Organic Halides

Natriuretic factor is a peptide hormone that regulates blood pressure. This peptide is encoded by a gene located on chromosome 10 and is made up of 28 amino acids. Natriuretic factor binds to the membrane of mitochondria and zymogen granules, causing them to release their contents into the cytosol. The resulting increase in cytosolic volume causes an increased diastolic pressure, as well as an increased glomerular filtration rate and cardiac output. Natriuretic factors have also been shown to stimulate the production of natriuretic peptides, which are involved in water balance and electrolyte homeostasis.

Please enquire for more information about Ovalbumin (257-264) (chicken) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Amino-6-chloropyrimidin-4(3H)-one (ACPP) is a betaine that has been shown to exhibit potent activity against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA). It is a mesomeric molecule, which means that it can exist as two different tautomers. The frequency of the absorption bands in the FTIR spectra for ACPP are characteristic of the carbenes and ethanolamine tautomers. The presence of these tautomers may be due to stabilization from the nucleophilic character of the nitrogen atom in betaines. Betaines are also able to form polymersized chains by reacting with themselves or other molecules, such as ethanolamine.

5-Bromo-2-(methylthio)pyrimidine is a synthetic compound that has been used to synthesize palladium complexes. It can also be used in the synthesis of vitamin B1, which is an essential nutrient for humans and animals. 5-Bromo-2-(methylthio)pyrimidine binds with magnesium and reacts with sulfoxide, nucleophilic attack and electronegativity. 5-Bromo-2-(methylthio)pyrimidine is activated by 2-chlorobenzothiazole and hydrogen chloride, which leads to nucleophilic attack on the electrophilic carbon atom. This causes a displacement reaction with the elimination of chlorine gas and production of dihydro.

4,5-Dibromo-1,2,6,7-tertahydro-8H-indeno[5,4-b]furan-8-one is a chemical reagent that is used for the debromination of ethyl cyanoacetate. The nucleophilic nature of the hydroxyl group in the target compound makes it an efficient substrate for this reaction. This reagent can be used to synthesize ramelteon which is a drug approved by the U.S. Food and Drug Administration (FDA) for insomnia treatment. This high yield synthesis highlights 4,5-dibromo-1,2,6,7-tertahydro-8H-indeno[5,4b]furan-8one's usefulness as a debrominating agent.

H-Phe-AMC Trifluoroacetate salt is a synthetic, protease inhibitor that inhibits the activity of serine and cysteine proteases. It binds to the active site of these enzymes and blocks their function. H-Phe-AMC trifluoroacetate salt has been used in food chemistry to hydrolyze proteins, and can be used to measure enzyme activities. This product also has been shown to have biological functions such as the inhibition of molting, physiological function, and the prevention of carcinogenesis.

Please enquire for more information about (D-Trp8)-Somatostatin-14 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Iron(II) tetrafluoroborate is a green-yellow crystalline solid that is soluble in water. It has been shown to have structural and optical properties that are similar to those of ferric chloride, but with the advantage of being less toxic. Iron(II) tetrafluoroborate is used as a homogeneous catalyst for organic reactions such as the hydrogenation of nitroarenes and the reduction of ketones. The catalytic activity of Iron(II) tetrafluoroborate arises from its ability to form hydrogen bonding interactions with other molecules and ions in solution.
Iron(II) tetrafluoroborate undergoes a number of reactions with other compounds, including cleavage products such as hydrogen sulfate and nitrogen atoms, which may be due to its chelate ligand. In coordination chemistry, Iron(II) tetrafluoroborate can form coordination complexes by reacting with potassium dichromate or calcium carbonate. These complexes are

4-Iodo-1-methyl-1H-imidazole is a trifluoroethylamine that inhibits the activity of tyrosine kinases. It binds to the active site of tyrosine kinase and prevents the binding of ATP, preventing phosphorylation and activation of downstream substrates. 4-Iodo-1-methyl-1H-imidazole has been shown to inhibit the proliferation of tumor xenografts in mice, as well as inhibiting headgroup binding and cellular proliferation in vitro. This agent also has a nanomolar range and high selectivity for protein kinases, which may make it suitable for therapeutic purposes.

4-Bromo-2-nitro-1H-imidazole (4BNI) is a synthetic drug that is used in the treatment of cancer. 4BNI inhibits the synthesis of DNA, which leads to cell death by preventing the production of proteins vital for cell division. When 4BNI is taken up by cells it becomes activated and binds to DNA, inhibiting the synthesis of RNA and protein. This process eventually leads to apoptosis (cell death). 4BNI has been shown to be effective against tumors in mice, but has not yet been tested on humans. The uptake of 4BNI in tumor tissue can be visualized using hypoxia imaging techniques such as positron emission tomography or magnetic resonance imaging.

4-Fluoro-3-nitroaniline is a chemical that can be used for industrial preparation. It is an efficient method for the production of 4-fluoroaniline, which is used in the manufacture of dyes and pharmaceuticals. The chemical ionization technique has been shown to be a good way to determine the presence of 4-fluoro-3 nitroaniline in animals. It has also been found to be active against infections caused by bacteria such as Salmonella enterica, Escherichia coli, and Klebsiella pneumoniae. This chemical may have adverse effects on testicular function and hematocrit levels in animals.

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

Please enquire for more information about PAR-2 (1-6) (mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about pTH (7-84) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (3R)-3-[(tert-Butoxycarbonyl)amino]-4-(2,4-difluorophenyl)butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

(±)-DoiHydrochloride is a serotonergic drug that belongs to the group of serotonin reuptake inhibitors. It affects the serotonergic system by inhibiting serotonin reuptake, which leads to increased synaptic concentrations of serotonin. This in turn activates signal pathways and increases levels of dopamine, norepinephrine, and epinephrine. (±)-DoiHydrochloride has antioxidative properties and can be used for the treatment of chronic schizophrenia. It was shown to be effective in patients with atrial fibrillation who were not responding well to other treatments.

6-Bromoindazole is a hydrogen bond inhibitor that has potential neuroprotective effects. It inhibits the enzyme DNA Gyrase, which is necessary for bacterial replication, and has antibacterial properties. 6-Bromoindazole interacts with the receptor tyrosine kinase axitinib and inhibits its activity. This interaction may be responsible for its neuroprotective effects.

Please enquire for more information about Fluorescein-6-carbonyl-Leu-Glu(OMe)-His-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page

NFAT Inhibitor trifluoroacetate salt H-Met-Ala-Gly-Pro-His-Pro-Val-Ile-Val-Ile-Thr-Gly-Pro-His-Glu-Glu (NFAT) is an inhibitor drug that has been shown to inhibit the nuclear factor of activated T cells (NFAT). NFAT is a transcriptional regulator that controls the expression of inflammatory genes in macrophages and other cell types. NFAT inhibitors have been shown to be effective for treating bowel diseases, such as ulcerative colitis and Crohn's disease, by inhibiting the activation of macrophages. NFAT inhibitors are also used in vitro as a tool for studying cellular signaling pathways. The most common type of NFAT inhibitor is fluconazole, which blocks calcineurin activity and prevents the activation of NFAT. However, other types of inhibitors are being developed, including mmp9 activity or

3-Amino-4-hydroxybenzoic acid hydrochloride (3ABA) is a crystalline compound with a molecular formula of C6H5NO2. It is an acidic compound that is soluble in water and alcohol, but not in ether. 3ABA has been used as the starting material for the synthesis of many other organic compounds. It can be obtained by reacting phenol with chlorobenzoyl chloride to form the chlorobenzoate salt, which on hydrolysis yields 3ABA. This compound has also been used as a reagent for synthesizing carbon nanotubes. The crystal structure of 3ABA was determined using X-ray diffraction data from crystallographic studies, and it was found to have three independent molecules per unit cell. Diffraction indicated that each molecule is composed of two benzene rings joined by a single bond between carbon atoms 1 and 2 and another bond between carbon atoms 2 and 3.

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

Please enquire for more information about Amyloid b-Protein (6-20) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about pTH (28-48) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Trimethylsulfoxonium Bromide is a fungicide that inhibits the growth of fungal cells. It binds to the sterol biosynthesis pathway and disrupts the production of ergosterol, which is an essential component for fungal cell membranes. Trimethylsulfoxonium Bromide has been shown to be effective against chronic bronchitis and other pulmonary diseases. This drug also has a horticultural use as a plant growth regulator. The chemical formula for Trimethylsulfoxonium Bromide is C1-C4-haloalkyl, profile, tebuconazole, fluconazole, triethyl orthoformate, chronic bronchitis, carbonyl group, hydroxyl group, anti-fungal.

Please enquire for more information about S-(-)-Nicotine-delta1’-(5’)-iminium diperchlorate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Undecafluorohexanoic acid is a perfluoroalkyl carboxylic acid that has been shown to disrupt steroidogenesis in vitro. It may be able to inhibit the transport of cholesterol, fats, and other lipids in cells, which causes disruption in steroidogenesis. This compound also has anti-cancer properties due to its ability to induce apoptosis and arrest cancer cell proliferation. Undecafluorohexanoic acid may also have developmental effects on animals because it can bind to estrogen receptors and disrupt the normal process of estrogen-mediated signaling pathways.

Endogenous heptapetide which causes vasodilation and has anti-hypertensive properties.

2,3,5-Trichlorobenzaldehyde is a chemical compound that has been shown to have anticancer and apoptotic effects. It inhibits the growth of bacteria by chelating iron ions and inhibiting bacterial dna synthesis. 2,3,5-Trichlorobenzaldehyde has also been shown to inhibit the growth of cancer cells in culture in an experimental study. This chemical has been used as a substrate for nmr spectroscopy to study its functional groups and radical scavenging activities. 2,3,5-Trichlorobenzaldehyde can be synthesized from phenacyl chloride and benzaldehyde in the presence of hydrogen chloride gas. The carbonyl group in 2,3,5-trichlorobenzaldehyde may cause metabolic disorders such as diabetes mellitus or hyperglycemia.

Trityl chloride resin is a chemical compound that is used as a model system for the study of trifluoroacetic acid and its reactions. Trityl chloride resin is insoluble in water and has been used as a reaction solution for transfer reactions. It has been shown to be an effective ligand for many types of receptors, with binding constants ranging from 10 M-1 to 10 M-10. Trityl chloride resin can also be chiral, which means that it may exist in two forms that are mirror images of each other. The physiological effects of this compound are not well understood, but it has been shown to have an effect on coordination geometry.

3-(2-Fluoroethoxy)Propanenitrile is a chemical with toxic properties. It is classified as a fluoroacetic acid and has been used in the production of other chemicals. Fluoroacetic acid is toxic to humans, showing signs of skin irritation, respiratory tract irritation, and kidney damage. 3-(2-Fluoroethoxy)Propanenitrile is not found naturally and has been sponsored by many companies.

Triethyloxonium tetrafluoroborate is an antimicrobial agent that inhibits the transfer of electrons from one molecule to another. It has been shown to be effective against methicillin-resistant Staphylococcus aureus and Mycobacterium tuberculosis. Triethyloxonium tetrafluoroborate binds to the bacterial enzyme, Jak1, which is involved in the formation of cytokines and interleukins. This binding inhibits the production of these molecules, leading to cell death by apoptosis. The use of triethyloxonium tetrafluoroborate as a research tool has facilitated its discovery as a potential anti-inflammatory drug for autoimmune diseases such as type 1 diabetes mellitus and rheumatoid arthritis. Triethyloxonium tetrafluoroborate can be used to inhibit amide synthesis, which may have applications in the study of carbohydrate chemistry and nitrogen atoms in biological systems. This compound has also been used

2,3-Bis(bromomethyl)quinoxaline is a nitrogenous heterocyclic compound that has a coordination geometry of square planar. It has been used as an inhibitor for the protein p21 and the nucleophile in palladium complexes. 2,3-Bis(bromomethyl)quinoxaline is also a model system for studying reaction mechanisms and chemical structures. The electron density map of the compound was obtained by X-ray crystal structure analysis. The reaction mechanism of this molecule is proposed to be through a chelate ring cross-coupling process.