Amino Acids (AA)

<p>Please enquire for more information about N-Methyl-1-(3,4,5-trimethoxyphenyl)methanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Phenylpiperazine is a piperazine derivative that can bind to the DNA of cervical cancer cells and inhibit their growth. It also has antihypertensive effects. 1-Phenylpiperazine is a white crystalline solid that is soluble in water, ethanol, ether, and chloroform. It binds to the hydrogen chloride ion (HCl) with high affinity and forms an equilibrium mixture with HCl gas. The binding constants of 1-phenylpiperazine to HCl are greater than those for piperazine. This compound has been shown to inhibit tumor cell growth in vitro through its ability to bind to DNA and prevent RNA synthesis. 1-Phenylpiperazine has been shown to have antihypertensive activity in rats by blocking alpha1-adrenergic receptors on vascular smooth muscle cells.br&gt;br&gt;<br>In addition, this molecule has been shown to have binding properties for amines which may be due to the presence</p>

<p>9-Methyl-b-carboline is a phytochemical that belongs to the class of protonated carbon disulphide. It has been shown to inhibit monoamine oxidase and is used in some medications. 9-Methyl-b-carboline has been shown to have physiological function, including growth factor activity and epidermal growth properties. It also inhibits hydroxylase, which is an enzyme that catalyzes the stepwise oxidation of tyrosine and phenylalanine. This compound can be found in plants belonging to the families of Fabaceae, Lamiaceae, and Solanaceae. The compound has been found to act as a secondary messenger in mitochondria by transferring electrons from NADH to coenzyme Q10.</p>

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

<p>Please enquire for more information about 3-(1-Ethyl-5-methyl-1H-pyrazol-4-yl)isoxazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Leu-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 1,1'-Methylene bis[theobromine] including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methyltryptamine is a tryptamine derivative that binds to the 5-HT2 receptors in the brain and blocks the action of serotonin. It has been proposed as a possible treatment for human immunodeficiency, but more research is needed to determine its efficacy. 2-Methyltryptamine acts as an agonist at 5-HT2 receptors and can be used in plate tests to detect histones deacetylase activity.</p>

<p>2-Bromo-4-methylacetophenone is a synthetic compound that inhibits bacterial growth through acetylation of the aromatic ring. It is used in the synthesis of imidazolidinones, which are a class of antibacterial drugs. 2-Bromo-4-methylacetophenone has shown inhibitory activity against MCF-7 breast carcinoma cells and mononuclear cells. It also has been synthesized from phenacyl bromide and potassium carbonate in anhydrous conditions. The crystal system for 2-bromo-4-methylacetophenone is tetragonal with space group P42/mnm.</p>

<p>3-(4-Chloro-phenyl)-7-hydroxy-chromen-4-one is an intermediate that is used in the research of Alzheimer's disease. It coordinates transition metals, such as copper (Cu), zinc (Zn), and nickel (Ni) to form a pharmacophore. This pharmacophore binds with flavones, which are compounds found in plants that have hypotensive and antihypertensive properties. 3-(4-Chloro-phenyl)-7-hydroxy-chromen-4-one has been shown to be an effective inhibitor of angiotensin II type 1 receptors and has a crystalline structure. 3-(4--Chloro---&gt;</p>

<p>Please enquire for more information about (R)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methyl pentanoic acid is a coordination complex that is synthesized by the condensation of propionyl chloride and 2-methylpentanoyl chloride. It has been shown to have anticancer activity against human cervical cancer cells, inhibiting the growth of cells in culture. The mechanism of action may be due to its ability to inhibit the production of mitochondrial proteins, leading to cell death. 2-Methyl pentanoic acid also has a strong affinity for fatty acids and can be used as an inhibitor of fatty acid synthase, which is an enzyme that catalyzes the synthesis of long chain fatty acids in mitochondria. 2-Methyl pentanoic acid can also be used as a treatment for seizures caused by divalproex sodium and isovaleric acid. It inhibits the production of 3-hydroxyisovaleric acid, which is responsible for these seizures, through competitive inhibition with valine at the 3 position on the enzyme's active site.</p>

<p>2,5-Dibromo-3-methylthiophene is a small molecule that has been shown to have anti-bacterial properties. It reacts with the bacterial cell membrane, disrupting the bacteria's ability to function and causing it to die. 2,5-Dibromo-3-methylthiophene can be used as an antibacterial agent in medicine or cosmetics. The chemical structure of 2,5-dibromo-3-methylthiophene is similar to that of oxadiazole and 5H-[1]benzothiazol[5,4,-d][1,2]oxazole and it has been shown that these compounds can also be used for antibacterial purposes. The anti-bacterial activity of 2,5-dibromo-3-methylthiophene is due to its functional groups which are reactive with metal ions such as Cu(II) and Fe(III).</p>

<p>2-Methylfuran is a compound that has been used as a catalyst in the synthesis of 2-methylpentane. The presence of nitrogen atoms in the molecule gives it some synergic effect with other catalysts, such as palladium and nickel. 2-Methylfuran can be detected at sensitivities of 10 parts per billion. A kinetic energy of ˜400 kJ/mole and a hydroxyl group give this compound the ability to react with laminar tissue culture cells. 2-Methylfuran is also a solid catalyst for methyl ethyl ketones, which are used in the production of solvents, plastics, and pharmaceuticals. Its transport properties are similar to those of isooctane, making it useful for studies on gas chromatography analysis.</p>

<p>Please enquire for more information about 5'-Amino-5'-deoxy-2',3'-O-(1-methylethylidene)-adenosine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Halosulfuron-methyl is a herbicide with a basic structure that inhibits the activity of protein synthesis by binding to the active site of the enzyme. Halosulfuron-methyl has been shown to have synergistic effects when used in combination with glyphosate, which may be due to its ability to inhibit renal bean protein synthesis at lower concentrations. Halosulfuron-methyl has also been shown to have antiangiogenic properties, which are thought to be caused by inhibition of choroidal neovascularization and pyrazole ring formation. The fluorescein angiography technique can be used for analytical purposes on both animals and humans. Halosulfuron-methyl is used as an analytical method for the determination of kidney bean concentrations in physiological levels. The sample preparation involves extraction using acetonitrile, followed by purification using high performance liquid chromatography (HPLC).</p>

<p>Please enquire for more information about Methyl (3S)-3-aminopent-4-ynoate hydrochloride 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 (S,S')-3-Methyl-1-(2-piperidinophenyl)butylamine, N-acetyl-glutamate 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 Acetyl-L-methionine sulfoxide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-2-Methylpyrrolidine is a synthetic quaternary ammonium compound that is a reaction yield enhancer. It has been shown to have histamine-lowering effects in vitro and in vivo. The pharmacokinetic properties of (R)-2-Methylpyrrolidine are characterized by moderate distribution and elimination half-life times. It is also active at the h3 receptors, which may be related to its wake-promoting effects. (R)-2-Methylpyrrolidine has been shown to increase the levels of amines in the brain, which may be associated with its antidepressant activity. This drug also has environmental effects such as increasing the absorption of heavy metal ions such as lead and cadmium.</p>

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

<p>2-Bromo-4-methoxybenzaldehyde is a cyclic, stereoselectively eliminable, acrylate that can be used in the asymmetric synthesis of sulfamidate and lactam. It can also be used to synthesize quinoline derivatives with aluminium chloride. This product has been shown to yield good yields when reacted with functional groups such as halides and nature. 2-Bromo-4-methoxybenzaldehyde is found in biomolecular reactions.</p>

<p>N-Chloroacetyl-L-tyrosine is a synthetic, proteolytic enzyme that hydrolyzes proteins containing the amino acid L-tyrosine. It has been shown to inhibit the growth of bacteria by inhibiting the activity of enzymes involved with protein synthesis and peptide bond formation. N-Chloroacetyl-L-tyrosine inhibits the activity of diazonium salt and conjugates, which are involved in polypeptide synthesis and DNA replication. It also has an inhibitory effect on functional groups, such as hydroxyl, amine, sulfhydryl, carboxylate, phosphate, and phosphoric acid.</p>

<p>1-Methyl-3-Propylbenzene is a type of aromatic hydrocarbon. It is used as a solvent, pesticide, and reagent in the chemical industry. The reaction time for this compound is about 15 minutes. 1-Methyl-3-Propylbenzene interacts with other compounds to form products that are easily identified by spectrometry, such as chromatographic science. This molecule has been shown to be an efficient method for creating phylogenetic trees based on fatty acids.</p>

<p>2-Methylbenzhydrol is an organic compound that belongs to the group of five-membered heterocyclic compounds. The crystal structure of 2-methylbenzhydrol has been determined by X-ray crystallography, and it reacts with a rhesus monkey in a stereoselective manner. It is also found as one of two diastereomers in the reaction between benzaldehyde and hydroxylamine. The molecular ion peak for 2-methylbenzhydrol can be detected using mass spectrometry, and the major product ions are ions corresponding to the loss of methanol (CHOH) from the molecule. Other functional groups present in this compound include an aldehyde and a hydroxy group. The reversed-phase high performance liquid chromatography (HPLC) plates used to separate 2-methylbenzhydrol from other similar compounds should be stable at room temperature, but will become unstable if heated to more than 40°C.</p>

<p>2-Methyl-3-buten-2-ol is a reactive oxygenated compound that can be found in the environment. It is produced by the oxidation of glyoxal, glycolaldehyde, and other simple sugars. 2-Methyl-3-buten-2-ol has been found to have toxic effects on wild type strains of Escherichia coli, including inhibition of growth and induction of cell death. In addition, 2-methyl-3 buten 2 ol has been shown to react with other molecules in the environment to produce epoxides. This compound can also be found in some foods and beverages as a result of its presence as a natural component or from contamination during processing. !-- END--&gt;</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>Please enquire for more information about 3-Methoxy methamphetamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>Please enquire for more information about 2-Methoxy-4-amino-5-ethylthiobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-NH-PEG8-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-PEG8-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>1-Methyl-1H-indole-3-carbohydrazide (MZ) is a potential anticancer drug that inhibits the growth of cancer cells. It binds to the colchicine binding site on the DNA, which prevents doxorubicin from binding and causing damage to the DNA. MZ has been shown to be effective against breast cancer and has been shown to inhibit tumor growth in mice by targeting cancer cells lines. MZ also inhibits proliferation of MDA-MB-231 cells in culture, as well as inhibiting cell cycle progression, leading to apoptosis. The molecular docking studies show that 1MZ binds to colchicine site on DNA with high affinity and specificity.</p>

<p>Fmoc-Thr-OPAC is a solid-phase peptide synthesis reagent. It is used to synthesize α-amino acid peptides. Fmoc-Thr-OPAC has been used in the preparation of various peptides, including polypeptide hormones such as insulin and vasopressin. The compound has also been used in the crystalline form for the synthesis of α-amino acid derivatives.</p>

<p>N,N,N',N'-Tetramethyl-p-phenylenediamine is a chemical compound that has been found to have a high affinity for proteins and nucleic acids. It interacts with these molecules by steric interactions and can change the phase transition temperature of water. N,N,N',N'-Tetramethyl-p-phenylenediamine reacts with surfactant sodium dodecyl (SDA) to produce protonated SDA species. These protonated SDA species are able to react with nucleophiles such as p-hydroxybenzoic acid (PHBA), which leads to an exchange reaction. The redox potentials of PHBA and N,N,N',N'-tetramethyl-p-phenylenediamine vary from -0.85 V to -1.05 V at pH 7.4, depending on the number of nitrogen atoms in the molecule. The x-ray</p>

<p>L-Serine amide hydrochloride is a synthetic, anti-HIV drug that is used as an antiviral agent. It inhibits the viral life cycle by inhibiting the activity of acyclic nucleoside phosphonates, which are vital to viral DNA synthesis. L-Serine amide hydrochloride binds to the cyclopentane ring of guanosine and prevents its interaction with the enzyme ribonucleotide reductase. This binding prevents the conversion of guanosine into GTP, thereby preventing HIV from using this molecule in their life cycle. L-Serine amide hydrochloride is not active against cellular proteins or prostaglandins.</p>

<p>N-Methyl-2,4-dinitroaniline is an organic compound that is used as a chemical intermediate. It is produced by the oxidation of N-methyl-2,4-dinitrophenylhydrazine with trifluoroacetic acid in the presence of amines and acetonitrile. It can be analyzed by gas chromatography for its oxidation products such as aldehydes and acetaldehyde. The sensitivity of this compound is insensitive to temperature and humidity, making it suitable for use in analytical chemistry.</p>

<p>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(2-Methyl-1H-imidazol-1-yl)ethanol is a synthetic intermediate that has been used to synthesize antibiotics and antiviral agents. It has a terminal half-life of about 2 days and its pharmacokinetics are linear with an oral dose range from 10 to 100 mg/kg. The fruit extract of Camptotheca acuminata contains alkaloids, which can be converted into 2-(2-methyl-1H-imidazol-1-yl)ethanol by alkalization. 2-(2-Methyl-1H-imidazol-1-yl)ethanol is effective against hordeolum, acne, and infectious diseases caused by viruses such as herpes simplex. This drug has antibacterial properties and can be used in the treatment of bacterial infections such as staphylococcal skin infections, streptococcal throat infections, or gonorrhea. Dehydration is an</p>

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

<p>(R)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid (BAAM) is a potent, orally bioavailable, and pharmacokinetically well-characterized inhibitor of blood coagulation that has been shown to be effective in animal models. BAAM inhibits the activity of tissue factor (TF), an enzyme that initiates the blood coagulation cascade. TF is important for hemostasis because it is activated by contact with blood and tissue factors such as collagen or thrombin. BAAM has shown some promise as a potential treatment for thrombosis, which can lead to heart attacks and strokes.</p>

<p>The tributylstannane group is a hypervalent group that contains three bonds and two lone pairs. 1,4-Phenylenebis[tributylstannane] belongs to the class of inorganic compounds that are semiconducting. It has been synthesized by cross-coupling with hydroxyl groups and trifluoromethanesulfonic acid. The synthesis of this compound is rather challenging due to its high reactivity, but it has been studied extensively for its potential use in organic electronics.</p>

<p>Eltrombopag olamine is an orally active drug that belongs to the class of thiazolidinones. It has been used for the treatment of thrombocytopenia in patients with chronic liver disease and myelodysplastic syndrome. Eltrombopag olamine inhibits platelet aggregation by binding to glycoprotein IIb/IIIa receptors on the surface of platelets. The drug is a prodrug that is metabolized in vivo to its active form, eltrombopag. This conversion is catalysed by CYP3A4 and CYP2D6 enzymes and can be inhibited by drugs that inhibit these enzymes, such as trifluoroacetic acid and hydroxyl group-containing compounds. Eltrombopag olamine binds to erythrocytes, which may be due to its ability to form intramolecular hydrogen bonds with nitrogen atoms. The synthesis of elt</p>

Please enquire for more information about (6a,11b,16a)-21-(Acetyloxy)-9-bromo-6-fluoro-11-hydroxy-16-methyl-pregna-1,4-diene-3,20-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Phenylacetic acid 2-phenylethyl ester is an ester of caproic acid and phenylethyl. It is used as a control agent in the manufacture of chemical substances, detergent compositions, and lemongrass oil. Phenylacetic acid 2-phenylethyl ester can be synthesized by reacting methyl anthranilate with benzoic acid in the presence of phosphotungstic acid. The required starting materials are available from commercial sources. The product has a structural formula that can be confirmed by nmr spectroscopy.</p>

<p>2-Methylbenzenesulfonamide is a chemical compound that has been shown to induce apoptosis in bladder cancer cells. It is an acid conjugate of the drug 2-methylbenzene-1,4-sulfonamide and it can be used for the treatment of bladder cancer. The compound binds to the apoptosis protein and inhibits its function, leading to cell death. The cytotoxic effects of 2-methylbenzenesulfonamide have been shown in short term toxicity studies in rats. In long term animal studies, this compound showed no adverse effects on the liver or kidneys, but did show some indication of reproductive toxicity. 2-Methylbenzenesulfonamide is not mutagenic and does not affect male fertility when given orally at doses up to 2000 mg/kg body weight for 90 days. 2-Methylbenzenesulfonamide binds to receptors on the surface of cancerous cells and induces apoptosis by inhib</p>

<p>Please enquire for more information about 1-BOC-2,3-Dihydropyrrole-4-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 5-methyl-2,4-dioxohexanoate is an intermediate in the preparation of cyclobutene. This compound can be prepared from triphenylphosphine and ethyl acetoacetate via a Wittig reaction. This process is intramolecular, meaning that the two molecules react to form one product without any molecules being lost or added. The Wittig Reaction was first discovered by Georg Wittig in 1953. Intramolecular reactions are often used to synthesize organic compounds with high yields because they do not require any external reagents or catalysts. Ethyl 5-methyl-2,4-dioxohexanoate has also been shown to be reactive with protonation and alkylation reactions.</p>

<p>2,5-Dichloro-4-methoxybenzoic acid is a synthetic herbicide that inhibits the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). This enzyme is necessary for the synthesis of aromatic amino acids. 2,5-Dichloro-4-methoxybenzoic acid is used as a selective herbicide in plants grown in vitro to eliminate weeds. It is also used to control populations of wild plants and grasses. 2,5-Dichloro-4-methoxybenzoic acid has been shown to inhibit the growth of glyphosate resistant weed species by inhibiting EPSPS activity.</p>

<p>Please enquire for more information about Nomega-(4-Methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Benzyl-phenol is a formaldehyde and aliphatic compound that is used as a chemical intermediate. It can be synthesized from 3-phenylglycine, which is an amino acid with the formula CH(CH)CONH. The hydroxyl group of 3-benzyl-phenol can be converted to a sulphonic or salicylic acid by hydrolysis with hydrochloric acid or salicylic acid respectively. 3-Benzyl phenol also catalyzes the reaction between paraformaldehyde and hexamine in the presence of water, yielding acetaldehyde and hydrogen gas.</p>

<p>Des-Gly10,D-Ala6,Pro-NHEt 9)-LHRH acetate salt Pyr-His-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-NHEt acetate (DGPRP) is a drug that is used to treat endometriosis. It is an agonist of the LHRH receptor and inhibits body formation by preventing the release of gonadotropin hormones. DGPRP has been shown to inhibit cell proliferation in cancer tissues and may be useful for the treatment of leukemia. This drug has also been shown to be biocompatible with polymer scaffolds and can be synthesized using methods such as solid phase peptide synthesis.</p>

<p>N-Methyl-L-valine hydrochloride is a synthetic molecule that binds to the CB2 receptor. It has been shown to have anti-inflammatory effects in mice by reducing the production of inflammatory mediators such as prostaglandins and cytokines. N-Methyl-L-valine hydrochloride has also been shown to reduce inflammation in several mouse models of autoimmune diseases, such as type 1 diabetes, multiple sclerosis, and rheumatoid arthritis. This drug was found to be effective in animal models for these diseases by inhibiting inflammatory mediator release from immune cells.</p>

<p>Z-L-Ala-NHS ester is a methyl ester that is used as a fluorescent probe for the detection of amines and other amino acids. It can be used to measure the pH of solutions, as well as in the detection of enzyme substrates and aldehydes. Z-L-Ala-NHS ester has been shown to have high fluorescence properties, which are sensitive to changes in pH.</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</p>

<p>Please enquire for more information about 2-Bromo-3-methylbutenoic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methyl-isoquinoline is a chemical compound that has been used as an intermediate in the synthesis of pharmaceuticals. It is also a useful building block for the production of other chemicals. This compound is soluble in water. 1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methyl-isoquinoline has shown to be a versatile and high quality reagent with many research applications.</p>

<p>The functional theory of 1-Boc-4-formyl piperidine (1BP) is that it activates the serine protease, which in turn inhibits the acetylcholine release. It also affects the 5-ht4 receptor, which is an important regulator of neuronal function and amine release. 1BP has been shown to have potent inhibitory activity against reactive molecules, including those that are involved in carcinogenesis. It also has a high affinity for the 5-ht4 receptor and can be used as a 5-ht4 receptor agonist.</p>

<p>4,4,4-Trifluorovaline is a chemical compound with a trifluoromethyl group that can be synthesized in an efficient method. It has been shown to have the ability to stabilize proteins and enzymes in recombinant systems. The enolate of 4,4,4-trifluorovaline reacts with amides to form allylations. The stereoselective synthesis of 4,4,4-trifluorovaline isomers produces two diastereoisomers that are separated by either chiral chromatography or crystallization. These methods allow for the introduction of 4,4,4-trifluorovaline into cellular systems without affecting the stability of the protein or enzyme.</p>

<p>Please enquire for more information about 5-Desmethyl-3-methyl leflunomide 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 Methyl 6-Bromo-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>Boc-Gly-Arg-Arg-AMC trifluoroacetate is a potent inhibitor of kinases, which are enzymes that play a crucial role in various cellular processes. It has been shown to effectively inhibit the activity of both Chinese and human kinases. This inhibitor has also demonstrated its efficacy as an anticancer agent by inducing apoptosis in cancer cells. Boc-Gly-Arg-Arg-AMC trifluoroacetate is a medicinal protein analog that can be used for the development of novel inhibitors with improved potency and selectivity. Its potential therapeutic applications make it a promising candidate for cancer treatment. Additionally, this compound can be detected in urine, making it an excellent biomarker for kinase activity in vivo.</p>

<p>Inhibitor of cathepsin</p>

<p>Please enquire for more information about (1R,2S)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenyl-1-propanol 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>Please enquire for more information about O-Benzyl-L-tyrosine methyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Methyl-1H-benzimidazole-2-carboxylic acid is a synthetic compound that can be used as an antiprotozoal. It has been shown to have good activity against intestinalis, vaginalis, and intestinalis species. 1-Methyl-1H-benzimidazole-2-carboxylic acid binds to the acetyl groups of the parasite's cell membrane and inhibits the formation of the cytoplasmic membrane. This prevents the parasite from synthesizing ATP, which causes them to die. 1-Methyl-1H-benzimidazole-2-carboxylic acid also has strong activity against Giardia lamblia, which is caused by its ability to inhibit protein synthesis in this organism.</p>

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

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<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>DL-4-Hydroxyphenylglycine is an active analogue of the natural amino acid L-glycine, which is a precursor in the biosynthesis of sulfamides. DL-4-Hydroxyphenylglycine has been shown to be active as an anti-infective agent against many bacteria and fungi that are resistant to other sulfa drugs. It is synthesized by reacting sodium carbonate and ammonia with the amide of 4-hydroxybenzeneacetic acid. The cyclic peptide is then hydrolyzed to form free DL-4-hydroxyphenylglycine. This drug has also been shown to have a strong inhibitory effect on fatty acid metabolism in liver cells, which may be due to its ability to bind to fatty acids and reduce their uptake by cells.</p>

<p>3-Methyl-1H-1,2,4-triazole-5-thiol is a coagulant agent that has been shown to be effective in the field of wastewater treatment. 3-Methyl-1H-1,2,4-triazole-5-thiol binds metal ions and prevents them from catalyzing reactions in the filtrate. It also has an inhibitory effect on polymerization reactions by binding to functional groups. 3MTH is used as a coagulant additive in many industries, such as papermaking, textile printing and dyeing, food processing and leather tanning. The use of 3MTH has been shown to reduce the amount of water needed during the production process. This product can also be used for coatings and other applications where it is necessary to prevent corrosion or environmental pollution by metal ions.</p>

<p>Please enquire for more information about 3,3'-[1,3-Phenylenebis(oxy)]dipropanoic 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 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>2,3,3-Trimethyl 5-methoxy indolenine (TMMI) is a fluorescent probe that has been used in photodynamic therapy. TMMI is chemically stable and has an unsymmetrical heterocycle with optical properties that allow it to be excited by green light at wavelengths of 540 nm. TMMI can be used to image hypoxic regions of the brain. This molecule has also been used as an enhancement agent for neovascularization and angiography. TMMI can be synthesized using mesoporous silica nanoparticles and halogens such as chlorine or bromine.</p>

<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>Please enquire for more information about Fmoc-O-tert-butyl-D-trans-4-hydroxyproline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Iodo-5-methylpyrimidine 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 beta-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 1-(Boc-amino)-4,9-dioxa-12-dodecanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>D-Leucine amide is a hydrophobic, carboxyamide amino acid that is found in the fungus Ochrobactrum anthropi. D-Leucine amide has been shown to catalyze the formation of tripeptides, such as d-alanine and d-tryptophan, from their monomers. The presence of this compound enhances the expression of genes encoding proteins involved in the synthesis of these amino acids. This compound also has been shown to enhance gene analysis by increasing the stability of DNA and RNA molecules.</p>

<p>5-[(2-Methoxyphenoxy)-methyl]-2-oxazolidinone is a pharmacological agent that is structurally similar to rapamycin. It has been shown to inhibit the production of creatine kinase in rat liver microsomes and has been used in studies on degenerative diseases. 5-[(2-Methoxyphenoxy)-methyl]-2-oxazolidinone inhibits the activity of polymerase chain reaction (PCR) by binding to the DNA polymerase and blocking the extension of an oligonucleotide primer. It has also been shown to be toxic to humans, as it can cause fatty acid accumulation and a clinical response. In addition, this drug is enantiopure, meaning that it is composed of only one type of molecule with a specific configuration. The analytical chemistry for this drug includes gas chromatography (GC) and high performance liquid chromatography (HPLC).</p>

<p>Beta-alanine amide HCl is a research chemical that belongs to the class of beta-amino acid derivatives. Beta-alanine amide HCl is an activator of nucleophiles and can be used in analytical chemistry as an indicator for chloride ions. It has been shown to react with asparagine, yielding beta-alanine and ammonia. The reaction system can be analysed by measuring the elimination of a hydrogen chloride ion from the beta-alanine amide HCl molecule and the subsequent increase in pH. The analytical method has also been used to measure concentrations of deamination reactions and redox potentials at high concentrations.</p>

<p>4-Hydroxy-N-isopropyl-N-methyltryptamine (4OHMIT) is an analytical chemical that has been shown to bind to various receptors in the rat brain. 4OHMIT has also been found to inhibit the binding of serotonin, dopamine and norepinephrine. This drug is a synthetic compound that has been detected in human urine samples.br&gt;br&gt;4OHMIT is a psychedelic substance that can be used for the acute treatment of depressive disorders and anxiety. It also has pharmacological treatments, such as analytical chemistry, which can be used to detect this drug in biological samples.</p>

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

<p>1-N-Boc-4-bromopiperidine is a Grignard reagent that is used for the preparation of amines. It can be prepared by reacting 1-bromo-4-methylpiperidine with magnesium metal in an ether solution. This compound has been shown to be efficient for the synthesis of biologically active molecules, such as dihydropyridones and isoquinolines. This product may cause skin irritation.</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>Please enquire for more information about 6a-Methyl hydrocortisone 21-hemisuccinate 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-Bromo-1-methyl-1H-imidazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide (AMIS) is an intermediate in the preparation of medicaments. It is a stable process and can be used as an intermediate for other compounds. AMIS is prepared by reacting methanesulfonic acid with methanol and ammonium carbonate, which produces methanesulfonamide, succinic acid and ammonium hydroxide. The reaction liquid is then heated to produce a crystalline solid. The crystals are then recrystallized to yield AMIS as a white solid.</p>