Composés apparentés aux enzymes, aux peptides et aux protéines

<p>Glyceryl monostearate is a white powder that is composed of glycerin and stearic acid. It has been shown to have high chemical stability in the presence of benzalkonium chloride, which is an antiseptic. Glyceryl monostearate can be used as a particle stabilizer in the preparation of some medications, such as sodium citrate and water vapor. Glyceryl monostearate may also have potential for use in the treatment of metabolic disorders like diabetes mellitus. The mechanism by which glyceryl monostearate may work to treat diabetes mellitus is not well understood. Glyceryl monostearate has also been shown to inhibit leukemia inhibitory factor and phase transition temperature, but its function in these areas is unknown.</p>

<p>Please enquire for more information about 3-Phosphoglyceric acid barium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5,6-Diamino-1,3-dimethyl uracil hydrate is a purine derivative that inhibits the growth of cancer cells by blocking the enzyme ribonucleotide reductase. This leads to a decrease in DNA synthesis, protein synthesis, and cell division. The anticancer activity of 5,6-Diamino-1,3-dimethyl uracil hydrate is due to its ability to inhibit the formation of ATP and the GTP cycle. It also has a potent inhibitory effect on the structural analysis of DNA and RNA. 5,6-Diamino-1,3-dimethyl uracil hydrate has been shown to produce apoptotic effects in many types of cancer cells. This drug also has specific agonist properties for G protein coupled receptors that are responsible for activating apoptosis.</p>

<p>Imipramine N-oxide hydrate is a polymer drug that belongs to the group of amines. It inhibits the activity of CYP450 enzymes and has been shown to be effective in treating inflammatory bowel disease (IBD). Imipramine N-oxide hydrate prevents adenosine A3 receptor activation and suppresses the production of dinucleotide phosphate, which may be responsible for its effectiveness in treating IBD. Imipramine N-oxide hydrate also has an effect on liver cells, which may lead to its effectiveness in treating infectious diseases. The drug is not active against autoimmune diseases, but it may have an effect on toll-like receptors.</p>

<p>L-Anserine nitrate salt is a soluble extract that contains nitrogen atoms, histidine, and primary amines. It is a natural substance found in animal tissue and can be used as a nutritional supplement for humans. L-Anserine nitrate salt has been shown to inhibit the activity of histamine release from mast cells in vitro, which may be beneficial in the treatment of hepatic steatosis. This extract has also been shown to increase levels of fatty acids in liver cells, which may reduce inflammation and improve insulin sensitivity. L-Anserine nitrate salt has also been shown to have antioxidant effects and inhibit DPP-IV activity, which may help treat drug sensitivity in animals.</p>

<p>Ammonium iron(II) sulfate hexahydrate is a salt that contains the metal ion ammonium and iron (II). It is used in cancer research as an electron-radiating agent. The drug molecules are encapsulated into the cavity of mesoporous silica nanoparticles by ionizing radiation. This process immobilizes the drug molecule and prevents it from diffusing away from the particle surface. Ammonium iron(II) sulfate hexahydrate has been shown to be effective against estrone and 17β-estradiol, which are types of estrogen.</p>

<p>Dimethylglyoxime is a pesticide that has been used to control insects and nematodes. It has been found to be effective in controlling mosquitoes, flies, and other pests. This compound is also used as an extractor in microextraction. Dimethylglyoxime is not toxic to humans and does not cause any adverse effects on the environment or human health. It can be used with chlorine for wastewater treatment.</p>

<p>Sodium metasilicate pentahydrate is a white powder that is soluble in water and alcohol. It is used as an acidity regulator, sequestering agent, and buffer in detergent compositions. Sodium metasilicate pentahydrate has been shown to inhibit the growth of bacteria by binding to fatty acids in their cell walls and preventing the formation of cell walls. The molecule also inhibits the polymerase chain reaction (PCR) by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. Electrochemical impedance spectroscopy has been used to measure the effect of this compound on particle size distribution and flow system performance.</p>

<p>Sodium tungstate dihydrate (STDH) is a sodium salt that has been shown to be effective against the MCL-1 protein. This protein is involved in regulating energy metabolism and cell death. STDH binds to the MCL-1 protein, preventing it from forming an oligomer with other proteins. This prevents the MCL-1 protein from translocating into the mitochondria and disrupting the mitochondrial membrane potential, which leads to cell death. STDH has been shown to be effective against wild-type strains of bacteria as well as against bacterial strains that have developed resistance to antibiotics such as molybdenum and tungsten. STDH also inhibits axonal growth in vitro and human serum, leading to physiological effects such as blood coagulation.</p>

<p>Calcium folinate pentahydrate is a drug that is used to treat overexertion. It is also used as a pharmacological treatment for cancer and as a drug repositioning agent. Calcium folinate pentahydrate has been shown to be effective in treating the symptoms of overexertion, including muscle cramps, pain, and fatigue. This drug binds to the casein in the bloodstream and forms calcium citrate, which is then excreted from the body. In cancer patients, this drug prevents tumor cells from dividing by inhibiting DNA synthesis and RNA synthesis. It does not affect normal cells because it cannot diffuse through membranes that are impenetrable by ions (e.g., cell membrane).</p>

<p>Ghrelin is a peptide hormone that is produced by cells in the stomach, but is also found in other tissues and organs. It regulates appetite and plays a role in glucose metabolism and energy homeostasis. Ghrelin is synthesized as a preprohormone with a molecular weight of 3,500 daltons. The trifluoroacetate salt has been shown to be useful as a building block for complex compounds with properties such as high purity, excellent solubility, and good stability.</p>

<p>o-Phenanthroline monohydrochloride monohydrate is a ligand that is used in crystallography to study the crystal structure of metal ions. It has been shown to be an efficient catalyst for the ring-opening of chloroformates, and can also be used as an analytical reagent that is capable of detecting chlorine in organic compounds. The hydrate form of o-phenanthroline monohydrochloride has a molecular formula of C12H14ClN3O4·2H2O and a molecular weight of 392.7 g/mol.</p>

<p>Thiamine monophosphate chloride dihydrate is a form of the vitamin thiamine. It has been used in control analysis to measure the activity of enzymes that require thiamine as a cofactor, such as transketolase and pyruvate kinase. Thiamine monophosphate chloride dihydrate has also been studied in biochemical properties, where it was found that this compound can be cleaved by picolinic acid to form thiazole phosphate. The matrix effect is an important factor in polymerase chain reactions and has been shown to be dependent on the presence of dinucleotide phosphate. This compound is an essential component of energy metabolism and plays a role in protein synthesis. Thiamine monophosphate chloride dihydrate also has toxicological studies, including a model system using wild-type strains of yeast. These studies have shown that this compound leads to physiological effects such as inhibition of glycolysis and lactic acid production.</p>

<p>N-Ethyl-N-(2-hydroxy-3-sulfopropyl)-3,5-dimethylaniline (NAHSDMA) is a coumarin derivative that inhibits protein synthesis and necrotic cell death. NAHSDMA was found to inhibit the growth of colorectal adenocarcinoma cells in culture and has been shown to have anti-inflammatory properties. NAHSDMA binds to the amine group of monoamine neurotransmitters, which are vital for brain function. This drug also has antimicrobial properties, inhibiting bacterial growth by binding to the enzyme DNA gyrase and topoisomerase IV, which maintain the integrity of bacterial DNA. Linear calibration curves were obtained in human serum with an IC50 value of 0.87 μM. NAHSDMA was shown to be metabolized through hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes,</p>

<p>4-Bromoveratrole is a triphenylene with a molecular weight of 454.42 g/mol and a melting point of 90°C. It has been shown that this molecule binds to the receptor for acetylcholine, which is found in the central nervous system and on muscles. The binding of 4-bromoveratrole to this receptor leads to the release of chloride ions from the cell, which increases the activity of acetylcholine. The detection sensitivity of 4-bromoveratrole in solution was determined by adding malonic acid or hydrochloric acid, which led to an increase in fluorescence intensity. This molecule also has fatty acid and hydroxyl groups that have been shown to have anti-inflammatory properties.</p>

<p>Alkaloid with anti-tumoral activity</p>

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<p>Potassium citrate is a salt of potassium and citric acid. It is used as an antacid to help relieve the symptoms of heartburn, sour stomach, and acid indigestion. Potassium citrate can also be used as a supplement when the body does not produce enough of this chemical on its own. It is usually taken with calcium pantothenate to provide additional relief for people who have low levels of these chemicals in their urine. The phase transition temperature for potassium citrate is approximately 33°C (91°F).</p>

<p>CYP17 enzyme inhibitor</p>

<p>Dimethyl fumarate (DMF) is a drug that acts as a prodrug for the active metabolite monomethyl fumarate (MMF). It is used in the treatment of psoriasis and other skin diseases, including erythema nodosum leprosum. DMF has been shown to significantly up-regulate the expression of proliferating cell nuclear antigen (PCNA), which is a response element for pdgf-bb. DMF also has antioxidant properties, which may be due to its ability to inhibit reactive oxygen species production. This drug also inhibits the activity of certain enzymes and blocks drug transporters that are involved in bowel disease.</p>

<p>Glycocholic acid sodium salt monohydrate is a compound that is used in the production of pharmaceuticals, agrochemicals, and other organic chemicals. It is also used as an intermediate to produce carboxylic acids, amino acids, and other building blocks. Glycocholic acid sodium salt monohydrate is soluble in water and has a high boiling point. It can be used for reactions with alcohols and amines to form esters or amides respectively. This compound can be used as a reagent for the synthesis of peptides, proteins, carbohydrates, and nucleosides. Glycocholic acid sodium salt monohydrate has been shown to have anti-inflammatory properties by inhibiting prostaglandin biosynthesis.</p>

<p>S-(-)-Tolterodine d-tartrate is a fine chemical that belongs to the class of organic compounds. It has been used as a useful scaffold in the synthesis of various complex compounds, such as reaction components and speciality chemicals. In addition, S-(-)-Tolterodine d-tartrate has served as an intermediate for the synthesis of other chemicals.</p>

<p>Dimethyl-D-tartrate is an enolate that has been synthesized using a stereoselective and l-tartaric acid. It has been shown to be pharmacologically active in micelles, which may be due to its ability to inhibit the accumulation of D-serine in the brain. Dimethyl-D-tartrate’s pharmacokinetic profile is characterized by a rapid elimination half-life and high clearance rate, which may be due to its metabolism by carbon tetrachloride. Dimethyl-D-tartrate has also been shown to have a strong affinity for l-phenylalanine and micelles, suggesting that it may act as an inhibitor of the enzyme phenylalanine hydroxylase.</p>

<p>1-Pentanesulfonic acid sodium monohydydrate (1PS) is the sodium salt of 1-pentanesulfonic acid. It is used as a fluorescent probe for atropine, which is a drug that blocks nerve impulses to muscles and produces paralysis. The concentration of 1PS can be determined by measuring the fluorescence intensity. This method can be used in conjunction with plates or quantifying with a spectrophotometer. Acetonitrile and dilution are required to produce the solution for measurement, which may then be injected into a chromatographic column for separation. Optical absorbance measurements are used to detect the presence of 1PS in the eluant from the column. Recoveries of 100% were obtained using this method on atropine sulfate in acetonitrile solutions containing 1-pentanesulfonic acid sodium monohydydrate at concentrations ranging from 0.01 to 10 mg/mL.</p>

<p>Apelin-17 trifluoroacetate is a reaction component, reagent and useful scaffold for the synthesis of complex compounds. It is a high quality, research chemical that is used in the synthesis of fine chemicals. Apelin-17 trifluoroacetate has versatile building block and can be used as a useful intermediate or as a speciality chemical. It also has high reactivity and is soluble in organic solvents.</p>

<p>Estradiol 17-butyrate is a fine chemical that can be used as a versatile building block or in the synthesis of complex compounds. This product is a research chemical, but it can also be used as a reagent or a CAS No. 18069-79-9. It has many applications in the field of chemistry, including being useful as an intermediate in organic synthesis and as a reaction component. Estradiol 17-butyrate is also useful for use as a scaffold for the preparation of other chemicals with similar properties.</p>

<p>Phosphotungstic acid hydrate is a white, crystalline solid that belongs to the group of phosphotungstates. It is soluble in methanol and water and has a low vapor pressure. Phosphotungstic acid hydrate is stable at room temperature and below, but decomposes above 100°C. The reaction mechanism for phosphotungstic acid hydrate is the formation of an acid complex with a proton from water, which can be written as<br>PW6O14(OH)2 + H2O <br>PW6O14(OH)3H+ + OH-<br>This reaction solution is acidic, with a pH of 2 or less. Hydroxyl groups on the phosphotungstate react with hydrogen fluoride to form tungsten hexafluoride gas. Hydrogen bonding interactions between the hydroxyl groups in phosphotungstic acid hydrate are responsible for its structural analysis. Oxidation catalysts such as magnesium salt</p>

<p>Copper(II) chloride dihydrate (CuCl2·2H2O) is a copper compound that can be used as an antimicrobial agent. It has been shown to inhibit the growth of bacteria, yeast and fungi by inhibiting cell division at the G1/S phase boundary. Copper(II) chloride dihydrate has also been shown to inhibit cyclin D2 production in HL-60 cells and to cause coumarin derivatives to react with DNA, leading to its structural analysis. It is soluble in water but insoluble in organic solvents. When exposed to air, it reacts with water vapor to form copper chloride (CuCl). Copper(II) chloride dihydrate is acidic and can react with bases such as amines or ammonia; this reaction may result in drug interactions.</p>

<p>ACTH(1-39) trifluoroacetate is a synthetic form of ACTH that is used for the diagnosis of autoimmune diseases and bowel disease. It is also used to assess the function of the adrenal gland in cases of suspected Cushing's syndrome. The blood sampling procedure involves withdrawing a small amount of blood from the patient and adding ACTH(1-39) trifluoroacetate to it, which causes an increase in cortisol concentration. ACTH(1-39) trifluoroacetate binds to corticotropin receptors on cells in the body, causing them to release basic proteins that are responsible for inflammation. This drug may be a potential biomarker for metabolic disorders such as obesity. It has been shown to have anti-inflammatory properties and can be used as a nonsteroidal anti-inflammatory drug (NSAID).</p>

<p>Venlafaxine is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) that is used to treat depression. Venlafaxine inhibits the reuptake of serotonin and norepinephrine into the presynaptic neuron, increasing their availability in the synaptic cleft. Venlafaxine has been shown to be effective in treating major depressive disorder and other depressive disorders, such as dysthymia and post-partum depression. The antidepressant effects of venlafaxine are believed to be due to its ability to block the uptake of serotonin and norepinephrine in the brain, resulting in an increased concentration of these neurotransmitters. Venlafaxine is metabolized by CYP2D6, CYP3A4, CYP1A2 and CYP2C19 enzymes, which may result in drug interactions with other drugs metabolized by these enzymes. To control for this effect, venlafaxine blood</p>

<p>Ergotamine D-tartrate is a drug that belongs to the group of nonsteroidal anti-inflammatory drugs. It is used in the treatment of migraine and other headaches. Ergotamine D-tartrate inhibits the production of nitric oxide, which has been shown to be involved in the process of angiogenesis. This drug also has long-term efficacy for headaches and migraines, as well as an anti-migraine effect. Ergotamine D-tartrate binds to specific receptors on neurons called alpha2 adrenergic receptors, which are located on blood vessels in the brain and have been implicated in migraine pathophysiology. These receptors are not present on vessels elsewhere in the body, which makes ergotamine a more selective drug for migraine than other nonsteroidal anti-inflammatory drugs.</p>

<p>Enalaprilat is an angiotensin-converting enzyme (ACE) inhibitor that prevents the formation of angiotensin II, a potent vasoconstrictor. It is used to treat high blood pressure and congestive heart failure. Enalaprilat is metabolized to enalapril, which has been found to act as an active inhibitor of DNA polymerase. This drug is also capable of inhibiting the synthesis of other proteins, such as those involved in protein transport and cell wall biogenesis.</p>

<p>Glycidyl butyrate is a chemical compound that is structurally similar to acetic acid. It has been shown to have antimicrobial properties, inhibiting the growth of bacteria by binding to surface-exposed fatty acids and hydroxyl groups. Glycidyl butyrate can also inhibit the enzyme activity of bacterial esterases, which are responsible for hydrolyzing esters. This property prevents the breakdown of glycidol, which can have toxic effects in humans and animals. The antimicrobial activity of glycidyl butyrate has been shown in vitro on a number of bacterial strains, including Streptococcus pyogenes (Group A streptococci), Bacillus subtilis (a spore-forming bacterium), Escherichia coli (a Gram-negative bacterium), Pseudomonas aeruginosa (a Gram-negative bacterium) and Staphylococcus aureus (a Gram-positive bacterium).</p>

<p>Metamizol sodium monohydrate is a nonsteroidal anti-inflammatory drug that is used as an analgesic and antipyretic. Metamizol sodium monerate is metabolized in the liver via cytochrome P450 (CYP) to form metamizole. It has been shown to inhibit chemiluminescence of polycyclic aromatic hydrocarbons using a dipyrone-treated biological sample, and the rate constant for this inhibition has been determined by the use of a chemiluminescence method. An analytical method for metamizol sodium monohydrate has also been developed using polymerase chain reaction (PCR) amplification of DNA sequences from human squamous cells, which can be used for forensic purposes. Metamizol sodium monohydrate has shown anti-inflammatory activity against rat paw edema and carrageenan-induced inflammation in rats, but it can cause side effects such as dizziness, drowsiness, headache, nausea,</p>

<p>Neuropeptide W-23 (human) is an antibody that recognizes the neuropeptide receptor, specifically the Neuropeptide Y receptor 1. The antibody binds to the Npy1 receptor and inhibits its activity. Neuropeptide W-23 (human) can be used as a research tool in cell biology and pharmacology studies.</p>

<p>Loratadine N-oxide is an organic chemical compound that is used as a reagent, complex compound, and useful intermediate. It has CAS No. 165739-62-8 and a molar mass of 280.2 g/mol. The solid form is white to pale yellow in color. It can be used as a building block for other compounds or as a versatile building block for reactions such as the synthesis of pharmaceuticals, pesticides, agrochemicals, and polymers. Loratadine N-oxide is also used in research chemicals and speciality chemicals due to its wide range of applications in various industries.</p>

<p>rec beta-Defensin 2 (human) is a recombinant peptide, which is a human-derived antimicrobial protein. It is sourced through recombinant DNA technology, enabling the production of a synthetic version of the natural peptide found in epithelial cells. Its mode of action involves disrupting microbial cell membranes, leading to cell lysis, in addition to modulating the immune response by interacting with immune cells and enhancing the production of cytokines.</p>

<p>4-Hydroxymandelic acid monohydrate is a chiral, herbicidal compound synthesized from mandelic acid and formaldehyde. It is often used as a coating additive in the synthesis of elastomers. 4-Hydroxymandelic acid monohydrate has been shown to have an interaction with elastomers by changing the flow rate of the elastomer and its parameters. The enantiomer of this compound is 2-hydroxymandelic acid monohydrate.</p>

<p>N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate is a molecule that regulates transcriptional activity. It can be used to isolate regulatory genes from different organisms and identify the specific genes that regulate the expression of other genes. The algorithm for this process is a stepwise, stereoselective, aerobic search. This process starts with an algorithm that identifies the best possible match between the gene sequence and the database sequences. The algorithm then transfers to another stepwise and stereoselective search of the database until it finds a match. The process ends when there are no more matches in the database or when all possible combinations have been searched. N-Benzyl-2,4,6-triphenyl pyridinium tetrafluoroborate has been shown to activate Staphylococcus aureus at very low concentrations but does not cause activation of mammalian cells at these concentrations.</p>

<p>Non-peptide renin inhibitor; anti-hypertensive</p>

<p>Please enquire for more information about Biotinyl-(Cys1,Lys(biotinyl)18)-Calcitonin (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Thyroxine sodium pentahydrate is an organic chemical compound that belongs to the group of thyroxine compounds. It is a white, crystalline solid with a molecular formula of C5H11NNaO4S. L-Thyroxine sodium pentahydrate is used in research as a reagent, scaffold, and intermediate, and can be used as a building block for other chemicals. This chemical has many different uses because it is versatile and reacts easily with other compounds.</p>

<p>Please enquire for more information about rec IL-4 (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ammonium oxalate monohydrate is a white crystalline solid that has a molecular weight of 104.096 g/mol and a melting point of 129°C. Ammonium oxalate monohydrate is a salt formed by the reaction of ammonium with oxalic acid. It is used as an experimental model for wastewater treatment, where it is able to remove ammonium ions from wastewater. This material also reacts with sodium salts to form hydrogen bonding interactions, which can be measured using analytical methods such as X-ray diffraction or electrochemical impedance spectroscopy.</p>

<p>Sodium nitroprusside dihydrate is an oxygen transport agent that works by inhibiting the enzyme cyclase. This inhibits the production of tnf-α and other inflammatory mediators, which reduces inflammation and pain. Sodium nitroprusside dihydrate is used to lower blood pressure in emergency situations, such as shock. It has been shown to be effective for treating pulmonary hypertension, chronic obstructive pulmonary disease, and other conditions related to oxygen transport. Sodium nitroprusside dihydrate is a metastable molecule that can be converted into a stable form (sodium nitroprusside) by ester hydrochloride or fatty acid esters.</p>

<p>Treatment of trypanosomiasis in heamolytic stage</p>

<p>Calcium dobesilate is a calcium salt that emits chemiluminescence in the presence of an oxidant. It has been used as a treatment for hypercalcemia, which is caused by high levels of calcium in the blood, and to prevent skin cancer. The experimental model was conducted on human serum and showed that calcium dobesilate reduced the enzyme activities in serum samples by 30% after 15 minutes of incubation. This reduction was statistically significant when compared to untreated groups. Calcium dobesilate also inhibited the growth of skin cancer cells in a pharmacological agent-induced experimental model.</p>

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<p>Dimethyl(methylthio)sulfonium Tetrafluoroborate (DMTSBF) is a synthetic, activated, nucleophilic reagent that has the ability to cleave disulfide bonds in proteins. DMTSBF is used for the synthesis of fatty acids and other organic compounds. It can also be used as an analytical reagent for determining the blood group of proteins. The chloride ion is necessary for this reaction. DMTSBF reacts with a nucleophile (e.g., hydroxyl, amine, thiol) to form a new bond and release sodium carbonate and silver trifluoromethanesulfonate.</p>

<p>Atrial natriuretic factor (ANF) is a hormone that plays an important role in the regulation of sodium excretion and blood pressure. It binds to two different receptor sites, which are located on the cell membrane. The ANF-A receptor is found in the atria of the heart and the ANF-B receptor is found in the kidneys. ANF has been shown to increase water excretion from the kidneys and decrease blood pressure by increasing sodium excretion from the kidneys and decreasing salt retention. Atrial natriuretic factor (4-28) is a disulfide form of ANF that has a high affinity for its receptors. This agent can be labeled with a radioactive atom for use as an experimental tool for determining binding sites. Atrial natriuretic factor (4-28) can also be chemically conjugated with polymers, such as polyethylene glycol, to make it more water soluble and therefore more useful as a drug candidate.</p>

<p>Tris(trimethoxysilyl)propyl isocyanurate (TTIPi) is an efficient method for the synthesis of conjugates. TTIPi can be used to prepare a variety of conjugates, such as those containing biomolecules such as proteins, peptides, nucleotides, and small molecules. The resulting conjugates can be visualized by microscopy and analyzed using the Anova statistical package. TTIPi has been shown to form covalent bonds with DNA bases and other substrates. It has also been shown to form coordination bonds with ethylene oxide or tetraethyl silane which are worthwhile for dispersive polymerization in organic solvents. The mesoporous silica support used in this process has been shown to be acidic or basic depending on the pH of the solution. This versatile technique is useful for preparing a wide range of conjugates.</p>

<p>Azatryptophan hydrate is an organic compound that is a useful building block, reagent, and intermediate in the synthesis of many complex compounds. Azatryptophan hydrate is soluble in water and reacts readily with a variety of other compounds. It can be used as a starting material to prepare complex molecules such as heterocycles and natural products. Azatryptophan hydrate has been shown to have high purity and quality and is often used as a research chemical or speciality chemical for commercial purposes.</p>

<p>Chelating agent used to detect aqueous copper ions by electrochemiluminescence</p>

<p>Aqueous soluble oxidant</p>

<p>Chloroplatinic acid hexahydrate is a chemical compound that is used to synthesize other chemicals, such as pharmaceuticals. It has a melting point of 810 degrees Celsius and a boiling point of 927 degrees Celsius. Chloroplatinic acid hexahydrate is soluble in water and reacts with copper chloride to form chloroplatinic acid monohydrate. It can be converted to hydrogen bonding interactions by adding hydroxyl groups or molecules, and it has been shown to have magnetic resonance spectroscopy properties.</p>

<p>2,5-Diphenyl-3-(4-methoxyphenyl)pyronium tetrafluoroborate is a chemical compound that can be used as a reagent or building block for the synthesis of other chemical compounds. It is also useful for research and as a versatile building block in organic chemistry. 2,5-Diphenyl-3-(4-methoxyphenyl)pyronium tetrafluoroborate is classified as a speciality chemical product. This compound has CAS Number 2907-20-2 and a molecular weight of 244.12 g/mol.</p>

<p>Methyl homoveratrate is a synthetic compound that belongs to the group of anticancer agents. Methyl homoveratrate inhibits the topoisomerase II enzyme, which is involved in DNA replication and transcription. It has been shown to have an inhibitory effect on the growth of cancer cells in cell culture and animal experiments. Methyl homoveratrate is also able to induce apoptosis by inhibiting fatty acid synthase, which contributes to its anti-cancer activity.</p>

<p>Methyl 6-nitroveratrate is an organic compound that is used as a reagent in organic synthesis. It is synthesized by the conversion of methyl 3-nitrobenzoate, an ester of benzoic acid, to methyl 6-nitrobenzoate with nitrous acid. Methyl 6-nitroveratrate has been shown to be metabolically stable and can be used in biochemical studies. Methyl 6-nitroveratrate also has protonation properties that are complementary to acetylcholine, which may account for its use as a comparator in pharmacological experiments. The molecule was postulated to have a role in synopses, but this has not been proven.</p>

<p>Metoprolol tartrate impurity N is an impurity of metoprolol succinate and has been shown to have photocatalytic activity. Metoprolol tartrate impurity N has been found in commercially available pharmaceutical products. It has been validated by both phase chromatography and hydrophilic interaction chromatography, with the latter providing a more detailed separation of the compound's various reaction intermediates. Impurities such as metoprolol tartrate impurity N may be present in commercial products due to the use of pyridinium salt as a solvent in the manufacturing process. The enantiomeric purity of metoprolol tartrate impurity N was determined to be 99%.</p>

<p>Cyclopentadienyldicarbonyl(tetrahydrofuran)iron(II) tetrafluoroborate is a chemical that is used as a building block in research and speciality chemical synthesis. The compound has been shown to be versatile, with many possible reactions, including the formation of a complex. This compound can also be used as an intermediate for another chemical or as a scaffold for other compounds. Cyclopentadienyldicarbonyl(tetrahydrofuran)iron(II) tetrafluoroborate is a high quality reagent that can be used in reaction processes with low toxicity.</p>

<p>Sodium ammonium phosphate tetrahydrate is an inorganic compound that is a salt. It is used as a test compound to measure the inhibition of viral growth. The test compound binds to the virus and prevents it from binding to cells, thus inhibiting viral replication. Sodium ammonium phosphate tetrahydrate can also be used as a means of preventing cavities by lowering the pH level in the mouth and inhibiting bacterial growth. Selenium compounds have been shown to have antiviral properties when tested on the typhimurium virus. Selenium compounds are not active against herpes simplex virus, but protocatechuic acid has been shown to inhibit herpes simplex virus replication in vitro and in vivo. Protocatechuic acid has also been shown to inhibit fatty acid synthesis and chloride ion uptake into cells, which may be responsible for its anti-viral properties.</p>

<p>Eotaxin is a human basic protein that belongs to the eosinophil cationic protein family. It stimulates the growth of cells and promotes tissue repair. Eotaxin also has a role in the immune response, as it is able to bind to and activate macrophages, neutrophils, and lymphocytes. Eotaxin is found in increased concentrations in inflammatory bowel disease (IBD), where it may play a role in the recruitment of inflammatory cells. The signal peptide sequence of eotaxin is cleaved by signal peptidase I and II during transit through the Golgi apparatus, yielding an active form that can be processed into mature eotaxin by several proteases. This active form can be detected by polymerase chain reaction (PCR) amplification of DNA isolated from human peripheral blood leukocytes or colonic biopsies. Eotaxin has been shown to have anti-inflammatory effects on both healthy tissues and those with</p>

<p>2-(4-Aminophenoxy)acetic acid hydrate is a synthetic, chlorine atom, primary amino compound that has been used as a lysine analogue in the production of lysine-deficient media. It also has been shown to be an inhibitor of the uptake of L-lysine by rat liver cells. 2-(4-Aminophenoxy)acetic acid hydrate can also be used to synthesize conjugates with other compounds such as fluorescein and luciferin. This compound is acidic and can form hydrogen bonds with other molecules. 2-(4-Aminophenoxy)acetic acid hydrate has shown novartis in fluorescence techniques, which may be due to its ability to emit light when excited at specific wavelengths.</p>

<p>Ethyl 4-coumarate is a versatile building block that is used in the synthesis of complex compounds. It is a reagent and can be used as a speciality chemical or useful scaffold in research chemicals. This chemical has been found to be a useful building block for the production of high quality and useful intermediates. Ethyl 4-coumarate is also a reaction component and can be used in the synthesis of fine chemicals.</p>

<p>Citric acid monohydrate is an organic compound that is used in biochemical research. It can be converted to citrate, which is a potential drug for chronic coughs. It has been shown to bind to toll-like receptor 4 and 5 (TLR4 and TLR5), reducing the activation of these receptors. Citric acid monohydrate also has a high rate constant, which makes it a good candidate for use in control analysis. This compound has been shown to have disease-modifying properties by altering iron homeostasis and ameliorating symptoms of inflammatory bowel disease. Citric acid monohydrate is also used as an analytical reagent for benzalkonium chloride in water samples.</p>

<p>Apomorphine hydrochloride is the salt form of apomorphine, a morphine derivative D2 dopamine agonist. The high selectivity for D2, D3, D4 and D5 receptors makes apomorphine hydrochloride a possible drug candidate and it is in clinical trials for diagnosis and treatment of Parkinsons disease. Moreover, apomorphine and apomorphine hydrochloride have been investigated in diverse studies for treating movement disorders.</p>

<p>Serotonin 5-HT4 receptor agonist</p>

<p>Resveratrol is a polyphenol found in the skin of grapes and red wine. It has been shown to have anti-inflammatory activity and has been used as a drug for treatment of coronary heart diseases. Resveratrol also activates the protein kinase AMPK by binding to toll-like receptor, which is involved in energy metabolism and inflammatory responses. Resveratrol can inhibit neuronal death induced by pharmacological agents such as glutamate or beta-amyloid peptide through activation of Ca2+ channels. Resveratrol also prevents cell death caused by ryanodine receptor activation by drugs such as isoproterenol or doxorubicin.</p>

<p>Homoveratramide is a synthetic drug that is used as an antibacterial agent. It has a broad spectrum of activity against bacteria, fungi, and protozoa. Homoveratramide has been shown to be effective against both Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Homoveratramide inhibits the synthesis of DNA by binding to the enzyme ribonucleotide reductase. This produces a bacteriostatic effect on the cell by halting DNA replication and transcription.</p>

<p>Hexadentate chelator</p>

<p>Dual antagonist of histamine H1 receptors and platelet-activating factor</p>

<p>Ethyl Isobutyric acid is a fatty acid that is produced by the fermentation of sugars with yeast. It is an oily liquid, which has a fruity smell and is soluble in water. Ethyl Isobutyric acid has been found to be present in human urine and plasma as well as in animal tissues. The most common form of this acid is ethyl iso-butyrate, which can be found in the diethyl succinate molecule. This compound can be used to synthesize other organic compounds such as caproic acid, malic acid, and diethyl succinate. These molecules have been shown to have many beneficial effects on humans and animals.</p>

<p>Sulfobromophthalein disodium salt hydrate is a fluorescent chemical that is used as a marker for renal function. It is most commonly used to assess the function of proximal tubules in the kidney and to assess the presence of cancer cells in various tissues. The uptake of sulfobromophthalein by the renal proximal tubules can be measured with an assay involving caco-2 cells. Multidrug resistance-associated protein (MRP) and other efflux pumps are expressed in these cells, which limits the amount of drug that can be absorbed into the cell. MRP also plays a role in multidrug resistance by pumping drugs back out of cells into the extracellular fluid, preventing them from being reabsorbed into circulation. This causes higher concentrations of drugs to accumulate inside the cell, leading to apoptosis.<br>Sulfobromophthalein has been shown to attenuate cancer progression, as well as reduce multidrug resistance</p>

<p>Please enquire for more information about rec IL-2 (human) 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 rec PDGF BB (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ghrelin is a peptide hormone that regulates appetite and has been shown to have potent anti-cachectic effects in animal models. It is thought to be an important regulator of body weight, insulin resistance, and metabolism. Ghrelin is synthesized in the stomach and released into the bloodstream when the stomach is empty. Ghrelin binds to ghrelin receptors in the hypothalamus, which stimulate growth hormone release from the pituitary gland. This hormone also binds to other cells in the hypothalamus, such as neurons that produce orexin, which may account for its effects on sleep patterns. Ghrelin has been shown to inhibit tumor growth by suppressing angiogenesis and inducing apoptosis. The molecular weight of ghrelin is 3497 Da. The sequence of ghrelin consists of 28 amino acids: Gly-Ser-Ser(octanoyl)-Phe-Leu-Ser-Pro-Glu-His-Gln-Lys-Ala</p>

<p>Alkaloid with anti-tumoral activity</p>

<p>1,1'-Dioctadecyl-3,3,3',3'-tetramethylindodicarbocyanine perchlorate (DiI) is a useful scaffold for the synthesis of complex compounds. It is a high-quality research chemical that is used in the synthesis of speciality chemicals and fine chemicals. DiI reacts with diazonium salts to produce blue or red fluorescent compounds. This compound can be used as a reagent for the production of amino acids or amines. It also reacts with other organic compounds to form complexes. The CAS number for DiI is 127274-91-3.</p>

<p>Brimonidine L-tartrate is a cyclase inhibitor that blocks the enzyme cyclic guanosine monophosphate (cGMP) phosphodiesterase. It has been shown to be effective in vivo in humans and has been shown to inhibit the production of neurotrophic factors in human HL-60 cells. Brimonidine L-tartrate is also effective as an anti-inflammatory agent and has long-term efficacy when used as a control analysis. This drug significantly reduced the rate constant of the 2-adrenergic receptor, which may lead to decreased risk of heart disease.</p>

<p>3-Methyl-2-benzothiazolinone hydrazone hydrochloride monohydrate is a diazonium salt that inhibits the activity of tyrosinase. It is used in pharmaceutical preparations as an inhibitor molecule to treat skin cancer. This compound has been shown to inhibit the production of melanin, which protects cells from damage by ultraviolet (UV) radiation. 3-Methyl-2-benzothiazolinone hydrazone hydrochloride monohydrate binds to tyrosinase and prevents it from forming radicals, which are necessary for the formation of melanin. The inhibition of this enzyme results in skin that is less susceptible to UV radiation and therefore less likely to develop skin cancer.</p>

<p>Acridin-9-amine hemihydrate is an organic compound that belongs to the class of acridine dyes. It has an acetylcholine receptor blocking property and is used in the treatment of dyskinesia. Acridin-9-amine hemihydrate has been shown to be effective in animal models for Alzheimer's disease. The structure of this molecule consists of a dipole, which has two tautomers, one with a hydrogen atom on nitrogen and another without it. The tautomeric form without the hydrogen atom is more stable than the other form in acidic conditions, but both forms are present in neutral or basic conditions. Acridin-9-amine hemihydrate is also an antitumour agent with activity against breast cancer cells.</p>

<p>Muscarinic antagonist</p>

<p>Bisoprolol hemifumarate is a selective beta-1 receptor blocker that has been used in the treatment of high blood pressure, heart failure, and other cardiovascular diseases. It is a prodrug that undergoes enzymatic hydrolysis to bisoprolol in the liver. Bisoprolol hemifumarate has been shown to be effective as an adjunctive therapy for patients with bowel disease and cardiac effects such as lowering blood pressure levels. This drug also has a positive effect on the heart by increasing the levels of natriuretic peptides and decreasing the level of atrial fibrillation (AF). Bisoprolol hemifumarate can be detected in human serum or plasma samples through an analytical method involving liquid chromatography (LC) coupled with tandem mass spectrometry (MS/MS), which can then be analyzed by multivariate logistic regression to control for confounding factors such as age, gender, ethnicity, alcohol intake, and smoking status.</p>

<p>1-Fluoro-2,4,6-trimethylpyridinium tetrafluoroborate is a reactive compound that is used in the synthesis of organic compounds. It can be used as a precursor to introduce fluorine into organic molecules. This reagent may also be used in reductive eliminations and dehydrogenative coupling reactions. 1-Fluoro-2,4,6-trimethylpyridinium tetrafluoroborate is thermodynamically stable and can be stored at room temperature for long periods of time.</p>