Deoxycytidine diphosphate
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Names | |
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IUPAC name
2′-Deoxycytidine 5′-(trihydrogen diphosphate)
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Systematic IUPAC name
[(2R,3S,5R)-5-(4-Amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxyoxolan-2-yl]methyl trihydrogen diphosphate | |
Identifiers | |
3D model (
JSmol ) |
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ChemSpider | |
MeSH | deoxycytidine+diphosphate |
PubChem CID
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UNII | |
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Properties | |
C9H15N3O10P2 | |
Molar mass | 387.177 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Deoxycytidine diphosphate is a
phosphoryl
group than CTP .
2'-deoxycytidine diphosphate is abbreviated as dCDP.[1]
Synthesis of Cytidine Nucleotides
Deoxycytidine diphosphate is synthesized through the oxidation-reduction reaction of cytidine 5'-diphosphocholine which is catalyzed by the presence of ribonucleoside-diphosphate reductase.[2] Additionally, ribonucleoside-diphosphate reductase is capable of binding and catalyzing both the formation of deoxyribonucleotides from ribonucleotide.[3]
See also
References
Further reading
- Kennedy, Eugene P.; Louise Fencil Borkenhagen; Sylvia Wagner Smith (1959). "Possible Metabolic Functions of Deoxycytidine Diphosphate Choline and Deoxycytidine Diphosphate Ethanolamine". Journal of Biological Chemistry. 234 (8): 1998–2000. PMID 13673002.
- Reichard, Peter (1962). "Enzymatic Synthesis of Deoxyribonucleotides: I. FORMATION OF DEOXYCYTIDINE DIPHOSPHATE FROM CYTIDINE DIPHOSPHATE WITH ENZYMES FROM ESCHERICHIA COLI". Journal of Biological Chemistry. 237: 3513–3519. PMID 13973714..