Alcoholes bencílicos

Applications Benzyl-2,3,4,5,6-D5 Alcohol is an isotopically labeled analog of Benzyl Alcohol (T536635), which is used in the synthesis of Cephalosporolide B as a versatile biomimetic synthetic precursor for chemical synthesis of other cephalosporides.
References Song, L. et al.: Org. Lett., 15, 5850 (2013);

3-Aminobenzyl alcohol is a prodrug that is metabolized to 3-aminophenol, its active form. It has immunomodulatory properties and can be used to treat population growth. 3-Aminobenzyl alcohol binds to specific receptors on the surface of lymphocytes, which inhibits the immune system's response to foreign antigens. This drug also has photochemical properties and can be used as a photosensitizer in photodynamic therapy. 3-Aminobenzyl alcohol is a hydrogen bond acceptor with acidic functional groups and has been shown to bind with proteins through hydrogen bonding interactions. The hydrogen bond strength between the drug and protein depends on the pH of the solution, which may affect its efficacy in different cell types.

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Synthetic building block; biomimetic anti-fungal

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3-Iodobenzyl alcohol is a pesticide that belongs to the class of halogenated benzaldehydes. It is a bioconjugate, which means that it can be coupled to an organic molecule to form a new molecule with improved properties. 3-Iodobenzyl alcohol is used in the synthesis of polymers and pharmaceuticals. In addition, 3-iodobenzyl alcohol has been studied as an anticancer drug candidate because it binds to DNA and inhibits DNA synthesis and repair in tumor cells. This compound has also been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) isolates.

3-Hydroxybenzyl alcohol is a fatty acid with a hydroxyl group. The clinical relevance of 3-hydroxybenzyl alcohol remains unclear. It has been used in acetate extract and ph optimum tests, as well as to study reaction solutions and nmr spectroscopic data. Hydrogen bonds have been observed between the molecule's hydroxyl group and the oxygen atoms in water molecules, which may explain its antifungal properties. 3-hydroxybenzyl alcohol also has an inhibitory effect on cyclic peptide synthesis, rotarod test performance, and analytical methods. It is a broad-spectrum antimicrobial that can be used against bacteria, fungi, protozoa and viruses. 3-hydroxybenzyl alcohol has an acidic character because it reacts with copper ions to form a copper complex.

3,4,5-Trimethoxyphenol is a fruit extract that has been shown to inhibit the activity of protein synthesis. It also inhibits the replication of hepatitis C virus in vitro by interfering with the acylation reaction and preventing the attachment of lipoproteins to cell membranes. 3,4,5-Trimethoxyphenol may be used as an analytical reagent for determining the degree of unsaturation in cinnamic acid derivatives.

3,4-Dimethoxyphenol is a compound that is structurally similar to p-hydroxybenzoic acid. It has been shown to inhibit fatty acid synthesis in rat liver microsomes by competitive inhibition of the enzyme β-hydroxylase. This inhibition may be due to its ability to form a stable complex with the enzyme and thereby preventing substrate binding. 3,4-Dimethoxyphenol can also be prepared by sulfonation of 3,4-dihydroxybenzaldehyde followed by chromatographic purification. The compound has been used as an analytical reagent for the determination of sulfonic acids, and it has been shown to have electrochemical methods with good sensitivity and selectivity.

2,6-Dimethyl-4-cyanophenol is a pyrimidine compound that has been used as a pharmaceutical drug to inhibit the replication of human immunodeficiency virus (HIV). It has also been shown to be effective against the strains of HIV that are resistant to other drugs. 2,6-Dimethyl-4-cyanophenol is an inhibitor of reverse transcriptase, which is an enzyme necessary for the production of viral DNA from viral RNA. This drug also inhibits bacterial growth by binding to bacterial DNA gyrase and topoisomerase IV. 2,6-Dimethyl-4-cyanophenol has a number of functionalities: it can act as an acid or base depending on its environment and it can form hydrogen bonding interactions with other molecules. This drug also has acidic properties that make it useful in the treatment of ph problems caused by trifluoroacetic acid.