3-Methyl-2-buten-1-yl Thiolacetate (CAS 33049-93-3)

3-Methyl-2-buten-1-yl Thiolacetate is a precursor to 3-Methyl-2-butenyl-1-thiol and is very prone to oxidation to the disulfide area. 3-Methyl-2-buten-1-yl Thiolacetate, also referred to as Prenyl Thioacetate, is a chemical compound renowned for its distinctive properties, making it highly valuable in scientific research. Belonging to the prenyl compound family, which encompasses compounds like farnesyl thioacetate and geranyl thioacetate, it holds significance for its ability to modify proteins and peptides. This characteristic renders it an indispensable tool in investigating diverse biological processes. With its broad range of scientific research applications, 3-Methyl-2-buten-1-yl Thiolacetate finds extensive use in modifying peptides and proteins to unravel their biological functionalities. Prenylation, a vital post-translational modification, plays a pivotal role in various biological processes such as signal transduction, protein-protein interactions, and membrane targeting. By utilizing 3-Methyl-2-buten-1-yl Thiolacetate, researchers can explore the impact of prenylation on protein function and localization. The process by which 3-Methyl-2-buten-1-yl Thiolacetate modifies peptides and proteins involves the addition of a prenyl group to a cysteine residue. This prenyl group, derived from isopentenyl pyrophosphate, forms a thioether bond with the cysteine residue. This modification has the potential to induce alterations in the biological activity, stability, and localization of the modified protein, enabling researchers to delve deeper into the intricacies of protein behavior.