Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2-(2,6-dimethyl-3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a reagent that is used in the synthesis of other compounds. It is a high quality research chemical and useful scaffold for the preparation of fine chemicals. This versatile building block is also used as an intermediate or building block in the synthesis of complex compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>3,3-Diphenylpropylamine is an organic compound that is used in the analytical method for infectious diseases. It has been shown to be stable under acidic conditions and can be hydrolyzed by enzymes to form 3,3-diphenylpropionic acid. This chemical is also an enantiomer of 2,2-diphenylpropanolamine. The hydrochloride salt of 3,3-diphenylpropylamine has been used as a pharmaceutical preparation for the treatment of gastric ulcers. This drug has pharmacokinetic properties that include a long half-life and low oral bioavailability.</p>

<p>2-Aminobenzaldehyde is an aromatic compound that contains a hydroxyl group, two nitrogen atoms, and an anhydrous sodium. It can be synthesized by the reaction of hydroxybenzaldehyde with trifluoroacetic acid or nitrobenzene. 2-Aminobenzaldehyde is used as a precursor to other compounds, such as 2-aminobenzonitrile and 2-aminophenol. It also reacts with anthranilic acid in the presence of sodium salts to give a variety of pyrazoles. This product has been shown to react with epidermal growth factor (EGF) in the presence of light to produce light emissions.</p>

<p>4,4-Dimethyl-1,2,3,4-tetrahydroquinoline (DMTH) is a synthetic compound that has been shown to stimulate pancreatic β-cells. DMTH is a prodrug that is converted into 4,4'-dimethoxy-1,2,3, 4-tetrahydroquinoline (DMT) by esterases in the body. DMT binds to the insulin receptor and increases insulin secretion from pancreatic β-cells. DMTH has been shown to be effective in treating patients with type 2 diabetes mellitus who are resistant to insulin. DMTH also reduces blood glucose levels in animal models of diabetes by stimulating the pancreas to produce more insulin and increasing the number of β cells in the pancreas. This drug may also prevent or reverse tissue damage caused by diabetes by inhibiting inflammatory processes and reducing oxidative stress on tissues.</p>

<p>2-(Hydroxymethyl)-3-methylfuran is a ketone with a ring system that contains one hydroxymethyl group and two methyl groups. It is also an adduct, which means that it is the product of a reaction between two substances. This compound can be used as a binder in pyrotechnics and polymers. 2-(Hydroxymethyl)-3-methylfuran has been proven to be stable under normal conditions, making it an excellent model compound for studying other compounds with similar structures.</p>

<p>4-Aminohippuric acid sodium (4AHA) is a drug that is used as a diagnostic tool for measuring renal plasma flow and renal function. The drug is administered intravenously and its optical properties are measured. 4AHA is filtered by the kidneys, which causes it to be excreted in urine. A sensor is placed on the patient's arm and measures the concentration of 4AHA in the blood flowing through the arm. This measurement can then be used to calculate renal plasma flow, which indirectly indicates kidney function. 4AHA can also be used to measure sodium levels in blood plasma, as it binds to sodium ions in solution. However, this application of 4AHA has been superseded by newer technologies such as ion-selective electrodes and magnetic resonance imaging, which offer improved accuracy at lower cost.</p>

<p>Eugenol is a phenolic compound and the main active ingredient of clove oil. Eugenol has been shown to have antioxidant, anti-inflammatory, analgesic, and antimicrobial properties. It also inhibits the growth of cancer cells in vitro (mcf-7 cells). The mechanism of eugenol’s activity is not well understood. It may involve activation of adenine nucleotide levels by inhibiting the production of p-hydroxybenzoic acid or by increasing nucleotide levels by inhibiting the conversion to p-hydroxybenzoic acid. Eugenol also inhibits bacterial DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. This inhibition leads to cell death by inhibiting protein synthesis. Eugenol has been shown to inhibit mineralization in petunia plants and may have a similar effect on human bone tissue.</p>

<p>4-[(1E)-3-Hydroxyprop-1-en-1-yl]phenol (4-HP) is a natural compound that belongs to the group of polyphenols. It is one of the main constituents of the plant extract, which is obtained from leaves of the plant Ferula communis. 4-HP has been shown to have antiinflammatory activity by inhibiting prostaglandin synthesis in 3T3-L1 preadipocytes. The synergic effect can be explained by a combination of its antioxidant and antiinflammatory properties. In an analytical method, 4-HP was found to be present in ferulic acid and p-hydroxybenzoic acid. 4-HP also inhibits dna polymerase activity and rna synthesis at low concentration levels. The mechanism of action may be due to the inhibition of bacterial dna gyrase and topoisomerase I, leading to bacterial cell death.</p>

<p>4-Amino-3,5-diiodobenzoic acid is a conjugate of the amino acid histidine with two iodine atoms. It is used as a radiopaque contrast agent for X-ray imaging and has been shown to be useful in distinguishing between normal tissue and cancerous lesions. The molecule can be modified to contain various functional groups that allow it to bind to other molecules such as proteins or DNA, which can alter its properties. 4-Amino-3,5-diiodobenzoic acid is also known as diaminobenzene diiodide and is soluble in water.</p>

<p>4-Acetoxyacetophenone is an organic compound that has a functional group with a hydroxyl group. It can undergo dehydration to form acetone and acetic acid, which are the reaction products. The reaction system is activated by a reactive or acid catalyst, and the reaction solution is made up of non-polar solvents. Hydrogenation reduction can be used to synthesize 4-Acetoxyacetophenone from 2-hydroxyacetophenone.</p>

<p>4-Acetamidobenzaldehyde is an organic compound that has been shown to exhibit inhibitory effects on influenza virus replication in cell culture. 4-Acetamidobenzaldehyde is a dihedral molecule with a p2 group and can be synthesized from benzaldehyde and acetamide. It has also been shown to have potential use in the treatment of tuberculosis. The biological properties of 4-acetamidobenzaldehyde are not well understood, but it is thought that uptake may occur through the imine nitrogen. This molecule has been detected in tissue samples such as lung, liver, and kidney.</p>

<p>4-Amino-3-methoxybenzoic acid is an inhibitor of the enzyme hydroxylase. It has been shown to inhibit cancer cell growth in nanomolar concentrations and may be a potential anti-cancer drug candidate. 4-Amino-3-methoxybenzoic acid inhibits the production of 3-methoxy-4-nitrobenzoic acid, which is an intermediate in the biosynthesis of cyclic peptides. This compound also has potent inhibitory activity against active enzymes involved in the biosynthesis of 3-methoxy-4-nitrobenzoic acid, such as hydroxylases, nitroreductases, and methyltransferases.</p>

<p>4-(Acetylamino)phenetole is a drug that belongs to the class of nonsteroidal anti-inflammatory drugs. It is a reactive, toxic chemical that has been shown to inhibit ATP binding cassette transporter (ABC) proteins and can be used for treatment of pain. 4-(Acetylamino)phenetole inhibits cellular energy metabolism by inhibiting an enzyme in the electron transport chain, which prevents the formation of reactive oxygen species necessary for cell growth. 4-(Acetylamino)phenetole also binds to DNA and reduces the transcriptional activity of certain genes. This drug has been found to show cytotoxicity in solid tumours and can be used as a chemotherapeutic agent.</p>

<p>5-Amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile (TCFP), also known as CX-546, is a photosynthetic activity enhancer that inhibits oxidative injury to chloroplasts. TCFP is a pyrazole ring with a sulfinyl group and a chlorine atom. TCFP has been shown to have no genotoxic or carcinogenic potential in vitro and in vivo studies. TCFP is not active against infectious diseases. TCFP can be used as an analytical reagent for the detection of cytochrome P450 activities in human serum.</p>

<p>Please enquire for more information about 5-Amino-4-bromo-2-fluorobenzoic acid 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 2-Amino-3-(furan-3-yl)propanoic acid hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A Hagedorn oxime used in the treatment of organophosphate poisoning.</p>

<p>5-Amino-1-phenylpyrazole-4-carboxamide (APC) is a synthetic compound that has been shown to have potential as an antitumor agent. This compound has been shown to inhibit the growth of cancer cells in vitro, with cytometric analysis showing that it inhibits DNA synthesis and cell proliferation. It also has antibacterial activity, which may be due to its ability to inhibit bacterial DNA gyrase and topoisomerase IV. APC has been found in wastewater at concentrations of 2.6 μg/L, indicating that it is currently being produced and used for industrial purposes. APC can be synthesized by reacting 1-(3-aminopropyl)piperazine with 3-(2H)-furanone and triethylamine to form 5-amino-1-[(2H)-pyridin-2-yl]pyrazole-4-- carboxylic acid chloride, which can then</p>