Amino Acids (AA)

<p>4-Hydroxy-3-methoxybenzoic acid ethyl ester is a synthetic compound that is converted to protocatechuic acid, an antioxidant found in wine. It has been shown to have antioxidative properties in inflammatory bowel disease by inhibiting the formation of reactive oxygen species. Protocatechuic acid also inhibits the growth of bacterial strains such as Listeria monocytogenes and Bacillus cereus, which are often resistant to antibiotics. The mechanism of action is not well understood, but it may be due to its ability to inhibit the production of p-hydroxybenzoic acid, a precursor for bacterial cell wall synthesis. Protocatechuic acid also has anti-inflammatory properties and can be used as a bioactive phenolic in topical preparations such as creams or ointments.</p>

<p>Prolintane hydrochloride is a drug that has been shown to inhibit the activity of enzymes in the inflammatory and immune responses. It also inhibits the uptake of caffeine, which may be due to its ability to bind with the toll-like receptor (TLR) and CB2 receptor. Prolintane hydrochloride has been used to treat bowel disease, depression, and autoimmune diseases such as rheumatoid arthritis. This drug has a depressant effect on the central nervous system, which may lead to symptoms such as drowsiness and fatigue. The drug is metabolized through a synthetic pathway that involves N-deacetylation by acetyltransferase enzymes. Prolintane hydrochloride also inhibits inflammatory bowel disease by reducing cytokine production in mice with colitis.</p>

<p>5-Fluoro-2-methylphenylhydrazine hydrochloride is a crystalline solid that is soluble in water. It is used as a reagent in organic synthesis, but it also has application as an intermediate in the production of calcium hydroxide and calcium fluoride. 5-Fluoro-2-methylphenylhydrazine hydrochloride reacts with methacrylate to produce an ultrafine powder, which can be difficult to hydrate because of its high molecular weight. The hydration reaction requires the addition of large amounts of water and heat. This process can be accelerated by adding a solution of calcium ions or calcium hydroxide to the reaction mixture. Hydrogen fluoride gas (HF) may also be generated during this process. Crystallization occurs when the solids are heated or placed in contact with a nonpolar solvent such as hexane.</p>

<p>Dihydro-5-methoxy-2,4(1H,3H)-pyrimidinedione is a high quality chemical and useful building block. It is a fine chemical and research chemicals as well as a versatile building block that can be used in synthesis of various compounds. Dihydro-5-methoxy-2,4(1H,3H)-pyrimidinedione has been shown to have activity against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens.</p>

<p>2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical &amp; Laboratory Equipment.</p>

<p>2-Phenoxybenzaldehyde is an organic compound that belongs to the heterocyclic aldehyde family. It is a white solid with a strong, pleasant odor. 2-Phenoxybenzaldehyde is used as an intermediate in organic synthesis, and has been shown to inhibit the receptor activity of human leukocyte antigen (HLA) class II molecules. The reaction mechanism for this inhibition is not known. The reaction of 2-phenoxybenzaldehyde with hydrochloric acid produces phenylhydroxylamine, which can be oxidized by inorganic acids to form phenyloxalic acid. This compound also inhibits the production of inflammatory cytokines such as TNFα and IL-1β in vitro and in vivo.</p>

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<p>17alpha-Methyl-19-nortestosterone (17MT) is an anti-cancer agent that has been used as a contraceptive. It inhibits the conversion of testosterone to dihydrotestosterone by competitive inhibition of the enzyme 3beta-hydroxysteroid dehydrogenase, which is responsible for the first step in the biosynthesis of androgens. 17MT has also been shown to inhibit angiotensin II formation, thereby reducing blood pressure. This drug acts as a structural analogue of progesterone and binds to progesterone receptors, as well as other steroid receptors, with high affinity. 17MT also inhibits fatty acid synthesis in cancer cells, leading to decreased tumor growth.</p>

<p>3-Phenyl-4-phthalazinone-1-acetic acid (3PPAA) is an organic compound that can be used to synthesize gold nanoparticles. Gold nanoparticles are ferroelectric and have a dipole moment. 3PPAA can be modeled using simulations with the panthera program, which is able to predict the effect of various parameters on the morphology of the particles. The shape of the gold nanoparticles can be controlled by changing the concentration of 3PPAA in water and by adding or removing a stabilizing agent such as sodium bicarbonate. 3PPAA has been shown to have a strong interaction with mitochondrial DNA, which could lead to death of cells by interfering with mitochondrial function.</p>

<p>Please enquire for more information about 7-Chloro-5-(2-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-2-methanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bis-Boc-amino-oxyacetic acid is an analog of goserelin acetate. It binds to the androgen receptor in prostate cancer cells, which leads to cytostatic effects. This drug has shown a low potency in human serum and does not bind to human serum proteins.<br>The uptake of Bis-Boc-amino-oxyacetic acid by prostate cancer cells was found to be significantly greater than that of goserelin acetate. The binding affinity of this drug for the androgen receptor is also lower than that of goserelin acetate, making it more selective for prostate cancer cells over other tissues.</p>

<p>3-Cyano-4-methylnitrobenzene is a nitro compound that can be prepared by the reaction of nitric acid with aniline. It has been shown to have a strong affinity for oxygen, which may be due to its pyran ring. 3-Cyano-4-methylnitrobenzene has been found to react with acetonitrile in an electrochemical experiment, leading to the formation of nitronium ion and nitrate ion. The mechanism for this reaction is not well understood, but it offers a convenient way of preparing 3-cyano-4-methylnitrobenzene from nitric acid and aniline.</p>

<p>N-Acetyl-L-methionine is a form of the amino acid methionine. It is an intermediate in the conversion of L-methionine to S-adenosylmethionine, which is involved in methylation reactions in cells. N-Acetyl-L-methionine has been shown to be effective against nitrite ion, a reactive nitrogen species that causes oxidative stress and damage to DNA, RNA, and proteins. It also has been shown to have biological properties for the prevention of ischemia reperfusion injury following cardiac arrest and liver transplantation. N-acetyl-L-methionine may also have benefits for individuals with high body mass index or rats with liver microsomes.</p>

<p>Lysine clonixinate is a non-steroidal anti-inflammatory drug (NSAID) that is used to treat pain, inflammation and fever. It is effective in the treatment of infectious diseases, statistically. Lysine clonixinate has been shown to have an antiviral effect against influenza virus and HIV. Lysine clonixinate also exhibits a protective effect against bacterial infections in animals with bowel disease.</p>

<p>1-Phenanthrol is a naturally occurring phenanthrene derivative that is used in the treatment of cervical cancer. It has been shown to be effective in the chemiluminescence method using urine samples, which indicates that it may have an effect on the body's metabolism. 1-Phenanthrol has also been shown to inhibit the production of s-phenylmercapturic acid, which is a metabolite of aromatic amines. This inhibition may be due to its receptor binding properties as it binds to and activates the peroxisome proliferator-activated receptor alpha (PPARα) and PPARγ. 1-Phenanthrol also inhibits angiotensin II type 1 receptors and can cause vasorelaxation by reducing blood pressure.</p>

<p>N6-Cbz-L-lysine is a compound that has been shown to inhibit the activity of enzymes involved in disulfide bond formation, such as protein tyrosine phosphatase (PTP), and other enzymes implicated in cancer. N6-Cbz-L-lysine binds to the enzyme bromoacetic acid complex, which is involved in the uptake of substances into cells. This compound also has a high resistance to ring-opening, making it a good candidate for cancer therapy. The structural biology and molecular modelling of N6-Cbz-L-lysine has shown that this drug may be an active substance with anti-cancer activities. Magnetic resonance spectroscopy studies have revealed that N6-Cbz-L-lysine may have potential as an antihypertensive agent.</p>

<p>Please enquire for more information about 9,10-Dihydro-5-methoxy-9-oxo-4-acridinecarboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminobenzoyl-L-glutamic acid (PABA) is a dinucleotide phosphate that can be found in human serum. It has been shown to have receptor activity for epithelial mesenchymal cells and is used as a model organism for folate, group p2 polymerase chain reactions (PCR). PABA is also involved in the reaction mechanism of linear calibration curves.</p>

<p>Please enquire for more information about (S)-2-Amino-5-methoxytetralin (S)-mandelate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methylnicotinic acid is a synthetic compound that belongs to the class of organic compounds. It is an amide with optical properties and reacts in aqueous solution with hydroxides to form salts. 5-Methylnicotinic acid has been shown to be effective against rupatadine fumarate, sodium hydroxide solution, transfer mechanism, and plasma samples.</p>

<p>Serotonin receptor 5-HT2A antagonist</p>

<p>Fmoc-L-aspartic acid beta-2-phenylisopropyl ester is a macrocyclic amino acid with conformational and anti-inflammatory properties. It has been shown to inhibit the proliferation of cancer cells in vitro, as well as the osteolytic, lymphoproliferative, and inflammatory activities in vivo. Fmoc-L-aspartic acid beta-2-phenylisopropyl ester also has antiarrhythmic effects on cardiac tissue that are caused by its ability to bind to chloride channels. This compound also inhibits the production of inflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin 6 (IL6).</p>

<p>H-gamma-carboxy-Glu-OH is a synthetic peptide with the amino acid sequence H-gamma-Carboxy-Glu. It is a glp-1 analogue and its function is to regulate glucose homeostasis. The protein has been shown to have antiapoptotic effects in human osteosarcoma cells. H-gamma-carboxy-Glu-OH has also been shown to regulate mitochondrial membrane potential, which is required for cell signaling pathways and calcium binding. H-gamma-carboxy-Glu-OH's receptor molecule is known as the GPCR, which plays an important role in the regulation of cell signaling pathways and calcium binding. H gamma carboxy Glu OH is a cyclic peptide that contains disulfide bonds. This compound has the basic structure of an alpha helix, which consists of many turns of amino acids bonded together by hydrogen bonds between individual amino acids</p>

<p>Please enquire for more information about 3-(tert-butyl)-4-(3-(4-nitrophenyl)prop-2-enylidene)-1-phenyl-2-pyrazolin-5-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Phenylbenzoic acid methyl ester is a bifunctional molecule that has been shown to be an effective antibacterial agent. It contains two oxadiazole moieties, which are structurally similar to sulfonamides and can form a stable amide bond with an amino group. The pharmacophore of 4-phenylbenzoic acid methyl ester is a four-member ring with two nitrogens and two carbons. This compound has been shown to have antibacterial properties by cleaving the magnesium bond in the enzyme methionine synthase, which catalyzes the formation of methionine from homocysteine and ATP. 4-Phenylbenzoic acid methyl ester is also able to cleave bonds in nonpolar solvents such as benzene, chloroform, and dichloromethane.</p>

<p>4-Bromo-2-methylbenzoic acid ethyl ester is a high quality and versatile building block. It is a useful intermediate in the synthesis of organic compounds, and can be used as a reaction component in the synthesis of complex compounds. 4-Bromo-2-methylbenzoic acid ethyl ester is also a useful scaffold for the construction of new chemical entities. It has been shown to react with potassium tert-butoxide to produce 4-(2,6-dimethylphenyl)piperidine (CAS No. 220389-34-4).</p>

<p>1-Linoleoyl-rac-glycerol is a lipid with a structure similar to that of linoleic acid. The compound is used as a substrate for the study of the effects of oxygenation on lipid metabolism. 1-Linoleoyl-rac-glycerol has been shown to have anti-inflammatory properties in chronic kidney disease and pancreatitis models, which may be due to its inhibition of pancreatic lipase. 1-Linoleoyl-rac-glycerol is also used as a reaction product in sample preparation techniques, such as thin layer chromatography and high performance liquid chromatography. A variety of reactions can be performed with this compound, including hydrolysis by thrombin or trypsin, esterification with methanol or chloroform, or oxidation by potassium permanganate. 1-Linoleoyl-rac-glycerol has been shown to inhibit the growth of human lung epithelial cells (thp1</p>

<p>N-(2-Chlorobenzyl)-1-phenylpropan-2-amine hydrochloride (CBP) is a potent stimulant drug that is used to treat chronic pain. It has been shown to be effective in the treatment of alopecia areata and inflammatory diseases, such as Crohn's disease, ulcerative colitis, and rheumatoid arthritis. CBP blocks protein synthesis by inhibiting the activity of the enzyme dinucleotide phosphate (DNP). This inhibition leads to the accumulation of adenosine monophosphate (AMP), which inhibits cyclic AMP production and protein synthesis. CBP also prevents the binding of DNP to RNA polymerase II at promoter sites, leading to a decrease in mRNA production. As a result, CBP may inhibit protein synthesis by preventing transcription or translation.</p>

<p>D-Ornithine hydrochloride is a synthetic amino acid that is used as a precursor for the synthesis of polyamines in the body. It is also used as an additive in food and animal feed. This amino acid has been shown to inhibit gramicidin production by inhibiting the enzyme acylase. D-Ornithine hydrochloride has also been shown to stimulate the production of ornithine by increasing ATP levels and activating enzymes such as pyruvate kinase, glutamic pyruvate transaminase, and phosphoenolpyruvate carboxykinase. In addition, it has been shown to have chemoenzymatic properties that allow for its use in reactions with fatty acids as substrates. The reaction yield increases with higher substrate concentrations, which can be achieved using immobilized cells or by adding cyclic peptides such as ornithine to the reaction mixture.</p>

<p>Cyclic(glycyl-L-tyrosyl) is a phenolic compound and the main metabolite of the dietary supplement resveratrol. It has been shown to have interactions with cellular transport, as well as the ability to activate a number of proteins that are involved in cellular transport. Cyclic(glycyl-L-tyrosyl) also interacts with hydroxyl groups on proteins and activates them, which may lead to the uptake of these proteins by cells. This interaction between cyclic(glycyl-L-tyrosyl) and hydroxyl groups on proteins may be due to its conformation and affinity for this residue. Cyclic(glycyl-L-tyrosyl) has been reported to inhibit the binding of glucosamine to NUDIX hydrolase, as well as preventing glucosamine from activating NUDIX hydrolase.</p>

<p>Please enquire for more information about 2-Amino-3-[[[4-(2-methylpropyl)phenyl]methylene]amino]-2-butenedinitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>L-Cysteine is a nonessential amino acid that has the ability to disrupt bacterial cell membranes. It can be produced by hydrolysis of human hair, feathers, and animal hides. L-Cysteine is used as a food additive and flavouring agent in human food and animal feed. It is also used as an additive in the manufacture of plastics, adhesives, and rubber products. L-Cysteine hydrochloride monohydrate (L-Cys HCl) is a white crystalline powder that dissolves readily in water. L-Cys HCl has been shown to have anti-inflammatory properties due to its ability to inhibit the production of prostaglandins.</p>

<p>(+/-)-6-Chloro-7,8-dihydroxy-3-allyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine HBr is a model system for Parkinson's disease that has been shown to have similar effects on locomotor activity as the dopamine antagonist haloperidol. The drug enhances dopaminergic and cholinergic transmission in the brain by binding to kappa opioid receptors. This leads to an increased release of dopamine and acetylcholine that can be blocked by drugs such as naloxone and atropine respectively. (+/-)-6-Chloro-7,8-dihydroxy 3-(allyl)-1-(phenyl) 2,3,4,5 tetrahydro 1H 3 benzazepine HBr has been shown to decrease camp levels in the caudate putamen region of rats</p>

<p>GABA is a neurotransmitter that is found in the brain and spinal cord. It is an analog of the amino acid gamma-aminobutyric acid and can be synthesized from glutamic acid. GABA has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis, which may be due to its ability to decrease the proliferation of T cells and macrophages. GABA also has been shown to promote growth of hybridomas, which are immune cells that produce antibodies.</p>

<p>Please enquire for more information about 3-((4-Acetylphenyl)amino)-2-phenylinden-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(Benzyloxy)-3-methoxyphenylacetonitrile is an anti-cancer drug that belongs to the class of dihydroisoquinolines. It is used as a monomer in the synthesis of other drugs and it has been shown to be an effective inhibitor of cancer cells when used with carbamic acid. 4-(Benzyloxy)-3-methoxyphenylacetonitrile is synthesised through the reaction of 2,4-dichloroisonicotinic acid and 3-fluoroacetamide in the presence of a strong acid catalyst. This compound has been shown to have a high level of stereoselectivity, which makes it useful for synthesising other compounds.</p>

<p>5-Amino-3-(4-methoxyphenyl)pyrazole (5AMPAP) is an anti-cancer agent that is effective against a number of different cancers, including breast, lung, and prostate. It selectively inhibits the growth of cancer cells by targeting enzymes in the mitochondria that are required for ATP production. 5AMPAP binds to the enzyme pyruvate dehydrogenase kinase, which has been shown to be involved in regulating cell proliferation and apoptosis. In addition, it has been demonstrated that this compound has anti-inflammatory properties. The regioselectivity of 5AMPAP was determined by x-ray crystallography and was found to form a pyrazolopyrimidine ring with two nitrogens on opposite sides of the ring. This regioselectivity is necessary for its anti-cancer activity.</p>

<p>Lysine(crotonyl)-OH is a versatile building block that has a variety of uses in the synthesis of complex compounds, research chemicals, and reagents. This compound can be used as a high-quality building block for the synthesis of useful intermediates, reaction components, and scaffolds.</p>

<p>H-Pro-Pro-OH·HCl is a fine chemical that is commonly used as a building block for organic synthesis. This compound is soluble in water, making it an ideal reactant for use in reactions involving peptides and proteins. H-Pro-Pro-OH·HCl is also useful as an intermediate, research chemical, or speciality chemical. It has been used as a reagent for the preparation of other chemicals and has shown high quality performance in reactions with nucleophiles.</p>

<p>7-Methylxanthine is a purine alkaloid that is the primary metabolite of caffeine. It is structurally related to theobromine, which is found in chocolate. 7-Methylxanthine has been shown to have hypoglycemic effects and may be useful for the treatment of myopia. The optimum concentration of 7-methylxanthine for inhibiting carotenoid biosynthesis has been determined as 10 μM. It also inhibits axial elongation in cultured chick retinal cells by reducing carotenoid levels and increasing p-hydroxybenzoic acid levels in the retina. The analytical method for quantifying 7-methylxanthine relies on high performance liquid chromatography with ultraviolet detection (HPLC/UV).</p>

<p>4-Phenyl-2-butanone is an organic compound that is used as a solvent. It has been shown to be effective against a wide range of bacteria, including Gram positive and Gram negative bacteria. 4-Phenyl-2-butanone disrupts the cell membrane by binding to glycol ether, which is an important part of the lipid bilayer. It also inhibits the synthesis of two important molecules in bacterial cells, dinucleotide phosphate and phospholipids. This process leads to bacterial cell death. 4-Phenyl-2-butanone also has antimicrobial properties due to its ability to destroy water vapor and inhibit growth of microorganisms on skin.</p>

<p>1-Phenoxyphthalazine is a n-oxide with life-threatening properties. It is used as a medication for high blood pressure and as an anxiolytic. 1-Phenoxyphazin has been shown to have receptor affinity for the dopamine, serotonin, and noradrenaline receptors. It also blocks the carboxylate ion channels of the central nervous system. 1-Phenoxyphthalazine has been shown to have peroxide and chloride properties, which may contribute to its antihypertensive effects.</p>

<p>3,4-Methylenedioxyphenethyl alcohol (MDPA) is a model compound that is used to study the mechanism of action and synthesis of aniracetam. It has been shown to be an antagonist of pentylenetetrazole, a convulsant drug. MDPA was also found to have anticonvulsant properties in mice. It was found that this compound had no effect on the inhibition of movement when administered at doses up to 100 mg/kg. This compound is an analog of liriodenine, which has been shown to have anti-inflammatory properties. 3,4-Methylenedioxyphenethyl alcohol is not active in the central nervous system due to its stereoselectivity; this means it can only bind to one stereoisomer within the brain and does not cross the blood-brain barrier.</p>

<p>4-Phenylazophenol is an organic azobenzene that has a specific treatment for the degradation of amines and mineralization. It has been shown to reduce the levels of phenols, fatty acids, and amines in wastewater. 4-Phenylazophenol is also used as an enzyme inhibitor in reactions with hydrogen bond formation and as a receptor α ligand. The natural compounds found in 4-phenylazophenol have borohydride reduction properties.</p>

<p>N-Fmoc-5-fluoro-L-tryptophan is a biologically active form of tryptophan that has been shown to have potent effects on the cardiovascular system. It is used as a tool for studying the function of angiotensin, collagen, and microstructural elements in the heart and lungs. N-Fmoc-5-fluoro-L-tryptophan has been shown to synergize with other heterocycles, maximizing its biological properties. This chemical is also effective at inducing muscle contraction in rats. N-Fmoc-5-fluoro-L-tryptophan binds to cardiothoracic proteins, causing changes in their structure that lead to increased muscle contractility. The covalent bond between this compound and the protein can be cleaved by enzymes such as proteases or nucleases, which can be useful for studying the interactions of drugs with these proteins.</p>

<p>9-Fluoro-3-methyl-7-oxo-10-(1-piperazinyl)-2,3-dihydro-7H-[1,4]oxazino[2,3,4-Ij]quinoline (FQ) is a fluoroquinolone antibiotic. It inhibits the DNA gyrase and topoisomerase IV enzymes that maintain the integrity of bacterial DNA. FQ has been used to treat urinary tract infections in humans and other animals. This drug is also effective against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. FQ binds to bacterial 16S ribosomal RNA and inhibits protein synthesis leading to cell death by inhibiting the production of proteins vital for cell division. The 9 position on the quinoline ring can be detected using UV detection at 260 nm.<br>FQ can be analyzed using mass spectrometry with fluor</p>

<p>1-palmitoyl-2-(10-(4-((trifluoromethyl)diazirinyl)phenyl)-8-oxadecanoyl)-sn-glycero-3-phosphocholine (PPC) is a liposome that induces necrotic cell death. It binds to the mitochondria and inhibits adenine nucleotide translocation, leading to the loss of mitochondrial membrane potential and the release of cytosolic calcium. This leads to activation of proapoptotic proteins, such as Bax and Bak, which initiates caspase-independent apoptosis. PPC also induces light emission from phospholipid hydroperoxide decomposition, which can be used as a biomarker for cellular physiology.</p>

<p>H-Tyr-Tyr-Tyr-OH is a synthetic compound that has been used to study the mechanism of lactoperoxidase. Lactoperoxidase is an enzyme that catalyzes the oxidation of thiocyanate to form hypothiocyanite, hydrogen peroxide, and a hydroxy group. The hydroxy group is formed by the reaction of two molecules of hydrogen peroxide with a molecule of thiocyanate. This reaction produces an oxygen atom, which then reacts with water to produce an acid. H-Tyr-Tyr-Tyr-OH has been shown to be a substrate for lactoperoxidase in horse serum and bovine serum. It has also been found to react with oxygen at neutral pH levels, forming a product that absorbs ultraviolet light at 280 nm.</p>

<p>Fmoc-D-allo-Thr(tBu)-L-Ser(Psi(Me,Me)pro)-OH is a reagent that is used as an intermediate in the synthesis of complex compounds. It is also a fine chemical that can be used to prepare speciality chemicals. Fmoc-D-allo-Thr(tBu)-L-Ser(Psi(Me,Me)pro)-OH has CAS No. and can be used as a reaction component in various reactions. This compound is versatile and can be used as a building block for other compounds.</p>

<p>O-Aminobenzoylglycyl-p-nitro-L-phenylalanyl-L-proline TFA salt is a synthetic, hydrophilic interaction chromatography (HIC) substrate. It has inhibitory properties and is used in biological assays to measure the activities of enzymes that catalyze the hydrolysis of the substrate. O-Aminobenzoylglycyl-p-nitro-L-phenylalanyl-L-proline TFA salt also has been shown to have bioactivities on blood pressure and cell monolayers.</p>

<p>(R)-Methyl 2-hydroxybutanoate is a synthetic chemical that is used in the esterification reaction to produce methyl esters and as an industrial solvent. This chemical can be synthesized by the reaction of (R)-methyl acetoacetate and hydrochloric acid. The technique for this chemical is a two-step process, which includes hydroxylation followed by hydrogenolysis. The yield rate for this chemical is about 98%.</p>

<p>Alanine anhydride is a purine derivative that can be used as a diagnostic agent. It contains a carbonyl group and a chloride, which are both low energy groups. Alanine anhydride is also a hydrogen bond acceptor, which allows it to bind to the amide backbone of proteins. The nitrogen atoms in this compound are diagnostic agents that can be used to identify the presence of cancer cells in urine samples. This chemical has been shown to have potential microbial infection-fighting effects.</p>

<p>(R)-(+)-2-Methoxypropionic acid is a derivatization agent that is used to label branched-chain amino acids. It has been shown to react with l-rhamnose, which is found in glycoproteins and polysaccharides.</p>

<p>Fmoc-a-Me-Trp(Boc)-OH is a fine chemical that is used as an intermediate in organic synthesis. It can be used as a versatile building block, useful reaction component, or speciality chemical. Fmoc-a-Me-Trp(Boc)-OH is an important compound for the production of complex compounds and is useful as a building block for high quality reagents. Fmoc-a-Me-Trp(Boc)-OH has CAS No. 1315449-98-9 and can be ordered from Sigma Aldrich at www.sigmaaldrich.com</p>

<p>D-Penicillamine is a nonsteroidal anti-inflammatory drug that is used to treat bowel disease, including ulcerative colitis and Crohn's disease. It has also been used as a treatment for schizophrenia that is unresponsive to other treatments. D-Penicillamine binds covalently to reactive oxygen species (ROS), thereby preventing their interaction with proteins and DNA. The binding of ROS by D-penicillamine can be monitored using electrochemical impedance spectroscopy (EIS). The compound has also been shown to reduce the expression of bcl-2 protein in human cells, which may result in increased oxidative injury and rates of cell proliferation. D-Penicillamine has been shown to have therapeutic benefits for patients with primary sclerosing cholangitis, myocardial infarcts, or preparative high performance liquid chromatography (HPLC) analysis.</p>

<p>Inhibitor of ornithine decarboxylase</p>

<p>Fmoc-Asp(OH)-OtBu is a synthetic, non-natural amino acid that has been used in the chemical synthesis of lipoproteins. It was incorporated into recombinant human low-density lipoprotein (LDL) and high-density lipoprotein (HDL) to study the effect of acidic hydrolysis on their composition. Fmoc-Asp(OH)-OtBu is a fluorescent compound that can be detected using spectroscopy. It is also used as an amino acid residue in solid-phase peptide synthesis to synthesize peptides with an aspartyl residue at the N terminus.</p>

<p>2,4-Dimethoxy-6-methylbenzaldehyde is a biomolecular that belongs to the class of depsidones. It is a tetracyclic compound that has been isolated from the fungus Antrodia camphorata and the lichen Xanthoria polycarpa. 2,4-Dimethoxy-6-methylbenzaldehyde has been shown to inhibit the growth of fungi by preventing oxidative phosphorylation in mitochondria. This compound also shows regioselectivity for phenanthrenes, which are aromatic hydrocarbons with two benzene rings and one or more methyl groups on each ring. The synthesis of 2,4-dimethoxy-6-methylbenzaldehyde is achieved through a Witting reaction between olefinic compounds and diethyl malonate in the presence of base. 2,4-Dimethoxy-6-methylbenzaldehyde can also be synthesized by oxidizing dib</p>

<p>L-Serine ethyl ester hydrochloride is a metabolite of L-serine that has been found to inhibit the growth of cancer cells. It has been shown to inhibit the proliferation of muscle cells and reduce the size of pancreatitis. L-Serine ethyl ester hydrochloride has also been shown to have an inhibitory effect on stenosis in animal models. This drug inhibits microbial growth by inhibiting protein synthesis in bacteria, which may be due to its hydroxyl group. L-Serine ethyl ester hydrochloride also enhances endothelial cell growth and prevents autoimmune diseases in mice.</p>

<p>3-Bromo-4-methoxybenzoic acid methyl ester is an isomer of 4-methoxybenzoic acid. It is a natural product that can be found in dihydroisoquinoline and in the ethyl formate oxidation products. There are two ways to synthesize this compound: by oxidation of diphenyl ethers or by hydrolysis of chloride acetaldehyde. 3-Bromo-4-methoxybenzoic acid methyl ester has been shown to have cellular toxicity against human cells and biphenyl.</p>

<p>2-Methylresorcinol, technical is the sodium salt of 2-methylresorcinol. It has been shown to be chemically stable at high temperatures and can be used in magnetic resonance spectroscopy. The nmr spectra of 2-methylresorcinol are different from those of other compounds. It is a molecule with a carbonyl group and one methyl group that reacts with hydrochloric acid to produce a reaction product with a chlorine atom, which reacts with trifluoroacetic acid or trifluoromethanesulfonic acid to produce an activated intermediate that can react with a second molecule to form another reaction product. This mechanism may be useful in the synthesis of anti-tuberculosis drugs.</p>

<p>2,2'-Dihydroxy-4-methoxybenzophenone (DHMB) is a chemical compound used in the manufacturing of sunscreens. It is also used as an antioxidant and antiinflammatory agent in topical preparations. The genotoxic effects of DHMB are well documented, but it is unclear whether these effects are due to UV radiation or other mechanisms. DHMB has been shown to be toxic to cells in vivo and in vitro. There have been reports of skin cancer developing on the ears of rats following chronic exposure to this chemical. DHMB binds to the estrogen receptor, which may be responsible for its genotoxic activity. This chemical has also been shown to inhibit the growth of bacteria such as Pseudomonas aeruginosa and Escherichia coli by binding with fatty acids on the cell membrane surface. DHMB is used for wastewater treatment because it can bind with heavy metals and remove them from water sources.</p>

<p>Fmoc-3-(2'-pyridyl)-L-alanine is an acid molecule that has been shown to have anti-cancer properties. It is a polysaccharide polymer used in the preparation of polyvinyl alcohol and polyvinyl acetate. The phosphatase activity of Fmoc-3-(2'-pyridyl)-L-alanine was first observed in the 1970s, when it was found to be an effective inhibitor of acid phosphatase. This structural study has also revealed the effects of Fmoc-3-(2'-pyridyl)-L-alanine on cancer cells, which may be due to its ability to prevent cell division and genetic control. Fmoc-3-(2'-pyridyl)-L-alanine is also known as a monoclonal antibody that can bind to specific structures on cancer cells, such as antigens and receptors, which may be responsible for these effects.</p>

<p>4-Methylpyrazole is a competitive inhibitor of alcohol dehydrogenase, which can be used to treat methanol and ethylene glycol poisoning. It is also used to inhibit the metabolism of ethanol by blocking the conversion of ethanol to acetaldehyde. 4-Methylpyrazole is metabolized into 4-methylpyridinium ion (4MP) by alcohol dehydrogenase, which prevents the conversion of acetaldehyde to acetic acid. This results in an increase in blood levels of acetaldehyde and a decrease in blood levels of acetic acid, leading to an accumulation of toxic metabolites such as formic acid. In addition, 4-methylpyrazole inhibits the enzyme glycol dehydrogenase that breaks down glycols into their harmless components. This leads to an accumulation of toxic intermediate products that are converted back into glycols.</p>

<p>4-Amino-3-methylbenzonitrile is a proton ionophore that can be used to prevent viral replication. It is a synthetic, aminobenzonitrile derivative that binds to the viral RNA polymerase and prevents the synthesis of new virus particles. 4-Amino-3-methylbenzonitrile has been shown to inhibit the growth of some strains of coxsackievirus, although it is less effective against other strains and viruses. 4-Amino-3-methylbenzonitrile inhibits the synthesis of viral proteins by binding to the viral RNA polymerase. This prevents viral transcription and replication, which leads to cell death.</p>

<p>Stable substitute for glutamine in cell culture media</p>

<p>Intermediate in the synthesis of sofosbubir</p>

<p>Please enquire for more information about (2-Amino-6-methylpyrimidin-4-ylthio)(diethylamino)methane-1-thione 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 Mca-Tyr-Val-Ala-Asp-Ala-Pro-Lys(Dnp)-OH trifluoroacetate 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 (2,6-dioxo-4-phenylcyclohexyl)-N-(3-(trifluoromethyl)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Phenyl-7-(Trifluoromethyl)-1,3-Dihydro-1,4-Benzodiazepin-2-One is a pyrethroid that has been shown to have an effective dose of 10 μg/kg in pharmacological tests. It has been shown to modulate hydrogen bond formation and the hydrophobic effects of diazepam. 5-Phenyl-7-(Trifluoromethyl)-1,3-Dihydro-1,4-Benzodiazepin-2-One is a monomer that can be used for the treatment of cancer. This active compound has been found to bind to the benzodiazepine binding site on GABA receptors in the brain and has been shown to induce digitonin release from nerve endings. It also binds with carbonyl groups which are found on proteins and nucleic acids.</p>

<p>N,N'-Bis-Boc-1-guanylpyrazol is a tetrapeptide that is used as a reagent in organic synthesis. It has been shown to have an inhibitory effect on the production and release of melanocortin and its related peptides, which are important for the regulation of body weight, appetite, and mood. N,N'-Bis-Boc-1-guanylpyrazol binds to sulfate groups on chondroitin sulfate proteoglycans. The inhibition of these sulfated proteoglycans leads to decreased levels of hyaluronic acid and a lack of water retention in the joints. This can cause symptoms such as pain and stiffness in joints, particularly those affected by osteoarthritis.</p>

<p>6-Amino-2-methylthio-4(3H)pyrimidinone is a potential antitumor drug with a radical mechanism of action. It inhibits the activity of the NS5B polymerase, an enzyme in the virus's RNA replication complex. The drug has been shown to inhibit proliferation of cancer cells in vitro and to have antiviral effects against a number of viruses, including influenza A and B. 6-Amino-2-methylthio-4(3H)pyrimidinone inhibits tyrosine kinases and also inhibits erythrocyte progenitors from differentiating into megakaryocytes. This drug is not metabolized by cytochrome P450 enzymes and does not bind to plasma proteins.</p>

<p>Cyclo(-Arg-Gly-Asp-D-Tyr-Lys) trifluoroacetate salt is a reagent that is used in organic synthesis as a building block to create complex compounds. It is also useful for research purposes, as it can be used to produce high quality products. Cyclo(-Arg-Gly-Asp-D-Tyr-Lys) trifluoroacetate salt is a chemical with CAS No. 217099-14-4 and has the chemical formula C17H21N3O2F3.</p>

<p>Please enquire for more information about Methyl 1-(2-chloro-4-fluorobenzyl)-3-formyl-6-methoxy-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2-Chloro-4-methylphenyl)hydrazine hydrochloride is a high quality reagent that is a useful intermediate for the synthesis of complex compounds. It has been used as a building block for the synthesis of speciality chemicals and research chemicals. This compound can be used to produce versatile building blocks and reaction components.</p>

<p>2-Hydroxy-5-methoxybenzyl alcohol (2HMB) is a methide that is used as an inductor in the synthesis of Taxol. 2HMB has been shown to induce apoptosis in MCF-7 cells and to promote the hydration of oxacycles. It can also be used in cancer research as a kinetic probe for the hydration of oxacycles. 2HMB activates MCF-7 cells and induces apoptosis, which may be due to its nucleophilic properties.</p>

<p>Amino acid; precursor to neurotransmitters, hormones, pigments, natural phenols</p>

<p>3-Amino-phenazin-2-ol is a pesticide that has been shown to have genotoxic effects on human lymphocytes in vitro. 3-Amino-phenazin-2-ol inhibits the growth of triticum aestivum, a type of cereal plant, by binding to the aminoacids in the cell wall and disrupting its structure. This leads to cell death and inhibits the synthesis of proteins necessary for cellular growth. The herbicide has also been shown to inhibit the growth of typhimurium at high concentrations and may be used as an herbicide or pesticide. The mechanism by which 3-amino phenazin 2-ol exerts its toxicity is not fully understood, but it may be due to its ability to activate cells that are exposed to low energy levels.</p>

<p>2-Methoxy-5-nitrophenol (2MNOP) is a compound that has been shown to inhibit the growth of bacteria in nutrient solutions by reducing the activity of glutamate pyruvate transaminase and pyridoxine hydrochloride. 2MNOP is a potent inhibitor of bacterial enzyme activities, such as neutral ph, hydrochloric acid, nitro, and toxicity studies. It is not active against eukaryotic cells or plants. The uptake of 2MNOP is enhanced by the presence of diamine tetraacetic acid and ethylene diamine. 2MNOP has also been shown to be effective against multi-walled carbon nanotubes.</p>

<p>2-Isopropyl-5-methylanisole is a natural compound that has been shown to have potent antimicrobial activity in a model system. It has been shown to inhibit the growth of bacteria by binding to the active site of bacterial DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. 2-Isopropyl-5-methylanisole has also been shown to be nontoxic in toxicity studies on various model organisms. 2-Isopropyl-5-methylanisole is absorbed through the skin when applied topically or taken orally, and can be used as an antibacterial agent for topical application or in foods.</p>

<p>Please enquire for more information about L-Lysyl-L-phenylalanyl-L-lysine trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Tyrosinol hydrochloride is a chiral molecule that is the hydrogenated form of L-tyrosine. It is an intermediate in the synthesis of L-dopa, which is used to treat Parkinson's disease. The enzymatic reaction that converts L-tyrosinol hydrochloride to L-dopa requires adenosine 5'-phosphosulfate as cofactor and histidine as a catalyst. The conversion of L-tyrosinol hydrochloride to L-dopa occurs with high yield and has been shown to be stereoselective. This synthetic pathway has been shown to have an activation energy of 53 kcal/mol and a reaction time of 30 minutes at room temperature.</p>