Alcoli

<p>3-Phenyl-1,2,4-oxadiazol-5-ol is a thione that has been shown to be conjugated with DNA and RNA. It is also able to form complexes with metal ions. This compound is spectroscopically active and can be used for the evaluation of biomolecules in vitro. 3-Phenyl-1,2,4-oxadiazol-5-ol can be used as an alternative to ethidium bromide for the detection of nucleic acids in agarose gel electrophoresis. It has been shown to inhibit protein synthesis in bacteria by binding to ribosomes and inhibiting protein synthesis.</p>

<p>Fibrinolysis Inhibiting Factor is a surface glycoprotein that belongs to the group of human serum proteins. It has been shown to be involved in the pathogenesis of bowel diseases and is a target for dextran sulfate. Fibrinolysis inhibiting factor binds to the surfaces of cells and blocks blood coagulation by interfering with the conversion of fibrinogen into fibrin. The protein also binds calcium ions and prevents them from being deposited on cell surfaces, thereby preventing inflammatory reactions such as inflammation of the bowel. Fibrinolysis inhibiting factor has been shown to activate monoclonal antibodies in vitro, which may explain its effect on inflammatory bowel disease.</p>

<p>Please enquire for more information about (3a,5a,17a)-19-Norpregnane-3,17-diol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Allopurinol-d2 is an inhibitor of xanthine oxidase, which is an enzyme that catalyzes the conversion of hypoxanthine to xanthine and then to uric acid. Allopurinol-d2 is used for the treatment of gout and hyperuricemia. The compound was expressed in Escherichia coli and purified by electrospray ionization mass spectrometry. It has been shown to inhibit methyltransferase activity, thereby decreasing the production of urate. Allopurinol-d2 has also been shown to decrease disease activity in animal models of colitis and ulcerative colitis.</p>

<p>(2-(Bromomethyl)phenyl)methanol is an acceptor of a palladium complex. It is used in the synthesis of amides and other functional groups, as well as in catalysis. 2-(Bromomethyl)phenyl)methanol can be quaternized with methyl iodide to form a bromoalkylamine. The reaction proceeds via an amide group on the bromoalkylamine and a hydrogen atom from the alkyl halide. This process is known as "supramolecular" or "intermolecular" hydrogen bonding. It has been found that 2-(Bromomethyl)phenyl)methanol forms complexes with palladium through intermolecular hydrogen bonding, which are more stable than those formed by other ligands such as phosphines and cyanides.</p>

<p>2-Methyl-2-propanethiol is an electron acceptor and a reagent that can be used for the synthesis of organic compounds. It is soluble in polar solvents, but insoluble in nonpolar solvents. 2-Methyl-2-propanethiol has been shown to react with thiols at concentrations below its optimum concentration. The reaction mechanism is believed to involve adsorption and intramolecular hydrogen transfer. The adsorption process occurs on the surface of the substrate and the intramolecular hydrogen transfer occurs through an intermolecular hydrogen bond with the substrate's hydroxyl group or disulfide bond. When 2-methyl-2-propanethiol reacts with a thiol, it forms a mercaptan group called p2 that contains two substituents, one on each carbon atom. This reaction produces a disulfide bond as well as an electrochemical detector signal known as "activated."</p>

<p>Potassium trimethylsilanolate is a chemical substance that has inhibitory properties. It is a trifluoroacetic acid derivative that inhibits the activity of certain enzymes, such as proteases and lipases. The compound's inhibitory properties are due to its ability to bind to cytochrome cb2 receptors by means of hydrogen bonding. The binding of potassium trimethylsilanolate to the receptor prevents the activation of apoptosis proteins and protein synthesis in cells. This substance also has an inhibitory effect on water vapor, inhibiting the formation of water molecules from hydrogen atoms and oxygen atoms. Potassium trimethylsilanolate can be used as an anti-cancer agent by preventing cell division in tumor cells and preventing cancer metastasis through inhibition of protease activity.</p>

<p>3,4-Dimethoxythiophenol is a chemical compound that is used as a fluorescence probe to study biological functions in cells. It reacts with hydroxyl groups and other reactive sites on proteins, including sulfhydryl groups, thiols, and amines. 3,4-Dimethoxythiophenol has been shown to inhibit the viability of cancer cells (e.g., prostate cancer cells) by interfering with the function of dehydrogenase enzymes. 3,4-Dimethoxythiophenol also inhibits growth of microglia (cells that protect neurons) in vitro. This inhibition is due to the production of reactive oxygen species by the microglial cells. The chemical structure of this compound includes a hydroxyl group and two methoxy groups.</p>

<p>Potassium methoxide is a strong base that reacts with methanol to produce potassium metal and methanol. It has been used as a model system for studying the reaction mechanism of metal carbonyls. The reaction solution is heated to produce glycol esters, which are catalyzed by the potassium metal. This process can be used to synthesize biologically active molecules, such as anti-inflammatory drugs, which are difficult to make using conventional methods. Potassium methoxide has also been shown to have protective effects against metabolic disorders in mice and has biological properties that may be useful in the treatment of infectious diseases.</p>

<p>3-O-Benzyl estriol is a synthetic estrogen that is used to treat menopausal symptoms. This drug has been shown to have a high affinity for the estrogen receptor, and it is also able to activate the estrogen receptor in cells. 3-O-Benzyl estriol has been shown to be more potent than other estrogens such as estrone or estriol and has been shown to increase the synthesis of proteins by increasing RNA synthesis. 3-O-Benzyl estriol is conjugated with glucuronic acid and excreted in the bile. It also has a number of metabolic transformations, including pyrolysis, which produces cyanamid and triethylamine.</p>

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<p>2-Cyclopentyl-4-chlorophenol is a synthetic fatty acid that is used as an antiviral agent. It inhibits the synthesis of fatty acids by inhibiting the conversion of 2,4-dienoyl CoA to 3-hydroxyacyl CoA. 2-Cyclopentyl-4-chlorophenol has been shown to be effective against a number of test organisms, including bacteria such as staphylococcus and virus such as herpes simplex virus. 2-Cyclopentyl-4-chlorophenol inhibits viral protein synthesis by blocking the action of host enzymes required for this process. The target cell for this drug is the host cell infected with a virus. This drug also has antihelminthic properties and can be used to treat parasitic infections caused by schistosoma haematobium and clonorchis sinensis worms. 2CPCP's structural formula is shown below:</p>

<p>3-Buten-1-ol is a reactive, anhydrous alcohol that can be used as a model system for hydrogen bonding. It can also be used to demonstrate the uptake of hydrochloric acid and hydroxyl group substitution reactions. 3-Buten-1-ol is soluble in organic solvents such as benzene and chloroform, but insoluble in water. The structural analysis of 3-buten-1-ol has been performed using spectroscopic techniques such as laser ablation and x-ray diffraction to determine its molecular formula. The reaction solution of 3-buten-1-ol with zirconium oxide has been shown to produce intramolecular hydrogen bonds and solid catalysts.</p>

<p>1,2-O-Dioctadecyl-sn-glycerol is a hydrogenated glycerol that can be used as an advance in synthetic chemistry. It can be hydrogenolyzed to produce choline and cyclic phosphatidylglycerols. The catalytic properties of 1,2-O-dioctadecyl-sn-glycerol are due to its ability to react with chloride or cadmium chloride to form dialkyl glycerols. This product is also used in the synthesis of cadmium.</p>

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<p>(2S,3S)-(+)-1,4-Bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol is a chiral phosphine ligand. It has been used as an optical catalyst for styrene polymerization and as a homogeneous catalyst for the electrochemical oxidation of cyclic aldehydes. This compound has also been used in preparative voltammetric studies of phosphines and diphosphines. (2S,3S)-(+)-1,4-Bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol can be obtained by reduction of bis-(diphenylphosphine)ethane with lithium aluminum hydride or sodium borohydride. This compound is soluble in solvents such as benzene and chloro</p>

<p>b-Gamma hexenol is a chemical compound that belongs to the group of odorants. It is a volatile compound that has been identified as an important component in the fragrance of many flowers, such as roses and lavender. b-Gamma hexenol has been found to have significant binding affinity for proteins and enzymes, which may be due to its ability to form soluble complexes at the interface between organic phases and aqueous solutions. b-Gamma hexenol is used in vitro assays as a pharmacological agent that blocks acetylcholine release from nerve endings, thereby reducing pain sensation. In addition, it is also used as an anion radical scavenger due to its high resistance against acid hydrolysis. !--</p>

<p>5alpha-Androst-16-en-3alpha-ol is a pheromone that is produced by the human body. It has been shown to be a potent inducer of transcriptional activation in mammalian cells. 5alpha-Androst-16-en-3alpha-ol also has biological properties that are similar to those of androstenol, another pheromone produced by the human body. 5alpha-Androstenol binds to the androgen receptor, which then regulates gene transcription and protein synthesis in target cells. This process can lead to changes in cell metabolism, proliferation, or apoptosis. It has been shown that 5alpha-androstenol can increase testosterone levels in humans as well as other primates such as rhesus monkeys. The odorant binding site of 5alpha-androstenol is unknown; however, it may be able to bind with odorant receptors through hydrophobic interactions.</p>

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<p>Tris(dimethylaminomethyl)phenol (TDAP) is a compound that has been used as an additive in detergents, paints, and sealants. TDAP is a reactive chemical with the potential to cause adverse effects in humans such as allergic reactions and environmental pollution. TDAP is classified as an extremely hazardous substance by the United States Environmental Protection Agency. TDAP can be found in many household products and building materials, including paint and sealants. TDAP can also be found in cosmetics such as shampoos, lotions, and deodorant. TDAP may also be found in some types of food packaging materials. Long-term exposure to TDAP may lead to calcium carbonate deposits on the lungs or kidney stones due to increased levels of boron nitride-induced calcium oxalate crystals in urine.</p>

<p>Please enquire for more information about R-(-)-3-Quinuclininol HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>This is a broad-spectrum antibacterial agent that inhibits bacterial DNA gyrase. It is active against atypical bacterial species, such as Chlamydia and Mycoplasma, and has been shown to be effective against certain strains of the methicillin-resistant Staphylococcus aureus (MRSA) bacteria. This drug also inhibits the growth of other bacteria by binding to their DNA. The drug is used in combination with other antibiotics to treat infections caused by Clostridium difficile, Helicobacter pylori, Borrelia burgdorferi, and Salmonella enterica. However, this drug does not work against Pseudomonas aeruginosa or Enterobacteriaceae infections.</p>

<p>Arjunolic acid is a hypoglycemic agent that belongs to the group of pharmacological agents. It is a reactive compound, which can be found in pueraria lobata and melaleuca alternifolia. Studies have shown that arjunolic acid has an effect on mitochondrial membrane potential, enzyme activities, and cardiac function. This compound also has anti-inflammatory activity and could be used for the treatment of inflammation. Arjunolic acid may have many other effects due to its ability to inhibit proinflammatory transcription factors such as NF-κB and AP-1.</p>

<p>3-Bromo-2-nitrophenol (3-BNP) is a brominating agent that can be used in the synthesis of a variety of compounds. It is prepared by the refluxing of 3-bromo-2-nitrobenzene with lithium chloride, followed by treatment with trifluoromethanesulfonic anhydride to yield 3-bromo-2-(trifluoromethyl)phenoxyacetic acid. The product can also be obtained from 2,4,6-trinitrophenol and NBS. 3-BNP has shown chemoselectivity for chlorides relative to iodides or fluorides. The yields are higher when it is used in coupling reactions and permutations with lithium or magnesium.</p>

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<p>4-Methyl estradiol is an estrogen that is a naturally occurring metabolite of estradiol. It has been shown to have weak estrogenic effects and may be used in low doses to treat breast cancer. 4-Methyl estradiol binds to the estrogen receptor with high affinity, which leads to its activation and subsequent translocation into the nucleus, where it binds to DNA and regulates gene transcription. The binding of 4-methyl estradiol to the receptor also stimulates the production of other hormones such as progesterone and estrone.</p>

<p>2,2-Dimethyl-1-propanol (DMPA) is an inorganic acid that can be used as a coagulant for wastewater treatment. It has been shown to be effective in removing malonic acid from water at pH 4.0 and below. The reaction mechanism of DMPA is not fully understood, but it is thought to involve the formation of a hydroxyl group on the methyl group of DMPA, which then reacts with the acid and releases hydrogen ions. The hydrogen ions react with sodium carbonate to form sodium bicarbonate and release water vapor. This process continues until all the DMPA has reacted or until there is no more acid present. Asymmetric synthesis of DMPA is possible using neopentyl alcohol and fatty acids as starting materials.</p>

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<p>2,3,4-Trifluorophenol is a chemical control agent that is used as an intermediate in the synthesis of organic compounds. It reacts with hydroxyl groups to form 2,3,4-trifluoroacetophenone from a proton. The compound has low light and x-ray absorption properties and is typically used in liquid crystal compositions. Chemical ionization experiments have shown that 2,3,4-trifluorophenol binds to copper oxide and forms copper trifluoride. This compound also has been found to be conjugated with neutral ph phenols and chlorinated with chlorine atom.</p>

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<p>Produces a fluorogenic signal in the presence of peroxidase</p>

<p>2-Hydroxyquinoline-4-carboxylic acid is a carboxylate that is structurally classified as a multidrug. It has been shown to inhibit bacterial efflux pumps and target enzymes, such as cancer cells and multidrug resistant bacteria. 2-Hydroxyquinoline-4-carboxylic acid also has potent antibacterial activity against Streptococcus faecalis, an opportunistic pathogen that causes infections in the urinary tract and on skin wounds. The fluorescence properties of this compound can be used for fluorescent labeling of biomolecules or for sensing applications.</p>

<p>3-Methyl-1H-1,2,4-triazole-5-thiol is a coagulant agent that has been shown to be effective in the field of wastewater treatment. 3-Methyl-1H-1,2,4-triazole-5-thiol binds metal ions and prevents them from catalyzing reactions in the filtrate. It also has an inhibitory effect on polymerization reactions by binding to functional groups. 3MTH is used as a coagulant additive in many industries, such as papermaking, textile printing and dyeing, food processing and leather tanning. The use of 3MTH has been shown to reduce the amount of water needed during the production process. This product can also be used for coatings and other applications where it is necessary to prevent corrosion or environmental pollution by metal ions.</p>

<p>3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone is a crystalline organic base. It is used as an intermediate in the synthesis of piperazine derivatives. 3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone can be used to acetylate phenols and amines. This compound also has been shown to be useful in the industrial production of carbostyril and other pharmaceuticals. 3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone is also a high yield coupling agent for the production of heterocyclic compounds such as 1,5,6,8-tetrahydropyrimidines and benzimidazoles.</p>

<p>5-Chloropentanol is a reactive compound that can be used as an epidermal growth factor. It has been shown to have potentiating effects on the production of epidermal growth factor in a biological sample. 5-Chloropentanol has also been shown to increase the rate of cell proliferation, which could be due to its ability to generate reactive chloroform in cells. It is not known whether 5-Chloropentanol has any carcinogenic properties.</p>

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<p>Naphthalen-2-ethanol is a primary alcohol that has been synthesized and immobilized onto boron nitride. It can be used as a synthetic reaction rate indicator. Naphthalen-2-ethanol is soluble in organic solvents such as methanol, which can be used to determine the concentration of methanol in solution by observing the change in absorbance at 230 nm. This compound has functional groups such as carbinols, which are characterized by their high reactivity and ability to form esters, ethers, amides, or nitriles. Naphthalen-2-ethanol also reacts with lipases to produce polyamines and with chromatography to produce substitutive nomenclature.</p>

<p>Chromagnol is a drug that inhibits the enzyme protein kinase C (PKC). It has been shown to have inhibitory properties on cardiac muscle cells and whole-cell recordings of heart cells. Chromagnol has also been shown to affect the function of bowel disease, including papillary muscle. Chromagnol has been shown to have effects on cardiac and atrial tissue. This drug may be a potential treatment for autoimmune diseases, such as multiple sclerosis, or other diseases that are caused by PKC overactivity. The mechanisms of action are not fully understood but it is believed that chromanol binds to the cytosolic Ca2+ ion channel, preventing it from opening and releasing Ca2+, which leads to an increase in intracellular Ca2+.</p>

<p>4-Hydroxy-7-methoxyquinoline is an anti-malarial drug that belongs to the class of trimethyl, trifluoromethyl group. It is a cyclic compound and its synthesis starts with cyclization of the methyl derivative, which forms a ring. This product is used in clinical practice as an inhibitor of malarial protozoa and has been shown to have mechanistic effects on the cytochrome bc1 complex containing red blood cells. 4-Hydroxy-7-methoxyquinoline also inhibits the growth of bacteria by binding to the enzyme methionine synthase, which is involved in the biosynthesis of methionine from homocysteine. The product also has an inhibitory effect on DNA synthesis and protein synthesis.</p>

<p>Please enquire for more information about 2-Amino-1-(2,3-dihydro-benzofuran-5-yl)-ethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Methyl-2-pyridylamino)ethanol (2MPE) is a small molecule that has been studied for its potential use as an inhibitor of the enzyme protein kinase C-alpha. The reaction mechanism of 2MPE with rosiglitazone, a drug used to treat type II diabetes mellitus, has been shown to be nucleophilic and proceeds through an addition-elimination mechanism. The kinetic parameters for this reaction have been determined by studying the effect of temperature on the reaction rate. Density measurements indicate that 2MPE is a low-molecular weight compound with a density of 1.08 g/mL at 25°C and 1 atm pressure. This study also found that microreactors are capable of producing high reaction yields in shorter amounts of time than larger reactors, making them well suited to the synthesis of small molecules such as 2MPE.</p>

<p>Rac-1,2-bis-palmitoyl-3-chloropropanediol is a dispersive molecule that is composed of a fatty acid and a chlorinated derivative of palmitic acid. It is used to calibrate the mass spectrometer and as an internal standard in quantitative analysis. Rac-1,2-bis-palmitoyl-3-chloropropanediol reacts with electrospray ionization with a dose-dependent response. It has been shown to be toxic to kidney cells at high doses but not at low doses. This chemical has been detected in food samples after being absorbed from the gastrointestinal tract. Rac 1,2-bis-palmitoyl 3 chloropropanediol can be found in the dipalmitate form or as formic acid.</p>

<p>Azacyclonol is a cytotoxic drug that prevents the proliferation of cancer cells, by inhibiting DNA synthesis. This drug has shown to be effective in treating bowel diseases, and is also used as a pharmacological agent for the treatment of infectious diseases. Azacyclonol has been shown to inhibit the growth of bacteria such as Mycobacterium tuberculosis, Listeria monocytogenes, and Haemophilus influenzae. It is also used to treat infections caused by HIV. The mechanism of action for azacyclonol is unknown; however, it may be due to its ability to bind with cell factor or stem cell factor.</p>

<p>7-Methylquinoline is an organic compound that can be used to synthesize antimalarial drugs. It is a quinoline derivative with a methyl group at the 7th position. The structure of 7-methylquinoline contains a nitrogen atom and hydrogen atoms, which are bonded to fluorine, chlorine, and bromine atoms. This molecule has been shown to be stable in the presence of Friedel-Crafts catalysts and chloride ions. The reaction mechanism for 7-methylquinoline is intramolecular hydrogen transfer from the chloroform molecule to the quinoline ring system. The formation rate for this compound is slow because it requires two steps: nucleophilic substitution and electrophilic addition reactions.</p>

<p>Please enquire for more information about 2-Valeryl-17'-estradiol 17-valerate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Pyridine-2,5-diol is a bacterial metabolite that is the product of the enzyme pyridoxal 5'-phosphate oxidase. This enzyme has been shown to be involved in microbial metabolism and enzymatic reactions, such as the conversion of picolinic acid to pyridine-2,5-diol. Pyridine-2,5-diol has been found to be expressed in wild type strains but not in mutant strains. The gene product for this enzyme has also been identified as maleate dehydrogenase.</p>

<p>Please enquire for more information about 2-[(4-Phenylpiperazin-1-yl)carbonyl]phenol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dodecane-1-thiol is a chemical that is used as an ingredient in the production of nanoparticles. It has been shown to have high resistance to sodium salts and is chemically stable. Dodecane-1-thiol can be synthesized by reacting dodecane with hydroxylamine and mercaptan, which are both highly reactive compounds. Dodecane-1-thiol has a hydroxyl group on the thiol group and a dimethyl fumarate molecule attached to it. The hydroxyl group reacts with mercaptan, while the dimethyl fumarate molecule attaches to the thiol group to provide stability. Dodecane-1-thiol can also be synthesized using polymerization reactions.</p>

<p>3,5-Dimethyl-1-hexyn-3-ol is a reactive chemical that is used as a polymerase chain reaction (PCR) substrate film. The film has an active surface and can be used to detect the presence of DNA by adding colloidal gold. 3,5-Dimethyl-1-hexyn-3-ol reacts with the glycol ether and surfactant to form a hydrophobic film on the surface of the substrate film. The hydrophobic films are nonpolar and do not mix with water, so they do not dissolve in water. This allows for detection of DNA by using plasma mass spectrometry or eugenol, which reacts selectively with double bonds in DNA. 3,5-Dimethyl-1-hexyn-3-ol is also used in wastewater treatment as an antimicrobial agent to control bacterial growth.</p>

<p>4-Cinnolinecarboxaldehyde is an organic compound that belongs to the group of cinnoline. It is a colorless liquid that can be used as a precursor in the production of aluminum metal. 4-Cinnolinecarboxaldehyde reacts with lithium aluminum hydride to form a compound that can be used as a reducing agent in organic chemistry. 4-Cinnolinecarboxaldehyde is also used as a precursor for preparing other compounds, such as lithium aluminum hydride and lithium aluminum trihydride.</p>

<p>2-Chlorothiophenol is a chemical compound that belongs to the group of fatty acids. It is synthesized by reacting phosphorus pentachloride with 2-chloroethanol in the presence of magnesium salt. The corresponding molecule has a diameter of 4.8 Å and a thermal expansion coefficient of 1.5×10 K−1, which is similar to the thermal expansion coefficients of fatty acids. 2-Chlorothiophenol reacts with carbonyl groups in the presence of oxygen to form 2-chlorophenol and hydrogen chloride gas, which are products that can be detected using spectroscopic techniques such as infrared or nuclear magnetic resonance spectroscopy. The reaction mechanism for this reaction is not well understood, but it is thought that the intramolecular hydrogen acts as an electron donor to form a pi bond between carbon atoms on adjacent molecules, leading to formation of an oxygenated molecule. 2-Chlorothiophenol also has protein</p>

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<p>1-Methyl-1H-benzimidazol-2-yl)methanol is a mononuclear, ligand anion with a sulfate group. The compound has a molecular weight of 180.07 and its chemical formula is C6H5NOSO3S. It is soluble in water and alcohols, but insoluble in ethers and chloroform. 1-Methyl-1H-benzimidazol-2-yl)methanol reacts with oxygen to form the corresponding peroxide, which has a boiling point of 228°C at 760 mm Hg pressure. This compound also reacts with nitric acid to form the corresponding nitrate salt, which can be precipitated by adding sodium chloride or ammonium chloride.</p>

<p>4-Pregnen-17a,20b-diol-3-one is a synthetic androgen with anabolic and androgenic activity. It has been shown in animal studies to increase maximal responses of the reproductive tract to gonadotropin stimulation. 4-Pregnen-17a,20b-diol-3-one binds to the activin receptor on the cell membrane, which leads to increased expression of a gene encoding for 3β-hydroxysteroid dehydrogenase (3βHSD), an enzyme involved in testosterone synthesis. This drug also increases the sensitivity of ovarian follicles to gonadotropins and decreases basal plasma levels of LH and FSH. 4-Pregnen-17a,20b-diol-3-one has not been found to be toxicologically significant at doses up to 10 mg/kg body weight per day.</p>

<p>2-(2-Methoxyphenoxy)ethanol (2-MPE) is a metabolite of propanediol, which is a precursor in the synthesis of polyurethanes. 2-MPE can be oxidized by monooxygenases to form syringyl and other reactive metabolites. Basic hydrolysis may also produce monomers such as phenols, alcohols, and carboxylic acids. Syringyl is one of the metabolic products of 2-MPE, which has been shown to be resistant to degradation by basidiomycete fungi.</p>

<p>Chlormadinol acetate is a stable complex of a fatty acid and an antibiotic that is used to treat infections caused by bacteria. It has been shown to have high resistance to antimicrobial agents, including amoxicillin-clavulanic acid, tetracycline, and multidrug efflux pumps. Chlormadinol acetate has also been shown to inhibit the growth of certain cancer cells in vitro and in vivo using gene therapy. This drug also inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit and preventing the formation of a functional 70S ribosome. Chlormadinol acetate has been shown to be clinically relevant in mice when used with amoxicillin-clavulanic acid or tetracycline.</p>

<p>CP 55940 is a cannabinoid receptor agonist that inhibits acetylcholine release in the brain and has been shown to cause neuronal death. CP 55940 binds to the α7 nicotinic acetylcholine receptor, which is important for memory and learning. The binding of this drug causes an increase in guanine nucleotide-binding protein (G protein) activity by reducing the rate of GTP hydrolysis, leading to inhibition of adenylyl cyclase activity and subsequent decrease in cAMP levels. CP 55940 has significant up-regulation of toll-like receptors following exposure, which leads to an increased immune response. This drug can also cause bowel disease or side effects such as seizures and psychotic symptoms. CP 55940 can interact with other drugs, including cannabinoids that may lead to serious side effects.</p>

<p>Dipalmitoylglycerol is a fatty acid that is naturally found in catfish. The optimal conditions for the synthesis of dipalmitoylglycerol from tripalmitin have been determined by surface methodology to be at pH 5 and at 0°C. Dipalmitoylglycerol has been shown to bind to the enzyme acetyl-CoA carboxylase, which is involved in the synthesis of fatty acids, and prevent its activation. As a result, there is no production of malonyl CoA, which is an important precursor in the synthesis of fatty acids. This may be beneficial for infants because it prevents them from developing allergies and asthma.</p>

<p>1-Docosahexaenoin-2-oleoyl 3-phosphocholine is a phospholipid compound that has shown promising potential in cancer research. This compound belongs to the steroid family and has been studied for its diagnostic capabilities in detecting breast cancer. It has also been investigated for its antiviral properties, particularly against HIV-1. Additionally, 1-Docosahexaenoin-2-oleoyl 3-phosphocholine has been researched for its use in diabetes management, with studies exploring its effects on insulin secretion and glucose metabolism. This compound has also been evaluated as a potential therapeutic agent for certain types of tumors due to its ability to inhibit tumor growth.</p>

<p>3-Methylether-estradiol is a naturally occurring estrogen that is found in humans and other mammals. It binds to estrogen receptors on the plasma membrane, which stimulates cell growth, protein synthesis, and modulates the immune system. 3-Methylether-estradiol has been shown to inhibit taurocholic acid induced hypertension in rats by blocking the conversion of angiotensin I to angiotensin II. In addition, this compound has been shown to have anti-inflammatory properties and can be used as an antihypertensive agent. 3-Methylether-estradiol has also been shown to increase blood pressure in pregnant rats when given at bolus doses. This drug should not be prescribed for use during pregnancy because it can cause fetal death.</p>

<p>Please enquire for more information about Midazolam-d4 maleate - 100 mg/mL in methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromoallyl alcohol is a halogenated aromatic hydrocarbon that is an analyte in the chemical analysis of soil. It is also used as a reagent for the debromination of 2-bromopropane and as a dehalogenating agent for the removal of bromine from organic compounds. 2-Bromoallyl alcohol can be distilled at high temperatures, but it will volatilize if heated to 80°C or higher. It has been reported that 2-bromoallyl alcohol was found to be present in all replicates analyzed. The recovery of this compound ranged from 83% to 114%. 2-Bromoallyl alcohol is used as a reagent in organic synthesis, such as in palladium catalyzed couplings with boronic acids and esters. This compound may also be used to synthesize N-(2-hydroxyethyl)hydroxylamines by reacting with sodium hydroxide</p>

<p>Octafluoro-1,6-hexanediol is a cyclic diol with the chemical formula C6F14O2. The compound is produced by the reaction of hexafluoropropylene oxide and hydrogen fluoride in the presence of a catalyst. This process can be repeated to produce higher molecular weight compounds such as octafluoro-1,8-octanediol (C8F18O2) and octafluoro-1,10-decanediol (C10F22O2). Octafluoro-1,6-hexanediol has been studied using spectroscopies and x-ray crystallography techniques. X-ray crystallographic studies have shown that this molecule has an intramolecular conformation with one hydroxy group on each end of the molecule. Octafluoro-1,6-hexanediol forms crystals that are colorless or light yellow in color. Crystals are monoclin</p>

<p>Sodium benzyloxide is an alkanoic acid with the chemical formula CH3C6H2O2. It is used as a matrix metalloproteinase inhibitor in the synthesis of bicyclic heterocycles. It is also used in asymmetric synthesis and as a substrate for enzyme inhibitors. Sodium benzyloxide has been shown to be effective against herpes simplex virus by preventing viral replication and inducing apoptosis.</p>

<p>4-(Butoxymethyl)-2-methoxyphenol is an antimicrobial agent that has been shown to be effective against Candida glabrata. It is a non-ionic surfactant with a C8 alkyl chain, which is derived from the reaction of butyl alcohol and phenol. 4-(Butoxymethyl)-2-methoxyphenol can be used in oral care products such as toothpaste or mouthwash. This product also has a control analysis for sodium citrate and root powder, which may be due to its fatty acid and magnesium salt content.</p>

<p>4-Hydroxy-17β-estradiol (4-OHE2) is a reactive metabolite of 17β-estradiol that binds to DNA and has been shown to have carcinogenic potential. The catechol-o-methyltransferase enzyme catalyzes the conversion of 4-OHE2 to 4-hydroxycatechol, which can then be further methylated by estrogen sulfotransferase or sulfatase to estrone and estrone sulfate. It has been shown that 4-OHE2 may be a potential biomarker for breast cancer. Experimental studies have shown that 4-OHE2 may act as an antioxidant in cancer tissues, but its activity has not been demonstrated in normal tissues. In order to demonstrate the ability of 4-OHE2 as an antioxidant, its activity was tested in vitro using human breast cancer cells (MDA MB 231). Results showed that 4-OHE2 decreased oxidative stress levels in these cells,</p>

<p>4-Amino-3-bromoisoquinoline is an isocyanide that reacts with nucleophilic heteroatoms such as the amino group. It also reacts with bromine to form a bromopyridine. The nitrile group of 4-amino-3-bromoisoquinoline can be reduced with sodium borohydride to produce 4-aminoquinoline. This compound has shown potential for use in chemotherapy and treating bacterial infections.</p>

<p>N-Acetyl-4-S-cysteaminylphenol is a tyrosinase inhibitor that is used in the treatment of skin disorders such as melasma and vitiligo. It slows the production of melanin by inhibiting tyrosinase activity and may be useful for treating some types of skin cancer. N-Acetyl-4-S-cysteaminylphenol also inhibits the growth of tumor cells, but not normal cells, which may be due to its ability to inhibit protein synthesis. This compound has been shown to inhibit cyclic nucleotide phosphodiesterases and cellular processes associated with the proliferation of cancer cells.</p>

<p>2,6-Dichlorophenol is a hydrogen-bond inhibitor that inhibits the reaction of receptors with their specific treatment. It has been shown to have an inhibitory effect on the light-induced activation of receptor cells and to inhibit the reaction mechanism of analytical methods. 2,6-Dichlorophenol has also been shown to be effective in synchronous fluorescence spectroscopy as a probe for detecting hydrogen bonds in biological samples. The chemical structure of 2,6-dichlorophenol is C6H4Cl2O. It is soluble in water and reacts with acids to form hydrogen chloride gas and 2,6-dichlorophenol hydrochloride (C6H3Cl2O).</p>

<p>2-Heptanol is a colorless liquid with a pungent odor. It is soluble in water and has a high boiling point. 2-Heptanol is an intermediate in the synthesis of fatty acids, which are used for the production of soaps, lubricants, and waxes. 2-Heptanol reacts with potassium hydroxide to produce potassium 2-heptoxide, which is soluble in water. The reaction products are caproic acid and hydroxy group. The transport properties of this compound are not well known.</p>

<p>Please enquire for more information about 7-Bromo-3-O-acetyl pregnenolone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(+)-Cis-abienol is a diterpene that is found in the leaves of the tobacco plant. It has been suggested to be involved in the synthesis of abscisic acid, which is an important hormone related to plant responses to water and salt stress. (+)-Cis-abienol may also have insecticidal properties and may play a role in resistance to insects. (+)-Cis-abienol has shown activity as an analytical reagent for the detection of hydroxyl groups, due to its UV absorption at 275 nm. The signal peptide sequence for this compound has been determined by analysis of tobacco sequences. This molecule's phase behavior can be predicted from its X-ray crystal structures and it is soluble in organic solvents such as benzyl alcohols or ethers. The mechanism for the reaction between (+)-cis-abienol and dehydroabietic acid has not yet been elucidated but it is thought that benzyl</p>

<p>8-Bromo-2-methylquinoline is a naphthalene derivative that has an oxidant function. It can be used as a solvent for chlorobenzene and as a catalyst for the production of bipyridines and piperazine. 8-Bromo-2-methylquinoline is also used as a ligand in the preparation of metal complexes. This compound reacts with methyl groups, chlorine, and halides to form methyl quinolines and dichloromethanes. 8-Bromo-2-methylquinoline may react with fatty acids to form polyunsaturated acid esters or with polyunsaturated fatty acids to form polyethers.</p>

<p>Tetrahydroquinoline-3-carboxylic acid is a crystalline, water-soluble compound. It is an intermediate in the synthesis of l-phenylalanine, paraformaldehyde and formaldehyde. Tetrahydroquinoline-3-carboxylic acid can be hydrolyzed to produce formic acid and hydrogen chloride. This product is also optically active and can be used as an indicator for hydroiodic acid.</p>

<p>1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methyl-isoquinoline is a chemical compound that has been used as an intermediate in the synthesis of pharmaceuticals. It is also a useful building block for the production of other chemicals. This compound is soluble in water. 1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methyl-isoquinoline has shown to be a versatile and high quality reagent with many research applications.</p>

<p>4-[(4-Chlorophenyl)phenylmethyl]-1-piperazineethanol dihydrochloride is a cholinergic drug that is used to treat allergic rhinitis in children and adults. It has been shown to be well tolerated in pediatric patients and geriatric patients, as well as being an innovative, labile, and biopharmaceutical compound. 4-[(4-Chlorophenyl)phenylmethyl]-1-piperazineethanol dihydrochloride is not metabolized by the liver and does not have significant side effects. It has a low potential for abuse because of its low solubility in water. It is an antihistamine that blocks the action of histamine at H1 receptors on smooth muscle cells in the nose, which helps reduce nasal congestion and sneezing.</p>

<p>Please enquire for more information about 11-Heneicosanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (7-bromo-2H-1,3-benzodioxol-5-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-[(4-Aminopiperidin-1-yl)methyl]phenol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (S)-1-(tert-Butoxycarbonyl)-2-azetidinemethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Indanol is a hydroxy compound that has a human immunodeficiency virus (HIV) replication inhibitor, antiviral activity, and structural formula. It has been shown to have anti-HIV activity in vitro at concentrations of 0.1 μM and 1 μM. 2-Indanol inhibits the process of reverse transcription by specifically binding to the hydroxyl group of the viral RNA polymerase and preventing it from making a hydrogen bond with the viral DNA template strand. 2-Indanol also slows down HIV replication by inhibiting protein synthesis. This inhibition is due to its ability to inhibit phosphorylation and dephosphorylation reactions in the host cell's ribosome machinery, which are required for protein synthesis. 2-Indanol has been shown to be active against covid-19 pandemic influenza viruses and has been used as an antiviral agent in mice infected with these viruses.</p>

<p>3-Nitro-benzene-1,2-diol is an inhibitor of catechol-o-methyltransferase (COMT), which catalyzes the transfer of a methyl group from S-adenosyl methionine to dopamine. This results in the formation of 3-O-(methylamino) catechol. COMT inhibitors are used as pharmaceutical preparations for the treatment of Parkinson's disease and other diseases involving dopamine. 3-Nitro-benzene-1,2-diol has been shown to inhibit COMT and prevent the breakdown of dopamine in the brain, which may be beneficial for treating Parkinson's disease and other nervous system diseases.</p>

<p>Please enquire for more information about [1-(3-Methylbutyl)-1H-benzimidazol-2-yl]methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Dimethylamino)ethanol is a colorless liquid that has a molecular weight of 78.1 g/mol and a boiling point of 176.1 °C. It can be found in many household products as well as cosmetics, pharmaceuticals, and chemical manufacturing. 2-(Dimethylamino)ethanol is a precursor to acetaldehyde and acetic acid, which are important intermediates in the production of polymers such as nylon. It can also be used to synthesize other chemicals such as dimethylformamide, ethylene glycol, and methyl methacrylate. This chemical reacts with calcium to form insoluble calcium 2-(dimethylamino)ethanolate (Ca(DMAE)). This reaction is reversible and the equilibrium can be shifted by changing the pH or adding another reactant such as hydrogen peroxide or hydroxide ions.</p>

<p>6-Heptyn-1-ol is a naturally occurring chemical compound that has been isolated from the human colon and shown to have potent cytotoxicity against human colon carcinoma cells. 6-Heptyn-1-ol inhibits the growth of cancer cells by inducing apoptosis, the process by which a cell commits suicide. It also inhibits pancreatic lipase, an enzyme involved in fat digestion. 6-Heptyn-1-ol has been shown to be a chiral molecule with two enantiomers that can be synthesized artificially. The (R) form of 6-heptyn-1-ol is more potent than the (S) form in inducing apoptosis and inhibiting pancreatic lipase activity.</p>

<p>(S)-1,2,3,4,5,6,7,8-Octahydro-1-[(4-methoxyphenyl)methyl]isoquinoline (acetate salt ) is a diphosphine that can be used as a catalyst to produce formic acid from methanol and carbon monoxide. This product is an enantiomer of picric acid and has been shown to be an effective additive in the crystallization of picric acid. The acetate salt is also optically pure.</p>

<p>Please enquire for more information about (S)-5,6,6a,7-Tetrahydro-6-methyl- 4H-dibenzo[de,g]quinoline-10,11-diol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>