Amines

2-Aminobenzhydrazide is a hydrogen bond donor that binds to the 5-HT2 receptor. It has been shown to be effective in treating infectious diseases such as malaria and dengue fever. 2-Aminobenzhydrazide inhibits the production of the inflammatory hormone prostaglandin E2 by inhibiting cyclooxygenase, which is responsible for converting arachidonic acid into prostaglandins. This drug also has anti-inflammatory properties because it blocks the action of amide and hydrazide receptors, which are associated with pain transmission. 2-Aminobenzhydrazide has been shown to inhibit the growth of bacteria and fungi in culture, with inhibition constants of 4.4 x 10 M for Escherichia coli and 8 x 10 M for Candida albicans.

Applications N-Alkyl(C12-16)-N-benzyl-N,N-dimethylammonium chloride, tech. (cas# 68424-85-1) is a useful research chemical.

O-(2-Aminoethyl)-O'-(2-azidoethyl)nonaethylene glycol is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. O-(2-Aminoethyl)-O'-(2-azidoethyl)nonaethylene glycol is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

Please enquire for more information about 1-Methyl-2-pyridin-4-yl-ethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-{2-(4-Chlorophenyl)-7-[(E)-2-(dimethylamino)vinyl][1,2,4]triazolo[1,5-a]pyrimidin-6-yl}ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-(Acetylamino)butanoic acid is a β-amino acid that inhibits the enzyme phosphotransferase. It is used as an inhibitor in biochemistry to study the mechanism of enzymes and to produce β-amino acids. 2-(Acetylamino)butanoic acid has been shown to inhibit the growth of corynebacterium glutamicum, a bacterium that produces enzymes that are necessary for cell growth. This compound also has asymmetric synthesis properties and can be used to produce enantiomers of other compounds. The reaction mechanism is thought to involve a chlorine atom attacking the double bond between carbons 1 and 2, forming an acyl chloride intermediate. This intermediate then reacts with hydroxide ion from the solution to form 2-(acetylamino)butanoic acid.

Hexadecyltrimethylammonium Perchlorate is a polycarboxylic acid that is used as an antibacterial agent. It inhibits the growth of bacteria by disrupting the permeability of bacterial membranes and inhibiting the synthesis of proteins. The compound is used in liquid crystal compositions, which are non-polymeric, and has been shown to be effective against gram-positive bacteria such as Staphylococcus aureus and Streptococcus pneumoniae. Hexadecyltrimethylammonium Perchlorate has also been found to have antifungal activity against Candida albicans.

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