5-iododeoxycytidine – CAS 611-53-0
5-iododeoxycytidine – CAS 611-53-0 is synthesised by Sigut Labs (Prague, Czech Republic).
Purity (LC-MS)
95%+
Package contents
5-iododeoxycytidine
This compound is for research use only. We do not sell to patients.
Amount
| 5 g | € 300 | Stock | ||
| 25 g | € 550 | Stock | ||
| Do you want custom amount? | Custom amount | |||
Amount
5 g
€ 300
Stock
25 g
€ 550
Stock
Do you want custom amount?
Custom amount
Characterisation
CAS: 611-53-0
IUPAC name: 4-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidin-2-one
Other names: ibacitabine; iododeoxycytidine
Molecular weight: 353.11 g/mol
Molecular formula: C9H12IN3O4
InChI: InChI=1S/C9H12IN3O4/c10-4-2-13(9(16)12-8(4)11)7-1-5(15)6(3-14)17-7/h2,5-7,14-15H,1,3H2,(H2,11,12,16)/t5-,6+,7+/m0/s1
Description
5-iododeoxycytidine (Ibacitabine) is an iodinated analog of deoxycytidine used topically in the treatment of herpes labialis.
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Payment
- Payment terms 30 days net
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References
- Creasey, W. A. (1963). Studies on the Metabolism of 5-Iodo-2′-deoxycytidine in Vitro: PURIFICATION OF NUCLEOSIDE DEAMINASE FROM MOUSE KIDNEY. Journal of Biological Chemistry, 238(5), 1772-1776.
- Münzel, M., Lischke, U., Stathis, D., Pfaffeneder, T., Gnerlich, F. A., Deiml, C. A., … & Carell, T. (2011). Improved synthesis and mutagenicity of oligonucleotides containing 5‐hydroxymethylcytosine, 5‐formylcytosine and 5‐carboxylcytosine. Chemistry–A European Journal, 17(49), 13782-13788.
- Cahová, H., & Jäschke, A. (2013). Nucleoside‐Based Diarylethene Photoswitches and Their Facile Incorporation into Photoswitchable DNA. Angewandte Chemie International Edition, 52(11), 3186-3190.
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