Date published: 2025-11-23

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Cytidine 5′-monophosphate (CAS 63-37-6)

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Alternate Names:
5′-CMP; 5′-Cytidylic acid; C-5′-P
Application:
Cytidine 5′-monophosphate is a nucleic acid constituent
CAS Number:
63-37-6
Purity:
≥95%
Molecular Weight:
323.20
Molecular Formula:
C9H14N3O8P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cytidine 5′-monophosphate (CMP) is a molecule present in living cells, serving as a precursor to fundamental molecules like DNA and RNA. As a nucleoside monophosphate, Cytidine 5′-monophosphate consists of a nucleoside linked to a phosphate group. Its significance lies in its involvement in cellular metabolism and the synthesis of molecules. Cytidine 5′-monophosphate finds extensive use in science, with diverse applications in vitro studies. Within cellular metabolism, Cytidine 5′-monophosphate assumes a role, participating in a wide array of biochemical processes. It contributes to the synthesis of DNA, RNA, proteins, and various other molecules. Cytidine 5′-monophosphate plays a role in regulating gene expression and signaling pathways.


Cytidine 5′-monophosphate (CAS 63-37-6) References

  1. Charge transfer complexes of adenosine-5'-monophosphate and cytidine-5'-monophosphate with water-soluble cobalt(II) Schiff base complexes in aqueous solution.  |  Boghaei, DM. and Gharagozlou, M. 2006. Spectrochim Acta A Mol Biomol Spectrosc. 63: 139-48. PMID: 15950536
  2. Structure of Staphylococcus aureus cytidine monophosphate kinase in complex with cytidine 5'-monophosphate.  |  Dhaliwal, B., et al. 2006. Acta Crystallogr Sect F Struct Biol Cryst Commun. 62: 710-5. PMID: 16880539
  3. Interactions of 1,12-diamino-4,9-dioxadodecane (OSpm) and Cu(II) ions with pyrimidine and purine nucleotides: adenosine-5'-monophosphate (AMP) and cytidine-5'-monophosphate (CMP).  |  Lomozik, L., et al. 2006. J Inorg Biochem. 100: 1781-9. PMID: 16899296
  4. Separation of cytidine 5'-triphosphate biosynthesized from cytidine 5'-monophosphate on ion-exchange resin and HPLC analysis of cytidine compounds.  |  Shi, LE., et al. 2008. Appl Biochem Biotechnol. 144: 1-14. PMID: 18415982
  5. Phosphorylation of uridine and cytidine by uridine-cytidine kinase.  |  Qian, Y., et al. 2014. J Biotechnol. 188: 81-7. PMID: 25160914
  6. Adsorption of nucleotides on biomimetic apatite: The case of cytidine 5' monophosphate (CMP).  |  Choimet, M., et al. 2015. J Colloid Interface Sci. 456: 132-7. PMID: 26117294
  7. Low energy secondary electron induced damage of condensed nucleotides.  |  McKee, AD., et al. 2019. J Chem Phys. 150: 204709. PMID: 31153208
  8. Efficient One-Pot Synthesis of Cytidine 5'-Monophosphate Using an Extremophilic Enzyme Cascade System.  |  Li, Z., et al. 2020. J Agric Food Chem. 68: 9188-9194. PMID: 32806118
  9. Tumor Microenvironments-Adaptive Apoptotic Effects of Cytidine 5'-monophosphate-Capped Gold Nanoclusters.  |  Zhang, CX., et al. 2022. ACS Appl Bio Mater. 5: 3452-3460. PMID: 35714365
  10. Adsorption separation of guanosine 5'-Monophosphate and cytidine 5'-Monophosphate by mixed-mode Resin HD-1: Experimental study and mathematical modeling.  |  Jiao, P., et al. 2022. J Chromatogr A. 1678: 463359. PMID: 35914411
  11. Crystal structure of 4,4'-(diazenediyl)dipyridinium nitrate perchlorate.  |  Qiu, QM., et al. 2022. Acta Crystallogr E Crystallogr Commun. 78: 897-899. PMID: 36072523
  12. The Full Cytosine-Cytosine Base Paring: Self-Assembly and Crystal Structure.  |  Li, Z., et al. 2023. Chemistry. 29: e202203979. PMID: 36757279
  13. Cell-free regeneration of ATP based on polyphosphate kinase 2 facilitates cytidine 5'-monophosphate production.  |  Teng, F., et al. 2023. Enzyme Microb Technol. 165: 110211. PMID: 36804179
  14. N-glycolylneuraminic acid as a carbohydrate cancer biomarker.  |  Wang, J., et al. 2023. Transl Oncol. 31: 101643. PMID: 36805917

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cytidine 5′-monophosphate, 5 g

sc-211159
5 g
$109.00