Álcoois

Fmoc-O-tert-butyl-L-threoninol is an aminoacyl chloroformate ester that is used in the synthesis of peptides. It has a conjugate acid chloride and a disulfide bond. The chloroformate group reacts with the carboxylic acid moiety of L-threonine to form an ester, which can then be cleaved by hydrolysis to yield L-threonine. This product is also used for the synthesis of peptides in which the threonine residue is conjugated to another amino acid such as cysteine or glutamic acid.
Fmoc-O-tert-butyl-L-threoninol is synthesized from l-threonine and isobutene via a phase chromatography process. The synthetic intermediate Fmoc-(S)-OH is reacted with trifluoroacetic acid (TFA)

2-Chlorobenzyl alcohol is a chemical compound that is used to synthesize other compounds. It is produced by the reaction of ethyl formate and hydrogen chloride in a reaction vessel. It reacts with benzoates to produce 2-chlorobenzoates, which are used as intermediates in the synthesis of pharmaceuticals. Hydroxyl groups can react with hydrogen fluoride to produce hydrofluoric acid, which is used as an industrial solvent. 2-Chlorobenzyl alcohol also reacts with hydroxide ions to produce ethylene glycol, which is used in making polyester fibers and plastics. This chemical compound has structural studies that show it has a proton and two hydroxyl groups that can react with hydrogen bond. Hydrogen bonds are important for the stability of DNA structures. The molecular structures of velvetleaf plants contain 2-chlorobenzyl alcohol, which may be due to its role in transferring oxygen from leaves to roots for respiration during

4-Isopropylresorcinol or 4-Isopropylbenzene-1,3-diol belongs to the family of alkylresorcinol. It is a synthetic molecule that has been shown to reduce tumor size and inhibit cancer cell growth in vitro and in vivo. It also inhibits the expression of heat shock protein (Hsp90), which is highly expressed in most tumor cells. A study done on human lung cancer cell lines showed that 4-isopropylresorcinol inhibited the growth of xenograft tumors with no side effects, by enhancing the sensitivity of lung cancer cells to photodynamic therapy, and arrests non-small cell lung cancer cells in the G1 phase with an associated increase in apoptosis. It also induces efflux transporters in tumor cells, which leads to a time-dependent pharmacokinetics.

Pycnogenol is a nonsteroidal anti-inflammatory drug that is derived from the bark of the French maritime pine tree. It has been shown to reduce bowel disease activity in animal models and has been found to be as effective as ibuprofen in human studies. Pycnogenol also inhibits the expression of toll-like receptor 4, which reduces inflammation in cells. Pycnogenol has also been shown to have an anti-inflammatory effect on human polymorphonuclear leukocytes and may be useful for treating various diseases such as cancer, cardiovascular diseases, or asthma. This compound also has natural antioxidant properties that are thought to protect against oxidative damage and help regulate blood pressure by inhibiting vascular smooth muscle proliferation.

3-Aminoquinoline is a chemical compound that inhibits the activity of the epidermal growth factor receptor (EGFR). It is a potent inhibitor of cell proliferation and has been shown to have antitumour activity. 3-Aminoquinoline has been shown to inhibit the proliferation of carcinoma cell lines. This drug binds to the EGFR receptor, preventing it from activating downstream signalling pathways that control cell growth. 3-Aminoquinoline also has biological properties, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, analytical chemistry, sample preparation, and Suzuki coupling reaction. The molecule is structurally analyzed using chemical structures and structural analysis techniques such as thermodynamic data or proton NMR spectroscopy. 3-Aminoquinoline also interacts with sugars through hydrogen bonding and oligosaccharides. These interactions are found to be high in value in some cases.

3-Phenyl-1,2,4-oxadiazol-5-yl)methanol is a versatile building block that has been used in the synthesis of complex compounds and research chemicals. It is also a reagent that can be used in the laboratory to synthesize other fine chemicals. 3-Phenyl-1,2,4-oxadiazol-5-yl)methanol is an intermediate that can be used to create high quality and useful building blocks for chemical reactions. This compound has many uses as a scaffold in organic synthesis and it can be used to make valuable products such as pharmaceuticals and pesticides. 3-(3'-phenyl)-1,2,4-oxadiazole 5'-amine is listed on the Chemical Abstracts Service (CAS) database with number 5543-33-9.

2-(2-Bromophenyl)ethanol is a functional group that contains a bromine atom and an ethoxy group. This compound is used to synthesize condensation products, such as the crystal x-ray diffraction of crystallized palladium complexes with acetaldehyde. The 2-(2-bromophenyl)ethanol analog was synthesized in order to study the synthesis and reactivity of a chelate ring. The hydroxyl group on this compound is useful for forming a magnesium salt or for using it as a synthetic reagent.

Please enquire for more information about 2-Indol-3-yl-2-oxo-N-(8-quinolyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page