Amino Acids (AA)

<p>Please enquire for more information about 7-Bromo-1-methyl-1H-imidazo[4,5-c]pyridine 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 (R,S)-Z-3-Amino-7-chloro-2-oxo-5-phenyl-1,4-benzodiazepine 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-Methyl-1H-imidazol-5-yl)methyl]amine 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 6-Chloro-1-methyl-1H-indole-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Please enquire for more information about Ethyl 6-bromo-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-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 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 L-Glutamic acid gamma-methyl ester alpha-tert-butyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>This is a high quality reagent that is a useful intermediate in the synthesis of complex compounds. It is also a fine chemical and a useful scaffold for the synthesis of complex molecules. Boc-glycine N-hydroxysuccinimide ester has many applications in research chemistry, such as being used as an intermediate in the synthesis of other organic compounds. It can also be used as a building block for creating diverse compounds with different reactive groups. Boc-glycine N-hydroxysuccinimide ester is soluble in water, making it suitable for use in reactions involving water. This versatile building block can be used to create drugs, pesticides, and other chemicals.</p>

<p>N-Acetyl-D-phenylalanine is a synthetic amino acid that is used as a building block in the synthesis of peptides and proteins. It is produced by the Friedel-Crafts reaction between benzene and acetic anhydride, which results in formation of the molecule with two phenyl groups. N-Acetyl-D-phenylalanine has been shown to react with water molecules to form supramolecular complexes, which may be immobilized for use as catalysts for chemical reactions. The rate of this reaction depends on the concentration of carbon source and substrate concentration.</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 Phg-Gly-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylbenzyl chloride is a reactive compound that has been shown to have inhibitory properties against cancer cells. It is an aromatic compound that is synthesized by the reaction of benzene and methyl chloride. This chemical appears as a white solid at room temperature. 2-Methylbenzyl chloride has been shown to have antimicrobial properties, which are due to its ability to react with fatty acids. The addition of 2-methylbenzyl chloride to fatty acid esters leads to the formation of hydroxylated derivatives, which are reactive and inhibit the growth of bacteria and fungi. This chemical also reacts with carbon disulphide, hydrogen chloride, and chloride in the presence of light or heat. The metabolic profiles of this chemical have not been well characterized, but it has been shown to be reactive with Mcf-7 cells.br&gt;br&gt; The following product details are for a product called "3DCTKP." br&gt;br</p>

<p>2-Bromo-D-phenylalanine is a precursor of l-DOPA, which is an amino acid that is used in the synthesis of dopamine. It is also used as a diagnostic agent for bladder cancer, where it is taken up by bladder cells and converted to radioactive 2-bromo-3′-deoxyuridine. This radioactive compound can be detected with a high performance liquid chromatography (HPLC) system. In addition, 2-Bromo-D-phenylalanine has been shown to inhibit the acid transporter in tumor cells, making it useful as an oncologic drug. 2 bromo d phenylalanine inhibits the acid transporter in tumor cells, making it useful as an oncologic drug</p>

<p>1-(2-Methoxybenzyl)piperazine (1-MBP) is a multitarget drug that has been shown to have medicinal properties. It inhibits the cholinergic system, which is involved in memory and cognition, as well as pathways such as the inflammatory response and amyloid production. 1-MBP has been shown to inhibit acetylcholinesterase, an enzyme that breaks down acetylcholine, thus increasing the amount of acetylcholine available for signaling. 1-MBP also inhibits cholinesterase, which increases the amount of acetylcholine in the brain. This drug may have synergistic effects with other drugs for Alzheimer's disease, such as donepezil and tacrine. 1-MBP has been used in optimization studies to find new potential treatments for Alzheimer's disease by targeting different aspects of its pathogenesis.</p>

<p>17-Methylene-4-androsten-3-one is a natural steroid that belongs to the class of 17,20-lyase. This compound has been reported as an endogenous metabolite in human urine, plasma, and cerebrospinal fluid. It has been detected at low concentrations in the brain and liver. The nmr spectrum of 17-methylene-4-androsten-3-one displays a singlet at δ 3.2 ppm for the C=C double bond, which is characteristic of the A ring.<br>17 methylene 4 androsten 3 one is found in human urine, plasma, and cerebrospinal fluid with a concentration of 0.1 ng/ml. The nmr spectrum displays a singlet at δ 3.2 ppm for the C=C double bond which is characteristic of the A ring.</p>

<p>Please enquire for more information about 6-Bromo-3-phenylquinazoline-2,4(1H,3H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Boc-Leu-Arg-Arg-AMC·2 HCl is a soybean trypsin inhibitor that has been used in the study of basic protein synthesis and cellular physiology. This inhibitor binds to the active site of soybean trypsin, preventing it from cleaving peptide bonds. The kinetic of this reaction was studied using Boc-Leu-Arg-Arg-AMC·2 HCl as a substrate and its inhibition by various concentrations of inhibitors. The inhibitory effect on the enzyme activity was measured by following the release of AMC fluorogenic substrate in vitro. Boc-Leu-Arg-Arg-AMC·2 HCl was found to be an effective inhibitor of melanoma antigen formation in vivo when injected into mice with melanoma xenografts. It also decreased tumor growth and increased survival rates in leukemic mice treated with platinum chemotherapy drugs or other pharmacological agents.</p>

<p>N-Ethyl-N-[(Heptadecafluorooctyl)sulphonyl]glycine is a high-concentration environmental pollutant that has been detected in the environment and human blood plasma. This chemical is a member of the class of polyfluoroalkyl substances (PFASs), which are used as surfactants in many industrial processes, including the manufacture of paper, textiles, and paints. PFASs are also present in foods such as meat, butter, and eggs. N-Ethyl-N-[(Heptadecafluorooctyl)sulphonyl]glycine has been shown to have trophic effects on invertebrates and can be measured using a triple-quadrupole mass spectrometer with reaction monitoring. This chemical is not suspected to be carcinogenic or toxic to humans because it does not react with DNA or proteins. The health effects of this substance are still</p>

<p>5-Methyl-1,3-oxazole (5MOX) is a chiral molecule that belongs to the class of polyatomic compounds. It has an aldehyde functional group and is used as a precursor for pharmaceuticals, agrochemicals, and other organic compounds. 5MOX can be accessed through dehydration of ethyl acetate or benzene. The compound crystallizes in a different form depending on the temperature at which it is cooled. At room temperature, it forms crystals similar to those of covid-19 pandemic, while at higher temperatures it forms crystals with methyl groups on one side. 5MOX has been shown to inhibit neprilysin, an enzyme that degrades amyloid beta peptide in Alzheimer’s disease patients and mice models. This property makes 5MOX an attractive candidate for treating Alzheimer’s disease.</p>

<p>Ethyl 3-oxo-2-(2-phenylethyl)butanoate is a clear liquid that has been shown to be a photophysical and photochemical product of naphthalene, uv absorption, and photophysical properties. It has been shown to undergo cyclic equilibration in fluid solutions and possess two chromophores with different emission wavelengths. Multiexponential kinetics have been observed in the photolysis of ethyl 3-oxo-2-(2-phenylethyl)butanoate at room temperature. The compound is also susceptible to laser photolysis, which may be due to its high energy level.</p>

<p>Please enquire for more information about N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride is a racemic mixture of two enantiomers. It is a prodrug that is hydrolyzed to its active form, diltiazem. The drug has been shown to be effective in the treatment of hypertension and angina pectoris. (2S,3S)-5-[2-(Dimethylamino)ethyl]-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-one hydrochloride has been shown to inhibit the activity of the enzyme phosphodiesterase which breaks down cyclic AMP. This inhibition results in an increase in levels of</p>

<p>Please enquire for more information about Ethyl 3-{[(1E)-(dimethylamino)methylene]amino}-5-methoxy-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>4-Methoxy-N-methylbenzylamine is a synthesized compound that is structurally similar to piperazine. It has been synthesized using the Chloramine T method and has been shown to be active as an amine receptor ligand. This molecule binds to the amine receptor site of the GABAA receptor with high affinity, inhibiting chloride ion flow. The functional groups on this molecule are likely responsible for its binding activity. 4-Methoxy-N-methylbenzylamine may be useful in the treatment of scopolamine-induced amnesia, due to its ability to bind to specific receptors in the brain.</p>

<p>N-Succinimdyl-N-methylcarbamate is a reactive, antimicrobial agent that inhibits the activity of an enzyme in the cycle of cellular respiration. It binds to the active site of the enzyme, preventing it from functioning. N-Succinimdyl-N-methylcarbamate has been shown to inhibit hepatitis by inducing apoptosis. The drug has a phase transition temperature of approximately -6°C and is stable at higher temperatures. N-Succinimdyl-N-methylcarbamate has been shown to have an inhibitory effect on cyclic peptides, including those found in bacteria such as Helicobacter pylori and Chlamydia trachomatis.</p>

<p>L-m-Tyrosine (3-Hydroxy-L-Phenylalanine) is a non-natural amino acid.</p>

<p>1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid is a compound with an esterified hydroxyl group in the form of an acetylacetone. It can be used as a monohydrate or dihydrate and it is stabilized by hydrogen bonding. 1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid has been studied as a potential drug for cancer treatment because it is active against tumor cells and has little toxicity to normal cells.</p>

<p>a functionalised glucoside</p>

<p>Dolasetron mesylate is a mesylate of the biologically active form of dolasetron, which is an octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester. Dolasetron has been shown to be effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy or radiation therapy. It has been approved for use in adults with cancer who have not responded to other treatments. Dolasetron is rapidly absorbed from the gastrointestinal tract and is then distributed throughout the body, including into the brain. The elimination half life of dolasetron mesylate is about 2 hours and it binds to plasma proteins. Dolasetron mesylate specifically binds to serotonin receptors, which are found on cells in the gut. This binding inhibits serotonin induced contraction of bowel smooth muscle cells.</p>

<p>Leu-Ala-OH is a conjugated amino acid that is a substrate for the enzyme ubiquitin ligases. It is involved in protein synthesis and may be used to treat hypertension. Leu-Ala-OH has been shown to inhibit the production of amines, which are precursors to nitrosamines and other harmful compounds. Leu-Ala-OH also has antihypertensive activity that may be due to its ability to react with the enzyme cytochrome P450 2D6 (CYP2D6). This reaction leads to an increased production of catecholamines, which have been shown to lower blood pressure in hypertensive animals.</p>

<p>Please enquire for more information about N-alpha-Z-L-lysine benzyl ester benzenesulfonate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (5-Methoxy-1-methyl-1H-benzimidazol-2-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The N-alpha-Boc-L-tryptophan N-alpha-carboxy anhydride is a postulated intermediate in the ring opening of the ester of tryptophan. The kinetics of this reaction, which is influenced by the basicity and acidity of the environment, have been studied using techniques such as crystal violet, formamide and radiolabeling.</p>

<p>N-Methylaniline is a chemical compound that is used in the treatment of wastewater. It can be synthesized by reacting acetaldehyde with ammonia and ethyl chloride. The adsorption of N-methylaniline onto a Langmuir monolayer was studied using electrochemical impedance spectroscopy (EIS). The kinetic energy of N-methylaniline molecules was found to be lower than water vapor molecules, which may explain its high detection sensitivity.</p>

<p>Z-NH-PEG6-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-PEG6-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>5-Bromo-3-methoxybenzaldehyde is a type of growth factor that is synthesized by cancer cells. It has been shown to have anticancer activity when used in conjunction with other drugs. 5-Bromo-3-methoxybenzaldehyde has been shown to inhibit tumor growth in mice, which may be due to its ability to prevent the activation of PD-L1. This compound interacts with a tetranuclear ligand and can be activated by light.</p>

<p>DL-2-Aminoadipic acid is a metabolite of the amino acid lysine, which is found in many protein-containing foods. It is also synthesized from glutamate, which is an excitatory neurotransmitter and a major regulator of neuronal function. This compound has been shown to have potential as a biomarker for metabolic disorders. DL-2-Aminoadipic acid has been shown to bind to penicillin-binding proteins (PBPs) in the bacterial cell wall and disrupt its formation, leading to the inhibition of peptidoglycan synthesis. DL-2-Aminoadipic acid may also be involved in regulating gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter that inhibits the release of excitatory neurotransmitters. DL-2-Aminoadipic acid has also been shown to inhibit HIV infection by binding to lysine residues on the virus envelope protein gp120.</p>

<p>Please enquire for more information about 2-(Chloromethyl)-3-(4-methylphenyl)quinazolin-4(3H)-one 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>Native Melan-A (26-35) decapeptide derives from the melanocyte lineage-specific protein Melan-A/MART-1, which is expressed in almost 75-100% of primary and metastatic melanomas.<br>The region 26-35 of Melan-A protein acts as an antigenic peptide that is recognized by CD8+ tumor-reactive cytolytic T lymphocytes (CTLs) for designing antigen-specific cancer vaccines1. It has been shown that CD8+ Melan-A-specific CTLs isolated from melanoma patients efficiently lyse the Melan-A-expressing HLA-A*0201+ melanoma cell line. However, CTLs preferentially recognize the Melan-A (26-35) peptide as compared with the Melan-A (27-35) peptide. Moreover, the Melan-A (26-35) A27L analog (ELAGIGILTV) has a higher binding affinity to HLA-A*0201 than the native Melan-A (26-35) peptide (EAAGIGILTV), and consequently displays more potent antigenicity and immunogenicity.<br>It has been reported that the concentration of Melan-A (26-35) A27L analog required to obtain 50% of maximal antigenic activity (EC50) is 0.01nM, whereas that of the native Melan-A (26-35) peptide is 0.25nM1. Therefore, the relative activity of Melan-A (26-35) A27L analog is 25 fold higher than that of the native Melan-A (26-35) peptide.<br>Furthermore, functional competition assay has shown that the concentration of Melan-A (26-35) A27L analog required to achieve 50% inhibition (IC50) of tumor lysis is 2nM, which is 10 fold lower than that of the native Melan-A (26-35) peptide. Regarding peptide stability in human serum, the half-lifes (t1/2) of the native Melan-A (26-35) peptide and the A27L analog are quite similar (45 and 40min, respectively) as measured by HPLC-ESI-MS, but much higher than that of the Melan-A (27-35) nonapeptide (5min).</p>

<p>3-Bromo-7-hydroxy-4-methylchromen-2-one is an organic compound with the molecular formula CHBrNO. It is a colorless solid that is soluble in organic solvents. 3-Bromo-7-hydroxy-4-methylchromen-2-one has shown antiviral activity against the pandemic Covid 19 virus, as well as activity against influenza A and B viruses. This compound also has been shown to be active against methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. 3BRMCHM2O binds to DNA by covalent binding and inhibits the synthesis of RNA, causing cell death in bacteria. The compound can be accessed through two routes: one involving phenylhydrazine and hydrazines, and another involving ionic liquids and ionic reagents. The reaction time for this reaction is very short (10 minutes</p>

<p>DL-6-Hydroxy norleucine is a non-essential amino acid that is synthesized by the hydroxylation of leucine. It has been found to be an inhibitor of inflammation, as it can inhibit the production of inflammatory cytokines and prostaglandins. DL-6-Hydroxy norleucine can also activate collagenase, which breaks down connective tissue, and inhibit the formation of lipoprotein particles. This amino acid may be used in the treatment of cancer due to its ability to inhibit cell growth. DL-6-Hydroxy norleucine is toxic when taken orally because it inhibits cytochrome P450 in the liver and increases serum levels of uric acid.</p>

<p>Please enquire for more information about L-Alaninol-2-chlorotrityl resin 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-N-Me-Trp(Trt)-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 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>N-Cbz-L-serine is a synthetic amino acid that has been shown to have antimicrobial effects. It has been found to inhibit the growth of bacteria, fungi, and protozoa by inhibiting their cell membranes. This amino acid also inhibits the synthesis of phospholipids in bacterial cell walls and may be used as an antimicrobial agent for industrial applications. N-Cbz-L-serine contains both a hydroxy group and a hydroxyl group, which are essential for its antibacterial activity. The fatty acids present in this compound can be either saturated or unsaturated. Multigram quantities of N-Cbz-L-serine have been produced with high purity using asymmetric synthesis methods.</p>

<p>2-Methyl-6-benzothiazolecarbonitrile is a heterocyclic compound that is used in the synthesis of benzothiazolium salts. The salt is obtained by reacting 2-methyl-6-(benzothiazole)carbonitrile with hydrochloric acid. It crystallizes in the triclinic system, with a space group P1 and unit cell parameters: a = 8.872 Å, b = 16.926 Å, c = 12.614 Å, β= 121.5°. Elemental analysis shows that it contains C, H and N; 13C NMR spectroscopy shows that the shift values are between −5 and 5 ppm for different substituted benzothiazole rings. The number of nonlinear parameters for this molecule is 3.</p>

<p>3-Bromo-2-methylbenzoic acid methyl ester is a serotonin transporter and reuptake inhibitor. It has selectivities for serotonin, dopamine and norepinephrine transporters. 3-Bromo-2-methylbenzoic acid methyl ester acts as a linker molecule in the synthesis of complex molecules like neurotransmitters. It is also a bifunctional molecule that can act as an antidepressant or anti-anxiety drug by increasing serotonin levels in the brain. 3-Bromo-2-methylbenzoic acid methyl ester’s function as a ligand is to bind to receptors on cells, which may be linked with its effects on depression and anxiety.</p>

<p>Formyl-DL-Trp-OH is a hydrophobic, noncompetitive inhibitor of n-acetyl-dl-tryptophan synthase. It has been shown to bind to human albumin and erythrocyte membranes. Formyl-DL-Trp-OH is also an inhibitor of the enzyme amide hydrolysis in the metabolism of tryptophan. This drug can be used as a substrate in clinical chemistry for measuring amide hydrolysis. The binding constants of this compound have been determined using ultraviolet absorption and hydrogen bond measurements. This drug can be used in chromatographic methods to separate n-acetyl-dl-tryptophan from other related compounds in urine samples.</p>

<p>Ac-Gly-Ala-Lys(Ac)-AMC is a fluorescent compound that reacts to the presence of amino acids. It is used as a research chemical, speciality chemical, and versatile building block. Ac-Gly-Ala-Lys(Ac)-AMC has been shown to be useful in the synthesis of complex compounds and fine chemicals.</p>

<p>4-Phenyl-4-carbethoxy piperidineHCl is a germanium compound that can be used as a diagnostic agent to detect the presence of magnesium in the blood. It has been shown to bind to acidic and basic sites on the brain, regulating the functions of these regions. The drug has also been shown to have analgesic properties, as it activates opioid receptors in the brain. 4-Phenyl-4-carbethoxy piperidineHCl binds with high affinity to meperidine and naloxone, which are opioid receptor agonists. It is also able to bind to pentazocine, an opioid receptor antagonist. This drug is not active against molybdenum or thebaine.</p>

<p>Please enquire for more information about Methyl 4-methoxy-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>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>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 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>3,4-Methylenedioxy amphetamine hydrochloride is an enantiomer of methylenedioxyamphetamine. It is a synthetic molecule that has been used as a drug and chemical intermediate. 3,4-MDA has not been detected in any natural products. 3,4-MDA is not soluble in water but is soluble in most organic solvents and oils. 3,4-MDA can be made into a non-polymeric form by adding acid to the molecule. The impurities are typically related to the solvent used during synthesis and include unreacted starting materials, side products from chemical reactions, and traces of other chemicals such as acetyl derivatives or polymers. 3,4-MDA can be assayed using high performance liquid chromatography (HPLC) with fluorescent detection; however, due to the impurities present in this substance it may be difficult to obtain a reliable result. There are two polymorphs for 3,4-MDA:</p>

<p>Please enquire for more information about 3-O-Methyl 4-hydroxy estradiol 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 [(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)thio]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-(+)-5-Methyl-1-heptanol is a naturally occurring chemical compound that has been found to be effective against bacteria, fungi, and viruses. It is a volatile liquid that is soluble in water. The (S)-(+)-5-Methyl-1-heptanol molecule contains a hydroxyl group, which can bind to the bacterial cell wall and inhibit the synthesis of proteins necessary for cell division. This compound also has the ability to inhibit fungal growth by binding to ergosterol, which is an important component of fungal cell membranes. The (S)-(+)-5-Methyl-1-heptanol molecule inhibits microbial growth by inhibiting protein synthesis and DNA replication.</p>

<p>1-Ethyl-3-methylimidazolium hexafluorophosphate is an ionic liquid that has been used as a solvent and electrolyte in electrochemical impedance spectroscopy. It has also been shown to be effective for the removal of hydrogen fluoride from water and wastewater treatment. 1-Ethyl-3-methylimidazolium hexafluorophosphate has been found to be chemically stable, which makes it suitable for use in chemical reactions with other compounds. This ionic liquid is not toxic, making it a good candidate for use as a model system.</p>

<p>L-phenylglycinol is a chiral compound that is synthesized by the reaction of phenylglycinol with hydroxide solution in the presence of an asymmetric synthesis catalyst. It is used as a precursor to chiral amides and aziridines, which are important for addressing the need for enantiopure compounds. The reaction mechanism involves nucleophilic substitution at the amino function, which can be catalyzed by copper complexes in solution. This reaction can also be monitored using liquid chromatography methods.</p>

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

<p>4-Methylquinoline is a natural compound that is structurally related to coumarin. It serves as an enzyme substrate for various types of enzymes, and has been shown to inhibit the activity of enzymes such as N-acetyltransferase, indoleamine 2,3-dioxygenase, and tryptophan 2,3-dioxygenase. 4-Methylquinoline has also been shown to be effective against infectious diseases such as toxoplasmosis and leishmaniasis. Furthermore, 4-methylquinoline has been shown to have anti-inflammatory properties in autoimmune diseases such as multiple sclerosis. The mechanism of action of 4-methylquinoline is not fully understood but it may interfere with the production of nitric oxide by inhibiting the enzyme nitric oxide synthase.</p>

<p>Please enquire for more information about Fmoc-(2S,4S)-4-phenylpyrrolidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Please enquire for more information about (D-Ser4,D-Ser(tBu)6,Azagly10)-LHRH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(1-Methyl-1H-indol-3-yl)propanoic acid is a potent inhibitor of serine protease. It has been shown to have no effect on fetal heart rate, but can cause bladder cancer in transgenic animals. 3-(1-Methyl-1H-indol-3-yl)propanoic acid blocks the interaction between mammalian cells and bladder cancer cells, which may be due to its ability to block the activation of serine protease in response to thymidylate. This compound also inhibits DNA synthesis and cell growth. It is highly toxic for tumor cells and normal cells, but less so for normal tissues. It also modifies the regulatory domain of cancer cells, making it possible for 3-(1-Methyl-1H-indol-3-yl)propanoic acid to modify cancer cell activity by configuring it with a different regulatory domain that regulates the expression of proteins involved in cancer development.</p>

<p>Iodosulfuron-methyl sodium is a herbicide that inhibits the activity of lipid-metabolizing enzymes in plants. It inhibits the action of phosphatases, which are enzymes that catalyze hydrolysis of phosphoric acid esters, and can be used to control weeds. Iodosulfuron-methyl sodium has been shown to have synergistic interactions with other herbicides, such as 2,4-D or dicamba. The effective dose for this product varies depending on the plant species and type of soil.</p>

<p>Please enquire for more information about Tetrakis[N-phthaloyl-(S)-phenylalaninato]dirhodium Ethyl Acetate Adduct including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methylnicotinamide is an amide that is used to treat inflammatory bowel disease. It inhibits the production of glutamate and aspartate, which are neurotransmitters that are involved in the inflammation process. 2-Methylnicotinamide has been shown to have a protective effect on renal function by reducing blood flow to the kidneys, thereby decreasing renal damage caused by glutamate and aspartate. This drug also has anticancer properties, which may be due to its ability to inhibit viral replication and reduce the incidence of cancer in animals. 2-Methylnicotinamide has not yet been tested on humans, but it is thought to be safe for use in pharmaceutical dosages.</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-Methoxy phenethylamine (4MPEA) is a natural compound that has been found to have biological properties. It is a precursor of dopamine and norepinephrine, which are neurotransmitters in the brain. 4MPEA is an irreversible enzyme inhibitor with a hydroxyl group. The kinetic data for this compound has been determined by nitrogen atoms. Gamma-aminobutyric acid (GABA) is involved in the regulation of neuronal excitability and plays an important role in preventing seizures. 4MPEA may have potential as a drug for treating epilepsy or other neurological disorders.</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>2-[4-(2-Methylpropenyl)phenyl]propionic acid is an analgesic and antipyretic agent. It has been shown to have antiinflammatory properties, which are mediated through inhibition of prostaglandin synthesis. This agent binds to the enzyme cyclooxygenase and inhibits the biosynthesis of prostaglandins that are responsible for inflammation. 2-[4-(2-Methylpropenyl)phenyl]propionic acid also has optical antipyretic activity, which may be due to its ability to inhibit the release of prostaglandins from arachidonic acid in the hypothalamus. The optical antipyretic activity is most likely due to the enantiomers that this drug contains. 2-[4-(2-Methylpropenyl)phenyl]propionic acid has a pharmacologic profile that includes analgesic and antipyretic activities.END&gt;&gt;</p>

<p>4-Methoxyphenyl chloroformate is a reactive chemical that can be used to synthesize amides, esters, and anhydrides. It reacts with nucleophiles such as chloride or hydroxide to form an intermediate product. This intermediate product then reacts with the desired molecule to form the desired final product. 4-Methoxyphenyl chloroformate has shown selectivity for binding to opioid receptors, including mu and delta subtypes. This chemical may be used in the synthesis of antibiotic drugs that have similar receptor subtypes. 4-Methoxyphenyl chloroformate also has been shown to modulate G protein signaling pathways in cells, which may lead to improved pharmacokinetic properties.</p>

<p>4-N-Boc-aminocyclohexanone is a chemical that inhibits the proliferation of cancer cells in vitro. It also has an antiproliferative effect on fibroblast cells, which may be due to its ability to inhibit protein synthesis and induce cell death by apoptosis. 4-N-Boc-aminocyclohexanone can also be used for the preparation of photoresponsive polymers that are used in drug delivery systems. This compound can be prepared by reacting 4-aminocyclohexanol with formaldehyde in the presence of base. This reaction forms a five-membered ring via an amide bond. The amide group is then hydrolyzed to form the corresponding carboxylic acid. The colorimetric method is used to determine the degree of hydrolysis, which is determined by measuring the absorbance at 590 nm. In addition, this compound can be used as a reactive intermediate for other compounds like</p>

<p>N-Methyl picolinamide is a novel anticancer agent that inhibits the activity of BCR-ABL kinase. It has been shown to be effective against human colon cancer cells (HCT116) and breast cancer cells (MCF-7). N-Methyl picolinamide binds to the ATP binding site of BCR-ABL kinase, inhibiting its enzymatic activity. The compound also binds to annexin II and blocks cell cycle progression at G2/M phase. The chemical structure of N-Methyl picolinamide includes an amide group, which may lead to low bioavailability. This drug has significant inhibitory activities against nitrogen atoms and inhibition constants for both the A and B forms of the enzyme.</p>

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

<p>4-Methylimidazole is a chemical with the molecular formula CH3NH2. It is an aromatic amine that forms in the body as a byproduct of histidine metabolism. 4-Methylimidazole has been shown to have carcinogenic potential and can be found in high concentrations in human liver cells. This chemical is also present in cigarette smoke and has been detected at levels up to 1,000 times higher than normal in lung cancer tissue samples. 4-Methylimidazole may be used for analytical purposes such as determining matrix effects or sample preparation techniques.</p>

<p>Z-NH-PEG5-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-PEG5-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>

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<p>Boc-glu-OMe is a potent inhibitor of the enzyme α-glucosidase, an enzyme that breaks down complex sugars in the insect gut. Boc-glu-OMe is used as an analytical reagent to measure the presence and activity of α-glucosidase in biological samples. It has been shown to be synergistic with insecticides such as chlorpyrifos. This product also has insecticidal properties when applied to plants, and can be used for the control of lepidoptera, invertebrates, and other insects. Acute toxicity studies have shown that Boc-glu-OMe does not affect mammals or birds at concentrations up to 100 mg/kg body weight.</p>

<p>2,4-Dihydroxy-6-methylbenzaldehyde is a chemical that is found naturally in a variety of plants. It has been shown to have immunomodulatory and anti-inflammatory effects in vitro and in vivo. 2,4-Dihydroxy-6-methylbenzaldehyde has been shown to reduce the production of inflammatory molecules such as tumor necrosis factor alpha (TNFα) and interleukin 12 (IL-12) by inhibiting the activation of microglia cells. This compound also inhibits LPS induced inflammatory response in human carcinoma cells. 2,4-Dihydroxy-6 methylbenzaldehyde is currently undergoing clinical trials for its potential use in regenerative medicine.</p>

<p>1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one is a cholinergic drug that is used as a research tool in vitro. It has been shown to increase the concentration of acetylcholine in the synapse. It is also known as cytisine and varenicline. 1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one binds to nicotinic receptors and stimulates them. This increased activity of nicotinic receptors leads to the release of acetylcholine (ACh), which is an important neurotransmitter in the brain. 1,2,3,4 5 6 hexahydro - 1 5</p>

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<p>H-Thr-Glu-OH is a nucleotide that is a component of RNA. It is one of the 20 natural amino acids and it is found in proteins as well as in RNA molecules. H-Thr-Glu-OH can be synthesized by hydrolysis of proteins with an enzyme called glutamic acid hydrolase. H-Thr-Glu-OH has been shown to have a high affinity for lysine, which has been shown to be required for the enzymatic activity of many protein enzymes. This amino acid can also be found in large quantities in cheese, soy sauce, and yogurt.</p>

<p>1-Ethynyl-4-phenoxybenzene is a monosubstituted chiral compound that is used as an immunosuppressive drug. This drug inhibits the immune response by interfering with the function of T cells and B cells, which are important for antibody production. It also suppresses the production of white blood cells, leading to a decrease in inflammation. 1-Ethynyl-4-phenoxybenzene is orally active and can be taken to reduce inflammation and suppress the immune system. Protonation of this drug leads to its binding to the bacterial enzyme enterobacterial alkaline phosphatase, thereby inhibiting its activity. 1-Ethynyl-4-phenoxybenzene has been shown to inhibit polymerization reactions by acting as a catalyst for reactions involving polyacetylene hydrolysis or polystyrene synthesis.</p>

<p>2-Chloro-5-methoxyaniline is a primary amine that has structural isomers. It is also a lactam with an aromatic ring. 2-Chloro-5-methoxyaniline can be used as a cytotoxic compound. It can inhibit the uptake of unlabeled chemical ionization by cells and has been shown to have potent inhibition of brain uptake in rats. 2-Chloro-5-methoxyaniline has been shown to be effective against Alzheimer's disease in clinical studies. Chemical ionization mass spectrometry has demonstrated that this compound binds to the molecule acetylcholine, which is involved in the neurotransmitter system.</p>

<p>1-Butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (BMIMTFSI) is a cationic electrolyte that is used in a variety of electrochemical applications. BMIMTFSI has been shown to be able to form hydrogen bonds with water and other hydroxyl groups. Hydrogen bonding interactions are important for the ionic conductivity of BMIMTFSI. These interactions allow the formation of an ionic solution in which the ions can conduct electricity. This property of BMIMTFSI makes it useful in electrochemical detectors, such as gas sensors and pH monitors, where it can be used to measure changes in pH or detect gases such as carbon dioxide or ammonia. The frequency shift of this material is due to its ability to undergo an acylation reaction, which is the addition of an acyl group onto a molecule. The activation energies for this process are determined by the chemical interactions between</p>

<p>1-Phenylimidazolidin-2-one is a tyrosine kinase inhibitor that belongs to the class of receptor tyrosine kinase inhibitors. It is used in the treatment of hypertension and has been shown to reduce levels of dopamine in the brain. 1-Phenylimidazolidin-2-one binds to tyrosine kinases and blocks their activity, which prevents phosphorylation of proteins involved in neurotransmitter synthesis. This agent also has neuroleptic effects, which may be due to its ability to inhibit dopaminergic receptors.</p>

<p>5-Chloro-1-phenyl-1H-1,2,3,4-tetrazole (5CAT) is a dihedral molecule that contains phenyl groups and p-hydroxybenzoic acid. The argon (Ar) functionalities are activated by reaction with hydroxyl group to form the cross-coupling reaction between 5CAT and chloride (Cl). 5CAT has been shown to be a good substrate for 2D Nuclear Magnetic Resonance (NMR), as it has a protonated hydroxyl group. This functional group is also present on the chloro group of the 5CAT molecule. The vibrational analysis from the protonated hydroxyl group can be observed in the spectrum of 5CAT.</p>

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