Peptide Synthesis

Please enquire for more information about H-Ile-Asn-OH trifluroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Fmoc-Val-Wang resin is a versatile tool used in peptide synthesis. It is commonly employed in the production of peptides for various applications, including research and pharmaceutical development. This resin facilitates the attachment of amino acids to create peptide chains with high precision and efficiency.

Fmoc-rink amide resin is a synthetic, radionuclide, and constant polymer. It is used in chemical ligation to produce peptides from amines and growth factors. Fmoc-rink amide resin also has antimicrobial properties due to its ability to inhibit the growth of bacteria and fungi by binding to their cell membranes. This polymer can be conjugated with growth factor or antimicrobial peptides for use as a therapeutic agent or used in the production of antibodies against a particular protein. Fmoc-rink amide resin has been shown to increase epidermal growth factor (EGF) uptake into cells by targeting EGF receptors on the cell surface.

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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.

N3-Orn(Boc) cyclohexylamine is a chemical intermediate that is used in the synthesis of complex compounds. It can be used as a building block or an intermediate in the synthesis of many fine chemicals, such as pharmaceuticals, agrochemicals, and fragrances. N3-Orn(Boc) cyclohexylamine is also used in reactions involving amines and alcohols to produce useful scaffolds. This chemical product has been shown to be safe for human use with no significant adverse side effects at doses up to 100mg/kg body weight.

Pexiganan acetate is the acetate salt form of a polymyxin B derivative that has potent antimicrobial activity against both Gram-positive and Gram-negative bacteria. It has been shown to be effective in the treatment of tissue infections, especially those caused by human pathogens such as Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. Pexiganan also has significant activity against Mycobacterium tuberculosis and other mycobacteria. The mechanism of action for pexiganan is not fully understood but it may involve the inhibition of bacterial cell wall synthesis, or the disruption of bacterial membranes. Pexiganan was originally isolated from a marine sponge off the coast of Australia in 1961. It had been classified as an antimicrobial peptide (AMP) because of its chemical structure, which includes a polymyxin B moiety. Pexiganan’s AMP classification was later challenged when researchers found that it did

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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%.

Please enquire for more information about L-Lysyl-L-phenylalanyl-L-lysine trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Crosslinker reacting rapidly with primary amines.  It is used as a protein crosslinker where it reacts with cysteine to yield specific conjugates.  The cyclohexane bridge confers added stability to the maleimide group making it ideal for maleimide activation of proteins.  It is soluble in water and many other aqueous buffers although it is less stable then in DMSO or DMF.

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.

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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.

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