Amino Acids (AA)

<p>Boc-Arg(Boc)2-OH is a protected derivative of the amino acid arginine. The Boc (tert-butyloxycarbonyl) groups shield both the amino group and the side chain's guanidine functionality. This protection scheme allows for its selective incorporation during peptide synthesis while offering stability under various reaction conditions. Boc-Arg(Boc)2-OH has been also used in the synthesis of amino acid prodrugs of cytotoxic anthraquinones, demonstrating its potential utility in developing targeted cancer therapies.</p>

<p>N,N-Diethyl-beta-alanine (DEBA) is a nucleophilic agent that reacts with epoxides. It has been synthesised and structurally studied using X-ray crystallography and electron diffraction techniques. DEBA has shown to have reactive properties and has been used in the synthesis of monoalkyl epoxides. The synthesis of DEBA was first reported by the research team of L1210 leukemia cells. This substance was found to be an effective inhibitor of growth in this cell line, which may be due to its ability to inhibit protein synthesis.</p>

<p>Please enquire for more information about 2-Chloro-1-(5-methoxy-1,2-dimethyl-1H-indol-3-yl)ethanone 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 2,4-Dichloro-6-methyl-Benzenesulfonylchloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 2-methylthiopropionate is an organic compound that is found in organisms and has been detected in the environment. It can be synthesized by the reaction of methane, carbon disulfide, and formaldehyde. Methyl 2-methylthiopropionate can also be produced by the reaction of β-unsaturated ketones with acid molecules. This substance is a potential precursor to ferrite. Methyl 2-methylthiopropionate has been shown to have physiological effects on fibrinogen and c-reactive protein levels in rats exposed to radiation. The production of this substance may lead to dry powder formation, which causes environmental pollution.</p>

<p>S-Methyl thiohexanoate is a fatty acid that is the product of the serine protease activity of the potato tuber. It has been shown to have a transcriptional regulatory effect on carbon source utilization and natural compounds production, which may be due to its ability to alter the phospholipid composition in plant cells. S-Methyl thiohexanoate can inhibit or induce natural compounds production depending on the concentration used. The effects of this compound are mediated by its ability to form hydrogen bonds with hydroxyl groups in phospholipids, altering their configuration and consequently disrupting membrane integrity. S-Methyl thiohexanoate also has been shown to act as an electron donor for covalent polymerization reactions catalyzed by DNA polymerases and reverse transcriptases. This may be due to its ability to form hydrogen bonds with phosphate groups in nucleic acids, altering their configuration and consequently disrupting DNA or RNA synthesis.</p>

<p>Please enquire for more information about 1-Methylindole-3-acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bradykinin acetate is a synthetic form of Bradykinin that is used as a nutritional supplement for people with chronic bronchitis. It is a solid-phase synthesis of bradykinin and has been shown to have the same effects on blood pressure as bradykinin b2. Bradykinin acetate has also been shown to cause vasodilation, which may be due to its ability to bind to the ryanodine receptor and activate calcium release from intracellular stores. This drug can be detected in test samples using laser ablation waveform analysis.</p>

<p>D-threo-methylphenidate hydrochloride (DL-threo-MPH) is an inorganic acid that has been shown to be effective in the treatment of symptoms associated with attention deficit hyperactivity disorder (ADHD) and narcolepsy. It has long-term efficacy, which means it can be taken for a long time without causing adverse effects. DL-threo-MPH is also used to treat alopecia areata, which is an autoimmune disease that causes hair loss. This drug works by increasing dopamine levels in the brain and blocking the reuptake of dopamine. DL-threo-MPH has been tested on mice and found to have pharmacokinetic properties that are similar to those of dextromethorphan, but is more potent and selective.</p>

<p>Please enquire for more information about H-Cys-Glu-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 4-(2-Chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-2-propanoic 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 (S)-(-)-3-(Benzoylthio)-2-methylpropanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(4-Phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one is a chromene derivative. It has been shown to suppress the production of inflammatory cytokines such as tumor necrosis factor and interleukin 4 in vitro. 4-(4-Phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one also inhibits the activity of protein phosphatase 1 (PP1) and PP2B, which are enzymes that regulate the activity of other proteins by dephosphorylating them. The compound also suppresses the production of cytokines in wild type mice by inhibiting macrophages from releasing proinflammatory cytokines. Microglia cells are also suppressed from producing inflammatory mediators. These properties make 4-(4-Phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one an attractive</p>

<p>4-Methylcyclohex-3-ene-1-carboxylic acid is an anionic compound that is used in the preparation of perfumes. This substance has been shown to have a cycloaddition reaction with nonionic detergents and isoprene, catalyzing the oxidation of terephthalic acid to ethylene. 4-Methylcyclohex-3-ene-1-carboxylic acid can also be used as a medicinal agent for aromatization or as a catalyst for the production of aldehydes.</p>

<p>2-Fluoro-5-methoxyaniline is a high quality reagent that is used as an intermediate in the synthesis of various complex compounds. The CAS number for this chemical is 62257-15-2 and it has been shown to be useful as a building block for the synthesis of fine chemicals, speciality chemicals, and research chemicals with many different uses. It is also a versatile building block that can be used in reactions involving amines, alcohols, thiols, and nitriles. 2-Fluoro-5-methoxyaniline may also be used as a reaction component in organic syntheses.</p>

<p>Dehydroalanine, also known as Z-dehydroalanine, is an intermediate in the synthesis of a variety of compounds. It has been shown to be an effective catalyst for asymmetric hydrogenation reactions. Dehydroalanine is used in the synthesis of phenyl phosphine, which can be used to catalyze asymmetric hydrogenation reactions. The formation and reactivity of dehydroalanine have been studied using NMR techniques.</p>

<p>1,1-Bis(4-hydroxyphenyl)-2-phenyl-1-butene (BPB) is a synthetic compound that is used to treat breast cancer. BPB binds to the estrogen receptor and inhibits the growth of breast cancer cells in culture. It has also been shown to inhibit aromatase, an enzyme that converts androgens into estrogens, thus inhibiting the synthesis of estrogens. BPB has been shown to have antiestrogenic activity in vitro studies and is being studied as a possible treatment for breast cancer in vivo.</p>

<p>Please enquire for more information about 1-(tert-Butoxycarbonyl)-4-methylpiperidine-4-carboxylic 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 N-Methylpiperidinyl-2-methyl benzilate 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 3-(Bromomethyl)-1-methyl-1H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 6-methylpyridine-2-carboxylate is a pyridine derivative that has a nitrogen at the 6 position. It is an anionic compound, which is soluble in methanol and dichloromethane. The compound can be used to synthesize pharmaceuticals or as a precursor for polymers. It has been shown to inhibit the growth of tumor cells by binding to type 1 receptor sites on the surface of cancer cells. It also binds to quinine and enolate groups, which are found in many drugs. These binding sites may be exploited for drug design purposes.</p>

<p>N-Phenyliminodiacetic acid (NPD) is an organic acid that functions as a monomer and polymerization initiator in polyanhydrides. It has been shown to function as a redox potential sensor, having a strong response to changes in the environment. NPD has been shown to be sensitive to reactive oxygen species, such as HCl, which can affect its fluorescence properties. This compound is also active against aneurysms and has been used in simulations of these lesions. NPD also chelates with metal ions and can be used in the treatment of heavy metal poisoning.</p>

<p>Please enquire for more information about N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The beta-Asp-Phe methyl ester is a sweetener that is used in many different food and drink products. It is a mixture of the amino acid phenylalanine, methylester and chrysanthemum petal extract. The beta-Asp-Phe methyl ester is used as a buffer to achieve the desired pH for the product. Beta-Asp-Phe methyl ester is also used as an anti-tumour agent, which has been shown to be effective against breast cancer cells. This compound can be synthesized using ammonium formate and chromatography to isolate the desired product.</p>

<p>Please enquire for more information about 5-(3-Methylphenyl)-1,3,4-oxadiazol-2-amine 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-O-tert-butyl-D-trans-4-hydroxyproline 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-[2-(4-Benzylpiperazin-1-yl)-2-oxoethyl]-N-methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-NH-PEG4-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG4-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-(2-Methoxyphenoxy)ethanol (2-MPE) is a metabolite of propanediol, which is a precursor in the synthesis of polyurethanes. 2-MPE can be oxidized by monooxygenases to form syringyl and other reactive metabolites. Basic hydrolysis may also produce monomers such as phenols, alcohols, and carboxylic acids. Syringyl is one of the metabolic products of 2-MPE, which has been shown to be resistant to degradation by basidiomycete fungi.</p>

<p>2,5-Dimethoxy-4-methylamphetamine hydrochloride is a molecule that belongs to the class of phenethylamines. It has a serotonergic activity and can be used in the treatment of depression. This drug also affects the dopaminergic system and 5-HT2 receptors. 2,5-Dimethoxy-4-methylamphetamine hydrochloride is an agonist for 5HT1A receptors and an antagonist for 5HT2A and 5HT2C receptors. It has been shown to have a significant effect on locomotor activity in humans. The effects of this drug are dose dependent, with high doses leading to hallucinogenic effects.</p>

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

<p>3-Amino-5-methylisoxazole is a chemical compound that is used in the treatment of wastewater. It belongs to the group of p2, which includes sulfamethoxazole and sulfa drugs. 3-Amino-5-methylisoxazole is activated by multi-walled carbon or fatty acid and has a neutral pH. It has been shown to have significant cytotoxicity against cancer cells and also has antibiotic combinations with other drugs. 3-Amino-5-methylisoxazole is a drug that can be used in chemotherapy, but it may cause drug reactions.</p>

<p>Hemokinin 1 is a protein that is encoded by the NK1R gene. It has been shown to be associated with insulin resistance, inflammatory diseases, and pain control. Hemokinin 1 is also a potential treatment for viral infections such as HIV and hepatitis C. Hemokinin 1 interacts with nicotinic acetylcholine receptors (nAChRs) in the brain and blood vessels, which leads to an increase in blood pressure. This protein also interacts with hematopoietic cells, which may be responsible for its function as an antinociceptive agent. Hemokinin 1 has been implicated in autoimmune diseases such as arthritis and atrial fibrillation. This protein is expressed mainly in the brain, liver, heart, kidneys and spleen.</p>

<p>N-alpha-Z-L-lysine 4-nitrophenyl ester hydrochloride is a protease that belongs to the family of serine proteases. It is produced by the biotechnological process of enzymatic extraction from the natural polysaccharide carrageenan. This product has been used in the production of high yield and purified enzymes for industrial applications. The enzyme has been shown to have cysteine and hydrolytic activity, as well as being able to break peptidic bonds in peptides. N-alpha-Z-L-lysine 4-nitrophenyl ester hydrochloride also has a high specificity for proteolytic cleavage of proteins at their carboxy terminal end.</p>

<p>2-Hydroxy-4-methylpyrimidine is a heterocyclic compound that is used in the synthesis of other heterocycles. It is prepared by the reaction of methylbenzene and nitrous acid, followed by hydrolysis to form an imine. This compound has been synthesized with various substituents at different positions on the ring and also as a series of homologues. The 2-hydroxy-4-methylpyrimidine molecule has four nitroso groups, which are substituted with methyl groups. X-ray crystallography studies have shown that the molecule can exist in two different forms: one with the methyl groups pointing "homotopically" towards each other and the other with them directed "heterotopically."</p>

<p>Please enquire for more information about N-alpha-Nim-Bis-Z-L-histidine 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 2-Methoxypyrimidine-5-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methylguanidine HCl is a denaturing agent that has been used in the determination of nitrogen atoms in organic compounds. It has also been shown to have biological properties, such as anti-inflammatory activity and modulation of nitric oxide synthase. 1-Methylguanidine HCl is used in medicine as an anti-inflammatory drug, but it is not currently approved for medical use. 1-Methylguanidine HCl may be used therapeutically to reduce serum levels of creatine, which is synthesized in the liver and excreted by the kidney.</p>

<p>Please enquire for more information about N-Nitroso-N-methyl-4-aminobutyric acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Chloromethyl)-1-methyl-1H-benzimidazole hydrochloride (CMMB) is a synthetic compound that inhibits the enzyme tyrosinase, which is responsible for catalyzing the production of melanin. The tetradentate ligand in CMMB binds to the active site of tyrosinase and prevents it from catalyzing reactions. The redox potentials of CMMB make it possible to oxidize and reduce the compound, which allows for an easy synthesis. The dihedral angle between the amine and pyrimidine rings in CMMB provides a biomimetic structure that can be used to synthesize other aromatic compounds.</p>

<p>(R,S)-1-Methyl-3-nicotinoylpyrrolidine is a nicotinic acid derivative with a pyrrolidine ring at the 1-position. It is used as an intermediate in the synthesis of other compounds and has been used as a stabilizer for cellulose. The stability study showed that the compound was stable to evaporation and oxidation products in ethanol solutions. The adsorption index (AI) was found to be 0.9.</p>

<p>100 - 200 mesh, loading value 0.3-0.8 mmol/gCross linker: 1%</p>

<p>Please enquire for more information about 4,5-Dihydro-5a-methoxy D-(-)-norgestrel including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-N-Me-Asn(Trt)-OH is a peptidomimetic that mimics the sequence of the serine protease. The Fmoc group on the N-terminal amino acid is used to protect against proteolytic degradation and its methyl ester group confers stability in biological fluids. The Fmoc-N-Me-Asn(Trt)-OH has been shown to have minimal effects on endogenous protein synthesis, while also being quantified with high sensitivity and specificity. This compound has been shown to inhibit protein-protein interactions by acting as a competitive inhibitor of serine proteases.</p>

<p>Ethacrynic acid L-cysteine adduct (EAC) is a non-competitive inhibitor of phosphatases. It is a β-unsaturated ketone that has been shown to inhibit the phosphatase activity of pepsin and other enzymes. EAC binds to glutathione, forming an inactive covalent bond. The glutathione conjugate is inactivated by incubation with aminopyrine and pepsin, which degrades the glutathione moiety. This leads to the formation of a phosphatase inhibitor that is catalytic and competitive in nature. EAC can be used as a reagent for cell culture media or tissue sections, where it inhibits the activity of phosphatases that might interfere with certain enzymatic reactions.</p>

<p>Please enquire for more information about 4-[1-(2-Methoxyethyl)-1H-indol-3-yl]butanoic 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 6-Benzyloxy-5-methoxyindole-2-carboxylic 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 4-Methoxy retinoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Methyl-2-pyridinemethanamine is an imine that is used in cancer therapy. It has been shown to have antitumor activity at nanomolar concentrations, which is a very low dose. 6-Methyl-2-pyridinemethanamine is not sensitive to the body's enzymes and does not show any signs of toxicity. This drug also has a pharmacokinetic profile that enhances the uptake of other drugs and can be used for the treatment of cancers that are resistant to chemotherapy. The mechanism of action of 6-methyl-2-pyridinemethanamine is constitutive activation, which means it binds to the constitutively active site on the protein target and inhibits its function.</p>

<p>Please enquire for more information about H-Glu(OtBu)-OBzl.HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Dansyl-D-phenylalanine is a polymer film that is used as a monolayer in chromatographic science. It has been shown to be an effective coating for paper and textiles. N-Dansyl-D-phenylalanine can also be used as a crosslinking agent in the synthesis of polymers, and its use has been demonstrated in the preparation of enantiomerically pure polymers. In addition, it has been used as a chiral stationary phase for chromatography and as an assay for amino acid analysis.</p>

<p>(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane is a potent and selective inhibitor of HIV protease. It binds to the active site of the enzyme and prevents the formation of an enzyme-substrate complex, which inhibits protein synthesis. (2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane has been shown to be a potent inhibitor for other serine proteases such as chymotrypsin and trypsin. This compound has also been shown to be effective in inhibiting a number of proteases from bacteria such as Bacillus subtilis and Pseudomonas aeruginosa. Inhibitors have also been found against nonenzymatic protein inhibitors such as bacitracin, polymyxin B, colistin sulfate, vancomycin, and daptomycin</p>

<p>Please enquire for more information about (S)-N-Boc-3-amino-1-butyne 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 4-Methoxy-N-methylbenzylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methoxyethanamine is a metabolite of the drug 2-methoxyethanol. It is an amine that can be found in urine samples. Its structure consists of a hydroxyl group, sodium carbonate, and an intramolecular hydrogen. 2-Methoxyethanamine inhibits the production of angiotensin II, which reduces blood pressure. This molecule has antihypertensive activity because it prevents the conversion of angiotensin I to angiotensin II in the kidneys. 2-Methoxyethanamine also has a stepwise mechanism for its synthesis from ethylene diamine and nitrogen atoms. It can be oxidized by hydrochloric acid or reduced by hydrogen bond or amines. The redox potential of this molecule is -0.06 V, which makes it a nucleophilic compound with an amide bond as its conjugate base.</p>

<p>Please enquire for more information about Fmoc-S-trityl-D-penicillamine 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 L-Cysteinesulfinic acid, monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Ethyl-2-phenylmalonamide (2-EPMA) is a metabolite of primidone that acts as an inhibitor of glutamate dehydrogenase and may be used in the treatment of epilepsy. It has been shown to be effective in treating seizures caused by carbamazepine, phenobarbital, or phenytoin. 2-EPMA is also used to measure enzyme activities in serum, which can be used as a diagnostic tool for liver diseases. 2-EPMA is typically prepared for use as an enzyme inhibitor by diluting it with high salt or human serum. This compound may have carcinogenic potential and should not be administered with single doses greater than 100 mg/kg body weight. 2-EPMA interacts with many other drugs such as phenobarbital, phenytoin, and carbamazepine.</p>

<p>T22 peptide, also known as [Tyr5,12,Lys7]-polyphemusin II peptide, is a short, positively charged peptide, analog of polyphemusin peptide which exerts a strong anti- HIV activity. Polyphemusins are known to inhibit the growth of gram-negative bacteria and some fungi such as Candida Albicans. T22 is a potent antagonist of CXCR4 (IC50 = 5.05 nM), a co-receptor used by HIV to penetrate cells.<br>It has been suggested that T22 exerts its effect against HIV-1 especially by blocking virus-cell fusion and that T22 might interact with HIV envelope protein (such as gp120 ) and T-cell surface protein. T22 antiviral activity has been shown on HIV-infected MT-4 cells with an IC50 of 0.008 µg/mL (2.6 nM). The cytotoxic concentration on HIV virus (CC50) of T22 is 54 µg/mL (17 mM).</p>

<p>Inhibitor of cathepsin</p>

<p>Fmoc-Asn-OPfp is an optical probe for the detection of epidermal growth factor (EGF). It has a hydroxyl group attached to a fatty acid with an amino group. The safety profile of Fmoc-Asn-OPfp has been shown in animal tests and it is not toxic to humans. This compound is also a long-term inhibitor of the enzyme that produces EGF, which can be used for the treatment of congenital heart diseases. Fmoc-Asn-OPfp is water soluble, which makes it convenient for use with optical systems such as microscopes. Fmoc-Asn-OPfp may be useful in the diagnosis and treatment of various other conditions, including human immunodeficiency virus (HIV) infection, cancer, and chronic kidney disease.</p>

<p>Reagent in the chemical synthesis</p>

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

<p>2-Hydroxy-3-methylcyclopent-2-enone is a chemical species that is commonly found in Chinese herbs. It has been shown to have a number of applications, including as an ingredient in wastewater treatment, light emission, and process optimization. 2-Hydroxy-3-methylcyclopent-2-enone can be synthesized by reacting hydrochloric acid with acetone and formaldehyde. The reaction mechanism is not yet fully understood. Clinical studies show that 2-hydroxy-3 methylcyclopentane carboxylic acid has the potential to treat cancerous tumors in vitro.</p>

<p>Please enquire for more information about D-2,4-Dichlorophenylalanine 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-Methyl-2-[[3-[(1e)-2-(2-pyridinyl)ethenyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]thio]benzamide 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 2-Amino-4'-methoxyacetophenone hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about tert-butyl (2S)-2-Methyl-4-oxopiperidine-1-carboxylate 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 anagliptin</p>

<p>Please enquire for more information about Boc-(4-pyridyl)-L-beta-homoalanine 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-(1H-Indol-4-ylmethyl)-N-[2-(4-methoxyphenyl)ethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Methoxypyridine-2-boronic acid is a boronate ligand that can be used to form coordination complexes with metals. It has been shown to interact with silver ions, which are the most effective ligands for enhancing the fluorescence of organic dyes. 6-Methoxypyridine-2-boronic acid is able to rigidify organic molecules by binding to their steric and electronic properties, making them more resistant to photodegradation. This property makes it an excellent candidate for the use in the development of fluorescent labels in analytical chemistry.</p>

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

<p>Please enquire for more information about 1-(4-Methoxy-pyridin-2-yl)-ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetradecafluoro-2-methylpentane is a fluorinated hydrocarbon that is used in synthetic chemistry. It has been shown to inhibit the growth of cancer cells and leaves. Tetradecafluoro-2-methylpentane has also been shown to be an anthropogenic emission and may contribute to global warming. The chemical is classified as a cyclic hydrocarbon, which means it contains two or more rings of carbon atoms. Cyclic hydrocarbons are generally toxic because they disrupt normal cellular function through interference with cell membranes, protein synthesis, and DNA replication.</p>

<p>Please enquire for more information about 4-Formyl-3-methoxy-phenyloxymethyl polystyrene 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 16-Phenoxy tetranor pgf2alfa cyclopropyl methylamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Arg-Gln-OH is a growth factor that has been shown to be effective in the genetic ablation of mice. This growth factor is taken up by cells via receptor activity and stimulates DNA synthesis and cell division. H-Arg-Gln-OH has been shown to be successful in the treatment of congenital heart disease. The onset latency is site specific and low energy, which means that it can be used for noninvasive treatments.</p>

<p>4-Chloro-2-phenylquinazoline is a ligand that inhibits the growth of bacteria by binding to their DNA. It has a molecular weight of 242.6 g/mol, and can be synthesized in two steps from 2-phenylaniline and o-chloroacetophenone. The pharmacokinetic properties of this compound have been studied using magnetic nanoparticles. 4-Chloro-2-phenylquinazoline has been shown to inhibit cancer cells and also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. This ligand binds to the nitrogen nucleophiles on the bacterial cell wall (e.g., trichophyton mentagrophytes) and prevents them from reacting with chlorine atoms in the environment, thus inhibiting bacterial growth.</p>

<p>Please enquire for more information about Methyl 3-formyl-4,6-dimethoxy-1-methyl-1H-indole-2-carboxylate 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(Ac)-D-Ala-D-lactic 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 2-Phenylpropan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The drug, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride (CGP 46660), is a competitive antagonist at the human histamine H3 receptor. It has been shown to bind to the histamine H3 receptor in the range of 0.001 to 1 μM and is selective for this receptor over other receptors. CGP 46660 is an optical sensor that can be used in titration calorimetry experiments to measure changes in heat production when it binds to histamine H3 receptors. The drug also has been shown to inhibit guanine nucleotide-binding protein (G protein) signaling pathways and brain functions such as memory formation, learning, and attention span. These effects were demonstrated in humans by measuring EEG activity. The optimum concentration of CGP 46660 for these effects was found to be between 0.01 and 10 μM.</p>

<p>Bis[(S)-1-phenylethyl]amine (BPEA) is an amide that is used as a synthetic intermediate in the process of alkylating and halogenating amines. BPEA is prepared by reacting phenethylamine with chloroacetic acid and phosphorous trichloride. It has been shown to have high efficiency in this reaction, with little impurities and a high yield. The product of this reaction can be purified using recrystallization or preparative thin-layer chromatography. BPEA is a ligand that contains a stereogenic center, which allows for the preparation of chiral compounds with great stereoselectivity. This synthetic intermediate can be used to prepare organometallic compounds in the presence of a phosphite ligand.</p>

<p>Please enquire for more information about 3-Methoxy-7a-methyl-estra-2,5(10)-dien-17-one 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 2-(4-Methoxyphenyl)-2-(1-hydroxycyclohexyl)ethylamineHydrochloride 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 3-Amino-6-bromo-2-methylquinazolin-4(3H)-one 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-alpha-Boc-Nomega,omega''-bis-Z-D-arginine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromo-3-methyl-1H-indazole is an organic compound that is synthesized from lithium diisopropylamide and lithium. 5-Bromo-3-methyl-1H-indazole is a white solid with a melting point of 151°C. It reacts with anhydrous hydrogen bromide to form 5,5'-dibromoindazole. The molecular weight of this compound is 202.2 g/mol.</p>

<p>Please enquire for more information about (Des-Gly77,Des-His78)-Myelin Basic Protein (68-84) (guinea pig) 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-D-glutamic acid-gamma-tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(5-Fluoro-2-methyl-1H-inden-3-yl)acetic acid (FMIAA) is a phase transfer catalyst that catalyses the condensation of alkyl esters. It can be used in the condensation of aromatic and aliphatic aldehydes in liquid phase with potassium as a reagent and organic solvent. The FMIAA is then removed by dehydrating the product, leaving it in solid form. FMIAA has been shown to be effective for the synthesis of a wide range of compounds, including pharmaceuticals such as cyclopentanone, aminomethylpiperidine, and 4-aminoquinoline.</p>

<p>Please enquire for more information about 1-(4-Isobutoxy-3-methoxybenzyl)piperazine 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-Boc-b-alanine ethyl ester 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-(R,S)-3-amino-N-1-carboxymethyl-2-oxo-5-cyclohexyl-1,4-benzodiazepine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Ac-Arg-pNA·HCl is a substrate that is activated by hydrogen fluoride to form a nitro group. This compound can be used in the synthesis of nitrobenzene and other aromatic compounds. Ac-Arg-pNA·HCl also has enzymic activity, which is catalyzed by an enzyme called benzyloxycarbonyl (Boc).</p>