Amino Acids (AA)

<p>N-alpha-Tosyl-L-lysine chloromethyl ketone HCl is a chemical compound that binds to DNA. It has been shown to induce neuronal death and caspase-independent cell death in HL60 cells. The compound can also be used as a biochemical probe to study the apoptosis pathway. N-alpha-Tosyl-L-lysine chloromethyl ketone HCl is currently being investigated as an antiinflammatory agent for chronic coughs due to its ability to inhibit proteases.</p>

<p>5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.</p>

<p>N-Boc-L-proline methyl ester is an organocatalyst that is synthesized through the condensation of proline with methylamine and a methylating agent. It is used as a synthetic intermediate in the synthesis of peptides, pharmaceuticals, and other organic compounds. The compound has been shown to be effective in asymmetric hydrogenation reactions. N-Boc-L-proline methyl ester has also been shown to be useful in the formation of imines and amides, which are important intermediates in organic synthesis.</p>

<p>1-(4-Methylphenyl)ethanol is a colorless liquid that has a low energy and functional groups. It can be used as a reaction product in vitro assays and rhizosphere. 1-(4-Methylphenyl)ethanol reacts quickly with high salt, phosphatase, and silicon. The rate of the reaction increases with an increase in temperature. 1-(4-Methylphenyl)ethanol is also used for cationic polymerization, which is used to detect cirrhosis, high salt, phosphatase, and silicon by optical properties.</p>

<p>4-(N-Boc-aminomethyl)aniline is a cavity-preventing agent that has been demonstrated to be neuroprotective in vitro. The drug also inhibits the growth of bacteria, fungi, and viruses in cell culture and animal models. 4-(N-Boc-aminomethyl)aniline is an innovative compound class that has shown potential for treating infectious diseases such as HIV, tuberculosis, and malaria. It has been shown to act by interfering with viral replication and inhibiting the production of inflammatory cytokines (e.g., tumor necrosis factor). Furthermore, 4-(N-Boc-aminomethyl)aniline can be used as a matrix effector or nucleophile to form hydrogen bonds with other molecules. It can also have an impact on nanomaterials when it is incorporated into their surface.</p>

<p>Suc-Gly-Pro-Leu-Gly-Pro-AMC (SGLP) is a synthetic substrate that is hydrolyzed by proteases and has been used as a model substrate in protease studies. It has been shown to be cleaved by a number of enzymes, including chymotrypsin, trypsin, elastase, and cathepsin D. The hydrolysis products are sucrose glycolate, glycerol phosphate, leucine amino acid ester, and proline amino acid ester. SGLP has been shown to have low bioavailability in human liver cells and heart tissue. Studies have also shown that SGLP can stimulate the production of myelocytic cells in vitro. This activity may be due to its ability to act as an immunomodulator or by targeting tissue enzyme activities.</p>

<p>(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide is a reagent and research chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile building block in organic chemistry. (E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide has been shown to be an effective intermediate for the synthesis of various complex compounds, such as pharmaceuticals and pesticides. This compound is also a useful scaffold for the synthesis of other fine chemicals.</p>

<p>(R)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid (cis) is an intermediate in the synthesis of a chiral drug. It is prepared by a ring-opening reaction with an alkyl substituent, followed by asymmetric synthesis to provide optically pure cis stereoisomers. This compound has been shown to be active as a desymmetrizer of esters and as an intermediate in the synthesis of biologically active compounds.</p>

<p>1,2-Dimyristoyl-rac-glycerol (1,2-DMG) is a monomolecular fatty acid that has been found to inhibit the replication of herpes simplex virus. It binds to the surface glycoprotein and inhibits the release of diacylglycerol from the lipid membrane. 1,2-DMG also inhibits the activity of acyl chain enzymes, which are necessary for the synthesis of fatty acids in trypanosomes. This inhibition prevents the growth and proliferation of lung fibroblasts and may be beneficial in treating cancer. The ionisation mass spectrum shows that 1,2-DMG has a molecular weight of 270 Da. The binding affinity between 1,2-DMG and water is 9 x 10 M at room temperature.</p>

<p>H-Glu-Val-OH is a coordination complex that contains the metal scandium. It is used as a ligand to form complexes with other metals and organic molecules. This compound is also used in peptide synthesis and has been shown to have a strong interaction with nitrate, serine, and formiate. H-Glu-Val-OH is soluble in solutions such as water or formiate. The tripeptide Ser-Gly-Val can be formed from this compound by hydrolysis of the hydroxo group.</p>

<p>Please enquire for more information about 3-((4-methylphenyl)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>L-Alaninamide hydrochloride is a hydrogen bond donor that has been shown to have anti-inflammatory properties. L-Alaninamide hydrochloride is able to crosslink hyaluronic acid, which can act as an immunosuppressant and inhibit the production of proinflammatory cytokines. In addition, L-alaninamide hydrochloride has been found to be effective in the treatment of amyloid protein aggregation diseases such as Alzheimer's disease. The drug binds to amyloid proteins by binding to their receptor site and inhibits the formation of amyloid fibrils by preventing cross-linking reactions between polypeptides. L-alaninamide hydrochloride also inhibits the formation of benzimidazole compounds, which are used in the treatment of rheumatoid arthritis.br&gt;br&gt;<br>The structure of L-alaninamide hydrochloride is an intramolecular hydrogen bond donor with a carbonyl group. It</p>

<p>2-Fluoro-4-methylbenzoic acid ethyl ester is a versatile building block that is used in the synthesis of complex compounds with a wide variety of biological and chemical properties. This compound has been used as a reagent for research, as well as in the production of pharmaceuticals and other speciality chemicals. It has also been found to be useful in the synthesis of compounds with high quality. 2-Fluoro-4-methylbenzoic acid ethyl ester can be used as an intermediate in reactions, or as a scaffold for further synthesis. The CAS number for this compound is 500579-61-3.</p>

<p>2-Chloromethyl-3,5-dimethyl-4-methoxypyridine is a drug substance that is used as a pump inhibitor. The optimal reaction conditions for the synthesis of this molecule are a Grignard reagent, chlorinating agent, and magnesium salt. Impurities may arise during the synthetic process due to chloride or inorganic acid catalyst. This drug substance is not soluble in water but can be dissolved in organic solvents such as ethers, chloroform, or benzene. It reacts with magnesium to form a chelate ring with an organic molecule.</p>

<p>2-(2-Methoxyphenoxy)ethylamine hydrochloride is a fine chemical with the CAS No. of 64464-07-9. It is a versatile building block that can be used as an intermediate for research chemicals, reaction components and specialty chemicals. This compound has been shown to work as a reagent in high quality synthesis.</p>

<p>Quinolin-2-yl-methylamine is an amine that is used in the synthesis of other compounds. It can be prepared by protonation of quinoline with methylamine, followed by crystallization. The yield of this reaction is dependent on the purity of the starting materials and the reaction conditions. This compound has a molecular weight of 169.07 g/mol and a melting point at 217 °C. The infrared spectrum for Quinolin-2-yl-methylamine shows peaks at 2900 cm−1, 1670 cm−1, and 1590 cm−1. It also has x-ray crystallography data (space group P21/c).</p>

<p>Macrophage-activating lipopetide-2 (MALP-2) is a TLR2 agonist and activator of  MyD88-dependent signaling pathways. It has potential as a vaccine adjuvant.</p>

<p>3-Amino-4-methoxybenzanilide is a white, crystalline solid that is soluble in organic solvents. It reacts with hydrochloric acid to form hydrogen chloride and 3-amino-4-methoxybenzoic acid. 3-Amino-4-methoxybenzanilide is used as an analytical reagent for determining the chloride content of various materials. The heat energy needed for the reaction to occur optimally is between 55 and 75 degrees Celsius. The optimal reaction system includes hydrochloric acid, an organic solvent, and diazonium salt activated by hydrogen chloride gas. The reaction time is 2 hours at room temperature and the analytical method used is titrimetric analysis using triticum aestivum as the particle.</p>

<p>[(1-Methyl-1H-indol-5-yl)methyl]amine acetate is a versatile building block that can be used in the preparation of a wide range of chemicals. This compound has been shown to react with a variety of reagents, such as phenyliodine diacetate and chloroacetic acid to give various products. [(1-Methyl-1H-indol-5-yl)methyl]amine acetate also reacts with potassium hydroxide (KOH) to produce indole. It is an important intermediate in the synthesis of other chemical compounds and has been reported in more than 200 scientific publications. The chemical formula for [(1-Methyl-1H-indol-5-yl)methyl]amine acetate is C13H14N2O4.</p>

<p>Cyclo(-Gly-L-Glu) is a cyclic dipeptide that has been analyzed using LC-MS/MS. It is a bioactive compound that can be found in the bioscience and biochemistry fields. Cyclo(-Gly-L-Glu) is used as an analytical method for determining the presence of dipeptides, which are small molecules composed of two amino acids linked together by a peptide bond. The cyclic form of the molecule allows it to bind to proteins and other molecules in order to stabilize them. Cyclo(-Gly-L-Glu) has also been shown to have potential as a therapeutic agent for cancer treatments, based on its ability to inhibit the activity of protein kinases involved in cell proliferation and apoptosis.</p>

<p>4'-Methylpropiophenone is a molecule that is used in pharmaceutical preparations. It has been shown to have a high affinity for the extracellular site of NMDA receptors and is an effective inhibitor of the ion channel. 4'-Methylpropiophenone also inhibits the activity of the enzyme acetylcholinesterase, which leads to increased levels of acetylcholine in the synaptic cleft. This results in increased neurotransmission and has been shown to be effective in vitro. The reaction solution can be prepared by reacting piperidine hydrochloride with propiophenone.</p>

<p>Fmoc-beta-Ala-4-amino-D-Phe(Boc)-OH is a fine chemical that can be used as a building block in research, as a reagent for chemical synthesis, or as a speciality chemical. It is also a versatile building block that can be used to create other compounds. Fmoc-beta-Ala-4-amino-D-Phe(Boc)-OH is an intermediate compound and scaffold. This compound has been shown to react with ethyl chloroformate to yield the corresponding beta amino ester.</p>

<p>4-(4-Aminophenyl)-3-methyl-4-oxobutanoicacid is a chemical substance that has been shown to be effective in treating insects. It is also used as an insecticide and herbicide. 4-(4-Aminophenyl)-3-methyl-4-oxobutanoicacid has been shown to have a high toxicity against insects, with a LD50 value of 5.6 mg/kg. This compound has been tested for its effects against the weevil species Rhinotia haemoptera, which is a pest that damages crops in Australia. 4-(4-Aminophenyl)-3-methyl-4-oxobutanoicacid was found to be highly toxic to this species of insect with an LC50 value of 0.1%.</p>

<p>Fmoc-di-n-butylglycine is a c1-8 alkyl that has been shown to have an antiinflammatory effect. It inhibits the phosphodiesterase enzyme, which is responsible for the degradation of cyclic adenosine monophosphate (cAMP), which increases levels of this molecule. This leads to increased activation of protein kinase A and protein kinase C, which are important in inflammatory pathways. Fmoc-di-n-butylglycine binds to the sodium channel, preventing it from opening and closing, thus inhibiting transmission of electrical signals. This drug has also been shown to inhibit potassium channels and hydrogen sulfate production by bacteria. Fmoc-di-n-butylglycine can be used as a model for the study of other drugs that act on sodium channels.</p>

<p>2-(4-tert-Butylphenoxy)-2-methylpropanoic acid is a versatile building block and reagent for the synthesis of complex compounds. It has been used in research as a possible treatment for inflammatory diseases, including asthma and rheumatoid arthritis. This product is also a useful scaffold for the development of new drugs. 2-(4-tert-Butylphenoxy)-2-methylpropanoic acid has been shown to have antiviral properties against human immunodeficiency virus (HIV) and hepatitis C virus (HCV).</p>

<p>Trichloroethylene is a chlorinated hydrocarbon that is primarily used as a solvent. The propionic acid is the monosodium salt of 3-(N-Methyl-N-pentylamino)propionic acid hydrochloride, which is an organic compound. The monohydrate and trichloride are two polymorphic forms of this substance. Acetone and unreacted Trichloroethylene are substances that may be formed during the chemical process. The alkaline form of Trichloroethylene may be obtained by refluxing the substance with sodium hydroxide in water or with potassium hydroxide in alcohol. This substance can also exist in a polymorphic form.</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>Bis[(5-ethyl-2-methyl-1,3,2-dioxaphosphorinan-5-yl)methyl] methyl phosphonate P,P'-dioxide (BEMPD) is a brominated organophosphorus chemical that is used as a pesticide. It is an effective flame retardant and can be used in the production of polyurethane foams. The main application of BEMPD is in the preparation of particulate matter for weather modification. This chemical has been shown to be an effective phase extraction agent for polychlorinated biphenyls (PCBs) and polybrominated diphenylethers (PBDEs). Florisil column chromatography has been validated as a clean, economical, and sensitive method for the analysis of BEMPD residues. The sampler must be carefully selected to avoid interference with the analytical results.</p>

<p>5-Methoxyindole-3-acetonitrile is a synthetic compound used as a reference for the synthesis of melatonin. It is produced by the addition of magnesium to 5-methoxyindole, followed by reaction with cyanide and nitrile. The synthesis of this compound was first published in 1938 and has since been used as a reference for many other studies. It has been shown that 5-methoxyindole-3-acetonitrile has high performance liquid chromatography properties, with a linear range from 0.5 to 50 mg/mL and an ultraviolet spectrum that falls within the region between 220 nm and 400 nm. A molecular modeling study was conducted on this compound, which showed that it conforms with 4-hydroxy indole ring systems found in natural products such as tryptophan and serotonin. This product also has fluorescent properties, which are caused by its electron withdrawing group (cyano).</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>Tos-Gly-Pro-Lys-pNA acetate is a peptide that has been shown to have inhibitory effects on serine proteases, such as fibrinogen. Tos-Gly-Pro-Lys-pNA acetate binds to the active site of serine proteases, which inhibits their activity and prevents them from cleaving fibrinogen. The rate of reaction is dependent on the concentration of enzyme inhibitors. For example, at low concentrations, the enzyme inhibitor will bind to only one or two sites on the serine protease, while at high concentrations it may bind to many sites. This molecule has been shown to be a potent inhibitor of human immunodeficiency virus (HIV) protease and is currently being studied for its use as a potential antiviral agent.</p>

<p>4,6-Dihydroxy-2-methylpyrimidine is a monomer that is used in the synthesis of polyurethanes. It is an intermediate in the reaction between hydrochloric acid and nitrous acid, which produces 4,6-dichloro-2-methylpyrimidine. The reaction mechanism involves transfer of a methyl group from an organic molecule to hydrochloric acid. This reaction can be carried out at either low or high pH values. The addition of magnesium salt increases the rate of the reaction by increasing the solubility of chloroformate in water. When ethyl esters are used as starting materials, a constant conversion rate can be obtained with a large excess of magnesium salt.</p>

<p>H-Asp-Asp-OH is a basic protein that is found in all organisms. It has been shown to have a role in the regulation of the immune system and in the development of cancer. H-Asp-Asp-OH has been studied for its use as an antigen for the production of monoclonal antibodies and as a potential therapeutic agent against infectious diseases and autoimmune diseases. The molecule consists of two amino acids, Aspartic acid and Asparagine, linked by an amide bond. The molecular weight is 212 daltons, which is too small to be filtered by size exclusion chromatography.</p>

<p>(+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine is an impurity of enalaprilat, which is a pharmaceutical drug used in the treatment of hypertension. Enalaprilat is manufactured by reacting 1-(S)-ethoxycarbonxyl-3-phenylpropane with L-alanine and triphosgene. This impurity has been shown to be a potent inhibitor of the enzyme angiotensin converting enzyme (ACE) and may cause adverse effects such as hypotension, cough, and dizziness. The chemical structure of (+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine consists of an aliphatic hydrocarbon chain with a maleate group at one end and a benzyl group at the other end. It also contains two amines, one on each side of the molecule.</p>

<p>Piperacillin is a β-lactam antibiotic that inhibits the synthesis of bacterial cell walls by binding to penicillin-binding proteins. It is used for the treatment of serious infections caused by gram-negative organisms such as Aerogenes, Enterobacter, and Klebsiella. Piperacillin has a high MIC90 value against Staphylococcus and other gram-positive bacteria, but it is not active against β-lactamase producing strains of bacteria such as E. coli or Klebsiella pneumoniae. The MIC90 values are determined through an analytical method on different strains of bacteria and validated with a sample preparation before use in clinical trials.</p>

<p>3-Methoxy-4-t-Butyl-Benzoic acid is a building block that can be used in the synthesis of a variety of organic compounds. This chemical has been used as a reagent, as well as in research and development. It is also used to synthesize complex compounds and may be used as a versatile building block or intermediate for reactions.</p>

<p>Please enquire for more information about 3-((3-chlorophenyl)methyl)-4-phenyl-1,2,4-triazoline-5-thione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cyclo(-L-Ala-L-Glu) is a versatile building block that belongs to the class of complex compounds. It can be used as a reagent, speciality chemical, or useful building block in organic synthesis. Cyclo(-L-Ala-L-Glu) has been shown to participate in a wide range of reactions, including condensation, esterification, and oxidation. Cyclo(-L-Ala-L-Glu) also has interesting properties that make it useful as an intermediate for the synthesis of other compounds. Cyclo(-L-Ala-L-Glu) can be heated with a strong acid such as nitric acid to produce cyclopropane derivatives. The high quality and usefulness of Cyclo(-L-Ala-L-Glu) makes it an excellent scaffold for synthetic chemistry.</p>

<p>Fosaprepitant is a drug that belongs to the class of drugs used for chemotherapy. It is a prodrug that is converted in vivo to aprepitant, its active form. Fosaprepitant acts as an antagonist of the neurokinin-1 receptor (NK-1R) and inhibits the binding of substance P, which leads to an anti-inflammatory effect. Fosaprepitant has been shown to inhibit the production of substance P in animal models, leading to a reduction in inflammation. In clinical trials, fosaprepitant has been shown to be safe and well tolerated when used with other drugs such as cisplatin and docetaxel in patients with cancer.</p>

<p>H-Tyr-Glu-OH is a fluorescent dye that has been used in assays to detect the uptake of polymers in bacterial cells. It is also used to study conformational properties of porphyromonas, which are bacteria found in the oral cavity. H-Tyr-Glu-OH reacts with the sugar alcohols in porphyromonas, causing a change in its optical properties. This change can be measured using spectroscopy methods such as fluorescence and absorption, which allows for monitoring of polymer uptake and other changes related to porphyromonas activity.</p>

<p>Please enquire for more information about 5-(4-methoxyphenyl)-2H-1,2,3-triazole-4-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3,4,5,6-Pentafluoro-L-phenylalanine (PFPA) is a substrate molecule that has been shown to inhibit the α1 subunit of the Na+/K+ ATPase in human heart cells. PFPA also inhibits the growth of bacteria in culture and is active against bacterial strains that have developed resistance to other antimicrobial agents. PFPA is also effective against bowel disease caused by H. pylori. PFPA has been shown to inhibit the production of an antimicrobial peptide by hl-60 cells in vitro and has been shown to be effective against a number of infectious diseases including tuberculosis and some autoimmune diseases.</p>

<p>2-Fluoro-3-methoxyaniline is a high quality chemical that can be used as an intermediate in the synthesis of complex compounds. It is a reagent and useful building block, with a CAS number of 801282-00-8. 2-Fluoro-3-methoxyaniline can be used to make speciality chemicals and research chemicals, as well as versatile building blocks for reactions. This compound is also a reaction component for the synthesis of other compounds.</p>

<p>5-Nitro-m-phenylenediamine is an organic compound that has the chemical formula CHNO. It is a white crystalline solid with a melting point of 158 °C. The compound is soluble in water and other polar solvents but insoluble in nonpolar solvents such as hexane. 5-Nitro-m-phenylenediamine can be prepared by nitration of m-phenylenediamine, which produces the desired product in about 30% yield and with impurities that must be removed by fractional crystallization. The compound is used as an intermediate for making dyes and pharmaceuticals.</p>

<p>N-Methyl-N-trimethylsilylacetamide is a bifunctional amide that can react with an electrophile, such as hexane, to form an N-methylated product. The amide group of the molecule can also be deprotonated by a strong base to form an enolate, which can then react with a nucleophile. The NMR spectra of this compound show that it has a multinuclear structure and contains two tautomers. It is used in analytical chemistry for sample preparation, chromatographic science for reaction intermediates, and chemical study for its reactivity.</p>

<p>L-glutamic acid di-tert-butyl ester hydrochloride is a synthetic glutamic acid conjugate that can be used in the treatment of cancer. L-Glutamic acid di-tert-butyl ester hydrochloride is a substrate for many enzymes, such as glutamate transporters and glutaminase, which are found in tumor cells. It has been shown to decrease the uptake of docetaxel by tumor xenografts in mice. The expression of L-Glutamic acid di-tert-butyl ester hydrochloride has been observed in tissues during cancerous growth and it is expressed at higher levels than in normal tissues.</p>

<p>3-Hydroxy-6-methylpyridine is a metabolite of the amino acid L-alanine. It has been shown to be hepatoprotective in a model system and to inhibit the allergic response. 3-Hydroxy-6-methylpyridine has also been shown to protect cells against oxidative damage by metal ions, as well as metabolic disorders such as diabetes. This compound is not active in competitive inhibition because it does not bind to the same site on the enzyme as the substrate. 3-Hydroxy-6-methylpyridine has also been shown to have neuroprotective effects, which may be due to its ability to inhibit acetylcholinesterase, an enzyme that breaks down acetylcholine, a neurotransmitter important for memory and learning.</p>

<p>6-Methyl-DL-tryptophan is a useful intermediate and building block for the synthesis of natural products, pharmaceuticals, and agrochemicals. It is also a versatile building block for organic synthesis as it can be used in the preparation of various types of compounds. 6-Methyl-DL-tryptophan has been shown to inhibit the production of nitric oxide by macrophages and microglia cells in response to proinflammatory cytokines. It is an inhibitor of protein biosynthesis, which may be due to its ability to inhibit tryptophan synthase.</p>

<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>2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol is a versatile chemical building block that can be used to synthesize a variety of compounds. It has been shown to be useful as a reaction component in the synthesis of pharmaceuticals and agrochemicals. The compound is also used as an intermediate for the preparation of other compounds. 2-[2-(2-t-Boc-aminoethoxy)ethoxy]ethanol is soluble in organic solvents, such as chloroform, ethanol, or acetone. It has a CAS number of 139115-92-7 and is relatively easy to purify by recrystallization from methanol.</p>

<p>2-Benzyloxy-6-methoxyacetophenone is a high quality and versatile chemical that can be used as a reagent or building block in organic synthesis. It is an important intermediate in the synthesis of fine chemicals, pharmaceuticals, and other complex compounds. 2-Benzyloxy-6-methoxyacetophenone has been shown to be useful as a scaffold for the synthesis of novel complex molecules, such as speciality chemicals. The compound also has potential applications in research and development of new drugs.</p>

<p>[(3-Methylphenyl)amino]acetic acid is a high quality chemical that can be used as a reagent, intermediate, or building block in the synthesis of other compounds. It is useful for the synthesis of complex compounds and has been shown to have a wide range of applications. This compound can be used in research chemicals and as an intermediate in the production of fine chemicals. [(3-Methylphenyl)amino]acetic acid is a versatile building block that can be used to synthesize different types of molecules with diverse properties. It also has many potential uses in medicine as it has been shown to inhibit protein kinase C (PKC), which may provide therapeutic benefits for some diseases.</p>

<p>(S)-2-Methoxy-2-(1-naphthyl)propanoic acid is a chiral molecule that can exist in two different forms, each of which has the same physical and chemical properties. The two enantiomers are not optically active, meaning they have the same degree of rotation when passed through a polarizing filter. It is an organic compound that is used as a flavoring agent in food chemistry and as a bioactive compound. (S)-2-Methoxy-2-(1-naphthyl)propanoic acid also has been shown to function as an attractant for hemipteran insects such as mosquitoes, although it is not clear if this property is due to its aromatic or enantiomeric structure.</p>

<p>1,2-Distearoyl-sn-glycerol (DAG) is a lipid molecule that is found in the cell membrane and can be used as an antimicrobial agent. DAG has been shown to inhibit the growth of bacteria by binding to their fatty acid chains. It also has been shown to bind to the receptor P2Y6, which is involved in mediating inflammatory responses, and inhibits its activity. This drug may be useful for treating diseases such as atherosclerosis and diabetes mellitus type 2.</p>

<p>4-Amino-1-Boc-piperidine is a potent inhibitor of the CCR5 receptor. It is an x-ray crystal structure with a hydroxide solution that inhibits the growth of cancer cells. The inhibitor binding site for 4-Amino-1-Boc-piperidine was determined to be the CCR5 receptor, which is located on the surface of hematopoietic cells. The compound has been shown to inhibit human T lymphocyte proliferation in vitro and inhibit HIV replication in infected patients. 4-Amino-1-Boc-piperidine is able to inhibit the growth of cancer cells by blocking the production of cytokines, such as interleukin 2, that are needed for cell division and growth.</p>

<p>3-Fluoro-2-methylbenzaldehyde is a colorless liquid that has a strong odor. It is used as an intermediate in organic synthesis, especially for the production of fluorine compounds. 3-Fluoro-2-methylbenzaldehyde is also used to study the bioconversion of aldehydes and reductases in fungi. This chemical can be detected by its spectra and its ability to react with fluorine. 3-Fluoro-2-methylbenzaldehyde can also be synthesized by reacting naphthalene with anisole and hydrogen fluoride gas.</p>

<p>N3-L-Leu-OH·BHA is a complex compound that has been used as a precursor to other compounds, such as pyrrolidines. It is an intermediate in the synthesis of various pharmaceuticals and research chemicals, such as 4-methylpiperidine. N3-L-Leu-OH·BHA has been shown to be useful in the preparation of various speciality chemicals, including building blocks for polymers and reagents for organic synthesis.</p>

<p>Methyl 4-methylsalicylate is a colorless liquid that has no odor. It can be synthesized by reacting ethyl bromoacetate with formaldehyde and anhydrous sodium acetate in the presence of hydrochloric acid. This product is used as an intermediate for various organic compounds, such as esters, ethers, amides, and nitriles. Methyl 4-methylsalicylate has been used in the synthesis of pharmaceuticals, perfumes, pesticides, herbicides, and other chemicals. Methyl 4-methylsalicylate is toxic to opportunistic fungal species but does not affect bacteria. The chemical reacts with DNA to form adducts that inhibit linear polymerase chain reactions (PCR). This inhibits DNA replication and transcription of DNA into RNA. The inhibition of protein synthesis by methyl 4-methylsalicylate also results in cell death.</p>

<p>Please enquire for more information about S-2-Propen-1-yl-L-cysteine ethyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4,6-Dimethyl-N-phenylpyrimidin-2-amine is a fungicide that is effective against the production of nitrite ion in the liver. It has been shown to be a potent inhibitor of hepatic steatosis. 4,6-Dimethyl-N-phenylpyrimidin-2-amine was also shown to have an inhibitory effect on the growth of fungal strains in vitro. This compound has been demonstrated to be active against a number of plant pathogens and may be useful in postharvest applications. 4,6-Dimethyl-N-phenylpyrimidin-2-amine interacts with the hippocampus formation and may play a role in preventing neurodegenerative diseases such as Alzheimer's disease or Parkinson's disease.</p>

<p>4-Methoxy-2-nitroaniline is a molecule that has been shown to be able to form an intramolecular hydrogen bond with the 5' carbon of the sugar ring. This reaction leads to the formation of an alkoxy radical, which reacts with chloride ions in acidic conditions. The formation of this intermediate product is reversible, and can be used for analysis of hydrochloric acid. 4-Methoxy-2-nitroaniline has also been shown to react with diazonium salt in the presence of acid, forming a molecule that contains two amines. This reaction can be reversed by adding hydrogen chloride to the solution and analyzing the solution's acidity.</p>

<p>N1-(2-Aminoethyl)-N1-methylethane-1,2-diamine is a chromatographic cross-linking agent that is used in the preparation of monoclonal antibodies. It contains two amino groups and two ethyleneamine groups. N1-(2-Aminoethyl)-N1-methylethane-1,2-diamine binds to calcium carbonate and forms a chelate ring with the metal ion. The compound has been shown to have diagnostic properties, as it can be detected by nmr spectra and by the use of monoclonal antibody.</p>

<p>The 4-Iodo-2-methylaniline is a synthetic molecule that belongs to the group of amines. It has been shown to bind to human protein and can be used for the synthesis of boronic acids and quinoline derivatives. 4-Iodo-2-methylaniline can be synthesized by reacting hydrochloric acid with sodium periodate, followed by addition of an aryl boronic acid. The reaction time is dependent on the nature of the reactant. The pharmacophore consists of a proton and an aryl boronic acid, which is responsible for binding with human protein.</p>

<p>4-Methyl-6-chloropyrimidine is an intermediate in the synthesis of 6-chloropurine, which is a dihydrochloride salt that can be hydrolyzed to form tetrapeptides. The nature of the reaction conditions employed for this conversion determines the yield of 4-methyl-6-chloropyrimidine. It can be synthesized by alkaline hydrolysis or by condensation of n-terminal amino acids with chloroacetic acid derivatives. This compound can also undergo hydrolytic cleavage to form oligopeptides and glycinates, which are n-substituted with dicyclohexylcarbodiimide.</p>

<p>2,2-Dimethyl-3-phenylpropanoic acid is a luteolytic agent that belongs to the group of phenylacetic acids. It has been shown to inhibit progesterone synthesis and induce regression of the estrous cycle in rats. 2,2-Dimethyl-3-phenylpropanoic acid is also able to bind with cytochrome P450 enzymes, which are involved in the metabolism of many drugs. This binding may lead to increased plasma concentrations of other drugs that are metabolized by cytochrome P450 enzymes, such as erythromycin and methyldopa.</p>

<p>Fmoc-S-tert-butoxycarbonylmethyl-L-cysteine is a polylactic residue with a propenone cyclic structure. It is soluble in organic solvents and has an aromatic heterocyclic ring. Fmoc-S-tert-butoxycarbonylmethyl-L-cysteine can be used to synthesize pesticides, nicotine, and immunogens.</p>

<p>Cyclo(-Pro-Tyr) is a natural product that belongs to the class of antimicrobial agents. It has been shown to inhibit the growth of colorectal adenocarcinoma cells by reducing mitochondrial membrane potential and inhibiting protein synthesis. Cyclo(-Pro-Tyr) also has antimicrobial properties against bacteria, including Enterococcus faecalis and Escherichia coli. The biological properties of Cyclo(-Pro-Tyr) have been investigated in vitro with tissue culture and acetate extracts, demonstrating its ability to inhibit the production of fatty acids, as well as its wound healing abilities. Cyclo(-Pro-Tyr) is a synthetase that uses methyl myristate as a substrate and etoac extract as an electron donor. The enzyme converts methyl myristate into cyclopropane fatty acid ester, which can be used for the synthesis of polymers such as polypropylene and polyethylene terephthalate.</p>

<p>6-Boc-hydrazinonicotinicacid is a cytotoxic compound that binds to hydroxyapatite and induces necrosis in cancer cells. This compound also has antimicrobial properties. 6-Boc-hydrazinonicotinic acid is conjugated with peptides for use as an immunoconjugate for the targeted delivery of drugs to cancer cells. It can be used to diagnose cancer by its uptake in human serum and inflammatory cells, as well as to identify cancerous tissues through its binding to hydroxyapatite. The biological studies have shown that 6-Boc-hydrazinonicotinic acid inhibits the growth of various types of tumour cells, including breast, prostate, colon, and lung cancers.</p>

<p>3-Bromo-2-methoxybenzyl alcohol is a reaction component that is used in the synthesis of a number of chemical compounds. It has been shown to be a useful scaffold, with versatile building blocks and intermediates. 3-Bromo-2-methoxybenzyl alcohol is an intermediate for the synthesis of complex compounds such as antihypertensive drugs, anti-inflammatory agents, and immunosuppressant drugs. This compound also has a variety of uses in research including as a reagent for the determination of enzyme activity and as an analytical reference standard.</p>

<p>Alpha-methylbenzyl alcohol is a fatty acid that is used as a chemical intermediate in the synthesis of pharmaceutical agents. It has been shown to inhibit phosphotungstic acid (PTA) hydrolysis and surface methodology, as well as to have carcinogenic potential. Alpha-methylbenzyl alcohol has also been found to be an inhibitor of phospholipase A2, which catalyzes the hydrolysis of glycerophospholipids into free fatty acids and lysophospholipids. Alpha-methylbenzyl alcohol inhibits the reaction by binding reversibly with the hydroxyl group on enzyme active site. The kinetic mechanism studies of alpha-methylbenzyl alcohol have revealed that it is a competitive inhibitor for enzymes such as protein kinase C and leucine aminopeptidase.</p>

<p>2-Methoxy-1-[(4-methylphenyl)sulphinyl]benzene is a reagent and useful intermediate that is used in the synthesis of complex compounds. This chemical has been shown to be a useful scaffold for the synthesis of natural products. It can also be used as a building block in the synthesis of speciality chemicals and research chemicals, as well as versatile building blocks in reactions.</p>

<p>Please enquire for more information about 2-(2-formyl-6-methoxyphenoxy)acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Phospho-L-arginine lithium salt hydrate is an arginine derivative that has a complex life cycle. It is used as a substrate for ATP synthesis, and also participates in the formation of disulfide bonds during protein folding. N-Phospho-L-arginine lithium salt hydrate is an important component of many enzymes, which are vital to the body's metabolic processes. This compound can be used to study biochemical properties of enzymes in biological samples and infectious diseases, which could lead to new treatments for these diseases.</p>

<p>H-D-allo-Threonine methyl ester hydrochloride is a speciality chemical that is used in research and development. It is an intermediate for the synthesis of other compounds, such as pharmaceuticals, pesticides, and fragrances. H-D-allo-Threonine methyl ester hydrochloride has been shown to be useful in the production of methanol and ethanol. This compound also has high quality and can be used as a reagent for other reactions.</p>

<p>4-Methylphenyl hydrazine hydrochloride is a chemical compound that has been shown to be an effective treatment for lung tumors. It has been shown to inhibit tumorigenesis in animal models by the inhibition of angiogenesis and tumor growth. This drug is administered as a subcutaneous injection and can cause hemorrhaging, inflammation, and necrosis at the injection site. 4-Methylphenyl hydrazine hydrochloride has also been postulated to have anti-tumorigenic properties in animals.<br>4-Methylphenyl hydrazine hydrochloride inhibits the production of adenomas and adenocarcinomas in rats when given orally or intragastrically, but not when given intravenously.</p>

<p>(S)-(+)-2-Phenylpropionic acid is an organic solvent that is catalyzed by a hydroxy group. It has been shown to be active against bacterial strains in the presence of borohydride reduction and immobilized on polystyrene beads. The enzyme activities were stereoselectively inhibited in the presence of (R)-(-)2-phenylpropionic acid, which is an enantiomer of (S)-(+)2-phenylpropionic acid. This inhibition may be due to the ability of this compound to form a more stable radical coupling with fatty acids such as oleic acid. The reaction temperature can affect the stereoselectivity, with higher temperatures favoring (R)-(-)2-phenylpropionic acid.</p>

<p>1-Methyl-1H-indole-2,3-dione is a chemical compound that belongs to the class of indole derivatives. It can be synthesized by reacting 2,3-dihydroxybenzaldehyde with 2,2'-azobis(2-amidinopropane) dihydrochloride and methyl iodide in the presence of copper (II) acetate. This reaction mechanism is similar to that of other reactions involving an intramolecular hydrogen transfer. The binding constants for 1-methyl-1H-indole-2,3-dione are very high and this compound has been shown to inhibit herpes simplex virus replication in vitro. 1MIDD binds to the active site of tryptophan fluorescence and synchronous fluorescence proteins. 1MIDD also binds to copper ions in a coordination geometry that is similar to that found for other compounds containing a carbonyl group.</p>

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

<p>L-Leucine methyl ester HCl is a monoclonal antibody that specifically binds to the hydroxyl group of human immunoglobulin. It is synthesized by reacting L-leucine with methylamine and hydrochloric acid, followed by hydrolysis of the ester and subsequent reaction with trifluoroacetic acid. The resulting product is purified by precipitation with ammonium sulfate and has a molecular weight of 476.3 Da. L-Leucine methyl ester HCl is used in pharmaceutical preparations for the treatment of amyloid protein-related diseases such as Alzheimer's disease, as well as cytosolic protein-related diseases such as leishmania and thp-1 cells.</p>

<p>Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(2-indol-3-ylethyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>This is a speciality chemical and is not intended for use in food, drug, or cosmetic applications. This fine chemical is a useful building block, which can be used to synthesize complex compounds. It has been shown to have high reactivity with a variety of reagents, making it an excellent research component.</p>

<p>Capryloyl glycine is a non-protein amino acid that has been identified as a potential biomarker for photosynthetic activity. Capryloyl glycine is a potent inhibitor of the growth of bacteria, fungi and yeasts. It was found to inhibit the growth of bacteria by blocking their ability to synthesize fatty acids in liver cells. Capryloyl glycine also inhibits the production of glycerides in skin cells, which may have therapeutic applications for certain skin disorders.</p>