Amino Acids (AA)

<p>Please enquire for more information about Biotinyl-(Glu1)-Gastrin I (human) Biotinyl-Glu-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-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 CKS-17 (7-12) 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 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>Please enquire for more information about Boc-Cys(Mbzl)-PAM 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 H-Gly-DL-Abu-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-Tyr-Ser-NH2·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</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 Biotinyl-pTH (44-68) (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(-Asn-Pro-Asn-Ala)6-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 Ac-Lys-Gln-Leu-Arg-AFC trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-Ala-Ala-Pro-OH is a tetrapeptide that is expressed in mammalian cells. It has been shown to have transcription-polymerase chain activity and can be used as a molecular modeling tool for the study of mutant enzymes. Boc-Ala-Ala-Pro-OH is an analog of the natural tetrapeptide Arg-Gly, which has been shown to be activated by proteolytic cleavage and complementarity with other tetrapeptides.</p>

<p>1,3,5-Tri(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl is a diphenyl ether derivative that has been synthesized from the reaction of methanol with a solution of benzimidazole. The compound is soluble in organic solvents such as chloroform and dichloromethane. The molecule absorbs UV light and emits visible light, which can be detected by photomultiplier tubes. It has chemical structures similar to other benzimidazole derivatives.</p>

<p>Please enquire for more information about (d(CH2)51,D-Ile2,Ile4,Arg8)-Vasopressin b-Mercapto-b,b-cyclopentamethylene-propionyl-D-Ile-Phe-Ile-Asn-Cys-Pro-Arg-Gly-NH2 (Disulfid e 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 H-Gly-Lys-OH·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc 8-Lys4-Lys2-Lys-b-Ala-PAM resin (200-400 mesh) is a versatile research chemical used in various applications. It contains aminooxyacetic acid, which is commonly used in the synthesis of fatty acids and other organic compounds. This resin is often employed in the purification and separation of target molecules, such as ochratoxin, collagen, synthetic cannabinoids, naphthalene derivatives, fatty acids, steroids, and more. Additionally, it can be utilized as an inhibitor for various enzymes or complexes like arp2/3 complex. The Boc 8-Lys4-Lys2-Lys-b-Ala-PAM resin has also been used in the synthesis of cefazolin sodium, an antibiotic widely used in medical settings. With its high-quality composition and fine particle size (200-400 mesh), this resin offers excellent performance and efficiency for biomass-related studies and other research endeavors.</p>

<p>Please enquire for more information about Vesicular Stomatitis Virus Nucleoprotein (52-59) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ser-Glu-Gly-OH is an atypical compound that has shown anti-cancer activity in vitro. It is a member of the family of compounds known as glycine receptor antagonists. H-Ser-Glu-Gly-OH has been shown to inhibit the proliferation of A549 lung cancer cells and to induce cell cycle arrest and apoptosis. The compound also inhibits the activation of signal regulated kinase (ERK) in A549 lung cancer cells, which may be due to its ability to inhibit the production of cytokines such as IL6, IL8, and TNFα. H-Ser-Glu-Gly-OH also has mitogenic and antiproliferative activities for a variety of nonmalignant cell lines including human umbilical vein endothelial cells (HUVEC), human embryonic kidney cells (HEK293), and mouse erythroleukemia cells (MEL).</p>

<p>Please enquire for more information about Fmoc-Glu(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>Glycosaminoglycans are polysaccharides that are made of repeating disaccharide units composed of a sugar and a uronic acid. Glycosaminoglycans serve as structural components in the extracellular matrix, where they provide tensile strength and elasticity to tissues. They also function as enzymes, providing energy for cellular processes. This glycosaminoglycan is found in human tissue, specifically the cervix and blood group antigens. It has been shown to have an effect on creatine kinase activity, which can be used as a screening tool for women who have had hysterectomies or biopsies done.</p>

<p>Hel 13-5 trifluoroacetate salt H-Lys-Leu-Leu-Lys-Leu-Leu-Leu-Lys-Leu-Trp-Leu-Lys-Leu-Leu-Lys-Leu-Leu<br>Hel 13 is a ternary anionic surfactant consisting of a helix and three head groups. The head groups are Lys, Leu, and Leu. Each of these three head groups have a hydrophilic polar group and two lipophilic chains. It is typically used as a surfactant in the pulmonary system to help maintain lung function. When Hel 13 is used in the pulmonary system, it helps to keep the alveoli open so that air can be exchanged with blood. Hel 13 also has been shown to reduce surface tension at high pressures and temperatures, which could potentially be used for industrial purposes such as oil drilling or nuclear power plants.</p>

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

<p>VIP is a potent vasoactive neuropeptide that is found in the heart, brain, and gut. It has been shown to be a potent inhibitor of guanethidine-induced contractions in the femoral vein, as well as atrial contractions. VIP also inhibits spontaneous contractions in the fundic region of the stomach and intestinal motility. VIP has been shown to inhibit vasoactive intestinal polypeptide-induced contractions in isolated rat ileum. VIP is expressed primarily in the enteric nervous system and throughout the gastrointestinal tract.</p>

<p>2-Phenylacetamide is a nitro, acetate extract that has been shown to have antimicrobial activity. It can inhibit HIV infection and has been investigated as an antiviral drug. 2-Phenylacetamide binds to the 2-adrenergic receptor, which is found in high concentrations in the brain and inhibits the release of neurotransmitters. It also binds to κ-opioid receptors and sodium carbonate, which are found on cells throughout the body. The biological properties of this substance have not been fully elucidated but some studies suggest that it may be able to inhibit microbial metabolism or stimulate monoamine neurotransmitters.</p>

<p>Ac-Met-AMC is a nucleoside analog that is an active inhibitor of the enzyme DNA polymerase. This drug has been shown to be effective in preventing the growth of cancer cells in tissue cultures, and it has also been used to study the relationship between isoforms and oxygenated species. Ac-Met-AMC binds to the cytosolic side of the enzyme, which reduces its activity, but this binding does not affect the enzyme's ability to bind substrate or ATP. Ac-Met-AMC has been shown to hydrolyze with a rate constant of 6 x 10 M(-1) s(-1).</p>

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

<p>Allatostatin is a type of allatotropin. Allatotropins are a family of neuropeptides that inhibit the release of other hormones, such as vitellogenin, which is a hormone that stimulates vitellogenesis in insect ovaries. Allatostatin inhibits the release of vitellogenin by binding to the receptor on the egg follicle cells and blocking its action. This drug has been shown to be effective at inhibiting mevalonate production in rat ganglia and is also found in high concentrations in holometabolous insects. It is synthesized from an amide precursor by a series of enzymatic reactions and can be desorbed from its storage site with mild acidification.</p>

<p>TRH-Gly Pyr-His-Pro-Gly-OH is a synthetic glucocorticoid that binds to the glucocorticoid receptor. It has been shown to be effective in inhibiting tumor growth and reducing the size of tumors in rats. TRH-Gly Pyr-His-Pro-Gly-OH has also been shown to reduce the release of calcium from intracellular stores, inhibit the biosynthesis of messenger RNA, and inhibit DNA synthesis in human tumor cells. It is used to treat patients with cancer and those with chronic obstructive pulmonary disease (COPD).</p>

<p>H-Gly-His-OH is a cationic surfactant that can be used as an emulsifying agent, dispersing agent, or wetting agent. It has been shown to form model complexes with hydrogen bond strength and the ability to bind to nitrogen atoms. H-Gly-His-OH has been detected in a detectable concentration of 0.01% in neutral pH and at least 0.1% in acidic pH. The chemical shift of the proton NMR spectra for H-Gly-His-OH are found at 8.5 ppm (δ) and 8.2 ppm (δ). Magnetic resonance spectroscopy performed on ternary mixtures containing H-Gly-His-OH show peaks at δ 2.6 ppm and δ 1.9 ppm from the amide protons of the His residue, which are characteristic for this molecule's chemical structure.</p>

<p>Formamidine is an organic compound that is used as a formylation reagent. It is a byproduct of the chlorination of formaldehyde and dimethylamine. Formamidine is produced by the reaction of chloride with formamide in the presence of dimethylamine, which leads to a high yield. Formamidine reacts with various imidazopyridines to produce a range of substituted imidazopyridines. The type and amount of substituent dictate the selectivity and reactivity of this reaction. The reagents are phosphorous pentachloride, oxalyl chloride, and N-methylformamide.</p>

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

<p>H-Gly-His-Arg-Pro-OH acetate salt is a synthetic monoclonal antibody that binds to fibrinogen. It has been used in the production of a model protein and as an anticoagulant. H-Gly-His-Arg-Pro-OH acetate salt has been shown to inhibit the growth of tissue plasminogen activator, which is a growth factor for cells involved in blood clotting. This drug also inhibits the release of acetylcholine from nerve cells, which may be due to its ability to bind to plasma proteins.</p>

<p>Please enquire for more information about Cytochrome C (88-104) (domestic pigeon) 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 Amyloid beta-Protein (1-46) 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-Arg-His-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 H-Leu-Arg-Arg-Arg-Arg-Phe-D-Ala-Phe-Cys(NPys)-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 Fmoc-Cys(StBu)-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 PYX-1 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Neurotensin is a peptide that regulates the activity of the hypothalamus and pituitary gland. Neurotensin is synthesized from prepro-neurotensin, which is cleaved to produce neurotensin (8-13) H-Arg-Arg-Pro-Tyr-Ile-Leu-OH. It is a member of the tachykinins family of neuropeptides, which are characterized by a conserved disulfide bond. Neurotensin has been shown to increase locomotor activity in mice and rats and may be involved in pain perception. Neurotensin also binds to receptors on nerve cells, including the enkephalin receptor, with high affinity. This binding leads to an inhibition of release of neurotransmitters such as dopamine, serotonin, and acetylcholine by neurons.</p>

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

<p>4-Fluoromethyl-alpha-methylbenzyl alcohol is a nonclassical molecule that has been synthesized. This molecule has been modeled computationally and the results indicate that it exhibits a planar geometry with a diastereomeric ratio of 1:1. The theoretical calculations show that the reaction of 4-fluoromethyl-alpha-methylbenzyl alcohol with water is exothermic, which would result in the formation of an intermediate hydroxide ion. Kinetic studies have shown that this molecule can undergo transfer reactions and dehydrogenation reactions, both of which are possible mechanisms for its reactivity.</p>

<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>H-Trp-Asp-OH trifluoroacetic acid is a protein that is localized in the kinase domain of the gene product. It has been shown to activate leishmania and human serum regulatory proteins. H-Trp-Asp-OH trifluoroacetic acid binds to guanine nucleotide binding proteins in the nuclear DNA, which may play a role in mitotic checkpoint control. This protein has also been shown to have basic properties and may be involved in plant metabolism.</p>

<p>Tos-Gly-Pro-OH is a fluorescent histone deacetylase (HDAC) inhibitor. It has been validated as a competitive inhibitor of HDACs by using a fluorescence assay to detect the deacetylated form of 7-amino-4-methylcoumarin. Tos-Gly-Pro-OH is used in the treatment of malignant tumors, such as leukemia and lymphoma, by inhibiting HDACs that are responsible for cellular proliferation. In addition, Tos-Gly-Pro-OH may be useful in the treatment of diseases caused by bacterial infection because it inhibits bacterial HDACs that are responsible for protein synthesis and chemotaxis. This drug also inhibits trypsin activity and can be used as an alternative to nonisotopic solvents for peptide synthesis.</p>

<p>Glycylglycine is a tetrapeptide antibiotic that belongs to the group of antibiotics. It is expressed in E. coli and has been shown to inhibit the growth of other bacteria through binding to metal ions, such as magnesium, which are necessary for their survival. Glycylglycine has also been shown to have a kinetic method with a high rate of inhibition. This compound was synthesized by an electrospray ionization process, and its enantiomeric form was detected using a spectrometer. The molecule has been found to be an overgrowth inhibitor in analytical chemistry studies.</p>

<p>N-Boc-4-piperidineacetaldehyde is a chiral, stable, and readily available aldehyde. It has been used in the synthesis of various biologically active molecules including imidazolidinones, which are important for their use as catalysts in organic chemistry. The synthesis of this molecule by the condensation of 4-piperidineacetic acid with acetaldehyde followed by reduction with sodium borohydride is an example of this type of reaction. N-Boc-4-piperidineacetaldehyde can be used to synthesize imines and linkers that are covalently bonded to the protein backbone. This molecule also has conformational stability and is not susceptible to oxidation or radiation damage.</p>

<p>Please enquire for more information about (Tyr0)-Stresscopin (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 Amyloid Bri Protein Precursor277 (89-106) 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-Uroguanylin (mouse, rat) 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 RecA-Like Protein (193-212) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>PTH-Related Protein (1-34) is a potent antagonist of the PTH/PTHrP receptor, which belongs to the family of peptide hormones. It can be used for the treatment of osteoporosis and certain types of cancer. It inhibits bone resorption by binding to the receptor in bone cells and blocking PTH/PTHrP-induced activation of phosphaturic acid phosphatase. This drug also inhibits the production of insulin-like growth factor I (IGF-I) and its receptors, which may lead to an anti-cancer effect. PTH-Related Protein (1-34) has been shown to have a high specificity for the PTH/PTHrP receptor, with moderate affinity for other receptors such as glucagon and somatostatin. The peptide is amphipathic, meaning it has both hydrophilic and hydrophobic regions. This characteristic allows it to penetrate cell membranes more easily than other</p>

<p>Nectofibrin Hexapeptide is a peptide that interacts with the antigen-binding site of an antibody. It has been shown to be able to bind to the ovary cells of rats and may have diagnostic value in autoimmune diseases such as idiopathic thrombocytopenic purpura. The sequence of this molecule is Arg-Gly-Asp, which shows complementarity with the receptor binding site on the ovary cells. This peptide could be used for immunotherapy or diagnostics in autoimmune diseases.</p>

<p>Alternariol-9-methyl ether is a natural compound that has been shown to have significant cytotoxic effects on murine hepatoma cells. This compound also synergizes with anti-retroviral drugs and has been found to be capable of inducing apoptosis in HIV-infected T cells at low concentrations. Alternariol-9-methyl ether is structurally related to the polycyclic aromatic hydrocarbons, such as alternariol, which are only weakly toxic to mice but are potent pro-apoptotic proteins when bound covalently to DNA. Structural analysis of this compound revealed that it inhibits the binding of a pro-apoptotic protein (Bid) to its target site on dsDNA, preventing Bid from initiating apoptosis. It is thought that this effect may be responsible for its synergistic interaction with active antiretroviral therapy.</p>

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

<p>Acetyl-(D-Lys2, Sar 3)-Melanotropin-Potentiating Factor acetate salt Ac-Lys-D-Lys-Sar-Glu-OH acetate salt is synthesized from a tetrapeptide. It has been shown to be neurotrophic and to stimulate the uptake of dopamine. Acetyl-(D-Lys2, Sar 3)-Melanotropin-Potentiating Factor acetate salt Ac-Lys-D-Lys-Sar-Glu-OH acetate salt has also been shown to be an analog of the growth factor nerve growth factor (NGF) and have similar effects on muscle tissue.</p>

<p>PAR-2 agonist is a synthetic peptide that activates PAR-2. It binds to PAR-2 receptors, which are present in the mesenteric vasculature and in various other tissues. Activation of PAR-2 leads to an increase in intracellular calcium concentration, activation of protein kinase C, cytosolic calcium ion release, phosphorylation of myosin light chain, muscle cell proliferation, transcription and translation initiation, and increased production of vasoactive intestinal peptide. This drug also has anti-inflammatory effects and stimulates epidermal growth factor (EGF) and thrombin receptor expression as well as growth factor production.</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>

<p>Please enquire for more information about VEGFR-KDR/Flk-1 Antagonist 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 H-Ser-Leu-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 Acetyl-Amylin (8-37) (mouse, rat) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3'-Methylacetophenone is an organic compound that belongs to the class of phenols. It has a number of reactions with other chemicals, including hydrogen chloride. The reaction between 3'-methylacetophenone and hydrogen chloride is an example of a nucleophilic substitution reaction. The rate of this reaction increases as the temperature rises, but slows down when the concentration of chloride ions increases. Kinetic studies have shown that the activation energy for this process is 12 kcal/mol, which is in agreement with previous results obtained from analytical methods and preparative experiments.</p>

<p>Trifluoroacetate salt</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>Suc-Gly-Pro-pNA is a proteolytic enzyme that hydrolyzes proteins. It has been shown to have potential for use as an anti-inflammatory agent. Suc-Gly-Pro-pNA has high proteolytic activity and can cleave peptide hormones such as angiotensin II and vasopressin. It also has thermal stability, and can tolerate high concentrations of salt and heat, making it suitable for therapeutic purposes. Suc-Gly-Pro-pNA binds to peptides with carboxy terminal residues by substrate binding, which may be the reason for its high degree of specificity. This enzyme is expressed in the cytosol and extracellular environment.</p>

<p>Z-Phe-Phe-diazomethylketone is a cathepsin inhibitor that has been shown to inhibit the proteolytic activity of various enzymes, including serine proteases and thrombotic thrombocytopenic. This compound inhibits the growth of Leishmania parasites in cell culture and has been shown to have a high affinity for carboxy terminal and proximal tubules. Z-Phe-Phe-diazomethylketone has a neutral pH, with an optimum at 7.0, which may be due to its ability to bind to proteins or other components of cells without affecting their functions.</p>

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

<p>H-[15N]Tyr-OH is a metabolite of tyrosine. It is the conjugate acid of propionic acid, and the conjugate base of 4-hydroxybenzyl. H-[15N]Tyr-OH is a phenylalanine and aromatic amino acid that has an aromatic ring with a phenyl substituent. This metabolite is hydroxy, which means it has one hydroxyl group on the phenyl ring. H-[15N]Tyr-OH binds to daphnia in vivo, causing death. The cause for this may be due to its ability to react with oxygen, forming reactive oxygen species (ROS).</p>

<p>Bradykinin is a peptide with a variety of physiological effects. It is formed by the cleavage of kininogen by kallikrein, and it is involved in the regulation of vascular tone and blood pressure, as well as responses to pain and inflammation. Bradykinin stimulates the release of histamine from mast cells, which causes an inflammatory response. Bradykinin also has been shown to stimulate the release of leukotrienes, prostaglandins, and cytokines from human lung tissue. The interaction between bradykinin and its receptors has been studied extensively using in vitro assays. The conformational changes in this peptide have been characterized by spectroscopic studies such as nuclear magnetic resonance (NMR) and circular dichroism (CD). In addition, bradykinin can be detected using luminescence techniques such as chemiluminescence or bioluminescence. Studies have shown that micromolar concentrations of bradykinin</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 Neuromedin S (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol is an impurity in hexane that is generated during the reaction of pyridine with acetonitrile. The impurity is removed by crystallizing it from methanol. 2-(4-Methyl-2-phenyl-1-piperazinyl)-3-pyridinemethanol has a high efficiency, and can be used to synthesize hexamethyldisiloxane. This product can be used as a metal catalyst for reactions involving alkali metals or metal halides. It can also be used as an alcohol solvent, but not hydrogenated.</p>

<p>Please enquire for more information about Insulin B (22-25) 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 1-Oleoyl-3-palmitoyl-rac-glycero-2-phosphoethanolamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>ACTH (4-10) trifluoroacetate salt is a cholinergic agent that belongs to the class of neurotransmitters. It is synthesized from the naturally occurring hormone ACTH, which is released by the anterior pituitary gland in response to a variety of stimuli. This compound has been shown to have physiological effects on various organs, including adipose tissue and locomotor activity. It also shows neuroprotective effects in animal models and has neurotrophic properties. The therapeutic potential of this compound for brain functions is currently being explored.</p>

<p>The H-Gly-Gly-Lys-Arg-OH acetate salt is a diagnostic agent that belongs to the group of active analogues. It is an analogue of sialin, a compound that has been shown to be involved in the molecular pathogenesis of cancer tissues. Sialic acid is an important component of many glycoproteins and glycolipids found in the human body. This compound is metabolized by sialidase enzymes, which are present in various tissues and organs such as the brain, kidney, liver, and plasma. The H-Gly-Gly-Lys-Arg-OH acetate salt inhibits these enzymes by binding to them and preventing their action. This drug also inhibits ATP dependent transport systems for neuronal cells.</p>

<p>Motilin is a gastrointestinal hormone that stimulates gastric motility and the release of pancreatic enzymes. It is also used to treat postoperative ileus, abdominal pain, and gastroduodenal ulcers. Motilin is administered nasogastrically to stimulate the movement of food through the stomach and intestines. The trifluoroacetate salt form is used in this application because it has a longer duration of action than other salts.</p>

<p>(S)-(-)-3-Chloro-1-phenyl-1-propanol is an efficient method for the synthesis of chiral propiophenone. It is synthesized by reacting a mixture of borane and tetrahydrofuran with (S)-(-)-3-chloro-1-phenylpropanol. This reaction produces the desired compound in good yield and high diastereoselectivity. The synthesis of this compound has been shown to be useful for the production of antidepressant drugs, such as κ-opioid receptor ligands, which are used to treat depression, anxiety, and chronic pain.</p>

<p>Please enquire for more information about Neuronostatin-19 (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 H-Lys-Gly-Gly-Lys-OH acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

<p>4-Methylsulphonylaniline is a reactive compound that can be used as an anticancer agent. It is a quinoline derivative and has been found to have potent antitumor activity against various cancer cell lines, including those resistant to other anticancer agents. The activation energy of this compound is high at 93 kcal/mol and it has been found to react with dimethylformamide (DMF) in the reaction mechanism. 4-Methylsulphonylaniline has also been shown to inhibit the growth of tumor cells in mice by inhibiting DNA synthesis. This molecule also causes DNA damage in cultured cells. 4-Methylsulphonylaniline may also cause environmental pollution because it reacts with sulfadiazine, which is a drug used for the treatment of chronic infections caused by bacteria such as Salmonella typhi and Mycobacterium tuberculosis, leading to the release of methyl sulfone, which can be toxic to aquatic</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>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>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>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 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>Please enquire for more information about H-D-Met-Met-Met-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 RVG-9R trifluoroacetate salt 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 HIV (gp120) Fragment (421-438) 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 Axltide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>