Dérivés d'acides aminés

<p>L-Tyrosine is a non-essential amino acid with versatile building block properties. It can be used as a reagent in organic synthesis, as a building block for complex compounds, and as a speciality chemical. L-Tyrosine is also useful as a reaction component in the synthesis of peptides and proteins. L-Tyrosine is an important intermediate in the production of pharmaceuticals, agrochemicals, dyes, flavors and fragrances. The CAS number for L-Tyrosine is 60-18-4.</p>

<p>D-Valinol is a fine chemical that has been used as an intermediate in the synthesis of other chemicals. It is also a versatile building block for organic reactions, such as condensation reactions. D-Valinol is a white solid and has CAS No. 4276-09-9. It can be used as a reagent or catalyst in the synthesis of pharmaceuticals, agrochemicals, and other speciality chemicals. D-Valinol is also useful as an intermediate in the production of high quality research chemicals and speciality chemicals.</p>

<p>Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in biological chemistry studies. Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in</p>

<p>Versatile small molecule scaffold</p>

<p>L-m-Tyrosine (3-Hydroxy-L-Phenylalanine) is a non-natural amino acid.</p>

<p>N-Chloroacetyl-L-tyrosine is a synthetic, proteolytic enzyme that hydrolyzes proteins containing the amino acid L-tyrosine. It has been shown to inhibit the growth of bacteria by inhibiting the activity of enzymes involved with protein synthesis and peptide bond formation. N-Chloroacetyl-L-tyrosine inhibits the activity of diazonium salt and conjugates, which are involved in polypeptide synthesis and DNA replication. It also has an inhibitory effect on functional groups, such as hydroxyl, amine, sulfhydryl, carboxylate, phosphate, and phosphoric acid.</p>

<p>5-Methyl-L-norleucine is an amide that is a natriuretic and has been shown to have physiological activities. It has been shown to have restenosis and tumor treatment properties, as well as antimicrobial resistance. 5-Methyl-L-norleucine also acts as a cyclic peptide, which may be due to its disulfide bond. This compound is not only effective in treating microbial infections, but it also has anti-inflammatory properties. 5-Methyl-L-norleucine is found in the genus of plants called "Acorus," so it can be used for plant physiology research.</p>

<p>Fmoc-β-azidoalanine is a cyclic peptide that is synthesized by the Fmoc solid phase peptide synthesis method. It is used as a model for serine proteases, and its ability to bind to other molecules has been shown using molecular modelling and validation. Fmoc-β-azidoalanine has an acidic side chain that can form a disulfide bond with cysteine residues on proteins. This property allows it to be used in crystallography and chemical biology studies. The molecule can also be used in the study of human serum biomolecules.</p>

<p>D-Histidinol dihydrochloride is a non-nucleoside inhibitor of phosphodiesterase enzymes. It has shown to be an effective inhibitor of topoisomerase II and topoisomerase IV, which are essential for DNA replication, repair and recombination. D-Histidinol dihydrochloride has been shown to inhibit the phosphodiesterase activity of several different types of cellular enzymes, including PDE1A4, PDE2A4 and PDE3A4. This drug also has shown to have some structural similarities with the nucleoside diphosphate analogs cAMP and cGMP. D-Histidinol dihydrochloride may be useful in the treatment of diseases that involve damage to DNA or cells.</p>

<p>N2-Lauroyl-L-glutamine is a surfactant that is used in skin care products. It is an amphiphilic molecule that has a hydrophilic head and lipophilic tail, which allows it to form micelles. This surfactant can be found as either the L or D isomer, which are mirror images of each other. The L form is more soluble and less hygroscopic than the D form. N2-Lauroyl-L-glutamine also contains fatty acids, polycarboxylic acid, and monomers. In addition to being used in skin care products, this surfactant can be found in cosmetics such as sunscreens and moisturizers. It also has a polymerization initiator function for silicone polymers and polyurethanes.</p>

<p>Please enquire for more information about O-Benzyl-L-tyrosine methyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Beta-alanine tert-butyl ester hydrochloride is a hydrogenated beta-amino acid ester that is used as a peptidomimetic. It has been shown to be absorbed by the intestine and it can be used to focus on chloride channels in the intestinal cells. Beta-alanine tert-butyl ester hydrochloride is an organic solvent and can also be used as an excipient for drug formulations. The molecule has a benzyl group and a chloride group, which are both substituted with hydrogen atoms.</p>

<p>Please enquire for more information about Fmoc-[D10]Leu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Selenocystine is a non-protein amino acid that belongs to the group of selenoamino acids. Selenocystine is found in plants and microorganisms, where it plays a role in bacterial metabolism. Selenocystine can be synthesized by bacteria from D-glutamate, cysteine, and hydrogen sulfide. It has been shown to have synergistic effects with other compounds such as carbon sources, hydroxyl ions, and subunits. Selenocystine has been shown to inhibit the growth of certain strains of bacteria that are resistant to antibiotics such as penicillin or erythromycin. These effects are mediated through the mitochondrial membrane potential and may also be due to its ability to inhibit microbial respiration.</p>

<p>DL-2-Aminoadipic acid is a metabolite of the amino acid lysine, which is found in many protein-containing foods. It is also synthesized from glutamate, which is an excitatory neurotransmitter and a major regulator of neuronal function. This compound has been shown to have potential as a biomarker for metabolic disorders. DL-2-Aminoadipic acid has been shown to bind to penicillin-binding proteins (PBPs) in the bacterial cell wall and disrupt its formation, leading to the inhibition of peptidoglycan synthesis. DL-2-Aminoadipic acid may also be involved in regulating gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that inhibits the release of excitatory neurotransmitters. DL-2-Aminoadipic acid has also been shown to inhibit HIV infection by binding to lysine residues on the virus envelope protein gp120.</p>