Amino Acids (AA)

<p>Glutaryl-Phe-pNA is commonly used as a substrate to measure the activity of proteases, which are enzymes that cleave peptide bonds. The cleavage of the Glutaryl-Phe-pNA substrate by proteases releases a colored 4-nitroaniline product, which can be detected and quantified spectrophotometrically to measure protease activity.</p>

<p>Please enquire for more information about (D-Arg2)-Dermorphin (1-4) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Fluoro-2-methoxyphenylacetone is a chemical with a wide array of applications in research and industry. It is a versatile building block, useful intermediate, and reagent for organic synthesis. This compound has been used as a starting material in the synthesis of other compounds. CAS No. 1017082-10-8</p>

<p>H-Pro-Pro-Pro-Pro-OH is a proteolytic enzyme that has been shown to have potential applications in drug design. The enzyme is able to cleave proteins, such as albumin, at different sites. It can be used to optimize the design of therapeutic drugs by highlighting the parameters that are important for successful protein cleavage. The enzyme has also been shown to have toxicological properties and interacts with serum albumin. H-Pro-Pro-Pro-Pro-OH is a protease that can be found in human serum.</p>

<p>3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.</p>

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<p>Please enquire for more information about Cortistatin-29 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-Gly-Gly-NH2 is a synthetic peptide that has been shown to inhibit the activity of phosphatases, which are enzymes that hydrolyze phosphate groups from phosphorylated substrates. It is a hydrophobic and metal chelator, which makes it suitable for use in chromaffin cells and dorsal root ganglia. Z-Gly-Gly-NH2 has been shown to be specific for inhibition of synaptic phosphatase (PP1). This compound also inhibits the enzyme inhibitor subtilisin, which is found in bacteria such as Streptomyces or Bacillus subtilis. Z-Gly-Gly-NH2 has been shown to have a high affinity for receptors.</p>

<p>Suc-Ala-Phe-Pro-Phe-pNA is a recombinant isomerase that has been shown to be an immunosuppressive agent. It is able to catalyze the conversion of cyclosporin A into its two inactive forms, as well as the conversion of cyclophilins A and B into their corresponding inactive forms. The enzyme has also been shown to have chaperone activity. Suc-Ala-Phe-Pro-Phe-pNA has been expressed in Escherichia coli and purified from inclusion bodies using an affinity column with immobilized recombinant cyclophilin A and B. The enzyme's activity was measured by catalysis of the conversion of pNPP, a substrate analogue, into pNPPdG, which can be detected spectrophotometrically at a wavelength of 340 nm. Suc-Ala-Phe-Pro-Phe-pNA shows exponential growth in the presence of</p>

<p>Boc-Pro-Gly-OH is a synthetic tetrapeptide that is used as a substrate molecule to study collagen hydroxylases. It has been shown to be an excellent substrate for the enzyme collagenase, and its chemical data indicates that it is bound by metal ions. The technique of dichroism was used to confirm the secondary structure of Boc-Pro-Gly-OH. This tetrapeptide has four amino acids, which are proline, glycine, histidine, and hydroxyproline.</p>

<p>Z-D-Phe-Phe-Gly-OH is a lysosomal carboxypeptidase that hydrolyzes peptides at the C terminus of proteins. It has a wide substrate specificity and can hydrolyze Z-D-Phe-Phe-Gly, Z-Arg-Lys, and L-Arg. This enzyme has been shown to have ion exchange chromatography activity. The elution profile for this enzyme on a sephadex G-100 column was found to have an optimum pH of 7.5 and elutes at a salt concentration of 0.5M NaCl. Carboxypeptidases are enzymes that cleave at the C terminus of proteins to produce smaller peptides or amino acids. They are involved in digestion, blood clotting, and cell signaling processes.</p>

<p>Leu-Enkephalin (sulfated) H-Tyr(SO3H)-Gly-Gly-Phe-Leu-OH is an endogenous opioid peptide that has been found in the central nervous system. It was first discovered by radioimmunoassays of brain tissue and then later found to be present in other tissues. Leu-enkephalin is not acidic, but it can form a salt with sulfonic acid or carboxylate, which may account for its ability to bind to receptors on cell membranes. The molecular weight of leu-enkephalin is 921.5 daltons and it contains one sulfonation group and one glycosylation site. Leu-enkephalin (sulfated) H-Tyr(SO3H)-Gly-Gly-Phe-Leu-OH can be synthesized from the amino acids Glycine, Tyr(SO</p>

<p>H-Val-Arg-Lys-Arg-Thr-Leu-Arg-Arg-Leu (HVLAHR) is a synthetic peptide that has been shown to have antiinflammatory properties. The peptide binds to the epidermal growth factor receptor (EGFR) and inhibits the production of proinflammatory cytokines and chemokines, such as IL1α, IL6, IL8, and TNFα. HVLAHR also binds to calmodulin and inhibits protein kinase C (PKC) activity. It has been shown that this peptide has neuroprotective effects in vitro by binding to neurogranin and inhibiting protein phosphorylation. HVLAHR can be used as a model organism in vitro to study protein kinase activity.</p>

<p>Ac-Ala-Ala-Pro-Phe-pNA is a serine protease inhibitor that has been shown to inhibit chymotrypsin, elastase, and other serine proteases. It is benzoylated to protect it from proteolytic degradation in the gastrointestinal tract and can be used as a therapeutic treatment for inflammatory bowel disease, pancreatitis, or other chronic diseases. Ac-Ala-Ala-Pro-Phe-pNA can be inactivated by thermal treatment (e.g., boiling) or by chemical reduction (e.g., sodium borohydride).</p>

<p>Please enquire for more information about 1b-(4-Fluorophenyl)hexahydro-',7-dihydroxy-7-(1-methylethyl)-1a-phenyl-7a-[(phenylamino)carbonyl]-3H-oxireno[3,4]pyrrolo[2,1-b][1,3] oxazine-3-butanoic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>HIV (gp41) Fragment H-Ala-Val-Gly-Ile-Gly-Ala-OH is a hydrophobic peptide fragment that is used as an antigen to induce immunity against HIV infection. The sequence of the peptide was obtained by sequencing the human immunodeficiency virus type 1 (HIV). The peptide contains glutamic acid and ornithine, which are necessary for the attachment of gp41 to the target cell surface and for the penetration of the virus into cells. The cyclic peptide induces mononuclear phagocytes to produce antibodies against gp41, which can inhibit infection by HIV.</p>

<p>Tat is a protein from the human immunodeficiency virus type 1 (HIV-1) that is responsible for the regulation of viral gene expression. Tat binds to a cellular receptor, CD4, and enters the cell. The Tat protein forms a ternary complex with transcription factors and RNA polymerase II. This complex then binds to promoter regions of HIV genes and initiates transcription. Tat has been postulated to modulate immune functions such as chemokine production, T-cell activation, and macrophage activation. The HIV-1 tat Protein (1-9) H-Met-Asp-Pro-Val-Asp-Pro-Asn-Ile-Glu-OH has been shown to have an effect on the immune system by affecting chemokines and other immune functions.</p>

<p>Please enquire for more information about Fmoc-Tyr(SO2(ONeopentyl))-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Lysyl-L-lysyl-L-lysyl-L-lysyl-L-lysine (LLLLLL) is an antibacterial agent that belongs to the class of pharmacological agents. LLLLLL has been shown to have antibacterial efficacy against oral pathogens, such as Streptococcus mutans and Porphyromonas gingivalis. LLLLLL binds to the bacterial cell wall by forming a covalent disulfide bond with cysteine residues on the peptidoglycan layer. This prevents cell wall synthesis, leading to cell death by inhibiting protein synthesis. LLLLLL has also been shown to have low toxicity in animal models for long periods of time, with high values in human serum.</p>

<p>1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) is a sodium salt that has the ability to form surfactant bilayers. DPPC is a model system for studying biochemical reactions and the phase transition of lipid bilayers. This compound has been used to study the effects of various drugs on cell membranes in biochemical research. In addition, DPPC has been shown to have hypoglycemic effects in animal models as well as having an anti-inflammatory effect.</p>

<p>Please enquire for more information about Mca-(Asn670,Leu671)-Amyloid beta/A4 Protein Precursor770 (669-674)-Lys(Dnp) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C-Peptide is a monoclonal antibody that binds to the β-cell and inhibits insulin release. It has been used in diagnosis of type 1 diabetes mellitus. C-Peptide is a hormone that regulates blood glucose levels by controlling the rate of glucose production in the liver, as well as by inhibiting the breakdown of glycogen in the liver. The C-terminal amino acid sequence Glu-Ala-Glu-Asp-Leu-Gln-Val-Gly-Gln-Val-Glu -Leu-Gly can be cleaved from the peptide by trifluoroacetic acid to yield free Gln, which can then be detected using mass spectrometry. Growth factors such as IGF1, FGF21, and HGF have been shown to increase C peptide levels in diabetic patients.</p>

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<p>Please enquire for more information about Bz-Nle-Lys-Arg-Arg-AMC 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 (Phe1,Ser2,Tyr6)-PAR-1 (1-6) 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 Boc-N-Methyl-gaMMa-aMinobutyric acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 3,5-dichloro-4-methoxybenzoate is a fine chemical and useful building block for research chemicals. It belongs to the class of speciality chemicals and can be used as a reagent in organic synthesis. Methyl 3,5-dichloro-4-methoxybenzoate is a versatile building block that has been reported in the synthesis of many complex compounds. This compound can also be used as an intermediate or scaffold for medicinal chemistry applications.</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>Racemic 3,11-dichloro-6,11-dihydro-6-methyl-dibenzo[c,f][1,2]thiazepine 5,5-dioxide is a hydrogen chloride salt of racemic 3,11-dichloro-6,11-dihydro-6-methyl dibenzo[c,f][1,2]thiazepine. Racemic 3,11 - dichloro - 6 , 11 - dihydro - 6 - methyl dibenzo [ c , f ] [ 1 , 2 ] thiazepine 5 , 5 - dioxide is used in the manufacture of high purity and high yield hydrogen chloride gas. Racemic 3,11 - dichloro - 6 , 11 - dihydro - 6 - methyl dibenzo [ c , f ] [ 1 , 2 ] thiazepine 5 , 5 - dioxide can be prepared by heating anhyd</p>

<p>Please enquire for more information about Boc-Asp(OcHex)-OSu including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-Cys(farnesyl)-OMe is a synthetic, methyl esterification product of farnesol and acetic acid. It is a protease activity inhibitor that has been shown to have bone resorption activity in rats. Ac-Cys(farnesyl)-OMe has been shown to inhibit the enzyme farnesyltransferase, which is involved in the posttranslational modification of proteins. This inhibition blocks the synthesis of sterols, which are necessary for bone resorption. Ac-Cys(farnesyl)-OMe has been shown to be active against multidrug resistant bacteria and may be used as an agent for treatment or prevention of heart disease.</p>

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<p>N-alpha-Z-L-ornithine (NALO) is an amino acid with the chemical formula CHNO, which is also known as 2-(aminoethoxy)ethanol. It is used to synthesize peptides and proteins. NALO has been shown to be a potent inhibitor of arginine biosynthesis in E. coli and yeast cells, but not in mammalian cells. This inhibition leads to an accumulation of L-ornithine, which is necessary for the synthesis of polyamines that are important for cell growth and replication.</p>

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

<p>Ac-Ala-Ala-OMe is a molecule that has conformational and interaction properties. It is an amide residue found in proteins. The amino acid sequence of Ac-Ala-Ala-OMe contains an elongating residue with a specific profile, which can be used as a molecule to study acylases. Acetamide, the precursor of Ac-Ala-Ala-OMe, is an acid methyl ester that has been shown to interact with chloride ions. When acetamide interacts with chloride ions, it undergoes a shift in its structure and produces the product Ac-Ala-Ala-OMe. This process may be due to solvent effects (i.e., the effect of water).</p>

<p>Please enquire for more information about Hippuryl-Cys(2-aminoethyl)-OH hydrochloride salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(D-Ala2)-Leu-Enkephalin H-Tyr-D-Ala-Gly-Phe-Leu-OH is a peptide that is a member of the endorphin family of endogenous analgesic compounds. It has been shown to have anti-inflammatory properties in clinical studies and to suppress bacterial growth in vitro. The compound has been implicated in the regulation of glucose homeostasis, as well as having an effect on body mass index and skin cells. (D-Ala2)-Leu-Enkephalin H-Tyr-D-Ala-Gly-Phe-Leu-(OH) is thought to modulate the activity of Toll like receptor 4, which is involved in inflammation and immune response.</p>

<p>Please enquire for more information about GLP-1 (7-37) (human, bovine, guinea pig, mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Used in treatment of nonspecific ulcerative colitis</p>

<p>Boc-D-Tyr(tBu)-OH is a natural product that is an amphipathic molecule with a cyclic structure. It has been shown to be able to inhibit the growth of bacteria, such as Staphylococcus aureus and Escherichia coli, by acting as an antibiotic. Boc-D-Tyr(tBu)-OH inhibits the synthesis of peptides by binding to the ribosome and blocking peptide elongation. This molecule also inhibits peptide synthesis by interacting with the aminoacyl site on the ribosome and preventing it from binding with amino acids. Boc-D-Tyr(tBu)-OH is synthesized in two stages: solid phase peptide synthesis and nucleophilic activation. The decapeptides are then purified and characterized based on their function.</p>

<p>Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe is a subunit of the endogenous opioid peptide Met-enkephalin. It is a proteolytic cleavage product of proenkephalin A and is also known as Tyr2, Phe2, or Arg6. Met-enkephalin has been shown to participate in signal transduction pathways that regulate blood pressure and exocrine secretion. Metenkephalin is an amide containing two cysteine residues with a hydrophobic side chain, which can bind metal ions such as calcium ions. Metenkephalin binds to the membrane of cells, altering membrane potential and naloxone binding sites.<br>Met enkephalin has been shown to be involved in serotonin release from platelets and inhibition of serotonin uptake by platelets.</p>

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

<p>H-Arg-Val-Leu-psi(CH2NH)Phe-Glu-Ala-Nle-NH2 is a compound which is structurally related to the amino acid histidine. It has been used as an indicator for Xanthochromia, a diagnostic for copper. H-Arg-Val-Leu-psi(CH2NH)Phe-Glu-Ala-Nle-NH2 has also been used in polyester production and as a monitoring agent for modifications of polylactic acid thermally.</p>

<p>4-Bromo-2-methylbut-1-ene is an alkylating agent that reacts with DNA, RNA and proteins. It has been shown to be effective in the treatment of bladder cancer. 4-Bromo-2-methylbut-1-ene is used as a trifluoride source for boron trifluoride etherate, which is then reacted with plant tissues. This reaction yields a prenyl group, which can be further processed to yield an alkynyl group. The alkynyl group can be reacted with anhydrous sodium to form a chloride salt. This salt can then react with carbon monoxide to form a carbone molecule, which is the final product of this chemical process.</p>

<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>Substance P is a tachykinin that is released from the nerve endings of the parasympathetic nervous system. It binds to receptors in the plasma membrane of cells and causes them to release acetylcholine, which is an inhibitory neurotransmitter. Substance P also has been shown to interact with muscle cells and cause contractions. The incubation of Substance P with muscle cells inhibits the release of calcium ions, which reduces the membrane potential and decreases the contractility of these cells.</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>

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<p>Suc-Ala-Pro-Ala-AMC is a synthetic peptide that is used as a fluorescent substrate to measure the activity of serine proteases. It is used in plant physiology and has been shown to be effective in the treatment of inflammatory diseases. Suc-Ala-Pro-Ala-AMC is an acidic molecule with a pKa of 3.1. This means it can exist as both a zwitterion, with a positive charge on one end and negative charge on the other, or as an ionized molecule with both ends having a negative charge. The zwitterionic form is more stable than the ionized form at low pH levels and will therefore be present at higher concentrations at lower pH values. Suc-Ala-Pro-Ala-AMC shows proteolytic activity against peptidases such as papain, bromelain, trypsin, and chymotrypsin. It also binds to neutroph</p>

<p>Please enquire for more information about Fmoc-Arg(Pbf)-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>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>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>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>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>H-Lys-Glu-Gly-OH is a polyelectrolyte that has high affinity for cationic dyes. It is synthesized by the reaction of a protonated amino acid with an epoxide. This molecule has been shown to counter act the effect of polystyrene particles in experiments, which may be due to its ability to form complexes with other substances and decrease their solubility. H-Lys-Glu-Gly-OH has been used as a reagent in solid phase synthesis to prepare peptides and it also appears to be active against glutamic acid.</p>

<p>H-DL-Val-Leu-Arg-pNA acetate salt is a natriuretic that is used to treat chronic kidney failure. It has an inhibitory effect on serine protease and epidermal growth factor, which are enzymes involved in the production of atrial natriuretic peptide (ANP). The drug also reduces blood pressure by inhibiting the activity of angiotensin II, which is a potent vasoconstrictor. H-DL-Val-Leu-Arg-pNA acetate salt has been shown to increase urea nitrogen levels by inhibiting the activity of alkaline phosphatase, which breaks down ammonia in the liver.</p>

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

<p>Hemokinin-1 is a hematopoietic cell growth factor that belongs to the group of neuropeptides. This protein has been shown to stimulate the production of white blood cells and is used as an adjuvant in vaccines. Hemokinin-1 stimulates the production of inflammatory cytokines and other proinflammatory substances. It also has been found to be involved in autoimmune diseases, cancer, and infectious diseases. The antigen binding site on Hemokinin-1 is located at residues Thr-Gly-Lys-Ala-Ser-Gln-Phe-Phe-Gly-Leu (TGLKSGPFGL) and the receptor binding site at residues Met-NH2. The receptor for Hemokinin 1 is the neurokinin 1 receptor (NK1R).</p>

<p>Please enquire for more information about H-Phe-Met-D-Arg-Phe-NH2 acetate 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 Acetyl-Neurotrophin Receptor (368-381) amide (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-DL-Phe-pNA is a synthetic derivative of the natural substrate Ac-Lys-pNA. It binds to the active site of serine proteases and blocks the release of their active form, which results in inhibition of collagen synthesis. The reaction is reversible and it can be hydrolyzed by chymotrypsin or elastase. Ac-DL-Phe-pNA has been shown to inhibit protein–protein interactions between epimastigotes and extracellular matrix proteins, leading to cell death. This compound has also been found to have an optimum pH of 6.5, which is neutral.</p>

<p>TRAP-5 is a peptide consisting of the amino acid sequence H-Ser-Phe-Leu-Leu-Arg. This peptide has been shown to have antiviral, anti-inflammatory, and anticancer properties. It has also been found to inhibit platelet activation in vitro and to reduce atherosclerotic lesions in mice. TRAP-5 has been shown to have therapeutic potential for diseases such as heart disease and lung diseases, although its efficacy has not yet been tested in humans.</p>

<p>Please enquire for more information about (Des-Gly10,D-Leu6,[13C6]Leu7,Pro-NHEt 9)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Methyl 6-methylnicotinate is a synthetic compound that has been shown to have cholinergic properties. It is an oxidation catalyst that can be used in the synthesis of methyl nicotinate, which is a drug for the treatment of influenza virus. Methyl 6-methylnicotinate also has been shown to inhibit the replication of influenza virus in vitro and in vivo. Methyl 6-methylnicotinate inhibits viral growth by binding to the antigenic site on hemagglutinin, preventing it from attaching to host cells. This compound also has been shown to inhibit the release of chloride ions in animal models and inhibits neuromuscular transmission. The molecular modeling studies revealed that methyl 6-methylnicotinate binds with high affinity to the active site of acetylcholinesterase enzyme and is able to form a covalent bond with its serine residue, thereby inhibiting its activity.</p>

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<p>H-Gly-D-Val-OH is a nonpolar amino acid that belongs to the group of amino acids. It is one of the 20 standard amino acids used by living cells and is found in proteins. The nitrogen atoms are located at the corners of a rectangle and are involved in hydrogen bonding. H-Gly-D-Val-OH is a component of fatty acids, which are molecules that form an important part of the human diet. Fatty acids are taken up by cells through endocytosis and metabolized within the cell cytoplasm by catabolism or anabolism. H-Gly-D-Val-OH has been shown to have kinetic properties in vitro and can be used as a ternary complex forming agent with glycine and D,L-valine when mixed with water. H Gly D Val OH also acts as a cyclic peptide, which can be synthesized from H Gly D Val OH with the help of</p>

<p>H-Ala-Gly-OH is a synthetic amino acid that is used to produce the peptide hormone luteinizing hormone (LH). It has been shown that H-Ala-Gly-OH is an antigen specific antibody response and has a hydrogen bond. The functional groups of H-Ala-Gly-OH include amine, carboxyl, and hydroxyl. Structural analysis of this compound was completed using a kinetic method. The conformational properties of H-Ala-Gly-OH were determined by nmr spectra and titration method. This synthetic amino acid may inhibit protein synthesis in vivo through treatment with carbohydrate.</p>

<p>Please enquire for more information about 2-(Aminomethyl)-2-methyl-1,3-propanediamine trihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-Leu-Val-Phe-aldehyde is a synthetic compound that inhibits the catalytic activity of carboxyl enzymes. It binds to the catalytic site of the enzyme via a noncovalent interaction with residues on the polypeptide chain, thereby preventing the formation of an active complex with other cofactors such as metal ions, amino acids, and ATP. Ac-Leu-Val-Phe-aldehyde can be used in analytical chemistry for determination of carboxyl groups in organic compounds or for determining protein content in biological samples. Ac-Leu-Val-Phe-aldehyde has also been shown to bind to antibodies which are specific for carboxyl groups.</p>

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<p>Please enquire for more information about Cyclo(-Gly-Asn-Trp-His-Gly-Thr-Ala-Pro-Asp)-Trp-Phe-Phe-Asn-Tyr-Tyr-Trp-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 H-D-Val-Leu-Lys-AMC acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-muramyl-Ala-D-Glu(Lys(stearoyl)-OH)-NH2 is a synthetic peptide that was designed to mimic the sequence of muramyl dipeptide (MDP), which is found in bacterial cell walls. Ac-muramyl-Ala-D-Glu(Lys(stearoyl)-OH)-NH2 binds to the protein albumin, which is an important component of human blood plasma and has been shown to be elevated in patients with autoimmune diseases. This peptide also inhibits the activity of metal hydroxides, such as aluminum hydroxide and calcium hydroxide, by binding to their surface, reducing their antimicrobial activity. The effect on locomotor activity has not been studied. Ac-muramyl-Ala-D-Glu(Lys(stearoyl)-OH)-NH2 may have effects on various cells types including macrophages and T</p>

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

<p>1-Methyl-1H-indazole-7-carbaldehyde is a 1,3,5-substituted indazole derivative that can be used as a building block for the synthesis of complex compounds. It is an intermediate in the synthesis of various pharmaceuticals and it has been shown to have potential applications in research chemicals. 1-Methyl-1H-indazole-7-carbaldehyde can be used as a versatile building block after conversion to other derivatives. This chemical is also being investigated as a possible treatment for Parkinson's disease and Alzheimer's disease.</p>

<p>H-Pro-Ser-Hyp-Gly-Asp-Trp-OH is a cyclic hexapeptide with a high activity against platelets. It is an antagonist of the cyclic RGD sequence, which is present in fibrinogen, fibronectin, vitronectin and other proteins. This peptide binds to the n-terminal residue of these proteins and prevents them from binding to their receptors on the surface of platelets. H-Pro-Ser-Hyp-Gly-Asp-Trp-OH has been shown to be specific for human platelets and does not bind to erythrocytes or leukocytes.</p>

<p>LymnaDFamide-1 is a neuropeptide that belongs to the family of c-terminal peptides. It is a dipeptide with a sequence of L-Pro-Tyr-Asp-Arg-Ile-Ser-Asn-Ser-Ala-Phe. This peptide was found in the nervous system of invertebrates, where it is believed to play an important role in the regulation of neurotransmitter release. In mammals, LymnaDFamide has been detected in the brain and in the gallbladder. It may be involved in regulating feeding behavior and gastric motility.</p>

<p>Please enquire for more information about pTH (1-37) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-D-Arg(Me)-OH is a peptide that has been shown to inhibit the proliferation of cancer cells in culture. It inhibits the growth of tumor cells by blocking the activity of the oxytocin receptor, which regulates cell adhesion and migration. The H-D-Arg(Me)-OH acetate salt has also been shown to promote the differentiation of basophilic leukemia cells into normal myeloid cells. This peptide is used as a control for incubated cell cultures, such as liver cells, and can be used to study protein synthesis.</p>

<p>Please enquire for more information about H-Tyr-Gln-Ser-Leu-Arg-Trp-NH2 acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Methyl-L-trans-4-hydroxyproline hydrochloride is a bioactive compound that is present in the leaves of Semecarpifolia. It has been found to have antioxidant and anti-inflammatory properties. The chemical structure of N-methyl-L-trans-4-hydroxyproline hydrochloride is cyclic, butanamide, hexane, ethanolic extracts, and semecarpifolia. The family Meliaceae includes species such as Eucalyptus, which produces the bioactive compound cineole. Solvents used in this process are hexane and ethanolic extracts.</p>

<p>Please enquire for more information about Exendin-4 (1-8) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,5-Diiodo-4-methoxybenzhydrazide is a high quality chemical that is useful in the preparation of complex compounds. This compound has been shown to be an excellent reagent and useful intermediate for the synthesis of various fine chemicals. It has been used as a precursor for the production of the antiviral drug Tamiflu, among other pharmaceuticals. 3,5-Diiodo-4-methoxybenzhydrazide is also a versatile building block that can be used in research or as a reaction component in organic synthesis.</p>

<p>Z-Phe-Ala-diazomethylketone is a molecule that belongs to the class of hydrolase inhibitors. It has been shown to have inhibitory properties against trichomonas vaginalis and proteolytic activity against liver cells. Z-Phe-Ala-diazomethylketone also has a kinetic energy of 11.2 kcal/mol, which is higher than most protease inhibitors. This molecule has been shown to be effective as a cell vaccine in wild-type mice and as a protease inhibitor in brain cells. The optimal ph for this molecule is 7.5, which corresponds to its pKa value of 5.1.</p>

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<p>Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate is an anticancer agent that belongs to the class of formamidines. It is synthesized by refluxing ethyl 4-hydroxyphenylacetic acid with hexamethylenetetramine and acetic acid in ethanol. After purification, it is converted to its active form by reacting with hydrochloric acid. Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate prevents the growth of cancer cells in culture by preventing DNA synthesis, which prevents RNA and protein synthesis. This agent has also been found to suppress paclitaxel production in cultured human breast cancer cells.</p>

<p>H-Pro-Phe-OH is a synthetic peptide that is used in the treatment of high blood pressure. It has been shown to decrease blood pressure by increasing the production of nitric oxide and by decreasing activity of angiotensin converting enzyme, which are factors that have an influence on blood pressure. H-Pro-Phe-OH has been shown to be effective for treating HIV infection and amyloidosis. H-Pro-Phe-OH binds to collagen and increases its production in tissues, which may be responsible for its antihypertensive effects. It also inhibits the growth of bacteria by binding to their cell walls and inhibiting their protein synthesis. The metabolic products of H-Pro-Phe-OH are not yet known, but it is thought that they may contain hydroxyproline or hydroxylysine residues.</p>

<p>Please enquire for more information about Acetyl-(Asn30,Tyr32)-Calcitonin (8-32) (salmon I) 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 Mastoparan 17 (free acid) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>