Nitro

<p>3-Nitroisonicotinaldehyde is a kinase inhibitor that binds to the ATP binding site of receptor tyrosine kinases. It inhibits the activation of these receptors and prevents the phosphorylation of tyrosine residues on the receptor. 3-Nitroisonicotinaldehyde has been shown to inhibit VEGFR-2, ABCG2, and efflux in human cancer cells. This drug has been shown to inhibit tumor growth in mice by inhibiting angiogenesis, which is a process that involves the formation of new blood vessels from pre-existing ones. 3-Nitroisonicotinaldehyde also inhibits tumor growth by blocking the production of vascular endothelial growth factor (VEGF) from angiogenic cells.</p>

<p>4-Methyl-3-nitrophenyl isocyanate (4MPN) is a chiral diisocyanate that can be used as an activated diisocyanate. 4MPN is prepared by the carbonylation of 3-nitrobenzaldehyde and xylene with hydrogen chloride in the presence of a catalyst. Impurities, such as chlorides or sulfurs, can be detected using surface methodology techniques. The feedstock for this compound is usually xylene, which has a high boiling point. This product contains reactive functional groups that can be used to modify surfaces and create polyurethane products.</p>

<p>The heterocycle alpha-chloro-2-nitrobenzaldoxime is a functional group that can be oriented in two different ways. The diversity of the product arises from the fact that it is possible to create new functional groups by substitution on the benzene ring and on the nitrogen. Heterocyclization of alpha-chloro-2-nitrobenzaldoxime can be achieved by using other heterocycles such as isoxazoles, which are readily available in large quantities, as building blocks. This reaction can be catalyzed by reductive means with sodium borohydride and methanol.</p>

<p>1-(3-Carboxyphenyl)-2-nitroethene is a reagent, speciality chemical, and versatile building block that is used in the synthesis of other compounds. It is also a useful intermediate or scaffold in many chemical reactions. 1-(3-Carboxyphenyl)-2-nitroethene has a CAS number of 98-36-4 and can be used as a high quality research chemical.</p>

<p>Please enquire for more information about N-Hydroxy-2-nitro-benzamidine 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 5-Chloro-4-nitrothiophene-2-sulfonylchloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is a fluorescent marker that can be used in immunohistochemical staining. It binds to endogenous vasoactive intestinal peptide, calcitonin and other proteins in tissues and can be detected using immunostaining. Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is optimised for use as a substrate for neutral endopeptidase and metalloendopeptidase enzymes, which are responsible for the degradation of vasoactive intestinal peptide.</p>

<p>Please enquire for more information about 4-(2,4-Dinitrophenyl)butanoicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxy-6-nitronaphthalene is a colourless, crystalline solid that is soluble in water and polar organic solvents. It has been used as a coupling agent for chromium compounds, such as dichromates and chromates. 2-Hydroxy-6-nitronaphthalene can be diazotised to form an orange compound. This reaction occurs under acidic conditions, but the product is stable at alkaline pH levels. The product of this reaction is an asymmetric monoazo dye that has trivalent chromium atoms covalently bonded to it. Hydrogen atoms are present on the nitrogen atoms of the molecule. 2-Hydoxy-6-nitronaphthalene can also be used to produce sulfate esters, which are typically used in organic synthesis reactions involving sulfuric acid or hydrogen sulfate ion donors.</p>

<p>Please enquire for more information about Methyl 6-nitropyrido[1,2-a]benzimidazole-8-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Pentachloronitrobenzene is a chemical that belongs to the group of nitrobenzenes. It is used as a biochemical reagent in enzyme assays, including methyl transferase, matrix effect, and chinese herb. Pentachloronitrobenzene can be used to detect single nucleotide polymorphisms (SNPs) in genes. The compound is also used as an analytical method for measuring acute toxicities and enzyme activities. In addition, pentachloronitrobenzene has been shown to have antibacterial properties against a wild-type strain of Escherichia coli with fluorescence probe.</p>

<p>Ethyl 5-Nitroindole-2-Carboxylate is a precursor to the anti-HIV drug Delavirdine. It is synthesized by condensation of ethyl pyruvate and urea derivative in the presence of thionyl chloride. This compound can be used as an intermediate in the synthesis of other compounds such as ethyl ester and ethyl pyruvate. The chemical reaction is carried out at room temperature using a chlorinated solvent such as methylene chloride or chloroform. Ethyl 5-nitroindole-2-carboxylate can also be used for the synthesis of other drugs, including antitumor agents.</p>

<p>4-Nitrophthalic acid is a white crystalline solid that has an acid and basic character. It has been shown to be antigenic, with a specific antibody able to bind to the 4-nitro group. The structure of 4-Nitrophthalic acid was determined using X-ray crystallography and NMR spectroscopy. The molecular weight of 4-Nitrophthalic acid is 177.2 g/mol, with a melting point of 174 °C and a boiling point of 341 °C. It is soluble in water and organic solvents such as ethanol, acetone, chloroform, ethyl ether, benzene, hexane, dichloromethane and ethyl acetate.</p>

<p>1-(3,4-Methylenedioxyphenyl) 2-nitropropene (1-MPNP) is a phosphatase inhibitor that is active against gram-negative bacteria by inhibiting enterotoxins and chlamydia. 1-MPNP inhibits the activity of tyrosine phosphatases, which are enzymes that play a major role in bacterial virulence. 1-MPNP competitively inhibits the activity of tyrosine phosphatases and prevents them from catalyzing the hydrolysis of polyphosphate substrates. This inhibition leads to an accumulation of polyphosphates in the bacterial cell membrane, which disrupts its permeability and leads to cell death.</p>