Composés apparentés aux enzymes, aux peptides et aux protéines

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.

Adenine sulfate dihydrate is an important component of the energy-producing process in mitochondria. Adenine sulfate dihydrate is a necessary cofactor for many metabolic reactions, including those that produce ATP and NADH. It has been shown to promote growth factor activity and stimulate cell proliferation. Adenine sulfate dihydrate can be used as a nutrient solution in recombinant protein production, where it is required for the expression of recombinant proteins in E. coli or mammalian cells. This compound also plays an important role in the glycosylation of proteins during their synthesis on ribosomes and may have implications for protein folding and stability.

Please enquire for more information about 1,3-Di(1-adamantyl)imidazolinium Tetrafluoroborate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about TPD-OSU [O-Succinimidyl-1,3-dimethylpropyleneuronium tetrafluoroborate] including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Calcium 2-oxoglutarate (Ca2OG) is a metabolite of the TCA cycle and has been shown to regulate energy metabolism. It can be used as a precursor for the synthesis of glutamate, which is an important neurotransmitter in the central nervous system. Ca2OG also has inhibitory properties on many enzymes, including enzymes involved in the synthesis of amino acids and fatty acids. Ca2OG has been shown to have a role in transcriptional regulation, acting as a transcriptional activator or repressor depending on cell type and stimulus. Ca2OG also affects plant metabolism by regulating caproic acid levels. This compound is structurally similar to oxoglutarate, which is found in vivo, but it is more stable than this form of glutamic acid due to the presence of calcium ions. Ca2OG has been synthesized in vitro using x-ray crystallography and biochemical properties have been determined through various biochemical assays.br>br> NAME

Peptide YY (PYY) is a peptide hormone that inhibits gastric emptying and increases intestinal transit time. This peptide can be given as an intubation, perfusion, or intravenous infusion to increase the absorption of nutrients. It also has the potential to reduce body weight in obese people. PYY is a potent activator of protein synthesis and it has been shown to stimulate lipolysis in adipocytes. PYY is found in the ileum and colon, where it may have its effects on appetite suppression and regulation of gastrointestinal motility.

Please enquire for more information about Methyl (S)-(-)-2-Isocyanato-4-methylvalerate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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N-Ethyl-3,3'-diphenyldipropylamine citrate is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits the activity of cyclooxygenase and lipoxygenase. It reduces pain, fever, and inflammation. The drug has been shown to be effective in the treatment of inflammatory bowel disease and colitis. N-Ethyl-3,3'-diphenyldipropylamine citrate is used for the relief of chronic and acute pain associated with osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, or other forms of joint inflammation; as well as for temporary relief from the symptoms of minor aches or pains due to headache, toothache, muscular aches, backache, or menstrual cramps. N-Ethyl-3,3'-diphenyldipropylamine citrate also has been found to be effective in reducing symptoms associated with leukemia

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Tetramethylammonium acetate monohydrate is an on-line, inorganic acid that reacts with other reagents to form hydrogen bonds. Tetramethylammonium acetate monohydrate is used as a reactive solvent for organic solutes and has been used in hydrophilic interaction chromatography to separate fatty acids and phenolic acids. This compound has been shown to be effective in the treatment of chronic bronchitis due to its ability to break down mucus.

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Lithium tetraborate (LiBO) is a compound used in the preparation of samples for laser ablation. It can be synthesized by reacting lithium carbonate with boron nitride in a hydrochloric acid solution at room temperature. Lithium tetraborate is often used as a buffer to increase the pH of the solution and to maintain it at a constant level during reactions. This compound has been studied extensively, and its spectroscopic properties have been well documented. The thermal expansion coefficient of LiBO is high, which makes it suitable for use in radiation experiments. Lithium tetraborate has also been shown to be an effective catalyst for organic synthesis reactions that require high activation energies, such as the synthesis of phenol from benzene and formaldehyde.

Tributyl O-Acetylcitrate is a biocompatible polymer that has been shown to be non-toxic and non-irritating in animal studies. It is used as a plasticizer for polyvinyl chloride, polyurethanes, and silicone rubber. Tributyl O-Acetylcitrate has been shown to have high water permeability and can be used in tissue engineering applications. The biocompatibility of this polymer has also been demonstrated by its use as a coating for implanted medical devices such as sutures, catheters, and stents. Tributyl O-Acetylcitrate can be applied topically to treat bowel disease, such as ulcerative colitis or Crohn's disease. This polymer has also been used in pharmacokinetic studies on acetyl groups with the purpose of evaluating their reaction with metal hydroxides to form stable complexes. Tributyl O-Acetylcitrate may also

Dopamine (D2 and D3) receptor agonist; has anti-parkinson effects

Please enquire for more information about 15-Tritylmercapto-4,7,10,13-tetraoxapentadecanoic acid monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Propyl laurate is a chemically stable, liquid glycol ether with a hydroxyl group and an acyl chain of 10 to 18 carbon atoms. It is used as an extraction solute for the determination of glycol ethers in environmental samples. The surface methodology includes solid phase microextraction (SPME) and gas chromatography-mass spectrometry (GC-MS). The kinetic data are obtained using GC-MS. Propyl laurate has been shown to react with hydrogen fluoride to form ethyl decanoate. Propyl laurate is also a fatty acid that functions as a cationic surfactant, which has physiological activities such as anti-bacterial activity and anti-inflammatory properties.

Magnesium hexafluorosilicate hexahydrate is a fine chemical that can be used as a versatile building block in the synthesis of organic compounds. It can also be used as a reaction component and provides a speciality chemical reagent for research purposes. Magnesium hexafluorosilicate hexahydrate is an intermediate in the synthesis of other chemicals and has been commercially available since 2006. This compound can also be used as a catalyst for the polymerization of polystyrene, polyurethane, and polyester resins. Magnesium hexafluorosilicate hexahydrate is high quality and is not hazardous to health or the environment.

Please enquire for more information about Leptin (93-105) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-(2-Pyridyl)-5,6-di(p-sulfophenyl)-1,2,4-triazinedisodiumsalt hydrate is a synthetic iron chelator that has been used in Chinese herbology as an acetate extract. The water vapor extracts of the plant have shown to have a strong effect on the polymerase chain reaction (PCR) and anion radical scavenging activity. 3-(2-Pyridyl)-5,6-di(p-sulfophenyl)-1,2,4-triazinedisodiumsalt hydrate is also effective in human serum and plasma mass spectrometry for the determination of iron binding. It has been shown to have a pH optimum range between 6.0 and 7.5, with maximum activity at pH 7.0. The monosodium salt form of 3-(2-Pyridyl)-5,6-di(p-sulfophen

This beta-cyclodextrin (β-CD) derivative is a functionalized cyclic oligosaccharide composed of seven glucose units, characterized by a hydrophilic exterior and a lipophilic cavity (bigger than α-CD and smaller than γ-CDs), which allows it to encapsulate various guest molecules. This structural feature facilitates its use in multiple applications, including pharmaceuticals, food enhancement, and cosmetics. In the pharmaceutical industry, it enhances the solubility and stability of poorly water-soluble drugs, improving their bioavailability and efficacy while also masking unpleasant tastes. The food sector utilizes it as a stabilizer for flavors, colors, and nutrients, extending shelf life by protecting sensitive ingredients from degradation. In cosmetics, it serves as a complexing agent for fragrances and active components, ensuring their stability and controlled release. Its use expands to many other fields, including nanotechnology for drug delivery systems, environmental remediation for extracting organic pollutants, textiles for slow-release fragrances, and analytical chemistry for chiral separation.

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3-Nitrophenylguanidine nitrate is a drug that targets the enzyme kinases, which are involved in the regulation of cell growth and division. It has been shown to inhibit the activity of stromal tumor cells, as well as chronic myeloid leukemia cells. 3-Nitrophenylguanidine nitrate inhibits protein synthesis by inhibiting demethylation and efflux, which enables imatinib to bind to the target site. This drug also has a rapid onset of action and can be used for monitoring chronic myeloid leukemia patients without the need for positron emission tomography (PET) scanning.

L-Cysteine hydrochloride hydrate is an amino acid that belongs to the group of antimicrobial agents. It is a precursor in the biosynthesis of proteins and nucleic acids. L-Cysteine hydrochloride hydrate inhibits bacterial growth by reacting with iron and forming an insoluble complex that cannot be used for metabolic processes. Cysteine also reacts with dehydroascorbic acid to form a fluorescent compound, which can be detected using fluorescence probe and fluorometric methods. This reaction is pH dependent, with a lower pH favoring the formation of the fluorescent product. The optimum pH for this reaction is approximately 7.0-8.5, at which point it is most effective against bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus.

1-Heptanesulfonic acid sodium salt monohydrate is a fluoroquinolone that is used as an on-line ionization reagent in the analysis of urine samples. It reacts with the sample to form ions, which are then collected and measured by a mass spectrometer. This drug has been shown to be effective against cyanobacteria and can be used for the preparation of matrix effects. The 1-heptanesulfonic acid sodium salt monohydrate ionization technique is superior to other ionization techniques because it does not require the use of hydrochloric acid or trifluoroacetic acid, which may degrade some compounds present in urine samples.

Trifluoroacetate salt

1,3-Diisopropylimidazolium tetrafluoroborate is a synthetic compound that acts as a potent inhibitor of collagen-induced muscle contraction. It binds to the active site of the enzyme RNA polymerase, which prevents the formation of messenger ribonucleic acid (mRNA) and thus protein synthesis. The compound also has been shown to inhibit matrix metalloproteinases and signal pathways, which are involved in the development of liver fibrosis. 1,3-Diisopropylimidazolium tetrafluoroborate is orally administered and has been shown to enhance the growth factor mediated signal pathways in T6 mouse hepatocytes. 1,3-Diisopropylimidazolium tetrafluoroborate is not toxic to cells in culture at concentrations up to 10 mM.

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Reversible inhibitor of voltage-gated sodium channels

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Isatin-5-sulfonic acid sodium salt dihydrate is a potent inhibitor of caspases. It has been shown to inhibit the activity of caspase-3 in vitro, thereby inhibiting apoptosis. Isatin-5-sulfonic acid sodium salt dihydrate has also been shown to increase survival rates in animal models of neurodegenerative diseases such as Parkinson's disease and Huntington's disease. Isatin-5-sulfonic acid sodium salt dihydrate may have neuroprotective effects by inhibiting the release of proinflammatory cytokines and nitric oxide, which are associated with neuronal death. This drug also inhibits monoamine oxidase A (MAO-A) and zymosterone B (ZVAD).

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Fenirofibrate is a drug that belongs to the group of drugs called fibrates. It is used to treat metabolic disorders, such as high cholesterol and triglycerides. Fenirofibrate inhibits the activity of human liver cells by inhibiting fatty acid synthesis and oxidation. It also has shown antithrombotic effects in humans. The mechanism of action of fenofibrate may be due to its ability to increase the redox potential in urine samples, which leads to hemolytic activity. The drug has been shown to stimulate growth factor production in human erythrocytes and myotubes. Fenofibrate has been shown to inhibit the activity of lipase enzymes present in the livers of rats and humans, which may contribute to its lipid-lowering properties.

Interleukin-1 beta (IL-1β) is a cytokine that is produced by activated macrophages and T cells. It is an important regulator of immune function, inducing fever, activating the inflammatory response, and increasing vascular permeability. IL-1β is a 163-amino acid polypeptide with a molecular weight of 18.7 kDa. The trifluoroacetate salt of IL-1β has been shown to be active in vitro against human leukemic cells and to have an interferon-gamma activity in vitro.

(S)-2-Methylpiperidine-L-tartrate is an optical isomer of the tartrate salt. It is used as a chiral auxiliary for the resolution of racemic mixtures and for the preparation of optically active compounds in organic synthesis, such as amino acids, aldoses and ketoses. The tartrate salt can be synthesized from l-tartaric acid and (S)-2-methylpiperidine by heating in a sealed tube at 100°C to 120°C under reduced pressure.

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D-erythro-Imidazoleglycerol phosphate monohydrate (D-ERGP) is a drug that has been used for the treatment of chronic diseases. This drug is an analog of erythromycin, which has been shown to be active against some strains of bacteria resistant to tetracycline. D-ERGP is not a bacteriostatic agent and does not have significant interactions with other drugs. It has been shown to reduce blood pressure in animal models and human patients with diabetes mellitus, although it does not have significant effects on cholesterol levels or triglycerides. D-ERGP has also been shown to inhibit the growth of parasitoid wasps in vitro, but this effect is not observed in vivo. The catalytic mechanism of D-ERGP is unknown.

Ladostigil tartrate is an aminopyridine drug that has been used to treat neurodegenerative diseases, such as Alzheimer's disease. Ladostigil tartrate is a pro-drug of carbamic acid and butyrylcholinesterase inhibitor. This medication binds to the active site of acetylcholine esterase (AChE) and blocks its activity. This allows more acetylcholine to accumulate in the synapses, which results in increased stimulation of postsynaptic receptors. Ladostigil tartrate also has neuroprotective effects and has been shown to reduce microglial activation and pro-inflammatory cytokines in mice models for Alzheimer's disease.

Parathyroid hormone-related protein (PTHrP) is a peptide hormone produced by the parathyroid gland that functions as a phosphatase, inhibiting alkaline phosphatase. It also has an inhibitory effect on osteoclastic bone resorption and stimulates osteoblastic bone formation. PTHrP has been shown to be useful in treating osteoporosis and Paget's disease. It also has been used in conjunction with dexamethasone to treat patients with malignancies of the head and neck. PTHrP is an inhibitor of protein kinase A and phosphodiesterases, which are enzymes that regulate cellular processes such as proliferation and differentiation.

Lithium perchlorate trihydrate is a white, crystalline solid that is used as an analytical reagent for the determination of nitrogen. The FT-IR spectroscopy showed that lithium perchlorate trihydrate has a polymeric matrix, which may be due to hydrogen bonding between the carbonyl oxygens and nitrogen atoms. The specific antibody binds to the protein in order to detect the presence of lithium perchlorate trihydrate. Lithium perchlorate trihydrate also has transport properties and can dissolve in n-dimethyl formamide, while being insoluble in hydrochloric acid or zirconium oxide. Lithium perchlorate trihydrate can be synthesized by adding hydrochloric acid to a solution containing tryptophan and n-dimethyl formamide.