Alcohols

DMPE; uncharged cell membrane phospholipid

Applications 1,2,10-Decanetriol (cas# 91717-85-0) is a compound useful in organic synthesis.

Bis-(1,3-diethylthiobarbituric acid)trimethine oxonol (BTTMO) is a compound class of drugs that inhibit the ATP-binding cassette transporter and block the transport of cellular metabolites across the mitochondrial membrane. This inhibition leads to a decrease in cellular ATP levels and an increase in cytosolic calcium. BTTMO has shown promising results in animal models for treatment of cervical cancer, which may be due to its ability to stimulate epidermal growth factor receptor signaling. BTTMO also inhibits energy metabolism by inhibiting mitochondrial membrane potential and blocking atp-sensitive potassium channels. It also induces gamma-aminobutyric acid release from neurons, leading to hyperpolarization of the cell membrane.

Trimethylsilylmethanethiol (TMSET) is a thiol that is used as a reagent in organic synthesis. It is soluble in water and it has a high boiling point, making it useful for reactions that require heat. TMSET has been shown to be an effective antiviral agent against hepatitis C virus (HCV) and influenza A virus by binding to the viral receptor on the cell surface and preventing its entry into the cell. TMSET also inhibits neuronal function by binding to the hydroxy group of proteins, thereby disrupting their structure and function.

Kushenol A is a natural product extracted from the Chinese herb Kushen. It is a white or off-white powder that has a molecular weight of 223.29 and consists of a hydroxyl group, three methoxy groups, and one methyl group. Kushenol A has been shown to have anti-inflammatory properties in vitro and in vivo by inhibiting the production of inflammatory cytokines such as IL-1β, IL-6, IL-8, TNFα, and MCP-1. This compound also has potent inhibitory activity against LPS-stimulated RAW264.7 cells with an IC50 value of 0.2 µM. Kushenol A is composed of several chemical structures including chlorogenic acids and plant families such as the Rosaceae family (which includes apples). Kushenol A has been found to be effective against infectious diseases such as listeriosis and SARS coronavirus infection in mice. This compound may be effective

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Please enquire for more information about 6-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

(2S,3R,4E)-2-Amino-4-tetradecene-1,3-diol is a compound that has been found to inhibit cancer cells. It was originally isolated from the leaves of the tropical plant Lepidoptera cinerascens and was shown to be effective against neuronal death in vitro. (2S,3R,4E)-2-Amino-4-tetradecene-1,3-diol is also able to induce autophagy in prostate cancer cells. This compound has a chemical structure similar to fatty acid and may have an effect on viruses such as HIV.

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2-(3-Benzyloxyphenyl)Octan-2-Ol is an analgesic agent that is used in the manufacture of other drugs. It is synthesized by methylation of heptanol with 3-benzyloxyacetophenone, followed by a Grignard reaction with hydrogen chloride and trimethylaluminum. The methyl group on the benzene ring is then replaced by the chloride group using a chlorination reaction. 2-(3-Benzyloxyphenyl)Octan-2-Ol has shown analgesic properties in animal studies, but further research is needed to determine its efficacy as a painkiller in humans.

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Conjugated linoleic acid is a conjugated fatty acid, consisting of a linoleic acid molecule with two or three double bonds. It has been shown to have inhibitory properties against pathogens such as Escherichia coli and Salmonella enterica. Conjugated linoleic acid also has anti-inflammatory effects on bowel disease and the energy metabolism in adipose tissue. It is thought that the action of conjugated linoleic acid on these processes is due to its ability to bind to enzymes involved in metabolic pathways. The following is an example of product description for eCommerce: Rifapentine is an anti-tuberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. Rifapentine inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity

4,4,4-Trifluoro-2-methyl-1-butanol is a chemical compound with formula CH3CF3OC(CH2)2OH. It can be produced by amination of acetone with hydrogen fluoride and ammonia in the presence of a palladium catalyst. The reaction is followed by bromination to yield 4,4,4-trifluoro-2-bromo-1-butanol. This compound can also be synthesized from alloisoleucine's natural precursor, methionine. Trifluoromethylation of 4,4,4-trifluoro-2-bromo-1-butanol leads to 4,4,4-(trifluoromethyl)-2-(methylthio)-1-(trifluoromethyl) butanal and finally 4,4,4-(trifluoromethyl)-2-(methylsulf

5-Chloroisoquinoline is a tryptic protease inhibitor that binds to the active site of the enzyme, preventing the hydrolysis of peptides. It has been shown to inhibit the activity of casein kinase and phosphorylate casein, leading to an increase in its solubility. 5-Chloroisoquinoline also interacts with dipoles in proteins, which leads to a change in charge distribution on the molecule. This can lead to changes in protein conformation and interactions with other molecules. In addition, this compound has been shown to interact with carboxy terminal amino acids on other proteins.

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Applications 3,3-Diethoxy-1-propanol is used as a reactant in the synthesis of nanoparticles. References Sumitani, Shogo, et al.: Reactive & Func. Polymers, 71(7), 684-693 (2011);Kanakubo, Yurie, et al.: Colloids and Surfaces, B, 78(1), 85-91 (2010)

6-Fluoroisoquinoline is a triazole with the molecular formula CHN. It is synthesized by reacting acetonitrile with an azide in the presence of ruthenium and ammonium nitrate. 6-Fluoroisoquinoline has been shown to enhance epoxidation reactions and also function as a sensor for nitrates.

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1-(Methylthio)ethanethiol (MTET) is a highly volatile, naphthenic compound that has been shown experimentally to be a sulfide and ethanal precursor. It is also an ethyl cinnamate solvent. MTET is soluble in organic solvents such as chloroform and benzene. MTET has been used to produce polymers by coating sensor surfaces with polymer film and evaporating the solvent. The fluorescence of MTET increases in the presence of oxygen, which may be due to its oxidation by air.

3-sn-Phosphatidylethanolamine is a phosphatidic acid that is used in the production of phospholipids and other lipid molecules. It is a component of the major phospholipid classes, including phosphatidylcholine, phosphatidylethanolamine, and sphingomyelin. 3-sn-Phosphatidylethanolamine can be obtained by hydrolysis of natural fats or synthesis from ethanolamine. The hydrolysis yields are dependent on the length of the fatty acid chains; for example, the yield for lauric acid is greater than that for palmitic acid. The ester linkage between the glycerol backbone and phosphate group is formed by an esterification reaction with ethanolamine.

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4-Pyridineethanol is a biocatalyst that can be immobilized on solid surfaces. It has been used in the catalytic oxidation of dimethylglyoxime to glyoxal and its derivatives, such as ethylene glycol, acetaldehyde, and formaldehyde. 4-Pyridineethanol is a ligand that binds to copper ions and is involved in the evolution of hydrogen peroxide from copper-tetraphenylporphyrin complexes. 4-Pyridineethanol also regulates the activity of enzymes by binding to pyridine nucleotides or cofactors or by acting as an electron donor in photochemical reactions.

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Fmoc-L-phenylalanine 4-alkoxybenzyl alcohol resin is a macroscopic matrix that can be used to visualize bioactive molecules. It is a linker that can be used in solid-phase peptide synthesis and is also used for the synthesis of cyclic peptides. Fmoc-L-phenylalanine 4-alkoxybenzyl alcohol resin has been experimentally shown to be selective for proteins with specific targets, such as the β2 adrenergic receptor.

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Piperonyl alcohol is an enzyme inhibitor that blocks the oxidation of piperonal, a chemical found in many plants and fruits. It has been used as a pharmaceutical preparation to treat skin conditions such as acne and psoriasis. Piperonyl alcohol can be used in food composition as a preservative and antioxidant. This compound is also used in the production of polymers for paints, plastics, and rubber. Piperonyl alcohol inhibits melanogenesis by inhibiting tyrosinase activity and interrupting the synthesis of melanin. The use of this compound to inhibit melanin synthesis has been approved for cosmetic use in Europe. Piperonyl alcohol was first synthesized by Ludwig Knorr in 1885 from piperonal, an aromatic organic compound found in many plants and fruits. The reaction solution obtained from the hydrolysis of piperonyl acetate with hydrochloric acid is reacted with cationic polymerization using sodium carbonate (NaCO) as a catalyst to produce

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