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N4-Acetylcytidine

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N4-Acetylcytidine Basic information

Product Name:
N4-Acetylcytidine
Synonyms:
  • 4-Acetyl-1-(beta-D-ribofuranosyl)cytosine
  • ACETYL CYTOSINE
  • N4-ACETYLCYTIDINE
  • 4-Acetylcytidine
  • Acetamide, N-(1,2-dihydro-2-oxo-1-beta-D-ribofuranosyl-4-pyrimidinyl)-
  • Acetylcytidine
  • N4-Ac-rC
  • n-acetyl-cytidin
CAS:
3768-18-1
MF:
C11H15N3O6
MW:
285.25
EINECS:
223-195-6
Product Categories:
  • Biochemicals and Reagents
  • Nucleoside Analogs
  • Nucleic acids
  • Nucleosides, Nucleotides, Oligonucleotides
  • Modified(deoxy)nucleoside
Mol File:
3768-18-1.mol
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N4-Acetylcytidine Chemical Properties

Melting point:
199 °C (dec.)(lit.)
Density 
1.72±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
DMSO (Slightly, Heated), Methanol (Slightly, Heated)
form 
Solid
pka
10.21±0.20(Predicted)
color 
White to Pale Yellow
PH
<1.5
λmax
247,297 (pH 7)
CAS DataBase Reference
3768-18-1(CAS DataBase Reference)
NIST Chemistry Reference
Cytidine, n-acetyl-(3768-18-1)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
36-36/37/39-26
WGK Germany 
3
HS Code 
29335990

MSDS

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N4-Acetylcytidine Usage And Synthesis

Description

N4-Acetylcytidine is a modified nucleoside and endogenous urinary nucleoside product of the degradation of tRNA. N4-Acetylcytidine is a biological marker for various cancers with elevated concentrations present in urine. tRNA has been shown to be excreted in abnormal amounts in the urine of cancer patients. tRNA from neoplastic tissue had a much more rapid turnover rate than the tRNA from the corresponding normal tissue. Evidence indicates that methylation of tRNA occurs only after synthesis of the intact macromolecule. Because there are no specific enzyme systems to incorporate the modified nucleosides into the macromolecular nucleic acid, these nucleosides once released in the process of tRNA turnover cannot be reutilized, nor are they further degraded, but are excreted in urine.
N4-Acetylcytidine is also a partially protected cytidine and therefore can be used as a synthetic building block to prepare further derivatized nucleosides such as 2’,3’-dideoxycytidine.

Uses

N4-Acetylcytidine (cas# 3768-18-1) is a nucleotide-derived metabolite used as biomarkers for diagnosis of inflammation-related diseases.

Definition

ChEBI: N(4)-acetylcytidine is cytidine in which one of the exocyclic amino hydrogens is substituted by an acetyl group. It has a role as a metabolite. It is a member of cytidines, a member of acetamides and a secondary carboxamide.

Biosynthesis

N4-acetylcytidine (ac4C) is a post-transcriptional modification of RNA that is conserved across all domains of life. All characterized sites of ac4C in eukaryotic RNA occur in the central nucleotide of a 5’-CCG-3’ consensus sequence. However, the thermodynamic consequences of cytidine acetylation in this context have never been assessed due to its challenging synthesis. Here we report the synthesis and biophysical characterization of ac4C in its endogenous eukaryotic sequence context. First, we develop a synthetic route to homogenous RNAs containing electrophilic acetyl groups. Next, we use thermal denaturation to interrogate the effects of ac4C on duplex stability and mismatch discrimination in a native sequence found in human ribosomal RNA. Finally, we demonstrate the ability of this chemistry to incorporate ac4C into the complex modification landscape of human tRNA, and use duplex melting combined with sequence analysis to highlight a potentially unique enforcing role for ac4C in this setting. By enabling the analysis of nucleic acid acetylation in its physiological sequence context, these studies establish a chemical foundation for understanding the function of a universally-conserved nucleobase in biology and disease.
Site-Specific Synthesis of N4-Acetylcytidine in RNA Reveals Physiological Duplex Stabilization
https://www.biorxiv.org/content/10.1101/2021.11.12.468326v1.full.pdf

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