Description
A pyrimidone that is cytosine bearing an N(4)-acetyl substituent.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C6H7N3O2 | 0 | 153.141 |
-acetylcytosine.svg)
Nomenclature
| IUPAC | SMILES | InChI | InChIKey | Synonyms |
|---|---|---|---|---|
| N-(2-oxo-1,2-dihydropyrimidin-4-yl)acetamide | O=C1NC=CC(=N1)NC(=O)C | InChI=1S/C6H7N3O2/c1-4(10)8-5-2-3-7-6(11)9-5/h2-3H,1H3,(H2,7,8,9,10,11) | IJCKBIINTQEGLY-UHFFFAOYSA-N |
|
Citations
- Malone, RJ, et al. 2003. Singlet excited-state lifetimes of cytosine derivatives measured by femtosecond transient absorption. Photochemistry and Photobiology. 77(2).
- Völkel, W, et al. 1998. Chlorothioketene, the ultimate reactive intermediate formed by cysteine conjugate beta-lyase-mediated cleavage of the trichloroethene metabolite S-(1,2-Dichlorovinyl)-L-cysteine, forms cytosine adducts in organic solvents, but not in aqueous solution. Chemical Research in Toxicology. 11(9).
- Wu, Z, et al. 2009. Stereoselective approach to the Z-isomers of methylenecyclopropane analogues of nucleosides: a new synthesis of antiviral synguanol. Nucleosides, Nucleotides & Nucleic Acids. 28(3).
- Zgierski, MZ, et al. 2005. Ab initio study of a biradical radiationless decay channel of the lowest excited electronic state of cytosine and its derivatives. The Journal of Chemical Physics. 123(8).
- Zhou, D, et al. 2013. Molecular structure and vibrational spectra of N4-acetylcytosine. Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy. 112.
- Zhou, S, et al. 2004. Synthesis and antiviral activity of (Z)- and (E)-2,2-[bis(hydroxymethyl)cyclopropylidene]methylpurines and -pyrimidines: second-generation methylenecyclopropane analogues of nucleosides. Journal of Medicinal Chemistry. 47(3).