Alcools

Please enquire for more information about 3-Keto petromyzonol-24-hemisuccinate including the price, delivery time and more detailed product information at the technical inquiry form on this page

1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol) 2000] (ammonium salt) is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol) 2000] (ammonium salt) is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

<p>Please enquire for more information about 1-Oleoyl-3-palmitoyl-rac-glycero-2-phosphoethanolamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Phenethyl glucosinolate potassium salt is a compound found in plants belonging to the Brassicaceae family. It has been shown to be highly toxic to larvae of the cabbage butterfly and other insects that feed on brassica plants. Phenethyl glucosinolate potassium salt has been shown to inhibit the development of these insects, probably by inhibiting protein synthesis in the insect's gut. The major sulfur-containing compound in this product is gluconasturtiin, which has been shown to inhibit growth of pekinensis at high temperatures. This compound also inhibits radiation-induced DNA damage and does not show significant effects on nonsignificant organisms such as yeast and mold.

2-Bromo-1-indanol is an industrial solvent used in the production of dyes, pigments, perfumes, pharmaceuticals, and other organic compounds. It is a chiral compound with two stereoisomers (R and S) that have different properties. The R isomer has a hydroxyl group on the 2 position of the indane ring, while the S isomer does not. The industrial process involves recycling of 2-bromo-1-indanol from the reaction mixture. This process can be monitored using mass spectrometric detection for bromine and hydrogen ions released during hydrolysis. 2-Bromo-1-indanol can be used to synthesize methoxybenzaldehyde with high regioselectivity, which can then be used to make some drugs such as amphetamine and methamphetamine.

<p>Please enquire for more information about 4-Chlorophenyl-2-pyridinylmethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Quinoline-4-carboxylic acid is a natural compound that is derived from the amino acid tryptophan. It has been shown to have antiinflammatory activity and to be an inhibitor of prostaglandin synthesis. Quinoline-4-carboxylic acid inhibits the growth of carcinoma cells in culture by inducing apoptosis, which is mediated by inhibition of protein synthesis. Quinoline-4-carboxylic acid also has pharmacokinetic properties, including a low volume of distribution, low clearance rate and high bioavailability.</p>

Cyclopent-2-en-1-ol is a reactive monomer that can react with chloride and hydroxyl groups. It can also undergo reaction with sodium carbonate to form a cyclic ester. Cyclopent-2-en-1-ol can be converted to an epoxide by the use of acid catalyst. This compound also has the ability to polymerize, forming polymers that are used in rayon production.

<p>2,2'-Biquinoline is a coordination compound that has been used as an analytical reagent in the determination of copper and nitrogen. It has been shown to be stable in a variety of matrices, including human serum and copper chloride. 2,2'-Biquinoline is also used as an antimicrobial agent against Gram-positive bacteria, including Staphylococcus aureus. The redox potentials of this compound are dependent on the number of nitrogen atoms present.</p>

3-(Aminomethyl)phenol is a potent inhibitor of growth factor receptor kinase (GRK) and protein kinase C. It has been shown to have inhibitory effects on cellular proliferation in mammalian cells and is being investigated as an adjuvant therapy for cancer treatment. 3-(Aminomethyl)phenol has also been shown to inhibit the enzyme cyclooxygenase-2, which is involved in the synthesis of prostaglandins. DISCUSSION: The carbonyl group of 3-(aminomethyl)phenol makes it a potent inhibitor of GRKs and protein kinases C. Kinases are enzymes that catalyze the addition of phosphate groups onto proteins, which affects their activity. As such, 3-(aminomethyl)phenol inhibits the activity of GRKs and protein kinases C by binding to the ATP-binding site, preventing ATP from binding and phosphorylating the enzyme's target proteins

<p>Schisanhenol is a natural drug that belongs to the class of fructus. It has been shown to have cytosolic calcium-lowering effects in vitro. Schisanhenol has been shown to inhibit polymerase chain reaction (PCR) and reverse transcriptase activity, which may be due to its ability to inhibit oxidative injury, such as free radicals. This drug also inhibits sulfa drugs and integrin receptors, which may be due to its antioxidant properties. Schisanhenol has been shown to inhibit the growth of cancer cells in vitro and has been used as an adjuvant treatment for adriamycin.</p>

<p>2-Bromo-6-methylpyridin-3-ol is a heterocyclic organic compound. It is a pyridine ring with two methyl groups attached to the ring at positions 2 and 6. The bromine atom is at position 3. This is an important intermediate in the Suzuki coupling reaction, which uses it as a starting material for the synthesis of many other compounds. The dieckmann condensation reaction produces this compound from 2,6-dichloropyridine and other reagents. Fluorescent when exposed to UV light, this compound has been used as a probe for chloride ions in solution using mass spectroscopy. This substance also yields dieckmann condensation products with alkynes and chlorine or bromine. 2-Bromo-6-methylpyridin-3-ol can be produced by treating pyridine with methylacrylate in the presence of catalysts such as copper(II)</p>

<p>2-Chlorophenyl)diphenylmethanol is an antifungal drug that blocks the function of a calcium ionophore in fungal cells. It has been shown to be effective against a variety of filamentous fungi, including Aspergillus fumigatus, Candida albicans, and Trichosporon cutaneum. This drug is used as a topical antifungal agent for treatment of skin infections caused by these fungi. 2-Chlorophenyl)diphenylmethanol has been shown to have anti-inflammatory properties in animal models of kidney fibrosis and cell binding. Clinical data suggests that it can be used for the prevention or treatment of stem cell transplantation complications such as graft versus host disease and leukemia.</p>

<p>(R)-(+)-3-Chloro-1-phenyl-1-propanol is a substrate for the lactamase of bacteria. The immobilized lipase catalyzes the hydrolysis reaction in which the lactam ring is broken, yielding a propiophenone intermediate. This intermediate can be converted to (S)-(+)-3-chloro-1-phenylpropanol by treatment with an alcohol oxidase or by hydrolysis with hydrogen peroxide. The product has been shown to have antidepressant activity and may modulate the dry weight of bacteria. In vivo studies show that this compound has a high concentration in rats and mice, but it is not active in humans.</p>

<p>2-Chloro-5-nitrobenzyl alcohol is a vibrational spectroscopy technique that can be used to study the interactions between molecules. The technique can be used to measure the population of molecules in a system and to determine the thermodynamic properties of systems. It has been shown that 2-chloro-5-nitrobenzyl alcohol is an inhibitor for macrocyclic compounds with electron withdrawing groups, such as carbonyl groups. This molecule has been studied using statistical strategies, which have been shown to be effective in predicting the binding affinity of 2-chloro-5-nitrobenzyl alcohol and other inhibitors for macrocyclic compounds.</p>

5-Iodo-2-methoxybenzyl alcohol (5IMB) is a conjugate that inhibits tubulin polymerization and mitochondrial membrane integrity. It has significant inhibitory effects on colchicine-induced apoptosis in colon cancer cells, inducing apoptotic cell death by the activation of caspase 3 and annexin. 5IMB also has an inhibitory effect on mitochondria, leading to mitochondrial membrane depolarization and apoptotic cell death. This conjugate also induces the death of human cancer cells, specifically mcf-7, which are involved in tumour growth and metastasis. The mechanism of action for 5IMB is through its ability to induce mitochondrial membrane depolarization, leading to apoptotic cell death.

<p>p-Xylene-α,α'-diol is a water-soluble polymer that can be prepared by the reaction of ethylene diamine with sodium citrate. The resulting product has a low molecular weight and high viscosity. The polymer is insoluble in water at pH values higher than 9.5 and soluble in acidic solutions. p-Xylene-α,α'-diol has been shown to exhibit good chemical stability and thermal expansion properties when exposed to temperatures of up to 300 °C. The polymer is soluble in organic solvents such as benzene, chloroform, acetone, ether, and carbon tetrachloride. The polymer has been shown to have transport properties for some drugs, such as ketoprofen and ibuprofen, with good kinetic data at various concentrations.</p>

3,4-Dichlorothiophenol is a chemical compound that belongs to the group of reactive compounds. It can be used as a chemical intermediate for the synthesis of other organic compounds. 3,4-Dichlorothiophenol is an inhibitor of methylating enzymes such as glyoxalase I and II and glyceraldehyde-3-phosphate dehydrogenase. This inhibition leads to the accumulation of methylglyoxal and 3-deoxyglucosone in cells, which are potent inhibitors of protein glycosylation. 3,4-Dichlorothiophenol also inhibits nucleophilic attack on DNA by epoxide hydrolases such as epoxide hydrolase 1 and 2. This inhibition results in the accumulation of reactive metabolites that are covalently adducted with DNA bases.

3-Chloro-2-nitrobenzyl alcohol is a chemical compound that has a molecular formula of C6H5ClNO2. This substance was synthesized by the reaction of 3-chloro-2-nitrobenzyl chloride with sodium hydroxide in methanol. The optimized geometry and vibrational frequencies were calculated using density functional theory (DFT) and theory of Raman scattering. The IR spectra were measured with Fourier transform infrared (FTIR) spectroscopy, which showed that the compound has a strong absorption in the region from 2,600 to 2,800 cm−1.

3-(3'-Trifluoromethylphenyl)propanol is a trifluoroacetic acid derivative that is used in acylation reactions to form esters. It can be obtained by the reaction of aluminium chloride, isopropyl alcohol, and phosphine with 3-trifluoromethylaniline. Impurities may include chloride and zirconium. The trifluoromethyl group on this molecule can react with the carbonyl group of an organic acid to form a trifluoroacetate ester.