Hydrazines

Please enquire for more information about (4-Bromo-3-methylphenyl)hydrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Formylhydrazinecarbothioamide is a bioactive molecule that has been shown to have antiviral and anticarcinogenic activity. It has been shown to inhibit the growth of animal viruses in cell culture, including influenza A, Newcastle disease virus, and vesicular stomatitis virus. 2-Formylhydrazinecarbothioamide also inhibits the production of carcinogenic molecules that are produced by tobacco smoke, such as nitrosamines and polycyclic aromatic hydrocarbons. The molecular structure of 2-formylhydrazinecarbothioamide is similar to ethionamide, which is an antituberculosis drug. This similarity may be responsible for its anti-tuberculosis activity. 2-Formylhydrazinecarbothioamide is structurally related to ethionamide (1) through hydrogen bonding with the amide nitrogen atoms in both molecules. The antibacterial activity of 2-formylhydrazinecarbothioamide

N-Phenylhydrazinecarbothioamide is a chemical compound that is used in wastewater treatment. It is an organic molecule that is composed of hydrophobic and hydrophilic parts. The hydrophobic part, which contains the phenyl group, binds to the hydrophobic region of the cell membrane and causes the cell to lyse. The hydrophilic part has an affinity for water and can be used as an electrode material in electrochemical impedance spectroscopy. N-Phenylhydrazinecarbothioamide also has been shown to have antibacterial properties against human pathogens, including Mycobacterium tuberculosis, Clostridium perfringens, and Escherichia coli O157:H7. The compound has been shown to inhibit cervical cancer cells by inhibiting protein synthesis through inhibition of ribosomal activity and fragmentation assay analysis showed that N-phenylhydrazinecarbothioamide binds to copper ions at a coordination geometry of

Please enquire for more information about 4-Fluoro-N-[4-(hydrazinocarbonyl)phenyl]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-Cyclohexylhydrazinecarbothioamide is a biochemical that belongs to the class of amides. It is a thione, which is an organic compound with a sulfur atom in the place of one or more hydrogens. The molecule has been shown to have anticancer activity and acts by inhibiting DNA synthesis, leading to cancer cell death. N-Cyclohexylhydrazinecarbothioamide also inhibits the biosynthesis of nucleic acids by binding to their enzyme's active site, thereby preventing hydrogen bonding interactions between amino acids that are necessary for protein synthesis. This drug binds to the DNA gyrase enzyme, which is vital for bacterial replication and transcription.

1,2-Bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyl)hydrazine is a magnetic resonance imaging (MRI) contrast agent that is used in the preparation of MRI contrast agents. It has an antioxidant effect that helps to protect cells from free radicals. 1,2-Bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyl)hydrazine can be used as a cross linking agent for polymers and other organic substances. It has been used as a water vapor barrier coating on paperboard in the manufacture of cigarette filters. This compound is also known to be a corrosion inhibitor and stabilizer for boron nitride which is used as an additive for steel production. 1,2-Bis(3,5-di-tert butyl 4 hydroxy hydrocinnamoyl)hydrazine reacts with p -

Please enquire for more information about N-Allyl-2-(3-hydroxybenzoyl)hydrazinecarbothioamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Fluorophenylhydrazine is a synthetic drug that has been shown to have antifungal activity in vitro. It is effective against a wide range of fungi, including Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus. 4-Fluorophenylhydrazine inhibits the growth of tumour cells by binding to cellular macromolecules such as RNA and DNA. This binding prevents the synthesis of proteins needed for cell division. The drug also inhibits prostaglandin synthesis by inhibiting caspase-2, which is an enzyme involved in the production of prostaglandins from arachidonic acid. 4-Fluorophenylhydrazine has been shown to be active against tuberculosis bacteria. It binds to the mycobacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 4-