Amino Acids (AA)

<p>Please enquire for more information about FA-Lys-Leu-OH 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-Asp(OtBu)-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>Intermediate in the synthesis of idelalisib (CAL 101)</p>

<p>Please enquire for more information about N-Boc-cis-3,4-methylene D-proline 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-Angiotensin I/II (1-7) Biotinyl-Asp-Arg-Val-Tyr-Ile-His-Pro-OH 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 Z-Gly-Gly-Phe-bNA 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 AMCA-Glu-Glu-Lys-Pro-Ile-Ser-Phe-Phe-Arg-Leu-Gly-Lys(biotinyl)-NH2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(4-Phenylbutoxy)benzoic acid is an organic compound that is produced by the reaction of 4-hydroxybenzoic acid with a Grignard reagent. The 4-hydroxybenzoic acid reacts with magnesium to form magnesium chloride and p-hydroxybenzoic acid, which then reacts with a Grignard reagent to form the desired product. This compound has been used in wastewater treatment and as an intermediate in the synthesis of dyes, perfumes, and pharmaceuticals. 4-(4-Phenylbutoxy)benzoic acid has also been used as a starting material for synthesizing other compounds such as chlorobenzene and p-hydroxybenzoic acid.</p>

<p>Please enquire for more information about LIP2 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ala-Asn-Phe-Leu-Val-Trp-Glu-Ile-Val-Arg-Lys-Lys-Pro is a monoclonal antibody that inhibits proliferation of endothelial cells. It binds to PDGF, which is a potent growth factor. This drug has been shown to inhibit the growth of vascular smooth muscle cells in vitro and in vivo by inhibiting cholesterol synthesis. H-Ala-Asn-Phe-Leu-Val-Trp has also been shown to have antagonist effects on basic fibroblast growth factor and cyclic AMP, which are important mediators of choroidal neovascularization and blood vessel formation.</p>

<p>Z-Phe-His-Leu-OH is a monoclonal antibody that is used in the diagnosis and treatment of prostate cancer. This drug binds to the extracellular domain of the human prostate epithelial cell antigen (PSA), which is overexpressed in prostate cancers. Z-Phe-His-Leu-OH can be used in combination with other drugs for the treatment of prostate hyperplasia, such as angiotensin II receptor antagonists or 5α reductase inhibitors. The conformational epitope of this antibody has been demonstrated by immunohistochemical analysis on human tissues.</p>

<p>Please enquire for more information about CART (55-76) (rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>D-Ala2,N-Me-Phe4,methionin(O)-ol5)-Enkephalin trifluoroacetate salt H-Tyr-D-Ala-Gly-N-Me-Phe-methionin(O)-ol trifluoroacetate salt is an analog of the endocannabinoid neurotransmitter, anandamide. It has been shown to be effective in the treatment of autoimmune diseases such as multiple sclerosis and inflammatory bowel disease. D-(3R)-3-[(1S,2R,3R,5R) -3-[2-(2,6 dichlorophenyl)ethenyl] -1H -indole]-1 -butanamine trifluoroacetate salt has been shown to inhibit the replication of a number of viruses including human immunodeficiency virus type 1 (HIV). This drug also inhibits the growth of organisms that are resistant</p>

<p>Bradykinin is a peptide hormone that has been found to act through the bradykinin receptor. It has also been found to be an antagonist of the receptor, as it inhibits the growth of cells that are stimulated by bradykinin. This drug can be used for the treatment of asthma and other inflammatory diseases. The sequence of this drug is D-Arg0, Hyp 3,D-Phe7)-Bradykinin trifluoroacetate salt H-D-Arg-Arg-Pro-Hyp-Gly-Phe-Ser-D-Phe-Phe-Arg-OH trifluoroacetate salt.</p>

<p>Lysine acetimidate is a reactive compound that can be activated by the addition of an acid. Lysine acetimidate is a potent activator of macrophages and other inflammatory cells. It has been used in experimental models to study bowel disease and repair mechanisms. In these models, lysine acetimidate has shown to have anti-inflammatory effects, which may be due to its ability to decrease the production of pro-inflammatory cytokines by immune cells. The metabolic disorder caused by lysine acetimidate is still being studied. Lysine acetimidate also has immunomodulatory effects, as it can inhibit the synthesis of epidermal growth factor (EGF) in lung cells and cause damage to alveolar type II cells in the lung.</p>

<p>IDR-1 is a peptide that is derived from the sequence of the human typhimurium protein. IDR-1 has been shown to have anti-inflammatory properties and modulates immune responses in mice. In particular, IDR-1 inhibits neutrophil chemotaxis by inhibiting formyl peptide receptor signaling. This peptide also inhibits bacterial chemokines, which are important for the recruitment of neutrophils. IDR-1 also has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and pertussis.</p>

<p>Please enquire for more information about H-Ala-Ala-Pro-Leu-pNA·HCl 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-His-Phe-bNA·2 HCl 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-Pro-His-Val-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dynorphin A (1-13) H-Tyr-Gly-Gly-Phe-Leu <br>Dynorphin A (1-13) H-Tyr-Gly-Gly-Phe is a synthetic substrate for κ opioid receptors. It also has antinociceptive properties and may be used as a potential analgesic drug. Dynorphin A (1-13) H-Tyr-Gly-Gly <br>Dynorphin A (1-13) H Tyr Gly Gly Phe Leu D Arg Arg Arg Ile Arg Pro Lys Leu Lys OH has been shown to be effective in the treatment of humans and rats with cardiac or physiological function problems. Dynorphin A (1 13) H Tyr Gly Gly Phe Leu D Arg Arg Arg Ile Arg Pro Lys Leu Lys OH increases serum prolactin levels in humans, which may indicate that it stimulates the hypothalamus to</p>

<p>Please enquire for more information about Boc-Val-Arg-AMC•HCl 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-N-Me-Asp(OBzl)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-6-methoxypyridine (2CMP) is a potent antagonist that binds to copper chloride, inhibiting its ability to activate aryl chlorides. This chemical has been shown to have anti-angiogenic effects in human cancer cells and can be used for the treatment of cancer. 2CMP has also been shown to be effective at blocking angiogenesis in mice with breast cancer. 2CMP is synthesized through an asymmetric synthesis process, which involves the use of a dipole and molecular docking analysis.</p>

<p>H-Phe-AMC Trifluoroacetate salt is a synthetic, protease inhibitor that inhibits the activity of serine and cysteine proteases. It binds to the active site of these enzymes and blocks their function. H-Phe-AMC trifluoroacetate salt has been used in food chemistry to hydrolyze proteins, and can be used to measure enzyme activities. This product also has been shown to have biological functions such as the inhibition of molting, physiological function, and the prevention of carcinogenesis.</p>

<p>H-Met-Glu-OH is a synthetic substance that inhibits the activity of cytochrome P450. It binds to cells, specifically platelets, and causes degranulation and activation of calcium ion channels. This leads to an increase in intracellular calcium ions that triggers blood clotting. H-Met-Glu-OH has been shown to be effective in treating cardiovascular diseases such as high blood pressure and heart arrhythmia. Clopidogrel is often used with H-Met-Glu-OH to prevent platelet aggregation, which would otherwise block the effectiveness of H-Met-Glu-OH.<br>H-Met-Glu has a high affinity for collagen and binds more efficiently to platelets than other cell types. This binding is reversible, which allows for repeated doses without causing toxicity or adverse effects on healthy cells.</p>

<p>Ac-Gly-Pro-AFC is a dipeptidyl peptidase inhibitor that inhibits the action of protein-degrading enzymes called peptidases. Ac-Gly-Pro-AFC has been shown to be effective in treating diabetes by inhibiting the activity of fibroblast activation protein, which is involved in the development of diabetes. Ac-Gly-Pro-AFC also has an inhibitory effect on the enzyme connect, which is involved in cellular proliferation and differentiation. Clinical trials have been conducted to evaluate the efficacy of this drug for treatment of diabetic nephropathy with promising results. Ac-Gly-Pro-AFC has also been shown to have a beneficial effect on collagen synthesis and inhibition of proinflammatory cytokine release from activated macrophages.</p>

<p>Ac-Ile-Glu-Pro-Asp-pNA is a synthetic peptide that has been shown to induce apoptosis in tumor cells. The peptide was found to cause cell lysis and necrotic cell death, which is associated with the activation of serine proteases. Ac-Ile-Glu-Pro-Asp-pNA also has been shown to have a toxicity profile similar to other apoptotic agents such as staurosporine, but it has not been tested for its ability to kill cancer cells without causing damage to healthy cells. Ac-Ile-Glu-Pro-Asp-pNA induces mitochondrial membrane depolarization and protein synthesis inhibition in K562 cells, which are human erythroleukemia cells. This peptide also has shown an ability to bind with monoclonal antibodies and inhibit the growth of casein.</p>

<p>Please enquire for more information about TRAF6 Control Peptide 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 Tyr-Lys-Gly-(Cyclo(Glu26-Lys29),Pro34)-Neuropeptide Y (25-36) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Tyr-Phe-OH is a peptide that is derived from the amino acid sequence of human epidermal growth factor and has been shown to inhibit HIV infection in vitro. H-Tyr-Phe-OH binds to the dna binding site on the protein gp120, which is essential for viral binding to cells and subsequent infection. The peptide has also been shown to bind to serum aminotransferase levels and produce an antibody response in humans. This peptide has biological properties that may be useful for treatment of many infectious diseases, such as hepatitis and HIV infection.</p>

<p>Edelfosine is a phospholipid that selectively binds to nuclear DNA, leading to apoptosis. It also binds to the G-protein coupled receptors and inhibits the release of Ca2+ from intracellular stores. Edelfosine has been shown to inhibit the growth of Leishmania in vitro as well as in vivo. This drug is being studied for its potential use in inflammatory bowel diseases, such as Crohn's disease and ulcerative colitis.</p>

<p>Please enquire for more information about (4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid 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-4-(neopentyloxysulfonyl)-Abu-OH (S)-2-(Fmoc-amino)-4-neopentyloxysulfonyl-butyric acid 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 (D-Trp6)-LHRH (2-10) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Suc-Val-Pro-Phe-SBzl is a synthetic subtilisin that has been modified to have an enhanced binding affinity for the enzyme's substrate. The enzyme's specificity and reactivity has been improved by adding a chloromethyl ketone group to the amino acid sequence. Suc-Val-Pro-Phe-SBzl is a serine protease inhibitor and has been shown to inhibit the activity of subtilisins, including subtilisin BPN' and Bacillus amyloliquefaciens subtilisin. It also inhibits peptidases and proteinases, which may be due to its ability to bind to the active site of these enzymes.</p>

<p>H-Gly-Gly-Met-OH is a hydrophobic amino acid with a decelerated reaction. It has been shown to modulate the growth of organisms, such as Staphylococcus aureus and Streptococcus pneumoniae. This molecule also has aspirin-like activity against S. aureus and can be used for cavity prevention. H-Gly-Gly-Met-OH is effective in inhibiting the growth of S. aureus, but not against Streptococcus pneumoniae. The test organism used in this study was Escherichia coli K12. H-Gly-Gly-Met-OH has been shown to have sequences that are similar to those found in kinetically slow peptides and tripeptides, which may explain its stability when encapsulated in liposomes for oral administration.</p>

<p>Please enquire for more information about H-Thr-Pro-OH·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Lys-Lys-Lys-Lys-OH acetate salt is a fatty acid that has been shown to form stable complexes with DNA and act as an intercalator. It also provides a repair mechanism for DNA, which may be due to its ability to bind to stem cell factor (SCF) and increase the proliferation of stem cells. H-Lys-Lys-Lys-Lys-OH acetate salt has significant cytotoxicity against viruses, such as human immunodeficiency virus type 1 (HIV1) and human papilloma virus type 16. This drug can also be used as an adjuvant in monoclonal antibody production by stimulating the production of antibodies from mouse spleen cells. H-Lys-Lys-Lys-Lys-OH acetate salt has been shown to inhibit the growth of E. coli K12 and Bacteria Corynebacterium diphtheriae, both of</p>

<p>The melanocortin-4 receptor (MC4R) is a G protein-coupled receptor that mediates the protective and cytoprotective activities of endogenous melanocortins. This receptor has been shown to be an important target for neuroprotective agents. The MC4R is expressed in the central nervous system, peripheral nervous system, and other tissues where it may have a role in regulating energy homeostasis. The N-terminal amino acid sequence of the human MC4R ligand is H-His-Phe-Arg-Trp-OH. This peptide has been shown to have potent agonist potency at the MC4R with a Kd of 0.2 nM and an EC50 of 2 nM.</p>

<p>For-Met-Phe-OH is a synthetic peptide that mimics the amino acid sequence of the human body's natural collagen. It is used as a building block for developing collagen gels, which are used in clinical pathology to identify and quantify cells. For-Met-Phe-OH has been shown to stimulate colony-stimulating factor, which regulates cell proliferation and differentiation. This peptide also plays a role in cell signaling pathways that regulate cell growth and differentiation. For-Met-Phe-OH has been shown to have anti-inflammatory effects by inhibiting the production of inflammatory cytokines.</p>

<p>Please enquire for more information about Z-Arg-Arg-pNA·2 HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Val-Tyr-Val-OH is a water soluble polymer that has a sulfamic acid group and a hydroxyl group. The polymer film is used as an additive for cellulose acetate, which is used in the manufacture of films, lacquers, and adhesives. H-Val-Tyr-Val-OH increases the solubility of the cellulose acetate in hydrochloric acid and reduces its tendency to dissolve in water. H-Val-Tyr-Val-OH also has a high degree of uv absorption. Constant techniques are used for analytical chemistry, such as gas chromatography and nuclear magnetic resonance spectroscopy, to study the surface properties of micelles formed from H-Val-Tyr-Val-OH.</p>

<p>Please enquire for more information about Gastric Inhibitory Polypeptide (1-30) amide (porcine) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The Fmoc-His(Boc)-OPfp is a synthetic peptide that has been shown to bind to angiotensin. It is chemically reactive and can be used in diagnostic assays for the detection of angiotensin. The Fmoc-His(Boc)-OPfp can also be used as a feedback control for sequence analysis, where it monitors the reaction sequence by binding to the last amino acid in the peptide. This binding prevents the formation of an enzyme with the enzyme reaction necessary for cell wall biosynthesis, inhibiting protein synthesis and cell division.</p>

<p>Please enquire for more information about IL-6 (88-121) (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 Acetyl-Hirudin (55-65) (desulfated) Ac-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Hydroxy-3-methylglutaric acid is an organic acid that is a valuable intermediate in the chemical production of epidermal growth factor. 3-Hydroxy-3-methylglutaric acid also has been shown to be useful as a reagent for the detection of bacterial strains, including E. coli, Salmonella enterica, and Pseudomonas aeruginosa. The enzyme activities of 3-hydroxy-3-methylglutaric acid are not well understood, but it has been shown to have effects on congestive heart failure and bowel disease. 3-Hydroxy-3-methylglutaric acid may be used in the treatment of inflammatory bowel disease due to its ability to inhibit certain enzymes responsible for inflammation and pain. The long term toxicity and symptoms associated with 3-hydroxy-3-methylglutaric acid have not yet been studied, but it has been shown to have no effect on cardiac function</p>

<p>Please enquire for more information about H-Hyp (Bzl)-OH·HCl 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 HCV NS4A Protein (22-33) (FDA strain) 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 (D-His2,D-Trp6)-LHRH 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 Met-Enkephalin acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Tyr-Trp-OH is a synthetic, constant ligand for nuclear receptors. It has been shown to be active in the cerebral cortex, with a brain concentration of about 1 µM at steady state. This compound has been shown to be an agonist of the transcription factor nuclear receptor peroxisome proliferator-activated receptor alpha (PPARα) and can be used as a potential therapeutic agent for Alzheimer's disease. H-Tyr-Trp-OH has also been shown to enhance phosphorylation of the microtubule protein tau in cultured cortical neurons, which may have implications for the treatment of Parkinson's disease.</p>

<p>Ac-His-His-Gly-His-OH is a lysine ligand with an acetyl group and two histidine residues. Acetylation of the hydroxyl group on the lysine residue is necessary for binding to metal ions, such as protonation. This molecule has been shown to have five different protonation states at neutral pH. The protonated form has been found to be more soluble in water than the deprotonated form. Acetylation of both lysines in the molecule leads to hydrolytic cleavage of the amide bond, which causes it to become insoluble in water. Acetylation also alters chemical properties, such as changes in color; for example, this molecule exhibits dichroism when viewed under polarized light.</p>

<p>Please enquire for more information about Oxyntomodulin (human, mouse, rat) 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 Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone 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 uPAR (84-95) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Gliadorphin is a peptide that occurs in cow's milk. It has been shown to be effective against bacterial translocation, which is the passage of bacteria from the gut into other parts of the body. Gliadorphin also has a safety profile, with no observed adverse effects in animal studies and dietary trials. The biological samples used for this study were casein and urine samples. The antibodies used were polyclonal antibodies and Gliadorphin was tested for its ability to bind to bacterial proteins in vivo. Hydration may be necessary for optimal absorption of gliadorphin, as dehydration can affect immune reaction. Gliadorphin does not have any known side effects or drug interactions, but it should not be used by people with an allergy to casein or those who are allergic to mammalian serine proteases (such as trypsin).</p>

<p>Please enquire for more information about N-(2-Amino-ethyl)-2-(benzyl-phenyl-amino)-acetamide 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 Adrenomedullin (11-50) (rat) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Leu-Leu-OMe·HCl is a reagent that is used as a reaction component. It is soluble in water and has a pH of 2.0. Leu-Leu-OMe·HCl is also useful for the synthesis of building blocks and fine chemicals with versatile applications, such as bioactive compounds and pharmaceuticals. This chemical has been shown to react with other molecules to form a variety of complex compounds, making it useful for research purposes. This compound can be used as an intermediate in the synthesis of many different products, including pharmaceuticals, pesticides, and insecticides.</p>

<p>Please enquire for more information about Ac-Lys-Tyr-Val-Nle-Gly-His-Phe-Arg-Trp-Asp-Arg-Phe-Gly-NH2 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 Gastric Inhibitory Polypeptide (6-30) amide (human) 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-Gly-Glu-Gly-Phe-Leu-Gly-D-Phe-Leu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Cyano-2-methylphenylboronic acid is a high quality compound that can be used as a reagent, intermediate, or building block in the synthesis of complex compounds. This chemical is also useful as a speciality chemical and research chemical. 3-Cyano-2-methylphenylboronic acid has versatile uses in organic synthesis due to its versatility in reactions and building blocks.</p>

<p>Please enquire for more information about Abz-Ala-Phe-Arg-Phe-Ser-Gln-EDDnp trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bicine, also known as N,N-Bis(2-hydroxyethyl)glycine, is a Bis(2-hydroxyethyl) amine buffer with an optimal pH range of 7.6-9.0 and a pKa of 8.26. This buffering agent forms metal complexes and is used in crystallization and enzymatic studies.</p>

<p>Please enquire for more information about Boc-Ala-Pro-Nva-4-chloro-SBzl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Val-Leu-OH·HCl is a hydrolytic cleavage product of the covalent adduct of valproic acid and HCl. It is an acidic compound that can be produced by hydrolysis or by exposure to alcohols. This compound is also known as ethylene glycol monobutyl ether, which is formed when ethylene reacts with butanol. H-Val-Leu-OH·HCl has been shown to cause termination in animal experiments and has been detected in humans following alcohol exposure. It also has some toxic effects on animals such as liver damage, kidney damage, and death.</p>

<p>Please enquire for more information about Fmoc-Nle-Wang resin (200-400 mesh) 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 Boc-Asn-o-nitrophenyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Nazumamide A is a cyclic peptide with inhibitory activity against serine proteases. It binds to the active site of thrombin and inhibits its action, thereby inhibiting the fibrinogen degradation in blood. Nazumamide A is also found to have neuroprotective properties, which may be due to its ability to inhibit nitric oxide production by binding to the enzyme nitric oxide synthase. It has been shown to have anti-inflammatory activities and can be used for the treatment of inflammation-associated diseases such as asthma and arthritis. Nazumamide A is a nonribosomal peptide that does not require any cofactors for synthesis.</p>

<p>Please enquire for more information about (D-Pro2,D-Trp6·8, Nle 10)-Neurokinin B including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Asp-Gly-OH is a peptide hormone that belongs to the group of hydroxylated aspartic acid. This peptide hormone has been shown to be a lymphocyte transformation factor in vitro and stimulates the production of collagen and other proteins. It has also been shown to have anticarcinogenic effects on bone cancer cells, which may be due to its ability to induce apoptosis. H-Asp-Gly-OH has a neutral pH and forms stable complexes with metal ions, such as copper and zinc, which are important for a variety of biological functions.</p>

<p>Please enquire for more information about Fmoc-Ser(tBu)-Thr(Psi(Me ,Me)pro)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The peptidomimetic H-Thr-Val-OH is a synthetic molecule that is hydrophobic. It has been shown to activate epidermal growth factor (EGF) through the transduction of a signal from outside the cell to inside the cell. This activation of EGF leads to increased levels of other molecules, such as cytosolic amide and hydrogen bond, which are important for cell growth. The amino acid sequence of H-Thr-Val-OH resembles that of EGF, allowing it to bind to the same receptor site on cells. This binding activates signalling pathways that lead to increased levels of proteins involved in cell proliferation, migration, and differentiation.</p>

<p>H-His-Met-OH is a histidine derivative that has been shown to have antioxidant properties. It is classified as an amide, and also acts as a chelating agent. The molecule can bind to metal ions and thereby scavenge free radicals. H-His-Met-OH has been shown to have anti-cancer activity in vitro and in vivo against kidney cancer cells. This compound also has the ability to inhibit the growth of Pseudomonas aeruginosa, which is an activated form of this bacterium, by preventing its respiration. H-His-Met-OH inhibits energy metabolism in cancer cells, which may be due to its ability to inhibit glucose uptake by inhibiting the glycolytic pathway.</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about H-trans-4,5-Dehydro-DL-Lys-OH·2 HCl 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-p-Chloro-Phe-D-Cys-b-(3-pyridyl)-Ala-D-Trp-N-Me-Lys-Thr-Cys-2-Nal-NH2 trifluoroacetate salt (Disulfide bond) 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 D-Threoninol 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 N-Et-Val-Leu-anilide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-2-methylthiophene is a linker that is used in the synthesis of metal carbonyls. It has been shown to be an efficient cross-linking agent for the preparation of polymers. 4-Bromo-2-methylthiophene can be isomerized to 2,5-dimethylthiophene by heating it with hydroxylamine. 4-Bromo-2-methylthiophene can also catalyze the alkylation of nucleophiles such as ammonia and dimethyl sulfate, as well as nucleophilic attack on carboxylic acid derivatives. This compound is acidic, due to its chloride substituent, which can react with basic groups such as hydroxyl groups or amines.</p>

<p>H-Met-Leu-Gly-OH is a tetrapeptide that has shown to have neuroprotective effects. It has been shown to be effective in the treatment of catalysis and inflammatory diseases. The peptidase activity of H-Met-Leu-Gly-OH is inhibited by the presence of lysine, arginine, and tryptophan. This inhibitory effect can be reversed by the presence of an acceptor such as histidine or cysteine. H-Met-Leu-Gly-OH also inhibits the production of nitric oxide in microglial cells and lung cells.</p>

<p>Please enquire for more information about H-Gly-Ala-Hyp-OH 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 FA-Ala-OSu including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Neuropeptide Y (18-36) trifluoroacetate salt H-Ala-Arg-Tyr-Tyr-Ser-Ala-Leu-Arg-His-Tyr-Ile-Asn-Leu-Ile-Thr-Arg -Gln is a peptide belonging to the family of neuropeptides. It has been shown to have potent vasoconstricting activity in rat and guinea pig hearts, as well as contractile activity in rat aortic rings. Neuropeptide Y (18 - 36) trifluoroacetate salt H -Ala -Arg Tyr Tyr Ser Ala Leu Arg His Tyr Ile Asn Leu Ile Thr Arg Gln Arg Tyr NH2 trifl uoroacetate salt also inhibits the cyclase activity of adenylate cyclase, which is responsible for generating the second messenger cAMP. This compound may be used to treat congest</p>

<p>Please enquire for more information about H-Ala-Ala-Ala-pNA·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-Val-Leu-OH is a model substrate for plant proteases, aminopeptidases and dipeptidases. It has been used as a standard to study the mechanism of hydrolysis by these enzymes. Z-Val-Leu-OH is hydrolyzed by these enzymes at optimally pH 8.0, with the rate increasing with temperature up to 45°C. The hydrolysis of Z-Val-Leu-OH by germination endosperm proteinase is inhibited by hemoglobin, which leads to increased levels of peptides in the endosperm.</p>

<p>N-Methyl-1-propanamine is a compound made up of ethylene diamine and activated chlorine. It has been used as a model system to study the biological properties of amines. This compound has been shown to have anti-cancer effects in human serum and is active against inflammation diseases. N-Methyl-1-propanamine is soluble in water, but not in ethanol or acetone. It has a pH optimum at 10 and decomposes at temperatures higher than 120°C. The activation energies for the reactions of this compound with hydrogen bond acceptors, such as alcohols and ethers, are relatively low (around 20 kcal/mol).</p>

<p>2-Bromo-6-methylpyridine-3-carboxaldehyde (BMPCA) is a pharmacological agent that belongs to the group of antagonists. It has been shown to be a potent antagonist at the NMDA receptor and may be used for treating neuropathic pain. BMPCA also has been shown to have competitive inhibition at the naphthyridine receptor, which may allow it to act as an antagonist or an agonist depending on its binding site. The regioisomeric analogs of BMPCA are 2-(2,5-dichloropyridyl)-6-methylpyridine-3-carboxaldehyde and 2-(2,5-dimethylpyridyl)-6-methylpyridine-3-carboxaldehyde. These analogs have been shown to inhibit the growth of tumor cells in vitro and in vivo.</p>