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Methylbenzenethonium chloride is an antimicrobial agent that has been shown to inhibit the growth of leishmania and other parasitic protozoa. It has a high affinity for acidic surfaces, such as those found in the human body. Methylbenzenethonium chloride adsorbs strongly to the surface of bacteria, thereby inhibiting the attachment of these organisms to mucosal surfaces and preventing their adhesion to host cells. This compound also inhibits bacterial surface-associated enzymes, including DNA gyrase and DNA topoisomerase IV. Methylbenzenethonium chloride has been shown to be active against both gram-positive and gram-negative bacteria and is considered safe for use in humans with acute toxicities below 1%.

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1-(3-Trifluoromethylphenyl)piperazine hydrochloride (TFMPP) is a derivative of the piperazine class of drugs. It is structurally similar to other drugs in this class, such as bromopropane, which acts as an agonist of the 5-HT1 receptor. TFMPP has been shown to be an agonist at 5-HT1 receptors and dopamine receptors. It has also been shown to inhibit serotonin uptake and release, and inhibits choline acetyltransferase activity in brain tissue. TFMPP is not active on the 5-HT2 receptor, but does have some affinity for the 5-HT2A receptor. TFMPP has high affinity for the serotonergic system, with selective binding to serotonin transporter proteins in vitro. TFMPP may also have some effect on cholinergic systems through its inhibition of acetylcholinesterase activity.

3-Fluoro-4-methylaniline is a synthesized compound that is used to produce anti-cancer agents. It is an amide and has anti-cancer properties. 3-Fluoro-4-methylaniline also binds to DNA and inhibits the synthesis of proteins in cancer cells. The binding constants for ligands are found to be high. 3-Fluoro-4-methylaniline can also bind with DNA through intercalation or hybridization, which prevents transcription of RNA from DNA, thereby inhibiting protein synthesis. This results in cell death by apoptosis.

Pentafluoroaniline is a pentavalent nitrogen-containing compound that is used in the synthesis of diazonium salts. It reacts with hydrogen fluoride to form a copper complex, which is a strong nucleophile. Pentafluoroaniline forms intramolecular hydrogen bonds between its nitrogen atoms and nonpolar solvent molecules. It binds to cholesterol esterase and inhibits the enzyme's function, thereby inhibiting the production of prostaglandins and leukotrienes. Pentafluoroaniline also has an inhibitory effect on proliferation by binding to amines in cells, preventing their activation by phospholipase A2 enzymes.

Arachidonoyl chloride is a chemical compound that belongs to the group of amides. It is used in biological studies for receptor binding and enzyme activities. Arachidonoyl chloride has been shown to inhibit insulin sensitivity by inhibiting the phosphorylation of tyrosine residues on insulin receptors, which are necessary for glucose transport into cells. The acyl chain of arachidonoyl chloride has a polyunsaturated fatty acid structure with two double bonds, which is important for its activity on the 2-arachidonoylglycerol (2-AG) pathway. The activation energy of arachidonoyl chloride is not yet known.