Aminas

2'-Aminoacetanilide is a colorless, crystalline compound that is soluble in water and has a bitter taste. It is used as an acidity regulator in food products, particularly bakery products. 2'-Aminoacetanilide can be found naturally in some microflora, such as lactic acid bacteria.
2'-Aminoacetanilide is an aromatic amine that contains both primary amino and functional groups. It is nucleophilic and reacts with proton by nucleophilic attack to form the corresponding amide or carbonyl group. 2'-Aminoacetanilide also has the ability to react with nitro compounds to form an amido-nitro adduct.

(R)-(+)-1,1-Naphthyl ethylamine is a molecule that belongs to the class of chromatographic compounds. It has a carbonyl group, which is a substrate for amine modifiers and other chemical reactions. (R)-(+)-1,1-Naphthyl ethylamine can be used as a model system for epidermal growth factor (EGF) and chelate rings. The molecule has been shown to have growth factor activity, which may be due to its ability to bind to EGF receptors on cells.

5,6-Diaminouracil sulfate is an amine that is used as a precursor in the production of the anti-cancer drug 5-fluorouracil. It can be synthesized from diaminopyrimidine and uracil. This compound has two amino groups, which are both substituted with hydrogens. The aminouracile group is substituted with a hydrogen and an amino group. 5,6-Diaminouracil sulfate has pyrimidone rings that are fused together to form a six-membered ring.

Thiamine tetrahydrofurfuryl disulfide is a thiamine derivative that has been shown to serve as a cofactor for enzymes such as peptidyl-prolyl cis-trans isomerase, which catalyzes the formation of peptide hormones. It also plays a role in the synthesis of polymers such as cellulose. Thiamine tetrahydrofurfuryl disulfide can be found in crystalline cellulose and is an important component of two-way crossover studies on peptide hormones. This drug has been shown to stimulate oxidative metabolism in cells and may have therapeutic potential for treating conditions associated with oxidative injury, such as stroke, head trauma, and heart attack.
Thiamine tetrahydrofurfuryl disulfide may also have a role in the development of inflammatory responses through its interaction with toll-like receptor 4 (TLR4).

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(R)-Amino carnitine is a pancreatic enzyme that is used as an experimental treatment for fatty liver disease. It has been shown to inhibit the synthesis of fatty acids, which are the main components of triglycerides. The inhibition of this enzyme leads to a decrease in the production of triglycerides and their accumulation in the liver, thereby reducing hepatic steatosis. (R)-Amino carnitine also has an inhibitory effect on protein synthesis, which is important for the conversion of amino acids into proteins essential for cell division and growth. This mechanism may explain its beneficial effects on insulin resistance, obesity, and diabetes.

2,2-Bis[4-(4-aminophenoxy)phenyl]propane is a monomer that is used in the production of polyurethanes. It has a number of alkyl substituents, including chloride, which are removed during the process. 2,2-Bis[4-(4-aminophenoxy)phenyl]propane reacts with chlorides to form hydrochloric acid and 2,2-bis(4-hydroxyphenyl)propane. The reaction time depends on the concentration of chloride and can be determined by gel permeation chromatography. This monomer has been shown to have a kinetic data that is dependent on temperature, as well as magnetic resonance spectroscopy and proton NMR data. The product also exhibits an increase in thermal expansion when compared to other monomers.

Aromatase inhibitor; anti-neoplastic

4-Aminophenylacetonitrile is a molecule that is structurally similar to nitrobenzene. 4-Aminophenylacetonitrile has been shown to be an efficient method for inhibiting faecalis growth and secretory phospholipase A2 (sPLA2) activity in vitro. It also inhibits the population growth of E. coli in vivo, which can be attributed to its ability to inhibit the enzyme catalysed by hydrogen bond formation.

2-(1H-Benzimidazol-1-yl)ethyl]amine dihydrochloride is a lead compound that has been shown to have antibacterial activity. It is a potent inhibitor of bacterial ribonucleotide reductase and thus inhibits DNA synthesis. The homology model of the enzyme shows that the chemical could bind to the active site and inhibit the production of ATP, preventing cell division. 2-(1H-Benzimidazol-1-yl)ethyl]amine dihydrochloride has been shown to have an effect on Clostridium and Bacillus anthracis, with MIC values of 1.0 µg/mL and 0.5 µg/mL respectively. This chemical also has potential for use as a drug in humans due to its lack of toxicity in mice at high doses (LD50 = 5 g/kg).

3-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-Heptadecafluorooctylsulfonylamino)Propyl-Trimethylazanium Chloride is a polyfluoroalkyl sulfonate (PFAS) that belongs to the group of substances. It is used in the manufacturing of electroplating and other chemical processes. PFAS are persistent organic pollutants that can accumulate in human and environmental tissues. The PFAS was originally synthesized as an analytical reagent for chromatography columns. 3-(1,1,2,2,3 ,3 ,4 ,4 ,5 ,5 ,6 ,6

N-Boc-hydroxylamine is an efficient method for the preparation of epoxides from carboxylic acids. The reaction system is a ruthenium complex in trifluoroacetic acid with an effective reaction time of 20 minutes and a stereoselective transfer mechanism. The carbamic acid group on the amine reacts with the epoxide to form a hydroxamic ester. Preparation of N-Boc-hydroxylamine can be accomplished by reacting hydroxylamine with a boc-protected alcohol, which then undergoes decarboxylation.

N-Acetyl-5-carboxymethoxy tryptamine is a versatile building block that is used as a reagent and in the synthesis of complex compounds. It can also be used as an intermediate or a reaction component in the synthesis of other compounds. This compound has been shown to have high quality and, when used as an intermediate, can serve as a useful scaffold for the synthesis of new molecules. N-Acetyl-5-carboxymethoxy tryptamine belongs to CAS No. 1397243-36-5, which is a speciality chemical that is not regulated by law.

2-Amino-5-chloro-2'-fluorobenzophenone is a phenoxazine that has been used as an analytical reagent. It is also a fluorescent compound and an anxiolytic drug. 2-Amino-5-chloro-2'-fluorobenzophenone can be found in urine samples, where it may be the result of biotransformation by bacteria in the intestine or chemical reactions with nicotine or hydrochloric acid. The molecular electrostatic potentials for 2-amino-5-chloro-2'-fluorobenzophenone are calculated from vibrational spectra and the crystal x-ray diffraction pattern of its crystals. The chromatographic conditions for 2-amino-5-chloro-2'-fluorobenzophenone are determined by clinical chemistry and biodegradability, which is assessed using nmr spectra.

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2,4,5-Trifluorophenylene-1,3-diamine is an isomer of 2,4,5-trifluorophenol. It is a colorless liquid that is soluble in ether and hexafluorobenzene. This compound can be used as a heat stabilizer in polymers and has been shown to yield high yields (over 95%) when polymerized with maleic anhydride. The compound also has the ability to coordinate to oxygen atoms and assemble into larger structures such as rings or chains. 2,4,5-Trifluorophenylene-1,3-diamine reacts with amines to form hydrogen bonds and exhibits amino groups on its structure that are important for calorimetry measurements.

5-Methoxygramine is a metabolic intermediate which is an analog of 5-hydroxytryptamine (5-HT). It has been shown to increase blood pressure and reduce the activity of the 5-HT2C receptor. This drug also has been found to inhibit the growth of some cancer cells in vitro, but it does not affect normal cells. It can be used as a tool for identifying compounds that may have similar effects. The binding affinity of 5-methoxygramine for the 5-HT2C receptor was measured by displacement experiments with 3H-spiperone. The effect of this compound on dopamine release from rat striatal slices was studied by measuring electrical activity in isolated heart preparations. The effect of this compound on leishmania infection was studied using infected mice and isolated heart preparations.

O-Aminobenzoylglycyl-p-nitro-L-phenylalanyl-L-proline TFA salt is a synthetic, hydrophilic interaction chromatography (HIC) substrate. It has inhibitory properties and is used in biological assays to measure the activities of enzymes that catalyze the hydrolysis of the substrate. O-Aminobenzoylglycyl-p-nitro-L-phenylalanyl-L-proline TFA salt also has been shown to have bioactivities on blood pressure and cell monolayers.

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.

Inhibitor of catalase; selection marker for  HIS3 systems; herbicide

2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide is an anticancer agent that inhibits the synthesis of proteins required for cell division. It has been shown to have anticancer activity and efficacy in vitro studies against human cancer cells, such as HCT116. This compound also induces apoptosis in infected cells by binding to viral particles and inducing the release of chloride ions. 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide has been found to be effective against influenza virus and particle production by inhibiting neuraminidase activity.