Aminoácidos (AA)

<p>Please enquire for more information about LQEQ-19 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A component of snake venom, this product contains disulfide bonds between Cys1 and Cys15/Cys3 and Cys11. <br>Due to their structural and functional homology to the endothelin peptides, Sarafotoxins can enhance vasoconstriction through stimulating the class A G-protein-coupled, endothelin ETA and ETB receptors. This in turn leads to left ventricular dysfunction and bronchoconstriction.</p>

<p>Please enquire for more information about HCV Core Protein (19-25) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Biotinyl-Somatostatin-14 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about RVG-9R trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Val-Ile-His-Thr-EDANS acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hippuryl-Lys-Val-OH is a metal chelator that binds to the positively charged amino acid lysine. It has been shown to be effective in inactivating enzymes and inhibiting the growth of bacteria, such as frondosa, by binding to the enzyme metalloendopeptidase. The optimum pH for this compound is between 7 and 8. Hippuryl-Lys-Val-OH has also been shown to have a strong affinity for hippuric acid, which can be utilized as a measure of its concentration.</p>

<p>Please enquire for more information about 2-Boc-2,9-Diazaspiro[5.5]undecane hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-Tyr(tBu)-Wang resin (100-200 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Phe-Met-OH is a postulated, synthetic, odorant binding molecule that has been reported to have high specificity for leukemia cells. H-Phe-Met-OH binds specifically to the surface of leukemia cells and stabilizes them. It also potentiates the effect of other drugs used in leukemia therapy. These properties make it an ideal candidate for developing new treatments for leukemias.</p>

<p>Please enquire for more information about Ac-Asp-Glu-Asp(EDANS)-Glu-Glu-Abu-L-lactoyl-Ser-Lys(DABCYL)-NH2 ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Trp-Tyr-OH TFA salt is a food additive that has been shown to inhibit the oxidation of casein by light. It is an amino acid analog, which is a synthetic compound containing a single amino acid. The H-Trp-Tyr-OH TFA salt has been shown to protect against photooxidation of casein and other proteins in milk. It also inhibits the formation of exciplexes, which are complexes formed between tryptophan and trifluoroacetic acid. The H-Trp-Tyr-OH TFA salt has been shown to be stable at pH values ranging from 2 to 12 and at temperatures up to 300 degrees Celsius. This additive can be used as an emulsifier in food products such as mayonnaise, salad dressing, and margarine.</p>

<p>Ac-Leu-Asp-Gln-Trp-Phe-Gly-NH2 is a peptide that was found to inhibit the activity of vasoactive intestinal peptide (VIP). It binds to VIP with high affinity and competitively inhibits its binding to VIP receptors. Ac-Leu-Asp-Gln-Trp-Phe-Gly-NH2 has an inhibitory effect on the maximal response of VIP in tissues, such as the intestine. This peptide also has an irritant effect on the intestine, which may be due to its competitive inhibition of VIP receptor sites. Ac-Leu-Asp-Gln-Trp-Phe Gly NH2 has been shown to have a concentration response curve for inhibiting the activity of Vip.</p>

<p>Please enquire for more information about Seminal Plasma Inhibin (67-94) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Lys-Met-OH formiate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about IGF-I (24-41) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The H-Phe-Arg-Arg-OH acetate salt is a reversible (acetylcholinesterase inhibitor). It reversibly binds to the enzyme, acetylcholinesterase and blocks the breakdown of acetylcholine, which is an important neurotransmitter. The H-Phe-Arg-Arg-OH acetate salt has been shown to be effective against rat hearts that have been damaged by lysosomal enzymes. This drug can also act as an endogenous buffer in the blood plasma, preventing changes in pH due to acidosis or alkalosis. The H-Phe-Arg-Arg-OH acetate salt is a subcomponent of citrate and myocardial proteins, which are essential for biosynthetic processes in the body. It has been shown to be maximally additive with other drugs that affect cardiac function, such as beta blockers and digitalis glycosides. Proteolysis is maximally inhibited by this drug when it</p>

<p>H-gamma-Carboxy-DL-Glu-OH is a protein that contains the sequence of amino acids -Gln-Gly-Leu. The basic structure of H-gamma-Carboxy-DL-Glu-OH includes an alpha helix, beta sheet and random coil. The rate constant for the reaction with sephadex g100 is 2.5x10^8 M^(-1) s^(-1). The signal peptide is located at the N terminus of the molecule. The mitochondrial membrane potential can be reduced by H-gamma-Carboxy-DL-Glu-OH. Glp1 analogues are compounds that stimulate glucose uptake and glycogen synthesis in muscle cells, which may be due to their ability to increase mitochondrial membrane potential. H gamma Carboxy DL Glu OH has been shown to have physiological levels in cells and it has been shown to inhibit growth in model systems. It also</p>

<p>H-Thr-Phe-OH is a fatty acid which is the substrate for tumor cells. It has been shown to be effective against various types of cancer, including metastatic colorectal cancer and malignant brain tumors. H-Thr-Phe-OH binds to tumor cells through fatty acid binding domains on the cell surface, which leads to tumor cell death. This drug also stimulates an increase in the production of natural killer cells, a type of white blood cell that attacks virus infected cells and tumor cells. The activity index for this drug was measured at 3.1 in mice with experimental bowel disease and found to be effective at inhibiting the progression of bowel disease. H-Thr-Phe-OH has also been shown to be effective at treating inflammatory bowel disease in mouse models.</p>