Alcohols

<p>1,10-Decanediol is an organic compound that belongs to the group of glycols. It has a melting point of 117°C and a boiling point of 285°C. 1,10-Decanediol is an asymmetric molecule with two different stereoisomers: cis-1,10-decanediol and trans-1,10-decanediol. The melting point for cis-1,10-decanediol is higher than that for trans-1,10-decanediol. This indicates that the cis form is more stable at room temperature than the trans form. 1,10-Decanediol can be used in the synthesis of fatty acids and dna duplexes. It has also been shown to inhibit the replication of HIV by binding to its reverse transcriptase enzyme and preventing it from functioning properly.</p>

<p>4-tert-Butyl-2,6-dinitrophenol is a yellowish solid that is soluble in organic solvents. It is used as an intermediate for the synthesis of dyes, pesticides and pharmaceuticals. 4-tert-Butyl-2,6-dinitrophenol has been shown to cause respiratory tract irritation and narcosis in animals. The toxic effects of 4-tert-Butyl-2,6-dinitrophenol are due to its high electrophilicity and nitro group (NO) which causes oxidative stress. The logistic regression analysis showed that the population growth of ciliates was negatively affected by the presence of halogens in the water.</p>

<p>2-(2,5-Dichlorophenyl)ethanol (2,5-DCPE) is an organic chemical that is used as a building block for the synthesis of fine chemicals and pharmaceuticals. 2,5-DCPE can be used as a reactant in synthesizing more complex compounds. It reacts with many different functional groups to form covalent bonds. The compound has been shown to have high quality and has been characterized by nuclear magnetic resonance spectroscopy and mass spectroscopy.</p>

<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>

<p>All-trans-retinol is a form of vitamin A that is an important component of the visual system and helps maintain healthy skin. Retinol is found in many animal products and can be taken as a dietary supplement. Retinol can react with other chemicals to form all-trans-retinoic acid, which has been shown to inhibit the growth of human carcinoma cells in culture by binding to the ATP binding cassette transporter. All-trans-retinol also inhibits the uptake of retinaldehyde and retinoic acid into cells, which may be due to its ability to bind to cell membranes or react with chemical inhibitors.</p>

<p>4-Amino-2-chlorophenol is an aminophenol that is used in the production of acetate, which is used in the manufacture of acetic acid. It is also used as a building block for organic synthesis. 4-Amino-2-chlorophenol reacts with acetyl chloride to form chloracetyl chloride, which can then be reacted with piperonyl butoxide to form 2-(4'-aminophenyl)-4,6-dichloropyridine. This reaction is catalyzed by hydrogen chloride and hydrogen bond formation with urea nitrogen. 4-Amino-2-chlorophenol has been shown to have long-term toxicity in animal studies and may be toxic when inhaled or ingested.</p>

<p>16-Dehydropregnenolone acetate is a synthetic compound that can be used in wastewater treatment. It reacts with phosphorus pentoxide to form an insoluble solid product. 16-Dehydropregnenolone acetate has been shown to inhibit the growth of human prostate cancer cells and breast cancer cells in vitro and in vivo. 16-Dehydropregnenolone acetate is also a specific agonist for the progesterone receptor, which may be due to its ability to bind to the stereospecific (S) binding site on this receptor. The optimum concentration for 16-dehydropregnanediol is 10 mM and it requires the presence of phosphotungstic acid for maximum activity. This substance has biological properties that are similar to those of natural progesterones, but it does not have any estrogenic properties.</p>

<p>Triphenylphosphonium is a reactive phosphonium salt that is used as an intermediate in the synthesis of 1,2,4-butanetriol. The synthesis of the triphenylphosphonium salt from the sodium salt of butyric acid and ferrocene is shown in this scheme. This synthetic route provides for planar chirality and an asymmetric synthesis. The byproduct, butyric acid, can be converted to its conjugate base with ammonium hydroxide or sodium hydroxide to provide cholic acid. Cholic acid is a hepatoprotective agent that has been used in the treatment of liver disease.</p>

<p>(S)-Glycerol 1-benzyl ether is a chiral, synthesised antidepressant drug that has shown to be effective in the treatment of depression. It binds to α-adrenergic receptors and blocks the binding of norepinephrine and epinephrine, preventing the production of stress hormones. (S)-Glycerol 1-benzyl ether is also used as a reagent for the synthesis of doxazosin and d-mannitol.</p>

<p>(+)-Dehydrodiconiferyl alcohol is a lignan, which is a type of phenolic compound naturally occurring in a variety of plant species, including those in the families Magnoliaceae, Lauraceae, and others. As a secondary metabolite derived from the oxidative coupling of coniferyl alcohol, it plays roles in plant defense and structural integrity.</p>

<p>3,5-Dibenzyloxybenzyl alcohol is a flavonoid that is used for the treatment of cancer. The compound inhibits the activity of cyclooxygenase-2 (COX-2) and has been shown to inhibit the production of prostaglandin E2, which is associated with inflammation. 3,5-Dibenzyloxybenzyl alcohol also inhibits metathesis reactions in an equilibration process that can be catalyzed by palladium or platinum. It has been found to have anti-inflammatory properties due to its inhibition of COX-2 and its ability to induce apoptosis in tumor cells. 3,5-Dibenzyloxybenzyl alcohol also has anti-cancerous properties, which may be due to its ability to inhibit cell proliferation through alkylation and spiroketal conjugation reactions. This compound also binds to tannins and fatty acids as well as monomers in a reversible manner</p>

<p>Fmoc-Cysteinol(Trt) is a versatile building block that can be used in the production of complex compounds and research chemicals. This compound is a high quality, useful building block that is used to synthesize many other compounds. It can also be used as a reagent or speciality chemical. Fmoc-Cysteinol(Trt) has been classified as a CAS No. 215954-72-6 and is a useful scaffold for chemical reactions.</p>

<p>1-(6-Chloropyridazin-3-yl)piperidin-4-ol (CPP) is an organic compound that is used as a corrosion inhibitor. It has been shown to be effective in the presence of hydrochloric acid and chloride ions in various media. The mechanism of CPP's anti-corrosion properties is due to its ability to form a protective film on metal surfaces, which can be attributed to its electron donating ability. This film prevents the occurrence of metal dissolution or metal oxidation, thereby preventing corrosion. CPP has been shown to inhibit the growth of bacteria by binding with DNA and RNA. It also inhibits protein synthesis through competitive inhibition of ribosomes.</p>

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<p>4,5-Dihydro-1H-pyrazol-3-ol hydrochloride (DHPE) is a potent inhibitor of the uptake and transport of serotonin in the rat brain. DHPE inhibits serotonin uptake by blocking the binding of serotonin to its transporter protein and also inhibits serotonin reuptake at the synapse. It is also an inhibitor of lysine hydroxylase, which converts lysine to catecholamine neurotransmitters. This inhibition leads to decreased levels of dopamine, norepinephrine and epinephrine, which can cause depression. DHPE binds to acidic amino acids such as glycine and glutamate, potentiating their actions on postsynaptic neurons. This effect may be due to increased synaptic activity or decreased inhibitory neurotransmitter release.br&gt;<br>br&gt;<br>The environment can affect the pharmacokinetics of DHPE. DHPE has been shown to have higher concentrations in acidic environments than basic environments because it is more soluble</p>

<p>4-Hydroxythiophenol is an organic compound with the molecular formula C6H4OHO. It is a white crystalline solid that is soluble in water and ethanol. 4-Hydroxythiophenol has been shown to inhibit the growth of bacteria by reacting with free intracellular hydroxyl groups, which are necessary for the biosynthesis of cell walls. This molecule also reacts with other biological molecules, such as nucleic acids and proteins, to form covalent bonds. 4-Hydroxythiophenol has been shown to be effective against both Gram-positive and Gram-negative bacteria in vitro assays.</p>

<p>Cetearyl alcohol is a type of fatty alcohol, which is derived from natural sources like coconut oil or palm kernel oil. It is a combination of cetyl and stearyl alcohols. This compound functions primarily through its emulsifying properties, allowing oil and water to mix effectively and form stable emulsions. It does this by reducing surface tension, thus facilitating the blending of disparate ingredients.</p>

<p>4-Phenylazophenol is an organic azobenzene that has a specific treatment for the degradation of amines and mineralization. It has been shown to reduce the levels of phenols, fatty acids, and amines in wastewater. 4-Phenylazophenol is also used as an enzyme inhibitor in reactions with hydrogen bond formation and as a receptor α ligand. The natural compounds found in 4-phenylazophenol have borohydride reduction properties.</p>

<p>(R)-2-Amino-1-phenylethanol is a molecule that has antimicrobial activity. It binds to the active site of bacterial enzymes, such as those involved in the synthesis of cell walls, and inhibits the growth of bacteria through competitive inhibition. This molecule also has a dihedral angle that is similar to that of other molecules with antibacterial activity. (R)-2-Amino-1-phenylethanol is an enantiomer, which means it can be synthesized from either (S)- or (R)-1-phenylethanol. The racemic form is more active than any individual enantiomer.</p>

<p>2-Methoxyresorcinol is a metabolite that is formed by the oxidation of resorcinol. It has two methoxy groups, which are functional groups that are usually found in organic compounds. 2-Methoxyresorcinol has been shown to inhibit the growth of tumour cells in vitro and in vivo. It also inhibits cell growth by decreasing protein synthesis and cell division. This compound is an analytical method for measuring hematocrit levels and can be used as a natural compound for the treatment of chronic kidney disease.</p>

<p>Calcipotriol is a vitamin D analogue that is used to treat psoriasis. It is classified as an aprotic solvent and is not soluble in water, but it dissolves in organic solvents. Calcipotriol binds to the receptor for nuclear factor kappa-B (NF-κB) and inhibits its activation, which suppresses the production of cytokines that are involved in inflammation and immune responses. The calcipotriol molecule has been shown to inhibit EGFR signaling, thereby suppressing tumor growth. This drug has also been shown to be effective in combination therapy with other drugs such as dithranol or anthralin for the treatment of psoriasis. Calcipotriol can be administered topically or by oral administration. It is usually applied twice daily and the dosage depends on the severity of the disease.</p>

<p>17alpha-Hydroxypregnenolone 3,17-diacetate is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. It is typically used as a reagent or speciality chemical for research purposes, but it also has applications in the production of pharmaceuticals, cosmetics, and other products. This compound has been shown to have high purity and is an excellent reaction component for the synthesis of new scaffolds.</p>

<p>20-Deoxo-23-deoxy-5-O-[3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranosyl]-20,23-di-1-piperidinyltylonolide is an antimicrobial agent that belongs to the group of chemotherapeutic agents. It is a fluorinated analog of tilmicosin. The low dose group was treated with this drug for five days, and the high dose group received 20 times the amount of drug. Fluorescence spectrometry showed that there was no significant difference in the fluorescence intensity between these two groups after 24 hours. This drug has been shown to have pharmacokinetic properties in rats and mice, but further optimization may be required to improve its process.</p>

<p>6-Amino-2,4-dichlorophenol is an organic solution that has been shown to inhibit the uptake of quinoline derivatives by lung fibroblasts. It also inhibits cellular targets such as flavin, blood pressure and v79 cells. 6-Amino-2,4-dichlorophenol has potent antibacterial activity and a reactive nucleophilic group that can form covalent bonds with proteins in the cell membrane. 6-Amino-2,4-dichlorophenol is a reactive agent that binds to DNA and RNA in the bacterial cell's cytoplasmic membrane and inhibits protein synthesis.</p>

<p>Emulgator; stabilizing surfactant used in cosmetics, pharmaceuticals, textiles</p>

<p>1,2-Distearoyl-sn-glycerol (DAG) is a lipid molecule that is found in the cell membrane and can be used as an antimicrobial agent. DAG has been shown to inhibit the growth of bacteria by binding to their fatty acid chains. It also has been shown to bind to the receptor P2Y6, which is involved in mediating inflammatory responses, and inhibits its activity. This drug may be useful for treating diseases such as atherosclerosis and diabetes mellitus type 2.</p>

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<p>4-Butoxybenzyl alcohol is a primary alcohol that is used as a solvent and reagent. It has been shown to disrupt the architecture of bacterial cell walls by destabilizing the molybdenum cofactor, which is essential for the enzyme xylose reductase. The destabilization of this cofactor leads to inhibition of cell wall synthesis and subsequent death of bacteria. 4-Butoxybenzyl alcohol also has antibacterial properties and can be used to inhibit the growth of Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis. This compound may also act by inhibiting amide formation or by binding to magnesium, aluminium, or amides in the bacterial cell wall.</p>

<p>2,4,5-Trimethylbenzyl alcohol (2,4,5-TMB) is an organic solvent that has been used as a photocatalyst. It has been shown to be an efficient and selective radical oxidation catalyst for the conversion of toluene to benzaldehyde. 2,4,5-TMB can also be used in UV irradiation as a sensitizer for the production of oxiranes from ethylene oxide and oxygen. 2,4,5-TMB is soluble in many common solvents such as ethers and chlorinated hydrocarbons. The reaction product is not known with certainty because it has not been isolated. However, it is thought that it may form radical anion radicals when irradiated with UV light or other forms of radiation.</p>

<p>2-(2-Aminoethyl)phenol is a monoamine oxidase inhibitor. It is a biogenic amine that is found in animals and plants. 2-(2-Aminoethyl)phenol has been found to have anti-inflammatory properties and can be used to treat mongolism.</p>

<p>1-O-Hexadecyl-rac-glycerol (1OHR) is a synthetic compound that has been shown to inhibit the growth of leukemia and other cells in vitro. It inhibits the activity of enzymes involved in carbohydrate chemistry, such as benzalkonium chloride, surface glycoprotein, monoclonal antibody, and enzyme activities. It also causes cytosolic Ca2+ release from intracellular stores and decreases the concentration of intracellular calcium. 1OHR has a minimal toxicity for mammalian cells and does not inhibit protein synthesis.</p>

<p>3-Bromo-2-methoxybenzyl alcohol is a reaction component that is used in the synthesis of a number of chemical compounds. It has been shown to be a useful scaffold, with versatile building blocks and intermediates. 3-Bromo-2-methoxybenzyl alcohol is an intermediate for the synthesis of complex compounds such as antihypertensive drugs, anti-inflammatory agents, and immunosuppressant drugs. This compound also has a variety of uses in research including as a reagent for the determination of enzyme activity and as an analytical reference standard.</p>

<p>DL-Phenylethanolamine is a hydroxy amine that is used in the synthesis of other chemicals. It is obtained by reacting phenylacetic acid with hydroxylamine. DL-Phenylethanolamine is an intermediate in the synthesis of the anti-inflammatory drug Indomethacin. This molecule contains a asymmetric carbon atom, which can be distinguished using infrared spectroscopy. The uptake of DL-phenylethanolamine into cells can be measured by detecting the release of amines from lysosomes and mitochondria. In addition, this molecule has conformational properties that can be detected by NMR spectroscopy, making it useful for detection sensitivity and identification purposes.</p>

<p>(1-Methylpiperidin-2-yl)methanol is a gaseous organic acid that belongs to the piperazine class of compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, including antipsychotics and antidepressants. (1-Methylpiperidin-2-yl)methanol has been shown to be an agonist of ganglion cells and can be used for the treatment of glaucoma. This compound also has shown to have anti-inflammatory properties, which may be due to its ability to inhibit nitric oxide production. Furthermore, (1-methylpiperidin-2-yl)methanol has been shown to inhibit 13c nuclear magnetic resonance spectroscopy with epoxides and hydroxyl groups. The reaction product is a crystalline solid with a molecular formula of C6H14O3N2, which corresponds to the molecular formula of 2-(dimethylam</p>

<p>Phenol red is a pH indicator that finds broad applications from chemistry to microbiology. Colour varies from yellow at pH&lt;6.8 (lmax 443nm) through to light red/pink at 6.8&lt;pH&lt;8.2 (lmax 570 nm) to vivid purple/red at pH&gt;8.2. It is widely used in cell culture to monitor pH and for colorimetric titration. For example, phenol red can be used to quantify Br- content in sea or fresh water. It is added to VTM as pH indicator, at the concentration of 10mg/ml, maintaining a pink colour at neutral pH.</p>

<p>Ingenol is a natural product, which belongs to the group of ingenol esters. It has been shown to have significant cytotoxic effects on solid tumours in vitro and in vivo. Ingenol is metabolized by esterases and glucuronidases, or hydrolyzed by esterases or glucuronidases, leading to the release of methyl ethyl erythritol tetranitrate (MEETN). The MEETN molecule is then converted into a nitrate radical that causes cell death. Ingenol is also effective against skin cancers. Studies have shown that it inhibits the growth of skin cancer cells through mitochondrial membrane potential and cytosolic calcium levels. This drug has a chemical stability of less than one week at room temperature.</p>

<p>4-Propylresorcinol is a potent tyrosinase inhibitor that has been shown to inhibit the activity of this enzyme in a synergistic interaction with metal chelators. The binding of 4-propylresorcinol to the active site of the enzyme inhibits the hydroxylation of L-tyrosine, preventing melanin production. This drug also inhibits the production of melanin by other pathways, such as by modulating cellular transcription. The inhibition of tyrosinase activity by 4-propylresorcinol has been shown to be specific and reversible.</p>

<p>3,4-Methylenedioxyphenethyl alcohol (MDPA) is a model compound that is used to study the mechanism of action and synthesis of aniracetam. It has been shown to be an antagonist of pentylenetetrazole, a convulsant drug. MDPA was also found to have anticonvulsant properties in mice. It was found that this compound had no effect on the inhibition of movement when administered at doses up to 100 mg/kg. This compound is an analog of liriodenine, which has been shown to have anti-inflammatory properties. 3,4-Methylenedioxyphenethyl alcohol is not active in the central nervous system due to its stereoselectivity; this means it can only bind to one stereoisomer within the brain and does not cross the blood-brain barrier.</p>

<p>4-Nitroquinoline-N-oxide is a polymerase chain reaction (PCR) inhibitor that blocks the activity of methyltransferases, which are enzymes involved in DNA replication and repair. The mechanism of action has been shown to be due to the inhibition of the activities of these enzymes in cancer tissues. The efficacy of 4-Nitroquinoline-N-oxide has been demonstrated using an experimental model system composed of cells from Candida glabrata and other cancers, as well as a model system for carcinogenesis in vitro. This compound also shows antiinflammatory activity and can be used as a natural compound for chemotherapy. Chromatographic analysis has revealed that 4-Nitroquinoline-N-oxide is not toxic to wild type strains, but it is toxic to cancer cells with mutations in their DNA repair mechanisms.</p>

<p>2,6-Dimethoxybenzyl alcohol is a synthetic compound that is a peroxidase substrate. It is used as an alternative for papaverine in the synthesis of penicillin and cephalosporin antibiotics. 2,6-Dimethoxybenzyl alcohol reacts with Mn2+ ions to form hydronium and hydrogen peroxide. This reaction has been shown to be more efficient than the decomposition of hydrogen peroxide by catalases or superoxide dismutases. 2,6-Dimethoxybenzyl alcohol also forms a reactive congener with erythrocytes and plasma proteins that can cause vasoconstriction in the blood vessels. The dimethoxybenzyl group (DMB) is a monosubstituted phenol group that binds to the active site of enzymes such as cytochrome P450s and glutathione reductase.</p>

<p>8-Nitroquinoline is a nitrogenous compound that has been used as an inhibitor of Leishmania, a parasite that causes leishmaniasis. 8-Nitroquinoline inhibits the growth of Leishmania by inhibiting the enzyme hepg2, which is involved in the synthesis of lipids and cholesterol. The inhibition of this enzyme leads to the accumulation of malonic acid, which inhibits the production of ATP. This inhibition may lead to cell death or inhibitory effects on other enzyme activities. 8-Nitroquinoline has been shown to be effective against Leishmania parasites in vivo.</p>

<p>Emax (230 nm) = 3113</p>

<p>4-(1-Adamantyl)-2-nitrophenol is a versatile building block that can be used to construct complex compounds. It is a research chemical that can be used as a reagent, as well as in the synthesis of pharmaceuticals and other chemicals. 4-(1-Adamantyl)-2-nitrophenol is soluble in water and ethanol, and has an odorless and colorless appearance. This chemical can be found under the CAS number 32599-84-1.</p>

<p>2-Amino-4-cyano-phenol is a compound that has been shown to have antitubercular activity. It modulates the activity of cromakalim, which is a drug used for the treatment of tuberculosis. 2-Amino-4-cyano-phenol is also an antibacterial agent and has been shown to activate bacterial DNA replication and protein synthesis. The mechanism of action of this compound is thought to be due in part to its ability to bind with the ribosomes on the outside surface of cells and inhibit their function. 2-Amino-4-cyano-phenol has also been shown to have structural similarities with phenylephrine, which inhibits bacterial growth by binding to DNA gyrase, thereby preventing transcription and replication.</p>

<p>Gestadienol is a synthetic, reconstituted drug that is used to treat congestive heart failure. Gestadienol is produced by reacting hydrochloric acid with isopropyl palmitate and diluent. The reaction yield of this process can be increased by implanting the drug into animal tissue for a period of time before extraction. Gestadienol binds to glucuronidated compounds in the blood, which may be due to its chemical similarity to estradiol. This binding prevents the glucuronidated compound from being excreted in urine and increases their concentration in the bloodstream. Gestadienol has been shown to increase postnatal development in rats, which may be due to its ability to bind progesterone receptors on cells and inhibit progesterone-mediated effects.</p>

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<p>4-Amino-3-nitrophenol is a reactive aminophenol that can be synthesized from hydrogen sulfate and diethyl ester. It is used in the synthesis of amines and other chemicals, as well as in analytical methods for determining the concentration of nitrates, nitrites, and aminophenols. 4-Amino-3-nitrophenol has been shown to have photocatalytic activity.</p>

<p>Estratetraenol is a synthetic estrogen that has the same structure as 17β-estradiol, but with three additional hydroxyl groups. It is used in research to study the effects of estrogens on humans and animals. Estratetraenol has been shown to activate the cell membrane receptors, which leads to a physiological response. This drug also causes an increase in oxygen consumption and inhibits ovulation. Estratetraenol binds to estrogen receptor cells and is metabolized by chemical substances in the liver into 17β-estradiol, which is then excreted by the kidneys. The drug does not bind to other types of receptor cells in humans or animals, such as those for progesterone or testosterone.</p>

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<p>2-(2,6-Dimethoxyphenoxy)ethanol is a cleavage agent that can be used for the synthesis of lignin model compounds. It is a benzylic ether that is catalyzed by laccase to produce 2,6-dimethoxybenzaldehyde. The compound can be used as a substrate for versicolor or peroxy cleavage reactions. Versicolor cleavage is performed with 1-hydroxybenzotriazole, while peroxy cleavage is performed with hydrogen peroxide. 2-(2,6-Dimethoxyphenoxy)ethanol has been shown to have radical properties and reacts with molecular oxygen and ethanone in the presence of deuterium gas to form 2,6-dimethoxyacetophenone.</p>

<p>3-Aminobutan-1-ol is an amine that is synthesized industrially by the reduction of soybean trypsin with borohydride. This chemical has been used as a substrate in asymmetric synthesis and can be detected by high detection sensitivity. 3-Aminobutan-1-ol binds to the carbonyl group of amino acid residues and causes a reaction with chloride ions for detection. The product of this reaction is an enantiomer, which can be separated from other reaction products by purified chiral stationary phases. 3-Aminobutan-1-ol is also involved in the biosynthesis of proteins and enzymes. It reacts with hydrochloric acid to form a salt, which can then be used as an enzyme inhibitor.</p>

<p>4-Ethoxyphenylethyl alcohol (4EPEA) is a non-invasive fluorescent probe that has been used in the study of nucleic acids. It is a small molecule that can be used to identify DNA and RNA sequences. 4EPEA terminates at a specific site on the DNA or RNA, where it forms a cavity with its hydroxyl group pointing outward. The cavity is then filled by the next base in the sequence, which reverses the orientation of 4EPEA and causes it to fluoresce. This process can be repeated to map the entire length of an RNA molecule or DNA strand. When 4EPEA is mixed with acetonitrile (ACN), it undergoes a transition from an amorphous state to a more crystalline state, which allows for better separation of 4EPEA from other compounds in ACN. The use of β-cyclodextrin as an additive further improves this separation as well as increasing the stability of</p>

<p>Intermediate in the synthesis of mirabegron</p>

<p>Precusor for preparation of indinavir; a chiral ligand for asymmetric synthesis</p>

<p>Impurity found in Primaquine diphosphate</p>

<p>1,1,3,3,4,4,4a,5,5,6,6,7,7,8,8,8a-Hexadecafluoro-2-(trifluoromethyl)decahydroisoquinoline is an organic solvent that has a very low boiling point and high volatility. It can be used in dry powder inhalers or as a component of hydrogel compositions for oxygen delivery to the lungs. The uptake of 1HF-2TFI into human colon carcinoma cells was found to be significantly higher than uptake by mammary carcinomas. This may be due to the difference in cell types and/or the phosphate group on the molecule. The binding constants of this molecule are also higher than those of other organic solvents such as acetone and ethanol. The results from a questionnaire study also indicated that 1HF-2TFI can be used for perfusion with oxygenated gas mixtures for</p>

<p>8-Hydroxyquinoline-2-carboxylic acid is a 3-hydroxyanthranilic acid derivative that is often used as a biomarker of urine. The 8OHQA can be synthesized from 3-hydroxyanthranilic acid by the action of xanthine oxidase and hydrogen peroxide, and it has been shown to be an inhibitor of protein synthesis. This inhibition may be due to its ability to form hydrogen bonds with the hydroxyl group on the ribose side chain and its ability to coordinate with metals. 8OHQA has been shown to have anti-inflammatory effects in bladder cancer cells, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>Heptadecafluoro-1-decanol is a chemical substance that has been used in wastewater treatment and as an odorant. It is also found naturally in human liver, heart tissue, and adrenocortical carcinoma. Heptadecafluoro-1-decanol can be chemically synthesized by the reaction of 1H,1H,2H,2H-heptadecafluorodecane with hydrogen fluoride. This chemical substance is known for its ability to bind to fatty acids and other organic compounds on the surface of water droplets. The hydroxyl groups on this molecule are able to form hydrogen bonds with water molecules, which may lead to increased surface tension. Heptadecafluoro-1-decanol has been shown to have anti-inflammatory properties in humans.</p>

<p>Extensive research has been conducted on the antimicrobial activity of 6-fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-(1,3)thiazeto(3,2a)quinoline-3-carboxylic acid (FPMT). FPMT is a levorotatory compound that is rapidly metabolized by esterases to 6FMT, which is also active against bacteria. FPMT inhibits bacterial growth, but does not inhibit mammalian cell growth. The main mechanism of action for FPMT is probably through its ability to inhibit the synthesis of bacterial DNA and RNA. This drug has been shown to be effective against sinusitis caused by bacterial rhinosinusitis and urinary tract infections caused by Escherichia coli and Pseudomonas aeruginosa. FPMT can be used as an alternative to prulifloxacin for the treatment of these types of infections</p>

<p>2-Oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid is a carboxylic acid that is an intermediate in the chemical synthesis of 2H and 3H tetrahydroquinolines. It can be synthesized by the oxidation of 2-(N,N-dimethylamino)benzaldehyde with hydrogen peroxide in methanol. The compound has been used to label animals for use in mass spectrometry studies and as a reactant in electron and nuclear magnetic resonance (NMR) spectroscopy experiments. In addition, 2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid has been used to study equilibrium and reversible reactions as well as to identify the abundances of different spectral peaks. 2-Oxo-1,2,3,4-tetrahydroquinoline-4</p>

<p>4-Bromo-2-(trifluoromethyl)phenol is a compound that belongs to the family of dialdehydes. It has been used in organic chemistry as an assembly reagent, a monomer in polymer synthesis, and as a building block for oligomers and duplexes. 4-Bromo-2-(trifluoromethyl)phenol is stable under basic conditions and can be used in the presence of chloroform. This compound functions as an intermediate for the synthesis of other functionalized molecules such as phosphine oxide, oxide, and diamines.</p>

<p>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.</p>

<p>18 carbon branched aliphatic alcohol mixture; component of cosmetic formulations</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>5-Hexen-2-ol is a constituent of various natural products such as the racemosum and macrocyclic lactones. It has been found to have a broad spectrum of biological activities, including antibacterial, antifungal, antiparasitic and antimalarial activity. 5-Hexen-2-ol has also been used in the synthesis of various macrocyclic lactones and macrolactones. This compound has been found to inhibit penicillium growth by competitive inhibition of ergosterol biosynthesis.</p>

<p>Propranolol is a beta-adrenergic receptor antagonist that is used to treat high blood pressure, chest pain and heart failure. It also has been shown to be effective in the treatment of inflammatory bowel disease (IBD). Propranolol blocks the binding of proprotein convertase subtilisin/kexin type 9 (PCSK9) to its receptors, which inhibits the production of LDL cholesterol. In humans, propranolol is metabolized through hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. The drug also has a synergic effect with other drugs such as erythromycin and phenobarbital. Propranolol binds to proteins in red blood cells and decreases diastolic pressure.</p>

<p>5-Pyridin-4-yl-1,3,4-thiadiazole-2-thiol is a molecule that is used as an immunosuppressant. It inhibits the production of cytokines and chemokines by inhibiting the activation of nuclear factor kappa B (NF-κB). This leads to less inflammation and a decrease in the ability of immune cells to proliferate. 5-Pyridin-4-yl-1,3,4-thiadiazole-2-thiol has been shown to have synergistic effects with other drugs, such as antifungal agents.</p>

<p>Cholestan-3b,5a,6b-triol is a naturally occurring fatty acid that has been shown to inhibit the synthesis of cholesterol and oxysterols in animal studies. It also acts as a receptor agonist for the LDL receptor. This compound is used in clinical trials to assess risk for cerebrotendinous xanthomatosis (CTX), a rare genetic disorder characterized by high levels of cholesterol and fatty acids in the brain and spinal cord. Cholestan-3b,5a,6b-triol is being studied as a potential treatment for atherosclerosis. The drug inhibits the uptake of cholesterol from macrophages and reduces the accumulation of atherosclerotic lesions in mouse models. Cholestan-3b,5a,6b-triol may be useful for treating patients with diabetes because it blocks the synthesis of fatty acids that can lead to diabetic complications such as retinopathy and nephropathy.</p>

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

<p>Bis-(4-chlorophenyl)-carbinol is a nonpolar compound with a linear plot. It is used as an intermediate in the synthesis of herbicides, insecticides, and pharmaceuticals. Bis-(4-chlorophenyl)-carbinol has been shown to bind to cylindrospermum, which is a type of marine algae that can be found in ecosystems such as the Great Barrier Reef. This binding reaction is the result of diphenylmethane, which is an aromatic compound that binds to bis-(4-chlorophenyl)-carbinol's electron-donating groups. The binding reaction was studied using dispersive solid-phase extraction (DSPE) and carbon source experiments on soil microorganisms. Cytochrome P450 enzymes are responsible for metabolizing bis-(4-chlorophenyl)-carbinol into unidentified metabolites.</p>

<p>2-Phenylquinoline-4-carbohydrazide is an antibacterial agent that binds to bacterial DNA gyrase and topoisomerase, which are enzymes that maintain the integrity of bacterial DNA. It also has significant anti-inflammatory activity and can be used for the treatment of skin disorders, such as acne. 2-Phenylquinoline-4-carbohydrazide has been shown to induce apoptosis in human dermal fibroblast cells. This drug has been shown to have anticancer activity in vitro and in vivo. The anticancer activity of this drug may be due to its ability to inhibit cancer cell proliferation by binding to DNA gyrase and topoisomerase, which are enzymes that maintain the integrity of bacterial DNA.</p>

<p>1-Hexadecanethiol (1-HDT) is a chemical substance that is used in the synthesis of polymers and as a reagent for surface modification. It has been shown to be an effective cationic surfactant with antimicrobial properties. 1-HDT has also been used to pattern surfaces and is found in water vapor, where it can react with oxygen to form 3-mercaptopropionic acid. 1-HDT reacts with thiols, alcohols, amines, and amino acids to form sulfides. In vitro assays have shown that 1-HDT can inhibit the growth of carboxy terminal protein polymer films. Chemical stability is dependent on the chemical species, which can be predicted by examining chemical structure and reactivity.</p>

<p>Resorcinol bis(2-hydroxyethyl)ether is a chemical compound that belongs to the class of polyols. It is a colorless liquid with a strong odor and has a molecular weight of 198.22 g/mol. Resorcinol bis(2-hydroxyethyl)ether is used in the production of polyester, polyurethane, and cellulose acetate butyrate. This chemical also has an anti-oxidant effect that can be utilized in industrial processes such as oxidation polymerization, dyeing, and curing agents. The synthesis methods for resorcinol bis(2-hydroxyethyl)ether include acetaldehyde condensation with glycerol or ethylene oxide followed by hydrolysis.</p>

<p>2-Bromo-4-(trifluoromethyl)benzyl alcohol is a versatile building block that can be used as a reactant in organic synthesis. It is also a useful intermediate and building block for complex compounds. This compound has been used as a reagent in the preparation of 2,2'-dipyridyldisulfide, which was shown to have potent antiproliferative activity against human cancer cells.</p>

<p>5β-Pregnane-3α,20α-diol is a human metabolite of estradiol that has been found to be an active inhibitor of the enzyme activity of GABA transaminase. It has been shown to have therapeutic potential in the prevention and treatment of cervical cancer, as well as other cancers. 5β-Pregnane-3α,20α-diol has also been found to inhibit ovarian activity. The diagnostic method for this metabolite is based on monoclonal antibody (MAb) reactivity with immunosorbent assay (ELISA) and gas chromatography/mass spectrometry (GC/MS). Women who have high values for this metabolite may be at risk for uterine cancer or breast cancer.</p>

<p>4-Methylthiophenol is a colorless liquid that is soluble in water. It has a molecular weight of 98.12 and an empirical formula of C6H7O2S. 4-Methylthiophenol is used as an analytical reagent, solvent, and chemical intermediate. It exhibits hydrogen bonding interactions with sodium carbonate and trifluoroacetic acid and forms a salt with sodium carbonate. The molecule's stability increases when it interacts with amines and the presence of nucleophiles such as water or alcohols. 4-Methylthiophenol has been shown to be effective at enhancing the fluorescence signal emitted by amines, which makes it useful for laser ablation mass spectrometry (LA-MS). 4-Methylthiophenol can also be used for kinetic energy measurements using FTIR spectroscopy because it will absorb infrared light at 1680 cm−1 from the CO2 laser beam.</p>

<p>1-(4-Nitrophenyl)glycerol has been shown to inhibit the growth of Gram-positive bacteria, including Streptococcus faecalis, and Gram-negative bacteria, including Pseudomonas aeruginosa. It is also used as a sample preparation for antimicrobial resistance testing.</p>

<p>2-Methoxy-4-vinylphenol is a chlorogenic acid that has been shown to inhibit the growth of Candida glabrata. It binds to ferulic acid and caffeic acids, which are natural compounds found in plants. The optimum concentration at which 2-methoxy-4-vinylphenol inhibits the growth of C. glabrata is between 0.5 and 1 mM. This compound can be readily analyzed using an analytical method with high selectivity for chlorogenic acids, such as liquid chromatography coupled with mass spectrometry (LC/MS). The binding of 2-methoxy-4-vinylphenol to ferulic acid and caffeic acid may also have implications for its use as an anti-inflammatory agent.</p>

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

<p>Propranolol hydrochloride is a prodrug that is converted to the active form, (S)-propranolol, by deesterification in vivo. Propranolol hydrochloride has been used for more than 50 years as a beta-blocker for the treatment of hypertension and angina pectoris. It is also used to treat other cardiovascular diseases such as arrhythmias and myocardial infarction. Propranolol hydrochloride inhibits the activity of human estrogen receptor (ER) and blocks the synthesis of proteins that are necessary for tumor growth. This drug has been shown to be effective against metastable polymorphs in urine samples and can be used as an analytical method to differentiate enantiomers.</p>

<p>2,4,5-Trimethoxybenzyl alcohol is a metabolite that is produced by the p. pastoris strain. It has been shown to be active against the enzyme glyceraldehyde-3-phosphate dehydrogenase and has been expressed heterologously in yeast. 2,4,5-Trimethoxybenzyl alcohol also has been shown to inhibit peroxidases and may have biochemical applications in pharmaceuticals as an inhibitor of lipid peroxidation.</p>