Enzyme, Peptide and Protein Related Compounds

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Anti-fungal agent; 14α-sterol demethylase inhibitor

Dibenzoyl-L-tartaric acid monohydrate is a chiral molecule that can be found in nature. It is soluble in organic solvents, but insoluble in water. Dibenzoyl-L-tartaric acid monohydrate has an affinity for carboxylate ligands and absorbs at 360 nm. The optical rotation of this compound is +20° to -50°, depending on the concentration and pH of the solution. This molecule is a potential pollutant because it can be degraded by oxidation or photolysis, yielding environmentally hazardous compounds. Its conformation may be changed by light or heat and, as a result, its properties may also change.

1,5-Dibenzyl glutarate is a beta-lactamase inhibitor that binds to the active site of bacterial enzymes in order to inhibit their activity. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. 1,5-Dibenzyl glutarate also inhibits tumor tissue growth by binding to the antigen surface and inhibiting tumor cell proliferation. This drug has been found to be safe for long-term use and does not produce any significant side effects.

Please enquire for more information about rec PDGF AA (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Please enquire for more information about (+/-)-ortho-nicotine diperchlorate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Bismuth citrate is an antimicrobial agent that is used to treat helicobacter pylori infections. Bismuth citrate may be an alternative to clarithromycin and metronidazole for the treatment of antibiotic-resistant strains of helicobacter. It has been shown to improve duodenal ulcer healing and reduce the incidence of gastric ulcers in a group of patients with duodenal ulcer disease. This drug has also been shown to significantly reduce the incidence of gastric cancer in patients with Helicobacter pylori infection. Bismuth citrate is a polymeric compound that is thought to bind to the bacterial cell wall and inhibit its growth through inhibition of protein synthesis, but this mechanism is not well understood. Bismuth citrate has been used as an antacid for decades, but it does not have any anti-inflammatory properties and should not be used for this purpose.

Hemokinin 1 is a protein that is encoded by the NK1R gene. It has been shown to be associated with insulin resistance, inflammatory diseases, and pain control. Hemokinin 1 is also a potential treatment for viral infections such as HIV and hepatitis C. Hemokinin 1 interacts with nicotinic acetylcholine receptors (nAChRs) in the brain and blood vessels, which leads to an increase in blood pressure. This protein also interacts with hematopoietic cells, which may be responsible for its function as an antinociceptive agent. Hemokinin 1 has been implicated in autoimmune diseases such as arthritis and atrial fibrillation. This protein is expressed mainly in the brain, liver, heart, kidneys and spleen.

Please enquire for more information about Osteostatin (1-5) (human, bovine, dog, horse, mouse, rabbit, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about 5-(H-Gly-Pro-Gly-Pro-amido)-9-[di-(3-sulfonylpropyl)amino]-benzo[a]phenoxazonium perchlorate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about Neuromedin S (rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Hydrocortisone-17-butyrate is a drug used for the treatment of inflammatory bowel disease and other infectious diseases. It is used in combination with other drugs to treat skin lesions, such as those that may be caused by an infection. Hydrocortisone-17-butyrate has been shown to be effective in treating cutaneous lesions in patients who are immunocompetent. The drug has also been shown to have significant cytotoxicity against human colon cancer cells. Hydrocortisone-17-butyrate is metabolized by hydroxylation, which can lead to unwanted side effects.

Please enquire for more information about Boc-L-Ile-OH hemihydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate (CDTA) is a chelating agent that has been shown to be effective in the treatment of some cancers. CDTA has been shown to inhibit the growth of tumor cells by binding to lysine residues on histones and DNA and inhibiting their acetylation. CDTA also prevents the genotoxicity induced by irradiation. CDTA can be used as an adjuvant in cancer therapy due to its ability to inhibit histone deacetylase activity. Trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate is synthesized from two amino acids: lysine and glutamic acid. This molecule is a polymeric compound composed of cyclic molecules linked together through amide bonds. These polymers are linear chains of

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Potassium vinyltrifluoroborate is a salt that contains the inorganic anion potassium and the organic ligand vinyltrifluoroborate. It is used as an electrolyte in electrochemical cells, such as fuel cells, to increase power output by increasing the conductivity of the electrolyte. This compound has been shown to be effective against chronic kidney disease and infectious diseases such as HIV and malaria. Potassium vinyltrifluoroborate also has anti-cancer properties due to its ability to inhibit cellular proliferation and induce apoptosis in cancer cells. The mechanism of action of this drug is still unclear but may be due to its ability to inhibit proteases, such as ns3 protease found in human erythrocytes.

5-Acetamido-6-amino-3-methyluracil hydrate (AAU) is a drug that is used as an analytical reagent in the determination of caffeine, 5-hydroxytryptophan, and other compounds. It can be used to assess interactions between drugs and enzyme activities. AAU has been shown to be a suitable substrate for many enzymes, including alcohol dehydrogenase, acetylcholinesterase, catalase, and glucose oxidase. The sample preparation procedure is performed by dissolving the compound in water or ethanol. The sample is then filtered before it is analyzed using high performance liquid chromatography (HPLC). The chemical properties of AAU are such that it can be easily transported from one place to another without undergoing significant changes in physical properties. AAU has been shown to have no effect on biological samples when exposed to radiation. AAU has been widely studied for its use as a monoclon

Reversible inhibitor of histone deacetylases (HDAC) that causes histone hyperacetylation, changes in chromatin structure and in gene expression. Sodium butyrate was shown to induce apoptosis in adenoma and carcinoma cell lines as well as to stimulate neurogenesis following cerebral ischemic injury. Sodium butyrate is present in large bowel as naturally occurring fatty acid and a by-product of bacterial fermentation of dietary fibres.

Estradiol hemihydrate is a synthetic estrogen. It binds to estrogen receptors, causing the activation of DNA transcription and synthesis of messenger RNA. Estradiol hemihydrate has been used for the treatment of various symptoms, such as menopause, osteoporosis, breast cancer, and metabolic disorders. The drug is most often administered by injection or in a polymeric matrix that dissolves slowly in the mouth. The recommended dose is between 0.5mg and 1mg per day. Estradiol hemihydrate can be detected in plasma using an analytical method called liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Polyoxyethylene stearate is a surfactant that functions as an emulsifier, dispersing agent, and wetting agent. It is used in personal care products, pharmaceuticals, and medical devices. Polyoxyethylene stearate has been shown to be effective in the treatment of allergic symptoms and eye disorders caused by glycols. The analytical method for measuring this compound involves metal hydroxides such as copper(II) hydroxide. Polyoxyethylene stearate has also been shown to have anti-infective properties in wastewater treatment systems. This chemical has been found to be toxic when given orally or injected into laboratory animals; however, it does not cause irritation at low concentrations when applied to the skin.

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Apelin-12 is a peptide hormone that belongs to the group of apelin family. It is an endogenous agonist for the apelin receptor and has been shown to affect metabolic and cardiovascular regulation. Apelin-12 has been found to increase systolic blood pressure, which may be due to its ability to inhibit the synthesis of nitric oxide in the heart. It also exhibits anti-inflammatory properties, which have been shown in vivo using a model of colitis induced by dextran sulfate sodium (DSS). The biological properties of this hormone are not yet fully understood. However, it is known that it has effects on cardiac contractility and myocardial infarct size in vivo. Further investigation into this protein's role in inflammatory diseases and metabolic disorders may lead to new treatments for these conditions.

Please enquire for more information about (Phe13,Tyr19)-MCH (human, mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Trans-Resveratrol-3,4'-disulfate is a sulfate conjugate of resveratrol, which is a natural polyphenolic compound. It is commonly derived from the metabolic processes involving resveratrol, a compound found in the skin of grapes, berries, and peanuts. As a metabolite, it is typically produced in the liver through sulfation, mediated by sulfotransferase enzymes. This conversion enhances the solubility and stability of resveratrol, potentially increasing its bioavailability compared to its parent compound. The mode of action of trans-Resveratrol-3,4'-disulfate involves interactions with various cellular pathways. It is believed to exert its effects through modulation of oxidative stress, regulation of inflammation, and activation of sirtuins, which are proteins associated with aging and metabolic regulation. Trans-Resveratrol-3,4'-disulfate has been studied for its potential applications in disease prevention and therapy. It is of particular interest in the fields of oncology, cardiology, and neuroprotection due to its antioxidant properties and ability to influence cell signaling pathways. Ongoing research continues to explore its utility in extending healthspan, as well as its capacity to mitigate the effects of various chronic diseases.

ACTH is a polypeptide hormone that regulates the release of cortisol from the adrenal cortex. ACTH (18-39) is a fragment of ACTH which binds to the glucocorticoid receptor with high affinity. The carboxy terminal sequence of ACTH (18-39) is identical to that of human ACTH and can be used as an immunogen to produce monoclonal antibodies against ACTH. The monoclonal antibodies can then be used in prognostic studies for patients with congestive heart failure, diabetic neuropathy, or k562 cells. ACTH (18-39) has an optimum pH level of 7.0 and can bind to cellular receptors at physiological concentrations. It also has a molecular weight of 4,000 Daltons and is soluble in trifluoroacetic acid and hydrogen fluoride, but not in water or methanol.

Please enquire for more information about Methyl-2-isocyanoisobutyrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ammonium magnesium phosphate hexahydrate is a compound that has been used in the treatment of wastewater and as an adsorbent for air emissions. It is also used to inhibit bacterial growth due to its potent antibacterial activity. Ammonium magnesium phosphate hexahydrate is a white powder with a molecular weight of 288.3 grams per mole. It has a strong adsorption capacity and can be used to treat urinary infections in women. The inhibition study revealed that the reaction products are mainly composed of ammonium ions, magnesium ions, and phosphates. The activation energies for this reaction are high, which may be due to the relatively high affinity between ammonium ions and water molecules. The morphology of this compound is crystalline or granular in nature with some amorphous regions present on the surface.

N-(4-Azido-2-nitrophenyl)-2-aminoethylsulfonate, sodium salt, dihydrate (NENPS) is a transport inhibitor that is used to study the transport properties of cells. This compound is a stilbene derivative with a sulfonic acid group at the 4 position. NENPS binds to the subunit of ATP synthase, which is responsible for the transport of ions and sugar into the cell. It irreversibly inhibits ATP synthase by binding to cysteine residues on the enzyme's F1 subunit. NENPS also binds to calcium ions in the cell membrane, which may be due to its ability to form disulfide bonds and compete for uptake sites on red blood cells.

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Potassium trifluoro(trifluoromethyl)borate is a reagent that is used in organic synthesis. It is an organometallic compound that can be prepared by the reaction of potassium with hydrogen fluoride and trifluoromethyl boric acid. The reagent has been shown to be scalable and viable for use in organic synthesis.

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.

Fibrinopeptide B is a linear peptide that is found in the human fibrinogen molecule. It has been shown to be bioactive and can be used as a specific molecular marker for thrombus formation. Fibrinopeptide B has an optimal wavelength of 280 nm, and can be detected using phosphoric acid-based electrophoresis. The peptides are typically only 10 to 20 amino acids long, although the length varies depending on the protein they are derived from.

Abiraterone is a fine chemical that can be used as a building block in the synthesis of complex molecules. It is also used as a reagent and speciality chemical in research and development. Abiraterone is an important intermediate in organic synthesis because it is versatile, easy to handle and has high quality. This compound can be used as a reaction component or scaffold for the preparation of useful molecules.

Sulfathiazole sodium sesquihydrate is an antibacterial drug that is used to treat infections caused by Clostridium perfringens and other bacteria. Sulfathiazole sodium sesquihydrate works by inhibiting the synthesis of folic acid, which is needed for the production of bacterial proteins. This drug has been shown to be effective against mastitis in cows and sinusitis in humans. Sulfathiazole sodium sesquihydrate may also be used for the treatment of necropsy lesions in horses, as well as throat infections in humans. The onset of symptoms usually occurs after a few days or weeks, but can occur within hours. Symptoms include fever, headache, nausea, vomiting, diarrhea, abdominal pain, distal muscle weakness and respiratory distress. In some cases this drug can cause death due to neurological problems (distal myopathy).

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Magnesium aspartate dihydrate is a chemical compound that is used to treat high blood pressure and heart disease. It is a salt of magnesium and L-aspartic acid, which are both active substances in the drug. Magnesium aspartate dihydrate has been shown to have a treatment effect on elevated levels of c-reactive protein (CRP) in men with normal kidney function. The drug has also been shown to be effective for the treatment of cavity, although it does not work for everyone. Magnesium aspartate dihydrate is chemically stable and can be used for diagnosis of magnesium deficiency, but it should not be given to women who are pregnant or breast-feeding. This drug may also inhibit the action of proton pumps, which are found in the body's cells that produce stomach acid.