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.

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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.

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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.

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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.

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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.

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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.

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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.

Zinc bromide dihydrate is a crystalline compound that is used as a catalyst for the conversion of metalloporphyrins to hydroporphyrins. This process is used in the production of vitamin B12. Zinc bromide dihydrate can also be used to inhibit the function of ion pumps, which are proteins that pump ions across membranes. The inhibition of these pumps may lead to a decrease in intracellular calcium levels and an increase in free radicals. Zinc bromide dihydrate has been shown to react with chlorophylls, vinylated heterostructures, and polyvinyl nonmetals. These reactions produce morphology changes in zinc bromide dihydrate crystals

(6R,7R)-3-[(4-Carbamoylpyridinio)methyl]-8-oxo-7-[2-(2-thienyl)acetylamino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrat e is an antimicrobial peptide that has been shown to have broad antimicrobial activity against a variety of bacteria, including methicillin resistant Staphylococcus aureus (MRSA), and many fungi and viruses. This peptide has also been shown to have antiinflammatory effects in mice with multiple sclerosis (MS). The mechanism for this effect is not known, but it may be due to the inhibition of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα).

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(-)-Diethyl-D-tartrate is an asymmetric synthesis of the thioether. It was synthesized from 1,4-dimethyl fumarate and diethyl ester in three steps. The first step involves the formation of the nitro compound by nitration of 1,4-dimethyl fumarate and then reduction to the corresponding alcohol with tetraisopropoxide. This alcohol undergoes a reaction with phosphorous acid to yield diethyl ester. In the final step, this diethyl ester reacts with alpha-tocopherol to form (-)-Diethyl-D-tartrate. (-)-Diethyl-D-tartrate has been shown to inhibit gastric acid secretion and reduce stomach ulcers in rats.

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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.

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3-Aminobenzamidinedihydrochloridehydrate is a serine protease inhibitor that has been shown to have high affinity for tumor cells. It is synthesized by the enzyme, thrombin, which is involved in blood clotting. 3-Aminobenzamidinedihydrochloridehydrate interacts with the protease activity of thrombin and prevents it from cleaving its substrate, thereby blocking the formation of fibrin clots. This inhibition of thrombin can lead to an increase in tumor cell proliferation, as well as an increase in antitumor activities.

Methyl Heptafluoroisobutyrate is a chemical compound that has an alkynyl group and a hydrocarbon group. It is produced by the reaction of silicon with ethylene oxide, followed by reaction of the product with chlorine gas. The methyl heptafluoroisobutyrate can be synthesized in a two-step process from methanol and chlorine. The first step is the synthesis of dichloromethane using methanol as a solvent and chlorination with chlorine gas. The second step is the addition of ethylene oxide to this product, followed by chlorination with chlorine gas. Methyl heptafluoroisobutyrate can also be made from fluorine in liquid hydrogen fluoride at low pressure and high temperature.

Ethyl 2-hydroxyvalerate is an organic compound that is a derivative of malic acid. It is used in the synthesis of fatty acids and ethyl esters, as well as in the production of amides. The compound has been shown to have a functional role in gabapentin metabolism by hydrolyzing it to form 2-hydroxygabapentin. The enzyme responsible for this reaction has been identified as citrate lyase, which also interacts with other compounds (e.g., citric acid) to regulate its activity. An experimental predictive model was developed using structural properties of the substrate and product, and validated using different chromatographic methods to generate a three-dimensional structure.

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Ochratoxin A is a mycotoxin that is found in cereals and cereal products. It can be detected by an analytical method that utilizes high performance liquid chromatography with fluorescence detection. Ochratoxin A has been implicated in the development of bowel diseases and has also been shown to inhibit catalase, peroxidase, and glucose-6-phosphate dehydrogenase activities. It also inhibits DNA polymerase, RNA polymerase, and mitochondrial enzymes involved in energy production. There is evidence that ochratoxin A may be genotoxic by inhibiting the repair of DNA damage caused by reactive oxygen species. The optimum concentration for ochratoxin A is between 0.1 and 1 micrograms per liter.br> Ochratoxin A is metabolized in plants via the phenylalanine pathway. This leads to increased levels of phenylalanine and p-hydroxybenzoic acid in the plant's tissues.br>

Strontium chloride hexahydrate is a chemical compound that belongs to the group of strontium compounds. It is used as an injection solution and reaction solution, and has been shown to have a beneficial effect on liver lesions in mice. Strontium chloride hexahydrate can be injected intravenously or intraperitoneally to treat patients with hypercalcemia or hypophosphatemia. This drug also has a toll-like receptor (TLR) agonistic effect, which may be due to its ability to stimulate the production of proinflammatory cytokines such as IL-1β, IL-6, IL-8, and TNF-α in macrophages. The optimum concentration for this drug is 1 mmol/L. Strontium chloride hexahydrate binds to plasma proteins through ionic interactions with chloride ions. This binding makes it difficult for the drug to pass through cell membranes, which limits its effectiveness.

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Please enquire for more information about 2-((e)-3-{5,5-dimethyl-3-[(e)-3-(1,3,3-trimethyl-1,3-dihydro-2h-benzo[g]indol-2-ylidene)-1-propenyl]-2-cyclohexen-1-ylidene}-1-prope nyl)-1,3,3-trimethyl-3h-benzo[g]indolium tetrafluoroborate including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Octanesulfonic acid sodium salt monohydrate is an animal drug that has been used for the long-term treatment of chronic exposure to animals. It can be used as a component of a chromatographic method for the analysis of dopamine in biological fluids. 1-Octanesulfonic acid sodium salt monohydrate has also been shown to have antipsychotic effects, which may be due to its ability to increase dopaminergic neurotransmission by inhibiting the reuptake of dopamine. This drug is not active against human cancer cells, but it does inhibit imatinib (the active form) and other tyrosine kinase inhibitors at micromolar concentrations, making it a potential candidate for use in pharmaceutical dosages as an adjunct therapy for chronic myeloid leukemia.

Estradiol is a form of the hormone estrogen that has been modified to be more lipophilic. It is used in combination with other drugs to treat menopausal symptoms and as an adjuvant for the treatment of breast cancer in women. Estradiol 17-valerate is also used in the treatment of schizophrenia, although not as often as estradiol valerate, because it has a shorter duration of action. The mechanism of action is thought to be due to its ability to increase the concentration of dopamine at nerve terminals by blocking reuptake or inhibiting its metabolism. This may result in relief from distal tubule dysfunction and an improvement in urinary tract symptoms associated with benign prostatic hypertrophy. There are many other possible mechanisms of action including the prevention of bone loss, increased bone age, and increased NMDA receptor binding potentials.

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Kisspeptin-54 is a mammalian peptide hormone that regulates the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus. Kisspeptin-54 has been shown to be potently immunogenic in humans and can be used as an antigen for the production of monoclonal antibodies. It is also a candidate drug for the treatment of obesity and may have neuroprotective effects. Kisspeptin-54 has been shown to reduce body mass index, which may be due to its ability to stimulate the immune system and promote antibody production against tumors. This peptide also has potent on-line binding properties that are useful in polymerase chain reactions.

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5-Amino-N-(3-amino-2,2-dimethyl-3-oxopropyl)-4-hydroxy-2-isopropyl-7-[4-methoxy-3-(3-methoxypropoxy)benzyl]-8-methylnonanamide fumar ate is a drug that inhibits the activity of angiotensin II, which is a hormone produced by the body. It is used as monotherapy for treatment of hypertension. 5AMINO has been shown to be effective in lowering blood pressure when administered alone and has been shown to be well tolerated. For this drug, the most frequently reported adverse reactions are nausea and dizziness. This drug should not be taken with other antihypertensive drugs or nonsteroidal antiinflammatory drugs such as ibuprofen (Motrin®). In addition, patients with diabetes should monitor their blood sugar levels carefully while taking this medication.

Tetramethylammonium fluoride tetrahydrate (TMF) is an ionic liquid that is a reaction product of tetraethylammonium and hydrochloric acid. TMF has been shown to react reversibly with water to produce aqueous hydrogen fluoride, which can be detected at low concentrations with a variety of analytical techniques such as gas chromatography. TMF has also been shown to have selectivities for the transport of silicon and calcium carbonate ions, which are useful in electrochemical studies. The activation energies for the reaction of TMF with water were determined by electrochemical studies to be around -0.4 eV.

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Polyethylene glycol monolaurate (PEGML) is a non-ionic surfactant that has been used in vitro to evaluate the effects of amines on cell viability. PEGML has been shown to be insoluble in water, but soluble in organic solvents and oils. PEGML is not cytotoxic at concentrations up to 100%. The correlation between the cytotoxicity of PEGML and the concentration of amines was evaluated by measuring the endpoint, irritancy, and sensitivity. The endpoints for this test are cell viabilities, which were determined using a MTT assay. Irritancy was assessed with an alamar blue assay, while sensitivity was determined by evaluating corneal epithelial cells for viability after exposure to different concentrations of PEGML.

1-Ethyl-3-methyl-imidazoliumtetrafluoroborate (EMIMBF) is an ionic liquid that has been shown to have a high solubility in water and organic solvents. The stability of EMIMBF has been shown to be greater than other ionic liquids and it is electrochemically inert. 1-Ethyl-3-methyl-imidazoliumtetrafluoroborate also has the ability to stimulate the production of growth factor β1, which promotes epidermal growth and wound healing. This compound is used in cosmetics as a solvent for polymers. It is also used as a component in mixtures with malonic acid and methylamine, which are used in the purification of human serum albumin.

Ferric chloride hexahydrate is a chemical compound that has the formula FeCl3·6H2O. It is composed of iron, chlorine, and water. Ferric chloride hexahydrate is used in wastewater treatment to remove organic compounds from the water. Ferric chloride hexahydrate reacts with sodium carbonate to form sodium citrate and ferrous chloride: FeCl3 + Na2CO3 → Fe(CO)2 + NaCl + 3H2O The reaction between ferric chloride hexahydrate and potassium dichromate produces the following products: FeCl3 + K2CrO4 → FeCrO4 + 2KCl In addition, ferric chloride hexahydrate can be used as an oxidizing agent in organic synthesis. The reaction mechanism for this process occurs when ferric chloride hexahydrate is mixed with a fatty acid such as octanoic acid: FeCl3 + C8H18

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ALPHA FACTOR SIGNALING PEPTIDE Yeast mating signaling pathway The life cycle of Saccharomyces cerevisiae, also known as the brewer’s and the baker’s yeast, is characterized by both haploid and diploid phases. Indeed, yeasts are organized in two haploid types, known as a and α cells (MATa and MATα), that can either proliferate individually, using mitosis, or fuse together to form MATa/MATα diploids. α factor - WHWLQLKPGQPMY peptide - CAS: 59401-28-4. Haploid, diploid cells For two haploid cells to mate, mating factors are needed. These pheromones induce G-Protein Coupled Receptor‘s (GPCR) conformational changes, which allow G-protein migration in the plasma membrane. GPCRs are present on both a and α yeast cells and turn into Guanine nucleotide Exchange Factors (GEF) upon G-protein release. The receptor’s « new activity » leads to guanosine diphosphate (GDP) exchange by guanosine triphosphate (GTP) on the G-protein, which will recruit STE 5 to allow Fus3 protein phosphorylation. Phosphate addition on Fus3 enables its fusion to the cell’s plasma membrane in order to activate formin proteins by phosphorylation. α factor - WHWLQLKPGQPMY peptide - CAS: 59401-28-4. Yeast mating signaling pathway Formin proteins being involved in the polymerization of microfilaments, their consequent growth within the cell will form shmoo projections to enable complete mating of MATa and MATα cells, towards MATa/MATα diploid cell that can undergo mitosis and meiosis to create new haploid spores. α factor - WHWLQLKPGQPMY - CAS: 59401-28-4. Yeast mating [CAS: 59401-28-4] α-factor pheromone - WHWLQLKPGQPMY To induce a yeast cells’ shmoo projection, WHWLQLKPGQPMY pheromone (or alpha mating factor) is produced by α yeast cells. This signaling peptide is part of the MFAL1_YEAST protein (UniProt: P01149) that excretes its active factor into the culture medium to act on the opposite mating type). α mating factor is a 13 residues peptide inducing the expression of necessary mating genes ( 200 genes - 3% of the yeast’s genome) to arrest yeast cell cycle in the G1 phase, while altering cell surface and nuclear determinants, towards MATa and MATα fusion. WHWLQLKPGQPMY interacts with its complementary pheromone, a-factor, which is a 12 residues peptide (YIIKGVFWDPAC) that is covalently attached to farnesyl to generate the appropriate response upon α pheromone activation. Alpha factor applications SB-PEPTIDE offers α mating factor WHWLQLKPGQPMY to study: Cell cycle Cellular morphology Transcriptional induction Signal transduction pathways

Quinoline N-Oxide Hydrate is a quinoline derivative with an intramolecular hydrogen bond. It has been synthesized to inhibit the enzyme, toxoplasma gondii, which is responsible for causing toxoplasmosis in humans and other animals. Quinoline N-Oxide Hydrate inhibits the enzyme by reacting with the hydroxyl group of one of its amino acids. Quinoline N-Oxide Hydrate also inhibits luminescence in Toxoplasma gondii cells and has an inhibitory effect on the growth of this parasite.

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Calcium nitrate tetrahydrate (CNT) is a calcium salt of nitric acid that has been used in the past to control insects. It is an oxidizing agent and is used as a fertilizer. CNT reacts with water to produce heat and water vapor, which can be used for heating or cooking. When heated, CNT decomposes into calcium nitrite and nitrogen dioxide. The structural analysis of CNT was carried out by X-ray diffraction and thermodynamic data were obtained by differential scanning calorimetry. The thermal expansion coefficient of CNT was determined by DTA experiments.