Alcohols

3-Amino-4-bromophenol is an industrial chemical that is used in the diazotization and reduction reactions. 3-Amino-4-bromophenol can be synthesized by reacting hydrazine with iron oxide and nitrite in a condition of acetone and sodium nitrite. The product yield for this reaction is about 90%. 3-Amino-4-bromophenol crystallizes from acetone as a white powder.

<p>1-Palmitoyl-rac-glycerol is a fatty acid that contains nitrogen atoms. It has hypoglycemic effects and is used to treat metabolic disorders. 1-Palmitoyl-rac-glycerol has been shown to have a protective effect on the liver by decreasing the levels of triglycerides in the blood and preventing lipid peroxidation. It also improves glucose metabolism and insulin sensitivity. 1-Palmitoyl-rac-glycerol is an important component of biological membranes, where it forms a hydrophobic region that helps maintain membrane structure. This compound also has hemolytic activity, which may be due to its ability to bind with phospholipids or cell membranes, leading to changes in their permeability or stability. The stability of 1-palmitoyl-rac glycerol can be tested by adding reagents such as sodium nitrite or potassium permanganate, which will cause a color change from yellow to brown if it reacts</p>

<p>1-Naphthyl ethanol is a chromatographic solvent that is used in the reaction rate of lipase. It consists of two hydroxyl groups, one on each naphthalene ring. The hydroxyl groups are separated by a carbonyl group and a sterically hindered boron nitride. This compound is synthesized using triflic acid in methanol and reacts with carbinols to form functional groups. 1-Naphthyl ethanol has been shown to have stereoselective reactions with alkenes and alkynes, which may be due to its ability to form hydrogen bonds.</p>

<p>1-(5-Isoquinolinesulfonyl)piperazine hydrochloride (1-ISOQ-PIP) is a chemical compound that has been shown to inhibit the growth of leukemia cells. It inhibits the expression of leukemia inhibitory factor, which may be due to its ability to introduce modifications into the sequence of DNA. 1-ISOQ-PIP also inhibits pluripotent stem cells and induces adipocyte differentiation. This substance can be used for cancer treatment by inhibiting the growth of leukemia cells and inducing differentiation.</p>

<p>1,3-Dibenzyloxy-2-propanol is a nucleophilic compound that has been shown to be effective against herpes simplex virus. This antiviral agent is also cytotoxic and has high molecular weight. It is acetylated to produce the corresponding acetate ester, which is scalable for industrial production. 1,3-Dibenzyloxy-2-propanol binds to the carbohydrate ligand on the surface of cells and inhibits the growth of viruses by trapping them in a hydrophobic environment. This drug has been shown to inhibit ganciclovir phosphorylation and can be used as an antiviral agent if combined with other drugs such as cannabinoids or nervous system agents. 1,3-Dibenzyloxy-2-propanol also reacts with endogenous ligands such as histidine, glutathione and dopamine receptors.</p>

<p>5-Nitroisoquinoline is a nitro compound that has been shown to be a potential biomarker for liver disease. 5-Nitroisoquinoline is synthesized from the reaction of hydroxylamine, sodium carbonate, and nitric acid. This chemical can also be found in human liver tissue. The titration calorimetry experiments performed on 5-nitroisoquinoline showed that the compound has a high heat of formation (194.1 kJ/mol) and low enthalpy of formation (-19.6 kJ/mol). Vibrational analysis revealed that there are four nitrogens in the molecule and two nitrogen atoms per molecule. X-ray crystal structures were obtained for 5-nitroisoquinoline with different solvents and hydrogen bonding was observed in all cases. Molecular modeling showed that there are five nitro groups, which would explain the name "5-nitro." The five nitrogen atoms coordinate to form a trigonal bip</p>

<p>2,6-Dichlorophenolindophenol is a redox indicator that can be used as an optical sensor for the measurement of hydrogen peroxide and other reactive oxygen species. It has been shown to inhibit caspase-independent cell death in carcinoma cells and is active against the opportunistic fungus Candida glabrata. The optimum concentration for this compound has been determined to be 1 mM.</p>

<p>Please enquire for more information about Gemcitabine monophosphate disodium monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,2,2-tribromoethanol or TBE derives from ethanol, where the hydrogen atoms from one carbon are substituted by bromine. 2,2,2-tribromoethanol is frequently used as initiator for synthesising functionalised polymers with end hydroxyl groups. In addition, 2,2,2-tribromoethanol is also often used in a labroatory setting to anaethetise mice.</p>

<p>cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. This compound is also a useful reagent, speciality chemical, and reaction component. cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride has been shown to be a valuable scaffold for research chemicals with high quality.</p>

<p>4-Methoxybenzyl alcohol is an inhibitor that inhibits the enzyme hydroxylase, which catalyzes the conversion of 4-methylphenol to 4-hydroxymandelic acid. The inhibition of this enzyme leads to a decrease in the production of pro-inflammatory factors, such as leukotrienes and prostaglandins. The inhibition of this enzyme also prevents the release of lysosomal enzymes, which may be a therapeutic target for degenerative diseases. Kinetic data has been collected by measuring the rate at which 4-methoxybenzyl alcohol reacts with hydroxylase in vitro and in vivo. This reaction was found to be second order with respect to substrate concentration, with a half-life of 2.8 hours at 37 degrees Celsius and pH 7.4.</p>

<p>Amodiaquine is a drug that belongs to the class of antimalarial agents. It is used for the treatment and prevention of malaria caused by erythrocytic forms of Plasmodium falciparum. Amodiaquine has shown synergistic effects with other drugs, such as sulfadoxine and pyrimethamine, for the treatment of malaria due to P. falciparum. The mechanism of action of amodiaquine is not well understood, but it may involve inhibition of the Toll-like receptor. Amodiaquine has been shown to inhibit polymerase chain reaction in a concentration-dependent manner and also inhibits polymorphonuclear leucocytes, which are important in innate immunity. In addition, amodiaquine is a hypoglycemic agent and can be used for the treatment of bowel disease.</p>

<p>Please enquire for more information about 5-(3-Methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

6-Methyl-16-dehydropregnenolone acetate (6MDA) is a versatile building block that is used in the synthesis of complex compounds. 6MDA is an intermediate for research chemicals and can be used as a reagent or as a speciality chemical. It has been shown to be useful in the synthesis of many complex compounds, including steroids, nonsteroidal anti-inflammatory drugs, and antibiotics. 6MDA has been shown to have high quality and is a useful scaffold for the synthesis of other compounds.

(R)-(+)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthalenediol is a synthetic compound that is used as a ligand for asymmetric catalysis. It is an optically active compound and can be used in catalytic reactions to produce compounds that are not available through other methods. (R)-(+)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthalenediol is a reactive compound and can be used as a ligand in Diels-Alder reactions. The synthesis of this product can be achieved with high yield by using the synthetic method described.

<p>Dobutamine is a beta-adrenergic agonist that causes the heart to contract and increase blood pressure. It is used for pharmacological treatment of congestive heart failure and ventricular arrhythmias, as well as during angiography of the coronary arteries. Dobutamine stimulates dopamine receptors in the heart, which increases the systolic pressure. Dobutamine has been shown to be effective in improving myocardial contractility, left ventricle function, and cardiac output in patients with chronic congestive heart failure. This drug also improves left ventricular regional wall motion, papillary muscle function, and mitral valve regurgitation. Dobutamine may cause side effects such as nausea, vomiting, headache, or chest pain.</p>

<p>Carboxyethylsilanetriol sodium salt - 25% in water is a reagent that is used to form complex compounds. It can be used as a reaction component or a building block to create more complex compounds, such as new medicines. Carboxyethylsilanetriol sodium salt - 25% in water has been shown to be an efficient and versatile scaffold for the production of fine chemicals and research chemicals. CAS No. 18191-40-7 is a speciality chemical that can react with other organic compounds to form new compounds for research purposes. Carboxyethylsilanetriol sodium salt - 25% in water is a useful intermediate and building block for various synthetic reactions because it can easily react with other organics to form new compounds which are useful in pharmaceuticals, agrochemicals, and other industries.</p>

<p>Medioresinol is a secondary metabolite found in plants belonging to the family Pinaceae. It is a fluorescent compound that can be seen with nmr spectroscopic data and has been identified as a fatty acid. Medioresinol has been studied for its effects on bacteria, fungi, and cancer cells. This compound has shown to inhibit the growth of the bladder cancer cell line 5637A and inhibit the growth of human leukemia cells by blocking protein synthesis. The mechanism of action of medioresinol is not yet well understood, but it may involve an interaction with p-hydroxybenzoic acid or secoisolariciresinol. Medioresinol is also known to have strong anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>3-Nitro-4-(trifluoromethyl)phenol is an amino acid that has been found in fossils of the proterozoic era. It is believed to have played a role in evolution and the onset of life because it was resistant to damage by oxygen free radicals. 3-Nitro-4-(trifluoromethyl)phenol has been shown to be damaging to mesenchymal cells, which are cells that form cartilage and bone, leading to cell death. The chemical damages mesenchymal stem cells, which can lead to diseases such as osteoarthritis or rheumatoid arthritis. Researchers believe that this chemical may have played a role in the orogeny, or mountain formation, that occurred during the late Proterozoic Era.</p>

<p>4,4'-Ethylidenebisphenol is a phenolic compound that has hydroxyl groups in its structure. It is used as a chemical intermediate in the production of resins and coatings. 4,4'-Ethylidenebisphenol is also used as an analytical reagent. It reacts with hydrogen peroxide to form a reactive radical intermediate that can be detected by electron spin resonance spectroscopy. The mechanism of this reaction involves the formation of an intermolecular hydrogen bond between the hydroxyl group on 4,4'-ethylidenebisphenol and the hydrogen peroxide molecule. The reaction solution contains 4-hydroxybenzaldehyde and 2,2-diphenyl-1-picrylhydrazyl radical as intermediates.</p>

<p>2-Phenyl-2-adamantanol is a deuterated analog of 2-phenyl-2-adamantane (C 10 H 16 ) with an isotopic weight of 128. The FTIR spectra show the presence of a new peak at 1728 cm−1, which is attributed to C=O stretching vibrations in the hydroxyl group. The IR spectrum of 2-phenyl-2-adamantanol shows that it has an azide group and two hydrogen bonds. It also interacts competitively with carbachol, but does not interact with atropine. Preparative oriented crystallization was used to isolate this compound from benzene.</p>

<p>3-Hydroxy-2,4,6-tribromobenzyl alcohol is a chemoenzymatic reagent that is used in the production of phenols. It is prepared from acetone and sodium bromide and catalyzes the bromination of phenols. This product has high yield and can be used as a source for 3-hydroxy-2,4,6-tribromobenzyl alcohol. 3-Hydroxy-2,4,6-tribromobenzyl alcohol is also an important reagent in the synthesis of polymers that are used in the production of paints and coatings.</p>

<p>11b-Hydroxy etiocholanolone is a major metabolite of 11-ketotestosterone. It is formed from the reaction of 11-ketotestosterone with either carbon disulphide or plasma cortisol. The physiological levels of 11b-hydroxy etiocholanolone are not well known, but it has been observed that there are higher levels in women than in men. This metabolite is an active form of testosterone and can be detected in urine samples. 11b-hydroxy etiocholanolone has been shown to have a biphasic response to testosterone treatment, where it increases at low concentrations and decreases at high concentrations. This metabolite is also involved in the synthesis of estradiol through the side chain cleavage, which leads to a chromatographic peak during gas chromatography analysis.</p>

<p>4-Hydroxy-5-iodo-3-methoxybenzyl alcohol is a polymer that has been synthesized as a model compound for lignin. It is a synthetic compound, which has not been found in nature. 4-Hydroxy-5-iodo-3-methoxybenzyl alcohol is toxic to bacteria and fungi, but not to mammalian cells. The metabolic products of this compound have not yet been identified.</p>

3-Amino-1-adamantanol hydrochloride (3AAAH) is a versatile building block that can be used for the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent, research chemical, speciality chemical, or useful scaffold in organic synthesis.

<p>Triamcinolone is a synthetic corticosteroid that reduces inflammation, suppresses the immune system, and relieves pain. It inhibits the production of cytokines and other inflammatory mediators by binding to specific receptors located in the cells of the immune system. Triamcinolone acetonide is an ester prodrug that is converted to triamcinolone in vivo. This drug has a long-term efficacy because it can be released slowly over time after intravitreal injection. The pharmacokinetic properties of triamcinolone are determined by its lipophilicity and water solubility. Triamcinolone acetonide has been shown to reduce inflammation in chronic arthritis, as well as reducing symptoms of eye disorders such as uveitis or glaucoma. This drug also prevents tumor growth by inhibiting protein synthesis and gene expression at the level of transcription, which leads to decreased cell proliferation or apoptosis.</p>

<p>Chemically a chlorinated salicylanilide, niclosamide is clinically used as an anthelmintic agent. The action of niclosamide has been proven to proceed by inhibiting the STAT3 signaling pathway. Recently, niclosamide, has been considered as an antiproliferative agent in cancer treatment, e.g. melanoma and colorectal cancer. In 2021, niclosamide has been tested for the treatment of COVID-19 patients.</p>

<p>1,6-Hexanediol diglycidylether is a reactive functional group that has been used in the production of polyurethane elastomers. It is also used as a cross-linking agent and polymerization initiator. The reactive functional group has been shown to form intramolecular hydrogen bonds, which are important for the formation of polyurethanes. 1,6-Hexanediol diglycidylether is an exothermic compound that reacts with deionized water, forming carbon dioxide and hydrogen gas. This product has been shown to cause allergic reactions in clinical studies.</p>

10-Azido-1-decanol is a non-polar solvent with reactive properties. It has been shown to cause cellular damage in proton and 6-chloropurine, which is a precursor for the synthesis of nucleic acids. 10-Azido-1-decanol has been used as an ultraviolet light absorber in strategies to protect tissues from ultraviolet light and it can also be used to study the effects of functional groups on optical properties. 10-Azido-1-decanol's hypochromic behavior makes it useful in bilayer studies because it can be easily distinguished from other solvents or water molecules.

<p>Progesterone is a hormone that regulates the menstrual cycle and plays a key role in pregnancy. It is produced by the corpus luteum, the placenta, and the ovaries. Progesterone is also involved in regulating other functions such as cell growth, fat metabolism, blood clotting, and water balance. The level of progesterone in urine has been shown to be a good indicator of follicular growth during ovulation. In women with metabolic disorders or lactogenic hormone deficiencies, low levels of progesterone can lead to infertility.</p>

<p>(4S)-2,2-Dimethyl-1,3-dioxane-4-methanol is a chemical with the CAS number 85287-64-5. It is used as a building block in organic synthesis. This chemical can be used in reactions to create more complex compounds. (4S)-2,2-Dimethyl-1,3-dioxane-4-methanol is also useful as a scaffold for larger molecules and as an intermediate in the production of other chemicals.</p>

<p>The active substances in LABD-8(17),14-dien-13,19-diol are hexane and diacetate. This product is analysed to be a decidua extract. Alcohols, coniferous extracts, oplodiol, epimanool and ozonization can also be found in this product. Structural analysis reveals that glycerides are the major component of this substance. A variety of other components were also detected in this substance such as methyl ester, aldehydes and diterpenes.</p>

Tetrabromobisphenols (TBB) are skin conditioners that are used in the cosmetic industry. They are derived from fatty acids and have a structural formula of C10H8Br4. TBBs have a fluorine atom at their central position and have been shown to react with bacterial strains and produce reaction products, such as hydrogen chloride, calcium carbonate, and carbonic acid. TBBs form hydrogen bonds with the membrane system of cells and affect physiological functions. TBBs are able to penetrate the skin and enter the bloodstream, which can lead to toxic side effects in humans.

Fepradinol is a potent inhibitor of microbial infection. It is a coordination complex that inhibits the growth of bacteria, fungi, and viruses by interfering with the synthesis of proteins required for the cell-wall biosynthesis. The diameter of this particle is between 10 and 100 nanometers, with an average particle size of 20 nanometers. It has been shown to be effective against eye diseases such as choroidal neovascularization due to its anti-inflammatory activity. Fepradinol has also been shown to inhibit the production of prostaglandins in animal models, which may be responsible for its anti-inflammatory activity.

<p>2,5-Dimethylresorcinol is a natural organic compound that has been shown to have the ability to inhibit the formation of reactive oxygen species. It is used in wastewater treatment and as an antioxidant. 2,5-Dimethylresorcinol has been shown to exhibit an inhibitory effect on lipid hydroperoxides and hydroxyl group binding. This compound can also be used as a substrate or product in catalytic domains. 2,5-Dimethylresorcinol is found in the form of usnic acid and orsellinic acid. The use of this compound as a catalyst for oxidation reactions has been studied extensively. It has also been shown to be an effective inhibitor for catalytic domains with a range of different metal ions.</p>

<p>All-E-Heptaprenol is a polyprenol compound, which is a key intermediate in the biosynthesis of terpenoids. It originates from bacterial sources, where it plays a crucial role in cellular processes. All-E-Heptaprenol functions primarily as a hydrophobic carrier molecule, facilitating the transport of sugar moieties across the lipid bilayer in the assembly of complex biopolymers.</p>

<p>3-Fluoro-4-methylphenol is a regiospecific, nature, activating, radiopharmaceutical, which is used in the synthesis of asymmetric formylation reagents. It can be synthesized from nitrobenzene and formaldehyde in the presence of sodium hydroxide. 3-Fluoro-4-methylphenol can be converted to 3-fluoroacetophenone by hydrogenation with palladium on charcoal. This compound has an electron withdrawing group and a nucleophilic group that are activated by a dihedral angle of 30° or less. The nitro group has the ability to accept electrons from other compounds or compounds such as ammonia or amines.</p>

4,6-Diaminoresorcinol dihydrochloride is a white solid that has viscosity and hydrochloric acid as its structural formula. It is soluble in water and reacts with proton, monosodium salt to form a precipitate. 4,6-Diaminoresorcinol dihydrochloride reacts with phosphorus pentoxide to form the sulfonation product. The thermal expansion of this material is 2.8 x 10^-5/K and it has shown chemical stability at high temperatures up to 450°C. This compound has been found to be an element analysis for chloride (Cl), hydrogen chloride (HCl) and morphology.

<p>4-Aminobenzyl alcohol is an ethylene diamine derivative that is insoluble in water. It has been shown to react with sodium carbonate in aqueous solution to form a polymer. The polymer has potential as a biomarker for the early detection of cancer and other diseases. 4-Aminobenzyl alcohol has low potency and is activated by caproic acid, which is used as an inhibitor of the enzyme epidermal growth factor (EGF). This compound also reacts with azobenzene to form a primary cell line.</p>

2-Methylresorcinol, technical is the sodium salt of 2-methylresorcinol. It has been shown to be chemically stable at high temperatures and can be used in magnetic resonance spectroscopy. The nmr spectra of 2-methylresorcinol are different from those of other compounds. It is a molecule with a carbonyl group and one methyl group that reacts with hydrochloric acid to produce a reaction product with a chlorine atom, which reacts with trifluoroacetic acid or trifluoromethanesulfonic acid to produce an activated intermediate that can react with a second molecule to form another reaction product. This mechanism may be useful in the synthesis of anti-tuberculosis drugs.

<p>(R)-(+)-Diphenyl-2-pyrrolidinemethanol is a chiral reagent that is used to catalyze the hydrogenolysis of esters and amides. This reaction yields a mixture of the corresponding alcohol and acid. The reagent can also be used to deprotonate azides, yielding diphenylprolinol. The product can then be hydrolyzed with an alkaline solution to form a methyl ester or an ester hydrochloride. This process is useful for the preparation of chiral alcohols and amines.</p>

<p>Darunavir is a HIV-1 protease inhibitor used orally in the treatment of patients with multi-drug resistant HIV-1 infection (Ghosh, 2007). It has also been shown to be effective against other infectious diseases such as hepatitis C virus and SARS coronavirus. Metabolized by cytochrome P450 3A (CYP3A) isoenzymes, darunavir is often administered together with ritonavir that prolongs its bioavaiability, giving a terminal elimination half-life (t1/2) of 15 hours (Back, 2008). The effect of darunavir on natural compounds such as matrix proteins and toll-like receptor activity has also been studied via high performance liquid chromatography (HPLC) experiments.</p>

<p>2-Phenoxybenzyl alcohol is an active compound that is a diarylamine with a phenoxy group. It has photochemistry activity, which can be used to form methanes and polyhalogenated phenoxy compounds. 2-Phenoxybenzyl alcohol has been found to react with amides and carbonyl groups in nature. This chemical also has the ability to undergo transfer and shift reactions.</p>

<p>3-Bromo-5-(trifluoromethyl)phenol is a versatile building block that is used as a scaffold for synthesis of complex compounds. It can be used as a reaction component in the synthesis of valuable chemical products, such as fine chemicals and research chemicals. 3-Bromo-5-(trifluoromethyl)phenol is also useful for the production of speciality chemicals. This chemical has been shown to have high quality and can be used as a reagent in organic synthesis.</p>

<p>1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol is a potent antihypertensive agent that is synthesized by the chemoenzymatic process. It differs from other antihypertensive drugs in that it incorporates an oxirane group, which makes it more hydrophobic than other drugs. 1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol is a crystalline solid with a melting point of 128°C and a density of 1.0 g/mL. The chemical name for this drug is 4-[(1E)-1-(chloromethoxy)propyl]phenol, which has potent antihypertensive activity and high enantioselectivity.</p>

<p>Xylene cyanol is a chemical compound that belongs to the group of phenols. It has been shown to be active in vitro against human skin cancer cells, and induces cell lysis. Xylene cyanol has also been found to bind to the BCR-ABL kinase domain, which is an enzyme that plays a crucial role in the development of leukemia and other autoimmune diseases. Xylene cyanol binds to dna binding domains on the protein surface and forms an adduct with bcr-abl kinase, which inhibits its activity. This inhibition prevents activation of this enzyme and leads to cell death by preventing DNA synthesis.</p>

<p>3-Bromo-5-methylphenol is an enolate that can be used to synthesize methicillin-resistant dibenzofurans. The synthesis of these compounds is a multistep process, which includes the formation of an enolate from 3-bromo-5-methylphenol and subsequent displacement with a variety of electrophiles. The use of 3-bromo-5-methylphenol as an enolate allows for high yields in the synthesis of dibenzofurans. Further, this compound has antibacterial properties and is effective against both gram positive and negative bacteria. 3-Bromo-5-methylphenol also has chloride and sulfonation properties, which have been used to make advances in the development of antibacterial agents.</p>

<p>1-(2,5-Dimethoxyphenyl)-2-nitroethanol is a chiral, asymmetric catalyst that has been shown to be effective in the enantioselective reduction of ketones. This process is important because it allows for the synthesis of chiral amino alcohols, which are then used in a variety of chemical reactions. The reaction can also be carried out with methyl amine as an amine source. 1-(2,5-Dimethoxyphenyl)-2-nitroethanol is an example of a catalyst that participates in catalysis through the lone pair on oxygen and nitrogen atoms.</p>

<p>2,6-Dichlorophenylmethyl carbinol is a synthetic oxidant that can be used in the oxidation of alcohols. It is used to convert alcohols into aldehydes and ketones with magnesium as a catalyst. 2,6-Dichlorophenylmethyl carbinol has been shown to be effective in the oxidation of cyclohexanone and styrene. It also has been shown to undergo homologation reactions, which are useful for the synthesis of natural products.<br>!--</p>

<p>2-Phenyl-4-quinolinecarboxylic acid is a nonsteroidal anti-inflammatory drug that is commonly used to treat bronchoconstrictor response and inflammatory bowel disease. It is also an antimicrobial agent, which can be used to treat infectious diseases. The compound was found to have structural similarity to other nonsteroidal anti-inflammatory drugs, such as ibuprofen and naproxen. 2-Phenyl-4-quinolinecarboxylic acid has shown the ability to inhibit leukemia inhibitory factor (LIF) production by lymphocytes, which may have a role in the development of leukemia. This drug also possesses antioxidative properties and has been shown to have high values in group P2 polymerase chain reactions.</p>