Date published: 2026-4-26

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5-Chloro-2′-deoxycytidine (CAS 32387-56-7)

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Application:
5-Chloro-2′-deoxycytidine is a tumor-selective radiosensitizer
CAS Number:
32387-56-7
Purity:
≥95%
Molecular Weight:
261.66
Molecular Formula:
C9H12ClN3O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-Chloro-2′-deoxycytidine is a modified nucleoside that is primarily used in the study of nucleic acid analogs and their incorporation into DNA. This compound is of particular interest in the field of molecular biology and genetics, where it is employed to understand the effects of halogenated nucleosides on DNA stability, replication, and repair mechanisms. As a cytidine analog, 5-Chloro-2′-deoxycytidine is useful in the synthesis of oligonucleotides with altered properties, which can be pivotal in studying protein-DNA interactions and the role of epigenetic modifications. Additionally, the chlorine substituent at the 5-position of the pyrimidine ring makes this compound a useful tool for probing the structural dynamics of DNA, as it can influence base-pairing and the overall conformation of the nucleic acid. Researchers also investigate the compound′s use in the labeling and detection of DNA, as it can provide insights into the localization and expression of specific genes.


5-Chloro-2′-deoxycytidine (CAS 32387-56-7) References

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  2. Plasma pharmacokinetics and oral bioavailability of 3,4,5,6-tetrahydrouridine, a cytidine deaminase inhibitor, in mice.  |  Beumer, JH., et al. 2008. Cancer Chemother Pharmacol. 62: 457-64. PMID: 18008070
  3. Ability of hypochlorous acid and N-chloramines to chlorinate DNA and its constituents.  |  Stanley, NR., et al. 2010. Chem Res Toxicol. 23: 1293-302. PMID: 20593802
  4. Chemical and cytokine features of innate immunity characterize serum and tissue profiles in inflammatory bowel disease.  |  Knutson, CG., et al. 2013. Proc Natl Acad Sci U S A. 110: E2332-41. PMID: 23754421
  5. Radiation, pool size and incorporation studies in mice with 5-chloro-2'-deoxycytidine.  |  Santos, O., et al. 1990. Int J Radiat Oncol Biol Phys. 19: 357-65. PMID: 2394614
  6. Selective radiosensitization and cytotoxicity of human melanoma cells using halogenated deoxycytidines and tetrahydrouridine.  |  Lawrence, TS. and Davis, MA. 1989. Int J Radiat Oncol Biol Phys. 16: 1243-6. PMID: 2715074
  7. Validation of a sensitive LC/MSMS method for chloronucleoside analysis in biological matrixes and its applications.  |  Noyon, C., et al. 2016. Talanta. 154: 322-8. PMID: 27154681
  8. In vitro and in vivo radiation sensitization by the halogenated pyrimidine 5-chloro-2'-deoxycytidine.  |  Russell, KJ., et al. 1986. Cancer Res. 46: 2883-7. PMID: 3698014
  9. Sensitization to X ray by 5-chloro-2'-deoxycytidine co-administered with tetrahydrouridine in several mammalian cell lines and studies of 2'-chloro derivatives.  |  Perez, LM. and Greer, S. 1986. Int J Radiat Oncol Biol Phys. 12: 1523-7. PMID: 3759575
  10. Five-chlorodeoxycytidine and biomodulators of its metabolism result in fifty to eighty percent cures of advanced EMT-6 tumors when used with fractionated radiation.  |  Greer, S., et al. 1995. Int J Radiat Oncol Biol Phys. 32: 1059-69. PMID: 7607927

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Chloro-2′-deoxycytidine, 1 mg

sc-284602
1 mg
$213.00

5-Chloro-2′-deoxycytidine, 2 mg

sc-284602A
2 mg
$421.00