Building Blocks

9-Azabicyclo[3.3.1]nonane N-oxyl (ABNO) is a reaction component in copper catalysed aerobic oxidation of alcohols. ABNO is a less hindered nitroxyl radical that exhibits an enhanced reactivity compared with TEMPO. Low catalyst loading (1 mol%) of ABNO can efficiently catalyse oxidation of alcohols in the presence of a Cu+ species and atmospheric oxygen to give the corresponding aldehyde or ketone.

<p>Azobenzene is an azobenzene that binds to the actin filaments and inhibits their polymerization. It has been shown to inhibit the polymerization of actin filaments in human serum, which may be due to its ability to react with the nitrogen atoms in actin. Azobenzene has also been shown to have a thermal expansion coefficient of 0.015x10-5/°C, which is much larger than that of most other compounds. The molecular geometry of azobenzene is planar and symmetrical, with two hydrogen atoms on each nitrogen atom on both sides of the molecule. This symmetry leads to a low intramolecular hydrogen bonding energy. The molecule’s photochemical properties are also interesting because it has a long lifetime and can be excited by wavelengths between 400-500 nm.</p>

5-Aminopyrimidine is a synthetic compound that has been shown to have inhibitory effects on the nervous system. The structural formula of 5-aminopyrimidine is C6H4N3O2. It is a structural analogue of pyrimidine and can be used as an anticancer drug. 5-Aminopyrimidine can also be used in the treatment of diseases such as diabetes and Parkinson’s disease. The reaction mechanism of 5-aminopyrimidine begins with the formation of an unstable diazonium salt, which then reacts with a chloride ion to form an alloxan intermediate. This intermediate then reacts with phosphate group to form a product that is soluble in water.

3-Amino-2-hydroxybenzoic acid (AAHB) is a nonsteroidal anti-inflammatory drug that belongs to the group of pharmaceutical preparations. It inhibits the enzyme dehydroascorbate reductase, which is involved in the production of hydrogen peroxide and other reactive oxygen species by phagocytes. Hydrogen peroxide and other reactive oxygen species can cause DNA damage and lead to cancer development. AAHB may also have antimicrobial effects, as it has been shown to inhibit bacterial growth and cell adhesion. AAHB interacts with fatty acids in a similar manner as aspirin does, but with a lower potency. It has been shown to inhibit prostaglandin synthesis by inhibiting lipoxygenase activity. The binding of AAHB at these sites prevents the formation of arachidonic acid from linoleic acid and blocks the conversion of arachidonic acid into prostaglandin H2 (PGH2).

<p>2-Amino-3-methylbenzoic acid is an organic compound with the formula H2CCH(NH2)(COOH). It is a white solid that is soluble in water. The molecule has a planar geometry, and the copper ion is coordinated by four oxygen atoms and three nitrogen atoms. This coordination geometry can be seen in the crystal structure of the molecule. 2-Amino-3-methylbenzoic acid has been shown to have antifungal activity against Aspergillus niger. It also inhibits 5-nitrosalicyclic acid and sodium carbonate, which are involved in the synthesis of nicotinamide adenine dinucleotide phosphate (NADPH) and ATP respectively. 2-Amino-3-methylbenzoic acid has also been shown to inhibit ryanodine receptor channels, which are important for calcium release from endoplasmic reticulum.</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 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>4-Aminopyridine N-oxide is a white, crystalline solid that is soluble in water and alcohol. It has a molecular weight of 128.2 and formula weight of 135.2. 4-Aminopyridine N-oxide reacts with acid solutions to produce nitrous acid and ammonia gas. The rate of the reaction depends on the concentration of aminopyridine and aniline, as well as the pH of the solution. The acetylation, diazotisation, and kinetics have also been studied extensively for this compound. Nitrous acid can react with amides to form azulene, which can then react with amines to form a molecule containing nitrogen, oxygen, carbon, hydrogen and one other element or compound from each group (e.g., NHCOCH). This reaction is reversible when solvents are present.br&gt; 4-Aminopyridine N-oxide may be used as a precursor for other organic</p>

<p>4-Aminoindole hydrochloride is a white crystalline solid that can be used as a versatile building block in organic synthesis. It is also used as an intermediate in the production of various pharmaceuticals and other chemical compounds. 4-Aminoindole hydrochloride is soluble in most polar solvents, but insoluble in ethers and oils. This compound is also a useful reagent for the conversion of nitrobenzenes to aminobenzoic acids. CAS Number 174854-93-4</p>

<p>Arg-Gly-Asp TFA salt is a molecule that is used as a prodrug, meaning it is inactive until it has been converted to the active form. It has been shown to be effective when injected subcutaneously or intramuscularly and is hydrophilic. Arg-Gly-Asp TFA salt has been shown to have problematic effects on polymerization when exposed to heat. The molecule has an active form that can be absorbed into the body through injection sites and then hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. Arg-Gly-Asp TFA salt also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>

<p>5-Amino-2-nitrobenzoic acid is a drug that has been shown to inhibit the activity of proteases. It has been used to detect the presence of protease activity in urine samples, as well as to study the inhibition of protease activity by other drugs. 5-Amino-2-nitrobenzoic acid is an inhibitor of chymotrypsin, trypsin, and elastase. This drug has been shown to be effective in inhibiting these enzymes at low concentrations, with a detection sensitivity of approximately 0.1 μM. 5-Amino-2-nitrobenzoic acid inhibits the growth of bacteria by binding to them and preventing protein synthesis. The compound also inhibits the enzyme dihydrolipoamide dehydrogenase in mitochondria, which is required for cellular respiration and energy production.</p>

<p>Aniline derivative; analgesic; anti-pyretic; electroosmotic flow marker</p>

<p>AP1867 is a small molecule that targets the protein–protein interactions of lipid kinases. It is being developed for the treatment of cancers, including breast, prostate and lung cancer. AP1867 has been shown to inhibit the growth of human cancer cells in tissue culture and animal models, with some effects on cell viability. AP1867 has also demonstrated an ability to induce genetic ablation in cultured cells and to modulate signal detection pathways. Target gene expression profiling has identified a number of potential molecular targets for this drug.</p>

Versatile small molecule scaffold

<p>4-Azidopiperidine hydrochloride is a chemical compound that is used as a versatile building block in the synthesis of complex chemical compounds. It is also used as a reagent or speciality chemical, and has many applications in research, such as being an intermediate for the synthesis of other chemicals. 4-Azidopiperidine hydrochloride can be used to make useful building blocks, reaction components, and scaffolds for chemical reactions.</p>

2-(7-Chloro-1H-indol-3-yl)ethanamine hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. It is a high quality, useful intermediate and reaction component in the synthesis of speciality chemicals and research chemicals. 2-(7-Chloro-1H-indol-3-yl)ethanamine hydrochloride has been shown to be a useful scaffold for the synthesis of pharmaceuticals and agrochemicals.

<p>Questiomycin A is a sesquiterpene lactone that is an antimicrobial agent. It has been shown to modulate the immune system by inhibiting the production of cytokines and altering the expression of genes related to autoimmune diseases. Questiomycin A also inhibits cell growth in myeloma cells, which is due to its ability to inhibit dinucleotide phosphate (NADPH) reductase, an enzyme required for mitochondrial membrane potential maintenance and other cellular functions. In addition, questiomycin A has been shown to induce apoptosis in liver cells as well as carcinoma cell lines. This drug can also be used for body formation, as it stimulates bone growth and inhibits osteoclast activity.</p>