2-Thio-UTP

From WikiMD's Wellness Encyclopedia


2-Thio-UTP is a modified nucleotide analog of uridine triphosphate (UTP) where the oxygen atom at the 2-position of the uracil base is replaced by a sulfur atom. This modification imparts unique biochemical properties to the molecule, making it a valuable tool in biochemical and pharmacological research.

Structure and Properties[edit | edit source]

2-Thio-UTP is structurally similar to UTP, with the primary difference being the substitution of a sulfur atom for an oxygen atom at the 2-position of the uracil ring. This substitution can affect the molecule's ability to participate in hydrogen bonding and can alter its interaction with proteins and enzymes.

The chemical formula of 2-Thio-UTP is C9H15N2O14P3S, and it has a molecular weight of approximately 508.2 g/mol.

Biological Activity[edit | edit source]

2-Thio-UTP is known to act as an agonist for certain subtypes of P2Y receptors, which are a class of G protein-coupled receptors (GPCRs) that respond to nucleotides like ATP and UTP. The presence of the thio group can enhance the stability of the nucleotide against enzymatic degradation, making it a useful tool for studying receptor activation and signaling pathways.

Applications in Research[edit | edit source]

2-Thio-UTP is used in various research applications, including:

  • Receptor Studies: It is used to study the activation and signaling of P2Y receptors, particularly in the context of cardiovascular and neurological research.
  • Enzyme Inhibition: The thio modification can make 2-Thio-UTP a potent inhibitor of certain enzymes that normally process UTP, allowing researchers to study enzyme function and regulation.
  • Molecular Biology: It can be used in studies involving RNA synthesis and modification, as the thio group can affect the incorporation and stability of the nucleotide in RNA strands.

Synthesis[edit | edit source]

The synthesis of 2-Thio-UTP typically involves the chemical modification of UTP. The process includes the introduction of a sulfur atom at the 2-position of the uracil base, often using thiolation reagents under controlled conditions to ensure specificity and yield.

Safety and Handling[edit | edit source]

As with many biochemical reagents, 2-Thio-UTP should be handled with care. It is important to follow appropriate safety protocols, including the use of personal protective equipment (PPE) and working in a well-ventilated area or fume hood.

Also see[edit | edit source]

Template:Nucleotides



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Contributors: Prab R. Tumpati, MD