Amino Acids (AA)

<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>1-(4-Hydroxyphenyl)-2-phenyl-1-butanone is a versatile building block that is used in the synthesis of many complex compounds. It has been used as a reagent or speciality chemical and can be used to synthesize a wide range of organic compounds. The compound also exhibits high quality and can be used as an intermediate in the synthesis of pharmaceuticals, herbicides, pesticides, and other research chemicals. 1-(4-Hydroxyphenyl)-2-phenyl-1-butanone is also a useful scaffold for the synthesis of natural products such as alkaloids, terpenes, and other research chemicals.</p>

<p>Please enquire for more information about 2-Hydroxy-5-iodo-3-methoxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methylcrotonyl glycine is a metabolite of carnitine that has been shown to be an effective marker for detection of creatine kinase (CK) deficiency in patients with infantile mitochondrial encephalomyopathy. 3-Methylcrotonyl glycine is used for the diagnosis of metabolic disorders such as fatty acid oxidation defects, enzyme deficiencies, and inherited metabolic disorders. 3-Methylcrotonyl glycine can be used for the diagnosis of various symptoms including muscle weakness, fatigue, developmental delay, and seizures in children. The sensitivity of 3-methylcrotonyl glycine as a biomarker can be increased by using gas chromatography coupled with mass spectrometry.</p>

<p>6-Methylmercaptopurine is an important metabolite of 6-methylmercaptopurine, which is a vital component of the nucleotide synthesis pathway. It is used in analytical methods to determine levels of nucleotides, as well as in biological studies for its effect on autoimmune diseases. 6-Methylmercaptopurine can inhibit replication by inhibiting the methyltransferase enzyme.</p>

<p>3-(Boc-amino)propyl bromide is an antimicrobial agent that has been shown to be a potent inhibitor of cancer cell growth in vitro. The mechanism of action of 3-(Boc-amino)propyl bromide is not yet known, but it may be due to its ability to inhibit the uptake of radiotracers by mda-mb-231 cells. 3-(Boc-amino)propyl bromide has also been shown to have a high affinity for proteins and is able to hydrogen bond with them. This property may explain the high salt requirement for its solubility, as well as its toxicity towards bacteria and other microorganisms.</p>

<p>Please enquire for more information about Methyl 3-amino-6-methylthieno[2,3-b]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-((2,3-dimethyl-5-oxo-1-phenyl(3-pyrazolin-4-yl))amino)-2-(1,3-dioxoindan-2-ylidene)ethanenitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>[5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetic acid is a reaction component that can be used in organic synthesis as a reagent. This chemical has been shown to have high quality, and is useful for research purposes. It is also a versatile building block and useful intermediate, which can be used in the production of complex compounds. [5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetic acid has CAS number 345637-71-0, and is a fine chemical that is useful for chemistry research.</p>

<p>Benzoyl-L-tyrosine amide is a reaction intermediate that is a competitive inhibitor of serine proteases. It binds to the active site of the enzyme and inhibits the breakdown of proteins by blocking the access of other reactants. Benzoyl-L-tyrosine amide has been shown to inhibit proteolytic activity in subtilis, an enzyme isolated from Bacillus licheniformis. The amino acid composition and binding properties are similar to those found in natural substrates. Benzoyl-L-tyrosine amide has been synthesized and its binding affinity towards histidine residues has been determined by titration calorimetry and fluorophosphate assay.</p>

<p>4-(1-Methyl-1-phenylethyl)phenoxyacetic acid is a versatile building block that is used in the synthesis of a variety of fine chemicals and drugs. 4-(1-Methyl-1-phenylethyl)phenoxyacetic acid is an intermediate in the synthesis of a number of complex compounds, including research chemicals, reagents, and speciality chemicals. This compound can also be used as a reaction component for the synthesis of other chemical compounds or as a scaffold for larger molecules.</p>

<p>Please enquire for more information about N-[(1-Methyl-1H-indol-3-yl)methyl]cyclohexanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 3-methyl-2-nitrobenzoate is a chiral, catalytic, and magnetic additive. It is used in the production of alkyl chlorides, cinnolines, and cyclic compounds. Methyl 3-methyl-2-nitrobenzoate can be used as a diagnostic for chloride ions or chlorine gas in water. It also has an important application in wastewater treatment by removing organics from wastewater effluent. Methyl 3-methyl-2-nitrobenzoate can be synthesized from allylic oxidation of methyl benzoate with sodium hypochlorite in the presence of copper sulfate catalyst. The reaction proceeds through an addition–elimination mechanism to produce the desired product and copper(II) chloride as a byproduct. The process occurs on a mesoporous material to increase surface area for the reaction to proceed more quickly and efficiently.</p>

<p>L-Histidine methyl ester dihydrochloride is a β-amino acid with the chemical formula HNCH2CH(CH3)CO2H. It has the functional group of an isopropyl group and a chloride ion. L-Histidine methyl ester dihydrochloride has been shown to bind to receptors in the central nervous system that are involved in pain perception. As a result, it can be used for the treatment of neuropathic pain, chronic pain, and cancer pain. This drug also inhibits nitric oxide production by binding to iron ions or copper ions. L-Histidine methyl ester dihydrochloride has been shown to have antiinflammatory effects as well as antioxidant properties.</p>

<p>Extensive research has been conducted on the antimicrobial activity of 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2a)quinoline-3-carboxylic acid (FPMT). FPMT is a levorotatory compound that is rapidly metabolized by esterases to 6FMT, which is also active against bacteria. FPMT inhibits bacterial growth, but does not inhibit mammalian cell growth. The main mechanism of action for FPMT is probably through its ability to inhibit the synthesis of bacterial DNA and RNA. This drug has been shown to be effective against sinusitis caused by bacterial rhinosinusitis and urinary tract infections caused by Escherichia coli and Pseudomonas aeruginosa. FPMT can be used as an alternative to prulifloxacin for the treatment of these types of infections</p>

<p>N-α,ε-Bis-Fmoc-D-lysine is a protease inhibitor that inhibits the protease activity of a number of proteases, including trypsin, chymotrypsin and elastase. It is an immunogenic protein. N-α,ε-Bis-Fmoc-D-lysine has been shown to be effective in preventing the immune response against peptides when used as an adjuvant for vaccines. This protein has also been shown to have proton nmr spectral properties that are similar to those of natural amino acids and therefore may not be detected by the immune system as a foreign antigen. N-α,ε-Bis-Fmoc-D-lysine has been postulated to act as a cell maturation agent through its ability to inhibit protein synthesis or cellular growth.</p>

<p>Please enquire for more information about N-Hydroxy-2-(4-methoxyphenoxy)ethanimidamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-methylbenzamide (2AMB) is a potent inhibitor of the enzyme dihydropyrimidine dehydrogenase and is used in cancer research for its ability to inhibit tumor cell line growth. 2AMB has been shown to inhibit the synthesis of DNA, RNA, and protein in various human cell lines. The mechanism of this inhibition is not well understood, but it may be due to its ability to inhibit the activity of synthetases involved in nucleotide biosynthesis or by inhibiting the reaction system that converts hydration into ATP.</p>

<p>Poly-L-lysine hydrobromide is a polymer that consists of repeating lysine monomers. It has a molecular weight range of 1000 to 5000 Daltons. Poly-L-lysine hydrobromide is used for intramolecular hydrogen bonding, which increases its resistance to thermal and kinetic energy. Poly-L-lysine hydrobromide is also used in the structural analysis of proteins, because it can be easily purified from human serum by dialysis. This polymer has been shown to be effective against carcinoma cell lines, amide bonds, terminal residues, and ester linkages. There is also evidence that poly-L-lysine hydrobromide may have anticancer properties in vitro and in vivo.<br>Poly-L-lysine hydrobromide has been shown to have antiangiogenic properties due to its ability to block the interaction between tumor cells and endothelial cells. This can lead to tumor regression and decreased metastasis</p>

<p>5-Methyl-2,3-hexanedione is a chemical compound that has been shown to be effective against avian influenza and the influenza virus. 5-Methyl-2,3-hexanedione inhibits the growth of influenza viruses by binding to the virus particles and preventing them from attaching to cells in the respiratory tract. This chemical also prevents the release of infectious viral particles from infected cells. The rate of encapsulation was determined by measuring the amount of 5-methyl-2,3-hexanedione that was adsorbed onto tylosin particles in a plate test. The encapsulation rate is greater than 80%. 5-Methyl-2,3-hexanedione has also been shown to inhibit tylosin resistance in vitro.</p>

<p>Niacin receptor 1 (NIACR1) antagonist; lipid lowering</p>

<p>(R)-(+)-Methylsuccinic acid is a catalysed, synthetic, asymmetric synthesis of the methylsuccinic acid skeleton. It is a liquid crystal compound that has been shown to be spontaneously racemic and have enantiopure versions of itself. The stereoisomers are an important part of its biological activity.<br>Methylsuccinic acid plays a role in the biosynthesis of butanol, which can be used as a biofuel or for industrial purposes.</p>

<p>1-(3-Benzyloxy-4-methoxyphenyl)-2-nitroethene (1BMN) is an ethanamine that has a skeleton of five benzene and one methoxybenzene rings. It is an analogue of lamellarin, which has been shown to have efficient synthetic and biological properties. 1BMN is biologically active as a lamellarin analog and may be useful for the treatment of diseases such as cancer, malaria, hypertension, hyperglycemia, hypercholesterolemia, and ulcerative colitis. 1BMN is synthesized from 2-nitroethanol by reacting with 3-bromobenzaldehyde in the presence of sodium hydroxide. This reaction results in the formation of 1BMN in high yield with few side reactions.</p>

<p>2-Bromo-4-methylbenzylamine hydrochloride is a fine chemical that is used as a building block for other chemicals or as a reagent in research. It has CAS No. 1293323-97-3 and can be used in reactions where an amine is needed. This product is high quality, versatile, and useful for many different types of reactions.</p>

<p>3-Chloro-4-methoxybenzoic acid methyl ester is a potent antiproliferative agent that inhibits the growth of cancer cells and bacteria. It is an amide, which has been synthesized by equilibration between two equivalents of 3-chlorobenzoic acid and methylamine. The copulatory proton profile for this compound has been determined using liquid chromatography with mass spectrometry detection (LCMS). This compound is also a weak inhibitor of tyrosine kinases, but is more potent as an inhibitor of protein kinase C. Sorafenib and dasatinib are examples of compounds that have been shown to be linked to this drug. 3-Chloro-4-methoxybenzoic acid methyl ester can induce the production of TNF-α in thp-1 cells at micromolar concentrations.</p>

<p>Fmoc-His(Trt)-OH is an amino acid with the chemical formula HOOC-CH2-CH2-N(CH3)2. It has broad-spectrum antimicrobial activity and can be used as a chemosensor for trifluoroacetic acid. Fmoc-His(Trt)-OH also showed anticancer activity, which may be due to its ability to inhibit protein synthesis in cancer cells by inhibiting histidine decarboxylase. Fmoc-His(Trt)-OH is synthesized through a chemical reaction using trifluoroacetic acid, which reacts with His and Trt residues on the surface of the resin.</p>

<p>4-Isopropyl-4'-methylchalcone (4'MCH) is a versatile building block that can be used for the synthesis of complex compounds. 4'MCH is an intermediate in the synthesis of various pharmaceuticals and research chemicals, such as cholesterol esters, sterols, and steroids. It also has been used to produce speciality chemicals including herbicides, pesticides, and fungicides. 4-Isopropyl-4'-methylchalcone is a high quality chemical with CAS No. 205688-50-2 that has a wide range of applications.</p>

<p>Please enquire for more information about 3-Methyl-5-pyrrolidin-2-ylisoxazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Fluoro-5-methoxybenzonitrile is a useful chemical intermediate that can be used in organic synthesis. It is a versatile building block with a high quality and it is easy to use in the synthesis of complex compounds. 3-Fluoro-5-methoxybenzonitrile has been shown to react as a nucleophile, and it has been used as a reagent for the production of other compounds. This compound also has potential applications in research, such as being an intermediate for the production of pharmaceuticals and agrochemicals. 3-Fluoro-5-methoxybenzonitrile is not classified as hazardous and does not pose any significant risk to human health or the environment.</p>

<p>Fmoc-4-amino-L-phenylalanine is a molecule with the amino acid, aminophenylalanine, that is used in devices to detect epithelial cells. It has been functionalized with a fluoro group and can be used as a fluorescent probe for the detection of epithelial cells. Fmoc-4-amino-L-phenylalanine can also be used to diagnose tumors and tumor cells by detecting their presence in urine samples. This peptide has been shown to have anti-tumor properties when it interacts with the tumor cell membrane, which may be due to its ability to inhibit protein synthesis and induce apoptosis.</p>

<p>N-alpha-Fmoc-Nepsilon-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-lysine is a synthetic amide with a peptide backbone. It has been shown to have anti tumor activity in vivo and in vitro against a variety of solid tumor xenografts. The compound was conjugated to the integrin receptor ligand RGD, which is expressed on the surface of various types of cancer cells. This modification increased the uptake of N-alpha-Fmoc-Nepsilon-1-(4,4 dimethyl 2,6 dioxocyclohex1 ylidene)ethyl L lysine by leukemia cells and solid tumor xenografts.</p>

<p>4-Bromo-3-methylbenzylamine hydrochloride is a synthetic chemical that can be used in the synthesis of various products. This compound is a useful scaffold for the preparation of complex compounds, and it has been used as a reaction component in organic chemistry. It is also a versatile building block that can be used to synthesize fine chemicals with high purity. 4-Bromo-3-methylbenzylamine hydrochloride has been assigned CAS No. 1955514-32-5 by the Chemical Abstracts Service (CAS).</p>

<p>5-Chloro-L-tryptophan (5CTP) is a chemical compound that belongs to the class of cyclic peptides. It is biosynthesized by plants and other organisms from 4-chloro-L-tryptophan. 5CTP is synthesized from 4CTP by a two step process, involving an oxidative decarboxylation followed by a deamination reaction. The oxidative decarboxylation converts the amino acid into an intermediate, which is then deaminated and converted into 5CTP. This compound has been shown to have potential as a drug against cancer cells, with its mechanism of action being related to its ability to form metal chelates with heavy metals such as copper and mercury. 5CTP has also been used in molecular modeling studies, genetic analyses, and biochemical investigations of substrate binding and enzyme catalysis.</p>

<p>The Val-Cit-PAB linker is an activated peptide linker that is cleaved by cathepsin B. It enables the selective intracellular release of attached drugs in ADC applications.</p>

<p>6-Methoxy-1-indanone is a chemical compound that can be found in the form of two structural isomers. They both have the same pharmacokinetic properties and are potent inhibitors of 5-HT1A receptors. 6-Methoxy-1-indanone also has potent inhibitory activity on the MT2 receptors, which are present in the central nervous system. This compound has been shown to be an active methylene group with neurodegenerative disease and has carbonyl groups.</p>

<p>2,3-Difluoro-4-methoxybenzoic acid is a versatile building block that can be used to make complex compounds. This compound is a high quality, useful intermediate and reaction component that can be used in the synthesis of pharmaceuticals and other chemical products. 2,3-Difluoro-4-methoxybenzoic acid is a reagent that can be used for research purposes or as a speciality chemical. It has been shown to have many uses as a scaffold for making new compounds with different structures.</p>

<p>L-Norvaline is a hydrophobic amino acid that is synthesized in the body from the essential amino acid valine. It is an important intermediate in the biosynthesis of other amino acids, such as L-leucine and L-isoleucine. L-Norvaline has been shown to inhibit bacterial growth and can be used as an antimicrobial agent. It also inhibits the polymerase chain reaction by binding to DNA and RNA, thereby blocking transcription. This drug has been shown to increase energy metabolism, improve renal function, and reduce metabolic disorders in animals. These effects are thought to be due to its ability to bind with carbonyl oxygens on lysine residues of proteins.</p>

<p>Ac-Gly-Lys-OMe acetate salt is a reactive chemical compound that is used in the synthesis of peptides. This salt is synthesized by reacting glycine with lysine and formaldehyde. Ac-Gly-Lys-OMe acetate salt has been shown to have hemolytic activity and can be used as a synthetic substrate for kinetic studies. It has also been found to activate complement, which may be due to its disulfide bond formation. Ac-Gly-Lys-OMe acetate salt has been shown to inhibit fibrinogen and nitrosylation, which may result in thrombotic disorders.</p>

<p>Phosphatidyl-L-serine (Ptd-L-Ser) is a glycerophospholipid consisting of the amino acid serine connected to glycerol via a phosphodiester linkage and 2 fatty acids attached to the primary and secondary hydroxyls of the glycerol via ester linkages. Phosphatidyl-L-serine is a phospholipid component of the cell membrane and plays a key role in cell cycle signalling, specifically in relation to apoptosis. It has been suggested that dietary supplements of phosphatidyl-L-serine may reduce the risk of dementia and cognitive dysfunction in the elderly.</p>

<p>2,4,5-Trihydroxy-DL-phenylalanine (2,4,5-THP) is a natural amino acid that has been found to have neurotrophic effects. It has shown to increase the levels of prolactin in the blood and tissues of experimental animals. 2,4,5-THP binds with dopamine or amines and can be used as a cofactor for enzymes involved in oxidative injury. 2,4,5-THP has also been shown to have antidepressant properties and to protect against neuronal death caused by pharmacological agents or fatty acids. 2,4,5-THP is structurally similar to tricyclic antidepressants such as imipramine and chlorpromazine.</p>

<p>Fmoc-O-phospho-L-tyrosine is a synthetic compound that belongs to the class of phosphatase inhibitors. It is a potent inhibitor of tyrosine phosphatases, which are enzymes that regulate cellular signaling. Fmoc-O-phospho-L-tyrosine has been shown to inhibit phosphorylation of the insulin receptor and may have an inhibitory effect on other tyrosine kinases. Inhibition of these enzymes results in increased levels of intracellular tyrosine, which can lead to inhibition of protein synthesis and cell proliferation. Fmoc-O-phospho-L-tyrosine has been shown to be effective against growth in cell culture, although more research is needed.</p>

<p>N-a-Z-L-Arginine HCl is a molecule that is the dihydrochloride salt of L-arginine. It has been shown to increase the permeability of cell membranes by interacting with the phospholipids, thus allowing more water to enter into the cell. N-a-Z-L-Arginine HCl has also been shown to interact with surfactants and positioning agents, which may be important for its function in model membranes. The mechanism by which this molecule works is not well understood, but it has been proposed that it may be due to its bonding properties and interactions with other molecules such as arginine.</p>

<p>O-Methyl-L-threonine is an analog of L-threonine. O-Methyl-L-threonine inhibits the production of fatty acids in resistant mutants, which are activated by the addition of a hydroxy group to their amino acid backbone. This analog has been shown to be effective at suppressing the growth of animal health bacteria and fungi, and has been used as a treatment for protein synthesis disorders in animals. O-Methyl-L-threonine is also used as a precursor for nicotinic acetylcholine synthesis. In vivo tests have shown that it has no toxic effects on mammalian cells, but does not inhibit photosynthesis in plants.</p>

<p>D-His(Bzl)-OH is a chromatographic ligand that has been used in the preparation of recombinant proteins and vaccines. D-His(Bzl)-OH is an amphipathic molecule with a hydrophilic head group and hydrophobic tail group. It has been shown to be an effective inhibitor of papillomavirus, as well as other viruses such as HIV, herpes simplex virus, poliovirus, and vesicular stomatitis virus. D-His(Bzl)-OH has also been shown to induce antibody production in micelles when conjugated to antigens. The binding of D-His(Bzl)-OH to the viral envelope protein can be increased by increasing pH or by adding ammonium sulfate or chloride ions. Increasing the flow rate during chromatography will also increase the progressions of D-His(Bzl)-OH through the column.</p>

<p>6-Chloro L-tryptophan is an aminotransferase inhibitor that is activated by the enzyme, aminotransferase. 6-Chloro L-tryptophan has been shown to inhibit the growth of tumour cells, which may be due to its ability to induce apoptosis and inhibit the production of tumour necrosis factor alpha (TNFα). This drug has also been shown to exhibit antiinflammatory effects and can inhibit the activation of microglia in human brain cells. 6-Chloro L-tryptophan is activated by liver cells and human macrophages, leading to the inhibition of 3-hydroxyanthranilic acid synthesis and the neutralization of acidic conditions. It also inhibits uptake in thp-1 cells, a type of white blood cell that lines blood vessels in lymph nodes. In addition, 6-chloro L-tryptophan has been shown to have antiviral effects</p>

<p>Hydrochloride salt</p>

<p>The H-Val-Ile-OH is an amino acid that is hydrophobic in nature. It has a molecular weight of 120.14 g/mol and a molecular formula of C6H11NO2. The H-Val-Ile-OH is classified as a cyclic amino acid due to the presence of a pyruvic acid ring and it can be found in organisms including humans, bacteria, fungi, and plants. The H-Val-Ile-OH can be found in the active site of proteases as well as subtilisin. This amino acid has been shown to have hydrolytic cleavage properties, which makes it suitable for use as an enzyme substrate for protein sequencing studies.</p>

<p>N2-Phenoxyacetyl guanine is a labile nucleoside that can be synthesized by the aminoacylation of guanosine with phenoxyacetic acid. It has been shown to have an important role in oxidative DNA damage, which may lead to mutagenesis and cancer. N2-Phenoxyacetyl guanine is stereoselective and binds preferentially to the GGC sequence, and it is also aminopropylated at its 2′ position. This nucleoside is not ionizing but can be degraded by radiation or enzymes such as deaminases.</p>

<p>Nilotinib is a small molecule that inhibits the tyrosine kinase activity of TK1, TK2, and TK3. It binds to the ATP-binding site of these kinases and prevents the phosphorylation of the cellular substrate. Nilotinib has been shown to inhibit the proliferation of leukemia cells in vitro, as well as to have antiproliferative effects in vivo. Nilotinib can be used for the treatment of chronic myelogenous leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). In addition, it has been shown to have synergistic effects with other drugs such as α1-acid glycoprotein inhibitors or methyltransferase inhibitors. Nilotinib can also be used for cases of hepatic steatosis.</p>

<p>2-[4-(4-Chloro-a-phenylbenzyl)-1-piperazinyl]-ethoxyacetic acid hydrochloride is a chemical compound that has been used to investigate the possible neuroprotective effects of cetirizine, an antihistamine. This drug was developed as a prodrug of cetirizine, which is converted in vivo to its active form. The main mechanism of action for this drug is inhibition of histamine release from mast cells and basophils by blocking H1 receptors. 2-[4-(4-Chloro-a-phenylbenzyl)-1-piperazinyl]-ethoxyacetic acid hydrochloride has also been shown to have beneficial effects on allergic symptoms and bowel disease in experimental models and clinical properties.</p>