Amino Acids (AA)

<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>5-Methyl-3-piperidin-4-yl-1H-indole hydrochloride is a synthetic chemical that is used as a building block for the synthesis of other compounds. It is a versatile intermediate, having been shown to react with amines, alcohols, phenols, and thiols. 5-Methyl-3-piperidin-4-yl-1H-indole hydrochloride can be used in the manufacture of pharmaceuticals and agrochemicals. This compound has been found to be an effective reagent for the preparation of cyclic peptides and can be used as a building block for the synthesis of other compounds. When reacted with 2-(trimethylsilyl)ethanol, it produces a high quality complex compound.</p>

<p>N-Boc-(R)-Nipecotic acid is a synthetic compound that is used in the treatment of lymphocytic leukemia, chronic lymphocytic leukemia, and other types of cancer. It is a dry powder that can be taken orally or subcutaneously. N-Boc-(R)-Nipecotic acid binds to p53 mutations and inhibits DNA synthesis. This drug has been shown to reduce the size of tumors in mice with subcutaneous tumors and has been found to be effective against leukemia cells in vitro. The development of this drug was rationalized on the basis of fluorescence profiles.</p>

<p>Please enquire for more information about L-Tryptophan-7-amido-4-methylcoumarin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-Pro-OH is a synthetic cyclic peptide with the amino acid sequence (Fmoc-Lys-Lys-Ala-Glu)n. Fmoc-Pro-OH binds to the androgen receptor and can be used as a research tool to identify other molecules that bind to the same receptor. It has been shown to inhibit the activity of ester hydrochloride, trifluoroacetic acid, and superparamagnetic iron in coordination complexes.</p>

<p>3-Phenoxybenzoic acid is a metabolite of nonsteroidal anti-inflammatory drugs (NSAIDs) and pyrethroid insecticides. It is an inhibitor of the enzyme matrix metalloproteinases, which are involved in the degradation of collagen. 3-Phenoxybenzoic acid was used as a model system to study the effects of NSAIDs on urinary excretion rates and to identify biomarkers for NSAID use. The metabolite can be detected in urine after ingestion by using analytical methods such as preparative high performance liquid chromatography or electrochemical impedance spectroscopy. 3-Phenoxybenzoic acid is also present in cells from human HL-60 cells and has been shown to inhibit the growth of human leukemia cells by interfering with protein synthesis.</p>

<p>4-Amino-3-methylbenzoic acid is a chemical compound that can be synthesized from 4-Methylbenzoic acid and sodium carbonate. It has been used in the treatment of cervical cancer and leishmania. The synthesis of this drug is an example of a chemical reaction in which a carboxylic acid is reacted with sodium carbonate to give an ester and sodium bicarbonate. This process requires the use of trifluoroacetic acid. The resulting drug also has antiviral properties, as it inhibits HIV infection by blocking reverse transcriptase activity. 4-Amino-3-methylbenzoic acid was also shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>Z-Phe-Arg-AMC·HCl is a fluorescent substrate for proteolytic enzymes. It has been shown to be a potent inhibitor of human immunoglobulin (Ig) secretion and protein synthesis in proximal tubules of the kidney, but this inhibition is not seen in the presence of other proteases. Z-Phe-Arg-AMC·HCl also inhibits the activity of soybean trypsin and hemolytic activity. This compound also has an optimum pH of 7.5 and is characterized by intermolecular hydrogen bonding as well as hydroxyl group interactions with enzyme active sites.</p>

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

<p>Please enquire for more information about 2-Chloro-N-(2-ethyl-6-methylphenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[3-(4,4,5,5-TetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]succinamic acid is an intermediate in the synthesis of a variety of compounds. It is also a useful building block in the synthesis of complex compounds. In addition to its use as a research chemical and reagent, N-[3-(4,4,5,5-TetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]succinamic acid can be used as a speciality chemical.</p>

<p>DL-alpha-Methyltryptophan is a metabolite of the amino acid tryptophan. It is a monoamine neurotransmitter that has been implicated in brain function and inflammatory lesions. DL-alpha-Methyltryptophan can be used as a potential drug target for the treatment of Parkinson's disease, depression, and anxiety disorders. The hydroxyl group on the indole ring of DL-alpha-Methyltryptophan gives it an increased reactivity with oxygen, which allows it to be oxidized by monoamine oxidase B (MAO B) to 3-hydroxyanthranilic acid. This reaction can be inhibited by MAO A inhibitors such as clorgyline or selegiline. The oxidation of DL-alpha-Methyltryptophan leads to increased concentrations of serotonin in the brain and increased activity of aminotransferases.</p>

<p>2-(Boc-amino)-3-methylpyridine is a cytotoxic agent that has been shown to inhibit the proliferation of cancer cells. It is a potent cytotoxic agent that can be used to treat cancer. 2-(Boc-amino)-3-methylpyridine inhibits the growth of cancer cells by inhibiting the activity of B-Raf, a protein involved in cell proliferation and apoptosis. The anticancer properties are due to its ability to inhibit protein synthesis in cells by inhibiting the enzyme carbinolamine N-methyltransferase, which is required for the synthesis of methionine. 2-(Boc-amino)-3-methylpyridine also inhibits DNA and RNA synthesis in cells. This drug has been shown to have antiangiogenic effects, which may be due to its ability to inhibit vascular endothelial growth factor (VEGF) production.<br>END&gt;</p>

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

<p>Luteolin-4'-O-glucoside is a flavonol glycoside that is found in plants such as licorice, celery, and parsley. Luteolin-4'-O-glucoside has been shown to inhibit the growth of Coccidioides neoformans by binding to the cell membrane surface and blocking the synthesis of phospholipids. It also inhibits cancer cells in culture by reducing their viability. The structural analysis of luteolin-4'-O-glucoside revealed an hydroxyl group on its aromatic ring, which may be responsible for its anti-inflammatory effects. Luteolin-4'-O-glucoside has been shown to be effective against inflammatory diseases, such as rheumatoid arthritis and asthma, and may also have a protective effect against certain types of cancer, such as cervical cancer. Luteolin-4'-O-glucoside has also been shown to</p>

<p>2-Amino-5-methylbenzonitrile (2AMB) is a molecule that has two nitrile groups. It has been shown to be effective in the treatment of cancer cells, and it also inhibits thymidylate synthase (TS), an enzyme involved in DNA synthesis. The crystallographic structure of this compound has been determined by x-ray diffraction studies, and 2AMB was synthesized and assayed for its anticancer activity on human lung cancer cells in culture. 2AMB is an intercalator that binds to DNA by inserting itself between base pairs, which then blocks the progression of DNA synthesis during replication. This type of inhibition causes cell death because the cell cannot divide or make new proteins. Naphthalene and pyrrole are two chemicals found in 2AMB that have been shown to have antibacterial properties.</p>

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

<p>Please enquire for more information about Racemic Fmoc-cis-3-phenyl-pyrrolidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromo-2-fluoro-3-methylpyridine is a fine chemical that is used as a scaffold for building more complex compounds. This chemical can be used in the synthesis of sulfonamides, thiocarbamates, and other organic compounds. 5-Bromo-2-fluoro-3-methylpyridine is also a versatile intermediate that can be used in the production of research chemicals and speciality chemicals. The purity of this compound is high and it has been shown to be a useful reagent in various reactions.</p>

<p>L-Cysteine hydrochloride hydrate is an amino acid that belongs to the group of antimicrobial agents. It is a precursor in the biosynthesis of proteins and nucleic acids. L-Cysteine hydrochloride hydrate inhibits bacterial growth by reacting with iron and forming an insoluble complex that cannot be used for metabolic processes. Cysteine also reacts with dehydroascorbic acid to form a fluorescent compound, which can be detected using fluorescence probe and fluorometric methods. This reaction is pH dependent, with a lower pH favoring the formation of the fluorescent product. The optimum pH for this reaction is approximately 7.0-8.5, at which point it is most effective against bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus.</p>