzymatic Actions and DNA Synthesis
Research has focused on the interaction of dCMP and its analogs with enzymes like DNA polymerases and deaminases, revealing their crucial roles in DNA synthesis and metabolism.
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