Grupos Protectores

Fmoc-L-Cys(StBu)-OH is a synthetic molecule that is used in pharmaceutical formulations. It can be synthesized from Fmoc-L-Cys and L-serine methyl ester by the chemical ligation of the two molecules. The chloride group at the end of this molecule provides a functional group for conjugation with other biomolecules, such as fatty acids. This molecule has been shown to have high purity with an isolated yield of about 98%.

Cbz-L-glutamine is a water soluble compound that is used in the synthesis of pomalidomide. It is synthesized through a stepwise amide formation from methylamine and ethylene diamine. Cbz-L-glutamine has been shown to have an inhibitory effect on cancer cells, which may be due to its ability to break down hydroxamic acids. This chemical reaction causes the release of hydrogen ions, which leads to the disruption of various cellular processes, such as DNA replication and protein synthesis. The uptake of Cbz-L-glutamine by cancer cells has been shown in tissue culture experiments.

Fmoc-Thr(tBu)-D-Ser(Psi(Me,Me)pro)-OH is a speciality chemical that is used as a reagent for peptide synthesis. It is also useful in the synthesis of complex compounds and scaffolds. This compound has high quality with a CAS number of 56610-81-8. Fmoc-Thr(tBu)-D-Ser(Psi(Me,Me)pro)-OH is a versatile building block that can be used in reactions involving amines and carboxylic acids. Fmoc-Thr(tBu)-D-Ser(Psi(Me,Me)pro)-OH is an intermediate that can be used in the synthesis of many different compounds.

Fmoc-Cys-(CAMTrt)-OH is an amino acid derivative, which is a synthetic compound essential for peptide synthesis. It is derived from natural cysteine, an amino acid found in proteins, and is modified with an Fmoc (9-fluorenylmethoxycarbonyl) protective group and a CAMTrt (trityl sulfonium ion) moiety. This derivative is used primarily in solid-phase peptide synthesis, where the Fmoc group protects the amine during chain elongation, and the CAMTrt group safeguards the thiol function of cysteine, preventing unwanted side reactions during synthesis.

N-Cbz-L-homoserine is a synthetic amino acid that has been used in positron emission tomography (PET) studies to determine the uptake and utilisation of other amino acids by biological systems. It has also been used in biological studies to investigate the mechanism of nucleophilic attack by serine on Cbz-protected homoserine. N-Cbz-L-homoserine has been shown to have hepatotoxic effects and may be carcinogenic, but no evidence indicates it is mutagenic or teratogenic. It is highly reactive with acrylonitrile, which can cause it to produce hydrogen cyanide as a result of nitrile hydrolysis.