Heterocycles with Nitrogen (N)

<p>2-Cyano-3,4,5,6-tetrachloropyridine is a genotoxic compound that is used for the preparation of picolinic acid. It has been shown to induce DNA damage and cytotoxicity in vitro. The reaction products of this compound have also been found to be genotoxic in vitro and in vivo. This chemical has been shown to inhibit the growth of cells in culture as well as cause cell death by releasing hydrogen chloride gas. 2-Cyano-3,4,5,6-tetrachloropyridine is a potent mutagen and carcinogen that can be activated by fluorine or chlorine compounds. This chemical can also form chlorinated derivatives with chlorine. 2-Cyano-3,4,5,6-tetrachloropyridine reacts with phosphorus pentachloride to produce hydrogen chloride gas and other reaction products such as chloride (Cl) or sublimed (P</p>

<p>4,4'-Dithiopyridine is a reactive molecule that can be used in the synthesis of other organic compounds. It is a disulfide bond with a redox potential of -0.43 V, which makes it readily available for reaction. The structural analysis of 4,4'-dithiopyridine has been performed using NMR spectroscopy and gas chromatography/mass spectrometry (GC/MS). This compound is an inhibitor of sugar transport and can be used to study the p-nitrophenyl phosphate reductase enzyme in bacteria. The reaction product between 4,4'-dithiopyridine and NADPH cytochrome P450 produces the fluorescent molecule 2-aminopurine. This fluorescent molecule may be used as a probe to study transfer reactions in bacteria.</p>

<p>2,4-Diamino-5-nitropyrimidine is a synthetic molecule that belongs to the class of heterocyclic amines. It has been shown to be a potent antiproliferative agent and has been found to inhibit hepg2 cell growth in vitro. This compound was also found to inhibit cancer cells, including mcf-7. 2,4-Diamino-5-nitropyrimidine binds nucleophilic sites on proteins and inhibits enzymes involved in DNA synthesis. The inhibition of these enzymes leads to cell death by preventing the production of new proteins needed for cell division.</p>

<p>BQ-610 is a novel peptide that has been shown to reduce the severity of mucosal inflammation in animal models of inflammatory bowel disease. It functions by binding to myofibroblasts, which are cells that produce an extracellular matrix and collagen. BQ-610 also blocks signalling pathways that are responsible for the production of TNF-α, MMP-2, and other molecules involved in the pathogenesis of inflammatory bowel disease. BQ-610 is effective at reducing inflammation in animal models of colitis, but not in human colonic epithelial cells or human colonic tissue.</p>

<p>Please enquire for more information about Octahydro-2,6-naphthyridin-1(2H)-one acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>This compound is an optical sensor that can be used to detect the presence of metal ions. It has a labile nature and is sensitive to light, which makes it ideal for use in fluorescence microscopy. 2-(Bromomethyl)pyridine hydrobromide has been shown to bind to nitric oxide and produce a strong fluorescent signal when exposed to copper ions. This probe can also be used as a molecular model for studying the interaction of metal ions with other molecules.</p>

<p>Please enquire for more information about 1-Benzyl-4-((tert-butoxycarbonyl)amino)piperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Hydroxypiperidine is a molecule with a carbonyl group. It is the most active and selective CCR5 receptor antagonist that has been studied to date. 4-Hydroxypiperidine inhibits HIV infection by preventing the binding of HIV to its receptor on the surface of white blood cells, thereby preventing it from entering these cells. 4-Hydroxypiperidine also acts as an anti-inflammatory agent in chronic bronchitis patients, due to its ability to inhibit prostaglandin synthesis. The chemical ionization mass spectra of this molecule show peaks for methyl ethyl, malic acid, and hydroxyl groups. These properties make 4-hydroxypiperidine a useful candidate for drug development against inflammatory diseases and several cancers.</p>

<p>4-Amino-3,5,6-trichloropyridine-2-carboxylic acid (4ATC) is a herbicide that inhibits the activity of pyridoxal phosphate (PLP)-dependent enzymes. 4ATC has been shown to be more toxic to plants than temozolomide and is used in vitro to study the effects of herbicides on cells. It inhibits cell growth and induces apoptosis in human cancer cells. In addition, 4ATC has been shown to inhibit the enzyme activities of group P2 proteins and nucleic acid synthesis. 4ATC also inhibits protein synthesis by inhibiting RNA synthesis in eukaryotic cells. 4ATC is not active against bacteria or fungi.</p>

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<p>1-Dodecylpyridinium Chloride is a quaternary ammonium salt that is used as an antimicrobial agent in a variety of products, such as pharmaceuticals, cosmetics, and household products. It has been shown to be toxic to humans at doses above 0.5 mg/kg. At sublethal doses, 1-dodecylpyridinium chloride inhibits the growth of bacteria by binding to the cationic sites on their cell surfaces and preventing them from attaching to other cells or molecules in their environment. 1-Dodecylpyridinium chloride also binds to the enzyme p-nitrophenyl phosphate reductase, which is required for bacterial growth. This inhibition leads to cell death by preventing ATP production and protein synthesis.</p>

<p>2-Amino-6-chloropurine is a nucleophilic substituent that is used in the synthesis of 2-amino-6-chloropurine. It reacts with hydroxyl groups to form a palladium-catalyzed coupling reaction solution, which is then treated with hydrochloric acid and trifluoroacetic acid. The product is purified by crystallization and recrystallization. This compound has potent antitumor activity against carcinoma cell lines, but it has not been shown to have any effect against Mycobacterium tuberculosis.</p>

<p>2-Isobutyl-3-methoxypyrazine is a hydrophobic compound that is not soluble in water. It has a bound form and can be titrated with calorimetry. 2-Isobutyl-3-methoxypyrazine is synthesized by reacting 2,2,4-trimethylpentane with methoxyacetone in the presence of sodium methylate. The compound has been detected as an odorant in numerous plant species and is believed to play a role in plant physiology. 2-Isobutyl-3-methoxypyrazine has been shown to have potent antiviral activity against infectious diseases such as HIV, herpes simplex virus type 1 (HSV1), and varicella zoster virus (VZV). This specific antiviral activity may be due to its ability to bind fatty acids by hydrogen bonds, which may interfere with the synthesis of viral membranes.</p>

<p>3,5-Dimethyl-4H-1,2,4-triazol-4-amine is a crystalline compound with antiproliferative and anti-inflammatory properties. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not fully understood but may be due to inhibition of DNA synthesis or by inhibiting the activity of topoisomerase II. 3,5-Dimethyl-4H-1,2,4-triazol-4-amine can also act as an antioxidant by scavenging reactive oxygen species (ROS). 3,5-Dimethyl-4H-1,2,4-triazol-4-amine has been shown to have a low toxicity in animals and humans.</p>

<p>Please enquire for more information about Methyl 6-oxo-1,6-dihydropyridazine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Pyrimidine-carboxylic acid is a biologically active molecule that can be found in the human body. It is a derivative of pyrimidine, which belongs to the group of purines. 2-Pyrimidine-carboxylic acid has been shown to inhibit the nicotinic acetylcholine receptor and α7 nicotinic acetylcholine receptor, which are receptors for acetylcholine. This molecule also has antihypertensive activity and has been shown to have therapeutic effects in psychotic disorders. 2-Pyrimidine-carboxylic acid binds to picolinic acid, which is an important intermediate in the metabolism of tryptophan, and hydroxyl group, which is essential for many biological functions. It also reacts with copper ions and forms a complex that is x-ray crystal structure confirmed. This complex may be used as a herbicide resistance inducer or as a chemical species for receptor binding studies or chemical reactions.</p>

<p>3-Hydroxy-2-nitropyridine is a chemical compound that has been shown to be an inhibitor of nicotinic acetylcholine receptor. The compound has been found to have luminescence properties and can be used as a fluorescent probe in the study of molecular recognition processes. 3-Hydroxy-2-nitropyridine is also an effective antimicrobial agent and has been shown to have clinical potential for the treatment of neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and Huntington's disease. It binds to the nicotinic acetylcholine receptor by forming hydrogen bonds with functional groups on the receptor surface. This binding prevents the agonist from binding and activating the ion channel that leads to depolarization of nerve cells. 3-Hydroxy-2-nitropyridine also reacts with chloride ions in order to form hydrochloric acid, which then inhibits microbial growth by altering their cell membrane permeability. The reaction yield is determined</p>

<p>Pyridine-2-aldoxime is a chemical compound that is used as a pesticide. It is an inhibitor of acetylcholinesterase, and it can be toxic at low doses. Pyridine-2-aldoxime binds to the active site of acetylcholinesterase and prevents the breakdown of acetylcholine by this enzyme, leading to paralysis of the respiratory muscles. Pyridine-2-aldoxime has been shown to be effective against chronic oral exposure to sarin gas, with lethal dose (LD) values ranging from 0.5–1 mg/kg in rats.</p>

<p>4-[(4-Methylpiperazin-1-yl)methyl]benzoic acid is an organic compound. It is a white solid that is insoluble in water but soluble in organic solvents. The molecule has a molecular weight of 224.8 g/mol and contains a carbonyl group and amine functional groups. 4-[(4-Methylpiperazin-1-yl)methyl]benzoic acid can be prepared by the acylation of 4-(aminomethyl)-benzoic acid with imidazole hydrochloride in the presence of sodium carbonate as a base.</p>

<p>4,4'-Diamino-2,2'-bipyridine (DABP) is a redox-active compound that is synthesized to be used as a single-stranded DNA probe. It has been shown to have high affinity for nucleic acids and can be used in many applications including the detection of mutations in human ovarian carcinoma cells. DABP can also be used as a model protein for studying interactions with other biomolecules. The immobilization of DABP on an electrode surface allows for the study of its electrochemical properties. This includes the correlation between the redox potential and luminescence intensity and the dependence on pH or ionic strength. DABP can also be used to detect oxygen concentration or ATP levels in mitochondria through its ability to absorb light at wavelengths from 400 nm to 800 nm which is then converted into light at lower wavelengths by uv irradiation.</p>